Ficha | A Simple Apparatus for Efficient and Reliable Mating of Gamet es from Ulva | Øivind Nordby | 19 | 63-64 | 1218 | no completo | Sin asignar | ||
Ficha | Diversity within red algal species : variation in world-wide samples of Spyridia lamentosa (Ceramiaceae) and periclados (Rhodomelaceae) using DNA markers and breeding Murrayella studies | ZUCCARELLO GIUSEPPE C. , BERNADETTE SANDERCOCK AND JOHN A. WEST | 0 | NO | Rodofitas | ||||
Ficha | MULTIPLE CRYPTIC SPECIES: MOLECULAR DIVERSITY AND REPRODUCTIVE ISOLATION IN THE BOSTRYCHIA RADICANS B. MORITZIANA COMPLEX (RHODOMELACEAE, RHODOPHYTA) WITH FOCUS ON NORTH AMERICAN ISOLATES | Zuccarello Giuseppe C. & John A. West | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Towards a medically approved technology for alginate-based microcapsules allowing long-term immunoisolated transplantation | ZIMMERMANN H. and et. al. | 16 | 491-501 | NO | parcialmente completo con liga | Feofita | The concept of encapsulated-cell therapy is very appealing, but in practice a great deal of | |
Ficha | Delineation of Chondrus (Gigartinales, Florideophyceae) in China and the origin of C. crispus inferred from molecular data | Zimin, Hu, and et. al. | 3 | 145 - 154 | NO | no completo | Rodofitas | Biogeography, Chondrus Stackhouse, internal transcribed spacer, phylogeny, taxonomy | Complete nuclear ribosomal DNA (nrDNA) internal transcribed spacer (ITS) sequences were obtained for 18 Chondrus populations collected at 15 sites from eight countries worldwide. Pairwise comparisons with the multiple alignment revealed that intraspeci |
Ficha | Study on the ecological safety of algacides: a comprehensive strategy for their screening | Zhou Lihong , Xuehao Chen & Tianling Zheng | 22 | 803–811 | NO | no completo | General | Algacide . Ecological safety. Ratio of efficiency to safety . Aquatic organism . Toxicity | The ecological safety of 14 algacidal materials were appraised using algal growth inhibition tests as well as toxicity test for zooplankton and fish and prawn juveniles. In addition, an integrative analysis for evaluating their pote |
Ficha | NHþ 4 enrichment and UV radiation interact to affect the photosynthesis and nitrogen uptake of Gracilaria lemaneiformis (Rhodophyta) | Zhiguang Xu, Kunshan Gao | 64 | 99-105 | No | no completo | General | Ammonia Gracilaria lemaneiformis Nitrogen uptake Phycoerythrin Photosynthesis UV radiation | Solar ultraviolet radiation (UVR, 280–400 nm) is known to inhibit the photosynthesis of macroalgae, (280–315 nm) significantly |
Ficha | Carpospore early development and callus-like tissue induction of Chrysymenia wrightii (Rhodymeniaceae, Rhodophyta) under laboratory conditions | Zhao Fengjuan and et. al. | 22 | 195–202 | NO | no completo | Rodofitas | Callus-like tissue . Carpospores. Chrysymenia wrightii . Development . Filamentous fronds. Rhodophyta | Morphological and culture studies of germlings derived from carpospores of Chrysymenia wrightii (Harvey) Yamada were carried out under various treatments combining temperature and irradiance. Basal, main, and |
Ficha | A Three-Gene Dinoflagellate Phylogeny Suggests Monophyly of Prorocentrales and a Basal Position for Amphidinium and Heterocapsa | Zhang Huan and et. al. | 65 | 463-474 | NO | parcialmente completo con liga | Fitoplancton | cob cox1 Cytochrome b Cytochrome c oxidase I Dinoflagellates Phylogeny rDNA | Many outstanding questions about dinoflagel- robust phylogeny. To do this, we generated a data set of cytochrome c o |
Ficha | Mariculture of economically important red seaweeds in Baja California, México. | Zertuche-Gonzales, J. A. | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Situación actual de la industria de macroalgas productoras ficocoloides en America Latina y el Caribe. | Zertuche Gonzalez, J. A. | 1 A 65 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Environmental impactsw of seaweed farming in the tropics | Zemke-White W.L. | NO | General | |||||
Ficha | World seaweed utilisation: An end-of-century summary | Zemke-White W. Lindsey & Masao Ohno | 11 | 369–376 | NO | parcialmente completo con liga | General | culture, harvest, seaweed, phycocolloid, alginate, carrageenan, food, fertiliser, world utilisation | The data for worldwide seaweed production for the years 1994/1995 are summarised. At least 221 species of seaweed were used, with145 species for food and 101 species for phycocolloid production. 2,005,459 t dry weight was produced, with 90% coming from |
Ficha | LISTA DE ESPECIES Y VARIACION ESTACIONAL DEL FITOBENTOS MARINO DE PLAYA GUARDALAVACA, CUBA | Zayas Carmen R. and et. al. | 23 | 81-84 | NO | no completo | General | lista de especies; variaciones estacionales: fitobentos; ASW, Cuba | Se presenta la lista de especies y variación estacional del fitobentos marino de Playa Guardalavaca. Se determinaron 76 |
Ficha | Gelidiaceae (Rhodophyta) in Bahia de Banderas, Western Pacific, Mexico. | Zaragoza, S. E., Vargas, D. R., & González, J. G. | 45 A 50 | 3793 | no completo | Sin asignar | We present the results of a fioristic study of intertidal species of Gelidiaceae collected in ten localities in the Bahía de Banderas region . The study area is within an extensive overlapping transitional zone between the tropical and subtropical regions | ||
Ficha | Economic marine algae of tropical south and east Asia and their utilization. | Zaneveld, J. S. | 3 | 1 A 55 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Phenology of Gigartina skottsbergii (Gigartinaceae, Rhodophyta) in Ancud Bay, southern Chile | Zamora Jaime P. & Renato Westermeier H | 253-258 | NO | Completo | Rodofitas | Gigartina skottsbergii, management, seasonal variation, seaweed | ||
Ficha | The Southern Australian Species of Laurencia (Ceramiales: Rhodophyta) | Yuzuru Saito and H. B. S. Womersley | 815-874 | 1356 | no completo | Sin asignar | Australia; Costa; L. aldingensis, L. shephevdii, L. bvandenii y L. tumida, L. arbuscula y L. tasmanica, | Species of Lauvencia along southern Australian coasts are common and often ecologically important. Sixteen species are recognized from this region, of which L. aldingensis, L. shephevdii, L. bvandenii and L. tumida are newly described. While most speci | |
Ficha | Keys to the Genera of Marine Algae of Taiwan | Young-Meng Chiang | 17 | ago-13 | 1350 | no completo | Sin asignar | Taiwan, China | The following keys were prepared for the use of the students in the National Taiwan University for the identification of marine algae of Taiwan. The genera cited here are only those reporte don Taiwan and its offshore islands, so that generic distinctions |
Ficha | A Proposal on the Classification of the Phaeophyta | Yositeru Nakamura | 147-155 | 3106 | no completo | Sin asignar | Phacosporeae y Cyelosporeae | This paper deals with a revision of subclasses in the Phacophyta and the establishment of a new order Ralfsiales. On the basis of the life historory, the Brown algae can be divided into two classes, Phacosporeae and Cyelosporeae. The former shows an alt | |
Ficha | Assessing the ecological status in the context of the European Water Framework Directive: Where do we go now? | Yorick Reyjol and et. al. | 332-344 | NO | no completo | General | Aquatic ecosystems Bioassessment Science-policy interface State-of-the-art WFD | The Water Framework Directive (WFD) is now well established as the key management imperative in river | |
Ficha | DEFINING THE MAJOR LINEAGES OF RED ALGAE (RHODOPHYTA) | Yoon Hwan Su and et. al. | 42 | 482–492 | NO | Completo | Rodofitas | Bangiophyceae; Compsopogonophyceae; Cyanidiophyceae; Florideophyceae; Porphyridiophycae; red algal lineages; Rhodellophyceae; Rhodophyta; Stylonematophyceae | Previous phylogenetic studies of the Rhodophyta have provided a framework for understanding red algal phylogeny, but there still exists the need for a comprehensive analysis using a broad sampling of tax |
Ficha | A single origin of the peridinin- and fucoxanthin containing plastids in dinoflagellates through tertiary endosymbiosis | Yoon Hwan Su and et. al. | NO | Fitoplancton | |||||
Ficha | Morphological homoplasy in Japanese Plocamium species Plocamiales, Rhodophyta) inferres from the Rubisco spacer sequence and intracellular acidity | Yano T. and et. al. | 43 | 383-393 | NO | Completo | Rodofitas | ||
Ficha | Ulva Lactuca (cholorophyta, ulvales) In Hong kong interdital waters-its nitrigen and phosphorus contents and ots use as a bioindicator of europhication | Y.B. Ho | 4 | 97-102 | No | no completo | General | ||
Ficha | Influence of alkali treatment on agar from Gracilaria cornea from Yucatan, ? Mexico | Y. Freile-Pelegrín & D. Robledo | 9 | 533–539 | no completo | General | Gracilaria cornea, agar, alkali treatment, composition, yield | The effect of alkali treatments on the yield, rheological and chemical properties of agar from Gracilaria cornea | |
Ficha | Cytological Observations on some Chlorococcoid Green Algae | Y. B. K. Chowdary | 23 | 233-238 | NO | parcialmente sin liga | Sin asignar | Kirchneriella e Hydrodictyon; fisiológico | Species of Characium, Kirchneriella and Hydrodictyon have been investigated cytologically and their chromosome numbers determined are as follows: Characium aungustum forma minor (11); Kirchneriella lunaris (18) and Hydrodictyon reticulatum (18). Their com |
Ficha | Effects of temperature and irradiance on early development of Chondrus ocellatus Holm (Gigartinaceae, Rhodophyta) | Xiao LI , ZHAO Peng , WANG Gaoge, LI Dapeng, WANG Jicheng, DUAN Delin | 28 | 508-513 | NO | Completo | Rodofitas | Chondrus ocellatus; temperature; irradiance; early development | Chondrus is a type of commercially produced red seaweed that widely used for food and carrageen extraction. Although the natural life history of the alga had been well understood, the factors influencing developme |
Ficha | Spatial distribution pattern analysis of subtidal macroalgae assemblages by a non-destructive rapid assessment method | Xabier Guinda, José Antonio Juanes, Araceli Puente, Beatriz Echavarri-Erasun | 34-43 | NO | Liga perdida | Sin asignar | Subtidal; Seaweed; Variability; Mapping; Monitoring, Management | The extensive field work carried out over the last century has allowed the worldwide description of general distribution patterns and specific composition of rocky intertidal communities. However, the information concerning subtidal communities on hard su | |
Ficha | Comparison of two methods for quality assessment of macroalgae assemblages, under different pollution types | Xabier Guinda, Jose ? Antonio Juanes, Araceli Puente, Jose ? Antonio Revilla | 743–753 | NO | Liga perdida | Sin asignar | Ecological status assessment; Indices and indicators; Macroalgae; Intertidal; Marine pollution; Water framework directive | The selection of adequate methodologies for the assessment of different biological quality elements is urgently needed for the application of the water framework directive (WFD 2000/60/EEC). In the case of macroalgae in coastal waters of the North East At | |
Ficha | Introduction to the Classification of Green Algae | Wysor Brian, Ph.D. | NO | Clorofita | |||||
Ficha | Introduction to Turf Algae | Wysor Brian | NO | parcialmente completo con liga | Feofita | ||||
Ficha | Prionitis pterocladina sp. nov.(Halymeniaceae, Rhodophyta), a newly recognized alga in the western Gulf of Mexico. | Wynne, M. J. | 36 | 535-544 | NO | parcialmente sin liga | Sin asignar | Prionitis pterocladina sp. nov. (Halyrneniaceae, Rhodophyta) is described from the western Gulf of Mexico, where its occurrence appears to be restricted to the lower eulittoral to upper sublittoral zone of the artificial jetties constructed of granitic bo | |
Ficha | Gelidium omanense sp. nov. (Gelidiaceae, Rhodophyta) from the sultanate of Oman | Wynne M.J. and D. Wilson F. | 47 | 64–72 | NO | parcialmente completo con liga | Rodofitas | Arabian Sea; Gelidium; Gelidium omanense sp. nov; Rhodophyta; Oman. | A new species of the red algal genus Gelidium, G. omanense M.J. Wynne, is described from the Sultanate of Oman, northern Arabian Sea. This species is a very commonly occurring eulittoral seaweed on the Omani coast,&nbs |
Ficha | Stage de biologie marine | WÜEST Jean & Frédéric SINNIGER | NO | parcialmente completo con liga | General | ||||
Ficha | High-quality RNA preparation for cDNA library construction of the Antarctic sea–ice alga Chlamydomonassp. ICE-L | Wu Guangting and et.al. | 22 | 778-783 | NO | no completo | Clorofita | Sea–ice alga . Chlamydomonas sp. ICE-L . RNA extraction . Lauryl sodium sulfate (SDS) . cDNA library construction | To study the molecular mechanism of the Antarctic |
Ficha | Native species behaviour mitigates the impact of habitat-forming invasive seaweed | Wright JeVrey T. and et. al. | 163 | 527–534 | NO | no completo | General | Ecosystem engineers · Hypoxia · Infauna · Marine algae · Soft-sediment ecology | Habitat-forming invasive species cause large, novel changes to the abiotic environment. These changes may elicit important behavioural esponses in native fauna, yet little is known about mechanisms driving this behaviour and h |
Ficha | Growth-forms in Non-geniculate Coralline Red Algae (Corallinales, Rhodophyta | Woelkerling Wm. J. and et. al. | NO | Rodofitas | |||||
Ficha | Biologie et phylogenie des algues | Woelkerling W.J. | 43 | 114 | NO | no completo | General | ||
Ficha | Marine Algae of Dominica | Wm. Randolph Taylor and Charles F. Rhyne | 3 | ene-16 | NO | parcialmente sin liga | Sin asignar | One hundred forty-one species of marine algae are reported from Dominica, W.I., with field notes. An ecological description of twelve collecting localities is given. A discussion of the differences between Agardhiella tenera (J. Agardh) Schmitz of the Wes | |
Ficha | Marine Algae of The Smithsonian-Bredin Expedition to Yucatán-1960 | Wm. Randolph Taylor | 22 | 34-44 | 1371 | no completo | Sin asignar | Quintana Roo, México. | A list of over 80 species of marine algae collected by the Fourth Smithsonian-Bredin Expedition of 1960 is given. These came from the territory of Quintana Roo on the east side of the peninsula of Yucatan, Mexico, and substantially add to the records of M |
Ficha | Marine Algae of the Smithsonian-Bredin Expedition to the Society and Tuamotu Islands | Wm. Randolph Taylor | 27 | 37-43 | 1380 | no completo | Sin asignar | Francia | Short lists of the marine algae collected by the Smithsonian-Bredin Expedition to the Society and Tuamotu Islands are given. A detailed discussion and description of Giffordia indica (Sond.) Papenf. & Chihara is given. |
Ficha | Instructions to Naturalists in the Armed Forces for Botanical Field Work | Wm. Randolph Taylor | mar-18 | 756 | no completo | Sin asignar | |||
Ficha | Notes on algae from the Tropical Atlantic Ocean—V | Wm. Randolph Taylor | 6 | 145-156 | NO | parcialmente sin liga | Sin asignar | Océano Atlántico tropical; Rhodoehaete parvula, Gymnogongrus minutus (Dorninica) y Gelidium nova-grana-tensis (Colombia) como nueva especie, Pterocladia bartlettii var. musciformis (Jamaica),Pocockiella y Stypopodium | A new record for Rhodoehaete parvula Thuret in the Western Hemisphere is provided (Jamaica). Three little components of the intertidal algal felt from West Indian and Central American rocks are discussed: Gymnogongrus minutus (Dorninica) and Gelidium nova |
Ficha | A taxonomic and nomenclatural reassessment of Tenarea, Titanoderma and Dermatolithon (Corallinaceae, Rhodophyta) based on studies of type and other critical specimens | Wm. J. Woelkerling, Yvonne M. Chamberlain And Paul C. Silva | 24 | 317-337 | 3349 | no completo | Sin asignar | Tenareal Dermatolithon | The taxonomy and nomenclature of genera of the Tenareal Dermatolithon complex has been reassessed on the basis of a study of generitype and other critical specimens. The type specimen of Millepora tortuosa Esper, which is the type of Tenarea Bory 1832, pr |
Ficha | A taxonomic reassessment of Lithothamnium (Corallinaceae, Rhodophyta) based on studies of R. A. Philippi's original collections | Wm. J. Woelkerling | 18 | 165-197 | 2277 | no completo | Sin asignar | Lithothamnium Philippi (Corallinaceae, Rhodophyta) | Critical studies of the original collections upon which Lithothamnium Philippi (Corallinaceae, Rhodophyta) is based have revealed that none of the five species included in the initial presentation conforms to any modern concept of the genus. Two species a |
Ficha | Growth-forms in Non-geniculate Coralline Red Algae (Corallinales, Rhodophyta) | Wm J. Woelkerling, LInda M. Irvine and Adele S. Harvey | 6 | 277-293 | NO | Liga perdida | Rodofitas | Although differences in growth-form have been widely used in delimiting taxa of non-geniculate coralline red algae (Corallinales, Rhodophyta), there has been no consistent application of the more than 100 terms employed to | |
Ficha | Sketch of the Character of The Marine Algal Vegetation of The Shores of The Gulf of Mexico | Wm . Randolph Taylor | 55 | ND | 3167 | no completo | Sin asignar | ||
Ficha | Research note: Characterization of a cDNA encoding glutamine synthetase II from Gelidium crinale (Rhodophyta) | Wilson Freshwater D. and et. al. | 50 | 17–21 | NO | no completo | Rodofitas | Gelidium crinale, glutamine syn- thetase, Rhodophyta, RT-PCR, 5?-RACE, 3?-RACE. | A cDNA encoding glutamine synthetase (GS) was characterized from the red alga, Gelidium crinale (Turner) Gaillon, using reverse-transcriptase polymerase chain reaction and the 5′- and 3′-rapid amplific |
Ficha | A multigene phylogeny of the Gelidiales including nuclear large-subunit rRNA sequence data | Wilson Freshwater D. & J. Craig Bailey | 10 | 229–236 | NO | Completo | Rodofitas | Gelidiales phylogeny, gene evolution, LSU, rbcL, SSU | Partial sequences (1032 bp) of the nuclear-encoded large ribosomal RNA gene (LSU) were determined for 16 gelidialean species, and analyzed separately and in combination with plastid rbcL and nuclear SSU gene sequences. |
Ficha | A gene phylogeny of the red algae (Rhodophyta) based on plastid rbcL | WILSON FRESHWATER D. and et. al. | 91 | 7281-7285 | NO | Completo | Rodofitas | A phylogeny for the Rhodophyta has been inferred by parsimony analysis of plastid rbcL sequences representing 81 species, 68 genera, 38 families, and 17 orders of red algae; rbcL encodes the large subunit of | |
Ficha | International Caulerpa taxifolia Conference Proceedings | Williams Erin and Edwin Grosholz | NO | Clorofita | |||||
Ficha | Circadian Activity Rhythm in the Horn Shark, Heterodontus Francisci: Effect of Light Intensity | William O. Finstad and Donald R. Nelson | 74 | 20-26 | NO | parcialmente sin liga | Sin asignar | isla de Santa Catalina, California. | Activity onsets of horn sharks, Heterodontus francisci, were studied in the natural environment at Santa Catalina Island, California. The mean of activity onsets of these nocturnal sharks occurred 76 min after sunset which corresponded to an approximate l |
Ficha | Studies on Philippine Chlorophyceae-II. Survey of Literature and List of Recorded Species | William J. Gilbert | 73-79 | NO | Liga perdida | Sin asignar | |||
Ficha | Pseudobryopsis oahuensis in Hawaii | WILLIAM J. GILBERT | 1 | 32-36 | NO | no completo | General | ||
Ficha | ·Contribution to the Marine Chlorophyta of Hawaii, II Additional Records' | WILLIAM J. GILBERT | 19 | 482-492 | NO | no completo | General | ||
Ficha | Structural, Chemical and Ecological Studies on Iridescence in Iridaea (Rhodophyta) | William H. Gerioick and Norma J. Lang | 13 | 121-127 | 1488 | no completo | Sin asignar | cuticle; Iridaea; iridescence; Rhodophyta | Transmission electron microscopy of the iridescent algae Iridaea flaccida (S&G) Silva, Iridaea cordata (Turn.) Bory var. cordata and I. Cordata var. splendens (S&G) Abbott reveals a multilaminated cuticle covering the thallus. Eperimental results show the |
Ficha | The National Academy of Science Committee on the Ecology of the Interoceanic Canal | William A. Newman | 2 | 247-260 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The Phytoplankton of the J. W. Frisz Memorial Lagoon, Shades State Park, Indiana | William A. Daily, Jack McCormick | 10 | ND | 42 | no completo | Sin asignar | ||
Ficha | First reports for the algae Borzia, Aulosira and Asterocytis in Indiana | William A. Daily | 6 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The presence of gigartinine in a New Zealand Gracilaria species | Wilcox Sarah J., Stephen J. Bloor, Jacqueline A. Hemmingson, Richard H. Furneaux & Wendy A. Nelson | 13 | 409–413 | NO | Completo | Rodofitas | gigartinine, chemotaxonomic marker, nitrogen pulse, Gracilaria, New Zealand | Gigartinine, 5-(3-amidinoureido)-2-aminovaleric acid, serves as a chemotaxonomic marker to distinguish two species of Gracilaria with very similar morphologies. Gigartinine was identified by 13C-NMR spectroscopy and amino a |
Ficha | Impact of algal research in aquaculture | Wikfors G.H. and M. Ohno | 37 | 968-974 | NO | no completo | Cultivo | cultivation; culture; human food; macroalgae; mariculture; microalgae; seaweeds | Algal aquaculture worldwide is estimated to be a $5–6 billion U.S. per year industry. The largest por- production for human food in Asia, with increasing |
Ficha | Algas marinas y su distribucion en balsas de cultivo (cuerdas y colectores) de Mytilus chilensis (Chloe, Chile). | Westermeier, H. | 13 | 1009-1026 | NO | parcialmente sin liga | Sin asignar | En tres mitiliculturas de la Isla de Chiloé (42 30' lat. S Y 73 45' Lon g . W), se llevaron a cabo estudios sobre la composición florística, biomasa y distribución en profundidad que las algas presentan en dos sustratos frecuentes en las balsas de cu! t | |
Ficha | A pilot-scale study of the vegetative propagation and suspended cultivation of the carrageenophyte alga in southern Chile | Westermeier Renato; David J. Patiño; Pedro Murúa; Juan C. Quintanilla; Juan Correa;Alejandro H. Buschmann & Ismael Barros | NO | Rodofitas | |||||
Ficha | Westermeier Renato; and et. al. | NO | Rodofitas | ||||||
Ficha | A new approach to kelp mariculture in Chile: production of free-floating sporophyte seedlings from gametophyte cultures of Lessonia trabeculata and Macrocystis pyrifera | Westermeier R. and et. al. | NO | Kelp | |||||
Ficha | Towards domestication of giant kelp (Macrocystis pyrifera) in Chile: selection of haploid parent genotypes, outbreeding, and heterosis | Westermeier R. and et. al. | NO | Kelp | |||||
Ficha | Macrocystis mariculture in Chile: growth performance of heterosis genotype constructs under field conditions | Westermeier R. and et. al. | NO | Kelp | |||||
Ficha | Biological basis for the management of Gigartina skottsbergii (Gigartinales, Rhodophyta) in southern Chile | Westermeier R. , A. Aguilar, J. Sigel, J. Quintanilla & J. Morales | 137–147 | NO | Completo | Rodofitas | Gigartina skottsbergii, population studies, demography | Environmental and biological parameters were analysed for populations of Gigartina skottsbergii (Setchell & Gardner) at Calbuco, Llanquihue Province (sheltered environment) and Ancud, Chiloe Province (exposed environmen | |
Ficha | Sexual compatibility and hybrid formation between the giant kelp species Macrocystis pyrifera and M. integrifolia (Laminariales, Phaeophyceae) in Chile | Westermeier R. and et. al. | 19 | 215-221 | NO | no completo | Kelp | Chile . conspecific . gametophytes. hybridization . interspecific . mariculture | Two species of giant kelp inhabit the coast |
Ficha | VARIACIÓN MENSUAL DE LOS CONTENIDOS ENÉRGETICOS, PORCENTAJE DE RENDIMIENTO DE CARRAGENANOS Y ANÁLISIS QUÍMICO DE LOS CARRAGENANOS EN LAS FASES DEL CICLO DE VIDA DE Chondrachantus chamissoi (C.Agardh) Kutzing,1843 (Rhodophyta,Gigartinales) EN COQUIMBO CHIL | WESTERMEIER H. RENATO | NO | Rodofitas | |||||
Ficha | ESTUDIOS EXPERIMENTALES EN EL CULTIVO DE Macrocystis pyrifera (L. C. AGARDH), A PARTIR DE GAMETOFITOS PROCEDENTES DE CUATRO LOCALIDADES DEL SUR DE CHILE ( X –XII REGIONES).” | Westermeier H. R. | NO | parcialmente completo con liga | Feofita | Macrocystis pyrifera L.C. Agardh, 1820, alga parda perteneciente al orden de las | |||
Ficha | Investigación y Desarrollo Tecnológico del Cultivo de Algas y su utilización por Invertebrados Herbívoros en Chile | Westermeier H Renato | NO | Cultivo | |||||
Ficha | The life history of Petrocelis franciscana | West, John A. | 7 | 299-308 | NO | Completo | Rodofitas | Tetraspores from Petrocelisfranciscana Setch. et Gardn. collected at Rockaway Beach, San Mateo County, California, 11 January 1971 were isolated into unialgal culture with Provasoli's enriched seawater medium at 1 | |
Ficha | The life history in culture of Petrocelis cruenta J. Agardh (Rhodophyta)from Ireland | West John A. ; Alan R. Polanshek; Michael D. Guiry | 12 | 45-53 | NO | Completo | Rodofitas | Tetraspores of Petrocelis cruenta J. Agardh from County Waterford, Ireland gave rise to foliose, dioecious gametophytes in culture. Carpospores from this foliose phase gave rise to Petrocelis-like crusts that have not repro | |
Ficha | Bacterial induction and inhibition of a fast necrotic response in Gracilaria conferta (Rhodophyta) | Weinberger Florian, Hans-Georg Hoppe & Michael Friedlander | 9 | 277–285 | NO | Completo | Rodofitas | cefotaxim, epiphytic bacteria, Gracilaria, seaweed-microbe interactions, seaweed pathology, Van- comycin | Of 45 bacterial isolates from healthy tips of Gracilaria conferta (Schousboe ex Montagne) J. et G. Feldmann, 29% were identified as 'conditional inducers' of an apical necrosis. That is, the isolates induced necrotic t |
Ficha | Endogenous and exogenous elicitors of a hypersensitive response in Gracilaria conferta (Rhodophyta) | Weinberger Florian & Michael Friedlander | 12 | 139–145 | NO | Completo | Rodofitas | cellulose, epiphytic bacteria, Gracilaria conferta, oligosaccharide, peptide, plant-pathogen interactions | Certain forms of oligocellulose and certain bacterially excreted peptides were identified as endogenous and exogenous elicitors, respectively, of a tip bleaching response in Gracilaria conferta (Schousboe ex Montagne) J. et G. Feldmann. The half-m |
Ficha | New Blennothrix-species (Cyanophyceae/Cyanobacteria) from Nepal. | Watanabe, M., & Komárek, J. | 15 | 67-79 | NO | parcialmente sin liga | Sin asignar | A new species of the cyanophyte/cyanobacterial genus Blennothrix (B. Ganeshii) from running water in the Kathmandu Valley, Nepal, is describe. The morphology of trichomes and filaments, type of filament branching, life cycleand the fine structure of cells | |
Ficha | Effect of blue light on indoor seedling culture of Saccharina japonica (Phaeophyta) | Wang Wen-Jun and et. al. | 22 | 737-744 | NO | no completo | Feofita | Chlorophyll fluorescence . Gametophyte . Photosynthesis. Sporophyte . Zoospore | Saccharina japonica is a brown alga that has |
Ficha | Early development patterns and morphogenesis of blades in four species of Porphyra (Bangiales, Rhodophyta) | Wang Jinfeng and et. al. | 22 | 297–303 | NO | Completo | Rodofitas | Blade . Development . Morphogenesis. Porphyra . Temperature | Pigment mutants were used as genetic markers to study the early development and morphogenesis of blades in four species of Porphyra. In Porphyra haitanensis, P. yezoensis, and P. oligospermatangia, the first |
Ficha | The Algal Ridges and Coral Reefs of St. Croix, their structure and Holocene development | Walter H. Ady | ND | NO | parcialmente sin liga | Sin asignar | St. Croix, EE. UU.; Lithophyllum congestum, Porolithon pachydermum, Neogoniolithon | The shallow coral reef and algal ridge systems on the eastern shelf of St . Croix are described and mapped in some detail. Based on present reef morphology, a section through the barrier reef in a ship channel, numerous sand probes and C 14 dating, Holoce | |
Ficha | Walter H. Adey, Philip A. Lebednik | NO | parcialmente sin liga | Sin asignar | |||||
Ficha | Studies on the biosystematics and ecology of the Epilithic Crustose Corallinaceae of the British Isles | Walter H. Adey & Patricia J. Adey | 8 | 343-407 | 1703 | no completo | Sin asignar | ||
Ficha | Quantitative study of sediment contribution by epiphytic coralline red algae in seagrass meadows in Shark Bay, Western Australia | Walker D.I. and Wm. J. Woelkerling | 43 | 71-77 | NO | Completo | Rodofitas | Calcium carbonate on leave and within leaf clusters of the seagrass Amphibolis antaretica, resulting from the growth of epiphytic coralline red algae, was used to calculate the rate of accumulation and rate of deposition of | |
Ficha | Growth rates and agar properties of three gracilarioids in suspended open-water cultivation in St. Helena Bay, South Africa | Wakibia J.G. , R.J. Anderson & D.W. Keats | 13 | 195–207 | NO | Completo | Rodofitas | Gracilariopsis sp., Gracilaria gracilis, growth, agar, yield, gel strength, dynamic gelling and melting temperatures, 3,6-anhydrogalactose, suspended cultivation | Relative growth rates (RGRs), yields and agar characteristics of three gracilarioid isolates (Gracilariopsis sp. from St. Helena Bay, and Gracilaria gracilis isolates from Langebaan Lagoon and Saldanha Bay) were measured to |
Ficha | Reseña geologica de la Cuenca de Lerma. | Waitz, P. | 58 | 123-138 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | STUDIES ON SELECTED CORALLINACEAE (RHODOPHYTA) AND OTHER ALGAE IN A DEFINED MARINE CULTURE MEDIUM | W. J. Woeljerling, Kenneth G. Spencer and John A. West | 67 | 61-77 | NO | Liga perdida | Rodofitas | A marine culture medium (MCM) has been developed and shown to have the unique ability to support the growth of several coralline algae. The results of experiments designed to determine the effects of varying certa | |
Ficha | Colonization, succession and growth rates of tropical crustose coralline algae (Rhodophyta, Cryptonemiales) | W. H. ADEY AND J. MICHAEL VASSAR | 14 | 55-69 | NO | no completo | General | ||
Ficha | Cell Shape and Wall Pattern in Relation to Cytoplasmic Organization in Pediastrum simplex | W. F. Millington and S. R. Gawlik | 62 | 824-832 | 1189 | no completo | Sin asignar | P. simplex, P. boryanum | P. simplex is a single-pronged, fenestrated species of Pediastrum. Comparison is made in regard to cell differentiation and structure with P. boryanum, a 2-pronged, unfenestrated species, with emphasis on the origin of cell wall pattern and the regulation |
Ficha | Hydrichthys Pietschi, New Species, (Coelenterata) Parasitic on the Fish, Ceratias Holboelli | W. E. Martin | 74 | 01-may | NO | parcialmente sin liga | Sin asignar | Hawaii; Hyclrichlhys pietsclii | A new hydroid, Hyclrichlhys pietsclii, was found on a myctophid fish, Ceratias holboelli Krøyer, collected off the leeward shore of Oahu, Hawaii. The basal plate of thehydroid erodes the pigmented epidermis and underlying tissues of the host. The literatu |
Ficha | Culture of marine algae using a re-circulating sea water system | W. E. Jones and E. S. Dent | 20 | 70-78 | NO | parcialmente sin liga | Sin asignar | Agua de mar en laboratorio; Prasinocladus marinus, Pringsheimiella scutata, Enteromorpha spp, | 1. A description is given of a re-circulating sea water system used to supply water for the culture of algae. Sea water is stored in two large storage tanks. From these, water is pumped to a header tank and then flows by gravity to experimental benches in |
Ficha | Fossil Arthropods of California | W. Dwight Pierce | 44 | 1361 | no completo | Sin asignar | |||
Ficha | Hannemania (Acarina: Trombiculidae ) and their Anuran Hosts at Fortynine Palms Oasis, Joshua Tree National Monument, California | W. Calvin Welbourn, Jr., and Richard B. Loomis | 74 | 15-19 | NO | parcialmente sin liga | Sin asignar | California; Hannemania hylae, Tree Frog Hyla cadaverina Cope y Hannemania bufonis Loomis y Welbourn | The larval stage of Hannemania hylae (Ewing) embeds in the California Tree Frog Hyla cadaverina Cope and Hannemania bufonis Loomis and Welbourn parasitizes the Red-Spotted Toad, Bufo punctatus Baird and Girard at Fortynine Palms Oasis, San Bernardino Coun |
Ficha | Preservation of Some Algal Cultures by Lyophilization | W. A. Daily - J. M. McGuire | 11 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Evolution, species and fossils: how does life evolve?. | Vrba, E. S. | 61 | 61-84 | 3870 | no completo | Sin asignar | ||
Ficha | Ectocarpaceen-Studien VII Giffordia | Von Paul Kuckuck | 8 | 119-152 | 3278 | no completo | Sin asignar | ||
Ficha | Ectocarpaceen-Studien VIII Einige Arten aus warmen Meeren | Von Paul Kuckuck | 361-382 | 3331 | no completo | Sin asignar | |||
Ficha | Die Algenbesiedlung der Unterweser unter Berückisichtingung ihrer Zuflüsse | Von Karl Behre | 2873 | no completo | Sin asignar | ||||
Ficha | Die Algenbesiedlung einiger Seen um Bremen und Bremerhaven | Von Karl Behre | NO | parcialmente sin liga | Sin asignar | ||||
Ficha | Zur Algen- unid Pilzflora des Liesingbaches | Von Bruno | ND | 73 | no completo | Sin asignar | |||
Ficha | Die Gattung Diplocbloris KORSIKOV - The genus Diplocbloris KORSIKOV | Von BOHUSLAV FOTT | 56 | 139-146 | NO | parcialmente sin liga | Sin asignar | Diplochloris, Chlorococcales, taxonomy, systematic revision, new species. | The genius Diplochloris was established by Korširov in 1939 from Ukraine. The type-species D. decussata was again found in Czecholovakia and the further data about its morphological variability are presented. Two new species from the centralEuropean water |
Ficha | NIVELES DE METALES PESADOS EN SEIS ESPECIES DE ALGAS MARINAS DE LA PENINSULA ANTARTICA | Vodopívez, Cristian and et. al. | 0 | NO | no completo | Fitoplancton | metales pesados, algas, Antártida | Seis especies de algas antárticas (rojas y pardas) fueron examinadas con el objeto de | |
Ficha | Chlamydomonas reinhardtii: a convenient model systemfor the study of DNA repair in photoautotrophic eukaryotes | Vlbek Daniel · Andrea Kevbovibová · Barbara Svieqená ·Elinka Gálová · Eva Miadoková | 1–22 | NO | no completo | Clorofita | DNA repair · Chlamydomonas reinhardtii · Repair pathways · DNA repair-cell-cycle regulation | The green alga Chlamydomonas reinhardtii is a convenient model organism for the study of basic biological processes, including DNA repair investigations. This review is focused on the studies of DNA repair pathways in C. reinhardtii. Emp | |
Ficha | The Biology of the Social Spider Anelosimus Eximius (Araneae: Theridiidae) | Vincent Brach | 74 | 37-41 | NO | parcialmente sin liga | Sin asignar | The social spider Anelosimus eximius has evolved advanced subsocial behavior which increases the efficiency of web construction, the capture of large prey, and defense. Colonies were observed in the field and in the laboratory. Communication between colon | |
Ficha | Phytoplankton functional groups and harmful algal species in antropologenically impacted waters of the NW Mediterranean Sea | Vila M. and M. Maso | NO | parcialmente completo con liga | Fitoplancton | ||||
Ficha | Adiciones al catálogo de algas marinas bentónicas para el Archipiélago Canario III. | Viera-Rodríguez, M. A., Audiffred, P. A. J., Gil-Rodríguez, M. C., Prudhomme van Reine, W. F., & Afonso-Carrillo, J. | 17 | 227-235 | 3886 | no completo | Sin asignar | Se amplia el catálogo de algas marinas bentónicas para el Archipiélago Canario en once especies; tres Phaeophyta: Cylindrocarpus berikeleyi (Greville) Crouan frat., Liebmannia Ieveillei J. Argard y Dictyota dichotoma (Hudson) Lamouroux, var. intricata (C. | |
Ficha | Comparison of simple techniques for estimating chlorophyll a concentration in the intertidal zone using high spectral-resolution field-spectrometer data | Véronique Carrère, Nicolas Spilmont, Dominique Davoult | 274 | 31-40 | NO | no completo | General | Chlorophyll a · Reflectance spectra · Microphytobenthos · Intertidal · English Channel | We compared 3 simple techniques for estimating the concentration of microphytoben- |
Ficha | Effect of Light on Motility, Life-Span, and Respiration of Bovine Spermatozoa | Vernon W. Proctor | 130 | 624 | NO | parcialmente sin liga | Sin asignar | Exposure to light of bovine spermatozoa suspended in various media results in a progressive decline in metabolic activity followed by the premature death of the cells. The inhibitory and spermicidal effects of visible light resemble a photodynamic action; | |
Ficha | Parasitic Relationship between Two Culturally Isolated and Unrelated Lichen Components | Vernon Ahmadjian and Elisabet Henriksson | 130 | 1251 | NO | parcialmente sin liga | Sin asignar | The presence of numerous haustoria, with accompanying death of the algas cells, was noted in a mixed cuture of the fungal symbiont (mycobiont) of Coliema tenax (Sw.) Ach., em . Degel. And Trebouxia impressa Ahm., the algal partner (phycobiont) of Physci | |
Ficha | The Lichen Association | Vernon Ahmadjian | 63 | 250-254 | 32 | no completo | Sin asignar | ||
Ficha | Some New and Interesting Species of Trebouxia, a Genus of Lichenized Algae | Vernon Ahmadjian | 47 | 677-683 | NO | parcialmente sin liga | Sin asignar | Phycobiont Trebouxia | Four species of the phycobiont Trebouxia, 3 of which are new, have been described in this paper. On the basis of this study, the algal genus has been divided into 2 main groups depending on the position that the chromatophore assumes during its bipartitio |
Ficha | Investigations on Lichen Synthesis | Vernon Ahmadjian | 49 | 277-283 | NO | parcialmente sin liga | Sin asignar | Separated fungal and algal components of the lichen, Acarospora fuscata (Nyl.) Arn., were recombined under controlled laboratory conditions to form structures comparable to those of the naturally occurring lichen thallus. The primary condition for this ar | |
Ficha | A Contribution toward Lichen Synthesis | Vernon Ahmadjian | 51 | 56-60 | 33 | no completo | Sin asignar | ||
Ficha | Seasonal variation of agar from Gracilaria vermiculophylla, effect of alkali treatment time, and stability of its Colagar | Vergara-Rodarte et. al. | 22 | 753–759 | NO | Completo | Rodofitas | Gracilaria . Agar. Seasonal variation . Gel strength . Storage . Baja California Sur | Gracilaria vermiculophylla, from Baja California Sur, Mexico, was studied in order to determine the seasonal variation of yield and quality of native and alkaline agar during 2007–2008. The highest alka |
Ficha | Mangrove Macroalgae in Southeastern Brazil: Spatial and Temporal Patterns | Verena R. Eston, Nair S. Yokoya, Mutue T. Fujii, M. Rosário A. Braga, Estela M. Plastino and Marilza Cordeiro-Marino | 51 | 829-837 | 2614 | no completo | Sin asignar | Mangrove macroalgae; macroalgal dominance patterns; spatial and temporal patterns; Latin American mangals. | To increase the limited ecological observations on mangrove rnacroalgae, seasonal changes and spatial differences of macroalgal abundance on pneumatophores, plantlets and branches of dwarf trees were analysed in mangrove areas bordering 2 rivers of IIha d |
Ficha | Gametophyte-sporophyte coalescence in populations of the intertidal carrageenophyte Mazzaella laminarioides (Rhodophyta) | Vera César , Paulina Lobos & Héctor Romo | 20 | 883–887 | NO | Completo | Rodofitas | Frond demography . Gametophyte-sporophyte fusion . Gigartinaceae . Intertidal seaweed | Mazzaella laminarioides has consistently been reported as a typical coalescent/clump species with a triphasic life history of the Polysiphonia-type in which the haploid gametophyte is the predominant phase wi |
Ficha | DINÁMICA DE POBLACIONES DE Macrocystis integrifolia BORY (LAMINARIALES, PHAEOPHYTA) EN EL NORTE DE CHILE | Vega Reyes Juan Manuel Alonso | NO | no completo | Feofita | El objetivo general de esta tesis fue el estudio de los efectos del evento El Niño y de | |||
Ficha | Local processes compound the latitudinal variability in the collapse and recovery of Chilean Macrocystis integrifolia populations (Laminariales, Phaeophyceae) following the 1997-1998 El Niño | Vega J. M.Alonso and et. al. | 0 | NO | no completo | Feofita | An integrated synchronic study was made on the interactive effects of the El Niño Southern | ||
Ficha | Seasonal and Spatial Monitoring of Productivity and of Reproduction of Chondrus canaliculatus (Gigartinales, Rhodophyta) from Chile | Vega J. M. A. and I. Meneses | 44 | 571-581 | NO | Completo | Rodofitas | Chondrus canaliculatus (C. Agardh) Greville used to cover extensive areas at Puerto Aldea 308169 S, 718309 W), Tongoy Bay, Chile. The exploitation of this commercially-valuable alga without knowledge of its produc | |
Ficha | CULTIVO COMERCIAL DE MACROCYSTIS sp. EN MAR SISTEMA SUSPENDIDO”, CALETA FLAMENCO, COMUNA DE CHAÑARAL | Vecchiola Trabucco Rinaldo Mario | NO | Cultivo | |||||
Ficha | Long term variability in the structure of kelp communities in northern Chile and the 1997–98 ENSO | Vásquez, J. A., Vega, J. A., & Buschmann, A. H. | 505–519 | NO | Liga perdida | Kelp | |||
Ficha | Distributional patterns and diets of four species of sea urchins in giant kelp forest (Macrocystis pyrifera) of Puerto Toro, Navarino Island, Chile. | Vásquez, J. A., Castilla, J. C., & Santelices, B. | 19 | 55-63 | 3859 | no completo | Sin asignar | The distribution pattern of microhabitat and diet was studied in 4 species of sea urchins (Loxechinus albus, Pseudechinus magellanicus, Arbacia dufresnei, Austrocidaris canaliculata) in a forest of Macrocystis pyrifera in southern Chile. We conclude that: | |
Ficha | Comunidades de macroinvertebrados en discos adhesivos de Lessonia nigrescens Bory (Phaeophyta) en Chile central. | Vásquez, J. A., & Santelices, B. Comunidades de macroinvertebrados en discos adhesivos de Lessonia nigrescens Bory (Phaeophyta) en Chile central. Revista Chilena de Historia Natural 131-154 | 57 | 131-154 | NO | parcialmente sin liga | Sin asignar | Los discos de adhesión de Lessonia nigrescens, al igual que los discos de otras Laminariales, albergan gran cantidad de invertebrados. Aun cuando se conocen algunos aspectos de la comunidad de organismos que habitan estos discos, se desconocen sus variaci | |
Ficha | Distributional patterns and diets of four species of sea urchins in giant kelp forest (Macrocystis pyrifera) of puerto toro, Navario Island , Chile | Vasquez Julio A. and et. al. | NO | Kelp | |||||
Ficha | Limiting factors in optimizing seaweed yield in Chile | Vasquez Julio A. & Renato Westermeier | 313-320 | NO | parcialmente completo con liga | General | Biological, educational, economic, social, and management factors. | A number of factors influenced yield from natural beds of marine algae in Chile. These factors are related not only to biological and ecological knowledge of the algal resource, but also to external events, such as; (1) the pressure of internation | |
Ficha | Production, use and fate of Chilean brown seaweeds: re-sources for a sustainable fishery | Vásquez Julio A. | 20 | 457-467 | NO | no completo | General | Kelp . Chile . Lessonia . Macrocystis . Abalone | Chile is an important producer of brown sea- Chilean kelp fluctuated between 40,000 t.year−1 in the early |
Ficha | Chondracanthus chamissoi (Rhodophyta, Gigartinales) in northern Chile: ecological aspects for management of wild populations | Vasquez J.A. and J.M. Alonso Vega | 13 | 267-277 | NO | Completo | Rodofitas | Biomass production, Chile, Chondracanthus chamissoi, epiphytism, herbory, reproduction phenology, resource managment | Abiotic and biotic factors affecting seasonal variations in the biomass and reproductive condition of Chondracanthus chamissoi were evaluated in a population at La Herradura Bay, northern Chile. During spring, increase in t |
Ficha | Macroinvertebrados asociados a discos de adhesión de algas pardas: Biodiversidad de comunidades discretas como indicadora de perturbaciones locales y de gran escala | Vasquez J. A. and J. M. A. Vega | NO | parcialmente completo con liga | Feofita | ||||
Ficha | El Niño 1997-98 en el norte de Chile: efectos en la estructura y en la organización de comunidades submareales dominadas por algas pardas. | Vasquez J. A. and J. M. A. Vega | 119-135 | NO | no completo | Feofita | Macrocystis, lessonia, herbivoría, comunidades costeras submareales. | Este trabajo analiza los efectos de El Niño 1997-1998 en las comunidades submarea- los patrones de abundancia y distribuci&oacu | |
Ficha | Repopulation of intertidal areas with Lessonia nigrescens in northern Chile | Vasquez J. A. and F. Tala | 7 | 347-349 | NO | parcialmente completo con liga | Feofita | Lessonia, northern Chile, repopulation, intertidal | Intertidal rocky areas in northern Chile were repopulated experimentally with the brown alga Lessonia nigrescens |
Ficha | The ecological effects of mining discharges on subtidal habitats dominanted by macroalgae in northern Chile: population and community level studies | Vasquez J. A. and et. al. | 217-229 | NO | parcialmente completo con liga | Feofita | coastal pollution, copper pollution, iron pollution, heavy metals, macroalgae, macroinvertebrates, Lessonia, L. trabeculata | ||
Ficha | The effects of mining pollution on subtidal habitats of nortjern Chile | Vasquez J. A. and et. al. | 13 | NO | no completo | Feofita | |||
Ficha | Ecological effects of harvesting Lessonia (Laminariales, Phaeophyta) in central Chile | Vasquez J. A. and B. Santelices | 41-47 | NO | parcialmente completo con liga | Feofita | ecological effects, harvesting, kelp, Lessonia | Lessonia nigrescens and L. trabeculata are economically important canopy-forming kelps in Chile . Experi- allowing the development of a h | |
Ficha | Biomass, reproductive phenology and chemical characterization of soluble polysaccharides from Rhodymenia howeana Dawson, (Rhodymeniaceae, Rhodymeniales) in northern Chile | Vasquez J. A. and et. al. | 41 | 235-242 | NO | Completo | Rodofitas | ||
Ficha | Variables morfometricas y relaciones morfologicas de Lessonia trabeculata Villouta & Santelices, 1986, en un poblacion submareal del norte de Chile | Vasquez J. A. | 64 | 271-279 | NO | no completo | Feofita | Lessiona, macroalga ,manejo de recursos, ambientes submareales. | |
Ficha | Ecological effects of brown seaweed harvesting | Vasquez J. A. | 38 | 251-257 | NO | no completo | Feofita | ||
Ficha | estado de Tamaulipas, MéxicoPotencial económico de la flora ficológica del | Vargas López, V. R. and et. al. | 171-179 | NO | parcialmente completo con liga | General | ficología, potencial económico, tamaulipas | La flora marina de ocho localidades del estado de Tamaulipas, fue | |
Ficha | Spatial and temporal variation of photosynthesis in intertidal Mazzaella laminarioides (Bory) Fredericq (Rhodophyta, Gigartinales) | Varela Daniel A. and et. al. | 18 | 827–838 | NO | Completo | Rodofitas | Photosynthetic acclimation . Spatial variation . Latitudinal variability . Tidal level . Photoinhibition | The red alga Mazzaella laminarioides is an economically important species with an extended latitudinal distribution along the Chilean coast. Its populations form mid-intertidal stands, several meters wide, and the |
Ficha | Inhibition of Ectocarpus siliculosus infestations with copper chloride in tank cultures of Gracilaria gracilis | Van Heerden P. D. R. and et. al. | 9 | 255-259 | NO | no completo | Cultivo | copper chloride, Ectocarpus siliculosus, epiphyte control, Gracilaria gracilis, Haliotes midae, tank culture | This study investigated copper chloride as an inhibitor of infestations of Ectocarpus siliculosusin Gracilaria gracilis |
Ficha | Activated defense systems in marine macroalgae: evidence for an ecological role for DMSP cleavage | Van Alstyne K.L. and et. al. | 213 | 53–65 | NO | no completo | General | Acrylic acid · Activated defenses · DMSP · Herbivory · Macroalgae | Activated defenses against herbivores and predators are defenses whereby a precursor compound is stored in an inactive or mildly active form. Upon damage to the prey, the precursor is enzymatically converted to a |
Ficha | Limited evidence of interactive disturbance and nutrient effects on the diversity of macrobenthic assemblages | Valeska Contardo Jara, and et al. | 308 | 37-48 | No | no completo | General | Intermediate disturbance hypothesis · Species diversity · Nutrient enrichment · ‘Bottom-up’ · Fouling · Productivity · Species richness · Brazil | The causes and consequences of the coexistence of a number of species in a given habi- in this context, including the ‘intermediate dist |
Ficha | Using genetic tools for sutainable management of kelps: a literature review and the example of Laminaria digitata | Valero M. and et. al. | NO | Feofita | |||||
Ficha | Rapid assessment of epibenthic communities: A comparison between two visual sampling techniques | Valeriano Parravicini | 395 | 21-29 | NO | no completo | General | Epibenthos Mediterranean Sea Replication Rocky reef Sampling Underwater survey Visual census | Quantification and comparisons of the structure of subtidal marine communities are essential for answering |
Ficha | VARIACIÓN ESPACIAL Y TEMPORAL DE LA COMUNIDAD DE ALGAS EN EL ARRECIFE COSTERO DE BOCA DE CANASÍ, LA HABANA, CUBA | Valdivia A. A. & E. de la Guardia L. | 25 | 123-131 | NO | parcialmente completo con liga | General | macroalgae; spatial variations; temporal variations; ASW, Cuba. | A study on spatial and temporal variations of algae cover in the coral reef east of Canasí ?s river mouth was carried out from February to October 2000. Three stations parallel to the coast, were located at different |
Ficha | Siliceous microfossils (Bacillariophyceae, Chrysophyceae) form the Upper Lerma Basin, Mexico. | Valadez, F., Caballero, M., Rodríguez-Vargas, D. C. & Sugiura-Yamamoto, Y. | 118 | 79-93 | NO | parcialmente sin liga | Sin asignar | Siliceous remains (diatoms and Chrysophyte stomatocysts) from the lacustrine sediments of lake Chignahuapan, Upper Lerma Basin, are illustrated and briefly described. The diatom record from these sediments has been used for palaeolimnological reconstructi | |
Ficha | Life Forms in the Algae | V. J. Chapman and D. J. Chapman | 19 | 65-74 | No | no completo | General | A review of life-form schemes in the algae is given and a new one is proposed because no previous scherne has | |
Ficha | Marine Algal Ecology | V. J. Chapman | 320-350 | 2864 | no completo | Sin asignar | |||
Ficha | The Spihonocladales | V. J. Chapman | 76-82 | NO | Liga perdida | Sin asignar | |||
Ficha | Mise au Point D'une Méthode de Cartographie des Macroalgues Marines Application á la Région de Calvi (Corse) | V. Demoulin, M.-P. Janssen et M. Licot | 102 | ND | 3340 | no completo | Sin asignar | Calvi, Córcega, Francia; | Elaboration of a mapping method for seaweeds. Application to the Calvi area (Corsica). A technique for mapping seaweeds based on a sampling distributed along the coast is presented. It has been applied for some thirty species on about twelve km of coast n |
Ficha | Mitochondria and Plastids as Endosymbionts: A Revival of Special Creation? The similarities between cellular organelles and prokaryotes are probably primitive features retained independently from a common ancestor. | Uzzell, T., & Spolsky, C. | 62 | 334-343 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Geographical genetic structure and phylogeography of the Sargassum horneri/Wlicinum complex in Japan,based on the mitochondrial cox3 haplotype | Uwal S. and et. al. | 156 | 901-911 | NO | no completo | Feofita | The genetic structure and phylogeography of in Japan were studied based on the mitochondrial cox3 hap- clades in a st | |
Ficha | The vertical distribution and seasonal abundance of intertidal microalgae on a rocky shore in New South Wales. | Underwood, A. J. | 78 | 199-220 | NO | parcialmente sin liga | Sin asignar | The abundance of intertidal microalgal food resources was estimated on shores at Cape Banks (Botany Bay, New South Wales) by indirect assays of the concentration of chlorophyll on and in the surface of sandstone rocks. Examination of the relationships bet | |
Ficha | Colonisation primaire des murs de beton par und Chrysocapsa (Cyanobacterie) a pigment UV-protecteur. | Turian, Gilbert. | 16 | 43-48 | NO | parcialmente sin liga | Sin asignar | Primary stages of the seasonal co!onization of concrete by the epilithic and photophilous Cyanophyta Gloeocapsa dermochroa (Chrysocapsa) have been illustrated. The golden yellow pigment - considered as scytonernin - from its pericellular sheaths has been | |
Ficha | Composants différentiels des croûte lichénoïde noires colonisatrices des roches basiques (calcicoles) versus acides (silicoles). | Turian, Gilbert. | 11 | 19 A 26 | 3801 | no completo | Sin asignar | Leproplaca xantholyta is the lemon-yellow leproid lichen secondarily colonizing the basophilic black lichenoid crust cornposed of Gloeocapsa + cyanophilic form of Coniosporium on calcareous rocks. On the acidophilic black lichenoid crust composed of Pleur | |
Ficha | Traînées noires biotiques (Cyanobactéries) et abiotiques (suie) de roches murales en ville de Genève. | Turian, Gilbert. | 12 | 71-77 | 3807 | no completo | Sin asignar | At the base of the calcareous or sandstone walls of several buildings in the City of Geneva, the ascending black streaks are composed of abiotic sooting materials. In co ntrast, rhe desc ending black streaks on a sandstone wall are biotic with, in their r | |
Ficha | Cyanophyte dorée (Chrysocaspa) pionniere de la colonisation du béton. | Turian, Gilbert. | 14 | 69-77 | 3808 | no completo | Sin asignar | The colonies of 16-128 golden -yellow sheathed cells of the typus dermochroa Näg, of Gloeocapsa biformis Erceg, aggregate into blackish crusts which are primo-colonizers of the apparently still virgin surfaces of urban walls of concrete. The intensity of | |
Ficha | Interactions algo-fongiques dans le Pleurococcetum vulgaris corticole, étude en microscopie optique et électronique. | Turian, G. et Reymond O. | 89 | 278-287 | 3802 | no completo | Sin asignar | ||
Ficha | Algal biotechnology industries and research activities in China | Tseng C.K. | 13 | 375–380 | NO | no completo | General | algal biotechnology, China, Gracilaria, Dunaliella, Laminaria, Nostoc, Porphyra, Spirulina, Undaria | In old China there were very few people engaged in the study of the algae, but in new China, freshwater and marine algae are studied by over one hundred old and new phycologists. There is now an algal biotechnology industry consisting of an aquaculture |
Ficha | Isotopic and elemental indicators of nutrient sources and status of coastal habitats in the Caribbean Sea, Yucatan Peninsula, Mexico | Troy Mutchler and etal. | 74 | 449-457 | No | no completo | General | d15N; nutrients; seagrass; coral reefs; eutrophication; wastewater; Mexico; Yucatan | Nutrient inputs associated with coastal population growth threaten the integrity of coastal ecosystems around the globe. In order to assess the |
Ficha | SEAWEEDS | Trono C.G. | NO | General | |||||
Ficha | Sponge–seaweed associations in species of Ptilophora (Gelidiaceae, Rhodophyta) | Tronchin Enrico and et. al. | 54 | 140–148 | NO | Completo | Rodofitas | Gelidiaceae, Ptilophora, Rhodophyta, South Africa, sponge–seaweed association, surface proliferations. | Sponge–seaweed associations in the seaweed genus Ptilophora are poorly understood; therefore, 94 specimens, representing all 17 species of Ptilophora, were examined to detail this phenomenon. All but 2 Ptilo |
Ficha | Ptilophora leliaertii and Ptilophora coppejansii, two new species of Gelidiales (Rhodophyta) from South Africa | Tronchin EM and et. al. | 39 | 395-410 | NO | Completo | Rodofitas | Gelidiales, LSU, Protea Banks, Ptilophora, rbcL, Rhodophyta, South Africa, taxonomy | Ptilophora leliaertii Tronchin et De Clerck sp. nov. and Ptilophora coppejansii Tronchin et De Clerck sp. nov. are described from Protea Banks reef situated off the southern coast of the KwaZulu-Natal Province in South Afri |
Ficha | A Reassessment and Reclassification of Species in the Genera Onikusa Akatsuka and Suhria J. Agardh ex Endlicher (Gelidiales, Rhodophyta) Based on Molecular and Morphological Data | Tronchin E. M. and et. al. | 45 | 548–558 | NO | Completo | Rodofitas | The phylogenetic relationships and taxonomic status of the Gelidialean genera Onikusa Akatsuka and Suhria J. Agardh ex Endlicher were examined based on analyses of molecular and morphological characters. The DNA s | |
Ficha | A re-evaluation of the genera Beckerella and ptilohora (Gelidiales, rhodophyta)based on molecular and morphological data | Tronchin E M and et. al. | 42 | 80-89 | NO | Completo | Rodofitas | ||
Ficha | Ecological engineering in aquaculture: use of seaweeds for removing nutrients from intensive mariculture | Troell m. and et. al. | 11 | 89-97 | NO | no completo | Cultivo | ecological engineering, biofilter, aquaculture, seaweeds, mariculture, eutrophication, Gracilaria, shrimp farming, mangroves, ecological footprint | Rapid scale growth of intensive mariculture systems can often lead to adverse impacts on the environment. Intensive |
Ficha | Physical forcing and phytoplankton distributions | TREVOR PLATT and et.al. | 69 | 55-73 | NO | no completo | Fitoplancton | fitoplancton, pigmentos, sensores remotos, color del océano, diatomeas, huracan, provincias biogeoquímicas. | INFLUENCIA DE FACTORES FÍSICOS Y DISTRIBUCIÓN DE FITOPLANCTON. – A escalas global y regional, la distribu- |
Ficha | Population dynamics of an association between a coral reef sponge and a red macroalga | Trautmana Donelle A. and et. al. | 244 | 87–105 | NO | no completo | Rodofitas | Ceratodictyon spongiosum; Dispersal; Fragmentation; Haliclona cymiformis; Rhodophyta; Symbiosis | Sponges are often as abundant as corals on tropical coral reefs and many species are symbiotic with algae. These associations may contribute significantly to reef primary productivity. This paper describes the first study e |
Ficha | Epulo multipedes gen. Et sp. Nov. (Corallinaceae, Rhodophyta), a coralline parasite from Australia | Towsend R.A. and J. M. Huisman | 43 | 288-295 | NO | Liga perdida | Rodofitas | ||
Ficha | Characterization of marine macroalgae by fluorescence signatures | Topinka, J. A., Bellows, W. Korjeff and Yentsch, C. S. | NO | General | |||||
Ficha | Mesoherbivores reduce net growth and induce chemical resistance in natural seaweed populations | Toht G.B. and et. al. | 152 | 245–255 | NO | no completo | General | Ascophyllum - Gastropod - Littorina - Nutrients - Phlorotannins | Herbivory on marine macroalgae (sea- weeds) in temperate areas is often dominated by relatively small gastropods and crustaceans (mesoherbivores). The eVects of these herbivores on the perfor- mance of adult |
Ficha | A provisional classification of algal-characterised rocky shore biotopes in the Azores | Tittley Ian & Ana I. Neto | 440 | 19–25 | NO | parcialmente completo con liga | General | algae, Azores, biotope, community structure, rocky shores | Recent studies of the rocky shores of the Azores archipelago have provided information on community structure allowing provisional identification of plant-characterised biotopes (habitats and their associated communiti |
Ficha | Seasonal changes in water quality and Sargassum biomass in southwest Australia | Tin C. Hoang, Anthony J. Cole, Ravi K. Fotedar, Michael J. O’Leary, Michael W. Lomas, Shovonlal Roy | 63-79 | NO | Liga perdida | Sin asignar | Physicochemical parameters · Sargassum beds · Seasonality · Canopy cover · Mean thallus length | Sargassum C. Agardh is one of the most diverse genera of marine macroalgae, and commonly inhabits shallow tropical and sub-tropical waters. This study aimed at investigating the effect of seasonality and the associated water-quality changes on the distrib | |
Ficha | Tissue Type Matters: Selective Herbivory on Different Life History Stages of an Isomorphic Alga | Thornber, C., Stachowicz, J. J., & Gaines, S. | 2255-2263 | NO | Liga perdida | General | algae; gametophyte; herbivory; isomorphic life cycle; Mazzaella flaccida; population dynamics; sporophyte; Strongylocentrotus purpuratus; Tegula funebralis. | Selective grazing by herbivores can have large effects on the population dynamics and community structure of primary producers. However, the ecological impacts of within-species herbivore preference for tissues of | |
Ficha | Functional properties of the isomorphic biphasic algal life cycle | Thornber, C. S. | 46 | 605-614 | NO | Liga perdida | Kelp | Many species of marine algae have life cycles that involve multiple separate, free-living phases that frequently | |
Ficha | Spatial and temporal variation of haploids and diploids in populations of four congeners of the marine alga Mazzaella | Thornber Carol S. and Steven D. Gaines | 258 | 65–77 | NO | Completo | Rodofitas | isornorphic life cycle, Mazzaella capensis, Mazzaella flaccida, Mazzaella laminarioides, Mazzaella splendens, haploid, diploid, macroalgae | Many algal species have life cycles that involve an obligate alternation of generations between nearly identical, free-living haploid and diploid individuals. The percentages of haploids to diploids, and the spatial and tem |
Ficha | Population consequences of biomass loss due to commercial collection of the wild seaweed Postelsia palmaeformis | Thompson S. A. and et. al. | NO | Liga perdida | Kelp | ||||
Ficha | Seaweed Communities in Retreat from Ocean Warming | Thomas Wernberg, et.al. | 21 | 1828-1832 | NO | no completo | General | In recent decades, global climate change [1] has caused | |
Ficha | Submerged Aquatic Vegetation and Physico-Chemical Monitoring in the Florida Bay Mangrove Zone, Everglades National Park | Thomas Frankovich, James Fourqurean, | No | no completo | General | ||||
Ficha | The life histories and developmental morphology of two species of Gloiosiphonia (Rhodophyta: Cryptonemiales, Gloiosiphoniaceae) from the Pacific Coast of North America | Thomas C. DeCew, John A. West, and E.K. Ganesant | 20 | 415-423 | 3236 | no completo | Sin asignar | Baja California, México; Gloiosiphonia capillaris | In culture the development of carpospores of Gloiosiphonia capillaris from Baja California, Mexico results in a free living crustose tetrasporophyte similar to Cruoriopsis. However, California isolates of the same species demonstrate direct gametophytic r |
Ficha | Culture studies on the marine red algae Hildenbrandia occidentalis and H. prototypus (Cryptonemiales, Hildenbrandiaceae) | Thomas C. DeCew and John A. West | 25 | 31- 41 | NO | parcialmente sin liga | Sin asignar | Pacífico nororiental; Hildenbrandia occidentalis SETCHELL y H. prototypus NARDO (Cryptonemiales, Hildenbrandiaceae) | Tetraspores of the red algae Hildenbrandia occidentalis SETCHELL and H. prototypus NARDO (Cryptonemiales, Hildenbrandiaceae) from the northeastern Pacific were cultured. Isolates of both species appear to be apomeiotic, producing tetrasporangial crusts si |
Ficha | Investigations on the life histories of three F arLowia speCIes (Rhodophyta: Cryptonemiales, Dumontiaceae) from Pacific North America | Thomas C. DeCew and John A. West | 20 | 342-351 | 3235 | no completo | Sin asignar | Farlowia compressa, F. mollis y F. conferta | Cultures of Farlowia compressa, F. mollis, and F. conferta, begun with carpospores indicate that all three species have a life history in which upright gametophytes alternate with a crustose tetrasporophyte resembling Haematocelis and/or Cruoriopsis. Tetr |
Ficha | Investigations on the life histories of three Farlowia species (Rhodophyta: Cryptonemiales, Dumontiaceae) from Pacific North America | Thomas C. Decew and John A. West | 20 | 342-351 | 3225 | no completo | Sin asignar | Farlowia compressa, F. mollis y F. conferta | Cultures of Farlowia compressa, F. mollis, and F. conferta, begun with carpospores indicate that all three species have a life history in which upright gametophytes alternate with a crustose tetrasporophyte resembling Haematocelis and/or Cruoriopsis. Tetr |
Ficha | A sexual life history in Rhodophysema (Rhodophyceae): a re-interpretation | Thomas C. DeCew and John A. West | 21 | 67-74 | 3234 | no completo | Sin asignar | Rhodophysema | Previous studies of field collected and cultured plants of Rhodophysema from different localities have demonstrated the existence of tetrasporangial and male plants, whereas female plants were apparently absent. Re-investigation of R. elegans from Califor |
Ficha | A rapid, precise and sensitive method for the determination of total nitrogen in natural waters | Thomas A. Frankovich, Ronald D. Jones | 60 | 227–234 | No | no completo | General | nitrogen; water quality; automated analysis; instruments; quantitative analysis; combustion | A rapid, automated method is described for the accurate determination of total combined nitrogen TN in natural waters. Ž . |
Ficha | Benthic indicators: Analysis of the threshold values of ecological quality classifications for transitional waters | Thierry Ruellet, Jean-Claude Dauvin | 54 | 1707-1714 | NO | no completo | General | Benthic index; Ecological indicators; Thresholds; Intercalibration; WFD | The effect of the modifications of the threshold values generally adopted for the five EcoQ (Ecological Quality) classes recognized by |
Ficha | INTEGRATING SEAWEEDS INTO MARINE AQUACULTURE SYSTEMS: A KEY TOWARD SUSTAINABILITY | Thierry Chopin et.al. | 37 | 975–986 | no completo | General | assimilative capacity; bioremedia- tion; coastal health; environmental impacts; integrated aquaculture; integrated coastal management; nutrifi- cation; salmon; seaweeds; sustainability | The rapid development of intensive fed aquaculture (e.g. finfish and shrimp) throughout the world is associated with concerns about the environmental impacts of such often monospecific practices, especially where activities are highly geograp | |
Ficha | Rafting of benthic macrofauna: important factors determining the temporal succession of the assemblage on detached macroalgae | Thiel Martin | 503 | 49–57 | NO | no completo | General | rafting, reproduction, dispersal, benthos, macroalgae, debris | Rafting on biotic and abiotic substrata has been reported for many benthic marine invertebrates. Here, I describe important characteristics of common floating substrata and review published studies examining the succession of |
Ficha | Are kelp holdfasts islands on the ocean floor? – indication for temporarily closed aggregations of peracarid crustaceans | Thiel M. and J. A. Vasquez | NO | Kelp | |||||
Ficha | Defining and detecting undesirable disturbance in the context of marine eutrophication | Tett P. and et. al. | 55 | 282–297 | NO | no completo | General | ||
Ficha | Electron microscope observations on the nuclear division in Valonia ventricosa (Chlorophyceae, Siphonocladales) | Terumitsu Hort and S Achlto E Nomoto | 133-142 | NO | Liga perdida | Sin asignar | The process of nuclear division in a coenocytic, marine green alga, Valonia venrricosa J. Agardh, has been examined in the electron microscope. The mitotic (or meiotic) spindle is centric and totally closed throughout the nuclear division. Kinetochores ar | ||
Ficha | Phylogeographic analyses of the 30S south-east Pacific biogeographic transition zone establish the occurrence of a sharp genetic discontinuity in the kelp Lessonia nigrescens: Vicariance or parapatry? | Tellier F. and et. al. | NO | Kelp | |||||
Ficha | THE LESSONIA NIGRESCENS SPECIES COMPLEX (LAMINARIALES, PHAEOPHYCEAE)SHOWS STRICT PARAPATRY AND COMPLETE REPRODUCTIVE ISOLATION IN A SECONDARY CONTACT ZONE1 | Tellier F. and et. al. | NO | Kelp | |||||
Ficha | Ecosystem e?ects of ?shing in kelp forest communities | Tegner, M. J. and P. K. Dayton | NO | Kelp | |||||
Ficha | Algae Collected on the presidential cruise of 1938. | Taylor W. R. | 98 | 1 A 18 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Illumination or confusion? Dinoflagellate molecular phylogenetic data viewed from a primarily morphological standpoint | Taylor F. J. R. “Max” | 52 | 308-324 | NO | no completo | Fitoplancton | dinoflagellate, evolution, molecular phylo- geny, morphology, relationships. | Recent molecular sequencing results involving multi- methodologies and genes produce trees that are |
Ficha | ESTIMACION DEL EFECTO DE LA AUTOFERTILIZACION SOBRE LOS PARAMETROS REPRODUCTIVOS Y DE CRECIMIENTO EN LESSONIA NIGRESCENS BORY, 1825 (LAMINARIALES, PHAEOPHYCEAE) EN LABORATORIO” | Tala Gonzalez F. B. | NO | Feofita | |||||
Ficha | First estimates of productivity in Lessonia trabeculata and Lessonia nigrescens (Phaeophyceae, Laminariales) from the | TALA FADIA and M. Edding | NO | parcialmente completo con liga | Feofita | ||||
Ficha | Growth and loss of distal tissue in blades of Lessonia nigrescens and Lessonia trabeculata (Laminariales) | TALA FADIA and M. Edding | 82 | 39-54 | NO | parcialmente completo con liga | Feofita | Chile; Growth; Erosion; Lessonia; Macroalgae; Particulate organic matter; Tissue loss | Meristematic growth and loss of distal tissue from blades of two ecologically important species in |
Ficha | Aspects of the reproductive phenology of Lessonia trabeculata (Laminariales: Phaeophyceae) from three populations in northern Chile | TALA FADIA and et. al. | 38 | 255-266 | NO | no completo | Feofita | Phaeophyceae; Lessonia trabeculata; kelp; reproductive phenology; spore culture; Chile | Lessonia trabeculata is a brown sea- coast of central and northern Chile, where it is the dominant kelp, and an important species in commu- |
Ficha | Sedimentatlon Studles of Red Algal Spores | Takeo Okuda and Michael Neushul | 17 | 113-118 | 2688 | no completo | Sin asignar | Red algae; red algal reproduction; sinking rate of spores; spore; micro-video. | More than 1000 spores from 11 species of red algae were collected; their differences in size and sinking rateswere measured using a new micro-video technique. A relationship between size and sinking rates was shown with larger spores generally sinking fas |
Ficha | Contribution of environmental and spatial processes to rocky intertidal metacommunity structure | Takehiro Okuda et. al. | 36 | 413-422 | NO | no completo | General | b-Diversity Ecological traits Environmental heterogeneity Macro ecology Spatial structure Variation partitioning | It has been debated whether the community structure of an open system is more dependent on |
Ficha | NEW INSIGHTS IN THE TAXONOMY OF THE CERAMIUM SINICOLA COMPLEX: RESURRECTION OF CERAMIUM INTERRUPTUM (CERAMIACEAE, RHODOPHYTA) | Tae Oh Cho, S. F. et. al. | 39 | 775-788 | NO | parcialmente sin liga | Rodofitas | Ceramium; C. interruptum; C. sinicola; Ceramiales; morphology; phylogeny; Rhodophyta; rbcL; RUBISCO spacer; SSU rDNA; taxonomy | Phylogenetic relationships of the Ceramium sinicola complex (C. interruptum and C. sinicola) including C. codicola were studied using nucleotide sequences of rbcL and small subunit rDNA, and the RUBISCO space |
Ficha | CERAMIUM INKYUII SP. NOV. (CERAMIACEAE, RHODOPHYTA) FROM KOREA: A NEW SPECIES BASED ON MORPHOLOGICAL AND MOLECULAR EVIDENCE | Tae Oh Cho and et. al. | 39 | 236–247 | NO | no completo | Rodofitas | Ceramium; C. inkyuii; Ceramiales; phylogeny; rbcL; Rhodophyta; SSU rDNA; taxonomy | Ceramium inkyuii sp. nov. is newly described based on samples collected from the east coast of Korea and compared with similar species such as C. paniculatum and C. tenerrimum. The new species is characterized by pseudo-dichotomously branched |
Ficha | NEW INSIGHTS IN THE TAXONOMY OF THE CERAMIUM SINICOLA COMPLEX: RESURRECTION OF CERAMIUM NTERRUPTUM (CERAMIACEAE, RHODOPHYTA) | Tae Oh Cho and et. al. | NO | Rodofitas | |||||
Ficha | Fungi in Oceans and Estuaries | T.W. Johnson, Jr. and F.K. Sparrow, Jr. | 4 | ND | 3233 | no completo | Sin asignar | ||
Ficha | Influence of submarine springs and wastewater on nutrient dynamics of Caribbean seagrass meadows | T.J.B. Carruthers, B.I. van Tussenbroek, W.C. Dennison | 64 | 191-199 | No | no completo | General | nutrient sources; sewage; submarine springs; groundwater; eutrophication; Thalassia testudinum; d15N; nitrogen; phosphorus; iron; seagrass; conceptual diagrams | The east coast of the Yucatan Peninsula, Mexico, consists of highly permeable limestone, such that surface flow and rivers are |
Ficha | SUMMER GROWTH OF CZYORDARZA FLAGELLZFORMZS (O.F. Muell.) C. Ag.: PHYSIOLOGICAL STRATEGIES IN A NUTRIENT STRESSED ENVIRONMENT | T.A. PROBYN and A.R.O. CHAPMAN | 73 | 243-211 | No | no completo | General | The objective of this study was to determine the relative importance of mechanisms by which | |
Ficha | Spatial and temporal distributions of epiphytic diatoms growing on Thalassia testudinum Banks ex Ko ̈nig: relationships to water quality | T.A. Frankovich and etal. | 569 | 259–271 | No | no completo | General | diatoms, epiphytes, Florida Bay, NMDS, Thalassia testudinum, water quality | The spatial and temporal distributions of the epiphytic diatom flora on Thalassia testudinum was described |
Ficha | Primary succession of coral-reef algae: Differing patterns on fished versus unfished reefs | T. R. McClanahan | 218 | 77-102 | NO | no completo | General | Experimental coral plates were placed on four coral reefs to determine the effect that sea urchin and herbivorous fish grazing, and river sediments have on successional changes in algae. Algal functional-group composition, | |
Ficha | Micro-Organisms In The Water Circuits Exposed To Radiation Of The Nuclear Reactor Budapest - Csillebe Rc | T. Hortobagyi and J. Vlgassy | 18 | 151-160 | 375 | no completo | Sin asignar | Budapest, Hungría, | Living micro-organisms have been demonstrated in the waters of the 2.5 MW research atomic reactor of Csillebére: in the secondary circuit, in the primary circuit and in the water of th e container for the storage of the burnt out fuel elements. Four demon |
Ficha | A CONSIDERATION OF THE " SPECIES PLAN- TARUM" OF LINN-SEUS AS A BASIS FOR THE STARTING-POINT OF THE NOMENCLATURE OF CRYPTOGAMS' | T. G. FARLOW | 44 | No | no completo | General | |||
Ficha | Effect of Whey Wastes on Stabilization Ponds | T. E. Maloney, H. F. Ludwig, J. A. Harmon and L. McClintock | 32 | 1283-1299 | NO | parcialmente sin liga | Sin asignar | Estanques de aguas residuales | Experiments were carried out with pilot-plant sewage stabilization ponds to determine why full-scale sewage stabilization ponds, used in conjunction with a primary sewage treatment facility, were not operating in a satisfactory manner. Poor pond performan |
Ficha | Morphogenesis in Micrasterias I. Tip growth | T. C. Lacalli | 33 | 95-115 | 1270 | no completo | Sin asignar | Micrasterias rotata | Observations on lobe growth in the lateral wings of the developing primary cell wall in the desmid Micrasterias rotata are reported and discussed. Patterns of incorporation of methyl-[3H]-methionine and C-1-[3H] glucose into the primary wall as revealed i |
Ficha | Morphogenesis in Micrasterias II. Patterns of morphogenesis | T. C. Lacalli | 33 | 117-126 | 1271 | no completo | Sin asignar | M. rotata, M. radiata | The final form of the polar lobe and lateral wings of developing semicells of M. rotata results from combined action of three growth processes: tip growth, branching and lobe broadening. Tip growth unaccompanied by branching or broadening occurs during no |
Ficha | A Review of the Marine Plants of Panama | Sylvia A. Earle | 2 | 69-88 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | HIERARCHICAL SPATIAL STRUCTURE AND DISCRIMINANT ANALYSIS OF GENETIC DIVERSITY IN THE RED ALGA MAZZAELLA LAMINARIOIDES (GIGARTINALES, RHODOPHYTA) | Sylvain Faugeronand et.al. | 37 | 705-716 | NO | no completo | General | assignment test; seaweed dispersal; gene flow; Mazzaella laminarioides; population ge- netic structure; RAPD | Our study of the genetic structure of Mazzaella genetic diversity based on random amplified poly- |
Ficha | The Origin of Nitrogen Isotope Values in Algae | SWART PETER K. and et. al. | NO | General | |||||
Ficha | Rocky-shore communities as indicators of water quality: A case study in the Northwestern Mediterranean | Susana Pinedo et. al. | 55 | 126-135 | NO | no completo | General | Bioindicators; Quality assessment; Ecological status; Macroalgal communities; Water framework directive; Mediterranean sea | The collection of 152 samples from the upper sublittoral zone along the rocky coasts of Catalonia (Northwestern Mediterranean) was |
Ficha | Brown Algal Mastigonemes: Comparative Ultrastructure | Susan Loiseaux and John A. West | 89 | 524-532 | 778 | no completo | Sin asignar | ||
Ficha | Effects of unidirectional and oscillatory water flow on nitrogen fixation (acetylene reduction) in coral reef algal turfs, Kaneohe Bay, Hawaii | Susan L. Williams, Robert C. Carpenter | 226 | 293–316 | No | no completo | General | Algal turfs; Coral reefs; Hydrodynamics; Nitrogen fixation | Rates of acetylene reduction (nitrogenase activity) by algal turf communities from Kaneohe |
Ficha | Lista de las macroalgas marinas cubanas | Suarez A.M. | 26 | 93-148 | NO | no completo | General | lista de especies; macroalgas marinas; ASW, Cuba | En este trabajo, se hace un breve recorrido por el estudio de las macroalgas marinas en Cuba. Se hace la |
Ficha | Effects of herbivory, nutrient level, and introduced algae on the distribution and abundnace of the invasive macroalga Dictyosphaeria cavernosa in Kaneohe Bay, Hawaii | Stimson J. and et. al. | 19 | 343-357 | NO | no completo | Feofita | Coral reef-Dictyosphaeria cavernosa- Herbivory-Macroalgae-Nutrients- Non-nativve- Phase shift | |
Ficha | The origin of red algae: Implications for plastid evolution | STILLER JOHN W. AND BENJAMIN D. HALL | 94 | 4520–4525 | NO | Completo | Rodofitas | The origin of the red algae has remained an enigma. Historically the Rhodophyta were classified first as plants and later as the most ancient eukaryotic organisms. Recent molecular studies have indicated simi | |
Ficha | Vegetative growth rates of Pterocladia capillacea (Gelidiaceae, Rhodophyta). | Stewart, J. G. | 27 | 85-92 | 3865 | no completo | Sin asignar | Al though it has bcen shown car lier th at tha lli in sorne pop ulations u f Ptcrocludia capillace« gr ow slo wly ovc r periods 01' sc ve ra l years, an observ a rio n o f possibly more rap id gro wt l: in an intcrtidal habitat suggest c d that under cert | |
Ficha | Seasonal abundance patterns of diatoms on Cladophora in Lake Huron. | Stevenson, R. J., & Stoermer, E. F. | 8 | 169-183 | NO | parcialmente sin liga | Sin asignar | Rocks bearing Cladophora were collected from May to November 1979 at two locations near Harbor Beach, Michigan, in Lake Huron to document seasonal patterns ofepiphytic diatom abundance and diatom proportion ofthe Cladophora-epiphyte assemblage biomass in | |
Ficha | Fluid Mechanics of the Thallus of an Intertidal Red Alga, Halosaccion Glandiforme | Steven Vogel and Catherine Loudon | 168 | 161-174 | 2689 | no completo | Sin asignar | Halosaccion glandiforme | The elongate, ellipsoidal thalli of Halosaccion glandiforme (Gmei.) Rupr. are alternately exposed and immersed with tidal cycles. These sea water-filled thalli are penetrated, mainly in the distal third, by 5 to 15 pores. During emersion, water is lost by |
Ficha | THE EFFECT OF LIGHT INTENSITY AND LIGHT PERIOD ON THE DEVELOPMENT OF THALLUS FORM IN THE MARINE RED ALGA PLEONOSPORIUM SQUARRULOSUM (HARVEY) ABBOTT (RHODOPHYTA: CERAMIALES). I. APICAL CELL DIVISION - MAIN AXES | STEVEN N. MURRAY and PETER S. DIXON | 13 | 15-27 | No | no completo | General | An analysis and discussion of two mechanisms of apical cell division in filaments of Pleono- oblique orientation of cross-wall formation during | |
Ficha | Measuring Intertidal Wave Forces | Stephen R. Palumbi | 81 | 171-179 | NO | parcialmente sin liga | Sin asignar | Wave force; intertidal; wave measurement; exposure; fundamental niche | Wave force is regarded widely to be an important determinant of distribution and abundance of shallow water, marine organisms, but is seldom measured in ecological studies. Here I describe a small, inexpensive device that measures forces due to wave actio |
Ficha | Effects of herbivory and nutrients on the early colonization of crustose coralline and fleshy algae | Stephanie A. Belliveau*, Valerie J. Paul | 232 | 105-114 | No | no completo | General | Algae · Coral reefs · Crustose coralline algae · Eutrophication · Herbivory | The persistence of phase shifts from coral-dominated to macroalgae-dominated commu- on tropical coral reefs. The influence of reduced he |
Ficha | The caribbean's western-most algal ridges in Cozumel, Mexico | Steneck R.S. and et. al. | NO | General | |||||
Ficha | Kelp forest ecosystems: biodiversity, stability, resilience and future | Steneck R.S. and et. al. | NO | Kelp | |||||
Ficha | Efecto de la temperatura sobre las tasas de fotosíntesis, crecimiento y calcificación del alga coralina de vida libre Lithophyllum margaritae | Steller DL and et. al. | 33 | 441–456 | NO | Completo | Rodofitas | rodolito, algas coralinas, calcificación, fotosíntesis, Lithophyllum margaritae. | Las praderas de rodolitos son la vegetación subacuática calcificante dominante en algunos ambientes costeros alrededor del mundo pero se cuenta con poca información cuantitativa acerca de su fisiolog&ia |
Ficha | The culture collection of algae at the university of Texas at Austin | Starr R. | 47-100 | NO | parcialmente completo con liga | Cultivo | |||
Ficha | Isozymes in macroalgae (seaweeds): genetic differentiation, genetic variability and applications in systematics | SOSA PEDRO A. AND SANDRA C. LINDSTROM | 34 | 427-442 | NO | no completo | General | allozymes, electrophoresis, genetic identity, genetic structure, genetic variability, isozymes, population genetics, seaweeds, systematics | Use of isozymes (including allozymes) in studies of population genetics and systematics of seaweeds has increased sufficiently in the last |
Ficha | Genetic structure of natural populations of Gelidium species: A re-evaluation of results | Sosa P. A. and et. al. | 10 | 279–284 | NO | Completo | Rodofitas | Canary Islands, electrophoresis, F-statistics, Gelidium canariensis, Gelidium arbuscula, genetic distance, genetic structure, isozymes | Twenty-two loci were re-evaluated to assess genetic variation and differentiation in three natural populations (two from Gran Canaria and one from Tenerife) of Gelidium (G. canariensis and G. arbuscula). The new data using |
Ficha | A new species of Basicladia on Australian freshwater turtles | Sophie C . Ducker | 157-174 | 2768 | no completo | Sin asignar | Australia; Basicladia ramulosa | 1 . A new species of the genus Basicladia is described . It occurs on the Australian freshwater turtle, Chelodina longicollis (SHAW). 2 . This species differs from those hitherto described, because it has profusely branched upright filaments, hence the ch | |
Ficha | Effect of nutrient enrichment on the source and composition of sediment organic carbon in tropical seagrass beds in the South China Sea | Songlin Liu, et. al. | 110 | 274-280 | NO | no completo | General | Seagrass bed Sediment organic carbon Source Composition Nutrient Microbial biomass carbon | To assess the effect of nutrient enrichment on the source and composition of sediment organic carbon (SOC) be- sediment, pri |
Ficha | The red alga Porphyra dioica as a fish-feed ingredient for rainbow trout (Oncorhynchus mykiss): effects on growth, feed efficiency, and carcass composition | Soler-Vila Anna and et. al. | 21 | 617–624 | NO | no completo | Rodofitas | Rainbow trout . Feed ingredient . Seaweed . Porphyra dioica . Pigment | Porphyra dioica meal was added at levels of 5, 10 and 15% to a diet for rainbow trout formulated to be isonitrogenous and isolipidic. The control diet was a commercial trout diet without seaweed meal. The exp |
Ficha | BENTHIC DIATOM COMMUNITY STRUCTURE IN BOREAL STREAMS. DISTRIBUTION PATTERNS ALONG ENVIRONMENTAL AND SPATIAL GRADIENTS | Soininen Janne | NO | no completo | Fitoplancton | The past decade has seen growing appreciation of the role of regional influences in | |||
Ficha | Organismic determinants and their effect on growth and regeneration in Gracilaria gracilis | Smit Albertus J. & John J. Bolton | 11 | 293–299 | NO | Liga perdida | Rodofitas | organismic determinants, Gracilaria gracilis, Rhodophyta, regeneration, growth, mariculture | The growth of Gracilaria gracilis (Stackhouse) Steentoft, Irvine et Farnham was examined by studying the effect of organismic determinants such as thallus length, position along the thallus and branching. Knowledge of these |
Ficha | SEM-analysis of colonies of the cyanophyte Nodularia water bloom from Baltic Sea. | Šmarda, J., Komárek, J., & Hübel, H. | 319-330 | 3770 | no completo | Sin asignar | The microcolon y structure of the cyanophytes Nodularia spumigena and Nodularia sp. forming blooms in the Baltic Sea, was studies by scanning electron microscopy. The morphnlogy of the dominant Nodularia filaments is described. Their colonies represent a | ||
Ficha | Contribuiç?o ao Estudo da Reproduç?o de Champia Minuscula (Rhodophyta-Rhodymeniales) | Silvia Maria Pita de Beauclair Guimar?es | 2 | 17-41 | 1529 | no completo | Sin asignar | This papel describes the development of reproductive structures of Champia minuscula. Detailed informations about thallus organization, early stages and position of the procarp and also the development of the carposporophyte till maturity are given. Male | |
Ficha | MACROALGAS FLOTANTES Y EPIFITAS ASOCIADAS CON Zostera marina L. EN BAHIA SAN QUINTIN (B.C., MEXJCO), DURANTE VERHNO-OTOÑO . 1982: BIOMASA Y COMPOSICION TAXONOMICA | Silvia E. Ibarra Obando, Raúl Aguilar Rosas | 11 | 89-104 | No | no completo | General | De junio a diciembre de 1982 se tomaron muestras mensuales para la determinación de la San Quintin. Se instalaron tres tra | |
Ficha | A reappraisal of the order Corallinales (Rhodophyceae). | Silva, P. C., & Johansen, H. W. | 23 | 245-254 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | DRIFT AND EPIPHYTIC MACROALGAE ASSOCIATED WITH Zostera marina L. IN SAN QUINTIN BAY (B.C., MEXICO) DURING SUMMER-AUTUMN 1982: BIOMASS AND TAXONOMIC COMPOSITION | Silva E. Ibarra Obando and Raúl Aguilar Rosas | 11 | 89-104 | NO | no completo | General | From June to December 1982, monthly samples were taken to determine the biomass of drift and epiphytic macroalgae in a Zostera marina meadow, in Babia Falsa, San Quintin. Three transects were determined: -0.95 m. (1), | |
Ficha | Predation, competition and prey communities: A review of field experiments | Sih A. and et. al. | NO | Kelp | |||||
Ficha | Drachiella liaoii sp. nov., a new member of the Schizoserideae (Delesseriaceae, Rhodophyta) from Taiwan and the Philippines | SHOWE-MEI LIN and et. al. | 37 | 93-102 | NO | no completo | Rodofitas | Ceramiales, Delesseriaceae, Drachiella liaoii sp. nov., LSU rDNA, Philippines, phylogeny, Rhodophyta, Schizoserideae, Taiwan | A new member of Delesseriaceae (Ceramiales, Rhodophyta) is described from Southern Taiwan and the Philippines. On the basis of comparative vegetative and reproductive morphology, and phylogenetic analysis inferred from nuclear-encoded large-subunit rib |
Ficha | Stressed, but not defenceless: no obvious inXuence of irradiation levels on antifeeding and antifouling defences of tropical macroalgae | Shirin Appelhans Y. and et. al. | 157 | 1151–1159 | NO | no completo | General | The production of defence metabolites is defend themselves chemically against herbivory and foul- | |
Ficha | Life history and molecular phylogenetic relationships of Asterocladon interjectum sp. nov. (Phaeophyceae) | Shinya Uwai and et. al. | 40 | 179-194 | NO | parcialmente completo con liga | Feofita | anisogamy, Asterocladon interjectum, Asterocladon lobatum, Asterocladon rhodochortonoides, Asteronema, isomorphic life history, Phaeophyceae, pyrenoid, stellate chloroplast arrangement | A small prostrate filamentous brown alga, isolated from the warm temperate Pacific coast of Japan, was cultured to |
Ficha | New records of Gelidiella pannosa, Pterocladiella caerulescens and Pterocladiella caloglossoides (Rhodophyta, Gelidiales) from Japan | Shimada Satoshi and Michio Masuda | 48 | 95–102 | NO | no completo | Rodofitas | Gelidiales, Gelidiella pannosa, Japan, molec- ular phylogeny, morphology, Pterocladiella caerulescens, Pterocladiella caloglossoides, Rhodophyta, secondary rhizoidal attachment, SSU rDNA sequences. | Three gelidialean species, Gelidiella pannosa (Feldmann) Feldmann et Hamel, Pterocladiella caerulescens (Kützing) Santelices et Hommersand and Pterocladiella caloglossoides (Howe) Santelices, are newly report |
Ficha | Phylogenetic affinities of general Acanthopeltis and Yatabela (Gelidiales, Rhodophyta) inferres from molecular analyses | Shimada Satoshi and et. al. | 38 | 528-540 | NO | Completo | Rodofitas | ||
Ficha | Two new species of Gelidium (Rhodophyta, Gelidiales), Gelidium tenuifolium and Gelidium koshikianum, from Japan | Shimada Satoshi and et. al. | 48 | 37–46 | NO | Completo | Rodofitas | Gelidiales, Gelidium koshikianum sp. nov., Gelidium tenuifolium sp. nov., Japan, molecular phylogeny, morphology, rbcL gene, Rhodophyta, secondary rhizoidal attachment. | Two new marine red algae, Gelidium tenuifolium sp. nov. and Gelidium koshikianum sp. nov. (Gelidiales, Gelidiaceae) are described from Japan. Gelidium tenuifolium with large-sized thalli (up to 30 cm tall)&nb |
Ficha | Reassessment of the taxonomic status of Gelidium subfastigiatum (Gelidiales, Rhodophyta) | Shimada S. and M. Masuda | 51 | 271-278 | NO | Completo | Rodofitas | Gelidiales, Gelidium elegans, Gelidium sub- fastigiatum, ITS1 sequence, Japan, molecular phylogeny, morphology, Rhodophyta. | The taxonomic relationship between Gelidium elegans Kützing and Gelidium subfastigiatum Okamura, two morphologically similar species of the red algal genus Gelidium (Gelidiaceae) growing in the north-wes |
Ficha | First report of Gelidlella ligulata (Gelidiales, Rhodophyta) in Japan | Shimada Satoshi and Michio Masuda | 47 | 97-100 | NO | no completo | Rodofitas | Gelidiales, Geiidieiia indica, Geiidieiia iiguiata, Japan, morphology, Pacific, Rhodophyta, secondary rhizoidal attachment. | A gelidialean red alga that was newly found in Japanese waters is referred to as Gelidielia liguiata Dawson, It is characterized by erect lanceolate blades developing from a creeping axis that are relatively large in t |
Ficha | Taxonomy of the family Batrachospermaceae (Batrachospcrmalcs, Rhodophyta) | Shigeru Kumano | 41 | 253-274 | 2805 | no completo | Sin asignar | Batrachospermum; Batrachospermaceae; Rhodophyta; Nothocladus; Sirodotia; Tuomeya; taxonomy. | In this review some reappraisals of the classification system of the family Batrachosper- maceae are introduced. An aspect of morphological relationships among the sections and the genera and a check list of the hitherto-described 104 taxa of the family B |
Ficha | The genus Chaetoceros (Bacillariophyta) from Peter the Great Bay, Sea of Japan | Shevchenko Olga G. and et. al. | 49 | 236-258 | NO | no completo | Fitoplancton | Chaetoceros; diatoms; morphology; Sea of Japan. | Several studies in the Sea of Japan have dealt with the taxonomy, morphology and ecology of Chaetoceros spe- recorded between 1991 and 2004 from the phytoplank- |
Ficha | Seasonality of macroalgae and epilithic diatoms in spring-fed streams in Texas, USA | Sherwood Alison R. & Robert G. Sheath | 390 | 73–82 | NO | no completo | General | diatoms, macroalgae, seasonality, springs, streams, Texas | A seasonal study of two spring-fed stream systems in south-central Texas was undertaken over a 15-month period and several phys |
Ficha | SYSTEMATICS OF THE HILDENBRANDIALES (RHODOPHYTA): GENE SEQUENCE AND MORPHOMETRIC ANALYSES OF GLOBAL COLLECTIONS | Sherwood Alison R. and Robert G. Sheath | 39 | 409-422 | NO | Completo | Rodofitas | 18S rRNA gene; Apophlaea; Hilden- brandia; Hildenbrandiales; morphometrics; rbcL gene; systematics | Fifty-seven collections of marine and freshwater Hildenbrandia from North America, South America, Europe, and Africa were compared with 21 type and historically important specimens using multivariate mor |
Ficha | A New Species of Paleocene Chimaeroid from California | Shelton p. Applegate | 74 | 27-30 | NO | parcialmente sin liga | Sin asignar | California; Chimaeroid del Paleoceno | A new species of Chimaeroid from the Paleocene of California is described which is the first New World record for the genus Ischyodus. The relationships of the present new species within the genus Ischyodus is discussed. |
Ficha | Size, survival and the potential for reproduction in transplants of Mazzaella splendens and M. linearis (Rhodophyta) | Shaughnessy Frank J. and Robert E. DeWreede | 222 | 109–118 | NO | Completo | Rodofitas | Biomechanics · Common garden · Mazzaella splendens · Mazzaella linearis · Reproduction · Survivorship | Biomechanical models of red algae have been developed that make predictions about blade survivorship based on tissue strengths, drag coefficients, and blade surface areas. The first 2 objectives of the present fie |
Ficha | CONTRASTING PATTERNS OF ALLOMETRY AND REALIZED PLASTICITY IN THE SISTER SPECIES MAZZAELLA SPLENDENS AND MAZZAELLA LINEARIS (RHODOPOHYTA) | Shaughnessy Frank J. | 40 | 846–856 | NO | Completo | Rodofitas | allometry; genetic differentiation; Mazzaella; phenotypic plasticity; reproduction; survivorship | Phenotypic differences between the low wave exposure Mazzaella splendens (Setchell et Gardner) Hommersand and the high exposure Mazzaella linearis (Setchell et Gardner) Fredericq could be due to plasticity or gene |
Ficha | Seasonal Variation in Understory Kelp Bed Habitats of the Strait of Juan de Fuca | Shaffer J. Anne | NO | Kelp | |||||
Ficha | Caracterización ficológica de la laguna de Bojórquez, Quintana Roo, Mexico. | Serviere-Zaragoza, E., Collado-Vides, L. I. G. I. A., & González-González, J. | 28 | 126-133 | 3753 | no completo | Sin asignar | Se estudiaron las algas de la laguna de Bojórquez y áreas adyacentes. Se hicieron seis colectas en 14 estaciones, desde Mayo 1985 a Octubre 1986. Se identificaron 52 taxones que incluyen 28 especies de la división Chlorophyta, 22 de la Rhodophyta y 2 de l | |
Ficha | Tissue nitrogen and phosphorus in seaweeds in a tropical eutrophic environment: What a long-term study tells us | Sergio O. Lourenço, et. al. | 18 | 389-398 | NO | no completo | General | dissolved nutrients, seaweeds, trophic status, tissue nitrogen, tissue N:P ratio, tissue phosphorus | Percentages of nitrogen and phosphorus in 10 species of seaweeds (6 green and 4 red algae) were monitored from |
Ficha | El Sargazo Gigante (Macrocystis Pyrifera) y su Explotación en Baja California | Sergio A. Guzmán del Próo, Sara de la Campa de Guzmán, José Luis Granados Gallegos. | 32 | 15-49 | 1465 | no completo | Sin asignar | Baja California, México; Macrocystis pyrifera | 1. A partir de fotografias aéreas de la costa occidental de Baja California, se elaboraron mapas que establecen la localizacion precisa de los mantos de "sargazo gigante" (Macrocystis pyrifera) en la peninsula de Baja California. Se confirma que el limite |
Ficha | Flora macroscópica asociada a los bancos de abulón (Haliotis spp.) en algunas áreas de la costa occidental de Baja Califonia. | Sergio A. Guzmán del Prado, Sara de la Campa de Guzmán y Jorge Pineda Barrera | 257-263 | 2806 | no completo | Sin asignar | Baja California, México; algas rojas, algas pardas, algas verdes; | El desarrollo de un programa de prospección abulonera en la costa occidental de Baja California, ha permitida hacer un estudio preliminar de la flora acompañante de las diversas especies de abulón (Haliotis spp.) que son explotadas regularmente en la zona | |
Ficha | Sobre la actividad antibiótica de ciertas especies de algas del Mediterráneo. | Serarols, M. D., Herna?dez, M. C., & Seoane, J. A. | 13 | 919-927 | 3839 | no completo | Sin asignar | The study of algae antibiotic activity is on the complete increase, and there is bibliographic information about the activity of a great number of species that also live in our coasts. The purpose of the present work, is to open this li- ne of investigati | |
Ficha | On the possibility of culturing Gelidium sesquipedale by vegetative propagation. | Seoane-Camba, J. A. | 48 | 59-68 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Sobre una rodofícea parásita de Gelidiáceas. | Seoane Camba, J. A. | 13 | 911-918 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Aportació al coneixement de les algues marines de les costes del País Valencià. | Seoane Camba, J. A. | 13 | 767-775 | NO | parcialmente sin liga | Sin asignar | In this survey we present the first results about the seaweed flora in the area of Valencia. The plants, that we have succeeded in picking up and classify until this moment, come from sixteen places of the coast that we are studying, located between Penis | |
Ficha | Proposals for Palisada poiteaui var. gemmifera comb. nov.and Palisada corallopsis comb. nov. (Rhodomelaceae,Rhodophyta) | Sentíes Abel and Jhoana Díaz-Larrea | 51 | 69–70 | NO | Liga perdida | Rodofitas | Ceramiales; Laurencia complex; nomenclatural proposals; Palisada. | Since Chondrophycus poiteaui var. gemmiferus and C. corallopsis fall within the new recently validated segregate genus Palisada K.W. Nam, two new nomenclatural combinations are proposed: Palisada poiteaui var. gem |
Ficha | CYANOPHYTA y CHLOROPHYTA Nuevas para la Argentina | Sebastian Guarrera y Guillermo Tell | 94-101 | 94 | no completo | Sin asignar | In the present paper, four species of Cyanopbyta (Gloeocapsa magma, Lyngbya spiralis, Microcoleus acutissimus, Tolypothrix campylonenroides), and one species of Chlorophyta (Sphaeroplea africana) are studied. Also, the presence of the genus Tetracystis (C | ||
Ficha | ESTIMACION DEL EFECTO DE LA AUTOFERTILIZACION SOBRE LOS PARAMETROS REPRODUCTIVOS Y DE CRECIMIENTO EN LESSONIA NIGRESCENS BORY, 1825 (LAMINARIALES, PHAEOPHYCEAE), EN LABORATORIO | Sebastián Andrés Godoy Báez | no completo | Feofita | Las macroalgas pardas del orden Laminariales son un recurso natural | ||||
Ficha | Demographic models to simulate the stable ratio between ecologically similar gametophytes and tetrasporophytes in populations of the Gigartinaceae (Rhodophyta) | Scrosati Ricardo and Robert E. DeWreede | 47 | 153–157 | NO | Completo | Rodofitas | demography, gametophyte, Gigartinaceae, matrix models, Rhodophyta, tetrasporophyte. | In populations of the Gigartinaceae (Rhodophyta), gametophytes often predominate numerically over tetrasporophytes. Several hypotheses have been proposed to explain this dominance, based on the usually implic |
Ficha | Effects of elevation, wave exposure, and year on the proportion of gametophytes and tetrasporophytes in Mazzaella parksii (Rhodophyta, Gigartinaceae) populations | Scrosati Ricardo & Benita Mudge | 520 | 199-205 | NO | Completo | Rodofitas | elevation, gametophyte, Gigartinaceae, Mazzaella, tetrasporophyte, wave exposure | We investigated the effects of elevation, wave exposure, and year on the proportion of gametophytes and tetrasporophytes in populations of the intertidal red seaweed Mazzaella parksii (= M. cornucopiae, Gigartinaceae) |
Ficha | Review of studies on biomass-density relationships (including self-thinning lines) in seaweeds: Main contributions and persisting misconceptions | Scrosati Ricardo | 53 | 224–233 | NO | no completo | General | clonal, interspecific biomass-density rela- tionship, self-thinning rule, ultimate biomass-density line, unitary. | Ecological models relating biomass and density are |
Ficha | Ramet dynamics for the clonal seaweed Pterocladiella capillacea (Rhodophyta): A comparasin with Chondrus crispus and with Mazzaella cornucopiae (Gigartinales) | Scrosati R. and E. Servire-Zaragoza | NO | Rodofitas | |||||
Ficha | Population structure and dynamics of the clonal alga Mazzaella cornucopiae (Rhodophyta, Gigartinaceae ) from Barkley Sound, Pacific Coast of Canada | Scrosati R. | 41 | 483-493 | NO | Completo | Rodofitas | ||
Ficha | Crowding in clonal seaweeds: Does self-thinning occur in Mastocarpus papillatus shortly before stand biomass peaks? | Scrosati R. | 84 | 233–238 | NO | Completo | Rodofitas | Clonal; Crowding; Gigartinales; Mastocarpus; Petrocelidaceae; Self-thinning; Size inequality | Fronds from crowded stands of clonal seaweeds, particularly those in which holdfasts are mostly perennial and are the major source of new fronds every year, are thought not to undergo self-thinning during the growth season, |
Ficha | Interannual variation of the abundance of Mazzaella cornucopiae (Rhodophyta, Gigartinales) from Pacific Canada in relation to changes in abiotic variables | Scrosati R. | 13 | 457–460 | NO | Completo | Rodofitas | abiotic variables, carrageenophyte, Gigartinales, interannual variability, intertidal zone, Mazzaella cornucopiae, population dynamics, Rhodophyta | The seaweed Mazzaella cornucopiae (Postels & Ruprecht) Hommersand is common in rocky intertidal areas from Pacific Canada and is a potential economic resource. In both 1993 and 1994, the abundance of M. cornucopiae from |
Ficha | Morphological plasticity and apparent loss of apical dominance following the main apex in Pterocladiella capillacea (Rhodophyta, Gelidiales) fronds | Scrosati R. | 41 | 96-98 | NO | Completo | Rodofitas | ||
Ficha | Mechanisms of recolonization of the clonal intertidal alga Mazzaella cornucopiae (Rhodophyta, Gigartinaceae) after disturbances | Scrosati R. | 76 | 1717–1724 | NO | Completo | Rodofitas | demography, disturbance, Gigartinaceae, Mazzaella cornucopiae, mortality, recolonization, recruitment. | The recolonization of the clonal intertidal alga Mazzaella cornucopiae (Postels et Ruprecht) Hommersand is considered here, as part of a larger project on its population ecology. Recolonization in Barkley Sound, Pacific Can |
Ficha | Demography of gnenets of clonal red seaweeds: current limitations and solutions using genetic markers from experimental populations | Scrosati R. | NO | Rodofitas | |||||
Ficha | The relationship between stand biomass and frond density in the clonal alga Mazzaella cornucopiae (Rhodophyta, Gigartinaceae) | Scrosati and et.al. | 259-265 | NO | Completo | Rodofitas | biomass-density relationship, Gigartinacaea, Mazzaella cornucopiae, seaweed, self-thinning | ||
Ficha | Dynamicsof the biomass-density relationship and frond biomass inequality for Mazzaella cornucopiae (Gigartinaceae, Rhodophyta): implications for the understanding of frond interactions | Scroati R. and R. E. Dewreede | 36 | 506-516 | NO | Liga perdida | Rodofitas | ||
Ficha | Persistence of gametophyte predominance in Chondrus crispus (Rhodophyta, Gigartinaceae) from Nova Scotia after 12 years | Scroasati R. & B. Mudge | 519 | 215–218 | NO | Completo | Rodofitas | Chondrus, gametophyte, Gigartinaceae, G:T ratio, long-term study, tetrasporophyte | Gametophytes predominated clearly over tetrasporophytes in an intertidal population of Chondrus crispus at Tor Bay (Nova Scotia, Canada) in the summer of 1991. Since this species is perennial and the rocky substrate is stab |
Ficha | Notes on the marine algae of the Bermudas. 7. Additions to the flora including Chondracanthus saundersii sp. nov. (Rhodophyta, Gigartinaceae)based on rbcL sequence analysis | SCHNEIDER CRAIG W. AND CHRISTOPHER E. LANE | 44 | 72–83 | NO | Liga perdida | Rodofitas | Ten species are added to the benthic marine algal flora of the Bermuda islands: Caulerpella ambigua, Champia salicornioides, Chondracanthus saundersii sp. nov., Dictyota pinnatifida, Gelidiella lubrica, Gelidiopsis planicau | |
Ficha | A synoptic review of the classification of red algal genera a half century after Kylin’s ‘‘Die Gattungen der Rhodophyceen’’ | Schneider Craig W. and Michael J. Wynne | 50 | 197–249 | NO | Completo | Rodofitas | classification; genera; Kylin; red algae; Rhodoplantae. | Classification of the red algae (Rhodoplantae) has undergone significant change since the seminal work of Harald Kylin, ‘‘Die Gattungen der Rhodophyceen,’’ a half century ago. The number of |
Ficha | CEVA. | Schereiber, M. & Cavaloc, E. | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Water quality in the Great Barrier Reef region: responses of mangrove, seagrass and macroalgal communities | Schaffelke Britta and et. al. | 51 | 279-296 | NO | no completo | General | Pollution; Mangroves; Seagrass; Macroalgae; Nutrients; Herbicides | Marine plants colonise several interconnected ecosystems in the Great Barrier Reef region including tidal wetlands, seagrass |
Ficha | Assessing red algal supraordinal diversity and taxonomy in the context of contemporary systematic data | Saunders Gary W. and Max H. Hommersand | 91 | 1494-1507 | NO | Liga perdida | Rodofitas | Bangiophyceae; Compsopogonophyceae; Cyanidiophyta; Eurhodophytina; Florideophyceae; Metarhodophytina; Rhodophyta; Rhodoplantae. | The wondrously diverse eukaryotes that constitute the red algae have been the focus of numerous recent molecular surveys and remain a rich source of undescribed and little known species for the traditional taxonomist. Molec |
Ficha | Small-subunit rDNA sequences from representatives of selected families of the Gigartinales and Rhodymeniales (Rhodophyta). 3. Delineating the Gigartinales sensu stricto | Saunders Gary W. and et. al. | 82 | 43–74 | NO | Completo | Rodofitas | Corynocystaceae, Cryptonemiales, Florideophyceae, Gigartinales, Rhodymeniales, systematics. | Nuclear small-subunit ribosomal DNA sequences were determined for 65 members of the Gigartinales and related orders. With representatives of 15 families of the Gigartinales sensu Kraft and Robins included for the first |
Ficha | A chronicle of the convoluted systematics of the red algal orders Palmariales and Rhodymeniales (Florideophyceae, Rhodophyta) | SAUNDERS GARY W. | ene-16 | NO | Completo | Rodofitas | Acrochaetiales, Camontagnea, Florideophyceae, Meiodiscus, Palmaria, Palmariaceae, Palmariales, phylogeny, Rhodophysema, Rhodophysemataceae, Rhodophyta, Rhodothamniella, Rhodothamniellaceae, systematics | ||
Ficha | Late Hauterivian coralline algae (Rhodophyta, Corallinales) from the Iberian Chain (E Spain). Taxonomy and the evolution of multisporangial reproductive structures | Sara Tomás, Julio Aguirre, Juan C. Braga, Carles Martín-Closas | 53 | 79-95 | NO | Completo | General | Hauterivian . Corallines . Rhodophyta . Maestrat Basin . Phylogeny . Taxonomy | Upper Hauterivian reefal carbonates of the Llacova Formation (Maestrat Basin, Iberian Chain, E Spain) contain Sporolithon phylloideum (Bucur and Dragastan) Tomas, Aguirre, Braga and Mart ? ??n-Closas comb. no |
Ficha | Population modelling of Gelidium sesquipedale (Rhodophyta, Gelidiales) | Santos R. & M. Nyman | 10 | 261–272 | NO | Completo | Rodofitas | Gelidium sesquipedale, population models, demography, population growth rate, elasticity analysis, projection matrix model, Stella model | A matrix population model of Gelidium sesquipedale, a commercial agarophyte from the Northeast Atlantic, was developed based on demographic data obtained during two years in a commercial stand of Cape Espichel, Portugal. G. |
Ficha | SIZE INCREMENTS DUE TO INTERINDIVIDUAL FUSIONS: HOW MUCH AND FOR HOW LONG? | Santelices, B., Alvarado, J. L., & Flores, V. | 46 | 685-692 | NO | Liga perdida | Rodofitas | axis differentiation; coalescence; Gracilaria; growth after fusion; interindividual fusions; marginal meristem; Mazzaella | Size increments following interindividual fusions appear as a general benefit for organisms, such as coalescing seaweeds and modular invertebrates, with the capacity to fuse with conspecifics. Using sporeling |
Ficha | Water movement and seasonal algal growth in Hawaii. | Santelices, B. | 43 | 225-235 | 3858 | no completo | Sin asignar | The biomass distribution of frondose algae on a Hawaiian reef varied from a period of minimum biomass (635 g wet weight m-2) during July-September to a period of maximum biomass (1,554 g m-2) during February-May. The pattern of variation had no significan | |
Ficha | Patterns of organizations of intertidal and shallow subtidal vegetation in wave exposed habitats of central Chile. | Santelices, B. | 192 | 35-57 | NO | parcialmente sin liga | Sin asignar | Wave-exposed rocky intertidal habitats of central Chile exhibit zonation of algal morphologies rather than strict patterns of species zonation. In low shore areas, there is a vertical sequence of perennial belts of calcareous crusts, kelp-like forms and e | |
Ficha | Contact responses between spores and sporelings of different species, karyological phases and cystocarps of coalescing Rhodophyta | Santelices Bernabe and et. al. | 143 | 381–392 | NO | Completo | Rodofitas | Coalescence is a well documented event in many red algal orders. However, it is as yet unknown if genetic compatibility and phylogenetic relationships could be factors limiting coalescence. Using controlled&n | |
Ficha | Competitive algal community organization in exposed intertidal habitats from central Chile | Santelices Bernabé and et. al. | 6 | 267-276 | NO | parcialmente completo con liga | General | Measurements of cover in the field indicate that most of the lower intertidal wave- Codjum d~rnorphum. Summer bleaching of the C. dimorphu | |
Ficha | Banks of microscopic forms and survival to darkness of propagules and microscopic stages of macroalgae | Santelices Bernabe and et. al. | 75 | 547-555 | NO | no completo | General | benthic algae, dark tolerance, germination, growth, microscopic forms. | Previous studies have found that the number of species conforming a bank of microscopic forms in tide pools in central |
Ficha | A bank of microscopic forms on disturbed boulders and stones in tide pools | Santelices Bernabé and et. al. | 129 | 215-228 | NO | no completo | General | Banks of microscopic forms - Disturbance - Diversity - Seaweed - Species-area relationship | Disturbed marine habitats contain banks of microscopic forms that develop into macro- |
Ficha | The fate of overgrown germlings in coalescing Rhodophyta | Santelices Bernabe and et. al. | 43 | dic-18 | NO | Completo | Rodofitas | The overgrowth of young sporelings by older and larger thalli is often assumed to result in death of the overgrown individual. However, if sporelings and larger conspecifics are able to coalesce, the fate of the overgr | |
Ficha | The effects of coalescence on survival and development of Mazzaella laminarioides (Rhodophyta, Gigartinales) | Santelices Bernabé and et. al. | 23 | 395–400 | NO | Completo | Rodofitas | Coalescence . Cluster of initials . Erect axis formation . Growth long-term effects. Mazzaella . Survival | The potential benefits associated with coalescence in red algae have been best documented with early stages of development. In this study, we report on the effects of the original number of spores on branching and |
Ficha | Field testing of inter- and intraspecific coalescence among mid-intertidal red algae | Santelices Bernabé and et. al. | 250 | 91–103 | NO | Completo | Rodofitas | Chimerism · Coalescence · Competition · Algae shape · Intertidal habitats · Mazzaella · Nothogenia · Red seaweeds | Although spores, sporelings and juveniles of many ecologically important and competitively dominant seaweed species inhabiting intertidal and shallow subtidal habitats may coalesce, it is unknown whether coalescence am |
Ficha | RECENT ADVANCES IN FERTILIZATION ECOLOGY OF MACROALGAE | Santelices Bernabé | 38 | 04-oct | NO | no completo | Cultivo | broadcasters; brooders; gene flow; fertilization frequency; massive gamete release; sea- weeds; polyspermy blocks; sperm competition; win- dow of opportunity | Our understanding of natural patterns of fertiliza- last 10 years due to new approaches and methods to characterize the nature and frequency of fertiliza- |
Ficha | A comparison of ecological responses among aclonal (unitary), clonal and coalescing macroalgae | Santelices Bernabe | 300 | 31– 64 | NO | no completo | General | Aclonal seaweeds; Body size; Clonal seaweeds; Coalescing seaweeds; Chimerism; Competition; Ecological responses; Herbivory | Based on growth patterns, regeneration capabilities and genetic make up, benthic macroalgae |
Ficha | Isabella Aiona Abbott (obituario) | Santelices Bernabe | NO | parcialmente completo con liga | General | ||||
Ficha | Mosaicism and chimerism as components of intraorganismal genetic heterogeneity | Santelices Bernabe | 17 | 1187–1188 | NO | parcialmente completo con liga | General | ||
Ficha | Taxonomic review of the species of Pterocladia (Gelidiales, Rhodophyta) | Santelices Bernabe | 10 | 237–252 | NO | Completo | Rodofitas | Gelidiella, Gelidium, Pterocladia, Pterocladiella, taxonomy | Segregating Pterocladiella from Pterocladia stimulated new taxonomic studies of the species originally assigned to Pterocladia. A total of 28 species are ascribed to the genus, one of them with doubts. Thirteen of the 27 na |
Ficha | Implications of clonal and chimeric-type thallus organization on seaweed farming and harvesting | Santelices Bernabe | 13 | 153–160 | NO | no completo | General | clones, coalescence, harvesting, farming, seaweeds | Clonal seaweeds are capable of regrowing from thallus fragments, while unitary seaweeds lack this capacity. This |
Ficha | Parviphycus, a new genus in the Gelidiellaceae (Gelidiales, Rhodophyta) | Santelices Bernabe | 25 | 313-326 | NO | Completo | Rodofitas | Algae, Gelidiales, Gelidiellacaea, pannosa-type stichidia, Parviphycus, Rhodophyta | |
Ficha | The discovery ofkelp forests in deep-water habitats oftropical regions | Santelices Bernabe | NO | Kelp | |||||
Ficha | Intra-elonal variation in the red seaweed Gracilaria chilensis | Santelices B.& D. Varela | 116 | 543-552 | NO | parcialmente completo con liga | Rodofitas | The phenotypic plasticity often found in seaweed populations has been explained only from the perspective of inter-population or inter-individual differences. However, many seaweeds grow and propagate by fragmentation of ge | |
Ficha | A harvesting strategy for Iridaea Laminarioides in central Chile | Santelices B. and R. Norambuena | 329-333 | 2637 | Completo | Rodofitas | seaweed, Iridaea, harvesting, Iridaea prodiction, carrageenan production | ||
Ficha | DEMOGRAPHIC CONSEQUENCES OF COALESCENCE IN SPORELING POPULATIONS OF MAZZAELLA LAMINARIOIDES (GIGARTINALES, RHODOPHYTA | Santelices B. and J.L. Alvarado | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Recruitment, growth and survival of Lessonia nigrescens (Phaeophyta) at various tidal levels in exposed habitats of central Chile | Santelices B. and F.P. Ojeda | 19 | 73-82 | NO | parcialmente completo con liga | Feofita | Mortality effects of ecological factors have generally not been tested in field population | |
Ficha | CONVERGENT BIOLOGICAL PROCESSES IN COALESCING RHODOPHYTA | Santelices B. and et. al. | 35 | 1127–1149 | NO | Completo | Rodofitas | Ahnfeltiopsis; chimeric individuals; Chondrus; coalescing Rhodophyta; Gracilaria; Mazzaella; Sarcothalia; sporeling coalescence | Sporeling coalescence in Gracilaria chilensis Bird, McLachlan et Oliveira produces genetically polymorphic, chimeric individuals. If this is common in red algae, it may have significant biological consequences. In |
Ficha | Sporeling coalescence and intraclonal variation in Gracilaria chilensis (Gracilariales, Rhodophyta) | Santelices B. and et. al. | NO | Rodofitas | |||||
Ficha | Group recruitment and early survival of Mazzaella laminarioides | Santelices B. and D. Aedo | 18 | 583–589 | NO | Liga perdida | Rodofitas | coalescence, recruitment, Mazzaella, Ca++, spore abundance | Several phycocolloid-producing Rhodophyta of significant economic importance are coalescing species, able to fuse with conspecifics during recruitment, reach larger sizes and increase their survival. In these species spores |
Ficha | Causes and implications of intra-clonal variation in Graciaria chilensis (Rhodophyta) | Santelices B. , D. Aedo & D. Varela | 7 | 283-290 | NO | no completo | Rodofitas | intra-clonal variation, Gracilaria, spore coalescence, strain selection | Strain selection studies in Gracilaria chilensis detected significant levels of intra-clonal variation. These findings motivated more detailed studies on the causes and implications of intra-clonal variation in these and ot |
Ficha | Persistence of intraclonal variation in Gracilaria chilensis Bird, McLachlan & Oliveira (Gracilariales, Rhodophyta) through successive generations of cuttings | Santelices B. & A. Gonzalez | 75-80 | NO | no completo | Rodofitas | generation of cuttings, genetic instability, Graciñaria, intraclonal variation, somaclonal variation | ||
Ficha | A conceptual framework for marine agronomy | Santelices B. | 15-23 | NO | no completo | Cultivo | agronomic ordination, farming productivity, multi-step farming, seaweeds, site fertility | Between the late 1960s and the early 1980s, several generations of phycologists in Hawaii and the Philippines, as- This study re | |
Ficha | Mecanismo estructurados de comunidades de algas intermareales. Estudio de caso en Chile continental | Santelices B. | NO | parcialmente completo con liga | General | ||||
Ficha | How many kinds of individual are there? | Santelices B. | 14 | 152-155 | NO | no completo | General | The concept of the individual links population biology with darwinian selection. | |
Ficha | Advances in the study intraclonal variation in Gracilaria chilensis (Rhodophyta) | Santelices B. | 42 | 39-44 | NO | Completo | Rodofitas | Intra-clonal variation, Gracilaria, sporeling coalescence, genetic variability, chimeric tissues. | The search for causes of intra-clonalvariation in Gracilaria chilensis has lead to studying the effects of physiological and development factors, pathogenic infections, genetic instability and sporeling coalescence on this |
Ficha | A dichotomous species of Codium (Bryopsidales, Chlorophyta) is colonizing northern Chile | Santelices | 77 | 293-304 | NO | no completo | Clorofita | Codium, introduced species, Chlorophyta, seaweed, northern Chile. | In late 2001 and early 2002, a dichotomous species of Codium appeared colonizing the low intertidal and |
Ficha | Field testing of seaweed-pom relations: algae get a dusting | Santelices | NO | parcialmente completo con liga | Feofita | ||||
Ficha | Centrocerocolax ubatubensis Joly (Ceramiacea, Rhodophyta): A new reported parasitic form the Canary Islands. | Sansón, M., Gil-Rodríguez, M. C. & Wildpret De la Torre, W. | 1 | 151-154 | NO | parcialmente sin liga | Sin asignar | Centrocerocolax ubatubensis Joly (Ceramiaceae, Rhodophyta): una nueva especie parásita de las Islas Canarias. Centrocerocolax ubatubensis Joly, una especie parásita de la familia Ceramiaceae (Rhodophyto) es citada por primera vez para el Atlántico Orienta | |
Ficha | Datos sobre la colonización de sustratos rocosos intermareales en Las Caletillas (Tenerife, Islas Canarias). | Sanson, M., Chacana, M., & Gil-Rodríguez, M. C. | 19 | 19 A 27 | NO | parcialmente sin liga | Sin asignar | Se aportan datos sobre la colonización de superficies denudadas en la zona intermareal de Las Caletillas (S de Tenerife) yse describe la secuencia se especies instaladas en ellas a lo largo de un año y medio de estudio. Los experimentos se realizaron en l | |
Ficha | Considerations on the genus Callithamnion (Ceramiaceae, Rhodophyta) in the Canary Islands. | Sansón, M., & Gil-Rodríguez, M. C. | 159 | 139-142 | 3898 | no completo | Sin asignar | After a critical revision of the records of the Callithamnion species from the Canary Islands as well as the study of new material, the presence of six species of this genus is confirmed: C. byssoides, C. corymbosum, C. decompositum, C. hookeri, C. tetrag | |
Ficha | Usefulness of tissue nitrogen content and macroalgal community structure as indicators of water eutrophication | Sangil Kim et. al. | 26 | 1149-1158 | NO | no completo | General | Community structure . Macroalgae . Nutrient enrichment . Sewage effluent . Tissue nitrogen content | We tested the hypothesis that the community |
Ficha | Bottom–up and cascading top–down control of macroalgae along a depth gradient | Samuli Korpinen, Veijo Jormalainen, Tuija Honkanen | 343 | 52–63 | No | no completo | General | Baltic Sea; Eutrophication; Fish predation; Herbivory; Macroalgal control; Trophic cascade | On marine rocky shores, macroalgal herbivory is often intense, such that the cascading effects of fish predation may contribute |
Ficha | Identificação e Importância dos Principais Gêneros de Algas de interêsse para o Tratamento de Àguas e Esgotos | Samuel Murgel Branco, Wilma Cardinale Branco, Helena A. Dos Santos Lima, Maria Therezinha Martins | mar-59 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Dados sôbre a variaçào do nivel do Plâncton, causada pelas alteraçòes de temperatura e viscosidade da àgua | SAMUEL M RGEL BRANCO | 21 | 45-46 | 24 | no completo | Sin asignar | ||
Ficha | CULTIVO DE OSTIONES Y MACROALGAS, EN BAHÍA INGLESA Y CALETA MORA | Salinas Blanco René Horacio | NO | Cultivo | |||||
Ficha | Cultivo de Macroalgas en Bahía Inglesa, III Región | Salinas Blanco Rene Horacio | NO | Cultivo | |||||
Ficha | Cultivo de macroalga en Caleta Mora III Región | Salinas Blanco R. H. | NO | Sin asignar | |||||
Ficha | Community-wide distribution of predator–prey interaction strength in kelp forests | Sala Enric and Michael H. Graham | NO | Kelp | |||||
Ficha | morphology, molecular phylogeny and taxonomy of Nitella comptonii (Charales, Characeae) | Sakayama et. al. | 45 | 417-421 | NO | parcialmente completo con liga | Clorofita | AtpB gene; charales; charophyceae; internal transcribed spacer region; Japanesse taxa; Morphology; Nitella; comptonii; Oospores; psaBgene, rbcL gene, scanning electron microscopy, Taxonomy | |
Ficha | The role of the secondary attachment disc in the vegetative propagation of Chondracanthus chamissoi (Gigartinales; Rhodophyta) | Saez Felipe and et. al. | 01-mar | NO | Completo | Rodofitas | Carrageenan; Chile; Chondracanthus chamissoi; Propagule; Seaweed; Vegetative propagation | The reattachment and vegetative growth of tetrasporophytic and cystocarpic fronds of Chondracanthus chamissoi by means of secondary attachment discs was evaluated in vitro. Our results show that both the reattachment of fro | |
Ficha | Discos secundarios de crecimiento C. chamisoi | Saez and et. al. | 0 | NO | Rodofitas | ||||
Ficha | Culture studies of Dictyosphaeria (Chlorophyceae, Siphonocladales) II. Morphological analysis of segregative cell division in Dictyosphaeria cavernosa | Sachito Enomoto, Terumitsu Hori, and Kazuo Okuda | 103-112 | NO | Liga perdida | Sin asignar | Chlorophyceae ; coenocyte ; Dictyosphaeria cavernosa ; segregative cell division; Siphonocladales. | The entire process of " segregative cell division " characteristic of the siphonocladalean algae was followed in the laboratory cultured material of the coenocytic marine green alga Dictyosphaeria cavernosa. Cell divisions both in the unicellular vesicles | |
Ficha | Culture studies of Dictyosphaeria (Chlorophyceae, Siphonocladales) I. Life history and morphogenesis of Dictyosphaeria cavernosa | Sachito Enomoto and Kazuo Okuda | 225-236 | NO | Liga perdida | Sin asignar | Chlorophyceae; Dictyosphaeria cavernosa; life history, morphogenesis; reproduction; Siphonocladales ; Valoniaceae. | The life history of the marine green alga Dictyosphaeria cavernosa (FORSSK.) BOERGESEN from the southwestern part of Japan was studied by laboratory culture experiments and field observation. Plants from the field kept in sterilized sea water produced rep | |
Ficha | Culture studies on artificially induced aplanospores and their development in the marine alga Boergesenia forbesii (Harvey) Feldmann (Chlorophyceae, Siphonocladales) | SACHITO ENOMOTO AND HIROYUKI HIROSE | 119-122 | NO | Liga perdida | Sin asignar | When the vegetative thallus of the gigantic unicellular marine alga, Boergesenia forbesii, is either placed in concentrated sea-water (X2.0) or subjected to mechanical stimulation (pinching with a pincette or probing with a fine glass needle), its protopl | ||
Ficha | On the Life-History of A.nacdyomene wrightii with Special Reference to the Reproduction, Development, and Cytological Sequences | Sachito Enomoto and Hiroyuki Hirose | 270-280 | NO | Liga perdida | Sin asignar | The sexual and asexual reproduction, development and cytology of a marine alga, Anadyomene wrightii have been studied by culture experiments. The plants produced and liberated swarmers at 23°, 2500 lux, 14 hr light, 10 hr dark condition. There are three t | ||
Ficha | A Plastid of Probable Green Algal Origin in Apicomplexan Parasites | Sabine Köhler et. al. | 275 | 1485-1489 | NO | no completo | General | Protozoan parasites of the phylum Apicomplexa contain three genetic elements: the nuclear and mitochondrial genomes characteristic of virtually all eukaryotic cells and a 35-kilobase circular extrachromosomal DNA. | |
Ficha | A New Approach for Detecting and Mappaing Sewage Impacts | S.D. Cstanzo and et. all. | 42 | 149-156 | No | no completo | General | Bioindicator; enviromental impact; isotopes; nutrients; pollution monitoring; sewage. | |
Ficha | Presencia de Porphiridium Cruentium (Smith y Sowerby) Näg. en Argentina | S.A. Guarrera | ND | 55 | no completo | Sin asignar | |||
Ficha | PHOTOSYNTHETIC PIGMENTS OF SYMBIOTIC DINOFLAGEL LATES (ZOOXANTHELLAE) FROM CORALS AND CLAMS | S. W. JEFFREY AND F. T. HAXO | No | no completo | General | 1. The photosynthetic pigments of the brown symbiotic algae (zooxanthellae) | |||
Ficha | Field determination of the critical nutrient concentrations for cladophora in streams and their importance in waste load management | S. L. Wong and B. Clark | No | no completo | General | Many streams in Southern Ontario are seriously infested with | |||
Ficha | EFFECTS OF NUTRIENTS, HERBIVORY, AND DEPTH ON THE MACROALGAL COMMUNITY IN THE ROCKY SUBLITTORAL | S. KORPINEN, V. JORMALAINEN, AND T. HONKANEN | 88 | 839–852 | No | no completo | General | Baltic Sea; bottom-up; community control; depth gradient; eutrophication; Fucus vesiculosus; macroalgal colonization; macroalgal consumption; nutrient enrichment; sublittoral herbivory; top-down. | We studied the interacting roles of nutrient availability and herbivory in |
Ficha | A Checklist of the Seaweeds of the Mediterranean and Atlantic Coasts of Morocco. IV. Rhodophyceae – Ceramiales | S. Benhikssoune et. al. | 46 | 55-68 | NO | Liga perdida | General | A checklist of Moroccan Ceramiales (Rhodophyceae), based on both literature records and some original data, is presented. The distribution of each taxon for this region (12 Mediterranean and 26 Atlantic localities)&nbs | |
Ficha | Effect of water motion on the cultivation of the economic seaweed Gracilaria parvispora (Rhodophyta) on Molokai, Hawaii | Ryder Erin and et. al. | 238 | 207–219 | NO | Completo | Rodofitas | Seaweed; Gracilaria; Water motion; Spores; Molokai | A cage culture system was previously developed for the red alga Gracilaria parvispora Abbott on Molokai, HI; however, yields have shown marked variation, even among cages with identical stocking rates and fertiliz |
Ficha | Classes, Collections, and Individuals | Ruth Barcan Marcus | 11 | 227-232 | 2761 | no completo | Sin asignar | ||
Ficha | Virus-Like Particles and Nuclear Inclusions in The Red Alga Porphyridium Purpureum (Bory) Drew et Ross | Russell L. Chapmun and Norm a J. Lang | 9 | 117-122 | 1487 | no completo | Sin asignar | Porphyridium purpureum | Ultrastructural examination of the unicellular red alga Porphyridium purpureum has revealed cytoplasmic and nuclear inclusions termed concentrrosomes. These bodies are morphologically distinct from the irregular membranous inclusions previously reported b |
Ficha | Grazer biomass correlates more strongly with production than with biomass of algal turfs on a coral reef | Russ G.R. | 22 | 63–67 | NO | parcialmente completo con liga | General | Algal turfs - Biomass - Coral reefs - Grazers - Production | The biomass of large herbivorous grazing fish |
Ficha | Intraspecific reproductive variation in Gelidium pusillum (Stackh.) Le Jol. (Gelidiales, Rhodophyta) from Europe | Rueness Jan & Stein Fredriksen | 10 | 253–260 | NO | Completo | Rodofitas | Gelidium, reproductive biology, chromosome number, life history, female sterility, sporeling survival | Interfertility has been demonstrated in vitro between isolates of G. pusillum from Norway, France and the British Isles, but anomalies in reproductive behaviour were observed in the two Norwegian isolates. In one of th |
Ficha | How to turn inside out | Rüdiger Schmitt and Manfred Sumper | 424 | 499-500 | NO | no completo | General | The discovery that a molecular motor of the kinesin family is involved in turning a multicellular green alga inside out might have implications for similar events in animal development. | |
Ficha | Species of Nostoc Vaucher Occurring in the Sonoran Desert in Arizona | Roy E. Cameron | 81 | 379-384 | NO | parcialmente sin liga | Sin asignar | Desierto de Sonora, Arizona; N. ellipsosporum Rabenh., N. microscopicum Carm., N. muscorum Ag., N. parmelioides Kuetz., N. pruniforme (L.) Ag. Y N. verrucosum (L.) Vauch | Seven species of Nostoc Vauch. were found in the area of the Sonoran Desert in Arizona. These included Nostoc commune Vauch., N. ellipsosporum Rabenh., N. microscopicum Carm., N. muscorum Ag., N. parmelioides Kuetz., N. pruniforme (L.) Ag., and N. verruco |
Ficha | Some aspects of the origin of diatoms and their subsequent evolution. | Round, F. E. | 14 | 483-486 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The taxonomy of the Chlorophyta. II, British | Round F.E. | 6 | 235-264 | NO | no completo | Clorofita | The taxonomy of all the algal groups possessing both chlorophyll a and b is discussed for the | |
Ficha | The taxonomy of the Chlorophyta, British | Round F.E. | NO | Clorofita | |||||
Ficha | EFFECT OF TEMPERATURE AND GRAZING ON GROWTH AND REPRODUCTION OF FLOATING MACROCYSTIS SPP. (PHAEOPHYCEAE) ALONG A LATITUDINAL GRADIENT1 | Rothausler Eva and et. al. | 45 | 547-559 | NO | no completo | Feofita | Chile; detachment; floating; graz- ing; growth; macroalgae; Macrocystis; rafting; reproduction; temperature | Macroalgal rafts frequently occur floating in oceans. These rafts are considered important dis- development. However, |
Ficha | Rotating Algal Turf Contactor Simulator | Rotating Algal Turf Contactor Simulator | 0 | NO | Cultivo | ||||
Ficha | Turf algal/sediment (TAS) mats: A chronic stressor on scleractinian corals in akumal, M | Roshan E.A.R. | NO | parcialmente completo con liga | General | ||||
Ficha | Index to the Brazilian Cryptogamic Literature | Rosa Maria Teixeira Bicudo – Carlos Eduardo de Mattos Bicudo | 5 | 125-129 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Bioprocess engineering of cell and tissue cultures for marine seaweeds | Rorrer a Gregory L. and Donald P. Cheney | 32 | nov-41 | NO | parcialmente completo con liga | Cultivo | Cell and tissue culture; Macroalgae; Photobioreactor | Seaweeds are a rich source of valuable compounds including food additives and biomedicinals. The |
Ficha | Growth of the commercial carrageenophyte Sarcothalia crispata (Rhodophyta, Gigartinales) on suspended culture in central Chile | Romo Hector and et. al. | 13 | 229–234 | NO | Completo | Rodofitas | carrageenophyte, Chile, field culture, germlings, growth, in vitro culture, irradiance, Sarcothalia crispata, temperature | Laboratory and field studies on growth of Sarcothalia crispata, which is one of the most important carrageen ophytes of Chile, were made in to assess its viability and growth in a system of suspended culture. In vitro& |
Ficha | Culture of Gigartina skottsbergii (Rhodophyta) in southern Chile. A pilot scale approach | Romo Hector and et. al. | 18 | 307-314 | NO | Completo | Rodofitas | carrageenophyte, cultivation, Gigartina, growth, Rhodophyta | In the last 10 years studies on the management and exploitation of Chilean carrageenophytes have proliferated in response to the increasing development of the local processing industry. One of the most important sources of |
Ficha | Culture of Gigartina skottsbergii (Rodophyta) in southern Chile. A pilot sacle approach | Romo Hector and et. Al. | NO | Cultivo | |||||
Ficha | Frond Size Distributions and the Effects of the Algal Canopy on the Behaviour of Ascophyllum Nodosum(L.) Le Jolis | Roger Cousens | 92 | 231-249 | 2630 | no completo | Sin asignar | Population; behaviour; canopy; laterals; initiation; mortality; growth; light; Ascophyllum | Stand sampling, field and laboratory experiments were conducted in order to examine the relationship between stand structure and individual frond behaviour in Ascophyllum nodosum (L.) Le Jolis. Size-frequency distributions were found to be extremely skewe |
Ficha | Chara connivens Salzm. ex Braun, un nuevo taxón para la flora ficológica de las Islas Canarias. | Rodríguez, M. C. G., Tejera, E. B., & Wildpret De la Torre, W. | 11 | 51-56 | NO | parcialmente sin liga | Sin asignar | In this paper the finding of a new taxon of the genus Chara L. Em. Ag., A.Br., C. Connivens Salzm. & Braun, in the islands of tenerife and Lanzarote, is announced. | |
Ficha | The epiphyte community of mangrove roots in a tropical estuary: distribution and biomass. | Rodriguez, C., & Stoner, A. W. | 36 | 117-126 | 3834 | no completo | Sin asignar | The algal community associated with roots of the red mangrove Rhizophora mangle L. bordering Laguna Joyuda estuary in Puerto Rico was investigated during June and July 1986. With a total of eight macroalgal species collected, species richness in the lagoo | |
Ficha | Consumption of drift kelp by intertidal populations of the sea urchin Tetrapygus niger on the central Chilean coast: possible consequences at different ecological levels | Rodriguez S.R. | NO | Kelp | |||||
Ficha | Gelidiales (Rhodophyta) en las costas del Pacifico mexicano con enfasis en las especies tropicales | Rodriguez D., López, N.López y J. González-González | 3 | NO | no completo | Rodofitas | |||
Ficha | RAPD differentiation of Grateloupia lanceola and the invasive Grateloupia turuturu (Gigartinales, Rhodophyta) in the Iberian Peninsula | Rodolfo Barreiro and et.al | 45 | 213-217 | NO | no completo | General | Grateloupia lanceola, Grateloupia turuturu, Iberian Peninsula, invasive seaweeds, RAPD markers | |
Ficha | Assessment of macroalgal nitrogen limitation in a seasonal upwelling region | Rodney M. Fujita, Patricia A. Wheeler, Robert L. Edwards | 53 | 293-303 | No | no completo | General | The relationship between nitrogen (N) availability and the growth of macroalgae in a | |
Ficha | Nutritional value of micro-algal mass cultures to the oyster Ostrea edulis L. | Rodhouse, P. G., Roden, C., & Somerville-Jacklin, M. E. | 32 | 11 A 18 | NO | parcialmente sin liga | Sin asignar | Mass cultures of natural phytoplankton were bloomed in outdoor tanks following nutrient enrichment. Once a bloom developed, tanks were enriched with nutrients daily and renewed at rates of 20%, 45% and 70% day-‘. The 20% flow rate culture was grown withou | |
Ficha | The Genus Codium (Codiales, Chlorophyta) at Lord Howe Island (N.S.W.) | Rod Jones and Gerald T. Kraft | 253-276 | NO | Liga perdida | Sin asignar | Five species of Codium have been found on the world's southernmost coral reef at Lord Howe Island, New South Wales (3l033'S.,159"03'E.). The genus forms, along with the brown algal order Dictyotales, a dominant marine algal group on the island. One specie | ||
Ficha | Algal Virus: Isolation | Robert S. Safferman, Mary-Ellen Morris | 140 | 679-680 | 21 | no completo | Sin asignar | Lynbya, Plectonema y Phormidium | Fresh water blue-green algae of the genera Lynbya, Plectonema, and Phormidium are susceptible to a virus recently isolated from a wastestabilization pond. Electron micrographs of a partially purified preparation show that the viral particle has an icosahe |
Ficha | The Continuing Search for Order | Robert R. Sokal | 126 | 729-749 | 2756 | no completo | Sin asignar | In this paper I review the principles for forming biological classifications and summarize recent findings concerning optimality criteria for classifications. Natural taxa are recognized as polythetic and related to concept formation in cognitive psycholo | |
Ficha | Terrestrial Plants of Panama | Robert L. Dressler | 2 | 179-186 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Distribution and ecology of Papenfussiella callitricha (Rosenv.) Kylin (Phaeophyceae, Chordariaceae) | Robert Hooper and G. Robin South | 16 | 153-157 | NO | parcialmente sin liga | Sin asignar | The range of PapenJussiella callitricha, previously regarded an endemic to south-west Greenland, is extended to include Newfoundland and Nova Scotia. Phenology and distribution of the species correlate with temperaturas below 8°C in eastern Canada, while | |
Ficha | Distribution and ecology of Papenfussiella callitricha (Rosenv.) Kylin (Phaeophyceae, Chordariaceae) | Robert Hooper and G. Robin South | 16 | 153-157 | NO | parcialmente sin liga | Sin asignar | Terranova y Nueva Escocia, Canadá; Papenfussiella callitricha | The range of Papenfussiella callitricha, previously regarded an endemic to south-west Greenland, is extended to include Newfoundland and Nova Scotia. Phenology and distribution of the species correlate with temperatures below 8°C in eastern Canada, while |
Ficha | Epiphytes on Cladophora Glomerata in The Great Lakes and St. Lawrence Seaway with Particular Reference to The Red Alga Chroodactylon Ramosum (=Asterocytis Smargdina) | Robert G. Sheath and Mary O. Morison | 18 | 385 -391 | 2821 | no completo | Sin asignar | Asterocytis; Chroodactylon; Cladophora; epiphytes; Great Lakes; Rhodophyta; St. Lawrence Seaway | The range of Cladophora glomerata along the east and north shorelines of the Great Lakes and St. Lawrence Seaway extends form just east of Montreal to Thunder Bay on Lake Superior. However, it does not occur at sites sampled in Georgia Bay, the North Chan |
Ficha | On Habitat Predictability and Algal Preadaptation to Novel Chemicals | Robert A. Michaels | 113 | 942-945 | 1455 | no completo | Sin asignar | ||
Ficha | Predation on the Isopod Crustacean Porcellio Scaber by the Theridiid Spider Steatoda Grossa | Robert A. Barmeyer | 74 | 30-36 | NO | parcialmente sin liga | Sin asignar | Pacific Grove, California | A population of the theridiid spider Steatoda grossa in Pacific Grove, California was studied to observe its predatory behavior towards the terrestrial isopod Porcellio scaber and subsidiary prey items. The isopod and spider are both found to be noctumall |
Ficha | Macroalgal communities of intertidal rock pools in the northwest coast of Portugal | Rita Araújo, I. Sousa-Pinto, I. Bárbara, V. Quintino | 192 – 202 | NO | Liga perdida | Sin asignar | Rock pools; Macroalgae; Environmental variables; Intertidal; NW Portugal | Macroalgal communities in littoral rock pools of the Northwest coast of Portugal were stu-died along 60 km of coastline. Thirty-eight pools were sampled twice between March and August 2003. Rhodophyta were the dominant algue group, whether the pools were | |
Ficha | Characterization of polysaccharides extracted from brown seaweeds | Rioux L.E. and et. al. | 69 | 530-537 | NO | no completo | Feofita | Laminaran; Fucoidan; Sodium alginate; Ascophyllum nodosum; Fucus vesiculosus; Saccharina longicruris; Polysaccharides; Seaweeds | The structural characteristics of polysaccharides extracted from Quebec’s seaweed have not been fully established to date. Ascophyl- |
Ficha | Phenology and small-scale distribution of some rhodomelacean red algae on a western Mediterranean rocky shore | Rindi Fabio & Francesco Cinelli | 35 | 115-125 | NO | Completo | Rodofitas | algal turfs, Boergeseniella, distribution, Lophosiphonia, Mediterranean Sea, phenology, Polysiphonia, Womersleyella | Distribution and phenology of some filamentous species of Rhodomelaceae in the low littoral and shallow sublittoral zones of an exposed, western Mediterranean rocky shore were studied for 1 year. The spatial distribution of |
Ficha | Effects of environmental factors on net photosynthesis and growth of intertidal specie of the genus Gelidium (Gelidiaceae, Rhodophyta) in northern Spain | Rico J.M. and S. Fredriksen | NO | Rodofitas | |||||
Ficha | Morphology and systematics of gelidiella tenuissima (Gelidiales, Rhodophyta)from Gran Canaria(CanaryIslands, Spain) | Rico J.M. and et. al. | 41 | 463-469 | NO | Completo | Rodofitas | ||
Ficha | Museums as Environmental Data Banks: Curatorial Problems Posed by an Extensive Biological Survey | Richard S. Cowan | 2 | 59-68 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Antarctic Marine Flora: Uniquely Devoid of Kelps | Richard L. Moe and Paul C. Silva | 196 | 1206-1208 | 1543 | no completo | Sin asignar | Himantothallus, Phyllogigas y Phaeoglossum. | The discovery of embryonic stages of the common large Antarctic brown seaweed Himantothallus has led to the conclusion that this plant, hitherto assigned equivocally to the Laminariales (kelps), is a member of the Desmarestiales. Moreover, field study of |
Ficha | Morphological and taxonomic studies on Antarctic Ceramiaceae (Rhodophyceae). II. Pterothamnion antarcticum (Kylin) comb. nov. (Antithamnion antarcticum Kylin) | Richard L. Moe & Paul C. Silva | 15 | ene-17 | 3247 | no completo | Sin asignar | Rhodophyceae Pterothamnion antarcticum (Kylin) peine. nov. Antithamnion antarcticum (Kylin) | Reproductive structures in Antithamnion antarctieum Kylin (Rhodophyceae: Ceramiaceae) are described for the first time. Tetrasporangia are cruciately divided and sessile, replacing first- or second-order branchlets of major and minor whorl-branches. Sperm |
Ficha | Morphological and taxonomic studies on Antarctic Ceramiaceae (Rhodophyceae). III. Georgiella and Plumariopsis (Tribe Ptiloteae) | Richard L. Moe & Paul C. Silva | 18 | 275-298 | 3218 | no completo | Sin asignar | Estructura y reproducción de Georgiella confluens (Reinsch) Kylin; Rhodophyceae | Knowledge of the structure and reproduction of Georgiella confluens (Reinsch) Kylin, the type of its genus, is amplified and clarified. The apical cell is not overtopped by lateral branches. Indeterminate axes are formed mainly from first-formed branches. |
Ficha | Minium parvum gen. et sp. nov., a crustose member of the Rhodymeniales (Rhodophyta) | Richard L. Moe | 18 | 38-46 | NO | parcialmente sin liga | Sin asignar | Minium parvum gen. et sp. nov. exists in all stages as a crust, a growth form previously unknown in the order to which it belongs-the Rhodymeniales. While members of this order exhibit a diversity of thallus form and anatomy, only erect or decumbent types | |
Ficha | Gainia and Gainiaceae, a new genus and family of crustose marine Rhodophyceae from Antarctica | Richard L. Moe | 24 | 419-428 | 3318 | no completo | Sin asignar | Antártida; Rhodophyceae marinas crustosas. | Gainia mollis gen. et sp. nov. es un alga costrosa, suave y resbalosa, de color rojo oscuro que crece en la zona infralitoral de la Península Antártica y en Antártica del Este. Los fragmentos del talo se separan fácilmente cuando se sujetan bajo presión. |
Ficha | Control of palmelloid formation in the green alga Pediastrum | Richard J. Ellis | 13 | 663-672 | 1233 | no completo | Sin asignar | Pediastrum tetras | Pediastrum tetras, normally a non-motile colony of eight cells, aggregates into large masses of up to 1500? in diameter when grown in certain nutrient media. These masses ("palmelloids") can be prevented from forming or can be dissociated into separate co |
Ficha | The Status of Knowledge of Panamanian Echinoids, 1971, with Comments on Other Echinoderms | Richard H. Chesher | 2 | 139-158 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Notes on Marine Algae of Washington and Southern British Columbia | Richard E. Norris and John West | 18 | 766 | no completo | Sin asignar | Washiington, y Sur de Columbia Británica; Thuretellopsis, Porphyropsis y Platysiphonia | Marine algae on the Pacific Coast of North America often show interesting distribution patterns beca use typicall y southern species are absent or rarely found in northern regions and northern species usually do not occur in southern waters. In recent yea | |
Ficha | Notes on Marine Algae of Washington and Southern British Columbia, II | Richard E. Norris and John A. West | 19 | 111-116 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Homothallism In Golenkinia Minutissima | Richard C. Starr | 43254 | 92 | no completo | Sin asignar | |||
Ficha | Brackish Water Species of Vaucheria (Xanthophyceae, Vaucheriales) from Louisiana and Texas | Richard A. Pecora | 6 | 25-29 | 1494 | no completo | Sin asignar | Región costera del Golfo de México; Vaucheria compacta, V. dillwynii, V. erythrospora y V. longicaulis | lnvestigations of algal mats at 10 locations along the northwestern coast of the Gulf of Mexico from Grand Terre Island, Louisiana, west to Redfish Bay, Texas, were conducted from February 1975 to July 1976. Data on distribution, habitat preference, and m |
Ficha | La Flora Bentonicamarina del Caribe de Costa Rica (Notas Preliminares) | Ricardo Soto y David L. Ballantine | 123-162 | 2514 | no completo | Sin asignar | Algae, Caribbean, Costa Rica, Taxonomy, Distribution | This paper presents an updated checklist of the benthic alqas of the Caribbean Coast of Costa Rica. A total of 262 species are included; 163 Rhodophyta, 40 Phaeophvta and 60 Chlorophyta. We report 60 new taxa: 33 species of Rhodophyta, 9 Phaeophyta incht~ | |
Ficha | RAMET DYNAMICS FOR THE CLONAL SEAWEED PTEROCLADIELLA CAPILLACEA (RHODOPHYTA): A COMPARISON WITH CHONDRUS CRISPUS AND WITH MAZZAELLA CORNUCOPIAE (GIGARTINALES) | Ricardo Scrosati and Elisa Servière-Zaragoza | 36 | 1061-1065 | NO | Completo | Rodofitas | allometry; Chondrus; clonal; Gelidiales; Gigartinales; Mazzaella; population ecology; Pterocladiella; ramet; Rhodophyta | Little is known about the dynamics and the ecological interactions among ramets (fronds) from populations of clonal red seaweeds. Small ramets are very difficult to tag, so their growth cannot be monitored di |
Ficha | DEMOGRAPHY OF GENETS OF CLONAL RED SEAWEWDS: CURRENT LIMITATIONS AND SOLUTIONS USING GENETIC MARKERS FROM EXPERIMENTAL POPULATIONS | Ricardo Scrosati | 11 | 145-155 | NO | Liga perdida | Rodofitas | clonel; demography; Gelidiales; genet; genetic markers; Gigartinales; Gracilariales; ramet; Rhodophyta | |
Ficha | The clonal seaweed Chondrus crispus as a foundation species | Ricardo A. Scrosati | 31 | 41-48 | NO | no completo | General | Chondrus; community structure; foundation species; Gigartinales; intertidal | The clonal seaweed Chondrus crispus (Rhodophyta, Gigartinales) forms extensive stands at low intertidal elevations on |
Ficha | Phylogenomics and its Growing Impact on Algal Phylogeny and Evolution | Reyes-Prieto Adrian and et. al. | 21 | 01-oct | NO | parcialmente completo con liga | General | algal evolution, endosymbiosis, genome database, genomics, phylogenomics | Genomic data is accumulating in public database at an unprecedented rate. Although presently dominated by the |
Ficha | Coastal groundwater discharge – an additional source of phosphorus for the oligotrophic wetlands of the Everglades | René M. Price, Peter K. Swart & James W. Fourqurean | 569 | 23-36 | No | no completo | General | coastal groundwater discharge, Everglades, phosphorus | In this manuscript we define a new term we call coastal groundwater discharge (CGD), which is related to |
Ficha | Biological bases for managment of Iridaea laminarloides Bory in southern Chile | Renato Westermeier et. al. | 313-328 | NO | Liga perdida | Rodofitas | Seaweed, Iridaea laminarioides, harvesting, regeneration, resource managment | ||
Ficha | A pilot-scale study of the vegetative propagation and suspended cultivation of the carrageenophyte alga Gigartina skottsbergii in southern Chile | Renato Westermeier et. al. | NO | Completo | Rodofitas | Carrageenophyte . Cultivation . Gigartina skottsbergii . Regeneration . Rhodophyta . Southern Chile | Different propagation techniques for cultivation of vegetative Gigartina skottsbergii fronds were tested using a system of suspended ropes, to which inoculants were attached. Our results showed that triangular fragments obt | ||
Ficha | The Anthropology of Eastern Panama | Reina Torres De Araúz | 2 | 229-246 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | A Metapopulation Perspective on the Patch Dynamics of Giant Kelp in Southern California | Reed Daniel C. and et. al. | NO | Kelp | |||||
Ficha | Algal Metabolism | Raven J.A. | NO | General | |||||
Ficha | Raúl Aviles - José Saúl Canjura | 1 | NO | parcialmente sin liga | Sin asignar | Hay varios artículos en este pdf pongo uno por uno o sólo la revista????? | |||
Ficha | Halodule wtigbtii ASCHERS (Potamogetonaes: Cymodoceae) EN LA BAHIA TOPOLOBAMPO, SINALOA, MEXICO | Raúl Aguilar Rosas yJesús López Ruelas | 11 | 87-91 | No | no completo | General | ||
Ficha | NUEVOS REGISTROS Y ALGUNAS NOTAS PARA LA FLORA ALGAL MARINA DE LA COSTA NOROCCIDENTAL DE BAJA CALIFORNIA, MEXICO | Raúl Aguilar Rosas et. al | 10 | 149-158 | NO | no completo | General | Se realizaron colectas de algas en la zona de entremareas en varias localidades de Baja California, en repetidos periodos de muestreo a partir de julio de 1978 hasta septiembre de 1983.Se observó la presencia de 21 e | |
Ficha | NEW REGISTERS OF MARINE ALGAE FOR THE FLORA OF BAJA CALIFORNIA, MEXICO. | Raúl Aguilar Rosas and Marco Antonio Aguilar Rosas | 12 | 17-20 | NO | no completo | General | As a result of a series of collects and ohscrrationsalong the northwestern coast uf Baja California from 1978 to the present (Aguilar Rosas et al., 1984) we found fine marine algae species which are new regis | |
Ficha | Sargassum muticum (YENDO) FENSHOLT (FUCALES, PHAEOPHYTA) IN BAJA CALIFORNIA COASTS, MEXICO. | Raúl Aguilar Rosas and Luis E. Aguilar Rosas | 11 | 127-129 | NO | no completo | General | ||
Ficha | Haloduk wrigbtii ASCHERS (Potamogetomdes: Cymodoceae) IN TOPOLOBAMPO BAY, SINALOA, MEXICO. | Raúl Aguilar Rosas and Jesús López Ruelas | 11 | 87-91 | NO | no completo | General | We report new evidente on the presente of Halodue wtightii Aschers., in the southem part of the Gulf of California (Sea of Cortes) The population found in Topolobampo Bay, Sinaloa, is 490 km south of the first and | |
Ficha | NUEVOS REGISTROS DE ALGAS MARINAS PARA LA FLORA DE BAJA CALIFORNIA, MEXICO. | Raúl .4guilar Rosas y Marco Antonio 4guilar Rosas | 12 | 17-20 | No | no completo | General | ||
Ficha | IS THERE AN ECOPHYSIOLOGICAL EXPLANATION FOR THE GAMETOPHYTE– TETRASPOROPHYTE RATIO IN GELIDIUM SESQUIPEDALE (RHODOPHYTA)? | Raquel Carmona and Rui Santos | 42 | 259-269 | NO | no completo | General | ecophysiological differentiation; frond re-attachment; gametophyte: tetrasporophyte ratio; Gelidium sesquipedale; recruitment; spore vital rates | In the fall, when 61% of the fronds of the Gelid- located in Albufeira (southern Portugal) were re- |
Ficha | Notes on Three Bermudian Marine Algae | Randolph Taylor | 277-283 | NO | Liga perdida | Sin asignar | |||
Ficha | Pacific marine algae of the allan hancock expeditions to the Galapagos Islands | Randolph T. W. | NO | parcialmente completo con liga | General | ||||
Ficha | Relative effects of grazers and nutrients on seagrasses: a meta-analysis approach | Randall Hughes A. | 282 | 87–99 | NO | no completo | General | Seagrasses · Meta-analysis · Epiphyte · Nutrients · Grazers · Management · Eutrophication · Top-down/bottom-up | Recent large-scale seagrass declines have prompted experimental investigations of potential mechanisms. Although many studies have implicated eutrophication or reductions of epi- |
Ficha | La vegetación acuática vascular de seis lagos-crater del estado Puebla, México. | Ramírez-García, P., & Novelo, A. | 46 | 75-88 | NO | parcialmente sin liga | Sin asignar | Las aguas de los seis lagos presentan una elevada concentración de sales y fueron divididos en dos grupos de acuerdo a la concentración de las mismas: el primero, denominado "concentrados" o "salinos'', formado por los lagos Alchichica y Atexcac y el segu | |
Ficha | Flora algal de rios templados en la zona occidental de la cuenca del Valle de Mexico | Ramirez V.M. and E.A. Cantoral Uriza | 74 | 143-194 | NO | no completo | General | ríos, algas, Rhodophyta, Xanthophyceae, Cyamoprokaryota, Chlorophyta, Bacillariophyceae, nuevos registros, Cuenca del Valle de México, México. | |
Ficha | Microhabitat and morphometric variation in two species of Prasiola (Prasiolales, Chlorophyta) from streams in central Mexico | Ram?rez Rodr?guezRoc?o and et. al. | 41 | 161-168 | NO | no completo | Clorofita | Ecology Freshwater algae Microhabitat Morphometric variation Temperate streams Mexico | Prasiolales are characterized by high morphological plasticity. This problem in taxo- of environment heterogeneity. Habitat character- |
Ficha | Phycology | Ralph A Lewin, Michael A Borowitzka | 01-oct | NO | Liga perdida | Sin asignar | The study of algae is generally called ‘phycology’, from the Greek word phykos meaning ‘seaweed’. Just what algae are is difficult to define, because they belong to many different and unrelated classes including both prokaryotic and eukaryotic representat | ||
Ficha | Tissue culture and regeneration of thallus from callus of Gelidiella acerosa | Rajakrishna Kumar G. and et. al. | 43 | 596-602 | NO | no completo | Rodofitas | ||
Ficha | A molecular phylogeny of the marine red algae (Rhodophyta) based on the nuclear small-subunit rRNA gene | RAGAN MARK A. and et. al. | 91 | 7276-7280 | NO | Completo | Rodofitas | Bangiophycidae - Florideophycldae - taxonomy - Kishino-Hasegawa test - Tempkton-Felsenstein test. | A phylogeny of marine Rhodophyta has been inferred by a number of methods from nucleotide sequences of nuclear genes encoding small subunit rRNA from 39 species in 15 orders. Sequence divergences are relative |
Ficha | Biological bases for management of iridaea laminarioides Bory in southern Chile | Ragan M.A. and C.J. Bird | NO | Rodofitas | |||||
Ficha | The ups and downs of benthic ecology: considerations of scale, heterogeneity and surveillance for benthic–pelagic coupling | Raffaelli Dave and et. al. | 191– 203 | NO | no completo | General | |||
Ficha | The non symbiotic origin of mitochondria. | Raff, R. A., & Mahler, H. R. | 177 | 575-582 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | En Defensa de la Taxonomía | Rafael Lamothe-Argumedo | 52 | 481-483 | 2754 | no completo | Sin asignar | ||
Ficha | Botanic Gardens and Arboreta | Radford | 2755 | no completo | Sin asignar | ||||
Ficha | A comparison of two rearing sites of the giant kelp Macrocystis integrifolia in Sitka Sound, Alaska | Rabung Samuel H. | NO | Kelp | |||||
Ficha | DESMIDS FROM UGADA AND LAKE VICTORIA | R0LF GR0NBLAD, ARTHUR M. SC0TT AND HANNAH CROASDALE | No | no completo | General | ||||
Ficha | The role of nutrients in regulation and promotion of harmful algal blooms in upwelling systems | R.M. Kudela, S. Seeyave, W.P. Cochlan | 85 | 122–135 | No | no completo | General | The Core Research Project on HABs in upwelling systems, as a component project of the international sci- | |
Ficha | Physiological Ecology of Four Polysiphonia Species (Rhodophyta, Ceramiales) | R.A. Fralick and A.C. Mathieson | 29 | 29-36 | NO | parcialmente sin liga | Sin asignar | New Hampshire, EE. UU.; Polysiphonia | Photosynthesis and respiration of 4 species of the marine red algal genus Polysiphonia were evaluated under a variety of light, temperature and salinity conditions. The manometric results were compared with the local distribution and abundance of each spe |
Ficha | Annulate Lamellae in Postfertilization Development in Polysiphonia novae-angliae (Rhodophyta) | R. Wetherbee, J.A. West, and M.J. Wynne | 49 | 401-404 | 780 | no completo | Sin asignar | Polysiphonia novae-angliae | Annulate lamellae (AL) are observed following fertilization in the red alga Polysiphonia novae-angliae. Intranuclear AL are single and scattered in the nucleoplasm. Cytoplasmic AL are single, stacked, or in a circular configuration. The AL are generally s |
Ficha | Seasonal variation in the concentrations of nutrients in two green macroalgae and nutrient levels in sediments in the R? ?as Baixas (NW Spain) | R. Villares, A. Carballeira | 58 | 887-900 | NO | no completo | General | Ulva; Enteromorpha; sediments; nutrients; eutrophication; Spain | Seasonal monitoring of the levels of carbon, nitrogen and phosphorus in two green macroalgae (Ulva and Enteromorpha) was |
Ficha | Experimental tank cultivation of Gracilaria chihsis in central Chile | R. Ugarte and B. Santelices | 101 | 7-16 | NO | no completo | General | Gracilaria chilensis was grown continuously in tanks over a 13-month period, changing the water only every I5 days, and adding CO2. air and nutrients. Biomass production was markedly seasonal, with a summer maximum of 100 g m-2 day-2 (wet) an | |
Ficha | Taxonomic Notes on Marine Algae from Malaysia III. Seven Species of Rhodophyceae | R. Terada, S. Kawaguchi, M. Masuda and S. M. Phang | 347-357 | NO | Liga perdida | Sin asignar | Six species of marine red algae are reported from Malaysia for the first time and their characteristic features are described: one species of the Halymeniaceae (Cryptonemiales), Cryptonemia crenulata (J. Agardh) J. Agardh; two species of the Solieriaceae | ||
Ficha | Preliminary Studies on the Growth of Selected ‘Green Tide’ Algae in Laboratory Culture: Effects of Irradiance, Temperature, Salinity and Nutrients on Growth Rate | R. Taylora, R. L. Fletcher and J. A. Raven | 44 | 327-336 | No | no completo | General | During the summer months, Langstone Harbour, a eutrophic inlet on the south coast of England, is | |
Ficha | Controlled Manipulations in the Marine Interdial Zone and their Contributions to Ecological Theory | R. T. Paine | NO | parcialmente sin liga | Sin asignar | ||||
Ficha | Cultural Observations on the Morphology, Reproduction and Cytology of a Freshwater Red Alga Compsopogon Mon. from India | R. Shyam and Y.S.R. K. Sarma | 32 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The Caribbean’s western- most algal ridges in Cozumel, Mexico | R. S. Steneck et. al. | 22 | 27-28 | NO | no completo | General | ||
Ficha | Observations on Phagocytosis of Coccomyxa parasitica (Coccomyxaceae; Chlorococcales) in Hacopecten magel/anicus l | R. N. STEVENSON AND G. ROBIN SOUTH | 25 | 307.-311 | No | no completo | General | Phagocytosis of Coccom~.xa parasilica in Placopecten magellanicus is described. Host phagocytosis occurs throughout the infective process and can also be demonstrated experi- | |
Ficha | Observations on Phagocytosis of Coccomyxa parasitica (Coccomyxaceae; Chlorococcales) in Placopecten magellanicus l | R. N. Stevenson and G. Robin South | 25 | 307-311 | NO | Liga perdida | General | Phagocytosis of Coccomyxa parasilica in Placopecten magellanicus is described. Host phagocytosis occurs throughout the infective process and can also be demonstrated experimentally using cultured algae. Agranular and g | |
Ficha | The Griffithsieae Group of the Ceramiaceae (Rhodophyta) and its Southern Australian Representatives | R. N. Baldock | 24 | 509-593 | NO | parcialmente sin liga | Sin asignar | G. corallinoides, G, tenuis C. Agardh y G. barbata C. Agardh, Anotrichium Naegeli | The genus Griffithsia C. Agardh, with its type species G. corallinoides (L.) Batters, is characterized by subdichotomous filaments of large multinucleate cells; by a fertile axis of three small discoid cells of which the subapical cell produces 1(-2) proc |
Ficha | Sobre dos supuestas Protofitas | R. Margalef | 1 | 06-jul | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The culture of benthic marine algae in the laboratory and the field | R. M. Smith and W. E. Jones | 20 | 62-69 | NO | parcialmente sin liga | Sin asignar | Anglesey, Reino Unido; Rhodophyceae | 1. Growth and development of algae from spores has been observed in the laboratory (Menai Bridge) and under field conditions at Ravenspoint (West coast of Anglesey). Attempts were made to culture all main components of the sub-littoral flora. Spore materi |
Ficha | Alternative Dynamic Regimes for Canopy-Forming Kelp: A Variant on Density-Vague Population Regulation | R. M. Nisbet and J. R. Bence | 134 | 377-408 | 2635 | no completo | Sin asignar | Different populations within at least some species show a range of qualitatively different population dynamics. Motivated by such an observation for giant kelp, we ask if a single set of underlying biological processes could be responsible for the differe | |
Ficha | Sporangia in the brown algal genus Desmarestia with special reference to Antarctic D. Ligulata | R. L. Moe and P. C. Silva | 25 | 159-167 | 1545 | no completo | Sin asignar | A critical review of the literature on sporangia in Desmarestia revealed scanty but important information. Variation in sporangial development and disposition ranges from the direct metamorphosis of scattered superficial cortical cells to the production o | |
Ficha | A Contribution on the Toxicity of Algae | R. E. Wheeler, James B. Lackey and Stuart Schott | 57 | 1695-1701 | 5 | no completo | Sin asignar | 1. Freshly collected Microcystis aeruginosa was found to be somewhat toxic for mice and guinea pigs when given parenterally but to be slightly, if at all, toxic when given by mouth. 2. Frozen, or frozen and vacuum dried, Microcystis aeruginosa was found t | |
Ficha | Gametangial Constants of Extant Charophyta for Use in Micropaleobotany | R. D. Wood | 33 | 186-194 | No | no completo | General | Descriptive data on extant species of Charophytes have been compiled, | |
Ficha | Illustrated Revised Classification of the Characeae | R. D. Wood | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | http://biomar.fciencias.unam.mx/Sobretiros/2019/informacion%202019/1.%20LITERATURA%20NUTRIENTES%20BAJO%20AN%c3%81LISIS/1.%20CARPETAS%20SIN%20DATOS%20-%20130%ef%80%a8/Long%20time%20studies-%203/2010.%20Babcock%20etal.%20Decadal%20trends%20in%20marine%20res | R. C. Babcocka, etal. | 1-6 | No | no completo | General | fishing effects | interactions | time lags | trophic cascade | marine protected area | Decadal-scale observations of marine reserves suggest that indirect | |
Ficha | Decadal trends in marine reserves reveal differential rates of change in direct and indirect effects | R. C. Babcocka, etal. | 1-6 | No | no completo | General | fishing effects | interactions | time lags | trophic cascade | marine protected area | Decadal-scale observations of marine reserves suggest that indirect | |
Ficha | Unusual mitosis in the red alga Porphyridium purpureum | R. Bronchart, V. Demoulin | 268 | 80-81 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Reevaluation of mitosis in the red alga Porphyridium purpureum | R. Bronchart, V. Demoulin | 283 | 409-410 | 3339 | no completo | Sin asignar | ||
Ficha | Molecular biotechnology of marine algae in China | Qin Song and et. al. | 512 | 21–26 | NO | parcialmente completo con liga | General | genetic engineering, marine algae, molecular biotechnology, molecular genetic marker | Molecular biotechnology of marine algae is referred to as the biotechnology on the identification, modification, |
Ficha | Algal Chloroplasts | Purton Saul | 01-sep | NO | no completo | General | A great diversity of chloroplasts is found amongst the various algal groups. This diversity | ||
Ficha | Valuable products from biotechnology of microalgae | Pulz Otto and Wolfgang Gross | 65 | 635-648 | NO | parcialmente completo con liga | Fitoplancton | The biotechnology of microalgae has gained | |
Ficha | Decalcification during epithallial cell turnover in Jania adhaerens (Coralinalles, Rhodophyta) | Pueschel C.M. and et. al. | 44 | 156-162 | NO | Liga perdida | Rodofitas | Epithallial cells of the coraline red algae are characterized by structural specializations that include deep invarginations of the dista cell surface, and by a unique developmental pattern that culmunates in senescence, sh | |
Ficha | Specialized calciferous cells in the marine alga Rhodogorgon carriebowensis and their implications for models of red algal calcification | Pueschel C. M. and et. al. | 166 | 89- 98 | NO | Liga perdida | Rodofitas | Calcification; Calcium carbonate; Rhodogorgon; Red algae. | Calcification in Rhodogorgon carriebowensis J. Norris et Bucher was associated with a particular cell type in the cortex. Calciferous cells were 4-6 times the length of cortical assimilatory cells. The distal two- |
Ficha | Polyphysa parvula (Solms-Laubach) Schnetter & Bula Meyer (Dasycladaceae, Chlorophyta) en la Región Macaronesica. | Prud'homme van Reine, W. F., Gil-Rodríguez, M. C., Hauroum T., R., Carrillo, J. M. A., & Wildpret De la Torre, W. | 13 | 219-224 | 3880 | no completo | Sin asignar | The distribution of Polyphysa parvula (Solms-Laubach) Schnetter G Bula Meyer, Dasycladaceae has been ampliates to three Archipelagos of Marconesian region (Madeira, Canary Islands and Cape verde Islands) being collected until now only in the island of Gra | |
Ficha | Tracking the invasive history of the green alga Codium fragile ssp. Tomentosoides | PROVAN JIM, SUSAN MURPHY and CHRISTINE A. MAGGS | 14 | 189-194 | NO | no completo | Clorofita | Codium fragile, invasive species, phylogeography | The spread of nonindigenous species into new habitats is having a drastic effect on natural ecosystems and represents an increasing threat to global biodiversity. In the marine environ- |
Ficha | Universal plastid primers for Chlorophyta and Rhodophyta | PROVAN JIM, SUSAN MURPHY AND CHRISTINE A. MAGGS | 39 | 43-50 | NO | parcialmente completo con liga | Clorofita | Chlorophyta, chloroplast, genetic markers, plastid, Rhodophyta, universal primers | To date, the majority of molecular genetic studies in algae have utilized a fairly limited range of markers such as the plastid |
Ficha | A subtidal algal turf community | Preskitt L. | NO | Fitoplancton | |||||
Ficha | Estudio citogenetico de macroalgas marinas con posibilidad de explotacion | Ponce-Marquez M.E. | NO | parcialmente completo con liga | General | ||||
Ficha | Antifouling activity as a function of population variation in Sargassum vulgare from the littoral of Rio de Janeiro (Brazil) | Plouguerné Erwan and et. al. | 22 | 717-724 | NO | no completo | Feofita | Antifouling . Biofilms . Sargassum vulgare . Perna perna . Geographical variation . Polyphenols | The brown seaweed Sargassum vulgare is abun- conducted, in which algae were collected at five locations |
Ficha | Physical forcing and phyutoplankton distributions | Platt T. and et. al. | NO | Fitoplancton | |||||
Ficha | MODIFICACION DE PROYECTO TECNICO: CULTIVO DE Macrocystis pyrifera EN SISTEMA SUSPENDIDO | PLANCTON ANDINO LTDA | NO | Cultivo | |||||
Ficha | ESTUDIO POBLACIONAL DE MACROCYSTIS PYRIFERA (L.) C. AGARDH (LAMINARIALES: PHAEOPHYTA) EN AMBIENTES PROTEGIDOY EXPUESTO AL OLEAJE EN TIERRA DEL FUEGO | Plana J. and et. al. | 71 | 66-75 | NO | no completo | Feofita | Macrocystis pyrifera, Phaeophyta, estudio poblacional, Estrecho de Magallanes, Chile. | Se realizó un estudio poblacional sinóptico en poblaciones de Macrocystis pyrifera considerando distintos regímenes |
Ficha | EVALUACION DE UNA TECNICA DE ENSILADO PARA EL ALGA Macrocystis pyrifera Y OBSERVACION DE SU CONSUMO POR PARTE DE ABALON ROJO (Haliotis rufescens) | Pizarro Tonioni Cristian | NO | parcialmente completo con liga | Feofita | Se describe la evaluación de una técnica de ensilado para algas, adaptada | |||
Ficha | Nitrogen and phosphorus removal rates using small algal turfs grown with dairy manure | Pizarro C. and et. al. | 14 | 469–473 | NO | Completo | General | Algal turf scrubbers, Dairy manure, Nitrogen, Periphyton, Phosphorus | Conservation and reuse of nitrogen (N) and phosphorus (P) from animal manure is increasingly important as crops of algae on the N |
Ficha | An economic assessment of algal turf scrubber technology for treatment of dairy manure effluent | Pizarro C. and et. al. | NO | no completo | General | Algal turf scrubber, Dairy manure, Phytoremediation, Algae, Nitrogen, Phosphorus, Organic fertilizer | Controlling the input of nitrogen (N) and phosphorus (P) from dairies and other livestock challenges to the agricultural community. The purpose of this p | ||
Ficha | Changes in biomass and botanical composition of beach-cast seaweeds in a disturbed coastal area from Argentine Patagonia | Piriz M.L. and et. al. | 15 | 67–74 | NO | no completo | General | Argentine Patagonia, Beach-cast seaweeds, Bioinvaders, Eutrophication, Seaweed wracks, Ulva, Undaria | Trends in wrack composition and biomass, and its relationship with the anthropogenic impact were studied along a coastal area in Nuevo Gulf (south Patagonia) in front of Puerto Madryn city. Beach-cast macroalgae compo- |
Ficha | Macroalgae blooms and d15N in subtropical coastal lagoons from the Southeastern Gulf of California: Discrimination among agricultural, shrimp farm and sewage effluents | Piñón-Gimate A. and et. al. | 58 | 1144–1151 | NO | no completo | General | Macroalgae blooms d15N, Nitrogen content, Nitrogen sources | Macroalgae blooms of Gracilaria vermiculophylla, Hypnea spinella and Spyridia filamentosa have been found contribute anthropogenic |
Ficha | Effect of nutrient inputs on growth, chlorophyll, and tissue nutrient concentration of Ulva reticulata from a tropical habitat | Pimchanok Buapet and etal. | 34 | 245–252 | No | no completo | General | Ulva, nutrient uptake, eutrophication, luxury accumulation, green tides | “Green tides” caused by overgrowth of Ulva species are an increasing problem in tropical areas. The effect of |
Ficha | The genera Melanothamnus Bornet & Falkenberg and Vertebrata S.F. Gray constitute well-defined clades of the red algal tribe Polysiphonieae (Rhodomelaceae, Ceramiales) | Pilar Díaz-Tapia, et.al. | 52 | ene-30 | NO | no completo | General | Biogeography; evolution; molecular systematics; morphology; phylogeny; Polysiphonia; red algae; time calibration | Polysiphonia is the largest genus of red algae, and several schemes subdividing it into smaller taxa have been proposed since |
Ficha | Sur Cinq Espéces d´Ulvella | Pierre Dangeard | 48 | ND | 1035 | no completo | Sin asignar | ||
Ficha | Quelques algues d'eau douce des tourbières à sphaignes de la région de Laigle (Orne) | Pierre Bourrelly | 93 | 338-345 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Early patterns of Caulerpa racemosa recovery in the Mediterranean Sea: the in£uence of algal turfs | Piazzi Luigi and et. al | 83 | 27-29 | NO | no completo | Clorofita | Variability in recovery of the introduced green alga Caulerpa racemosa has been investigated on a subtidal | |
Ficha | The Freshwater Cladophoraceae | Phinney, H. K. | ND | 3740 | no completo | Sin asignar | |||
Ficha | Estimates of nuclear DNA content in 98 species of brown algae (Phaeophyta) | Phillips N. and et. al. | NO | no completo | Feofita | Background Brown algae are critical components of marine ecosystems around the world. However, the | |||
Ficha | Marine macroalgal biodiversity hotspots: why is there high species richness and endemism in southern Australian marine benthic flora? | Phillips J. | 10 | 1555-1577 | NO | parcialmente completo con liga | Feofita | Australia, biodiversity, biogeography, endemism, marine macroalgae, species richness | The southern Australian marine macroalgal flora has the highest levels of species richness and endemism of any regional macroalgal flora in the world. Analyses of species composition and dis- |
Ficha | Ecological differences between the isomorphic phases of Mazzaella lilacina (Rhodophyta, Gigartineceae): 1. Spore production, 2. Recruitment specialization, 3. Resistance to removal by Wave Action | Phillips B. | NO | Rodofitas | |||||
Ficha | Observations on the Ecology of The Caribbean and Pacific Coasts of Panama | Peter W. Glynn | 2 | 13-30 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Marine biological community baselines in unimpacted tropical ecosystems: spatial and temporal analysis of reefs at Howland and Baker Islands | Peter S. Vroom, et. al. | 19 | 797-812 | NO | no completo | General | Algae Coral reef Fish Monitoring Phase shift | Howland and Baker Islands are two small, isolated reef and sand islets located |
Ficha | Spatial heterogeneity of benthic community assemblages with an emphasis on reef algae at French Frigate Shoals, Northwestern Hawai‘ian Islands | Peter S. Vroom and et. al. | 24 | 574–581 | NO | Completo | Rodofitas | Coral reef - Ecozone - Geomorphic zone - PRIMER - Monitoring - Rapid ecological assessment | Reefs in tropical atoll systems have historically been described on a geomorphic basis, and segregated into loosely defined fore-reef, back-reef, and lagoonal reef zones. However, recent oceanographic monitor |
Ficha | A CRITIQUE OF THE TAXONOMY OF MARINE ALGAE* | Peter S. Dixon, Ph.D. | 617-622 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Growth and Reproduction in Red Algae in Relation to Light and Dark Cycles | Peter S. Dixon and W. Norma Richardson | 764-777 | 1303 | no completo | Sin asignar | |||
Ficha | In situ spore germination in Erythrotrichia carnea | Peter S. Dixon & John H. West | 3 | 253-255 | 819 | no completo | Sin asignar | ||
Ficha | Studies on Marine Algae of The British Isles: The Genus Ceramium | Peter S. Dixon | 39 | 331-374 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Variation and Speciation in Marine Rhodophyta | Peter S. Dixon | 51-62 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Taxonomic and Nomenclatural Notes on the Florideae, IV. | Peter S. Dixon | 117 | ND | NO | parcialmente sin liga | Sin asignar | Rhodophyta | The present notes are concerned with problems of nomenclature and taxonomy which have discovered during the preliminary work for the preparation of the volumen on Rhodophyta for the proposedFlora of Bristish Marine Algae. |
Ficha | The Origin of Nitrogen Isotope Values in Algae | PETER K. SWART & SAMANTHA EVANS | No | no completo | General | The fractionation accompanying assimilation of NO3 | |||
Ficha | Life History Studies of Selected British Ceramium Species | Peter Edwards | 9 | 181-184 | 1286 | no completo | Sin asignar | Ceramium shuttleworthianum, C. rubrum y C. pedicellatum | Ceramium shuttleworthianum, C. rubrum, and C. pedicellatum demonstrated a Polysiphonia type of life history without deviations in unialgal culture. The reported absence of fertile gametophytic plants of C. shuttleworthianum and C. flabelligerum from north |
Ficha | Field and Cultural Studies on The Seasonal Periodicity of Growth and Reproduction of Selected Texas Benthic Marine Algae | Peter Edwards | 14 | 59-114 | NO | parcialmente sin liga | Sin asignar | siliculosus Ectocarpus, Giffordia mitchelliae, fascia Petalonia, Erythrocladia subintegra, Goniotrichum alsidii, Bangia fuscopurpurea, Porphyra leucosticta, Acrochaetium crassipes, A. flexuosum, Ceramium strictum, Centroceras clavulatum y Polysiphonia bol | Seasonal observations in nature in the Port Aransas, Texas area in the Gulf of Mexico have been combined with cultural studies on the laboratory in an attempt to elucidate the casual factors of the distinctive seasonal alteration of the benthic marine alg |
Ficha | CULTIVO EXPERIMENTAL DE ALGAS PARDAS EN LA IV REGION, COQUIMBO, CHILE | PESQUERA SAN JOSE S.A. | NO | Cultivo | |||||
Ficha | The prostrate system of the Gelidiales: diagnostic and taxonomic importance | Perrone Cesira and et. al. | 49 | 23–33 | NO | Completo | Rodofitas | attachment; Gelidiales; Pterocladiaceae; rhizoids; rhizines; taxonomy. | Despite numerous recent studies on the Gelidiales, most taxa belonging to this order are still difficult to distinguish when in the vegetative or tetrasporic state. This paper describes in detail the morpholo |
Ficha | Principales tipos de vegetación bentónica y su zonación en el litoral comprendido entre las Rías de Camariñas y de Corme y Lage (Costa de Camelle, La Coruña). | Pérez-Cirera, J. L., & Maldonado, J. L. | 13 | 893-910 | NO | parcialmente sin liga | Sin asignar | En este trabajo se realiza un estudio sobre las algas beníonícas de las costas de Camelle (La Coruña, NO. de Espolia), describiendo los principales tipos de vegetación y comunidades, así como su distribución vertical o zonación en el espacio intermareal. | |
Ficha | Cistocarpos en el tetrasporofito de Polysiphonia macrocarpa (Rhodomelaceae, Rhodophyta). | Perez-Ciera, J. L. | 13 | 887-891 | NO | parcialmente sin liga | Sin asignar | The occurrence of cystocarps and tet casporangia on the same thallus is reported in Polyaiphonia macrocarpa Harvey in Mackay from Ría de Corme y Lage (La Coruña, Spain). This species is characteristic of the communities of Ceramium shuttleworthinum and C | |
Ficha | Estudios en las especies canarias de Galaxaura y Tricleocarpa (Galaxauraceae, Rhodophyta). | Pérez, L., & Carrillo, J. M. A. | 22 | 35-63 | NO | parcialmente sin liga | Sin asignar | De acuerdo con los criterios taxonómicos más recientes cuatro especies pertenecientes a la familia Galaxauraceae han sido referidas para Canaria: Galaxaura rugosa (Ellis & Solander) Lamouroux, G. obtusata (Ellis & Solander) Lamouroux, Tricleocarpa cylindr | |
Ficha | Temperature effects on the microscopic haploid stage development of Laminaria ochroleuca and Sacchoriza polyschides, kelps with contrasting life histories | Pereira T.R. and et. al. | 52 | 395-403 | NO | no completo | Feofita | Kelp l Temperature l Growth rate l Fecundity l Haploid gametophyte l Demography | Kelp forests are one of the most diverse and productive ecosystems worldwide. Global climate change and human |
Ficha | A comparative analysis of phycocolloids produced by underutilized versus industrially utilized carrageenophytes (Gigartinales, Rhodophyta) | Pereira Leonel and et. al. | 21 | 599–605 | NO | Completo | Rodofitas | Seaweed . Cultivation . Phycocolloids. Carrageenan . FTIR-ATR . FT-Raman | Carrageenan (E-407) and semi-refined carrageenan (E-407a) are some of the main additives used by the food industry for their gelling, emulsifying, thickening, and stabilizing properties. These are natural ingredie |
Ficha | Interactions Between Wave Action and Grazing Control the Distribution of Intertidal Macroalgae | Per R. Jonsson, Lena Granhag, Paula S. Moschella, Per A ? Berg, Stephen J. Hawkins, and Richard C. Thompson | 1169–1178 | NO | Liga perdida | Sin asignar | breaking waves; breakwaters; climate change; dislodgment; Fucus spp.; grazing; hydrodynamic drag; limpets; Patella vulgata; transplantation; Ulva sp.; wave exposure. | Canopy-forming macroalgae are key species on temperate rocky shores. However, there is a lack of understanding of how the relative balance of physical and biological factors controls the establishment and persistence of intertidal macroalgae. Here we pres | |
Ficha | Estudio fitosociológico de una zona intermareal en la Bahía de Málaga, costa pacífica colombiana. | Peña, E. J., Palacios, M. L., & Mejia, A. | 4 | 12 A 21 | 3766 | no completo | Sin asignar | ||
Ficha | Evaluación preliminar de polisacáridos en el alga roja Catenella caespitosa (Gigartinales) en el pacífico colombiano. | Peña, E. J., Benitez R. & Colmenares, A. J. | 612- 619 | 3765 | no completo | Sin asignar | |||
Ficha | Macroalgas marinas bénticas asociadas al manglar de la Costa Pacífica colombiana. | Peña, E. J., & Palacios, M. L. | 500 - 505 | 3762 | no completo | Sin asignar | |||
Ficha | Influence of alkali treatment on agar from Gracilaria cornea from Yucat´an, M´exico | Pelegrin Y. Freile & D. Robledo | NO | parcialmente completo con liga | Cultivo | ||||
Ficha | Nutrient content of macroalgae with differing morphologies may indicate sources of nutrients for tropical marine systems | Peggy Fong, Krista Kamer, Katharyn E. Boyer, Karleen A. Boyle | 137-152 | NO | Liga perdida | Sin asignar | Macroalgae · Tropics · Nutrients · Morphological forms · Puerto Rico | To investigate whether tissue N and P content of morphologically distinct macroalgae reflect different processes controlling nutrient availability, we measured water column nutrients and collected 5 species of algae for tissue N and P analysis from 18 sta | |
Ficha | El Proyecto Macroalgas del Pacífico Mexicano y sus avances. II . Estrategia General del Trabajo. | Pedroche, Francisco F. | 1 A 11 | 3760 | no completo | Sin asignar | |||
Ficha | El Proyecto Macroalgas del Pacífico Mexicano y sus avances. I . Programación y Desarrollo. | Pedroche, Francisco F. | 1 A 14 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Response of macroalgae and macroinvertebrates to anthropogenic disturbance gradients in rocky shores | Pedro Almeida Vinagre, Antónia Juliana Pais-Costa, Rui Gaspar, Ángel Borja, João Carlos Marques, João Magalhães Neto | 850-864 | NO | Liga perdida | Sin asignar | Marine, Intertidal, Nutrient enrichment, Biological quality elements, Comparative response, Opportunist/sensitive taxa | The compliance of macroalgal and macroinvertebrate assemblages to anthropogenic disturbance gradients (e.g.,nutrient enrichment) was investigated atintertidal rocky shores.Macroalgae and macroinvertebrates presented parallel behavior, both showing shifts | |
Ficha | Simple and rapid RNA extraction from freeze-dried tissue of brown algae and seagrasses | PEARSON GARETH and et. al. | 41 | 97-104 | NO | parcialmente completo con liga | Feofita | brown algae, Fucus, lyophilization, plastid gene expression, rbcL, RNA extraction, seagrass | An inexpensive and rapid RNA extraction protocol for brown algae and seagrasses is presented, based on homogenization |
Ficha | PATTERNS OF REPRODUCTION, GENETIC DIVERSITY, AND GENETIC DIFFERENTIATION IN CALIFORNIA POPULATIONS OF THE GENICULATE CORALLINE ALGA LlTHOTHRIX ASPERGILLUM (RHODOPHYTA) | Pearson Elizabeth A. and Steven N. Murray | 33 | 753-763 | NO | Completo | Rodofitas | Corallinales; coralline algae; genetic variation; isozyme electrophoresis, Lithothrix aspergillum; reproduction; Rhodophyta; seaweeds | The reproductive composition and genetic diversity of populations of the red seaweed Lithothrix aspergillurn Gray (0. Corallinales) were studied at three southern California sites (Shaw's Cove and Treasure Island, |
Ficha | Water relations of the dune grasses Ammophila arenaria and Elymus mollis on the coast of Oregon, USA. | Pavlik, B. M. | 45 | 197-205 | NO | parcialmente sin liga | Sin asignar | Predawn water potentials of Ammophila arenaria and Elymus mollis were never more negative than -0.2 MPa and midday minima did not drop below -2.0 MPa dur- ing the May to October study period. Both species were probably rooted in a salt-free water table th | |
Ficha | A cladistic analysis of Rhodophyta: Florideophycidean orders | Paul W. Gabrielson and David J. Garbary | 22 | 125 -138 | NO | parcialmente completo con liga | Rodofitas | A cladistic analysis of the orders of red algae is presented that concentrates on relationships among florideophyte taxa. The data matrix comprises 35 characters and 15 taxa. Biochemical and ultrastructural characters as we | |
Ficha | Algae as indicators of environmental change | Paul V. McCormick & John Cairns | 6 | 509-526 | NO | no completo | General | environmental monitoring, algal indicators, environmental change, indicator organisms, pollution, microbial ecology | Despite an increased awareness by governments and the general public of the need for protecting all types of |
Ficha | Algae as indicators of environmental change | Paul V. McCormick & John Cairns | 6 | 509-526 | NO | no completo | General | environmental monitoring, algal indicators, environmental change, indicator organisms, pollution, microbial ecology | Despite an increased awareness by governments and the general public of the need for protecting all types of |
Ficha | Rhizoid formation in Valonia (Siphonocladales, Chlorophyceae) | PAUL ROMMEL ELVIRA, SATOKO SEKIDA AND KAZUO OKUDA | 51 | 391-402 | NO | no completo | General | WORDS: Actin, FITC-labeled lectin, Microtubule, Polysaccharide, Rhizoid induction, Valonia | Rhizoids were artificially induced by the contact or approach of substrata toward Valonia macrophysa, V. fastigiata and |
Ficha | Has the Biological Species Concept Outlived Its Usefulness? | Paul R. Ehrlich | 10 | 167-176 | 2762 | no completo | Sin asignar | ||
Ficha | The ultrastructure of an alloparasitic red alga Choreocolax polysiphoniae | Paul Kugrens and John A. West | 12 | 175-186 | 758 | no completo | Sin asignar | Choreocolax polysipiloniae | An alloparasite, Choreocolax polysipiloniae, apparently represents one of the most evolved parasitic red algae. Chloroplasts are highly reduced and consist of double membrane limited organelles lacking any internal thylakoid development. The uninucleate c |
Ficha | The effect of acidification on the determination of organic carbon, total nitrogen and their stable isotopic composition in algae and marine sediment | Paul Kennedy*, Hilary Kennedy and Stathis Papadimitriou | 19 | 1063-1068 | No | no completo | General | We investigated the effects of sample acidification on the stable carbon and nitrogen isotopic com- an algal culture and a marine sediment. | |
Ficha | Experimental Evaluation of Ecological Dominance in a Rocky Intertidal Algal Community | Paul K. Dayton | 45 | 137-159 | NO | parcialmente sin liga | Sin asignar | Actinians; algae; asteroid; community organization; competition; dominance; echinoid; grazing; intertidal; obligate relationships; predation; succession. | The mechanisms by which various species exert influence disproportionate to their abundance or mass on the structure of a lower intertidal algal community were evaluated experimentally. These functional roles were evaluated by various controlled manipulat |
Ficha | The Generic Name Hormidium as Applied to Green Algae | Paul C. Silva, Karl R. Mattox, Will H. Blackwell and Jr. | 21 | 639-645 | NO | no completo | General | Hormidium Kiitzing 1843 (non Lindley ex Heynhold 1840, Orchidaceae) is shown to have been lectotypified with H. velutinum, a chizogoniaceous alga. Hormidium sensu Klebs 1896 comprises ulotrichaceous algae. Although in | |
Ficha | Remarks on Algal Nomenclature II | Paul C. Silva | 8 | 60-64 | NO | no completo | General | ||
Ficha | Remarks on Algal Nomenclature. III | Paul C. Silva | 9 | 18-25 | NO | no completo | General | ||
Ficha | Remarks on Algal Nomenclature. IV | Paul C. Silva | 16 | 941-945 | No | no completo | General | ||
Ficha | Remarks on Algal Nomenclature V | Paul C. Silva | 21 | 199-205 | No | no completo | General | ||
Ficha | Remarks on Algal Nomenclature VI | Paul C. Silva | 29 | 121-145 | NO | no completo | General | Thirty-nine generic names of living algae are formally proposed for conservation. Two new combinations are made, Hormiscia gregaria (Braun) P. C. Silva, replacing H. neglecta Kornmann in connection with the proposal to cons | |
Ficha | Thallobionta | Paul C. Silva | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Chlorophycota | Paul C. Silva | ND | NO | parcialmente sin liga | Sin asignar | This division includes all algae that have chlorophyll a and b. exce pt the Euglenophyceae, which in all other respects are so different as to suggest a separate origin of their photosynthetic pigments. Three classes are recognized: the Chlorophyceae, Cha | ||
Ficha | Review of the Taxonomic History and Nomenclature of the Yellow-Green Algae | Paul C. Silva | 121 | 20-63 | NO | no completo | General | The taxonomic history of the yellow-green algae is reviewed with emphasis on classification above the rank of genus. Numerous nomenclatural situations in need of rectification or clarifieation are discussed. At the ord | |
Ficha | REVEALING GENETIC MARKERS IN GELIDIUM VAGUM (RHODOPHYTA) THROUGH THE RANDOM AMPLIFIED POLYMORPHIC DNA (RAPD) TECHNIQUE | Patwary Mohsin U. and et. al. | 89 | 216-222 | NO | Completo | Rodofitas | amplification fragment length polymorphism; DNA amplification fingerprinting; Gelidium ; genetic marker; polymerase chain reaction (PCR); random amplified polymorphic DNA (RAPD); Rhodophyta | The recently developed random amplified polymorphic DNA technique was evaluated as n method for characterizing isolates of the agarophyte Gelidium vagum Okamura. Reaction conditions for single primer polymerase ch |
Ficha | Responses to nutrient enrichment, wave action and disturbance in rocky shore communities | Patrik Kraufvelin | 262–274 | NO | Liga perdida | Sin asignar | Mesocosm; Nutrient enrichment; Canopy gap formation; Rocky intertidal; Algal colonisation; Marine biodiversity | A high degree of resistance against nutrient enrichment has previously been demonstrated for macroalgal-dominated rocky shore communities in the presence of moderate to large amounts of macroinvertebrate grazers. To experimentally examine, under controlle | |
Ficha | Nutrient Mass Flux between Florida Bay and the Florida Keys National Marine Sanctuary | Patrick J. Gibson & Joseph N. Boyer & Ned P. Smith | 31 | 21-32 | No | no completo | General | Florida Bay . Florida Keys. Nutrients. Nutrient loading . Volume transport . Nitrogen . Phosphorus | There is a net discharge of water and nutrients |
Ficha | The Ascidians of South Australia III. Northern Sector of the Great Australian Bight and Additional Records | Patricia Kott | 99 | ene-20 | NO | parcialmente sin liga | Sin asignar | Gran Bahía de Australia; Euherdmaniinae y Botryllinae | An account is given of 58 species of the Ascidiacea from South Australia, of which 7 species are new, including two assigned to new genera in the sub families Euherdmaniinae and Botryllinae. Records of 22 species from the northern part of the Great Austra |
Ficha | Growth of members of Cladophorales in experimental culture. | Patel, R. J. | 10 | 40-53 | NO | parcialmente sin liga | Sin asignar | Chaetomorpha melagonium Kütz., Rhizoclonium riparium Harv. y Pithophora keioensis Wittr | The effects of different ternperatures, light for different lengths of time and different quantities of light on growth of Chaetomorpha melagonium Kütz., Rhizoclonium riparium Harv. and Pithophora keioensis Wittr. have been described. The lower ternperatu |
Ficha | Facultative Heterotrophy in Some Chlorococcacean Algae | Parker, B.C., Bold, H.C. & Deason, T.R | 133 | 761-763 | NO | parcialmente sin liga | Sin asignar | Bracteacoccus, Spongiochloris, Diciyochloris, Neochloris y Spongiococcum; morfológico. | All know species of the genera Bracteacoccus, Spongiochloris, and Diciyochloris, and some of the species of Neochloris and Spongiococcum are capable of growing heterotrophically in darkness in glucose-salts médium. In contrast, all know species of Chloroc |
Ficha | Quelques stations francaises de Geitleria calcarea, Cyanophycde cavernicole | Par P. Bourrelly and P. Dupuy | 35 | 136-140 | NO | no completo | General | The atmophytic, lime-incrusting alga Geitleria calcarea (Cyanophyta, Stigonemataceae), discovered in 1955 by Friedmann in two caves of Israel, has been found in six caves in France. Ecological conditions at all habitats are | |
Ficha | Tank cultivation of the red alga Palmaria palmata: Effects of intermittent light on growth rate, yield and growth kinetics | Pang Shaojun & Klaus Lüning | 16 | 93-99 | NO | no completo | Cultivo | intermittent light, growth rate, growth kinetics, Palmaria palmata, photoinhibition, tank cultivation, yield | Tank cultivation of marine macroalgae involves air-agitation of the algal biomass and intermittent light conditions, |
Ficha | Application of SSR and AFLP to the analysis of genetic diversity in Gracilariopsis lemaneiformis (Rhodophyta) | Pang Qiaoqiao and et. al. | 22 | 607–612 | NO | Completo | Rodofitas | Genetic diversity. Gracilariopsis lemaneiformis. SSR | The agarophyte Gracilariopsis lemaneiformis is both important for biological research and of significant economic value. However, the genetic diversity of wild populations of the alga has not been studied. We |
Ficha | Removal of phosphate by the green seaweed Ulva lactuca in a small-scale sewage treatment plant (Ios Island, Aegean Sea, Greece) | Panagiotis Tsagkamilis, et.al. | 22 | 331-339 | NO | no completo | General | Biofilter. Chlorophytes. Phosphate absorption . Sewage effluent . Ulva | In the present study, the use of seaweeds for |
Ficha | Signal transduction during fertilization in the unicellular green alga, Chlamydomonas | Pan Junmin and William J Snell | 3 | 596-602 | NO | no completo | Clorofita | Sexual reproduction in the green alga, Chlamydomonas, is | |
Ficha | Preliminary Screening for Potential Algicides | Palmer, C. Mervin; Maloney, Thomas E. | 55 | 01-ago | NO | parcialmente sin liga | Sin asignar | Microcystis, Nitzschia, Gomphonema, Scenedesmus, Chlorella y Cylindrospermum | A comparatively simple procedure for the preliminary screening of chemical compounds for algicides is described together with results obtained with the first 76 substances tested. As groups, inorganic and organic salts, rosin amine compounds, and antibiot |
Ficha | Algae in Water Supplies of Ohio | Palmer, C. Mervin | 62 | 225-244 | 12 | no completo | Sin asignar | ||
Ficha | Efectos de la contaminación sobre la diversidad genética de Mazzaella laminarioides (Bory) Fredericq (Gigartinales, Rhodophyta) en bahías | Palma Mario and et. al. | 64 | 24-32 | NO | Completo | Rodofitas | sod-1, Mazzaella laminarioides, diversidad genética, contaminación. | Se determinó y comparó la variabilidad genética interpoblacional de Mazzaella laminaroides (Bory) Fredericq presente en Bahía Coliumo, Bahía San Vicente y Bahía Concepción, l |
Ficha | DESARROLLO DE GAMETÓFITOS Y ESPORÓFITOS DE MACROCYSTIS PYRIFERA (L.) C. AGARDH (LAMINARIALES: LESSONIACEAE) DE LA REGIÓN DE MAGALLANES EN CONDICIONES DE LABORATORIO | Palacios M. and A. Mansilla | NO | parcialmente completo con liga | Feofita | ||||
Ficha | Exploring the potential of clay in mitigating Pyrodinium bahamense var. compressum and other harmful algal species in the Philippines | Padilla Larry V. and et. al. | 22 | 761–768 | NO | no completo | General | HAB mitigation . Clay . Red tide . Pyrodinium . Cell removal efficiency | Harmful algal bloom occurrences worldwide and mitigate their detrimental effects. This study inves- |
Ficha | Agricultural fertilizers as alternative culture media for biomass production of Chondracanthus squarrulosus (Rhodophyta, Gigartinales) under semi-controlled conditions | Pacheco-Ruíz I. and et. al. | 240 | 201–209 | NO | Completo | Rodofitas | Biomass production; Agricultural fertilizers; Chondracanthus squarrulosus; Nutrients | The red alga Chondracanthus squarrulosus was cultured under semi-controlled conditions to evaluate growth (biomass production) with agricultural fertilizers (ammonium nitrate, ammonium sulphate and urea) vs. analytical grad |
Ficha | Reclutasmiento in situj y fertilidad der fases nucleares de Gelidium robustum (Rhodophyta) | Pacheco-Ru?z I. and et. al. | NO | Rodofitas | |||||
Ficha | Biogeografia e historia de vida de dos especies de Porphyra (Rhodophyta) endemica del Golfo de California, Mexico | Pacheco R.I. | NO | Rodofitas | |||||
Ficha | Host-specificity of Endophyton ramosum (Chlorophyta), the causative agent of green patch disease in Mazzaella laminarioides (Rhodophyta) | Pablo C. Sánchez and et.al. | 31 | 173-179 | NO | Completo | Rodofitas | disease, Endophyton, host-specificity, infection, Mazzaella | The level of host-specificity of Endophyton ramosum, the causative agent of green patch disease in Mazzaella laminarioides, was experimentally tested in the laboratory. Cross-infection trials demonstrated that the endophyte |
Ficha | Atmospheric nitrogen deposition from a remote source enriches macroalgae in coral reef ecosystems near Green Turtle Cay, Abacos, Bahamas | P.J. Barile, B.E. Lapointe | 50 | 1262–1272 | No | no completo | General | Atmospheric deposition; Nitrogen; Macroalgae; Coral reefs; Bahamas | Over the past several decades, the fixation of ‘‘new’’ nitrogen to the biosphere has doubled. For the early 21st century, the most |
Ficha | Invasion of Codium fragile ssp. tomentosoides in northern Chile: A new threat for Gracilaria farming | P.E. Neill, O. Alcalde, S. Faugeron, S.A. Navarrete, J.A. Correa | 259 | 202-210 | no completo | General | Algal farming; Invasion ecology; Marine invasion; Non-indigenous species; Seaweed; South America | Invasive species are key components of the burgeoning global change in ecological communities. The green alga Codium fragile | |
Ficha | EFFECTS OF SELF-FERTILIZATION IN THE GIANT KELP, MACROCYSTIS PYRIFERA | P. T. RAIMONDI, D. C. REED, B. GAYLORD, AND L. WASHBURN | 85 | 3267-3276 | No | no completo | General | California, USA; competition; dispersal; inbreeding; kelp; Macrocystis pyrifera; outcrossing; self-fertilization; spores. | The costs of self-fertilization were evaluated for the giant kelp, Macrocystis stage is the 1N spore generation. Once spores settle, they grow into |
Ficha | Changing Patterns of Distribution in Marine Algae | P. S. Dixon | 14 | 109-115 | 1497 | no completo | Sin asignar | ||
Ficha | Cost of reproduction in Fucus distichus | P. O. Ang, Jr | 89 | 25-35 | 2668 | no completo | Sin asignar | Reproductive effort (ratio of fertile to total plant dry weight) was measured in Fucus distichus L. emend. Powell. On average, 12.7 % of plant dry weight is in reproductive biomass and this amount is relatively constant over most months. Reproductive effo | |
Ficha | Interaction of top down and bottom up factors in intertidal rockpools: Effects on early successional macroalgal community composition, abundance and productivity | P. Masterson, and et. al. | 363 | dic-20 | NO | no completo | General | Grazing Macroalgae Nutrient enrichment Rockpools Top down/bottom up control | Increasing levels of eutrophication in coastal waters and recognition of natural variation in supply of nutrients, |
Ficha | The Maintenance of Species-Richness in Plant Communities: The Importance of The Regeneration Niche | P. J. Grubb | 52 | 107-145 | 2765 | no completo | Sin asignar | I. According to ‘Gause’s hypothesis’ a corollary of the process of evolution by natural selection is that in a community at equilibrium every species must occupy a different niche. Many botanists have found this idea improbable because they have ignored t | |
Ficha | Nouvelles observations sur deux Coccolithophoracees marines: Cricosphaera roscoffensis (P. Dangeard) comb. nov. et Hymenomonas globosa (F. Magne) comb. nov. | P. Gayral et J. Fresnel | 15 | 339-355 | 1732 | no completo | Sin asignar | ||
Ficha | Notes on Sexual Reproduction in Desmids. Experiencies with Conjugation Experiments in Uni-algal Cultures | P. F. M. Colsfl and R. M. Y. Teixeira | 23 | 603-611 | 1258 | no completo | Sin asignar | losterium Iimneticum Lemn. Cl. moniliferum Bory ex Ralfs, y Micrasterias papilifera Breb. De CI. limnetieum no zygoporas; fisiológico | Over 120 randomly selected strain helonging to 16 genera and to more than 80 species of Desmids were brought into uni-algal culture and subjected to condition, provoking conjugation. Only 3 isolates - all homothallic - exhibited sexual reproduction: Clost |
Ficha | On the Term Character | P. Dearte Rodrigues | 35 | 140-141 | 2758 | no completo | Sin asignar | ||
Ficha | CODIUM AMPHIBIUM: A SPECIES OF DOUBTFUL VALIDITY | P. C. SILVA AND D. E. G. IRVINE | 39 | 631-636 | NO | no completo | General | Plants agreeing in habit with the material originally described as Codium | |
Ficha | Evaluación de Lactuca Sativa y Selenastrum Capricornutum como Indicadores de Toxicidad en Aguas | P. Bohórquez-Echeverry, C. Campos-Pinilla | 83-98 | NO | Liga perdida | Sin asignar | bioensayos, contaminación del agua, Lactuca sativa y Selenastrum capricornutum, toxicidad | El bioensayo con Selenastrum capricornutum ha sido utilizado como herramienta de valoración de la contaminación del agua, debido a su habilidad para detectar efectos adversos a mezclas complejas de sustancias químicas. El objetivo de este estudio fue comp | |
Ficha | Scandinavians who have contributed to the of the Knowledge flora of North America. | P. A. Rydberg | 6 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | A method for determining the surface area of corals | Ove Hoegh-Guldberg | 7 | 113-116 | NO | no completo | General | Although there are several techniques available damicorn | |
Ficha | De Algi et Characeis | OTTO XORDSTEDT. | 25 | 43132 | 19 | no completo | Sin asignar | ||
Ficha | A multivariate analysis of morphological variation in the Hemizygia bracteosa complex (Lamiaceae, Ocimeae) | Otieno D. F. and et. al. | 261 | 19-38 | NO | no completo | Feofita | Hemizygia bracteosa complex, phenetics, cluster analysis, discriminant analysis, principal component analysis. | The variation and recognition of taxa examined using multivariate techniques. Morpho- H. |
Ficha | Seasonal changes in abundance and shifts in dominance of life history stages of the carrageenophyte Sarcothalia crispata (Rhodophyta, Gigartinales) in south-central Chile | Otaiza Ricardo D. and et. al. | 13 | 161–171 | NO | Completo | Rodofitas | Chile, gametophytic dominance, Gigartinaceae, life history, resorcinol, Sarcothalia crispata, selfseeding | The population dynamics of the carrageenophyte Sarcothalia crispata is described from subtidal beds at two localities in south-central Chile. Seasonal fluctuations in total density and biomass were not evident. Fronds were |
Ficha | Composición Nutricional y Funcional de las Algas Clorofíceas Chilenas: Codium fragile y Ulva lactuca | Ortiz V. Jaime | ene-25 | NO | no completo | Clorofita | Existen pocos antecedentes científicos referente a la composición químico-nutricional y de componentes funcionales de las diferentes macroalgas que proliferan en las amplias costas chilenas, en vista a la necesidad de&nbs | ||
Ficha | PARTHENOGENESIS IN THE BROWN ALGA LESSONIA NIGRESCENS (LAMINARIALES, PHAEOPHYCEAE) FROM CENTRAL CHILE | Oppliger L.V. and J. A. Correa | 43 | 1295-1301 | NO | no completo | Feofita | DNA quantification; flow cytom- etry; Lessonia nigrescens; parthenogenesis; Phaeo- phyceae | Parthenogenesis, the development of female gam- brown algae, although limited quantitative informa- is reported for the firs |
Ficha | SEX RATIO VARIATION IN THE LESSONIA NIGRESCENS COMPLEX (LAMINARIALES, PHAEOPHYCEAE): EFFECT OF LATITUDE, TEMPERATURE, AND MARGINALITY | Oppliger L. V. and et. al. | 46 | NO | no completo | Feofita | cryptic species; gametophyte; latitude; Lessonia nigrescens; marginal populations; Phaeophyceae; sex determination; sex ratio; tem- perature | Little is known about variation of sex ratio, the proportion of males to females, in natural popula- of the mating system. The observation of sexual | |
Ficha | Brazilian mangal vegetation with special emphasis on the seaweeds. | Oliveira, E. C. | 55-65 | 3824 | no completo | Sin asignar | |||
Ficha | Physiological Responses of Phytoplankton to Major Enviromental Factors | Olga v. H. Owens and Wayne E. Esalas | 27 | 461-483 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Role of colonization in spatio-temporal patchiness of microgastropods in coralline turf habitat | Olabarria C. | 274 | 121-140 | NO | Completo | Rodofitas | Australia; Intertidal rocky shore; Microgastropods; Artificial turf; Colonization; Patchiness | The ability of benthic macrofauna to disperse and colonize new habitats throughout their life may contribute substantially to small-scale patchiness in abundances in different habitats. Microgastropods in coralline turf on |
Ficha | Seaweeds and their uses in Japan. | Okazaki, A. | 1-165 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Marine biotoxins and harmful algal blooms in mexico's pacific littoral | Ochoa J.L.and et. al. | 0 | NO | General | ||||
Ficha | Underwater Disturbances | O. L. Martin Jr. | 53-60 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Wind-induced long term increase and short term fluctuations of shallow water suspended matter and nutrient concentrations, Ringkøbing Fjord, Denmark | O. B Pedersena, C. Christiansena & M. B. Laursenb | 273-287 | NO | Liga perdida | Sin asignar | The terrestrial supply of nutrients to the shallow lagoon Ringkøbing Fjord has shown a significant downward tendency for phosphorus during the past 10 years. In spite of a decreasing supply, there is at the same time an increase in nutrient concentrations | ||
Ficha | Observaciones traoficas y de distribucion espacial de peces asociados a un bosque submareal de Lessonia trabeculata | Nuñez M. L. and J. A. Vasquez Castro | NO | parcialmente completo con liga | Kelp | ||||
Ficha | Forces on intertidal organisms due to breaking ocean waves: Design and application of a telemetry system | NOTES | 27 | 178-183 | NO | parcialmente sin liga | Sin asignar | A new telemetry system measures the direction and magnitude of the forces imposed on intertidal organisms by individual breaking waves. Cast epoxy replicas of organisms are mounted on three transducers embedded in an exposed rock surface. Force data are e | |
Ficha | A simple device for recording the maximum force exerted on intertidal organisms | NOTES | 28 | 1269-1274 | 2683 | no completo | Sin asignar | A new dynamometer records the magnitude and direction of the maximum force imposed on individual organisms by rapid water flow. These measurements allow “exposure” to be accurately quantified, and maximum water velocity to be estimated. The device is rugg | |
Ficha | Rhodogorgon, an anamolous new red algal genus from the Caribbean Sea. | Norris, J. N., & Bucher, K. E. | 102 | 1050-1066 | NO | parcialmente sin liga | Sin asignar | Rhodogorgon (Rhodophyta) a new genus with two species , R. carriebowensis and R. ramosissima, superficially resembling some gorgonian soft corals, is described frorn the Caribbean Sea. Studies of vegetative morphology, male reprcductive structure, pigment | |
Ficha | A New Species of Basicladia from the Snail Viviparus Malleatus Reeve | Normandin, Robert F.; Taft, Clarence E. | 59 | 58-62 | 2767 | no completo | Sin asignar | Basicladia vivipara | In June 1956 a specimen of the snail Viviparus malleatus Reeve was obtained from a pond on South Bass Island, Lake Erie. An alga growing on the snail shell was identified with the Genus, Basicladia described by Hoffman and Tilden (1930). This habitat is n |
Ficha | An Empirical Comparison of Microcomputer Parsimony Programs,II | Norman I. Platnick | 5 | 145-161 | 2771 | no completo | Sin asignar | The effectiveness and efficiency of J.S. Farris new microcomputer parsimony program (Henning86. version 1.5) are evaluated with reference to 60 data sets, including those used to benechmark earlier mainframe and microcomputer packages. By overcoming the | |
Ficha | Vegetative and reproductive morphology of the type species of Gloiocladia, G. Furcata (Faucheaceae, Rhodophyta)Se ha habilitado la compatibilidad con lectores de pantalla. | Noemí Sánchez and Conxi Rodríguez-Prieto | 44 | 222-233 | NO | Liga perdida | Sin asignar | The type species of Gloiocladia, G. furcata, is described in detail, and its characters are compared with those of other species currently accepted in Gloiocladia. The presence of a subcortex of ovoid, angular or stellate cells, connected by secondary | |
Ficha | Halogenated Monoterpene Derivatives from Desmia (Chondrococcus) japonicus | Nobutaka ICHIKAWA, Yoko NAPA, and Sachito ENOMOTO | 562-565 | NO | Liga perdida | Sin asignar | |||
Ficha | Purification of phycoerythrin from Porphyra yezoensis Ueda (Bangiales, Rhodophyta) using expanded bed absorption | Niu Jian-Feng and et. al. | 22 | 25–31 | NO | Completo | Rodofitas | Porphyra yezoensis. R-phycoerythrin . Hydrophobic interaction chromatography . Expanded bed absorption . Ion-exchange chromatography . Streamline column | R-phycoerythrin was purified by means of phenylsepharose expanded bed absorption and DEAE-sepharose ion-exchange chromatography from Porphyra yezoensis, one of the largest and important aquaculture species in Chin |
Ficha | Systematics and Paleobiology | Niles Eldredge and Michael J. Novacek | 11 | 65-74 | 2769 | no completo | Sin asignar | Systematics, ostensibly the "old" paleontology, actually plays a central and crucial role in modern paleobiology. We argue that a revised ontology has recently darified the nature of species and has expressly added monophyletic groups to the roster of spa | |
Ficha | Field and morphological observations of Gelidium longipes (Gelidiales, Rhodophyta), a rare endemic red alga from northern New Zealand | NELSON W. A. and T. J. FARR | 41 | 707–713 | NO | no completo | Rodofitas | Gelidiales; Gelidium longipes; northern New Zealand | Field observations of the little known, New Zealand endemic red alga Gelidium longipes (Gelidiales, Rhodophyta) indicate that this species has a highly restricted distribution in northern New Zealand. Pr |
Ficha | Invasion of Codium fragile ssp. tomentosoides in northern Chile: A new threat for Gracilaria f | Neil and et. al. | 0 | NO | Clorofita | ||||
Ficha | Nuevos registros de macroalgas para el Atlántico mexicano y riqueza florística del Caribe mexicano | Neidy Pauline Cetz-Navarro et. al. | 18 | nov-19 | NO | no completo | General | Arrecifes de coral, Caribe mexicano, ficoflora, Península de Yucatán, Quintana Roo. | Se revisaron muestras de macroalgas de un hábitat pocas veces analizado (colindante a la parte basal del tejido vivo |
Ficha | Evolvability, Modularity, and Individuality During the Transition to Multicellularity in Volvocalean Green Algae | Nedelcu Aurora M. and Richard E. Michod | ene-30 | NO | no completo | Clorofita | evolvability, germ line, green algae, immortality, individuality, modularity, totipotency, Volvox | During evolutionary transitions in the units of evolution, individuality emerges at a new and | |
Ficha | ECOLOGICAL DISTRIBUTION OF STREAM MACROALGAL COMMUNITIES FROM A DRAINAGE BASIN IN THE SERRA DA CANASTRA NATIONAL PARK, MINAS GERAIS, SOUTHEASTERN BRAZIL | NECCHI-JÚNIOR, O. and et. al. | 63 | 01-dic | NO | parcialmente completo con liga | General | ecological distribution, macroalgae, mountain stream, highland grassland. | Twelve stream segments were sampled four times in 1998-1999 (one sampling per season) in the drain- 45’-21o |
Ficha | Germination in Pithophora akinetes. | Neal, E. C., & Herndon, W. R. | 87 | 525-527 | 3728 | no completo | Sin asignar | ||
Ficha | The Entomology of Panama | Neal A. Weber | 2 | 187-198 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Algas: Un importante recurso natural. | ND | ND | 3725 | no completo | Sin asignar | |||
Ficha | Ley de Aguas Nacionales | ND | 22 A 44 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Flora ficologica de México. | ND | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Flora Ficológica de Riscos | ND | 1 A 6 | NO | parcialmente sin liga | Sin asignar | Este documento representa el proyecto preliminar de investigacióll sobre algas mariras bentonicas presentes en los "Riscos o Peñascos" a lo Larqo del Pacífico Tropical Mexicano. Forma parte del proyecto "Macroalgas del Pacífico Mexicano", que integra junt | ||
Ficha | Cryptophyta, Euglenophyta and Pyrrhophyta. | ND | 262-269 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | DINÁMICA DE LAS INTERACCIONES ALGA-CORAL EN DOS BAHÍAS DE LA REGIÓN DE SANTA MARTA (CARIBE COLOMBIANO) CON DISTINTO GRADO DE INFLUENCIA ANTROPOGÉNICA | Nazira Mejía–Niño y Jaime Garzón–Ferreira. | 32 | 243-261 | NO | no completo | General | Arrecifes coralinos, Algas, Interacciones, Santa Marta, Colombia, Caribe. | Para contribuir al conocimiento del impacto potencial de las macroalgas sobre las comunida- interacciones alga-coral en co |
Ficha | Iridaea cordata (Gigartinales, Rhodophyta): responses to artificial UVB radiation | Navarro Nelso P. and et. al. | 22 | 385–394 | NO | Completo | Rodofitas | Carpospores . Germlings. Morphological alteration . Mortality . UVB effects | The effects of UVB radiation on the different developmental stages of the carrageenan-producing red alga Iridaea cordata were evaluated considering: (1) carpospore and discoid germling mortality; (2) growth r |
Ficha | UVB effects on early developmental stages of commercially important macroalgae in southern Chile | Navarro N.P. and et. al. | 20 | 897–906 | NO | no completo | General | Commercial seaweeds . Spores. UVB impact | High levels of ultraviolet-B radiation (UVB) |
Ficha | New Species of Gelidium on The Pacific Coast of North America | Nathaniel Lyon Gardner | 13 | 273-318 | 3240 | no completo | Sin asignar | ||
Ficha | Selectivity of Ingestion and Digestion in the Chrysomonad Flagellate Ochromonas malhamensis | Nathan Dubowsky | 21 | 295-298 | NO | parcialmente sin liga | Sin asignar | Ochromonas malhamensis; digestion; Gomori stain; ingestion; phagotrophy; electron microscopy. | Ochromonas malhamensis cells were allowed to feed on autoclaved Aerobacter aerogenes, biochemically inert polystyrene latex particles of comparable size, shape and density, or a combination of these to determine if this protozoan is capable of phagotrophi |
Ficha | The Structure and Reproduction of the Genera Ceramium and Campylaophora in Japan with special Reference to Criteria of Classification | Nakamura, Yositeru | 4 | 15-62 | 1383 | no completo | Sin asignar | 1. In the species examined, the mean diametel of the tetraspore is smaller than that of the carpospore, and both spores of Ceramium are smaller than those of Campylaephora in the mean diameter respectively. The mode of germination of the spores shows both | |
Ficha | Taxonomic notes on Caribbean Neosiphonia and Polysiphonia (Ceramiales, Florideophyceae): five species from Florida, USA and Mexico | Nadya R. Mamoozadeh and D. Wilson Freshwater | 54 | 269-292 | NO | no completo | General | Caribbean Mexico; Florida; molecular-assisted identification; Neosiphonia; Polysiphonia. | Molecular-assisted identification using plastid-encoded rbcL Mexico samples. Morphological character states were exam-< |
Ficha | Competitive Relationships in Natural and Artificial Algal Communities | Nabivailo Yu. V. and E. A. Titlyanov | 32 | S21–S31 | NO | parcialmente completo con liga | General | competition, seaweeds, mechanisms, community. | Modern data on competitive relationships and their role in the succession of natural and artificial |
Ficha | Identification, definition and quantification of goods and services provided by marine biodiversity: Implications for the ecosystem approach | N.J. Beaumont, M.C. Austen, J.P. Atkins, D. Burdon, S. Degraer, T.P. Dentinho, S. Derous, P. Holm, T. Horton, E. van Ierland, A.H. Marboe, D.J. Starkey, M. Townsend, T. Zarzycki | 253–265 | NO | Liga perdida | Sin asignar | Marine biodiversity; Goods and services; Ecosystem Approach; Environmental management | This paper identifies and defines ecosystem goods and services provided by marine biodiversity. Case studies have been used to provide an insight into the practical issues associated with the assessment of marine ecosystem goods and services at specific l | |
Ficha | Rhodophyceae | N. Svedelius | ND | 3149 | no completo | Sin asignar | |||
Ficha | The Clinging Mechanism of Pseudophryne Bibroni (Anura: Leptodactylidae) to an Alga on Glass | N. Gradwell | 99 | 31-34 | NO | parcialmente sin liga | Sin asignar | Despite the absence of an oral sucker, tadpoles of all stages from 26 to 40 (of Gosner 1960) were found to be capable of clinging by their jaws to an alga on vertical glass. When the glass was wiped clean of the alga, Phyllobium sp., tadpoles were no long | |
Ficha | Possible role of a mitochondrial genome rearrangement in maintaining the spatial segregation of two cryptic species of the Lessonia nigrescens species complex | Myriam VALERO2,3 and Sylvain FAUGERON4 | 52 | 371-383 | NO | Liga perdida | Kelp | Heteroplasmy l Kelp l Mitochondria l Parapatric distribution l Range edge l Speciation | In numerous taxa, studies have reported the co-occurrence of several copies for a single mitochondrial marker |
Ficha | Using genetic tools for sustainable management of kelps: a literature review and the example of Laminaria digitata | Myriam VALERO et. al. | 52 | 467-483 | no completo | Feofita | Seaweed harvesting l Spatial and temporal genetic variation l Population connectivity l Conservation strategy | Kelp forests are threatened by human activities that result in habitat loss or deplete natural stocks, but little is | |
Ficha | Algas | Myriam Krasilchik | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Stictosiphonia Kelanensis (Grunow Ex Post) King & Puttock (Rhodomelaceae, Rhodophyta): A New Record from Atlantic Mangroves | Mutue Toyota Fujii, Nair Sumie Yokoya y Marilza Cordeiro-Marino | 17 | 93-97 | 2618 | no completo | Sin asignar | Stictosiphonia kelanensis, mangrove, new record, Atlantic. | Stictosiphonia kelanensis (Grunow ex Post) King & Purtock (Rhodomelaceae, Rhodophyta): a new record from Atlantic mangroves. During a study of the algae in mangroves of Rio Sítio Grande, Ilha do Cardoso (25°03'S; 47°55'W), Sao Paulo State,Brazil, plants b |
Ficha | QUANTIFICATION OF THE EFFECTS OF SPORELING COALESCENCE ON THE EARLY DEVELOPMENT OF GRACILARIA CHILENSIS (RHODOPHYTA)' | Munoz Alejandro A. and Bernabe Santetices | 30 | 387-392 | NO | parcialmente completo con liga | Rodofitas | coalescence; ecology; Gracilaria chi- lensis; Rhodophyta; sporeling coalescence; sporeling growth | Sporeling coalescence in species of Gracilariales and Gigartinales is predicted to result in larger basal areas of growing disks as well as earlier initiation, increased abundance, and faster growth rales of |
Ficha | Seasonal Variations in the Vertical Distribution of Benthic Microalgae in the Upper Sediment of the Mdloti Estuary, South Africa | Mundree Sarasvathi and et. al. | 46 | 323–331 | NO | no completo | General | chlorophyll-a; light; microphytobenthos; nutrients; pheopigments, temporarily-open estuary; vertical distribution. | A 12-month survey investigated seasonal variations in the vertical distribution of benthic microalgal biomass |
Ficha | Effects of wave exposure on the proportion of gametophytes and tetrasporophytes of Mazzaella oregona (Rhodophyta: Gigartinales) from Paci¢c Canada | Mudge Benita and Ricardo Scrosati | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Morphologische und physiologische Studien an der Cladophoracee Pithophora. | Mothes, K. | 48 | 110-121 | 3732 | no completo | Sin asignar | ||
Ficha | The influence of environmental factors on the distribution of freshwater algae: an experimental study: II. The role of pH and the carbon dioxide-bicarbonate system. | Moss, B. | 61 | 157-177 | NO | parcialmente sin liga | Sin asignar | Oligotrophic species of algae would not grow at pH values above 8 6-8 85, whilst eutrophic ones grew at pH values above 9, and at considerably higher bicarbonate levels than did the former. The results are interpreted in terms of the available free CO2 at | |
Ficha | The influence of environmental factors on the distribution of freshwater algae: An experimental study: III. Effects of temperature, vitamin requirements and inorganic Nitrogen compounds on growth. | Moss, B. | 61 | 179-192 | NO | parcialmente sin liga | Sin asignar | Growth rates of fifteen species of algae were measured at temperatures between 40 C and 360 C. The maximum growth rates of oligotrophic species tended to be smaller than those of eutrophic species. Temperature optima for growth under the conditions used d | |
Ficha | Macroalgal morphology mediates particle capture by the corallimorpharian Corynactis californica | Morrow Kathleen M. and Robert C. Carpenter | 155 | 273–280 | NO | Liga perdida | Rodofitas | The shallow kelp forest at Santa Catalina Island, California (33.45 N, ¡118.49 W) is distinguished by several canopy guilds ranging from a floating canopy (Macrocystis pyrifera), to a stipitate, erect u | |
Ficha | Responses to desiccation stress by Klebsormidium rivulare (Ulotrichales, Chlorophyta) from a Rhode Island stream. | Morison, M. O. & Sheath, R. G. | 24 | 129-145 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Macro- and mesoherbivores prefer native seaweeds over the invasive brown seaweed Sargassum muticum: a potential regulating role on invasions | Monteiro C. A. and et. al. | 156 | 2505-2515 | NO | parcialmente completo con liga | Feofita | Herbivory has a strong impact on algal distribu- species. In this study, we assess the potential regulating role | |
Ficha | Mazzaella laminarioides spp. Tres especies cripticas con hsitorias demograficas dsitintas en Chile | Montecinos A. | NO | General | |||||
Ficha | TETRASPOROGENESIS IN Gelidium floridanum (GELIDIALES, RHODOPHYTA): CYTOCHEMICAL STUDY | Monte-Domecq, F. A. and et. al. | 12 | 21-22 | NO | Completo | Rodofitas | Gelidium is a genus of red algae with a very wide geographic range. It is an economically valuable seaweed used in agar production. The taxonomy of red algae is based on the complexity of reproductive structures and life hi | |
Ficha | Areal and vertical distribution of Cladophora glomerata biomass in western lake Erie. | Monaco, M. E. & Herdendorf C. E. | 84 | 78 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | GRAZING IMPACT OF, AND INDIRECT INTERACTIONS BETWEEN MESOGRAZERS ASSOCIATED WITH KELP (LAMINARIA DIGITATA) | Molis M. | NO | Kelp | |||||
Ficha | Phylogenetic Position of Siphonocladiales | Mohammed Nizamuddin | 83 | 282-290 | NO | parcialmente sin liga | Sin asignar | Thirteen species of tardigrades were colleted primarily from the Appalachian Mountains of North and South Carolina. A few collections from Virginia and Vermont are included also in the study. Additional collections records are cited for Echiniscus (Echini | |
Ficha | Phytogeography of the Fucales and their Seasonal Growth | Mohammed Nizamuddin | 13 | 131-139 | NO | Liga perdida | General | ||
Ficha | Algal Taxonomy: Historical Overview | Moestrup Øjvind | NO | parcialmente completo con liga | General | 01-jun | |||
Ficha | Algae: Phylogeny and Evolution | Moestrup Øjvind | 01-may | NO | no completo | General | Ideas on the phylogeny and evolution of the algae are presently based on a combination of | ||
Ficha | Hymenocladiopsis crustigena (Rhodymeniaceae), a new genus and species of marine Rhodophyceae from the Antarctic Peninsula. | Moe, R. L. | 25 | 1 A 9 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Notophycus fimbriatus (Solieriaceae), a new genus and species of marine Rhodophyceae from the Antarctic Peninsula. | Moe, R. L. | 25 | 544-550 | 3918 | no completo | Sin asignar | ||
Ficha | Recherches sur les Céramiacées (Rhodophycecs-Cernmiales) et leur morphogéuèse, l. Structure de I´appareil végétatif et des organes reproducteurs. | Mme M.-Th. L'Hardy-Halos | 77 | 211-287 | 1372 | no completo | Sin asignar | Atlántico frances; Antithamnion plumula, Spyridia filamentosa, morfológica. | This work is the study of the vegetative strcture and of the reproductive organs of a few Ceramiaceae from the French Atlantic and Chanel Coasts. The typical cladomian structure (Chadefaud, 1952) is detailed for Antithamnion plumula v. plumula where we ha |
Ficha | Recherches sur les Céramiacées (Rhodophycecs-Cernmiales) et leur morphogéuèse, Il. Les modalités de la croissance et Ies remaniements cellulaires. | Mme M.-Th. L'Hardy-Halos | 78 | 201-256 | 1370 | no completo | Sin asignar | Callithamnion tetragonum, Spyridia filamentosa, Corynospora pedicellata | Growth of Ceramiaceae is generally typically monopodial, but certain species show a different pattern difficult to explain. Thus, Callithamnion tetragonum shows monopodially developed eladomian axes and the growth of Spyridia filamentosa and of Corynospor |
Ficha | Recherches sur les Céramiacées (Rhodophycées-Céramiales) et leur morphogénèse. III.Observations et recherches experimentales sur la polarité cellulaire et pour la hiérarchisation des elements de la fronde. | Mme M.-Th. L'Hardy-Halos | 78 | 407-491 | 1427 | no completo | Sin asignar | ||
Ficha | Les Ceramiaceae (Rhodophycaea Florideae) des côtes de Bretagne 1.- Le genre Antithamnion Nägeli | Mme M.-Th. L'Hardy-Halos | NO | parcialmente sin liga | Sin asignar | ||||
Ficha | La morphogénèse chez les Ceramiaceae: Organisation hiérarchique de la fronde | Mme M.-Th. L'Hardy-Halos | 115 | 142-148 | NO | parcialmente sin liga | Sin asignar | Spyridia filamentosa (Wulf.) Harv. y Callithamnion tetragormm (con) C. Ag. | The indeterminate and determinate branches which constitute the Ceramiaceae's thallus depends upon regulation and inter-relation phenomena which can be studied experimentally. Sorne species show branches, the nature and part played in the morphologie orga |
Ficha | Characterization of carbohydrate combining sites of Bryohealin, an algal lectin from Bryopsis plumosa | Min Gui Jung & et. al. | 22 | 793-802 | NO | no completo | Clorofita | Bryopsis plumosa . Algae . Bryohealin . Lectin . N-acetyl-D-galactosamine . N-acetyl-D-glucosamine . Sugar binding site . Chemical modification | Bryohealin is a lectin involved in the wound- In the previous purification study, it has been shown that |
Ficha | Ingestion and transformation of algal turf by Echinometra mathaei on Tiahura fringing reef (French Polynesia) | Mills Suzanne C. and et. al. | 254 | 71–84 | NO | no completo | General | Sea urchins; Bioerosion; Grazing; Ingestion; Coral reef | The sea urchin Echinometra mathaei is the most abundant herbivore on many tropical reefs. We studied the ingestion and digestion diel rhythms, transformation of algal turf and bioerosion attributable to this species on the |
Ficha | New records of marine benthic algae from the Lagon Sud-Ouest of New Caledonia, South Pacific | Millar Alan J. K. and Claude E. Payri | 54 | 154–170 | NO | parcialmente completo con liga | General | biogeography, New Caledonia, new records, Macroalgae, taxonomy. | As part of an ongoing project to substantially increase |
Ficha | New records of marine benthic algae from New South Wales, eastern Australia | Millar Alan J. K. | 52 | 117–128 | NO | parcialmente completo con liga | General | Australia, Caulerpa taxifolia, Laurencia platyclada, Lord Howe Island, marine algae, new records, New South Wales. | Twenty-four species of marine macroalgae are recorded Ocean. Include |
Ficha | Morphology and molecular phylogeny of the marine algal order Gelidiales (Rhodophyta) from New South Wales, including Lord Howe and Norfolk Islands | Millar A.J. and D. Wilson F. | 18 | 215-263 | NO | no completo | Rodofitas | Fifteen species in seven genera of the marine benthic red algal order Gelidiales are reported from the New South Wales coast including Lord Howe Island and Norfolk Island. Critical sampling, a re-examination of herbarium sp | |
Ficha | Comparative Reproductive Patterns in Culture of Different Gigartina Subgenus Mastocarpus and Petrocelis Populations from Northern Japan | Michio Masuda, John A. West, Yukimasa Ohno and Munenao Kurogi | 97 | 107-125 | 3164 | no completo | Sin asignar | Gigartina subgenus Mastocarpus - Hybridization - Life hitory - Petrocelis - Rhodophyta. | Samples of the Gigartina pacifica-ochotensis complex were collected at 21 localities around Hokkaido and northern Honshu. The carpospore and blade tip cultures showed 3 reproductive patterns. (1) 237 (86.8%) of the 273 cultured isolates derived from singl |
Ficha | Setting nutrient thresholds to support an ecological assessment based on nutrient enrichment, potential primary production and undesirable disturbance | Michelle Devlin, Suzanne Painting, Mike Best | 55 | 65–73 | No | no completo | General | Nutrients; Primary productivity; Water Framework Directive; Classification | The EU Water Framework Directive recognises that ecological status is supported by the prevailing physico-chemical conditions in each water body. This paper describes an approach to providing guidance on setting thresholds for nutrients taking a |
Ficha | Polyneuropsis stolonifera gen. and sp. nov. (Delesseriaceae, Rhodophyta) from the Pacific Coast of North... | Michael Wynne and John A. West | 6 | 243-253 | NO | parcialmente sin liga | Sin asignar | Santa Cruz Conty en el centro de California hasta Vancouver Island, British Columbia; Delesseriaceae (Ceramiales, Rhodophyta), Polyneuropsis stolonifera gen. et sp. nov., | A new taxón of the red algal family Delesseriaceae (Ceramiales, Rhodophyta), Polyneuropsis stolonifera gen. et sp. nov., is described and recorded from sites ranging from Santa Cruz Conty in central California to Vancouver Island, British Columbia. This m |
Ficha | Definition, Character, and Other Equivocal Terms | Michael T. Ghiselin | 33 | 104-110 | 2759 | no completo | Sin asignar | ||
Ficha | Dominance and Distribution of Benthic Macrophyte Assemblages in a North Florida Estuary (Apalachee Bay, Florida) | Michael S. Zimmerman and Robert J. Livingston | 29 | 27-40 | 1516 | no completo | Sin asignar | Laurencia poitei, Digenia simplex, Gracilaria verrucosa, Gracillaris joliifera | A comparative analysis was made concerning the distribution of benthic macrophyte assemblages in shallow portions of Apalachee Bay (north Florida). This included a comparison of areas affected by bleached kraft mill effluents (BKME) (the Fenholloway River |
Ficha | Temporal variation and succession in an algal-dominated high intertidal assemblage | Michael S. Foster, Eric W. Nigg, Laurie M. Kiguchi, Dane D. Hardin, John S. Pearse | 15 – 39 | NO | Liga perdida | Sin asignar | Ecological generalization; Endocladia muricata; Grazing; Mastocarpus papillatus; Succession; Recovery rate; Rocky intertidal; Seasonality | We determined whether temporal variation and succession were similar among sites with similar species composition by sampling unmanipulated and cleared plots in a high intertidal assemblage dominated by Endocladia muricata and Mastocarpus papillatus. Samp | |
Ficha | A method to determine which nutrient is limiting for plant growth in estuarine waters—at any salinity | Michael Neill | 50 | 945–955 | No | no completo | General | Limiting; Nutrient; Estuary; Nitrogen; Phosphorus; Carbon; Plant; Phytoplankton; Salinity | A method, utilising overlaid graphs for nutrients vs salinity, was developed in order to determine which nutrient is limiting for |
Ficha | Structure and Significance of Crueiate Flagellar Root Systems in Green Algae: Comparative Investigations in Species of Chlorosarcinopsis (Chlorosarcinales) | Michael Melkonian | 130 | 265-292 | 2861 | no completo | Sin asignar | Chlorophyceae, Chlorosarcinopsis, C. pseudominor, C. gelatinosa, C. auxotrophica, C.minor, C. dissociata.--Comparative ultrastructure, zoospores, flagellar root system, function, taxonomy. | The ultrastructure of biflagellate zoospores in seven species of the green alga Chlorosarcinopsis (Chlorosarcinales) was studied, particularly the cruciate flagellar root system, and a comparative approach was attempted. The seven species constitute four |
Ficha | Life History and Systematic Studies of some Pacific North American Phaeophyceae (Brown Algae) | Michael James Wynne | 50 | ND | NO | parcialmente sin liga | Sin asignar | Pacífico de América del Norte; Ectocarpales, Chordariales, Dietyosiphonales y Seytosiphonales | Members of four orders of brown algae (Ectocarpales, Chordariales, Dietyosiphonales, and Seytosiphonales), occurring along the Pacific Coast of North America, were investigated using culture techniques. The purpose of the study was to contribute to a bett |
Ficha | Studies on the Life Forms in Nature and in Culture of Selected Brown Algae | Michael J. Wynne | ND | NO | parcialmente sin liga | Sin asignar | América del Norte (California a Alaska); Petalonia, Seytosiphon lomentaria, C. bullosa de C. peregrina, C. sinuosa f. tuberculatta, | Petalonia fascia and Seytosiphon lomentaria have been collected from various locations along the west of North America (California to Alaska), and cultures have been established in an effort to determine what morphological and life-history attributes may | |
Ficha | Culture studies of Pacific coast Phaeophyceae | Michael J. Wynne | 119 | 129-144 | NO | parcialmente sin liga | Sin asignar | Syringoderma abyssicola, the little known type spedes of an apparently dictyotalean genus, is reported on after field and culture observations. Fungal infestations of the genus Eurychasma produce conspicuous sporangia which give the appearance of reproduc | |
Ficha | Inorganic nutrition in pond cultivated Gracilaria conferta (Rhodophyta): nitrogen, phosphate and sulfate | Michael Friedlander | 13 | 279-286 | NO | Completo | Rodofitas | agar, Gracilaria conferta, nitrogen, nutrition, phosphate, sulfate | The experience gained in the outdoor cultivation system of Gracilaria conferta in Israel suggests three main inorganic variables: inorganic carbon, macronutrients and micronutrients. The effects of the macronutrients nitrog |
Ficha | Life History and Hybridization Studies on Gigartina Stellata and Petrocelis Cruenta (Rhodophyta) in The North Atlantic | Michael D. Guily and John A. West | 19 | 474-494 | 3162 | no completo | Sin asignar | Carrageenan; Gigartina; hybridiuition; life history; north Atlantic; Petrocelis; photoperiod; Rhodophyta; tetrasporogenesis. | Fourteen isolates of the crustose marine red alga Petrocelis cruenta J. Agardh from various localities in the British Isles, France (including the type locality), Spain and Portugal gave rise in culture to dioecious foliose plants identifiable as Gigartin |
Ficha | Photosynthetic activity of benthic diatoms in response to different temperatures | Mi Sun Yun & Sang Heon Lee & Ik Kyo Chung | 22 | 559-562 | no completo | Fitoplancton | Benthic diatoms. Temperature . Photosynthesis. SA/V ratio . Chlorophyll fluorescence | The photosynthetic activities of benthic diatoms | |
Ficha | Stasis or kinesis? Hidden dynamics of a rocky intertidal macrophyte mosaic revealed by a spatially explicit approach | Menge Bruce A. and et. al. | 314 | 3 –39 | NO | parcialmente completo con liga | General | Competition; Disturbance; Grazing; Macrophyte mosaics; Oregon; Phyllospadix scouleri | Macrophyte mosaics, or tile-like assemblages of turfy marine macroalgae and surfgrass (Phyllospadix scouleri), are |
Ficha | Gracilaria and Polycavernosa (Rhodophyta) from Micronesia. | Meneses, I. S. A. B. E. L., & Abbott, I. A. | 20 | 187-200 | 3845 | no completo | Sin asignar | Three species of the red algal genus Gracilaria (Gracilariaceae) and four entities, one a new species, of the closely related genus Polycavernosa are recognized from material dcposited in the University of Guam herbarium. Gracilaria salicornio, widely rep | |
Ficha | Strain selection and genetic variation in Gracilaria chilensis (Gracilariales, Rhodophyta) | Meneses I. & B. Santelices | 11 | 241-246 | NO | parcialmente completo con liga | Rodofitas | DNA polymorphism, Gracilaria chilensis, genetic variability, strain selection | Strain selection processes in seaweed often have assumed that sterile clones could be maintained for long periods in a diversity of environments without major genetic changes. However, clonal species such as Gracilaria chil |
Ficha | Integración florística de las algas marinas de la costa sur de Jalisco, México | Mendoza-González A. Catalina and et. al. | 82 | 19-49 | NO | no completo | General | Cyanophyta, Rhodophyta, Heteroconthophyta, Chlorophyta, riqueza específica. | Se presentan los resultados obtenidos en un estudio sobre las algas marinas bentónicas en 7 localidades de |
Ficha | Estudio preliminar de las algas marinas bentónicas de la costa de Jalisco, México. | Mendoza, A. C., & Mateo, L. E. | 37 | 9 A 25 | NO | parcialmente sin liga | Sin asignar | Se presentan los resultados preliminares de un estudio sobre la flora marina bentónica de las costas de Jalisco, en aguas del Pacífico tropical de México. La lista florística se acompaña de datos relativos a la distribución de las especies en el área de e | |
Ficha | Speciation and Mating Behavior in Eudorina | Melvin Goldstein | 11 | 317-344 | 1474 | no completo | Sin asignar | A comparative morphological study was made of 73 clones of Eudorina isoated from 44 natural populations and grown under controlled environmental conditions. Utilizing the information obtained in this study in association with the existing taxonomic and ex | |
Ficha | Se busca Caulerpa Taxifolia | Meinesz, A., De Vaugelas, J. & CNS de Caulerpa Taxifolia | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Survival strategies in Polysiphonia adamsiae and P. strictissima (Rhodophyta, Rhodomelaceae) subjected to sediment deposition and grazing pressure | Mei Junxue and David R. Schiel | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Phylogeny of Oedogoniales (Chlorophyceae, Chlorophyta) inferred from 18S rDNA sequences with emphasis on the sequencesrelationships in the genus Oedogonium based on ITS-2 | Mei H. , W. Luo, G. X. Liu, and Z. Y. Hu | 265 | 179-191 | NO | no completo | Clorofita | Oedogoniales, Oedogonium, Oedocladium, Bulbochaete, 18S rDNA, ITS-2, phylogeny, systematics. | The phylogeny of Oedogoniales was |
Ficha | Preparation of galactans from Gracilaria debilis and Gracilaria salicornia (Gracilariales, Rhodophyta)of Indian waters | Mehta Gaurav K. and et. al. | 22 | 623–627 | NO | Completo | Rodofitas | Gracilaria debilis. Gracilaria salicornia . Galactans. 13C NMR . GC-MS | Superior quality non-methylated and low-sulphated galactans were extracted from two Indian agarophytes namely Gracilaria debilis and G. salicornia growing naturally along the west coast of India, using an eco |
Ficha | Algal d15N values detect a wastewater effluent plume in nearshore and offshore surface waters and three-dimensionally model the plume across a coral reef on Maui, Hawai‘i, USA | Meghan L. Dailer and etal. | No | no completo | General | d15N Wastewater Nitrogen Algal bioassay Coral reefs | The coral reef at Kahekili, Maui is located 300 m south of the Lahaina Wastewater Reclamation Facility | ||
Ficha | The ecology of intertidal algal crusts: variation within a functional group | Megan N. Dethier | 37-71 | NO | Liga perdida | Sin asignar | Crustose algae; Disturbance; Functional group; Herbivory; Morphology; Stress | Encrusting marine algae are found at all depths in the photic zone from polar to tropical seas worldwide, yet little is known about their ecology. Crusts (including red, brown, and green algae as well as lichens and Cyanobacteria) tend to predominate in a | |
Ficha | Refining cryptophyte identification: matching cell fixation methods to FISH hybridisation of cryptomonads | Medlin Linda K. & Sabine Strieben | 22 | 725-731 | NO | parcialmente completo con liga | Fitoplancton | Cryptophytes. Fixation methods. Flow cytometry . FISH hybridisation | The Division Cryptophyta, Class Cryptophyceae, |
Ficha | In situ net primary productivity and photosynthesis of Antarctic sea ice algal, phytoplankton and benthic algal communities | McMinn Andrew and et. al. | 157 | 1345–1356 | NO | no completo | General | Primary production at Antarctic coastal sites is | |
Ficha | A selected bibliography on seaweed aquaculture research and development in the tropical pacific | McLachlan J.L. and et. al. | NO | Cultivo | |||||
Ficha | Ultrastructure and differentiation in Cladophora glomerata. I. Cell division. | McDonald, K. L., & Pickett-Heaps, J. D. | 63 | 592-601 | NO | parcialmente sin liga | Sin asignar | Cladophora glomerata, | Cladophora glomerata is a coenocytic, fresh-water green alga in which mitosis and cyto- kinesis occur independently. The mitotic spindle is centric, closed, and develops from two half- spindles which form from amorphous but well-defined MTOCs at each pole |
Ficha | Responses of algae, corals and fish to the reduction of macroalgae in fished and un fished patch reefs of glovers reef atoll, belize | McClanahan T.R. and et. al. | 19 | 367-379 | NO | no completo | General | Algae, coral reef fishes, disturbance, fishing, herbivory, marine protected areas, | |
Ficha | Algal growth and species composition under experimental control of herbivory, phosphorus and coral abundance in Glovers Reef, Belize | McClanahan T.R. and et. al. | 44 | 441-451 | NO | no completo | General | Algal growth; Cage experiments; Herbivory; Nutrients; Phosphorus; Pollution | The proliferation of algae on disturbed coral reefs has often been attributed to (1) a loss of large-bodied herbivorous fishes, (2) |
Ficha | The Marine Algae of Oregon part I. Chlorophyta and Phaeophyta | Maxwell S. Doty | 3 | ene-68 | 1287 | no completo | Sin asignar | ||
Ficha | Rocky Intertidal Surfaces | Maxwell S. Doty | 67 | 535-585 | 2808 | no completo | Sin asignar | ||
Ficha | Recent devlopments in the sustematics of the Gigartinaceae (Gigartinales, Rhodophyta) based on rbcL sequence analysis and morphological evidence | Max H. Hommersand et. al. | 47 | 139-151 | NO | Completo | Rodofitas | Biogeography, cysticarp, Gigartinaceae, Gigartinales, molecular systematics, red algae, Rhodophyta, seaweeds | |
Ficha | SOLVING TAXONOMIC AND NOMENCLATURAL PROBLEMS IN PACIFIC GIGARTINACEAE (RHODOPHYTA) USING DNA FROM TYPE MATERIAL | Max H. Hommersand et. al. | 37 | 1091-1109 | NO | Liga perdida | Rodofitas | Chondracanthus; DNA; Gigartina- ceae; herbarium specimens; Iridaea; ITS 1; Mazzaella; PCR; red algae; RUBISCO spacer; type material | Molecular data obtained by a procedure for extracting PCR-amplifiable nuclear and chloroplast DNA from old and formalin-fixed red algal herbarium specimens were used to elucidate problems in the systematics of Pac |
Ficha | Max H. Hommersand and Richard B. Searles | 1736 | no completo | Sin asignar | |||||
Ficha | DESARROLLO DE GAMETÓFITOS Y ESPORÓFITOS DE MACROCYSTIS PYRIFERA (L.) C. AGARDH (LAMINARIALES: LESSONIACEAE) DE LA REGIÓN DE MAGALLANES EN CONDICIONES DE LABORATORIO. | Mauricio Palacios & Andrés Mansilla | 31 | 43-53 | no completo | Feofita | Macrocystis, cultivo, Tierra del Fuego | El objetivo del presente estudio consiste en describir y evaluar el desarrollo de gametófitos | |
Ficha | Life history studies in culture of a Mastocarpus species (Rhodophyta) from central Japan. | Masuda, M., West, J. A., & Kurogi, M. | 14 | 11 A 38 | 3846 | no completo | Sin asignar | Mastocarpus plants (= Gigartina mammillosa sensu MIKAMI) were collected at 9 localities covering its whole geographical range in Japan. A total of 286 plants were studied in laboratory culture using unialgal strains each derived from individual plants, in | |
Ficha | The induction of reproductive cell formation of Ulva pertusa Kjellman (Ulvales, Ulvophyceae) | Masanori Hiraoka and Sachito Enomoto | 199-203 | NO | Liga perdida | Sin asignar | induced reproduction, maturation inhibitor, reproductive cells, Ulva pertusa, zooid for-mation. | Synchronous zooid formation in Uiva pertusa Kjellman was induced in excised disks maintained in sterilized seawater at 20°C, 12:12 h L: D cycle and fluorescent light at 100 ?mol photons m -2 S-1 Zooids were reieased from mature disk tissue on the morning | |
Ficha | Production of antibacterial substances by benthic Tropical Marine Algae | MARY BELLE ALLEN AND E. YALE DAWSON | 79 | 459-460 | NO | parcialmente sin liga | Sin asignar | Laminaria angustata, Undaria pinnatifida y Rhodomela larix | Methanol extracts of three benthic algae from Japanese waters, Laminaria angustata, Undaria pinnatifida, and Rhodomela larix, have been shown to inhibit several species of bacteria. |
Ficha | RECOVERY AND GENETIC DIVERSITY OF THE INTERTIDAL KELP LESSONIA NIGRESCENS (PHAEOPHYCEAE) 20 YEARS AFTER EL NIÑO 1982/83 | Martinez E.A. and L. Cardenas | 39 | 504-508 | NO | no completo | Feofita | Massive mortality in kelp beds of the Pacific | |
Ficha | Selective mortality on haploid and diploid microscopic stages of Lessonia nigrescens Bory (Phaeophyta, Laminariales) | Martinez E.A. and B. Santelices | 229 | 219-239 | NO | parcialmente completo con liga | Feofita | Complex life-histories; Haplo–diploid phases; Herbivory; Laminariales; Lessonia; Microscopic algal stages; Size selection; Wave impact | In seaweeds, potential selective events on juveniles are particularly important because the |
Ficha | Clasificación de Asociaciones Vegetales Bentónicas por Métodos Objetivos. Aplicación al Mediolitoral de una Playa Rocosa. | Martín A. Hall y Alicia L. Boraso | ND | 1345 | no completo | Sin asignar | Several methods commonly used for objetive description of plant communities were teste don a rocky shore (Punta Cavendish, Puerto Desead, Argentina); this site permitted assessinets of the discriminating power of the methods in severe conditions. The quan | ||
Ficha | El Agar | Martha Ma. Ortega | 9 | ND | 842 | no completo | Sin asignar | ||
Ficha | Estudio de las Algas comestibles del Valle de México. | Martha Ma. Ortega | 14 | 85-97 | NO | parcialmente sin liga | Sin asignar | Valle de México, Lago; Cyanophyta Phormidium tenue (Menegh) Gomont y Chroococus turgidus (Kuetz) Naegeli | Se exponen los antecedentes históricos del “tecuítlatl” o “cocolin” y “amomoxtle” que constituían un suplemento alimenticio humano en las épocas del florecimiento y esplendor de los pueblos del Anáhuac. Se describe la evolución del gran Lago del Valle de |
Ficha | Consideraciones Taxonómicas sobre Diatomeas Epifitas del Intermareal Rocoso Marplatense. II | Martha E. Ferrario and Eugenia A. Sar | 88 | nov-27 | 2542 | no completo | Sin asignar | Diatomeas, taxonomía, ecología, distribución. | Catorce especies y variedades de diatomeas epífitas de macroalgas intermareales fueron estudiadas usando microscopio óptico y electrónico de barrido. La distribución ecológica de Navicula tripunctata (Müller) Bory es ampliada a ambientes marinos litorales |
Ficha | Marine Diatoms from Chubut (Argentina Republic) Centrales II-Thalassiosira | Martha E. Ferrario and Eugenia A. Sar | 48 | 421-429 | 2540 | no completo | Sin asignar | Thalassiosira, taxonomy, morphology, drstribution. | Eight species of Thalassiosira from the coastal wáter of the Province of Chubut, Argentina, were studied using both light and scanning electron microscope. Th. minima Gaarder represent a new record for the South Atlantic Coast and Th. minuscula Krasske a |
Ficha | Diatomeas Pennadas de la Ria de Puerto Deseado (Provincia de Santa Cruz, Argentina) I. Araphidales. | Martha E. Ferrario | 193 | 135-176 | 58 | no completo | Sin asignar | Santa Cruz, Argentina; Rhaphoneis amphiceros, Licmophora flabellata (Carmichael) Agardh, Grammatophora hamulifera Kiitzing, Rhabdonema arcualum. | Se han estudiado las Diatomeas correspondientes al orden Araphidales, en la Ría de Puerto Deseado. Se identificaron 8 géneros y 16 especies, las cuales, con excepción de Rhaphoneis amphiceros, son nuevas para el área revisada. Dos de ellas: Licmophora fla |
Ficha | Notes on New or Little-Known Marine Algae from Brazil Se ha habilitado la compatibilidad con lectores de pantalla. | Marshall Avery Howe and William Randolph Taylor | jul-33 | NO | Liga perdida | Sin asignar | |||
Ficha | Deepest Known Plant Life Discovered on an Uncharted Seamount | Mark M. Littler, Diane S. Littler, Stephen M. Blair, James N. Norris | 227 | 57-59 | 3263 | no completo | Sin asignar | The discovery of abundant autotrophic macrophytes living below 200 meters indicates their importance to primary productivity, food webs, sedimentary processes, and as reef builders in clear oceanic waters. Estimates concerning minimun light levels for mac | |
Ficha | BLOOM OF THE GIANT ANADYOMENE GIGANTODICTYON SP. NOV. (ANADYOMENACEAE, CLADOPHORALES) FROM THE OUTER SLOPE (25–50 m) OF THE BELIZE BARRIER REEF | Mark M. Littler and Diane S. Littler | 48 | 60-63 | No | no completo | General | algal bloom Anadyomene; Anadyo- menaceae; Anadyomene gigantodictyon; Belize Barrier Reef; Cladophorales | A giant form of Anadyomene, most similar to Ana- diminutive alga endemic to Florida, appeared as up |
Ficha | Assessment of coral reefs using herbivory/nutrient assays and indicator groups of benthic primary producers: a critical synthesis, proposed protocols, and critique of management strategiesy | MARK M. LITTLER and DIANE S. LITTLER | 17 | 195–215 | No | no completo | General | coral reefs; eutrophication; management; relative-dominance model; monitoring; indicator groups; herbivory; nutrients | 1. Rapid assessment protocols for determining and monitoring the status of any given coral reef |
Ficha | Species as 'noise' in community ecology: do seaweeds. block our view of the kelp forest? | Mark E. Hay | 9 | 414-416 | 2694 | no completo | Sin asignar | ||
Ficha | THE FUNCTIONAL MORPHOLOGY OF TURF-FORMING SEAWEEDS: PERSISTENCE IN STRESSFUL MARINE HABITATS1 | Mark E. Hay | 62 | 739-750 | NO | no completo | General | competitiom; desiccation; Dictyota; fringing reef; Halimeda; herbiory; Laurencia; morphology; productivity; seaweeds; turf. | Many seaweeds that occur in physically stressful habitats or habitats subject to mod- form is energetically expensive (the net production |
Ficha | Simulation of alternative management strategies for red algae, luga roja, (Gigartina skottsbergii Setchell and Gardner) in southern Chile | Marin S.L. and et. al. | NO | Kelp | |||||
Ficha | Ficologia Marinha Bentónica no Brasil: Situaç?o Actual e perspectiva | Marilza Cordeiro Marino | ene-23 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Observations on Two Species of Hyperiid Amphipods Associated with the Ctenophore Pleurobrachia Bachel | Marilyn Flores and Gary J. Brusca | 74 | oct-15 | NO | parcialmente sin liga | Sin asignar | Hyperoche medusarum y H. mediterranea | Two species of hyperiid amphipods (Hyperoche medusarum and H. mediterranea) were found in symbiotic associations with the ctenophore Pleuiobrachia bachei. H. mediterranea has not previously been reported from this ctenophore. Adult amphipods were most fre |
Ficha | Les difficultes de la phylogenie chez les Algues Corallinacées | Marie Lemoine | 19 | 1319-1325 | 3288 | no completo | Sin asignar | Archaeolitholhamnium | Investigations concerning Corallinaceous phylogeny encounters serious impediments since fossilization tends to destroy some important cell Wall characters. In addition, a structural type may, at different periods, be associated to two unlike reproductive |
Ficha | 15N MEASUREMENTS OF AMMONIUM AND NITRATE UPTAKE BY ULVA FENESTRATA (CHLOROPHYTA) AND GRACILARIA PACIFICA (RHODOPHYTA): COMPARISON OF NET NUTRIENT DISAPPEARANCE, RELEASE OF AMMONIUM AND NITRATE, AND 15N ACCUMULATION IN ALGAL TISSUE1 | Mariachiara Naldi and Patricia A. Wheeler | 38 | 135-144 | No | no completo | General | ammonium; Gracilaria; isotope dilution; macroalgae; 15N; nitrate; Ulva; uptake | Ammonium and nitrate uptake rates in the mac- were determined by 15N accumulation in algal tissue |
Ficha | Nitrate uptake and storage in the seaweed Ulva rigida C. Agardh in relation to nitrate availability and thallus nitrate content in a eutrophic coastal lagoon (Sacca di Goro, Po River Delta, Italy) | Mariachiara Nald, Pierluigi Viaroli | 269 | 65 – 83 | No | no completo | General | Coastal lagoon; Eutrophication; Nitrate; Ulva rigida; Uptake | The seasonal cycle of biomass and tissue composition of Ulva rigida C. Agardh, in relation to |
Ficha | Feofíceas do Litoral Norte do Estado do Rio De Janeiro, Brasil | Maria Teresa Menezes de Szechy y Marilza Cordeiro-Marino | 18 | 205-241 | 2616 | no completo | Sin asignar | Brown algae, marine flora, taxonomic survey. | Phaeophyceae from the Northern coast of Rio de Janeiro State, Brazil. From September 1982 to March 1984, a survey of the brown algae of Northern coast of the Rio de Janeiro State was carried out. Within this region, 7 collecting stations were established, |
Ficha | Fitobentos de Arrecife de Lanzarote, Reserva de la Biosfera (Islas Canarias) | María Elena Guadalupe, María Candelaria Gil-Rodríguez y María del Carmen Hernández-González | 16 | 33-46 | 2645 | no completo | Sin asignar | Phytobenthos, Arrecife de Lanzarote, Canary Islands. | Se presenta un catálogo de 200 especies de vegetales marinos bentónicos: 9 Cyanophyta, 109 Rhodophyta, 34 Phaeophyta, 44 Chlorophyta, 2 Eumycota y 2 Magnoliophyta recolectadas entre Playa del Reducto e Islote del Francés (Arrecife, SE Lanzarote) durante e |
Ficha | Studies on the Development, Life History and Taxonomy of the Ectocarpales (Phaeophyta) in Southern Australia | Margaret N. Clayton | 22 | 743-813 | NO | parcialmente sin liga | Sin asignar | Feldmannia, Giffordia y Hecatonema; Morfológico | The morphology, development and life history of filamentous brown algae, in particular species of the commoner genera Feldmannia, Giffordia and Hecatonema, are described. Morphogenetic differences parallel the well known n~orphological distinctions betwee |
Ficha | A study of variation in Australian species of Coipomenia (Phaeophyta, Scytosiphonales) | Margaret N. Clayton | 14 | 187-195 | 1183 | no completo | Sin asignar | Australia; Colpomenia peregrina (Sauvageau) Hamel y Colpomenia sinuosa (Roth) Derbes & Solier | Morphological and anatomical variation exhibited by Colpomenia in Australia has been studied using a hybrid index method and by analysis of variance. Some of the characteristics commonly used to distinguish the species are found to be variable and provide |
Ficha | THE ROLE OF CHARACEAN ALGAE IN THE MANAGEMENT OF EUTROPHIC SHALLOW LAKES | Marcel S. van den Berg, and et al. | 34 | 750-756 | No | no completo | General | Charaphytes; freshwater; Lake Veluwe- meer; shallow lake restoration | Characeae (charophytes or stoneworts) are ana- is divided into two tribes, the Chareae and Nitelleae, |
Ficha | Un Nuevo Equipo de Muestreo Cuantitativo para la Colecta de Organismos Asociados al Fitobentos Marino | Manuel Ortiz, Ana María Suárez | 4 | 93-104 | 2621 | no completo | Sin asignar | Thalassia; Cuba. | Se describe y ofrece Ie forma de operar un nuevo equipo para el muestreo de organísmos asociados a los vegetales bentósicos de aguas someras. Se presentan además los resul-tados obtenidos mediante los muestreos efectuados en dos localidades de la platafor |
Ficha | Algas Asociadas a Laurencia implicata (Ceraiviiales. Rhodophyta) en la Cayeria De Bocas De Alonzo, Cuba | Manuel Brito y Ana M. Suarez | 15 | 93-98 | 2620 | no completo | Sin asignar | Asociaciones ecológicas, Laurencia implicata, ASW, Cuba. | Se realizó una investigación sobre las algas asociadas a las masas del alga roja Laurencia implicata. Se encontraron 29 especies, las cuales 13 son Rhodophyta, 12 Chlorophyta, 2 Phaeophyta y 2 Cyanophyta. La biomasa de L. implicata varió de 551.1 g/m2 en |
Ficha | Growth and survival performance of the gametophyte of Gigartina skottsbergii (Rhodophyta, Gigartinales)under defined nutrient conditions in laboratory culture | Mansilla A. and et. al. | 20 | 889–896 | NO | Completo | Rodofitas | Gigartina skottsbergii . Growth . Nutrient requirements | Gigartina skottsbergii is a commercially important carrageenan producer that has been suffering severe extraction pressure in Chile’s Magellan Region and Cape Horn Archipelago since 1998. In order to create |
Ficha | Morphology and composition of mineral deposits of Lithophyllum byssoides (Lamarck) Foslie (Corallinales, Rhodophyta) from the Island of Ustica | Mannino A. M. | 137 | 203-214 | NO | Completo | Rodofitas | chemical-mineralogy, Coralk'naceae, Lithophyllum byssoides, morphology, southern Tyrrhenian Sea | The present study is based on the analysis of thalli of Lithophyllum byssoides (Lamarck) Foslie (Corallinales, Rhodophyta) collected from the Islandof Ustica (southern Tyrrhenian Sea). Both the composition of |
Ficha | The species concept in diatoms | Mann D.G. | 38 | 437-495 | NO | no completo | Fitoplancton | ||
Ficha | Chemical extraction techniques to free fossil silicoflagellates from marine sedimentary rocks. | Mandra, Y. T., Brigger, A. L., & Mandra, H. | 39 | 273-284 | NO | parcialmente sin liga | Sin asignar | silicoflagelados fósiles | Techniques of extracting fossil silicoflagellates and other siliceous micro- fossils from marine sedimentary rocks are described. The extraction is achieved by dissolving and chemically disaggregating all the rock, (or the cementing agents of the rocks) e |
Ficha | Paleoecology and taxonomy of silicoflagellates from an upper Miocene diatomite near San Felipe, Baja California, Mexico. | Mandra, Y. T., & Mandra, H. | 99 | 1 A 35 | NO | parcialmente sin liga | Sin asignar | Baja California, México. | Surface or near-surface temperatures at time of deposition probably were between 8°and 13° C. Systematics, camera lucida drawings, optical micro- scope photographs, and scanning electron micrographs are included. The slides and specimens used in this stud |
Ficha | Seasonal accumulation of metals by red alga Gracilaria verrucosa (Huds.)Papens. from Thermaikos Gulf, Greece | Malea P. & S. Haritonidis | 11 | 503–509 | NO | Liga perdida | Rodofitas | accumulation, Gracilaria verrucosa, metals, seasonal variation | Concentrations of Fe, Pb, Cu, Zn and Cd were determined during one season in the red alga Gracilaria verrucosa, sediment and seawater from the Thermaikos Gulf, Greece. This region has been subject to change due to increases |
Ficha | Molecular systematics of red algae: building future structures on firm foundations structures on firm foundations | Maggs Christine A. | 103-122 | NO | Completo | Rodofitas | Red algal systematics has a solid morphological foundation, based on analyses of female reproductive structures and post-fertilization development by Kylin and other workers. Recognition of the value of pit-plug ultras | ||
Ficha | YET ANOTHER NEW RED ALGAL ORDER? | Maggs Christine A. | 38 | 619–620 | NO | Completo | Rodofitas | ||
Ficha | Algal Spores | Maggs C.A. & M.E. Callow | NO | General | |||||
Ficha | Gelidiella calcicola sp. nov. (Rhodophyta) from the British Isles and Northern France | Maggs C. A. and M. D. Guiry | 22 | 417 - 434 | NO | Liga perdida | Rodofitas | Gelidiella caleicola sp. nov. (Gelidiales, Gelidiaceae) is described from plants growing on loose-lying subtidal coralline algae and shells on southern, western and northern shores of the British Isles, and from Roscoff in | |
Ficha | COMPETITION STUDIES OF MARINE MACROALGAE IN LABORATORY CULTURE | Maggs & Cheney | 26 | 18-24 | NO | parcialmente completo con liga | Cultivo | ||
Ficha | Phytoplankton functional groups and harmful algal species in anthropogenically impacted waters of the NW Mediterranean Sea | MAGDA VILA and MERCEDES MASÓ | 69 | 31-45 | no completo | Fitoplancton | asociaciones fitoplanctónicas, grupos funcionales, dinoflagelados tóxicos, mar Mediterráneo. | GRUPOS FUNCIONALES DE FITOPLÁNCTON Y ESPECIES TÓXICAS O NOCIVAS EN AGUAS DEL MEDITERRANEO NORDOC- | |
Ficha | A classic Caribbean algal ridge, Holandes Cays, Panama: an algal coated storm deposit | Macintyre Ian G. and et. al. | 20 | 95-105 | NO | Completo | Rodofitas | Algal ridge. Storms deposits. Submarine lithification. Crustose coralline algae. | Twenty-seven radiocarbon dates of cores covered from six drill holes indicate that the relief of the ridge on the seaward edge of the Holandés Cays, San Blas. off the Caribbean coast of Panamá, was formed by s |
Ficha | Vegetative propagation and spore-based recruitment in the carrageenophyte Chondracanthus chamissoi (Gigartinales, Rhodophyta) in northern Chile | Macchiavello Juan E. A., Cristian R. Bulboa C. and Mario Edding V. | 51 | 45-50 | NO | Completo | Rodofitas | Chile, Chondracanthus chamissoi, frond re- attachment, recruitment, reproduction, spores. | In the present study we compared vegetative and spore-based propagation for Chondracanthus chamissoi (C. Agardh) Kützing. Monthly field observations were made over a 1-year period at Puerto Aldea, Tongoy |
Ficha | Genetic structure of the giant kelp Macrocystis pyrifera along the southerastern Pacific | Macaya E.C. and G. C. Zuccarello | NO | parcialmente completo con liga | Kelp | ||||
Ficha | PRESENCE OF SPOROPHYLLS IN FLOATING KELP RAFTS OF MACROCYSTIS SPP. (PHAEOPHYCEAE) ALONG THE CHILEAN PACIFIC COAST | Macaya E.C. and et. al. | 41 | 913-922 | NO | no completo | Kelp | Chile; detachment, dispersal; float- ing; kelp rafts; Macrocystis; Pacific Coast; sporophylls | Some species of macroalgae continue to live for the presence of sporophylls (w |
Ficha | VARIACIÓN MENSUAL DE LOS CONTENIDOS ENÉRGETICOS, PORCENTAJE DE RENDIMIENTO DE CARRAGENANOS Y ANÁLISIS QUÍMICO DE LOS CARRAGENANOS EN LAS FASES DEL CICLO DE VIDA DE Chondrachantus chamissoi (C.Agardh) Kutzing,1843 (Rhodophyta,Gigartinales) EN COQUIMBO CHIL | Macarena Herrera Abaroa Valdivia | ene-66 | NO | Liga perdida | Rodofitas | Chondrachanthus chamissoi, Rhodophyta endémica del extremo Sur de Sudamérica, es intensamente extraída debido a que sintetiza polisacáridos sulfatados de muy buena calidad, que pertenecen a la fa | ||
Ficha | Ficoflora del Sustrato Rocoso dentro de las Costas del Golfo de México, México | Ma. Elena Sáncez Rodríguez | 29 | 347-350 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Nutrient manipulation methods for coral reef studies: A critical review and experimental field data | M.M. Littler, D.S. Littler, B.L. Brooks, B.E. Lapointe | 336 | 242–253 | No | no completo | General | Algae; Corals; Coral reefs; Methods; Nutrients | The results reported in this paper demonstrate suboptimal experimental designs in some of the previously published |
Ficha | Observacion Sobre la Estructura Valvar de Thalassiosira Tumida (Janisch) Hasle, Presente en Bahia Margarita (Antartida) | M.E. Ferra rio y E.A. Sar | 363 | 01-jul | 2539 | no completo | Sin asignar | Bahía Margarita (Antártida), Argentina; Thalassiosira tumida (Janisch) | Thalassiosira tumida (Janisch) Hasle proveniente de bahía Margarita (Antártida) fue estudiada usando Microscopio de Luz y Microscopio Electrónico de Barrido. La presencia de especímenes con contorno valvar triangular, es señalada por primera vez para la e |
Ficha | Succession in an intertidal benthic community affected by untreated sewage effluent: A case of study in the SW Atlantic shore | M.E. Becherucci and et. al. | 109 | 95-103 | NO | no completo | General | Benthic assemblages Recovery time Marine pollution Berkeleya sp. Boccardia proboscidea Brachidontes rodriguezii | A study of benthic succession related with sewage pollution was conducted in a warm-temperate coastal area of |
Ficha | Seasonal variation in growth and carrageenan content of Calliblepharis jubata (Rhodophyceae, Gigartinales) from the Normandy coast, France | M. Zinoun & J. Cosson | 8 | 29-34 | NO | no completo | General | Rhodophyceae, Calliblepharis jubata, growth, carrageenan | Study of the seasonal variation in the quality and content of iota carrageenan in Calliblepharis jubata from the |
Ficha | Algal Succession in a Macrocystis pyrifera Forest | M. S. Foster | 32 | 313-329 | NO | parcialmente sin liga | Sin asignar | Macrocystis pyrifera, | Algal succession within a subtidal forest of the giant kelp Macrocystis pyrifera was studied by following colonization and community development on concrete blocks fastened to the bottom. Sets of blocks were placed in the bed at 3-month intervals. Subsequ |
Ficha | Regulation of Algal Community Development in a Macrocystis pyrifera Forest | M. S. Foster | 32 | 331-342 | 870 | no completo | Sin asignar | Submareal; Macrocystis pyrifera | The effects of small and large-scale roughness, overstory development, competition for space with sessile animals, and grazing on algal community development in a subtidal Macrocystis pyrifera forest were examined using specially prepared concrete blocks |
Ficha | Seasonal patterns of tidepool macroalgal assemblages in the North of Portugal. Consistence between species and functional group approaches | M. Rubal, P. Veiga, R. Vieira, I. Sousa-Pinto | 66 | 187-194 | NO | no completo | General | Seasonal Pattern Tidepool Macroalgae Functional Groups Monitoring Grateloupia Turuturu | Macroalgae are useful organisms to monitor the environmental quality and to detect impacts due to |
Ficha | Vegetation of the intertidal zone of the lagoon of Aldabra, with particular reference to the photosynthetic prokaryotic communities | M. Potts and B.A. Whitton | 208 | 13-55 | 2167 | no completo | Sin asignar | ||
Ficha | pH and Eh On Aldabra Atoll 2. Intertidal Photosynthetic Microbial Communities Showing Zonation | M. Potts & B . A. Whitton | 67 | 99-105 | 2154 | no completo | Sin asignar | pH, Eh, mangrove forest, intertidal sediments, Chromatium, Hyella balani, diatoms | An account is given of changes taking place in intertidal photosynthetic microbial communities during every 14-day tidal cycle on Aldabra Atoll . These changes are apparently a consequence of movement of water with low Eh values from mangrove forest passi |
Ficha | Entéromorphes | M. Pierre Dangerard | 01-abr | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Entéromorphes | M. Pierre Dangerard | 01-abr | NO | parcialmente sin liga | Sin asignar | |||
Ficha | A List of Marine Algae from Libya | M. Nizamuddin, J. A. West and E. G. Menez | 22 | 465-476 | NO | Liga perdida | General | Based on published records of earlier collections, a list of marine algae was compiled totaling 178 species: Chlorophyta-15 genera, 29 species, Phaeophyta-19 genera, 34 species, Rhodophyta-76 genera, 112 species, Cyanophyta | |
Ficha | Taxonomic Notes on Marine Algae from Malaysia. V. Five Species of Rhodymeniales (Rhodophyceae) | M. Masuda, K. Kogame, S. Kawaguchi and S. M. Phang | 81-88 | NO | Liga perdida | Sin asignar | Five species of the red algal order Rhodymeniales are reported from Malaysia for the first time and their characteristic features are described: Chamaebotrys boergesenii (Weber-van Bosse) Huisman (Rhodymeniaceae), Coelarthrum sp. (Rhodymeniaceae), two spe | ||
Ficha | Unusual linear arrays of the coral reef macrophyte Halimeda incrassata in the Bahamas | M. M. Littler, B. E. Lapointe | 26 | 817-818 | No | no completo | General | ||
Ficha | Notes on The Genus Pseudomalaxis Fischer (Mollusca: Gastropoda) and its Fossil Species in Australia | M. F. Buonaiuto | 99 | 21-29 | NO | parcialmente sin liga | Sin asignar | Australia y Nueva Zelanda; | Two fossil species of Pseudomalaxis Fischer are discussed; P. asculpturatus Maxwell (Late Eocene) and P. praemeridionalis (Chapman) (Early Middle Miocene). The former is a new discovery in Australia and is one of a few forms common to both Australia and N |
Ficha | Distribution of the Marine Benthic Flora of the Caribbean Sea | M. Díaz - Piferrer | ND | 1293 | no completo | Sin asignar | A paper on the distribution of the benthic marine flora of the Caribbean and neighboring áreas was presented at the Symposium on Investigations and Resorces of the Caribbean Sea and Adjacent Regions which was held at Willemstad, Curaçao, Netherlands Antil | ||
Ficha | Cladograms Should Be Called Trees | M. D. Hendy and David Penny | 33 | 245-247 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Reinstatement of the Genus Mastocarpus Kützing (Rhodophyta) | M. D. Guiry, J. A. West, D.-H. Kim and M. Masuda | 33 | 53-63 | 3163 | no completo | Sin asignar | Morfología; historia de vida; caracteres bioquímicos; género Mastocarpus. | Morphological, life history and biochemical characters are used to show why the genus Mastocarpus should be reinstated for four widely distributed species of Gigartina (Gigartinaceae). Mastocarpus species have channelled thalli on which the female reprodu |
Ficha | Gelidieila minima sp. nov. (Rhodophyta) from Victoria, Australia: Implications for the Generic Classification of the Gelidiaceae | M. D. Guiry & H. B. S. Womersley | 27 | 165-176 | NO | no completo | General | Gelidiella minima sp. nov. (Gelidiaceae, Gelidiales) is described from the shallow subtidal of Point Lonsdale, Victoria, Australia, where it grows on shell fragments and both calcareous and non-calcareous encrusting algae. | |
Ficha | Mangrove Macroalgal Communities of Latin America: The State of Art and Perspectives | M. Cordeiro-Marino, M. R. A. Braga, V. R. Eston, M. T. Fujii, and N. S. Yokoya | 51-64 | 2613 | no completo | Sin asignar | |||
Ficha | Morphological and Cytological Studies on Brazilian Laurencia. 1: L. Arbuscula Sonder (Rhodomelaceae, Rhodophyta) | M. Cordeiro-Manno, M.T. Fujii y N. Yamaguishi-Tomita | 10 | 29-39 | 2617 | no completo | Sin asignar | Laurencia arbuscula Sonder (Rhodomelaceae, Rhodophyta); morfológico. | Morphological studies on Laurencia arbuscula Sonder (Rhodomelaceae, Rhodophyta) were carried out to provide a more detailed description for this species. L. arbuscula was classified in the genus Laurencia, subgenus Laurencia, section Laurencia. This speci |
Ficha | South African Parasitic Florideae and their Hosts 3. Four Minute Parasitic Florideae | M. A. Pocock | 167 | nov-41 | NO | parcialmente sin liga | Sin asignar | Sudáfrica; Choreonema thureli, Episporium centroceratis, Falkenbergieila caespitosa, Polysiphonia incompla, | Four small parasitic florideae are recorded and observations on their structure, development, reproduction and occurrence described. The cosmopolitan Choreonema thureli is recorded for the first time from South Africa, where it is widespread and of compar |
Ficha | Hydrodictyon in South Africa. With Notes on The Known Species of Hydrodictyon. | M. A. Pocock | 24 | ND | 1424 | no completo | Sin asignar | ||
Ficha | On the Origin of Mitosing Cdls | Lynn Sagan | 14 | 225-274 | 2825 | no completo | Sin asignar | ||
Ficha | Grateloupia huertana sp. nov. (Halymeniaceae, Rhodophyta), a peculiar new prostrate species from tropical Pacific Mexico | LUZ ELENA MATEO-CID and et. al. | 44 | abr-16 | NO | no completo | General | Grateloupia huertana sp. nov. is newly described from Oaxaca, Pacific Mexico on the basis of comparative morphology | |
Ficha | Development of commercial Kappaphycus production in the Line Islands, Central Pacific | Luxton David M. & Patrick M. Luxton | 477-486 | NO | no completo | Cultivo | Kappaphycus, seaweed production, socio-economics, Kiribati, Pacific Islands | Kappaphycus alvarezii (basionym Eucheuma alvarezii) was introduced to the Line Island atolls of Kiritimati | |
Ficha | Manual de microscopia electrónica, ultraestructura y citología vegetal. | Lux, Alexander | 1 | 1 A 7 | 3869 | no completo | Sin asignar | ||
Ficha | Mass cultivation of seaweeds: current aspects and approaches | Lüning Klaus and Shaojun Pang | 15 | 115-119 | NO | no completo | Cultivo | Epiphytes, Integrated cultivation, Seaweed cultivation, Seaweeds | A word-wide overview is presented of the current state of mass cultivation of seaweeds. In comparison with a |
Ficha | DESICCATION PROTECTION AND DISRUPTION: A TRADE-OFF FOR AN INTERTIDAL MARINE ALGA1 | Luke J. H. Hunt and Mark W. Denny | 44 | 1164-1170 | NO | no completo | General | desiccation protection; desicca- tion tolerance; Endocladia muricata; fairy rings; marine algae; thermotolerance | For marine algae, the benefits of drying out are |
Ficha | A key to the genera of the Marine Chlorophyta from Puerto Rico | Luis R. Almodóvar, Hugo L. Blomquist, Alida Ortiz, and Edgardo Ortiz | 1094 | no completo | Sin asignar | ||||
Ficha | NEW RECORDS AND RANGE EXTENSIONS FOR MARINE ALGAE OF THE PACIFIC COAST OF BAJA CALIFORNIA, MEXICO. II | Luis Ernesto Aguilar Rosas and Isaí Pachéco Ruiz | 11 | 67-76 | NO | no completo | General | Continuing collections of the ben& marine flora on the Pacific Coast of the Baja California Peninsula, we report new distribution range for nine species of which four have not been found previously in Baja California. T | |
Ficha | GREEN ALGAE (CHLOROPHYTA) FROM TODOS SANTOS BAY, BAJA CALIFORNIA, MEXICO. | Luis Ernesto Aguilar Rosas and Hans Bertsch | 9 | 111-123 | NO | no completo | General | We made occasional intertidal and subtidal collections throughout the different habitats of Todos Santos Bay, Baja California, México, from November 1975 to December 1982. Fro | |
Ficha | OCURRENCIA DE ALGAS CAFES (PHAEOPHYTA) EN LA BAHIA TODOS SANTOS, BAJA CALIFORNIA. | Luis Ernesto Aguilar Rosas | 8 | 25-34 | NO | no completo | General | Se llevaron a cabo 6 muestreos de algas bentónicas en la zona de entremareas en 6 zonas dentro de la Bahía Todos Santos, mediante los cuales se determinó la presencia de 24 especies de algas caf&ea | |
Ficha | Mapping of Posidonia oceanica beds around Elba Island (western Mediterranean) with integration of direct and indirect methods | luigi Piazzi, Stefano Acunto Francesco Cinelli | 23 | 339-346 | NO | no completo | General | Posidonia oceanica / seagrass / algae / mapping / airborne teledetection / Mediterranean | Direct and indirect methods were used for mapping Posidonia oceanica beds around Elba Island. Side scan sonar and a visual infra red scanner were used to detect the extension of beds. Also, direct observations were adopted |
Ficha | Growing the reproductive cells (carpospores) of the seaweed,Kappaphycus striatum, in the laboratory until outplanting in the field and maturation to tetrasporophyte | Luhan Maria Rovilla J. & Hananiah Sollesta | 22 | 579-585 | NO | parcialmente completo con liga | Clorofita | Carposporophyte . Temperature . Tetrasporophyte . Grow-out . Growth | Carposporophytes of the seaweed, Kappaphycus |
Ficha | Effects of ocean acidification on macroalgal communities | Lucia Porzio, Maria Cristina Buia, Jason M. Hall-Spencer | 400 | 278-287 | NO | no completo | General | Ocean acidification Macroalgal communities Marine biodiversity Functional ecology | There are high levels of uncertainty about how coastal ecosystems will be affected by rapid ocean acidification |
Ficha | Plant species diversity in a marine intertidal community: Importance of herbivore food preference and algal competitive abilites | Lubchenco J. | 112 | 23-39 | NO | no completo | General | ||
Ficha | Reproductive development and classification of the red algal genus Ceratodictyon (Rhodymeniales, Rhodophyta) | LR. Price and G.T. Kraft | 106-116 | NO | Liga perdida | Sin asignar | Ceratodictyon spongiosum Zanardini (Rhodymeniales, Rhodophyta) is a widely distributed tropical Indo-Pacific species, the thalli consisting of a reticulate network of algal axes surrounded and covered by a sponge symbiont. Several important reproductive f | ||
Ficha | GREEN ALGAE AND THE ORIGIN OF LAND PLANTS | LOUISE A. LEWIS AND RICHARD M. MCCOURT | 91 | 1535–1556 | no completo | Clorofita | Chlorophyta; Charophyta; DNA; Mesostigma; Streptophytina; ultrastructure. | Over the past two decades, molecular phylogenetic data have allowed evaluations of hypotheses on the evolution of green algae based on vegetative morphological and ultrastructural characters. Higher taxa are now generally recognized on the basis | |
Ficha | Can Sewage be Converted to Human Food? | Louis G. Williams | 2 | ND | 53 | no completo | Sin asignar | ||
Ficha | Morphological and growth responses of geographically isolated Macrocystis integrifolia populations when grown in a common environment | Louis D. Druell and Lindley Kemp | 60 | 1409-1413 | 2632 | no completo | Sin asignar | Macrocytis integrifolia Bory | Changes in blade morphology and growth characteristics of Macrocytis integrifolia Bory from four geographically separated populations growns in a common environmet were followed over two growth seasons. Initial differences in blade morphology and rate of |
Ficha | Universitarios estudian comunidades de algas y arrecifes | Lopez N. & H. Leon | 0 | NO | parcialmente completo con liga | General | |||
Ficha | The ubiquitous diatom–a brief survey of the present state of knowledge. | Lohman, K. E | 258 | 180-191 | 3715 | no completo | Sin asignar | Diatoms have distinctive and highly diversified tests or shells, similar to but not identical with opal in composition, accouting for their preservation as fossils in many kinds of sedimentary rocks and their importance to the geologist. The problem of un | |
Ficha | Characterization of the UDP-glucose pyrophosphorylase gene from the marine red alga Gracilaria gracilis | Lluisma Arturo O. & Mark A. Ragan | 10 | 581-588 | NO | parcialmente completo con liga | Rodofitas | UDPglucose pyrophosphorylase, polysaccharide biosynthesis, red algae | UDP-glucose pyrophosphorylase (UGPase) is a key enzyme in carbohydrate metabolism, particularly polysacchar- gene of the agar |
Ficha | Expressed sequence tags (ESTs) from the marine red alga Gracilaria gracilis | Lluisma Arturo O. & Mark A. Ragan | 9 | 287-293 | NO | parcialmente completo con liga | Rodofitas | EST, expressed sequence tag, Gracilaria, carbohydrate biosynthesis | Expressed sequence tags (ESTs) are partial sequences of cDNAs, and can be used to characterize gene expression |
Ficha | Occurrence of closely spaced genes in the nuclear genome of the agarophyte Gracilaria gracilis | Lluisma Arturo O. & Mark A. Ragan | 11 | 99-104 | NO | parcialmente completo con liga | Rodofitas | genome structure, genome organisation, red algae, synteny | Little is known about the structure and organisation of nuclear genomes in red algae. In particular, it is not known |
Ficha | Identification of a glucose-6-phosphate isomerase involved in adaptation to salt stress of Dunaliella salina | Liuqing Cui & Yurong Chai & Jie Li & Hongtao Liu & Lei Zhang & Lexun Xue | 22 | 563-568 | NO | no completo | Clorofita | Dunaliella salina . Glucose-6-phosphate isomerase . Halotolerance . Salt stress. Two-dimensional gel electrophoresis | The unicellular green alga Dunaliella salina is a recognized model for studying plant adaptation to high salinity. To isolate some salt-induced proteins at proteomics levels and to identify their expressions at gene levels, algal ce |
Ficha | Development of expressed sequence tag-derived microsatellite markers for Saccharina (Laminaria) japonica | Liu fuli and et. al. | 22 | 109-111 | NO | no completo | Feofita | Phaeophyta . Microsatellite . EST. Molecular marker | Expressed sequence tag-derived microsatellite |
Ficha | QTL Mapping for Frond Length and Width in Laminaria japonica Aresch (Laminarales, Phaeophyta) Using AFLP and SSR Markers | Liu fuli and et. al. | 12 | 386-394 | NO | parcialmente completo con liga | Feofita | Laminaria japonica Aresch . Genetic linkage map . QTL mapping . Marker-assisted selection . AFLP. SSR | In Laminaria japonica Aresch breeding practice, |
Ficha | The dominant Ulva strain of the 2008 green algal bloomin the Yellow Sea was not detected in the coastal waters of Qingdao in the following winter | Liu Feng & et. al. | 22 | 531-540 | NO | no completo | Clorofita | Ulva prolifera . Green tides. Internal transcribed spacer.rbcL . Enteromorpha . Phylogenetic analyses | The region of Qingdao, China, experienced the |
Ficha | Intertidal macrophyte communities from Pacific Baja California and the upper Gulf of California: relatively constant vs. environmentally fluctuating systems. | Littler, M. M., & Littler, D. S. | 4 | 145-158 | NO | parcialmente sin liga | Sin asignar | The adaptive features of marine macrophyte communities in a markedly fluctuating environment (the northern Gulf of Californis) were contrasted with those characteristic of a climatically more constant system (the Pacific coast of yhe Baja Peninsul | |
Ficha | Effects of stochastic processes on rocky-intertidal biotas: an unusual flash flood near Corona del Mar, California. | Littler, M. M., & Littler, D. S. | 86 | 95-106 | NO | parcialmente sin liga | Sin asignar | A localized storm on 9 May 1977 produced deluge-level quantities of rain (2.56 cm within 3 h) causing flooding of the rocky shoreline at Corona del Mar, California. Unlike the patterns observed throughout 1975 and 1976 and at a comparable site 40 km to th | |
Ficha | Morphological form and photosynthetic performances of marine macroalgae: tests of a functional/form hypothesis. | Littler, M. M. | 23 | 161-166 | NO | parcialmente sin liga | Sin asignar | Net and gross prodution rates were determined in the field at light intensities above 20,000lux for 45 species of marine macroalgae from four different enviroment in southwestern North America. Thin sheetlike and finely branched thallus-forms showed great | |
Ficha | An undescribed fungal pathogen of reef-forming crustose coralline algae discovered in American Samoa | Littler M.M. and D.S. Littler | 17 | 144 | NO | no completo | Rodofitas | ||
Ficha | Competition between macroalgae and corals: effects of herbivore exclusion and increased algal biomass on coral survivorship and growth | Lirman D. | 19 | 392-399 | NO | no completo | General | Coral-algal, competition, Caging, Grazer, exclusion, Algal overgrowth, Florida reef tract | |
Ficha | CRYPTIC DIVERSITY AND PHYLOGENETIC RELATIONSHIPS WITHIN THE MASTOCARPUS PAPILLATUS SPECIES COMPLEX (RHODOPHYTA, PHYLLOPHORACEAE) | Lindstrom Sandra C. | 44 | 1300-1308 | NO | no completo | Rodofitas | cryptic species; Mastocarpus; North Pacific; nuclear ribosomal internal transcribed spacer; Phyllophoraceae; phylogeny; rbcL gene | Mastocarpus papillatus (C. Agardh) Ku ?tz. is a com- coast of North America from Baja California to rbcL gene and the nuclear ri |
Ficha | Producción y Explotación de Algas en Chile | Linda Joyce y Bernabé Santelices | 10 | mar-26 | NO | no completo | Cultivo | ||
Ficha | Macroalgal bioindicators (growth, tissue N, d15N) detect nutrient enrichment from shrimp farm effluent entering Opunohu Bay, Moorea, French Polynesia | Lin David T. and Peggy Fong | 56 | 245–249 | NO | parcialmente completo con liga | General | Aquaculture; Effluent; Bioindicators; Nutrient enrichment; Stable isotopes; Macroalgae; Shrimp farming | Nutrient enrichment from shrimp aquaculture poses an increasing environmental threat due to the industry’s projected rapid growth |
Ficha | Molecular differentiation of two morphological variants of Gracilaria salicornia | Lim Phaik-Eem and et. al. | 13 | 335-342 | NO | no completo | Rodofitas | Gracilaria salicornia, molecular taxonomy, random amplified polymorphic DNA (RAPD) | Xia in 1986 combined Gracilaria salicornia, G. canaliculata (G. crassa), G. cacalia and G. minorinto one species: |
Ficha | Lista preliminar de fitoplancton del Puerto de la Libertad. | Lila Aida Gutiérrez A., & Menjívar, R. F. | 3 A 35 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | UNA REVISIÓN TAXONÓMICA DEL GÉNERO Udotea EN EL CARIBE MEXICANO Y CUBANO | Ligia Collado-Vides, Ana María Suárez y Rubén Cabrera | 30 | 145-161 | no completo | General | morfología; taxonomía; Udotea; ASW, México, Cuba. | Se hizo una revisión de la bibliografía para la región del Caribe mexicano y cubano con la finalidad de conocer la | |
Ficha | A history and annotated account of the benthic marine algae of Taiwan. | Lewis, E. J., & Norris, N. J. | 29 | 1 A 38 | NO | parcialmente sin liga | Sin asignar | Records of the benthic marine algae of the Island of Taiwan and neighboring islands have been organized in a floristic listing. All publications with citations of benthic marine green algae (Chlorophyta), brown algae (Phaeophyta), and red algae (Rhodophyt | |
Ficha | An Attempt to Determine Possible Taxonomic Significance of the Properties of Water Extractable Pulysaccharides in Red Algae | Leonard Stoloff and Paul Silva | 11 | 327-330 | 1546 | no completo | Sin asignar | More than sixty species of red algae have been described as containing significant quantities of polysaccharide hydrocolloids. There seem to be three major types of these polysaccharides. It is the purpose of this paper to determine the degree of correlat | |
Ficha | Macroalgas de Oaxaca. | León-Tejera, H., & González-González, J. | 486-498 | NO | parcialmente sin liga | Sin asignar | Las macroalgas marinas de Oaxaca se estudian a partir de 1847 por 13 investigadores. En 30 obras se reportan 166 especies de 21 localidades, quedando aún franjas considerables de litoral por estudiarse. El conocimientoque se tiene es incompleto y algunas | ||
Ficha | Evolution, development, and the units of selection | Leo W. Buss | 80 | 1387-1391 | NO | parcialmente sin liga | Sin asignar | The "Modern Synthesis" forms the foundation of current evolutionary theory. It is based on variation among individuals within populations. Variations within individuals are believed to hold no phylogenetic significance because such variation cannot be tra | |
Ficha | A highly sensitive cell assay for validation of purificationregimes of alginates | Leinfelder U. and et. al. | 24 | 4161-4172 | NO | no completo | General | Alginate; Apoptosis; Bacterial spores; Implantation; Fibrosis; Immune reaction | Among the hydrogels used for microencapsulation of cells and tissues, alginate has been and will continue to be one of the most |
Ficha | Individualistic Classes | Leigh Van Valen | 43 | 539-541 | 2763 | no completo | Sin asignar | ||
Ficha | Isotopic disequilibrium in marine calcareous algae | Lee D. and S. J. Carpenter | 17 | 307-329 | NO | Completo | Rodofitas | Calcareous algae; Calcification; Vital effects; d 13C and d 18O values | A survey of the d |
Ficha | CENTRO DE CULTIVO DE MACROCYSTIS sp | LECAROS GALAZ XIMENA PILAR | NO | Cultivo | |||||
Ficha | Trophic and biotic interactions in Laminaria digitata beds: wich fators could influence the persistence of marine kelp forests in northern Brittany? | Leblanc C. and et. al. | NO | Kelp | |||||
Ficha | Diversity and biomass dynamics of marine algae in Biosphere II’s tropical reef macrocosm | Leah Bymers, Edward P. Glenn, Stephen G. Nelson, Kevin Fitzsimmons | 442–456 | NO | Liga perdida | Sin asignar | Biosphere II; Coral reef restoration; Seaweed; Biodiversity; Succession; Intermediate disturbance; Paradox of the plankton; Chaos; Functional form hypothesis; Niche diversification | Macrocosms can be used to study complex ecological processes in a small physical space, but the validity of the studies depends on how well the macrocosm simulates natural ecosystem functions. We measured the standing crop of macroalgae and nutrient level | |
Ficha | Liste des algues marines de Cherbourg | Le Jolios A. | NO | General | |||||
Ficha | Poblaciones, biomasas y producciones fitoplanctónicas del Lago Titicaca. | Lazzaro, X. | 23-63 | NO | parcialmente sin liga | Sin asignar | El objeto de este estudio es el Lago Menor o Huiñaimarca (el área ubicada al sur del estrecho de Tiquina en el lago Titicaca) como ambiente de poblaciones de fitoplancton. Las influencias climáticas, particularmente la gran amplitud térmica en áreas monta | ||
Ficha | Comparative Habitat Diversity and Faunal Relationships Between the Pacific and Caribbean Panamanian Decapod Crustacea: A Preliminary Report, With Some Remarks on the Crustacean Fauna of Panama | Lawrence G. Abele | 2 | 125-138 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Carregeenan | Laurel Treviño??? | mar-19 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Ready-Serve Desserts | Laurel Treviño??? | ene-20 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Stabilization of Fermented and Directly Acidified Sour Milk Drinks | Laurel Treviño??? | ene-33 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | A complex-systems approach to predicting effects of sea level rise and nitrogen loading on nitrogen cycling in coastal wetland ecosystems | Laurel Larsen and et al. | 5 | 67-92 | No | no completo | General | To effectively manage coastal ecosystems, we need an improved understanding of how tidal marsh ecosys- existing literature to be | |
Ficha | Macroalgas y pasto marino, útiles bioindicadores de contaminación por hidrocarburos fósiles en sistemas acuáticos | Laura Georgina Calva B. y Rocío Torres Alvarado | 68 | 38-46 | NO | no completo | General | policyclic aromatic hydrocarbons, ma- croalgae, seagrass, coastal lagoon, bioaccumulation, traslocation. | The present work describe the importance like bioin- grass in coastal environments, with emphasis in pe- study of polycycl |
Ficha | Macroalgas y pasto marino, útiles bioindicadores de contaminación por hidrocarburos fósiles en sistemas acuáticos | Laura Georgina Calva B. y Roc ??o Torres Alvarado | 68 | 38-46 | NO | no completo | General | hidrocarburos arom ?aticos polic ??cli- cos, macroalga, pasto marino, laguna costera, bio- acumulaci ?on, traslocaci ?on. | En el presente trabajo se ejemplifica la importan- bioindicadores de contaminantes en ambientes cos- la bioacumulaci ?on de hi |
Ficha | Algae anathomy, biochemistry and biotechnology | Laura Barsanti, Paolo Gualtieri | 1-301 | NO | no completo | General | This book is an outgrowth of many years of research aimed at studying algae, especially micro- | ||
Ficha | Distribution and morphological variation of low-shore algal turfs | Laura Alroldi | 138 | 1233-1239 | NO | no completo | General | The distribution of three functional groups of algae (filamentous, corticated terete and calcareous articulated) was investigated in low-shore, turf-forming assemblages from rocky shores in the western Mediterranean Sea (It | |
Ficha | Responses of turf-forming algae to spatial variations in the deposition of sediments | Laura Airoldi, Massimiliano Virgillo | 165 | 271-282 | NO | no completo | General | Pelagic-benthic coupling . Sedimentation . Spatial variab~hty Experimental scale Colonisation . Algal turf. Polysiphonia setacea - Rocky subtidal shore | Responses of a turf-forming, filamentous, algal assemblage to spatial variation in the |
Ficha | Nutrient availability to marine macroalgae in Siliciclastic versus carbonate-Rich coastal waters | Lapointe B.E. & M.M. Littler | 15 | 75-82 | NO | parcialmente completo con liga | General | ||
Ficha | Nutrient thresholds for bottom-up control of macroalgal blooms on coral Jamaica and southeast Florida | Lapointe B.E. | NO | General | |||||
Ficha | PHYLOGENETIC ANALYSES OF THE BRYOPSIDALES (ULVOPHYCEAE, CHLOROPHYTA) BASED ON RUBISCO LARGE SUBUNIT GENE SEQUENCES | Lam Daryl W. and Frederick W. Zechman2 | 42 | 669-678 | NO | no completo | Clorofita | Bryopsidales; Caulerpales; Chlorophyta; Phlyogeny; rbcL; RUBISCO; taxonomy; Ulvophyceae | Current taxonomy of the Bryopsidales recogniz- Halimedineae. This concept was supported by early |
Ficha | Functional divergence in heat shock response following rapid speciation of Fucus spp. in the Baltic Sea | Lago-Leston A. and et. al. | 157 | 683-688 | NO | no completo | Feofita | In the Baltic Sea, the broadly distributed brown | |
Ficha | Resistance of benthic intertidal communities to multiple disturbances and stresses | Laetitia Joseph, Mathieu Cusson | 49-64 | NO | Liga perdida | Sin asignar | Community structure · Functional response · Multiple stressors · Resistance · Canopy disturbance · Grazers · Nutrient addition · Rocky intertidal | Many ecosystems are facing biodiversity loss and environmental change due to anthropogenic activities, with these impacts occurring within the context of natural disturbance. Understanding ecosystem functioning and the response of communities to these imp | |
Ficha | Giant kelp (Macrocystis pyrifera) survival in deep water (25–40 m) during El Niño of 1997–1998 in Baja California, Mexico | Ladah L. B. and J. A. Zertuche-Gonzalez | 47 | 367-372 | NO | parcialmente completo con liga | Kelp | deep water macroalgae; El Nin ? o; ENSO; giant kelp; internal waves. | During the 1997–1998 El Nin ? o, we examined seasonally coast of Northern Baja California. Though most popula- |
Ficha | Correlated light and electron microscope studies on brown algae | L.V. Evans and M. Susan Holligan | 71 | 1161-1172 | NO | no completo | General | ||
Ficha | Marine algae from the Gulf of Santa Clara, Sonora, Mexico | L.E. Aguilar-Rosas, R. Aguilar-Rosas, L.E. Mateo-Cid & A.C. Mendoza-Gonzalez | 477 | 231-238 | NO | no completo | General | marine algae, seaweed, distribution, seasonality, taxonomy, Gulf of Santa Clara, Mexico | Four sites in the Gulf of Santa Clara, northwestern coast of Sonora, Mexico, were sampled seasonally during |
Ficha | Effect of current on mineral uptake and respiration by a fresh-water alga. | L.A. Whitford and G.J. Schumacher | 423-425 | NO | parcialmente sin liga | Sin asignar | P32 uptake and CO2 evolution by Oedogonium kurzii Zeller were compared in the laboratory in still and moving water. An “inherent current demand” by this lotic species was indicated a) by x10 increase in P32 uptake at current equivalents of 18 cm/see; and | ||
Ficha | Correlated Light and Electron Microscope studie on Brown Algae I. Localization of alginic Acid and Sulphated Polysaccharides in Dictyota | L. V. Evans and M susan Holligan | 1161-1172 | NO | Liga perdida | Sin asignar | By electron microscopy and light microscope histochemical techniques, alginic acid and sulphated polysaccharides (probably largely fucoidan) have been located in the cell walls of Dictyota dichotoma. The cell walls of the vegetative thallus and those of m | ||
Ficha | Response of intertidal macrobenthic communities to long term human induced changes in the Eo estuary (Asturias, Spain): Implications for environmental management | L. de Paz, J.M. Neto, J.C. Marques, A.J. Laborda | 66 | 288-299 | NO | no completo | General | Benthos Long-term Shellfish culture Ecosystem disturbance Environmental impact Eo estuary Cantabric sea | Long term macrobenthos data together with physical habitat parameters were analysed to investigate |
Ficha | Bostrychia calliptera (Montagne) (Rhodomelaceae, Rhodophyta), Registro Nuevo para el Centro del Golfo de México | L. Collado-Vides y J.A. West | 22 | 47-55 | NO | parcialmente sin liga | Sin asignar | Bostrychia calliptera, México, distribución, algas marinas, manglares. | Bostrychia calliptera (Montagne) Montagne, recolectada en los manglares de la laguna de Sontecomapan (Veracruz, México), es un registro nuevo para el centro del golfo de México. Bostrychia calliptera difiere de su aliada más cercana, Bostrychia pinnata J. |
Ficha | Gelidiales. | Kylin, Harald. | 24 A 29 | 3818 | no completo | Sin asignar | |||
Ficha | Photosynthesis in Codium fragile (Chlorophyta)from a Nova Scotia estuary: responses to desiccation and hyposalinity | Kwang Young Kim Æ David J. Garbary | 151 | 99-107 | NO | no completo | Clorofita | Codium fragile ssp. tomentosoides from Gulf of St. Lawrence, was extremely tolerant to stres- | |
Ficha | Studies on Hypneocolax, with a discussion on the origin of parasitic red algae | Kung-Chu Fan | 3 | ND | 935 | no completo | Sin asignar | ||
Ficha | Morphological Studies of the Gelidiales | Kung-Chu Fan | 32 | 315-368 | 1072 | no completo | Sin asignar | Gelidiaceae, Gelidiellaceae, Pterocladia, P. lindaueri, Pierocladia, Gelidium, Pierocladui, Suhria, Porphyroglossum, Acropeltis,Ptilophora, morfológica. | The order Gelidiales is here considered to comprise two families, the Gelidiaceae and the newly established Gelidiellaceae. The family Gelidiellaceae includes only the genus Gelidiella . A new species of Pterocladia, P. lindaueri, is described on the basi |
Ficha | Advances in APPLIED PHYCOLOGY | Kumar Gupta R. & V. Dhar Pandey | NO | parcialmente completo con liga | General | ||||
Ficha | Some observations on Batrachospermum intortum Jao and B. sinense Jao (Rhodophyta, Nemalionales) from Szechwan in China. | Kumano, S. | 32 | 221-226 | 3796 | no completo | Sin asignar | ||
Ficha | Red Algal Parasites Occurring on Members of the Gelidiales | Kukg-Chu Fan and George F. Papenfuss | 15 | 33-38 | 942 | no completo | Sin asignar | ||
Ficha | Nutrient Limitation of the Macroalga Enteromorpha intestinalis Collected along a Resource Gradient in a Highly Eutrophic Estuary | KRISTA KAMERI, | 27 | 201-208 | No | no completo | General | We conducted a laboratory experiment to quantify nutrient (nitrogen and phosphorus) limitation of ma- nutrient-rich system | |
Ficha | Nutrient Addition to Experimental Rocky Shore Communities Revisited: Delayed Responses, Rapid Recovery | Kraufvelin Patrik and et. al. | 9 | 1076–1093 | NO | no completo | General | mesocosm; coastal eutrophication; intertidal communities; canopy algae; green tides; marine biodiversity; nutrient enrichment; long-term experiment. | Coastal eutrophication may alter the dominance patterns of marine macroalgae, with potential con- ecosystem. Benthic macroalgae and animals in |
Ficha | Biomass, diversity and production of rocky shore macroalgae at two nutrient enrichment and wave action levels | Kraufvelin P. and et.al | 157 | 29-47 | NO | no completo | Cultivo | The littoral zone of temperate rocky shores is | |
Ficha | Review of the genus Polyedriopsis Schmidle, incl. Tetraedorn bi-ridens Beck Mannagetta 1926 = P. bitridens (Beck-Mannag.) comb. novak | Kova?ik, L. | 117 | 246-252 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | A new Contribution to the Alien Red Macroalgal Flora of Greece (Eastern Mediterranean) with Emphasis on Hypnea Species | Konstantinos Tsiamis & Marc Verlaque | 393-410 | NO | Liga perdida | Sin asignar | Alien / Botryocladia madagascariensis / Greece / Hypnea anastomosans / Hypnea valentiae / macroalgae / Mediterranean / taxonomy | Three alien Rhodophyta, Botryocladia madagascariensis, Hypnea anastomosans and Hypnea valentiae, were recorded and illustrated for the first time from Greece (Aegean Sea and nearby areas). Previously reported from Karpathos Island, B. madagascariensis was | |
Ficha | Vetenskaps-akademiens förhandlingar | Kongl, Ö | 49 | 199-206 | 1276 | no completo | Sin asignar | ||
Ficha | Epigloeosphaera, a new cyanophyte genus from Nordic lakes. | Komárková-Legnerová, J. | 62 | 7 A 12 | NO | parcialmente sin liga | Sin asignar | A new genus Epigloeosphaera with one species is described from slightly dystrophic and eutrophicated lakes (South Sweden, North Russia and Cariada). The genus belongs to chroococcalean type with rod-like cells, localized on the surface of mucilaginous sph | |
Ficha | Primary production and functioning of algae in the fishpond littoral. | Komarkova, J., & Marvan, P. | 28 | 321-334 | 3781 | no completo | Sin asignar | ||
Ficha | Polynuclearity of vegetative cells in coccal green algae from the family Neochloridaceae. | Komárek, R. | 137 | 255-273 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Review of the genus Dictyosphaerium (Chlorococcales). | Komárek, J., & Perman, J. | 233-297 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | What is «Spirulina platensis» in fact?. | Komárek, J., & Lund, J. W. | 58 | 1 A 13 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Trichome structure of fourAphanizomenon taxa (Cyanophyceae) from Czechoslovakia, with notes on the taxonomy and delimitation of the genus. | Komárek, J., & Ková?ik, L. U. | 164 | 47-64 | 3745 | no completo | Sin asignar | The dimension and variation range of terminal and intercalary cells, heterocysts, and akinetes of four Aphanizomenon taxa occurring in Czechoslovakia were studied. Statistical and graphical procedures were used for evaluation. With regard to A. flos-aquae | |
Ficha | The genus Chlorotetraedron McEntee et al.(Protosiphonales, Chlorophyceae). | Komárek, J., & Kova?ik, L. | 57 | 289-297 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The genus Ecdysichlamys (Chlorellales). | Komárek, J., & Comas, A. | 56 | 13 A 28 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Areas of distribution of coccal green algae in relation to the algal flora of Cuba. Phycol. Lat. Amer | Komárek, J., & COMAS, A. | 2 | 133-167 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Species concept in coccal green algae. | Komárek, J. | 437-471 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Metacladistics | Kluge, A. G. | 5 | 291-294 | 3717 | no completo | Sin asignar | ||
Ficha | Carotenoid fluorescence in Dunaliella salina | Kleinegris Dorinde M. M. and et. al. | 22 | 645-649 | NO | no completo | Clorofita | ?-carotene . Carotenoids . Dunaliella salina . Fluorescence microscopy. Globules | Dunaliella salina is a halotolerant green alga that |
Ficha | The Atlantic Barrier Reef Ecosystem at Carrie Bow Cay, Belize, I Structure and Communities | Klaus Riitzler and Ian G. Macintyre | 12 | ND | 3256 | no completo | Sin asignar | Barrera coralina del Caribe cerca de Carrie Bow Cay, Belice; | Riitzler, Klaus, and Ian G. Macintyre, editors. The Atlantic Barrier Reef Ecosystem at Carrie Bow Cay, Belize, I: Structure and Communities. Smithsonian Contributions to the Marine Sciences, number 12, 539 pages, frontispiece, 232 figures, 5 plates, 47 ta |
Ficha | Biological interactions and their role in community structure in the rocky intertidal of Helgoland (German Bight, North Seat) | Klaus Janke | 219-263 | NO | Liga perdida | Sin asignar | Over 3 successive seasonal cycles (April 1986 to October 1988), field experiments were established within 3 intertidal levels in the sheltered rocky intertidal of Helgoland (North Sea, German Bight). Competitors for space (A4ytilus edulis, macroalgae), he | ||
Ficha | Seasonal growth and carbon and nitrogen content in canopy and first-year plants of Laminaria hyperhorea (Laminariales, Phaeophyceae) | KJERSTI SJ0TUN, STEIN FREDRIKSEN AND JAN RUENESS | 35 | 1-8 | No | no completo | General | The seasonal growth pattern of canopy plants has been compared with that of first-year plants. Large, canopy-forming | |
Ficha | Ecological significance and commercial harvesting of drifting and beachcast macroalgae and seagrasses in Australia: a review | Kirkman Hugh & Gary A. Kendrick | NO | General | |||||
Ficha | Observations of relic intertidal assemblages in an inland marine-spring of Eyre Peninsula, South Australia | Kiran Liversage | 46-56 | NO | Liga perdida | Sin asignar | Benthos; disturbance; saline lake; invertebrate; boulder habitat | Marine-springs containing relic intertidal species can be used to observe how assemblages usually found only on open coasts are structured when free from disturbances associated with water movement. This study tested if two previously described patterns f | |
Ficha | List of Marine Algae collected in Caroline and Mariana Islands, 1915. | Kintaro Okamura, Rigakuhakushi | 77-96 | NO | Liga perdida | Sin asignar | |||
Ficha | A taxonomic study on the Bostrychia tenella complex (Rhodomelaceae, Rhodophyta). | King, R. J., Puttock, C. F., & Vickery, R. S. | 27 | 10 A 19 | 3805 | no completo | Sin asignar | Four closely related taxa in the genus Bostrychia (B. tenella, B. binderi, B. binderi f. terrestris and B. flagelhfera) are investigated and re-assessed using multivariate analyses. Continuous variation was found in all but one of the characters measured | |
Ficha | Morphological and taxonomy of Bostrychia and Stictosiphonia (Rhodomelaceae/Rhodophyta). | King, R. J., & Puttock, C. F. | 2 | 1 A 73 | NO | parcialmente sin liga | Sin asignar | The genus Bostrychia Montagne s.l. is reassessed. Two genera are recognised, Bostrychia and Stictosiphonia J. D. Hooker et Harvey, differing from each other by the number of tiers of pericentral cells per axial cell, the mode of cortication and the number | |
Ficha | Bostrychia pinnata J. Tanaka et Chihara in Australia. | King, R. J., & Puttock, C. F. | 12 | 17 A 24 | 3823 | no completo | Sin asignar | Bostrychia pinnata was described by TANAKA and CHIHARA (1984 a) from mangrove forests in Japan. The species is now recognized in northern Australia. To the original description we now add descriptions of male and female plants, as well as the carposporoph | |
Ficha | Macroalgae associated with the mangrove vegetation of Papua New Guinea. | King, R. J. | 55-62 | NO | parcialmente sin liga | Sin asignar | The macroalgae associated with the mangrove vegetation of Papua New Guinea, a region which is phycologically poorly known, is investigated. The flora includes the characteristic 'Bostrychia-Caloglossa' association, and a complement of algae which may be r | ||
Ficha | Germination and Photo-Induction of Polarity in the Spherical Cells Regenerated from Protoplasm Fragments of Boergesenia forbesii | Kimiraru Ishizawa, Sachito Enomoto and Shunji Wada | 173-186 | NO | Liga perdida | Sin asignar | The processes of rounding (spheration) and cell wall formation of extracellular protoplasm fragments of Boergesenia forbesii were examined. This spheration depended on the presence of Ca n+ in the medium, and was accelerated exponentially with increasing | ||
Ficha | A new melobesioid alga Synarthrophyton chejuensis sp. nov. Corallinales, Rhodophyta) including comparison with Mesophyllum cystocarpideum | Kim Ji Hee and et. al. | 43 | 501-520 | NO | Completo | Rodofitas | ||
Ficha | Pulse feeding with nitrate and phosphate in relation to tissue composition and nutrient uptake by some macroalgae from the Red Sea at Ghardaqa (Egypt) | Kh. Abou Aisha, Effat F. Shabana, M. S. El-Abyad, I. A. Kobbia, F. Schanz | 135-145 | NO | Liga perdida | Sin asignar | This investigation aimed at determining the effects of experimental enrichment with either N or P or both elements on the tissue nutrient levels, and on the internal N: P molar ratios of three macroalgal species collected in the vicinity of Ghardaqa, Red | ||
Ficha | STRUCTURAL EVOLUTION IN THE FLAGELLATED CELLS OF GREEN ALGAE AND LAND PLANTS* | KENNETH D. STEWART and KARL R. MATTOX | 10 | 145--152 | No | no completo | General | ||
Ficha | Experimental transplantations of coralline algal turf to demonstrate causes of differences in macrofauna at different tidal heights | Kelaher B.P. and et. al. | 282 | 23-41 | NO | Completo | Rodofitas | Rocky shore; Macrofauna; Coralline turf; Transplantation | On rocky intertidal shores, dense fronds of coralline algal turf provide habitat for diverse assemblages of macrofauna. There are large differences in these assemblages and in the physical structure of coralline turf betwee |
Ficha | Cytomorphogenesis in cenoytic green algae. V. Segregative cell division and cortical microtubules in Dictyosphaeria cavernosa (Siphonocladales, Chlorophyceae) | Kazuo Okuda and et.al. | 45 | 189-196 | NO | no completo | General | cenocytic green alga, cortical microtubules, Dictyosphaeria cavernosa, protoplasmic contration, segregative cell division, Siphonocladales, wound responses. | |
Ficha | Seaweeds Fisheries Management in France, Japan, Chile and Norway | Katia FRANGOUDES | 52 | 517-525 | NO | no completo | General | Seaweeds l Management l France l Japan l Chile l Norway | Coastal communities have long gathered seaweeds for their own consumption, for animal feed and for fertilizer. |
Ficha | Natural pigments from algae: algae represent an untapped renewable resource for a number of useful products. | Karuna-Karan, A., & Schick, B. | 105 | 79-88 | 3723 | no completo | Sin asignar | ||
Ficha | Annual cycle of microphytoplankton from the coasts of the tropical Mexican Pacific | Karina ESQUEDA-LARA et.al. | 46 | 335-345 | no completo | Fitoplancton | Diatoms, Dinoflagellates, Diversity, Net phytoplankton, Succession, Tropical Mexican Pacific. | Despite the length of littorals, studies of annual cycles for phytoplankton in the Mexican Pacific are rare, espe- S | |
Ficha | Nutrient limitation of the Macroalga, Penicillus capitatus, Associated with Subtropical Seagrass Meadows in Bermuda | KAREN J. MCGLATHERY, ROBERT W. HOWARTH, ROXANNE MARINO | 15 | 18-25 | No | no completo | General | Nutrient limitation of the rhizophytic macroalga Penicillus capitatus found associated with sub- The photosynthetic response of P. ca | |
Ficha | Nuclear DNA Content Estimates in Multicellular Green, Red and Brown Algae: Phylogenetic Considerations | KAPRAUN DONALD F. | 95 | 7–44 | NO | no completo | General | C-value enigma, Chlorophyta, DNA C-values, eukaryotic algae, nuclear genome size, Phaeophyta, Rhodophyta. | Background and Aims Multicellular eukaryotic algae are phylogenetically disparate. Nuclear DNA content |
Ficha | Red algal polysaccharide industry: economics and research status at the turn of the century | Kapraun Donald F. | jul-14 | NO | no completo | Rodofitas | co-production, cyclic production, mariculture, sustainable development | Commercial research priorities target production cost reduction and expansion of new applications for established | |
Ficha | Optimization of certain physical parameters for the mariculture of Gracilaria edulis (Gmelin) Silva in Minicoy lagoon (Laccadive Archipelago) | Kaladharan P. and et. al. | 139 | 265-270 | NO | no completo | Cultivo | Gracilaria edulis; Mariculture; Optimum parameters | |
Ficha | Isolation and characterisation of a fourth hemagglutinin from the red alga, Gracilaria verrucosa, from Japan | Kakita Hirotaka and et. al. | 11 | 49-56 | NO | no completo | Rodofitas | hemagglutinins, Gracilaria, sulphated polysaccharide, carbohydrate specificity, seaweed, elec- trophoretic behaviour | Isolation and characterisation of marine algal hemagglutinins or lectins are essential for their potential industrial application as specific carbohydrate affinity ligands. The phosphate buffer extract of the red alga, Gracilaria verru- |
Ficha | Environmental factors associated with the spatial distribution of crustose coralline algae on the Great Barrier Reef | K. Fabricius - G. De´ath | 19 | 303-309 | NO | Completo | Rodofitas | Crustose coralline algae - Corallinales - Rhodophyta - Sedimentation - Turbidity | Crustose corralline algae (CCA) fulfill two key functional roles in coral reef ecosystems: they contributesignificantly to reef calcification, and they induce larval settlement of many benthic organisms. Percentage cover of CCA, and environmental condi |
Ficha | Listado Ficofloristico Preliminar de Playa San Telmo, Mich., Mex. | K. Dreckmann Estay & L. González Pérez-Sandi | 01-mar | NO | parcialmente sin liga | Sin asignar | |||
Ficha | New records of benthic marine algae from the Canary Islands (eastern Atlantic Ocean): morphology, taxonomy and distribution | Julio Afonso-Carrillo, Marta Sansón, Carlos Sangil and Tania Díaz-Villa | 119–127 | NO | Liga perdida | Sin asignar | Acrochaetium; Canary Islands; Colaconema hallandicum; Gelidiella; Lomentaria chylocladiella; Parviphycus setaceus; Pseudotetraspora marina. | Four species of marine algae are reported from the Canary Islands for the first time. Our report of the western Atlantic Gelidiella setacea (Gelidiales, Rhodophyta) is the first from the eastern Atlantic Ocean. Pseudotetraspora marina (Tetrasporales, Chlo | |
Ficha | MACROINVERTEBRADOS ASOCIADOS A DISCOS DE ALGAS PARDAS: BIODIVERSIDAD DE COMUNIDADES DISCRETAS COMO INDICADORA DE PERTURBACIONES LOCALES Y DE GRAN ESCALA | Julio A. Vásquez & J. M. Alonso Vega | no completo | Feofita | El Niño Oscilación del Sur (ENOS), disco de adhesión, Lessonia, comunidad de macroinvertebrados, contaminación minera, Norte de Chile, deshechos orgánicos. | Los discos de adhesión de Lessonia trabeculata, alga parda que forma huirales submareales, son | |||
Ficha | Macroinvertebrados asociados a disco de adhesión de algas pardas: Biodiversidad de comunidades discretas como indicadora de perturbaciones locales y de gran escala | Julio A. Vásquez & J. M. Alonso Vega | 429-450 | no completo | Feofita | ||||
Ficha | Variables morfométricas y relaciones morfológicas de Lessonia trabeculata Villouta & Santelices, 1986, en una población submareal del norte de Chile | julio A. Vasquez | 64 | 271-279 | NO | no completo | Feofita | Lessonia, macroalgas, manejo de recursos, ambientes submareales | |
Ficha | Mariculture of Kappaphycus alvarezii (Rhodophyta, Solieriaceae) color strains in tropical waters of Yucatan, Mexico | Julieta Muñoz, Yolanda Freile-Pelegr?n, Daniel Robledo | 239 | 161 – 177 | no completo | General | Carrageenan; Kappaphycus alvarezii; Mariculture; Yucatan | Three color strains of the n-carrageenan producing red alga Kappaphycus alvarezii were | |
Ficha | Chondracathus chamissoi (Rhodophyta, Gigartinales) in northern Chile: ecological aspects for management of wild populations | Julia A. Vasquéz & J. M. Alonso Vega | 13 | 267-277 | NO | Completo | Rodofitas | biomass production, Chile, Chondracathus chamissoi, epiphytism, herbivory, reproduction phenology, resource management | |
Ficha | Sur Deux Formes Nouvelles de Micrasterias | Jules Brunel | 03-jun | NO | parcialmente sin liga | Sin asignar | |||
Ficha | The Benthic Algal Composition, Standing Crop, and Productivity of a Caribbean Algal Ridge | Judith L. Connor and Walter H. Adey | ND | 1712 | no completo | Sin asignar | The distribution and standing crop of benthic algal species on a Caribbean algal ridge (St. Croix) and its associated carbonate pavements is discussed and contrasted with that of other eastern Caribbean algal ridges and a Pacific algal ridge. Mean standin | ||
Ficha | Healing and regeneration responses in Gigartina skottsbergii (Rhodophyta, Gigartinales): optimization of vegetative propagation for cultivation | Juan A. Correa, Jessica Beltrán, Alejandro H. Buschmann & Renato Westermeier | 315-327 | NO | Liga perdida | Sin asignar | Gigartina skottsbergii, regeneration, wound healing, vegetative propagation | The red alga Gigartina skottsbergii is becoming increasingly valuable as a resource to providing the raw material for the carrageenan industry established in Chile and elsewhere. As a result, wild stocks of the species are subject to intense harvesting by | |
Ficha | Produccion y explotacion de algas en Chile (1967-1975) | Joyce L. & B. Santelices | NO | parcialmente completo con liga | Cultivo | ||||
Ficha | Contribution of Receptacles from the Fucoid Ascophyilum nodosum to the Detrital Pool of a North Temperate Estuary | Josselyn, M. N., & Mathieson, A. C. | 1 | 258-261 | 1748 | no completo | Sin asignar | Ascophyllum nodosum | The fucoid brown alga Ascophyllum nodosum (L.) Le Jolis annually produces lateral repro- ductive branches (i.e. receptacles) approximately equal in weight to its vegetative thalli. The receptacles are shed within a single month during the spring. The esti |
Ficha | Bactrophora irregularis, a New Brown Alga from Australia | Josephine E. Tilden and Anna Parker Fessenden | 381-386+388 | NO | Liga perdida | Sin asignar | |||
Ficha | Dispersal of Fresh-Water Algae by Migratory Water Birds | Joseph S. Gots, Jacob Goldstein | 130 | 623 | NO | parcialmente sin liga | Sin asignar | Texas y Oklahoma, EE.UU. | Many migratory water birds killed in Texas and Oklahoma contained viable fresh-water algae in the lower digestive tracts. Such birds are thought to play a significant role in the long-range dispersal of certain algae, particularly those species easily kil |
Ficha | A Preliminary Survey of the Algal Flora of Soils of Certain Areas of Texas | Joseph Cain | 9 | 166-170 | NO | parcialmente sin liga | Sin asignar | Texas; taxonómico. | A listing is given of the microscopic algal flora obtained from 71 soil collections made in Central, North, and West Texas. Consideration is given to the ubiquity of certain genera and to the difficulty encountered in attempting a determination of the spe |
Ficha | Phenotypic plasticity in a mutualistic association between the sponge Haliclona caerulea and the calcareous macroalga Jania adherens induced by transplanting experiments. I: morphological responses of the sponge | José Luis Carballo, Enrique Ávila, Susana Enríquez, Leonardo Camacho | 467–478 | NO | Liga perdida | Sin asignar | The mutualistic association between the sponge Haliclona caerulea and the calcareous red macroalga Jania adherensis conspicuous on shallow rocky regions of Mazatla ?n Bay (Eastern tropical Pacific, Mexico). Transplanting experiments were carried out to ex | ||
Ficha | Analisis Preliminar de los Datos de la Campaña Antartica de Verano 1992/93 Proyecto Oceanografía Costera Brown | José Gallo, Martha Ferrario, Eugenia Sar, Gabriela Tosonotto, Miguel Segura y Daniel Molina | 426 | ene-50 | 2548 | no completo | Sin asignar | Antártida, Argentina. | Durante la Campaña Antártica de Verano 92/93, en el marco del Proyecto Oceanografía Costera, fue realizado un muestreo intensivo en el área de Bahía Paraíso. Los datos físicos, químicos, meteorológicos y biológicos recogidos recibieron un análisis prelimi |
Ficha | Monitoring of sewage Outfalls in Northern Spain: Preliminary Studies of Benthic Communities | José A. Juanes and Juan C. Canteras | 289-295 | NO | Liga perdida | Sin asignar | Baseline; benthos; macroalgae; macrofauna; monitoring; multivariate analysis; rocky; sediments. | Baseline studies constitute, at the same time, the base and the reference point for the development of sitespecific monitoring programs. As a previous step in the analysis of the structure of benthic communities in the infralitoral off Avilés an Gijón, m | |
Ficha | Fouling mediates grazing: intertwining of resistances to multiple enemies in the brown alga Fucus vesiculosus | Jormalainen V. and et. al. | 155 | 559-569 | NO | no completo | Feofita | Macroalgae have to cope with multiple natural to them. Evolution of resistance is complicated by the inter- | |
Ficha | Evaluation of the health status of a coastal ecosystem in southeast Mexico: Assessment of water quality, phytoplankton and submerged aquatic vegetation | Jorge A. Herrera-Silveira, Sara M. Morales-Ojeda | 72–86 | NO | Liga perdida | Sin asignar | Coastal ecosystem condition; Eutrophication; Indicators; Phytoplankton; Seagrasses; Submerged aquatic vegetation; Water quality; Yucatan | The coastal environment of the Yucatan Peninsula (SE, Mexico) includes a wide variety of ecosystems ranging from mangroves to coral reefs, resulting in a heterogeneous landscape. Specifically, the marine system is characterized by environmental difference | |
Ficha | Algal Ecology of Southern Icelandic Hot Springs in Winter | Jon A. Sperling | 56 | 183-190 | No | no completo | General | Algae; algae, blue-green; algae, thernzophilic; algae, winter surv iv al; algal ecology; Iceland; Icelandic hot springs; Mastigocladus; photosynthetic efficiency; primary prodluctii'ity; winter light in high latitudes. | A survey of algal habitats of southern Icelandic hot springs (Hengill-Olfus |
Ficha | Coral–algal competition: macroalgae with different properties have different effects on corals | Jompa Jamaluddin and Laurence J. McCook | 258 | 87–95 | NO | no completo | General | Coral–algal competition · Algal functional groups · Filamentous algal turfs · Corti- cated algae · Life-history traits · Porites spp. · Corallophila huysmansii · Chlorodesmis spp. | Competition between hard corals and macroalgae is a key ecological process on coral reefs, especially during reef degradation, which often involves a ‘phase-shift’ from coral- to alga- |
Ficha | Contrasting effects of turf algae on corals: massive Porites spp. are unaffected by mixed-species turfs, but killed by the red alga Anotrichium tenue | Jompa Jamaluddin and Laurence J. McCook | 258 | 79-86 | NO | no completo | Rodofitas | Coral-algal competition ·Anotrichium tenue · Epilithic algal community · Filamentous algal turfs · Porites spp. | Competition between corals and algae is an important process on coral reefs, especially |
Ficha | Effects of competition and herbivory on interactions between a hard coral and a brown alga | Jompa J. and L.J. McCoook | 271 | 25-39 | NO | no completo | Feofita | Coral – algal competition; Coral reef; Herbivore exclusion; Lobophora variegata; Overgrowth; Porites cylindrica | Despite widespread acceptance of the negative effects of macroalgae on corals, very few studies |
Ficha | Calcification by Crustose Coralline Algae on the Northern Great Barrier Reef, Australia | John R. M. Chi~holml | 45 | 1476-1484 | NO | Completo | General | Calcification by four species of crustose coralline algae was estimated on the windward reef at Lizard Island, northern Great Banier Reef, Australia, by combining measurements of O?, pH, and total alkalinity with equat | |
Ficha | Physical Characteristics of the Proposed Sea-Level Isthmian Canal | John P. Sheffey | 2 | 31-40 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The red algal genus Coelarthrum B0rgesen (Rhodymeniaceae, Rhodymeniales) in Australian seas, including the description of Chamaebotrys gen. nov. | John M. Huisman | 95-112 | NO | Liga perdida | Sin asignar | The genus Coelarthrum presently includes eight species world-wide, of which three (c. muelleri (Sonder) B¢rgesen, C. cliftonii (Harvey) Kylin and C. boergesenii Weber-van Bosse) have been recorded from Australian seas. An examination of type and recent co | ||
Ficha | Vegetative and Reproductive Morphology of Nemastoma damaecorne (Gigartinales, Rhodophyta) from Western Australia | John M. Huisman | 721-728 | NO | Liga perdida | Sin asignar | The vegetative and reproductive morphology of the red alga Nemastoma damaecorne Harvey (Gigartinales) have been examined. Thalli are flattened and variously branched, either foliose with marginal proliferation or deeply incised. Structurally, the thallus | ||
Ficha | THE ECOLOGY OF RIVER ALGAE | John L. Blum | 22 | 291-341 | NO | no completo | General | ||
Ficha | A taxonomic and geographical catalogue of the seaweeds of the western coast of african and adjacent islands | John D.M. and et. al. | NO | General | |||||
Ficha | Pilayella Littoralis F. Rupincola from Washington: The Life History in Culture | John A. West | 3 | 150-153 | 866 | no completo | Sin asignar | Washiington; cultivo utilizando medios de agua de mar natural suplementados y diversos regímenes de temperatura; Pilayella littoralis f. La rupincola, morfológico. | The life history of Pilayella littoralis f. rupincola from Washington was studied in culture using supplemented natural seawater media and various temperatura, photoperiod, and light intensity regimes. Plants in nature exhibited characteristics typical fo |
Ficha | Observations on four rare marine microalgae from Hawaii | John A. West | 8 | 187-192 | 787 | no completo | Sin asignar | Hawai; Rhodosorus marinus, Coccolithus neohelis, Ochrosphaera verrucosa y Sarcinochrysis marina | Rhodosorus marinus, Coccolithus neohelis, Ochrosphaera verrucosa, and Sarcinochrysis marina were isolated into culture from coral fragments and are recorded as new for the benthic marine algal flora of Hawaii. The life histories and cytology of these spec |
Ficha | Environmental Regulation of reproduction in Rhodochorton Purpureum | John A. West | 213-230 | 783 | no completo | Sin asignar | Chile, California, Washington y Alaska; Rhodochorton purpureum | Isolates of Rhodochorton purpureum from Chile, California, Washington and Alaska were grown in unialgal culture. The effects of light intensity, daylength, temperature and salinity on reproduction were tested. The California, Washington and Alaska clones | |
Ficha | Environmental Control of Hair and Sporangial Formation in the Marine Red Alga Acrochaetium proskaueri sp. nov. | John A. West | 377-384 | NO | parcialmente sin liga | Sin asignar | An isolate of Acrochaetium proskaueri sp. nov. from Puget Sound, Washington, was grown in unialgal culture under defined conditions using Provasoli's enriched sea water medium. The effects of light intensity, day length and temperature on development and | ||
Ficha | Morphology and Reproduction of The Red Alga Acrochaetium Pectinatum in Culture | John A. West | 4 | 89-99 | NO | parcialmente sin liga | Sin asignar | Medios de agua de mar natural suplementados; Acrochaetium pectinatum, | The life history of the marine red alga Acrochaetium pectinatum (Kylin) Hamel was studied in unialgal culture using supplemented natural seawater media. The tetrasporophytes are larger than the gametophytes, have a compact filamentous basal system, and pr |
Ficha | Addendum to Microalgae Culture Collection 1986-1987 (No. NREL/SP-232-3079-a). | Johansen, J. R., Lemke, P., Nagle, N. J., Chelf, P., Roessler, P. G., Galloway, R., & Toon, S. (1987). | 1 A 23 | 3737 | no completo | Sin asignar | |||
Ficha | Flore Algale des iles Chausey | Joel Cosson et Chantal Billard | 106 | 63-72 | 1714 | no completo | Sin asignar | Rhodophyceae, Phaeohyceae y Chlorophyceae | The algal flora of Chausey in the Channel Islands has been listed in three different facies charateristic of the archipelago: a moderately exposed rocky shore located SW in the Main Island, a very sheltered muddy cove below the Gros Mont (Anse de la Truel |
Ficha | Action des conditions d'eclairement sur la croissance des gamétophytes de Laminaria digitata (L.) Lamouroux (Phéophycée, Laminariale) | Joel Cosson | 20 | 50-54 | 1715 | no completo | Sin asignar | Light is very important for the development of gametophytcs of Laminaria digitata. Light intensities of 1-2 W/m2 increase the number of mitosis and favour the growth of axis. Growth of gametophytes in greatly affected by intensities under 0,1 W/m2 or over | |
Ficha | Evolution de la fertilité des populations de Laminaria digitata (L.) Lamouroux (Phéophycée, Laminariale) au cours de l´année | Joel Cosson | 21 | 28-34 | 1717 | no completo | Sin asignar | It has been shown that fertility of populations of Laminaria digltata (L.) Lam. on the coasts of Calvados is maximum between June and October with regard to the number of thalli bearing sporocysts, the relative importance of sori and the quantity of spore | |
Ficha | Sur la Vegetanon Algale de L'etage Littoral dans la Region De Saint-Vaast- La·Hougue et la Presence D'une Espece Japonaise Nouvelle Pour Les Cotes Françaises | Joel Casson, Anny Duglet & Chantal Billard | 105 | 109-116 | 1713 | no completo | Sin asignar | St-Vaast-La Hougue, Francia | La vegetación de algas de la región de St-Vaast-La Hougue, que es mucho menos acomodada ahora que a principios del siglo XX, tiene anomalías con respecto a la zonación habitual encontrada en la costa de Calvados o Cotentin: inversión Cinturones de fucacea |
Ficha | Growth rate influence on the chemical composition of phytoplankton in oceanic waters | Joel C. Goldman, James J. McCarthy and Dwight G. Peavy | 279 | 210-215 | NO | no completo | General | The chemical composition of oceanic phytoplankton (by atoms) typically occurs in the proportions C106 N16 P1. Yet, in laboratory growth conditions these proportions are only observed for mar | |
Ficha | Culture Studies on the Marine Green Alga Halicystis parvula-Derbesia tenuissima. II. | Joanna Ziegler Page and John M. Kingsbury | 55 | 01-nov | 1509 | no completo | Sin asignar | Unialgal cultures of the macroscopic, vesicular, coenocytic gametophyte (Halicystis parvula Schmitz) of Derbesia tenuissima (DeNotaris) Crouan fr. Were grown under various enviromental regimes to elucidate the cytology of gamete formation and the factors | |
Ficha | Culture Studies on the Marine Green Alga Halicytis Parvuladerbesia Tenuissima. III. Control of Gamete Formation by an Endogenous Rhythm | Joanna Ziegler Page and Beatrice M. Sweeney | 4 | 253-260 | NO | parcialmente sin liga | Sin asignar | Derbesia tenuissima (De Notaris) Crouan fr. (Chlorophyceae), anteriormente conocido como Halicystis parvula | Evidence is presented for an endogenous rhythm which controls gamete formation in the coenocytic gametophytic stage of the marine alga Derbesia tenuissima (De Notaris) Crouan fr. (Chlorophyceae), formely Known as Halicystis parvula. The rhythm is present |
Ficha | Synopsis of Biological Data On Laminaria hyperborea | Joanna M. Kain | 87 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Seagrasses and eutrophication | JoAnn M. Burkholder, David A. Tomasko, Brant W. Touchette | 350 | 46–72 | No | no completo | General | Biomarkers; Eutrophication; Food webs; Grazers; Nitrogen; Phosphorus; Seagrass; Watershed | This review summarizes the historic, correlative field evidence and experimental research that implicate cultural eutrophication |
Ficha | Gelidiaceae (Rhodophyta) from the northern Gulf of California, Mexico | Joan G. Stewart and James N. Norris | 20 | 273-284 | NO | parcialmente sin liga | Sin asignar | Golfo de California, México; Pterocladia parva Dawson con P. Gelidium microphysa Setchell & Gardner resultó ser una forma de G. pusillum (Stackh.) | Extensive recent collections of Gelidiaceae (Rhodophyta) from the northern Gulf of Cali-fornia, Mexico were studied. Comparisons of field-collected and laboratory-grown thalli support the merger of Pterocladia parva Dawson with P.Gelidium microphysa Setch |
Ficha | BISCAYNE BAY CONCEPTUAL ECOLOGICAL MODEL | Joan A. Browder and etal. | 25 | 854–869 | No | no completo | General | Biscayne Bay, seagrass, dolphins, manatees, fish, pink shrimp, water quality, coastal wetlands, freshwater inflow | Biscayne Bay is a naturally clear-water bay that spans the length of Miami-Dade County, Florida, |
Ficha | Removal of Ammonia from Wastewater Effluent by Chlorella Vulgaris | Jinsoo Kim et.al. | 15 | 391-396 | NO | no completo | General | microalgae; Chlorella vulgaris; wastewater effluent; nitrogen removal | The capability of Chlorella vulgaris to remove nitrogen in the form of ammonia and/or ammonium Ohio, U.S.A.) was studied. The was |
Ficha | Understanding the role of ecological indicator use in assessing the effects of desalination plants | Jin-Soo Chang | 416-433 | NO | Liga perdida | Sin asignar | Seawater desalination; Ecological indicators; Environmental impact assessment; Environmental risk assessment; Ecosystem health assessment | Understanding the role of a global seawater desalination plant project using potential ecological indicators is important in assessing ecological risk and/or impact evaluations from observations at a molecular level. A marine health assessment of ecologic | |
Ficha | Blackwell Publishing, Ltd. Tracking the invasive history of the green alga Codium fragile ssp. tomentosoides | JIM PROVAN, SUSAN MURPHY and CHRISTINE A. MAGGS | 14 | 189–194 | NO | no completo | Clorofita | Codium fragile, invasive species, phylogeography | The spread of nonindigenous species into new habitats is having a drastic effect on natural ecosystems and represents an increasing threat to global biodiversity. In the marine environ- |
Ficha | Succession in Algal Mat Communities at Three Different Nutrient Levels | Jerry L. Wilhm and Joseph Long | 50 | 645-652 | NO | parcialmente sin liga | Sin asignar | The effect of three different levels of phosphates and nitrates on temporal variation of structural and functional parameters was studied in algal mat communities in microcosms. The experimental units contained 1 liter of water collected from a farm pond. | |
Ficha | Cell division in Klebsormidium subtilissimum (formerly Ulothrix subtilissima), and its possible phylogenetic significance | Jeremy Pickett- Heaps | 6 | 167-183 | 2859 | no completo | Sin asignar | Klebsormidium subtilissimum; taxonomía. | An ultrastructural study of cell division has confirmed that the Ulotrichalean alga previously classified as Ulothrix subtilissima, is correctly designated as Klebsormidium subtilissimum. The spindle is centric and open, and during anaphase the chromosome |
Ficha | Cell Division in Cosmarium Botrytis | Jeremy Pickell-Heaps | 8 | 343-360 | 1213 | no completo | Sin asignar | Cell division in Cosmarium is described. Premititic cells are very dense; the semicells, previously appressed to one another, separate slightly during entry into prophase. This separation coincides with deposition of a girdle of new Wall material around t | |
Ficha | Determining Spatial and Temporal Inputs of Freshwater, Including Submarine Groundwater Discharge, to a Subtropical Estuary Using Geochemical Tracers, Biscayne Bay, South Florida | Jeremy C. Stalker & René M. Price & Peter K. Swart | 32 | 694–708 | No | no completo | General | Groundwater. Isotopes . Trace metals. Geochemistry. Florida . Submarine groundwater discharge | Geochemical mixing models were used to deci- discharge, or groundwater discharge) to Biscayne Bay, an |
Ficha | Bioassessment Techniques for Monitoring of Eutrophication and Nutrient Limitation in Coastal Ecosystems | JENS ERIK LYNGBY, SVERRE MORTENSEN and NICK AHRENSBERG | 39 | 212-223 | No | no completo | General | nutrient limitation; eutrophication; ulva lac- tuca; phytoplankton; nitrogen; phosphorus. | Bioassesment by the use of the macroalga, Ulva lactuca L., |
Ficha | Nutrient and growth dynamics of Halimeda tuna on Conch Reef, Florida Keys: Possible influence of internal tides on nutrient status and physiology | Jennifer E. Smith and etal. | 49 | 1923–1936 | No | no completo | General | We conducted a manipulative nutrient enrichment study to examine the physiological and growth dynamics of | |
Ficha | The ecology of Sargassum pteropleuron Grunow (Phaeophyceae, Fucales) in the waters off South Florida I. Growth, reproduction and population structure | Jeffrey S. Prince and Steven W. O'neal | 18 | 109-114 | 1784 | no completo | Sin asignar | Key Largo, Florida; Sargassum pteropleuron Grunow | The seasonal growth (change in length), reproduction, and structure of a dense population of Sargassum pteropleuron Grunow off Key Largo, Florida are described. The maximum mean rate of increase in plant length occurred during the high water temperatures |
Ficha | The evolutionary relationships of man and orang-utans | Jeffrey H. Schwartz | 308 | 501-505 | NO | parcialmente sin liga | Sin asignar | Fósil Sivapithecus | Man shares uniquely few morphological features with either the chimpanzee or the gorilla, whereas there are many features thtat suggest affinities between man and the orang-utan, to whom the fossil Sivapithecus appears to be closely related. If these are |
Ficha | Benthic indicators: From subjectivity to objectivity – Where is the line? | Jean-Claude Dauvin a, Gérard Bellan, Denise Bellan-Santini | 947–953 | NO | Liga perdida | Sin asignar | Benthic indicators; Soft-bottom community; Subjectivity; Objectivity; Expert judgement | Over the last few years, the interest in using benthic indicators to assess marine environments has increased dramatically after a rather long period of relative stagnation, mostly due to the need to assess the status of coastal marine waters required by | |
Ficha | Algas... Glosario ilustrado | Javier Carmona Jiménez, Marco A. Hernández Muñoz, Mónica Ramírez Vázquez | ene-83 | NO | Liga perdida | Sin asignar | |||
Ficha | Tissue Nutrient Content of Gracilaria spp. (Rhodophyta) and Water Quality along an Estuarine Gradient | Janine L. Horrocks, George R. Stewart and William C. Dennison | 46 | 975-983 | No | no completo | General | Tissue nutrient content of Gracilaria spp. (Rhodophyta) was tested as a bioindicator of | |
Ficha | Physiological activity of Porphyra in relation to eulittoral zonation | Jang K. Kim, George P. Kraemer, Charles Yarish | 365 | 75–85 | No | no completo | General | Emersion Eulittoral Zonation Nitrogen Phosphate Porphyra | Eulittoral seaweeds at different tidal elevations are exposed to various frequencies and durations of |
Ficha | Structure, Persistence, and Role of Cqnsumers in a Tropical Rocky Intertidal Community (Taboguilla Island, Bay of Panama) | Jane Lubchenco, Bruce A. Menge, Stephen D. Garrity, Peggy J. Lubchenco, Linda R. Ashkenas, Steven D. Gaines, Richard Emlet, John Lucas and Sharon Strauss | 23-73 | NO | Liga perdida | Sin asignar | The physical environment and patterns of distribution and abundance of macroalgae, sessile and mobile animals are described for the littoral zone of Taboguilla Island, Bay of Panama. The substratum is basaltic and heterogeneous in both texture and topogra | ||
Ficha | Ecological Studies of the Salt Marsh Ecad Scorpioides (Hornemann) Hauck of Ascophyllum Nodosum (L.) Le Jolis | Jan S. Chocks and Arthur C. Mathieson | 23 | 171-190 | NO | parcialmente sin liga | Sin asignar | Hauck de Ascophyllum nodosum | The seasonal and spatial distribution of the free-living ecad scorpioides (Hornemann) Hauck of Ascophyllum nodosum (L.) Le Jolis are described from the Great Bay Estuary System of New Hampshire-Maine, U.S.A. The growth and distribution of ecad scorpioi |
Ficha | Ecological Studies of The Salt Marsh Ecad Scorpzozdes (Hornemann) Hauck of Ascophyllum Nodosum (L.) Le Jolis | Jan S. Chock and Arthur C. Mathieson | 171-190 | NO | Sin asignar | The seasonal and spatial distribution of the free-living ecad scorpioides (Hornemann) Hauck of Ascophyllum nodosum (L.) Le Jolis are described from the Great Bay Estuary System of New Hampshire-Maine, U.S.A. The growth and distribution of ecad scorpioides | |||
Ficha | Ecology and Species Diversity of Coral Reefs on Opposite Sides of the Isthmus of Panama | James W. Porter | 2 | 89-116 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Euglena Gracilis in Synchronous Division. II. Blosynthetic Rates Over the Life Cycle | James R. Cook | 270-289 | 2865 | no completo | Sin asignar | Euglena gracilis | 1. When grown autotrophically on an appropriate light-dark regimen, populations of the flagellate Euglena gracilis divide synchronously, an approximate doubling of cell number occurring in each dark period. 2. Growth of the average cell during the light p | |
Ficha | Some new records of marine aIgae from the R/V Proteus cruise to British Columbia | James N. Norris L and Isabella A. Abbott | 5 | 87-94 | NO | parcialmente sin liga | Sin asignar | Columbia Británica, Canadá; Chlorophyta, Phaeophyta, Rhodophyta, Ulotrichales. | Twenty-eight species of benthic marine algae are newly reported from northern British Columbia. They comprise three Chlorophyta, three Phaeophyta and 22 species of Rhodophyta. The green alga Acrochoete repens Prings. (Ulotrichales) is reported from the Pa |
Ficha | Articulated Coralline Algae of the Gulf of California, Mexico, I: Amphiroa Lamouroux | James N. Norris and H. William Johansen | 9 | ene-29 | NO | no completo | General | Norris, James N., and H. William Johansen. Articulated Coralline Algae of to the Marine Sciences, number 9, 29 pages, 18 figures, 1981.—Amphiroa (Coral-< | |
Ficha | Observations on The Genus Blidingia (Chlorophyta) in California | James N. Norris | 7 | 145-149 | NO | parcialmente sin liga | Sin asignar | California; Blidingia (Ulvales), | The green algal genus Blidingia (Ulvales), reported for the first time California only 4 years ago, is now found to be fairly widely distributed there as B. minima (Nägeli ex Kützing) Kylin var. minima. B. minima var. subsalsa (Kjellman) scagel is now rec |
Ficha | Marine Algae and Seagrasses from Carrie Bow Cay, Belize | James N. N orris and Kalina E. Bucher | 12 | 167-223 | 3257 | no completo | Sin asignar | Carrie Bow Cay, South Water Cay y Twin Cays en el arrecife de la barrera central, Belice; Chlorophyta, Phaeophyta y Rhodophyta | A total of 165 taxa of benthic marine algae and three of seagrasses (angiosperms) has been found in the intertidal and subtidal habitats of Carrie Bow Cay, South Water Cay, and Twin Cays on the central barrier reef, Belize. Of the algae, 52 are Chlorophyt |
Ficha | Macroalgae (Rhodophyta: Laurencia Spp.) as Habitat For Young Juvenile Spiny Lobsters, Panulirus Argus | James M. Marx and William F. Herrnkind | 423-431 | NO | Liga perdida | Sin asignar | Field surveys were conducted in the middle Florida Keys to better document habitat used by newly settled juvenile spiny lobsters, Panulirus argus. Early benthic stages were most numerous in locations where they resided in or beneath macroalgal clumps of r | ||
Ficha | The distribution of benthic marine algae a bibliography for the British Isles | James H. Price | 3 | 305-315 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Ecology of understory kelp environments. I. Effects of kelps on flow and particle transport near the bottom | James E. Eckman, David 0. Duggins and Amy T. Sewell | 129 | 173-187 | 2633 | no completo | Sin asignar | Growth; Kelp; Recruitment; Sedimentation; Suspension-feeding; Transport | Because of their likely ecological importance, the effects of understory kelps on fluid and particulate transport near the bottom were assessed in waters of the San Juan Archipelago, Washington, U.S.A. Relative to more exposed rocky substrata at identical |
Ficha | Algal blooms and the nitrogen-enrichment hypothesis in Florida springs: evidence, alternatives, and adaptive management | James B. Heffernan and etal. | 20 | 816-829 | No | no completo | General | dissoved oxygen; eutrophication; Florida USA; herbivory; nitrate; precaution; rivers; springs; trophic structure. | |
Ficha | Physiologie Vegetale. - Resultats de la microanalyse des cristaux vacuolaires chez deux Chromopliytes unicellulaires marines: Exanthemachrysis gayraliae. Pavlova sp. (Prymnesiopliycees, Pavlovacees). | Jacqueline Fresnel, Pierre Galle et Paulette Gayral | 288 | 823-825 | 1725 | no completo | Sin asignar | Exanthermachrysis gayraliae y Pavlova sp | The microanalysis of the intravacoular crystals of Exanthermachrysis gayraliae and Pavlova sp, using a Castaing microprobe, has shown a high concentration of barium and sulphur elements and a much lower calcium concentration. |
Ficha | La structure hildenbrandiolde, strategie adaptative chez les Floridees | Jacqueline Cabioch et G. Giraud | 307-315 | NO | Liga perdida | Sin asignar | The structure of the encrusting thallus of Hildenbrandia prototypus shows a type of or-ganization quite similar to that found in the basal crust of a certain number of erect Rho-dophyta (Grateloupia filicina, Dermocorynus montagnei, Ahnfeltia plicata). Th | ||
Ficha | Étude Sur Les Corallinacées II. La Morphogenèse; Conséquences Systématiques et Phylogénétiques. | Jacqueline Cabioch | 13 | 137-288 | 3290 | no completo | Sin asignar | ||
Ficha | Expansion of a Central California Kelp Forest Following the Mass Mortality of Sea Urchins | J.S. Pearse and A.H. Hines | 83-91 | 2636 | Sin asignar | The mass mortality by disease of a localized population of sea urchins, Strongylocentrotus franciscanus, on the seaward side of a kelp forest was followed by the rapid seaward expansion of 4 species of brown algae, Macrocystis pyrifera, Laminaria dentiger | |||
Ficha | Expansion of a Central California Kelp Forest Following the Mass Mortality of Sea Urchins | J.S. Pearse and A.H. Hines | 51 | 83-91 | 2636 | no completo | Sin asignar | Macrocystis pyrifera, Laminaria dentigera, Pterygophora california, Nereocystis leutkeana y Cystoseira osmundacea. | The mass mortality by disease of a localized population of sea urchins, Strongylocentrotus franciscanus, on the seaward side of a kelp forest was followed by the rapid seaward expansion of 4 species of brown algae, Macrocystis pyrifera, Laminaria dentiger |
Ficha | Effects of enviromental factors on net photosynthesis and growth of intertidal species of the genus Gelidium (Gelidiaceae, rhodophyta) in northern Spain | J.M. Rico and S. Fredriksen | 60 | 265-273 | NO | Liga perdida | Rodofitas | Enviromental factors. Gelidium. Northern Spain. Physiology. Zonation | |
Ficha | On anadyomene and microdictyon, with the description of three new allied genera, discovered by Menzies in the Gulf of Mexico | J.E. Gray | 65-72 | NO | Liga perdida | Sin asignar | |||
Ficha | Response of different benthic indices to diverse human pressures | J.C. Dauvina, S. Alizier, C. Rolet, A. Bakalem, G. Bellan, J.L. Gomez Gesteira, S. Grimes, J.A. de-la-Ossa-Carretero, Y. Del-Pilar-Ruso | 143-153 | NO | Liga perdida | Sin asignar | Benthic indicators; Soft-bottom communities; Subjectivity; Objectivity; Human pressures; Site comparison | The interest in benthic indicators for soft-bottom marine communities has dramatically increased after a rather long period of relative stagnation due to the need for new tools to assess the status of marine waters, called for by the Clean Water Act and t | |
Ficha | The Life History of Rhadochorton membranaceum, an Endozoic Red Algal | J.A. West | 22 | 111-115 | NO | parcialmente sin liga | Sin asignar | Washington EE. UU.; Rhodochorton membranaceum Magnus | Two clones of Rhodochorton membranaceum Magnus were isolated into unialgal culture from hydroids collected subtidally in Puget Sound, Washington (USA) during July and August, 1972. Tetrasporangia were formed on the upright branches. The tetraspores produc |
Ficha | Macroalgae, a suitable indicator of the ecological status of coastal rocky communities in the NE Atlantic | J.A. Juanes, X. Guinda, A. Puente, J.A. Revilla | 8 | 351–359 | No | no completo | General | Ecological quality Intertidal Macroalgae Reefs Subtidal Water Framework Directive | Despite the great importance of shallow rocky communities (<30 m deep) due to their contribution to the biodiversity of coastal waters, most efforts in ecological status assess- |
Ficha | Dangerous Sea Life | J. W. Lermond | 25-34 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Peru Current | J. W. Lermond | 61-68 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Light- and Electron-Microscopic Studies of Growth and Reproduction in Cutleria (Phaeophyta) II. Gametogenesis in the Male Plant of C. hancockii | J. W. La Claire II and J. A. West | 101 | 247-267 | NO | no completo | General | Cutleria; Gametogenesis; Morphogenesis; Phaeophyta; Developmental ultrastructure. | Development of the plurilocular male gametangium in Cutleria hancockii Dawson is fundamentally similar to that of the female gametangium. However, the sequence of mitoses is less regular and the number of divisions is |
Ficha | Virus-Like Particles in the Brown Alga Streblonema | J. W. La Claire II and J. A. West | 93 | 127--130 | 1449 | no completo | Sin asignar | Streblonema sp.; Fisiológico | Ultrastructural examination of Streblonema sp. revealed icosahedral virus-like particles (135-150nm) throughout the cytoplasm of vegetative cells. The densely packed particles consist of an osmiophilic coat around a fibrillar core. Most cytoplasmic organe |
Ficha | Light- and Electron-Microscopic Studies of Growth and Reproduction in Cutleria (Phaeophyta) I. Gametogenesis in the Female Plant of C. hancockii. | J. W. La Claire II and J. A. West | 97 | 93-110 | 1448 | no completo | Sin asignar | Cutleria hancockii Dawson; fisiológico | Differentiation of the female gametangium in Cutleria hancockii Dawson is described. Four series of mitoses result in a 16-1ocule structure (four tiers of four cells each). The organelles in each locule become polarized after partitioning is complete, |
Ficha | Water Density and its Applications | J. W. Chanslor | 69-75 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Treasure from the Sea | J. W . Chanslor | sep-16 | NO | parcialmente sin liga | Sin asignar | The sea is "water " only in the sense that water is the dominant substance present, Actually, it is a solution of gases and salts in addition to vast numbers of living organisms, the majority of which are quite minute. Since the beginning, materials in so | ||
Ficha | Effects of herbivory, nutrients levels, and introduced algae on the distribution and abundance of the invasive macroalga Dictyosphaeria cavernosa in Kaneohe Bay, Hawaii | J. Stimson | 19 | 343-357 | no completo | Feofita | Coral reef; Dictyosphaeria cavernosa; Herbivory; Macroalgae; Nutrients; Non-native; Phase shift | ||
Ficha | A video recording and analysis system used to sample intertidal communities | J. S. Whorff and L. Grifting | 160 | 01-dic | 2670 | no completo | Sin asignar | Cover; Image analysis; Quadrat; Sampling; Video | A quantitative method for monitoring and analysing intertidal communities is presented. 60 quadrats from an intertidal field experiment on the effects of predation by Stramonita haemastoma (L.) were used as an example to describe the method. Camcorder rec |
Ficha | Variations of New England Estuarine Seaweed Biomass | J. S. Chock and A. C. Mathieson | 26 | 87 -97 | NO | parcialmente sin liga | Sin asignar | Seasonal and spatial biomass variations of estuarine intertidal macrophytes were recorded for 15 consecutive months at Cedar Point, Little Bay, New Hampshire, U.S.A. A typical seasonal cycle was recorded with maximum summer biomass (136-168 g dry weight 0 | |
Ficha | The Developmental Sequence of the Marine Red Alga Pseudogloiophloea in Culture | J. Ramus | 52 | ND | 1075 | no completo | Sin asignar | Chaetangiaceae, Nemaliales | The marine red alga Pseudogloiophloea confusa (Chaetangiaceae, Nemaliales) was isolated into unialgal culture from carpospores by means of a surface-sterilization technique. Carpospores give rise to minute, filamentous, irregularly branched, Acrochactium- |
Ficha | Utilization of Glutamate and Glucose for Heterotrophic Growth by the Marine Pennate Diatom Nitzschia laevis | J. Lewin and J.A. Hellebust | 47 | 01-jul | NO | parcialmente sin liga | Sin asignar | Pennate Nitzschia laevis | Nitzschia laevis Hustedt grew in the dark in the presence of either glutamate or glucose as substrate. Complex mixtures of yeast extract or tryptone plus lactate also supported good heterotrophic growth, while tryptone alone only supported very slow growt |
Ficha | The Problem of Later Starting Points in Algae | J. Komárek, Z. Pouzar and J. R?ži?ka | 8 | 86-88 | 30 | no completo | Sin asignar | ||
Ficha | Eutrophication and harmful algal blooms: A scientific consensus | J. Heisler and etal. | 8 | 3–13 | No | no completo | General | Eutrophication Harmful algal blooms HABs Management of nutrients Nutrient loading Nutrient composition Nutrient pollution US EPA Water quality | In January 2003, the US Environmental Protection Agency sponsored a ‘‘roundtable discussion’’ to |
Ficha | L'accessibilitié, Terme Nouveau en Phytogéographie | J. Heimans | NO | parcialmente sin liga | Sin asignar | For a better understanding of the causal relations between a certain unit of vegetation and its station the proposal is put forward to designate as accessibility factors the totality of conditions prevailing at a certain locality, that may influence the p | |||
Ficha | Gélidiales | J. Feldm Ann et G. Hamel | 9 | 85-129 | 3285 | no completo | Sin asignar | ||
Ficha | Morphogenesis and generic :concepts in coralline algae - a reappraisal | J. Cabioch | 493-509 | NO | Liga perdida | Sin asignar | In coralline algae, anatomy has long been used for generic definition, in addition to reproductive structures. Coralline anatomy is here analysed according to its two main components: cell behaviour and morphogenesis. The meristems and their function are | ||
Ficha | Étude historique et phytogéographique de la phycologie canadienne | J. Brunel | 842 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Observations on the Marine Unicellular Endophyte Chlorochytrium porphyrae (Chlorophyceae) | J. A. West, C. M. Smith and D. L. McBride | 31 | 299-305 | NO | Liga perdida | Clorofita | Chlorochytrium porphyrae Setchell et Gardner is an endophytic, unicellular green alga occurring in the intertidal red alga Porphyra perforata of Pacific North America. Chlorochytrium porphyrae appears to have a haplont | |
Ficha | The ecological effects of mining discharges on subdital habitats dominted by macroalgae in northern Chile: population and community level studies | J. A. Vásquez | 217-229 | no completo | Feofita | coastal pollution, copper pollution, heavy metals, macroalgae, macroinvertebrates, Lessonia, L. trabeculata | |||
Ficha | The Quantitative Role of 'Dark' Respiratory Processes in Heterotrophic and Photolithotrophic Plant Growth | J. A. Raven | 40 | 587-602 | 2871 | no completo | Sin asignar | The hypothesis that ATP and reductant generated in photosynthetic partial reactions can be used in vivo for energy-requiring reactions other than the photosynthetic carbón reduction cycle is supported by much experimental evidence. When such direct use of | |
Ficha | Effect of Gibberellins, Kinetin and other Factors on the Growth of Unicellular Marine Algae in Culture | J. A. Bentley-Mowat and S. M. Reid | 12 | 185-193 | 37 | no completo | Sin asignar | Nannochloris oculata, Gymmodinium splendens y Phaeodactylum tricornutum | The influence of gibberrellins A1, A2, A3 and A4 and kinetin was studied on the growth of laboratory cultures of Nannochloris oculata, Gymmodinium splendens, and Phaeodactylum tricornutum. Both growth??tomotion and inhibition was obtained according to con |
Ficha | Life Histories in the Florideophyceae and their Evolution | Isamu Umezaki | 28 | ene-18 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | RECLUTAMIENTO in situ Y FERTILIDAD DE FASES NUCLEARES DE Gelidium robustum (RHODOPHYTA) / RECRUITMENT in situ AND FERTILITY OF NUCLEAR PHASES OF Gelidium robustum (RHODOPHYTA) | Isaí Pacheco-Ruíz José A. Zertuche-González Mauricio Bustos-Barrera Edgar Arroyo-Ortega | 27 | 35-46 | NO | Liga perdida | Rodofitas | Gelidium robustum, esporas, supervivencia, reclutamiento. | Las plantas de Gelidium robustum liberan esporas todo el año. Sin embargo, sólo se observa reclutamiento in situ en verano. Se demuestra que existe desigualdad en la supervivencia de carposporas vs t |
Ficha | BIOMASS SEASONAL VARIATIONS AND ECOLOGICAL OBSERVATIONS IN porphura perforata J. AG. (RHODOPHYTA, BANGIALES) IN TODOS SANTOS BAY, BAJA CALIFORNIA MEXICO | Isaí Pacheco Ruiz, Zaúl García Esquivel, Rasaura Valenzuela Grijalva and Luis E. Aguilar Rosas | 12 | 62-69 | NO | no completo | General | in the present study monthly evaluations of biomass of Porphura perforata were made in two different zones in the Bahía de Todos Santos, from September 1980 to August 1981. The maximum values in biomass were found in | |
Ficha | CULTURE OF Gigatina candiculata HARV. JUVENILE GERMLINGS, BY MEANS OF MEDIA ENRICHED WITH DIGESTED COW MANURE | Isaí Pacheco Ruiz, Zaúl García Esquivel and Luis E. Aguilar Rosas | 13 | 51-58 | NO | no completo | General | Tetrasporophyte germlings of Gigartina canaliculata were cultivated with success during eight weeks using digested cow manure as nutrients source. Four different concentrations of the biodigested solution were use | |
Ficha | VARIACION ESTACIONAL DE BIOMASA Y OBSERVACIONES ECOLOGICAS EN Poqdym perforetu J. AG. (RHODOPHYTA, BANGIALES) EN LA BAHIA DE TODOS SANTOS, BAJA CALIFORNIA, MEXICO | Isaí Pacheco Ruíz | 12 | 62 - 69 | No | no completo | General | En el presente estudio se hicieron mediciones mensuales de biomasa de Porphym petfomta | |
Ficha | Marine Algae of California | Isabella A. Abbott and George J. Hollenberg. | 24 | 124-127 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Taxonomy and Nomenclature of the Type Species of Dumontia Lamouroux (Rhodophyta) | Isabella A. Abbott | 28 | 563-566 | NO | no completo | General | Dumontia contorta (Gmelin) Ruprecht is the earliest available name for the widely distributed northern hemisphere red alga, D. incrassata (Muller) Lamouroux, which has also been incorrectly known as D. filiformis (Hornemann | |
Ficha | THE USES OF SEAWEED AS FOOD IN HAWAII | Isabella A. Abbott | 32 | 409-412 | NO | no completo | General | Rapid and frequent air service to Hawaii has brought about a stronger westernization in food choices and food habits than was possible 30 or 40 years ago. The transport of more fresh foods from the Orient is also possi | |
Ficha | On Schimmelmannia from California and Japan | Isabella A. Abbott | ND | 937 | no completo | Sin asignar | |||
Ficha | Structure and Reproduction of Farlowia (Rhodophyceae) | Isabella A. Abbott | 2 | ND | NO | parcialmente sin liga | Sin asignar | Rhodophyceae; fisiológico. | In the two species of Farlowia (Dumontiaceae) which occur on the west coast of North America, the development of female reproductive structures is similiar to that previously reported in the Japanese species, F. irregularis. Farlowia resemble Dumontia in |
Ficha | Different levels of macroalgal sampling resolution for pollution assessment | Isabel Díez, Alberto Santolaria, José María Gorostiaga | 1779-1789 | NO | Liga perdida | Sin asignar | Biomonitoring; Data transformation; Functional groups; Intertidal assemblages; Recovery process; Taxonomic sufficiency | The effects of using reduced sampling resolutions to study macroalgal vegetation patterns have not been studied sufficiently. Here, we test the influence of taxonomic resolution level, removal of occasional species, aggregation of species abundances into | |
Ficha | Información médica | 2813 | no completo | Sin asignar | |||||
Ficha | Dasysiphonia chejuensis gen. et sp. nov. (Rhodophyta, Dasyaceae) from Korea | In Kyu Lee and John A. West | 4 | 115-129 | NO | no completo | General | Dasysiphonia chejuensis gen. et sp. nov., a marine red alga belonging to the Dasyaceae, Ceramiales, is described from Cheju Island on the southern coast of Korea. The thallus grows sympodially, forming an indeterminate or d | |
Ficha | Evaluating marine ecosystem health: Case studies of indicators using direct observations and modelling methods | I. Rombouts and et. al. | 24 | 353-365 | NO | no completo | General | Benthos Complexity Management Indicators Isotopes Phytoplankton Trophic models Zooplankton | A major challenge in ocean and coastal management is to find simple ways to evaluate the health of such |
Ficha | Growth-related intraclonal genetic changes in Gracilaria chilensis (Gracilariales: Rhodophyta) | I. Meneses, B. Santelices, P. Sánchez | 135 | 391-397 | NO | Completo | Rodofitas | Gracilaria chilensis exhibits noticeable intraclonal variation, some of which is presumed to result from mitotic recombinations or other types of DNA turnover associated with replication activities during cel | |
Ficha | Seaweed assemblage changes in the eastern Cantabrian Sea and their potential relationship to climate change | I. Díez, N. Muguerza, A. Santolaria, U. Ganzedo, J.M. Gorostiaga | 108-120 | NO | Liga perdida | Sin asignar | Bay of Biscay; diversity; global warming; indicators of change; macroalgae; subtidal vegetation | Rising sea-surface temperatures (SSTs) over the last three decades in the south-eastern part of the Bay of Biscay could be affecting phytobenthic assemblage distributions. This study assesses recent changes in species abundance and diversity along the wes | |
Ficha | A single origin of the peridinin- and fucoxanthin- containing plastids in dinoflagellates through tertiary endosymbiosis | Hwan Su Yoon, Jeremiah D. Hackett, and Debashish Bhattacharya | 99 | 11724–11729 | NO | no completo | Fitoplancton | The most widely distributed dinoflagellate plastid contains chlo- type, found in taxa such as Karlodinium micrum and Karenia spp., | |
Ficha | Phylogeny of Alariaceae, Laminariaceae, and Lessoniaceae (Phaeophyceae) Based on Plastid-Encoded RuBisCo Spacer and Nuclear-Encoded ITS Sequence Comparisons | Hwan Su Yoon and et. al. | 21 | 231-243 | NO | no completo | Feofita | kelps; Laminariaceae; Lesso- niaceae; Phaeophyceae; phylogeny; RuBisCo spacer; ITS. | Concatenated sequences from the plastid-encoded RuBisCo spacer and nuclear-encoded rDNA ITS re- the phylogeny of kelps (Pha |
Ficha | Deep-Sea Farming of Kappaphycus Using the Multiple Raft,Long-Line Method | Hurtado A.Q. and R. F. Agbayani | 45 | 438–444 | NO | no completo | General | Farming practices of Kappaphycus seaweed planters using the multiple raft, long-line method were assessed | |
Ficha | History, current status and future of marine macroalgal research in New Zealand: Taxonomy, ecology, physiology and human uses | Hurd C. L. and et. al. | 52 | 80-106 | NO | no completo | General | aquaculture, chemistry, human uses, inter- tidal and subtidal ecology, macroalgae, New Zealand, physiology, seaweed, taxonomy. | New Zealand has a rich and diverse macroalgal flora |
Ficha | DESICCATION PROTECTION AND DISRUPTION: A TRADE-OFF FOR AN INTERTIDAL MARINE ALGA | Hunt L.J. and M. W. Denny | NO | General | |||||
Ficha | The limits of cladism. | Hull, D. L. | 28 | 416-440 | NO | parcialmente sin liga | Sin asignar | Cladismo; clasificación; evolución; especies. | The goal of cladistic systematics is to discern sister-group relations (cladistic relations) by the methods of cladistic analysis and to represent them explicitly and unambiguously in cladograms and cladistic classifications. Cladists have selected cladis |
Ficha | A molecular study of Mazzaella (Gigartinaceae, Rhodophyta) and morphological investigation of the splendens clade from Pacific North America | Hughey J. R. and M.H. Hommersand | 49 | 113–135 | NO | Liga perdida | Rodofitas | Gigartinaceae, ITS, Mazzaella, Pacific North America, Phylogenetic analysis, rbcL | The delineation of species of Mazzaella remains problematic because of similarities in thallus shape and color. To better define species boundaries, molecular phylogenetic analyses and developmental studies of Mazzaella wer |
Ficha | Solving taxonomic and nomeclatural problems in pacific gigartinaceae (Rhodophyta) using DNA from type material | Hughey J. R. and et. al. | NO | Rodofitas | |||||
Ficha | Ecological significance and commercial harvesting of drifting and beach-cast macro-algae and seagrasses in Australia: a review | Hugh Kirkman & Gary A. Kendrick | 9 | 311–326 | NO | no completo | General | Australia, macro-algae, seagrasses, beach-cast, ecology, harvesting | This review provides an overview of aspects of the ecology of drifting and beach-cast macroalgae and marine |
Ficha | Factors affecting macroalgal distribution in a eutrophic tropical lagoon in Taiwan | Hsing-Juh lin & Jia-Jang Hung | 144 | 653–664 | NO | no completo | General | Factors affecting distribution of macroalgal | |
Ficha | Algen aus den Fischteichen von Buzsák I. Scenedesmus-Arten | Hortobágyi Tibor | 1 | 42-64 | 379 | no completo | Sin asignar | ||
Ficha | Algen aus den Fischteichen von Buzsák I. Scenedesmus-Arten | Hortobágyi Tibor | 1 | 42-64 | 379 | no completo | Sin asignar | ||
Ficha | A Szellidi -Szikesto Uj Harpochytrium-Fajáról | Hortobágyi Tibor | 48 | ND | 358 | no completo | Sin asignar | ||
Ficha | A Szellidi -Szikesto Uj Harpochytrium-Fajáról | Hortobágyi Tibor | 48 | ND | 358 | no completo | Sin asignar | ||
Ficha | Algen aus den Fischteichen von Buzsák II. | Hortobágyi Tibor | 1 | ND | 384 | no completo | Sin asignar | ||
Ficha | Algen aus den Fischteichen von Buzsák II. | Hortobágyi Tibor | 1 | ND | 384 | no completo | Sin asignar | ||
Ficha | Magyarország halastavainak mikrovegetációja I | Hortobágyi Tibor | 95-99 | 360 | no completo | Sin asignar | |||
Ficha | Magyarország halastavainak mikrovegetációja I | Hortobágyi Tibor | 95-99 | 360 | no completo | Sin asignar | |||
Ficha | Adatok Magyarország Moszataihoz Iv. | Hortobágyi Tibor | 359-391 | 381 | no completo | Sin asignar | |||
Ficha | Adatok Magyarország Moszataihoz Iv. | Hortobágyi Tibor | 359-391 | 381 | no completo | Sin asignar | |||
Ficha | Diagnoses Algarum Novarum | Hortobágyi Tibor | 549-552 | 382 | no completo | Sin asignar | |||
Ficha | Hyalophacus Tiszae Hortob. n. sp. | Hortobágyi Tibor | 393-398 | 383 | no completo | Sin asignar | |||
Ficha | A Hortobágyi Halastavak Algál és A Vizsgált Halastavak Termelöképessége | Hortobágyi Tibor | 441-461 | 357 | no completo | Sin asignar | |||
Ficha | A Hortobágyi Halastavak Algál és A Vizsgált Halastavak Termelöképessége | Hortobágyi Tibor | 441-461 | 357 | no completo | Sin asignar | |||
Ficha | A Scenedesmus Oahuensis (Lemm.) Smith Új Taxonjai | Hortobágyi Tibor | 58 | ND | 378 | no completo | Sin asignar | ||
Ficha | Scenedesmus mirandus Hortob, n. sp. | Hortobágyi Tibor | 42 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Phacus concavus Hortob, nova species | Hortobágyi Tibor | 30 | 100 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Uj Phacusok. | Hortobágyi Tibor | 41 | ND | 373 | no completo | Sin asignar | ||
Ficha | Uj Phacusok. | Hortobágyi Tibor | 41 | ND | 373 | no completo | Sin asignar | ||
Ficha | A Scenedesmus verrucosus Roll zöldmoszatról. | Hortobágyi Tibor | 42 | ND | 370 | no completo | Sin asignar | ||
Ficha | A Scenedesmus verrucosus Roll zöldmoszatról. | Hortobágyi Tibor | 42 | ND | 370 | no completo | Sin asignar | ||
Ficha | Az Euglena okyuris Schmarda és az E. oxiyuris Schmarda f. Minor Defl. hazai elöfordulásáról. | Hortobágyi Tibor | 42 | ND | 371 | no completo | Sin asignar | ||
Ficha | Az Euglena okyuris Schmarda és az E. oxiyuris Schmarda f. Minor Defl. hazai elöfordulásáról. | Hortobágyi Tibor | 42 | ND | 371 | no completo | Sin asignar | ||
Ficha | Pediastrum-rendellenességek a Balatonból. Abnormitates generis Pediastrum e lacu Balaton (Hungria) | Hortobágyi Tibor | 42 | ND | 372 | no completo | Sin asignar | ||
Ficha | Pediastrum-rendellenességek a Balatonból. Abnormitates generis Pediastrum e lacu Balaton (Hungria) | Hortobágyi Tibor | 42 | ND | 372 | no completo | Sin asignar | ||
Ficha | Ferdenyakú Trachelomonas Cinkotáról | Hortobágyi Tibor | 44 | 367 | no completo | Sin asignar | |||
Ficha | Latest data to the microvegetation of lake Balton | Hortobágyi Tibor | 10 | ene-18 | 368 | no completo | Sin asignar | ||
Ficha | Latest data to the microvegetation of lake Balton | Hortobágyi Tibor | 10 | ene-18 | 368 | no completo | Sin asignar | ||
Ficha | ZWEI NEUE SIDEROCELIS-ARTEN AUS DEM BALATON. | Hortobágyi Tibor | 18 | 25-29 | 366 | no completo | Sin asignar | ||
Ficha | Az Euglena Ehrenbergii KIebs hazai elolordulása és bioszociológiai szerepe | Hortobágyi Tibor | 361 | no completo | Sin asignar | ||||
Ficha | Az Euglena Ehrenbergii KIebs hazai elolordulása és bioszociológiai szerepe | Hortobágyi Tibor | 361 | no completo | Sin asignar | ||||
Ficha | A Scenedesmus armatus Chod. val. Bogláriensis Hortob. két uj formája | Hortobágyi Tibor | 362 | no completo | Sin asignar | ||||
Ficha | A Scenedesmus armatus Chod. val. Bogláriensis Hortob. két uj formája | Hortobágyi Tibor | 362 | no completo | Sin asignar | ||||
Ficha | Coccomonas Éberii nova species A Balaton egy új Phytomonadinája | Hortobágyi Tibor | 9 | 22-27 | 363 | no completo | Sin asignar | ||
Ficha | Coccomonas Éberii nova species A Balaton egy új Phytomonadinája | Hortobágyi Tibor | 9 | 22-27 | 363 | no completo | Sin asignar | ||
Ficha | PLANKTONGOMBA A BALATON SESTONJÁBAN. | Hortobágyi Tibor | 7 | 364 | no completo | Sin asignar | |||
Ficha | PLANKTONGOMBA A BALATON SESTONJÁBAN. | Hortobágyi Tibor | 7 | 364 | no completo | Sin asignar | |||
Ficha | A CYANOPHYCEAK SEJTKILÖVELÉSES SZAPORODÁSA | Hortobágyi Tibor | 7 | 365 | no completo | Sin asignar | |||
Ficha | A CYANOPHYCEAK SEJTKILÖVELÉSES SZAPORODÁSA | Hortobágyi Tibor | 7 | 365 | no completo | Sin asignar | |||
Ficha | Adatok Magyarorszag Moszataihoz. Ii. Additamenta Ad Cognitionem Algarum Hungariae. Ii. | Hortobágyi Tibor | 47 | ND | 355 | no completo | Sin asignar | ||
Ficha | Adatok Magyarorszag Moszataihoz. Ii. Additamenta Ad Cognitionem Algarum Hungariae. Ii. | Hortobágyi Tibor | 47 | ND | 355 | no completo | Sin asignar | ||
Ficha | Nouvelles Observations Concernant La Multiplication Des Algues Bleues (Cyanophycees) | Hortobágyi Tibor | ND | 374 | no completo | Sin asignar | |||
Ficha | Nouvelles Observations Concernant La Multiplication Des Algues Bleues (Cyanophycees) | Hortobágyi Tibor | ND | 374 | no completo | Sin asignar | |||
Ficha | Adatok Magyarország moszataihoz. II. | Hortobágyi Tibor | 47 | 31-42 | 356 | no completo | Sin asignar | ||
Ficha | Adatok Magyarország moszataihoz. II. | Hortobágyi Tibor | 47 | 31-42 | 356 | no completo | Sin asignar | ||
Ficha | Algák A Balatonból | Hortobágyi Tibor | 26 | 329-342 | 380 | no completo | Sin asignar | ||
Ficha | Algák A Balatonból | Hortobágyi Tibor | 26 | 329-342 | 380 | no completo | Sin asignar | ||
Ficha | Recent developements in the systatics of the Gigartinaceae (Gipartinales, Rhodophyta) based on rbcL sequence analysis and morpjological evidence | Hommersand Max H. and et. al. | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | New perspectives in the taxonomy of the Gigartinaceae (Gigartinales,Rhodophyta) | Hommersand Max H. and et. al. | 105-120 | NO | Completo | Rodofitas | biogeography, Gigartinaceae, Gigartinales, Rhodophyta, seaweed, systematics | A revised description of the Gigartinaceae is provided, together with a key and short diagnosis of each genus and a list of the species examined. New combinations have been proposed where appropriate. Distinguishing cystoca | |
Ficha | Smithora | Hollenberg | 1 | 04-nov | 2483 | no completo | Sin asignar | Erythropeltidaceae | Smithora must be considered as a new genus in the Erythropeltidaceae. From Porphyra and closely related genera it differs in the origin of several blades from a common base, in the lack of rhizoidal processes in connection with the attachment organ, and e |
Ficha | Ulva descripcion | Hoffmman & Santelices | 0 | NO | parcialmente completo con liga | Clorofita | |||
Ficha | Effects of selected physicochemical factors on growth and zoosporogenesis of Cladophora glomerata (Chlorophyta). | Hoffmann, J. P., & Graham, L. E. | 20 | 1 A 7 | NO | parcialmente sin liga | Sin asignar | The effects of vitamin B1 and B12, temperature light intensity and Photoperiod on dry weight production and zoosporogenesis of Cladophora glomerata (L.) Kütz were investigated by factorial experiments. Statistical analysis showed all of the above factors | |
Ficha | Interactions of nitrate and phosphate on the development of microscopic stages of Lessonianigrescens Bory (Phaeophyta). | Hoffmann, A. J., Avila, M., & Antelices, B. | 78 | 177-186 | 3857 | no completo | Sin asignar | The effects of different concentrations of nitrate and phosphate on the microscopic stages of development of Lessonia nigrescens Bory were studied. Meiospores were cultivated under different concentrations of nutrients (0 to 100 pmol N. 1 - ‘, and 0 to 1. | |
Ficha | laminariales | Hoffmann A. and B. Santicelices | NO | Kelp | |||||
Ficha | Morphology and life history of Coelocladia artica (Dictyosiphonales, Phaeophyceae), new to Japan | Hiroshi Kawai | 183-187 | NO | Liga perdida | Sin asignar | Coelocladia artica; Dictyosiphonales; life history; morphology; Phaeophyceae. | The occurrence of Coelocladia artica Rosenvinge (Dictyosiphonales, Phaeophyceae) is reported for the first time in the Pacific Ocean, from Oshoro, Hokkaido, Japan. The field material was approximately 30 mm in height, up to 300 ?m in diameter, 2-3 times i | |
Ficha | A glossary of phycological terms for students of marine macroalgae | Hine, A. E. | 1 A 91 | 3714 | no completo | Sin asignar | |||
Ficha | Variability in the fractionation of stable isotopes during degradation of two intertidal red algae | Hill Jaclyn M. and Christopher D. McQuaid | 82 | 397-405 | NO | parcialmente completo con liga | Rodofitas | d13C d15N stable isotope analysis macroalgae fractionation decomposition Gelidium pristoides Hypnea spicifera | Macroalgae contribute to intertidal food webs primarily as detritus, with unclear implications for food |
Ficha | Characterization of tidal pool algae in the Mexican Tropical Pacific coast | Hilda Leon, Dalila Fragoso, Daniel Leon, Carlos Candelaria, Elisa Serviere & Jorge Gonzalez-Gonzalez | 197-205 | 2519 | no completo | Sin asignar | Tidal pools, algal characterization, Mexico | Tidal pools in the Mexican Tropical Pacific coast have received relatively little attention in spite of their considerable richness in species and wide distribution in the region. This paper presents the first characterization of the algal flora of this r | |
Ficha | Morphology, molecular phylogeny and taxonomy of Nitella comptonii (Charales, Characeae) | Hidetoshi Sakayama and et.al. | 45 | 417-421 | NO | no completo | Clorofita | AtpB gene; charales; charophyceae; internal transcribed spacer region; Japanesse taxa; Morphology; Nitella; comptonii; Oospores; psaB gene, rbcL gene, scanning electron microscopy, Taxonomy | |
Ficha | Culture Studies on Caulerpa (Caulerpales, Chlorophyceae) III. Reproduction, Development and Morpholo~,ical Variation of Laboratory-cultured C. racemosa var. peltata | HIDEO OHBA, HIROAKI NASHIMA AND SACHITO ENOMOTO | 105 | 589-600 | NO | no completo | General | Caulerpa racemosa var. laetevirens -- Caulerpa racemosa var. peltata -- Chlorophyceae -- Development -- Morphological Variation -- Reproduction | Reproduction, development and morphological variation of the marine green alga |
Ficha | Estimacion de la actividad total anadida y de la autoabsorcion en las determinaciones de produccion del fitoplancton con 14-C. | Herrera, J., & Margalef, R. | 30 | 37-44 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Chaetoceros bermejensis sp. nov., a new planktonic diatom from the Gulf of California. | Hernández-Becerril, D. U. | 34 | 521-526 | NO | parcialmente sin liga | Sin asignar | A new species of the diatom genus Chaetoceros Ehr., Ch. bermejensis sp. nov., is described and illustrated by light and electron microscopy, from net plankton samples frorm the Gulf of California. It is included within the subgenus Hyalochaete Gran, secti | |
Ficha | The morphology and taxonomy of the planktonic diatom Chaetoceros coarctatus Lauder (Bacillariophyceae). | Hernández-Becerril, D. U. | 6 | 281-287 | 3711 | no completo | Sin asignar | The diatom Chaetoceros coarctatus has been studied by light (LM) and electron microscopy (SEM, TEM), from preserved plankton samples collected in the Gulf of California and off the Pacific coast of Baja California. Observations include the finding of a nu | |
Ficha | Two new species of the diatom genusChaetoceros (Bacillariophyta). | Hernández-Becerril, D. U. | 181 | 217-226 | 3754 | no completo | Sin asignar | Two new planktonic diatom species of the genus Chaetoceros are described herein: Ch. octagonus and Ch. rectus, from material of Baja California coasts and the Gulf of California, respectively; Ch. rectus was also found in a sample from Australian waters. | |
Ficha | A new dinoflagellate from the Indian Ocean: A link between the genera Amphisolenia and Triposolenia (Dinophyceae? | Hernandez-Becerril David U and Ma Esther Meave del Castillo | 38 | 108-113 | NO | no completo | Fitoplancton | ||
Ficha | Note on the morphology of two planktonic diatoms: Chaetoderos bacteriastroides and C. seychyellarus, with comments on their taxonomy and distribution | Hernandez-Becerril David U | 111 | 117-128 | NO | no completo | Fitoplancton | Chaetoceros-diatoms-distribution-morphology-taxonomy | |
Ficha | Morphology and taxonomy of three little-known marine planktonic Chaetoceros species (Bacillariophyceae) | Hernandez-Becerril David U | 35 | 183-188 | NO | no completo | Fitoplancton | Chaetoceros, distribution, morphology, planktonic diatoms, taxonomy | Three marine planktonic species of the diatom genus Chaetoceros were studied by light and electron microscopy, from net samples |
Ficha | Morphological study of the marine planktonic diatom Chaetoceros okamurai (Chaetocerotales, Bacillariophyceae)from the Gulf of Mexico | Hernandez-Becerril David U | 46 | nov-15 | NO | no completo | Fitoplancton | Chaetoceros oi | Despite the numerous works on phytoplankton in the this area. The presence of the planktonic diatom Chae- |
Ficha | The dinoflagellate genus Prorocentrum along the coasts of the Mexican Pacific | Hernandez-Becerril D. U. and et. al. | 418 | 111-121 | NO | no completo | Fitoplancton | dinoflagellates, Prorocentrum, morphology, taxonomy, Mexican Pacific, red tides | We surveyed the dinoflagellate genus Prorocentrum Ehrenberg in Mexican Pacific waters, where it is rather com- and the Gulf of Cali |
Ficha | Coccolithophorids from the west coast of Baja California, Mexico | Hernandez-Becerril D. U. and et. al. | 452 | 31-45 | NO | no completo | Fitoplancton | coccolithophorids, phytoplankton, morphology, new records, Baja California | Studies on coccolithophorids in Mexico are rather scarce, probably due to the use of traditional methods for study- flora |
Ficha | Toxic and harmful marine phytoplankton and microalgae (HABs) in Mexican Coasts | Hernandez-Becerril D. U. and et. al. | 42 | 1349-1363 | NO | no completo | Fitoplancton | Biotoxins; harmful algal blooms; marine phytoplankton; Mexican coasts; microalgae. | Harmful Algal Blooms (HABs) are becoming an increasing problem to human health and environment (including effects on natural |
Ficha | Planktonic Silicoflagellates (Dictyochophyceae) from the Mexican Pacific Ocean | Hernandez-Becerril D. U. and E. Bravo-Sierra | 44 | 417-423 | NO | no completo | Fitoplancton | One hundred and sixty Formalin-preserved net samples were collected from different zones in the Mexican | |
Ficha | Sobre la presencia de Rhodophyllis divaricate (Stachkouse) Papenfuss (Rhodophyllidaceae Engler, Rhodophyta) en el Archipiélago Canario. | Hernández, M. L., Gill-Rodríguez, M. C. & Afonso-Carrillo, J. | 1 | 479-482 | 3901 | no completo | Sin asignar | La presencia en Canarias de talos fértiles de Rhodophyllis divaricata permite ampliar ligeramente el límite meridional de distribución de esta especie hasta ahora localizada en Marruecos. | |
Ficha | Estudio de la vegetación ficológica del litoral comprendido entre Cabezo del Socorro y Montaña de la Mar, Güímar, Tenerife. | Hernández, M. L., & Gill-Rodríguez, M. C. | 11 | 141-170 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Algal Establishment on Sterilized Soil Replaced in an Oklahoma Prairie | Herman S. Forest, Dan I. Willson and Robert B. England | 40 | 475-477 | 28 | no completo | Sin asignar | Cultures of algae from the surface soil in a natural prairie were compared with those from pots of sterilized soil which had been buried to ground-level and allowed to remain for one, three, and five-and-a-half months. The soil samples were cultured in mo | |
Ficha | Predicting the occurrence of rocky reefs in a heterogeneous archipelago area with limited data | Henna Rinne and et. al. | 138 | 90-100 | NO | no completo | General | macroalgae marine habitat mapping MPA SDM seabed geomorphic features shelf seas Baltic Sea Archipelago Sea | The lack of spatial distribution data on marine habitats often presents an obstacle to their protection. The |
Ficha | Seasonal Variation of Antifouling Activities of Marine Algae from the Brittany Coast (France) | Hellio C. and et. al. | 6 | 67-82 | NO | no completo | General | antifouling, settlement, bacteria, barnacle, diatoms, fungi. | The antifouling activity of extracts (aqueous, ethanol, and dichloromethane) of 9 marine macroalgae |
Ficha | Propagule banks, herbivory and nutrient supply control population development and dominance patterns in macroalgal blooms | Heike K. Lotze, Boris Worm and Ulrich Sommer | 89 | 46–58 | No | no completo | General | Destructive macroalgal mass blooms threaten estuarine and coastal ecosystems | |
Ficha | The Functional Morphology of Turf-Forming Seaweeds: Persistence in Stressful Marine Habitats | Hay Mark E. | NO | General | |||||
Ficha | The effects of nutrient availability on tolerance to herbivory in a brown seaweed | Hay K. B and et. al. | 99 | 1540-1550 | NO | no completo | Feofita | amphipods, herbivory, limiting resource model, macroalgae, phlorotannins, plant–herbivore interactions, resistance, Sargassum, trade-offs | 1. Plants can resist herbivory through mechanisms of resistance (traits that reduce the amount of |
Ficha | Vegetación bentónica del Roque de los Organos (Gomera). | Hauroum T., R., Rodríguez, M. G., Afonso-Carrillo, J., & Willdpret De la Torre, W. | 107-117 | NO | parcialmente sin liga | Sin asignar | Se realiza el estudio de la vegetación bentónica del Roque de Los Órganos, espectaculares acantilados situados al N de la isla de Gomera, con muy escasa pla- taforma litoral, accesibles únicamente por barco y sometidos a un violento oleaje que los hace vi | ||
Ficha | Estudio del fitobentos del Roque de los Órganos (Gomera): catálogo florístico. | Hauroum T., R., Gil-Rodríguez, M. C., Afonso Carrillo, J., & Wildpret de la Torre, W. | 13 | 259-276 | NO | parcialmente sin liga | Sin asignar | The marine algae inhabiting Roque de Los Organos have been studied. A total of 59 species have been collected, 21 of which represent new records for the island of Comera and 1 Phaeophyta, Giffordia intermedia (Rosenv.) Lund, and 2 Rhodophyta, Gelidium lat | |
Ficha | Phototrophic biofilms on the interior walls of concrete Iterson-type cooling towers | Hauer Tomas | 22 | 733–736 | NO | no completo | General | Cyanobacteria . Algae . Cooling towers. Biofilms. Concrete . Czech Republic | Algae and cyanobacteria form noticeable biofilms |
Ficha | The Marine Fisheries of Panama | Harvey R. Bullis and Edward F. Klima | 2 | 167-178 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | CHOREONEMA (CORALLINALES, RHODOPHYTA): 18S rDNA PHYLOGENY AND RESURRECTION OF THE HAPALIDIACEAE FOR THE SUBFAMILIES CHOREONEMATOIDEAE, AUSTROLITHOIDEAE, AND MELOBESIOIDEAE | Harvey A. S. | 39 | 988-998 | NO | Completo | Rodofitas | 18S rDNA phylogeny; Austrolithoid- eae; Choreonema; Choreonematoideae; Corallinaceae; Corallinales; Hapalidiaceae; Melobesioideae; Sporo- lithaceae | Phylogenetic analyses of 18S rDNA gene data for Choreonema thuretii (Corallinales, Rhodophyta) and available data for other coralline red algae indicated that Choreonema belongs to the same lineage as other&n |
Ficha | Escape responses and prey availability in a kelp forest predator-prey system | Harrold C. | 119 | 132-135 | NO | no completo | Kelp | ||
Ficha | A re-classification of the Acrochaetiales based on molecular and morphological data, and establishment of the Colaconematales ord. nov. (Florideophyceae, Rhodophyta) | Harper, James T. and Saunders, Gary W | 37 | 463-476 | NO | Completo | Rodofitas | Acrochaetiaceae, Acrochaetiales, Colaconemataceae fam. nov., Colaconematales ord. nov., Florideophyceae, large-subunit rDNA, molecular systematics, phylogeny, Rhodophyta, small-subunit rDNA | Systematics of the red algal order Acrochaetiales and related taxa was investigated using combined small- and large-subunit |
Ficha | Ecological differences between the isomorphic reproductive phases of two species of Iridaea (Rhodophyta: Gigartinales). | Hannach, G., & Santelices, B. | 22 | 291-303 | 3863 | no completo | Sin asignar | This study tests the hypothesis that species traditionally characterized as isomorphic exhibit similar physiological and ecological responses to different environmental factors, by comparingthe ecological and ecophysiological responses of reproductive pha | |
Ficha | Ecological differences between the isomorphic reproductive phases of two species of Iridaea(Rhodophyta: Gigartinales) | Hannach G. & B. Santelices | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Small-scale genetic structure in the sea palm Postelsia palmaeformis Ruprecht (Phaeophyceae) | Handojo T. and et. al. | 149 | 731-742 | NO | no completo | Feofita | Documenting the scale of movement among populations is an important challenge for marine ecol- palmaeformis Ruprech | |
Ficha | Macroalgae Blooms and their Effects on Seagrass Ecosystems | Han Qiuying and Liu Dongyan | 13 | 791-798 | NO | no completo | General | eutrophication; decline; seagrasses; macroalgae blooms | Seagrass decline caused by the macroalgae blooms is becoming a common phenomenon throughout temperate and direct an |
Ficha | Background Document for Maërl beds | Hall-Spencer Jason M. | mar-34 | NO | Liga perdida | Rodofitas | This Background Document on maërl beds has been developed by OSPAR following the inclusion of this habitat on the OSPAR List of threatened and/or declining species and habitats (OSPAR agreement 2008-6). The document pr | ||
Ficha | Effect of inorganic and organic nutrient addition on coral–algae assemblages from the Northern Red Sea | Haas Andreas and et. al. | 380 | 99–105 | NO | no completo | General | Coral–algae assemblage Coral pigmentation change Inorganic nutrients Organic nutrients Red Sea Turf algae | Previous studies in fringing reefs of the Northern Red Sea demonstrated that the in-situ competition of corals |
Ficha | Patterns of interactions among neighbor species in a high intertidal algal community | Ha Kim J. | 17 | 41-51 | NO | no completo | General | competition, facilitation, fucold, intertidal, macroalgae, microhabitat, neighbor distance, turf algae | |
Ficha | Use of clearing and fluorescence techniques in anatomical studies of the sporophyte of Macrocystis (Phaeophyceae, Laminariales) | H.L. Barrales, R.L. Peterson, D.J. Grenville And J.F. Gerrath | 392-396 | NO | Liga perdida | Sin asignar | Dried herbarium specimens of Macrocystis pyrifera were rehydrated, cleared by removing chlorophyll and other pigments with hot ethanol or acetone and then treating with hot alkali, and stained by a number of techniques. The distribution and structure of m | ||
Ficha | The Complementarity Principle in Biological and Social Structures | H.H. Pattee and J. R?czaszek-Leonardi, | 1 | 191-200 | 2760 | no completo | Sin asignar | Complementarity is an epistemological principle derived from the subject-object or observer-system dichotomy, where each side requires a separate mode of description that is formally incompatible with and irreducible to the other, and where one mode of de | |
Ficha | Janieae and Lithotricheae: two new tribes of articulated Corallinaceae (Rhodophyta) | H. William Johansen and Paul C. Silva | 17 | 413-417 | 1544 | no completo | Sin asignar | Rhodophyta | Evidence now available warrants segregating the genera of two subfamilies of articu- lated Corallinaceae (Rhodophyta) into tribes. Within the subfamily Corallinoideae, the tribe Janieae (comprising Jania, Holiptilon, and Cheilosproum) is distinguished fro |
Ficha | Conceptacles in the Corallinaceae | H. William Johansen | 114-119 | 3325 | no completo | Sin asignar | Corallinaceae | Although all conceptacles in the Corallinaceae consist of chambers opening by one or more pores, their ontogeny and anatomy, as well as the structure of their contents, is diverse. Several types may be distinguished by: (a) whether or not filaments arisin | |
Ficha | The Biological and Economic Importance of Algae, Part I | H. W. Johnston | 13 | ND | 1 | no completo | Sin asignar | This series of articles is designed to give those students previously unfamiliar with algae an introduction to their importance and uses. It is not intended to refer to all the published information available; but sufficient will be presented to generate | |
Ficha | The Biological and Economic Importance of Algae, Part 2 | H. W. Johnston | 14 | ND | NO | parcialmente sin liga | Sin asignar | In the first article of this series (Johnston 1965), we dealt with the importance of algae as producers of organic matter—the fuel of the biological world. While this is of fundamental importance to Man, it is not of such direct and personal concern as so | |
Ficha | Phycological Reviews 4 Current status of generic concepts in coralline algae (Rhodophyta) | H. W. Johansen | 15 | 221-244 | 3326 | no completo | Sin asignar | ||
Ficha | Some Aspects of Evolution in the Isogamous, Filamentous Chlorophyceae and Their Relation to the Classification of the Chlorophyceae | H. S. Forest | 83 | 141-150 | NO | parcialmente sin liga | Sin asignar | 1. Classification of the Chlorophyceae should be undertaken with the recognition that there is a closely knit phylogenetic sequence of isogamous green algae with ulotrichoid chloroplasts from the most rudimentary to the most advanced filamentous forms. No | |
Ficha | Biochemical Correlates of Seasonal Change in Marine Communities | H. Perry Jeffries | 113 | 643-658 | 1517 | no completo | Sin asignar | Plankton and benthos respond in different ways to seasonal change, but their patterns of fatty acid distribution are similiar. The general trend of chemical progression is toward longer chain lengths and increasing unsaturation. Thus, as a temperate commu | |
Ficha | Use of biotic indices in semi-enclosed coastal ecosystems and transitional waters habitats—Implications for the implementation of the European Water Framework Directive | H. Blanchet , N. Lavesque, T. Ruellet, J.C. Dauvin, P.G. Sauriau, N. Desroy, C. Desclaux, M. Leconte, G. Bachelet, A.-L. Janson, C. Bessineton, S. Duhamel, J. Jourde, S. Mayot, S. Simon, X. de Montaudouin | 360–372 | NO | Liga perdida | Sin asignar | Biotic index; European Water Framework; Directive; Benthic invertebrates; Semi-enclosed coastal ecosystems; Transitional waters | This study deals with the application of macrozoobenthos-based biotic indices (BI) within the frame of the implementation of the European Water Framework Directive. More precisely, this study aimed at assessing the performance of five recently developed m | |
Ficha | Marine Algae of the Solomon Islands | H. B. S. Womersley and A. Bailey | 257-352 | NO | Liga perdida | Sin asignar | An account is given of the benthic marine algae (and sea grasses) collected on the 1965 Royal Society Expedition to the Solomon Islands. The known algal flora is fairly typical of such a tropical area, comprising some 71 species of Chlorophyta, 27 of Phae | ||
Ficha | The Helminthocladiaceae (Rhodophyta) of Southern Australia | H. B. S. Womersley | 13 | 451-487 | NO | parcialmente sin liga | Sin asignar | Australia, Nemalion; Helminthora, H. lindaueri de Nueva Zelanda, Helminthocladia, H. beaugleholei sp. Nov. Y H. dotyi sp. Nov., Y Liagora, L. codii sp. Nov.); Taxonómico | The southern Australian Helminthocladiaceae, comprising Nemalion (one species), Helminthora (two species, including H. lindaueri from New Zealand), Helminthocladia (four species, with H. beaugleholei sp. nov. and H. dotyi sp. nov.), and Liagora (four spec |
Ficha | A Critical Survey of The Marine Algae of Southern Australia II. Phaeophyta | H. B. S. Womersley | 15 | 189-270 | NO | parcialmente sin liga | Sin asignar | A survey is given of the known Phaeophyta of southern Australia, including synonomy, references, type data, and critical notes. The following new taxa are described: Sphacelaria carpoglossi, Distromium flabellaturn, and D. multifidum. Many names are reduc | |
Ficha | Patterns of Genicular Development in Amphiroa (Corallinaceae) | H . William Johansen | 5 | 118-123 | 3327 | no completo | Sin asignar | Sudáfrica; Amphiroa. | Two types of genicular development (designated Types I and II) are present in South African species of Amphiroa. Genicula of both types originate when medullary tissue near branch endings softens by decalcification. In Type I decalcification does not prog |
Ficha | PHYSIOLOGICAL ADAPTATIONS IN TWO ECOTYPES OF FUCUS VESICULOSUS AND IN FUCUS RADICANS WITH FOCUS ON SALINITY | Gylle Anna Maria | NO | no completo | Feofita | Bothnian Sea, brackish, brown algae, D1, 77 K fluorescence emission, Fucus vesiculosus, Fucus radicans, light?harvest antenna, mannitol, marine, NMR, Norwegian Sea, quantum yield, photosynthetic maximum capacity (Pmax), photosystem, (PSI, PSII), PsaA, Rub | The in origin intertidal marine brown alga Fucus vesiculosus L. grow | ||
Ficha | Changes in Carbon and Hydrogen Stable Isotope Ratios of Macroalgae and Seagrass During Decomposition | Gwen E. Fenton and David A. Ritz | 26 | 429-436 | No | no completo | General | isotope ratios; decomposition; macroalgae; sea grasses; Tasmania | Stable isotope ratios of carbon and hydrogen were determined for six algae and |
Ficha | From Protoplasm to Swarmer: Regeneration of Protoplasts from Disintegrated Cells of the Multicellular Marine Green Alga Microdictyon Umbilicatum (Chlorophyta) | Gwang Hoon Kim, Tatiana A. Klotchkova and John A. West | 174-183 | NO | Liga perdida | Sin asignar | cell membrane; Microdictyon; protoplast regeneration; swarmers; wound-induced reproduction | Protoplast regeneration from extruded cytoplasm of the multicellular marine green alga Microdictyon umbilicatum (Velley) Zanardini (Cladophorales, Anady-omenaceae) was investigated. The early process of protoplast formation is comprised of two steps: aggl | |
Ficha | Factors affecting sporulation of Gracilaria cornea (Gracilariales, Rhodophyta) carposporophytes from Yucatan, Mexico | Guzman-Uriostegui Alberto & Daniel Robledo | 285-290 | NO | no completo | Rodofitas | carpospores, Gracilaria cornea, spore cultivation | Carpospore shedding was studied in Gracilaria cornea in order to determine maximum spore output potential for | |
Ficha | Evaluacion y manejo de praderas de feofitas en la provincia de Arauco | Guzman M. L. and G.Moreno P. | NO | Feofita | |||||
Ficha | Diagnóstico sobre las investigaciones y explotación de las algas marinas en México. | Guzmán del Proo, S. A., Casas-Valdez, M., Díaz-Carrillo, A., Díaz-López, M. L., Pineda-Barrera, J., & Sánchez-Rodriguez, M. E. | 3 | 1 A 63 | 3786 | no completo | Sin asignar | Los litorales de la República Mexicana cuentan con un gran número de especies de algas 1114 identificadas, sin embargo, sólo algunas pueden ser factiblemente explotadas. Hay 5 géneros que tienen importancia económica en la actualidad Macrocystis, Gelidium | |
Ficha | Farming of the giant kelp Macrocystis pyrifera in southern Chile for development of novel food products | Gutierrez Alfonso and et. al. | 18 | 259-267 | NO | no completo | Kelp | Macrocystis pyrifera, farming, food products, Chile | This study explores the potential cultivation of the giant kelp Macrocystis pyrifera (L.) C.A. Agardh in southern |
Ficha | Variacion Morfologica Estacional de Rhizosolenia Alata Brightwell en Bahia Paraiso, Antartida Occidental | Gustavo Ferreyra y Martha E. Ferrario | 300 | ene-18 | 2531 | no completo | Sin asignar | Bahia Paraiso, Antartida Occidental, Argentina; Rhizosolenia alata; morfológico | Se realizó el estudio al microscopio óptico y electrónico de la variación morfológica estacional de muestras de poblaciones que según criterios tradicionales podrían ser referidas a Rhizosolenia alata, Rh. inermis y sus respectivas subespecies. Se analizó |
Ficha | Systematicof Gracilariopsis (Gracilariales, Rhodophyta) based on rbcL sequence analyses and morphological evidence | Gurgel C.F.D. and et. al. | NO | Rodofitas | |||||
Ficha | European Journal of Phycology | Guiry Michael D. | NO | General | |||||
Ficha | Gelidiella minima sp. nov.(Rhodophyta) from Victoria, Australia: Implications for the generic classification of the Gelidiaceae | Guiry M. D. and H. B. S. Womersley | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Macroalgae (Seaweeds) | Guillermo Diaz-Pulido and Laurence J. McCook | NO | no completo | General | The Great Barrier Reef World Heritage Area has a highly diverse macroalgal | |||
Ficha | Effect of UV stress on the fatty acid and lipid class composition in two marine microalgae Pavlova lutheri (Pavlovophyceae) and Odontella aurita (Bacillariophyceae) | Guihéneuf Freddy and et. al. | 22 | 629-638 | NO | no completo | Fitoplancton | Pavlova lutheri . Odontella aurita . UV radiation . Lipid classes . n-3 fatty acids | Polyunsaturated fatty acids (PUFAs), especially |
Ficha | THE MESOZOIC RADIATION OF EUKARYOTIC ALGAE: THE PORTABLE PLASTID HYPOTHESIS | Grzebyk, Daniel and Oscar Schofield | NO | General | |||||
Ficha | Mosaic genetic structure and sustainable establishment of the invasive kelp Undaria pinnatifida within a bay (Bay of St- Malo, Brittany) | Grulois D. and et. al. | NO | Kelp | |||||
Ficha | Chlorophyll: Structure and Function | Grimm Bernhard | 01-ago | NO | no completo | General | Chlorophyll is the dominant pigment on Earth and serves as the light-trapping and energy | ||
Ficha | The thermal algae of the Philippines | Gregorio T. Velasquez | 11 | 137-147 | 48 | no completo | Sin asignar | This is the firet study of the thermal algae inthe Philippines. Seven species, one coccoid form of Chlorophyceae and the others Myxophyceae are herein reported. They are: Gloeocystis Grevillei (Berk) Dr. and Daily, Coccochoris stagnina Spreg., Phormidium | |
Ficha | Further study of the thermal algae of the Philippines | Gregorio T. Velasquez | 4 | 455-457 | 50 | no completo | Sin asignar | ||
Ficha | THE NUTRIENT ASSIMILATIVE CAPACITY OF MAERL AS A SUBSTRATE IN CONSTRUCTED WETLAND SYSTEMS FOR WASTE TREATMENT | GRAY SHALLA and et. al. | 34 | 2183-2190 | NO | no completo | General | Constructed wetlands, maerl, wastewater, phosphorus, nitrogen | This study evaluated the performance of maerl (calcified seaweed) as a substrate for artificial |
Ficha | Primary succession on a seasonal tropical rocky shore: the relative roles of spatial heterogeneity and herbivory | Gray A. Williams, Mark S. Davies, Sanjay Nagarkar | 203 | 81-94 | NO | no completo | General | Biofilm · Cyanobacteria · Herbivory · Hong Kong · Mucus · Spatial heterogeneity · Succession · Tropical rocky shore | Hong Kong is within the tropics and has a seasonal climate. In winter, shores support patches of ephemeral macroalgae and areas of seemingly bare rock close to crevices where mollus- |
Ficha | Emergent properties of kelp forests: flow-modification by kelp canopies couples propagule output to supply | Graham M.H. | 84 | 1250-1264 | NO | no completo | Kelp | kelp canopies, flow modification, propagule supply, giant kelp zoospores, Macrocystis pyrifera, population dynamics, reproductive coupling, scale-dependent dispersal | Propagule dispersal is fundamental in regulating the strength of demographic and genetic |
Ficha | Planktonic patterns and processes in the Giant Kelp Macocystis pyrifera | Graham M.H. | NO | Kelp | |||||
Ficha | Diversity and Dynamics of Californian Subtidal Kelp Forests | Graham M. H. and et. al. | NO | no completo | Kelp | ||||
Ficha | GLOBAL ECOLOGY OF THE GIANT KELP MACROCYSTIS: FROM ECOTYPES TO ECOSYSTEMS | Graham M. H. and et. al. | NO | Kelp | |||||
Ficha | COUPLING PROPAGULE OUTPUT TO SUPPLY AT THE EDGE AND INTERIOR OF A GIANT KELP FOREST | Graham M. H. | NO | Kelp | |||||
Ficha | CONFRONTING MULTICOLLINEARITY IN ECOLOGICAL MULTIPLE REGRESSION | Graham M. H. | 84 | NO | no completo | Kelp | multiple regression; confounding factors; multicollinearity; sequential regression; principal components regression; structural equation modeling | The natural complexity of ecological communities regularly lures ecologists to collect | |
Ficha | Short term monitoring of biotic change in Tasmanian marine reserves | Graham J. Edgar, Neville S. Barrett | 261–279 | NO | Liga perdida | Sin asignar | Fish; Invertebrates; Macroalgae; Marine reserve; Tasmania; Temperate reef; Visual census | Fishes, large invertebrates and macroalgae inside four marine reserves and at associated external reference sites off the eastern Tasmanian coast were censused between 1992 and 1993 shortly after the declaration of the reserves. Changes in several populat | |
Ficha | Expansive covers of turf-forming algae on human-dominated coast: the relative effects of increasing nutrient and sediment loads | Gorgula S.K. & S.D. Conell | 145 | 613-619 | NO | parcialmente completo con liga | General | Turf-forming algae form more extensive habi- coast of South Australia. This pattern is frequently ob- considered | |
Ficha | Effects of water motion on propagule release from algae with complex life histories | Gordon R. and S.H. Brawley | 145 | 21-29 | NO | no completo | General | Reproductive marine algae with complex life depending upon whether the spore-producing or gam- kelp Alaria esculenta (L.) | |
Ficha | Disturbance initiates diversity in recruitment of canopy-forming algae: interactive effects of canopy-thinning and substratum availability | GOODSELL PARIS J. AND SEAN D. CONNELL | 44 | 632-639 | NO | no completo | General | We assessed whether disturbance within monospecific canopies (Ecklonia radiata, Phaeophyta) increases diversity of ma- | |
Ficha | Estudio fenológico de cuatro especies de Cystoseira C. Agardh (Phaeophyta, Fucales) en Punta del Hidalgo, Tenerife (Islas Canarias). | González-Rodríguez, R. M., & Afonso-Carrillo, J. | 18 | 205-234 | 3875 | no completo | Sin asignar | The morphological and reproductive phenology of four species of Cystoseira in Punta del Hidalgo (Tenerife, Canary Islands). C. abies-marina (Cmelin) C. Agardhr, C. compressa (Esper) Gerloff & Nizamudin, C. FoenicuIacea ( L. ) GrevilIe and C. humilis var. | |
Ficha | Flora ficologica de México. | González-González, J. | ene-14 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Coalescence and chimerism in Codium (Chlorophyta) from central Chile | GONZALEZ A.V. AND B. SANTELICES | 47 | 468-476 | NO | parcialmente completo con liga | Clorofita | This study evaluates the natural occurrence of inter- and intracrust fusions of patches of a common species of Codium in | |
Ficha | Chlorophycées des côtes françasises | Gontran Hamel | 5 | 383-430 | 3102 | no completo | Sin asignar | ||
Ficha | Contribucion al estudio de las algas rojas de la isla de Tabarca (Alicante). | Gomez-Menor Robles, J. M., & Fuertes Lasala, E. | 13 | 865-872 | NO | parcialmente sin liga | Sin asignar | In this paper we include the List of the microscopic species of Cyanophyta, Phaeophyta and Chlorophyta, found in the sea around the island of Tabarca, also giving the possible reasons for apearence of hunger forms. | |
Ficha | Frond regrowth from basal disc in Iridaea laminarioides (Rhodophyta, Gigartinales) at Mehuin, southern Chile | Gomez Ivan M. and Renato C. Westermeier | 73 | 83-91 | NO | parcialmente completo con liga | Rodofitas | Red algae of the family Gigartinaceae, including the genus Iridaea, have recently become | |
Ficha | Nota sobre la variacion morfologica de Gelidium spathulatum en Mallorca. | Gómez Garreta, M., Ribera Siguán, M. A., & Seoane Camba, J. A. | 13 | 857-863 | NO | parcialmente sin liga | Sin asignar | En esta nota presentamos las variaciones morfológicas sufridas por Gelidium spathulatum (Kützing) Bornet a lo largo del año, en una población determinada de la cala de Portals Nous (Bahía de Palma). Estas variaciones quedan reflejadas en dibujos realizado | |
Ficha | Estudio fenológico de varias especies del género Cystoseira en Mallorca. | Gómez Garreta, M., Ribera Siguán, M. A., & Seoane Camba, J. A. | 13 | 841-855 | NO | parcialmente sin liga | Sin asignar | In this paper we studied the variations, both from the morphological and reproductive point of view, that occurred during a year in various species of Cystoseira. The observations were carried out monthly between fe- bruary 1978 and January 1979 in four l | |
Ficha | Constant short-day treatment of outdoor-cultivated Laminaria digitata prevents summer drop in growth rate | Gomez Ivan and Klaus Luning | 36 | 391-395 | NO | no completo | Cultivo | cultivation, daylength, growth rhythm, kelp, Laminariales, Laminaria digitata, photoperiod, seasonality, short days | Previous laboratory studies in species of the Laminariales have revealed that both the onset of growth in early winter and |
Ficha | The application of adaptive cluster sampling for rare subtidal macroalgae | Goldberg Nisse A. and et. al. | 151 | 1343–1348 | NO | no completo | General | Adaptive cluster sampling (ACS) is a tar- may be inadequately sampled with simple random | |
Ficha | Differential targeting of closely related ECM glycoproteins: the pherophorin family from Volvox | Godl Klaus and et. al. | 16 | 25-34 | NO | no completo | General | ECM glycoproteins - green algae - hydroxyproline-rich glycopotreins - pherophorins - Volvox | |
Ficha | Correlation between Gracilaria parÍispora Rhodophyta/biomass production and water quality factors on a tropical reef in Hawaii | Glenn Edward P. and et. al. | NO | Rodofitas | |||||
Ficha | Correlation between Gracilaria parvispora (Rodophyta) biomass production and water quality factors on a tropical reef in Hawaii | Glenn Edward P. and et. al | NO | Cultivo | |||||
Ficha | A sustainable culture system for Gracilaria parÍispora Rhodophyta/using sporelings, reef growout and floating cages in Hawaii | Glenn Edward P. and et. al | NO | Cultivo | |||||
Ficha | Spore culture of the edible red seaweed, Gracilaria parvispora (Rodophyta) | Glenn Edward P. and et. al | 142 | 59-74 | NO | no completo | Cultivo | Gracilaria; Carpospores; Tetraspora; Culture method | |
Ficha | Species Composition and Seasonal Periodicity of The Marine Benthic Algae of Galveston Island, Texas | Glenn C. Lowe,Jr. and El enor R. Cox | ND | 1429 | no completo | Sin asignar | Isla de Galveston, Estados Unidos; Chlorophyta, Phaeophvta, Rhodophyta, Xanthophyta | Sampling of benthic algae from selected sites on Galveston Island was carried out at regular intervals between June 1972 and August 1974 to determine the species composition and seasonal periodicity of the communities. Nineteen genera and twenty eight spe | |
Ficha | Experimental use of salt to control the invasive marine alga Caulerpa taxifolia in New South Wales, Australia | Glasby Tim M. , Robert G. Creese, Peter T. Gibson | 122 | 573-580 | NO | no completo | Clorofita | Control; Experimental; Introduced species; Management; Seaweed | Caulerpa taxifolia was first discovered in New South Wales, Australia, in April 2000 and is now present in nine waterways. Infes- |
Ficha | Mapping and biomass estimation for a harvested population of Gelidium sesquipedale (Rhodophyta, Gelidiales) along the Atlantic coast of Morocco | Givernaud T. et. al. | 44 | 66-71 | NO | Completo | General | The alga Gelidium sesquipedale is harvested by divers along the Atlantic coast of Morocco and used for agar production. Management of this natural resource has become necessary due to increasing industrial demand. Deta | |
Ficha | Mapping and biomass estimation for harveted population of Gelidium sesquipedale (Rhodophyta, Gelidiales) along the Atlantic coast of Morocco | Givernaud T. and et. al. | NO | Rodofitas | |||||
Ficha | MULTIPLE CRYPTIC SPECIES: MOLECULAR DIVERSITY AND REPRODUCTIVE ISOLATION IN THE BOSTRYCHIA RADICANS/B. MORITZIANA COMPLEX (RHODOMELACEAE, RHODOPHYTA) WITH FOCUS ON NORTH AMERICAN ISOLATES | Giuseppe C. Zuccarello and John A. West | 39 | 948-959 | NO | Completo | Rodofitas | Bostrychia moritziana, Bostrychia radicans, cox2-3 spacer, hybridization, phylogeography, reproductive isolation, Rhodophyta, RUBISCO spacer, SSCP | Red algae of the Bostrychia radicans/B. moritziana complex are common in warm temperate areas of North America. Phylogenetic analysis of both plastid and mitochondrial DNA sequence data revealed seven di |
Ficha | Diversity within red algal species: variation in world-wide samples of Spyridia filamentosa (Ceramiaceae) and Murrayella periclados (Rhodomelaceae) using DNA markers and breeding studies | Giusepe C. Zuccarello, Bernadette Sandercock and John A. West | 37 | 403-417 | NO | Liga perdida | Rodofitas | cox2-3 spacer, cryptic species, large subunit rRNA, Murrayella periclados, rbcL, reproductive compatibility, RuBisCo spacer, Spyridia filamentosa, Spyridia hypnoides | Molecular and breeding studies on two pan-tropical marine red algae reveal vastly different levels of genetic variation and reproductive isolation. Sequenced DNA regions from the nuclear, mitochondrial and plastid geno |
Ficha | The Seaweed Resources of kwaZulu-Natal, South Africa: The Current State of Our knowledge | Gillesitlie, R. D., Aingworth, J., & Critchley, A. T. | 186-193 | NO | Liga perdida | General | The coastline of KwaZulu-Natal, South Africa supports a substantial diversity of seaweeds which remains to a great extent | ||
Ficha | The phytoplankton of some artificial pools near Stockholm. | Gilbert Morgan Smith | 17 | 43313 | 46 | no completo | Sin asignar | ||
Ficha | The Preservation of Fresh Water Chlorophyceae | Gilbert Morgan Smith | 15 | 219-230 | 68 | no completo | Sin asignar | ||
Ficha | The historical significance of names applied to reproductive structures of algae. | Gilbert M. Smith | 3 | 217- 223 | NO | parcialmente sin liga | Sin asignar | Le faltan páginas al artículo | |
Ficha | Biological Results of The University of Miami Deep-Sea Expeditions. 93. Comments Concerning the University of Miami's Marine Biological Survey Related to the Panamanian Sea-Level Canal | Gilbert L. Voss | 2 | 49-58 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Halophila decipiens Ostenfeld (Hidrocharitaceae) una fanerógama marina nueva para el Atlántico Oriental. | Gil-Rogríguez, M. C. & Simó, T. C. | 11 | 207-216 | NO | parcialmente sin liga | Sin asignar | Whit the presence of Halophila decipiens Ostenfeld, in the Canary Archipelago, the pantropical area of the species has been amplified, which hitherto had not been recorded on the coasts of the Eastern Atlantic. Some remarks concernig the species´ecology | |
Ficha | Praderas marinas de Zostera noltii (Zosteraceae) en las Islas Canarias. | Gil-Rodríguez, M. C., Alfonso-Carrillo, J., & Wildpret De la Torre, W. | 17 | 143-146 | NO | parcialmente sin liga | Sin asignar | Se confirma la existencia de praderas de Zostera noltii Hormen. (Zosteraceae) en Lanzarote (Islas Canarias). Se enuncian brevemente las características más importantes de las praderas submarinas y se realizan algunos comentarios fitosociológicos. | |
Ficha | Adiciones a la flora marina: nuevas citas para la región Canaria. | Gil-Rodríguez, M. C., Afonso-Carrillo, J., & Cruz Simó, T. | 11 | 135-140 | NO | parcialmente sin liga | Sin asignar | Four species of marine algae have been recorded from Canary Islands for the first time: Sporochnus pedunculatus (Hudson) C.Ag. Nereia tropica (Taylor) Taylor, Cutleria multifida (Smith) Greville and Bornetia secundiflora (J. Ag.) Thuret. Ecological remark | |
Ficha | Sobre la estructura y reproducción de Cottoniella Boergesen (Rhodophyta, Ceremiales) en las Islas Canarias. | Gil-Rodríguez, M. C., Afonso Carrillo, J., Wildpret De la Torre, W., & Hauroum T., R. | 41 | 227-236 | NO | parcialmente sin liga | Sin asignar | Se describen por primera vez las estructuras sexuales del género Cottoniella en el endemismo macaronésico C. filamentosa (Howe) Boergesen var. fusiformis (Boergesen) Cormaci, Furnari & Scammacca y se detalla la estructura de las plantas canarias, resaltan | |
Ficha | Sobre la distribución de la familia Dasycladaceae (Chlorophyta) en las Islas Canarias. | Gil-Rodríguez, M. C., & Afonso-Carrillo, J. | 13 | 831-839 | NO | parcialmente sin liga | Sin asignar | The presence of the vegetal formation "maerl", wel l know n on the europea n coasts, has bee n detecte d of the E. coast of Te - nerife on the sea bed at a depth of between 20 to 60 m. It is compose d principall y of the accumulation of arbuscular stems o | |
Ficha | Contribución al estudio del género Cystoseira C. Ag. en el Archipiélago Canario. | Gil-Rodriguez, M. C. & Wildpret De la Torre, W. | 373-383 | NO | parcialmente sin liga | Sin asignar | Archipielago Canario; Cystoseira tamariscifolia (Huds.) Papenfuss., C. abies-marina (Tuner.) C. Ag., C. humilis Schousboe in Jützing., C. discors (L.) C. Ag., y C. compressa (Esper.) Gerloff et Nizann. | En el Departamento de Botánica de la Facultad de Ciencias de la Universidad de La Laguna, se está realizando un estudio exhaustivo de la vegetación algal del Archipiélago Canario. En este estudio aparte de confeccionar el catálogo e inventarios de las esp | |
Ficha | Contribución a la ficología de la Isla del Hierro. | Gil-Rodriguez, M. C. & Wildpret De la Torre, W. | 8 | 245-260 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The genus Laurencia (Rhodomelaceae, Rhodophyta) in the Canary Islands. | Gil-Rodriguez, M. C. & Haroun, R. | 159 | 113-117 | 3903 | no completo | Sin asignar | Up to now, only eight species of Laurencia have been reported on the Canarian Coasts. However, a revision of La Laguna University Herbarium (TFCPhyc.) and with fresh collections made from 1987 to 1989 in several locations along the Canarian Coasts, have a | |
Ficha | Adiciones a la flora marina y catálogo ficológico para la Isla de Lanzarote. | Gil-Rodriguez, M. C. & Afonso-Carrillo, J. | 10 | 58-70 | NO | parcialmente sin liga | Sin asignar | As a result of studies carried out on the coast of the island of Lan- zarote the ficological catalogue of this island has been a ugmented to 40 species, of which 4 represent new records for the Canary Archipe- lago. The general characteristics of the site | |
Ficha | Revisión taxonómica-ecológica del género Cystoseira C. Ag. en el archipiélago canario. | Gil-Rodriguez, M. C. | 9 | 115-148 | NO | parcialmente sin liga | Sin asignar | Duns la "polldre verte" corticol e, l' algue suba érienne Pleurococcu s vulgarts Naeg. entre en inter action de con tad du type bio troph ique avec les hy phes de la Dématiée Coniosporium aeroalgico lum Tu r. Dans la ,.pou drc noire" des éco rces d'a rbre | |
Ficha | Cenozoic coralline algal assemblage from southwestern Kutch and its importance in palaeoenvironment and palaeobathymetry | Ghosh Amit K. | 83 | 153-158 | NO | Completo | Rodofitas | Little contribution has been made on the study of coralline algae from the Cenozoic sediments of southwestern Kutch. Some of the limestone units belonging to Oligocene and Miocene sediments of southwestern Ku | |
Ficha | Composition and comunity structure of the coralline algal reefs from atol das rocas, South Atlantic, Brazil | Gherardi D.F.M. and D.W.J. Bosence | NO | Rodofitas | |||||
Ficha | STABLE ISOTOPE COMPOSITION OF BENTHIC CALCAREOUS ALGAE FROM BERMUDA | GEROLD WEFER AND WOLFGANG H. BERGER | 51 | 459-465 | No | no completo | General | Carbonate secreted by benthic algae from Bermuda (5 genera, 3 phyla) can be grouped into four types | |
Ficha | The morphology of Grateloupia intestinalis from New Zealand, with some thoughts on generic criteria within the family Cryptonemiaceae (Rhodophyta) | Gerald T. Kraft | 16 | 43-51 | NO | parcialmente sin liga | Sin asignar | Nueva Zelanda; Cryptonemiaceae, Rhodophyta; Morfológico. | The reproductive morphology of Grateloupia intestinalis (Cryptonemiaceae, Rhodophyta) from New Zealand is illustrated. Comparison is made to previous descriptions of Grateloupia and to Aeodes, a second genus of the family. Grateloupia intestinalis falls w |
Ficha | Studies of Marine Algae in the Lesser-known Families of the Gigartinales (Rhodophyta). I. The Acrotylaceae | Gerald T. Kraft | 25 | 97-140 | 1357 | no completo | Sin asignar | Acrotylus australis J. Ag., Hennedya crispa Harv., Amphiplexia hymenocladioides J. Ag. y A. racemosa (J. Ag.) comb, nov. | The Acrotylaceae is composed of Acrotylus australis J. Ag., Hennedya crispa Harv., Amphiplexia hymenocladioides J. Ag. and A. racemosa (J. Ag.) comb, nov. (all endemic to southern Australia), Reinboldia polyearpa Schmitz from South Africa and Ranavalona d |
Ficha | DETERMINACIÓN DE LA BIOMASA DE Macrocystis integrifolia (huiro canutillo), Lessonia trabeculata (huiro palo) y Heterozostera chilensis (pasto marino), MEDIANTE TÉCNICAS DE TELEDETECCIÓN AEROESPACIAL EN BAHÍA CHASCOS - REGIÓN DE ATACAMA” | Geosensing Ltda | NO | Feofita | |||||
Ficha | An unusual algal habitat | George J. Schumacher | 141-142 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Supplement to Smith´s Marine Algae of the Monterey Peninsula | George J. Hollenberg and Isabella A. Abbot | 19 | 61 | 782 | no completo | Sin asignar | ||
Ficha | An Account of the Species of Polysiphonia on the Pacific Coast of North America. I. Oligosiphonia | George J. Hollenberg | 772-785 | NO | Liga perdida | Sin asignar | |||
Ficha | A New Species of Malaconema (Rhodophyta) from the Marshall Islands | George J. Hollenberg | 2 | 169-172 | 1744 | no completo | Sin asignar | ||
Ficha | An Account of The Ralfsiaceae (Phaeophyta) of California | George J. Hollenberg | 5 | 290-301 | 1746 | no completo | Sin asignar | New taxa are described as follows: Ralfsia confusa sp . nov., Ralfsia integra sp. nov., Pseudolithoderma nigra sp. nov., Diplura simulans gen. et sp. nov., Endoplura aurea gen, et sp, nov. Lithodermataceae is included in Ralisiaceae. An emended descriptio | |
Ficha | Notes on Pacific coast Marine Algae | George J. Hollenberg | 155-162 | NO | Liga perdida | Sin asignar | |||
Ficha | Phycological Notes-I | George J. Hollenberg | 528-538 | NO | Liga perdida | Sin asignar | |||
Ficha | New Marine Algae from Southern California. II | George J. Hollenberg | 30 | 571-579 | NO | parcialmente sin liga | Sin asignar | Sur de California; Petroglossum, Rhodosiphonia, Sorella, Herposiphonia parva. | Petroglossum gen. nov. is closely related to Phyllophora, from which it differs chiefly in the nemathecial nature of the antheridial sori. Rhodosiphonia gen. nov. is a member of the Rhodomelaceae resembling Ophiocladus in a number of respects, including t |
Ficha | Culture Studies of Marine Algae. III. Porphyra perforata | George J. Hollenberg | 45 | 653-656 | NO | parcialmente sin liga | Sin asignar | Porphyra perforata | Culture studies of Porphyra perforata, which were previously reported in brief at the meetings of the Pacific Section of the Botanical Society of America at Pasadena, California in June, 1955, show that mature plants of this species probably produce no ne |
Ficha | New Genera in the Rhodomelaceae from the Central Pacific | George J. Hollenberg | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | A Morphological Study of Amplisiphonia: A New Member of the Rhodomelaceae | George J. Hollenberg | 101 | 380-390 | 67 | no completo | Sin asignar | Amplisiphonia; morfológico. | 1. Amplisiphonia represents a new member of the Rhodomelacea closet o Placophora in vegetative structure. It differs from that genus in size and habit, but chiefly in the fact that the tetrasporangia are borne in modified lobes of the thallus rathe |
Ficha | Some New Myxophyceae from Southern California | George J. Hollenberg | 66 | 489-494 | 1737 | no completo | Sin asignar | ||
Ficha | Culture Studies of Marine Algae. I. Eisenia arborea | George J. Hollenberg | 26 | 34-41 | 1747 | no completo | Sin asignar | The life cycle and the gametophyte plants of Eisenia arborea are essentially like those described for other members of the Laminariales. Low temperatures are not essential for culturing the sexual plants, which develop and fruit abundantly at ordinary roo | |
Ficha | Culture Studies of Marine Algae. II. Hapterophycus canaliculatus S. & G. | George J. Hollenberg | 28 | 676-683 | 1742 | no completo | Sin asignar | Hapterophycus | Although mature plants of Hapterophycus bear only unilocular sporangia, the zoids from these reproductive structures exhibit heteroblasty, giving rise to two distinct types of germlings. Cytological evidence indicates that meiosis occurs during the first |
Ficha | An Account of the Species of the Red Alga Herposiphonia Occurring In the Central and Western Tropical Pacific Ocean | George J. Hollenberg | 22 | ND | NO | parcialmente sin liga | Sin asignar | Océano Pacífico tropical central y occidental; H. arcuata, H. crassa, H. delicatula, H. dendroidea, H. dendroidea var. menor, H. dubia, H. nuda, H. obscura, H. parca var. interrupta, H. pacifica, H. trichia, H. variabilis, H. parca, H. subdisticha y H. te | Fourteen species of the genus Herposiphonia are described. The following species and varieties are new: H. arcuata, H. crassa, H. delicatula, H. dendroidea, H. dendroidea var. minor, H. dubia, H. nuda, H. obscura, H. parca var. interrupta, H. pacifica, H. |
Ficha | Phycological Notes III. New Records of Marine Algae From The Central Tropical Pacific Ocean | George J. Hollenberg | 20 | 74-82 | NO | parcialmente sin liga | Sin asignar | Océano Pacífico tropical central; Dermocorynus occidentalis, Ceramium panicumátum, C. hamatispinum, Spirocladia barodensis, Symphyocladia marchantioides, Lophosiphonia cristata, L. prostrata, ExophylIum. Goii. Las gamas de Ralfsia pangoensis y MurrayeIIa | Taxonomic and distributional notes are given for the following marine algae, which are reported for the first time from the central tropical Pacific Ocean: Dermocorynus occidentalis, Ceramium panicuIatum, C. hamatispinum, Spirocladia barodensis, Symphyocl |
Ficha | An Account of the Species of Polysiphonia of the Central and Western Tropical Pacific Ocean I. Oligosiphonia | George J. Hollenberg | 32 | 56-98 | NO | parcialmente sin liga | Sin asignar | Twenty-four tetrasiphonous species are described. The following species or varieties are new : Polysiphonia anomala, P. apiculata, P. delicatula, P. flaceidissima var. decimera, P. flaccidissima var. iki, P. flaccidissima var. lopi, P. hawaiiensis, P. her | |
Ficha | The morphology and taxonomy of the red alga Sarconema (Gigartinales: Solieriaceae) | George F. Papenfuss And Tikvah Edelstein | 13 | 31-44 | 763 | no completo | Sin asignar | Africa Oriental; Sarcollema | A study of the structure and reproduction of two species of Sarcollema from East Africa has shown that the genus is correctly placed in the Solieriaceae. The genus agrees with Solieria in that the auxiliary cell is indistinguishable before diploidization. |
Ficha | The morphology and systematic position of the green algae Ernodesmis and Apjohnia | George F. Papenfuss And Mitsuo Chihara | 14 | 309-316 | NO | parcialmente sin liga | Sin asignar | The monotypic genera Ernodesmis Børgesen and Apjohnia Harvey, which in habit resemble each other and which have been regarded as belonging to the Siphonocladaceae by most authors, are shown to be different genera. Neither appears to belong to the Siphonoc | |
Ficha | Review of the genera of Dictyotales (Phaeophycophyta) | George F. Papenfuss | 25 | 271-287 | NO | parcialmente sin liga | Sin asignar | Dictyopteris, Dictyota, Dictyotopsis, Dilophus, Distromium, Glossaphora, Lobophora, Lobospira, Microzonia, Pachydictyon, Padina, Pocockiella, Spatoglossum, Stoechosperrum, Stypopodium, Syringoderma, Taonia, Triplostromium y Zonaria | The composition of the Dictyotales has undergone much change since the appearance of the present author's chapter in the Manual of P hycology in 1951. In that paper I listed 21 genera as follows: Chlanidophora, Dictyerpa, Dictyopteris, Dictyota, Dictyotop |
Ficha | Notes On South African Marine Algae. V. | George F. Papenfuss | 34 | 267-287 | 761 | no completo | Sin asignar | La hojas están desordenadas | |
Ficha | Notes On South African Marine Algae. V. | George F. Papenfuss | 34 | 267-287 | 761 | no completo | Sin asignar | La hojas están desordenadas | |
Ficha | On the Geographical Distribution of Some Tropical Marine Algae | George F. Papenfuss | 45-51 | NO | parcialmente sin liga | Sin asignar | La páginas están desordenadas | A number of genera and some species of marine algae have a distributiun that extends from the Caribbean westward into the Pacific and Indian Oceans and in some instances all the way to East Africa, whereas a relatively small number of these taxa also occu | |
Ficha | Taxonomic and nomenclatural notes on three species of Brown Algae | George F. Papenfuss | 1 | 320-330 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Landmarks in Pacific North America Marine Phycology | George F. Papenfuss | 21-46 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Sur l´origine pseudo-endogène des rameaux verticillés tétrasporangifères du Griffithsia flosculosa (Ellis) Batt. | Geneviève Feldmann | 96 | 28-31 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Sur Quelques Ceramiacées de Nouvelle-Zélande | Geneviève Feldmann | 2 | 131-141 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Sur Quelques Ceramiacées de Nouvelle-Zélande (suite) | Geneviève Feldmann | 32 | 307-314 | 1523 | no completo | Sin asignar | ||
Ficha | Molecular divergence and morphological diversity among four cryptic species of Plocamium (Plocamiales, Florideophyceae) in northern Europe | Gary W. and Lehmkuhl, K. Virginia | 40 | 293 - 312 | NO | Completo | Rodofitas | cryptic species, Florideophyceae, large-subunit rDNA, molecular systematics, phylogeny, Plocamiaceae, Plocamium, Rhodophyta, small-subunit rDNA | The Plocamiaceae currently includes two genera: the free-living Plocamium and the adelphoparasite, Plocamiocolax. Plocamium includes ca. 40 species that are widely distributed throughout the world’s oceans. Most speci |
Ficha | Cellular Organization, Mitosis, and Cytokinesis in the Ulotrichalean Alga, Klebsormidium | Gary L. Floyd, Kenneth D. Stewart, and Karl R. Mattox | 8 | 176-184 | 2858 | no completo | Sin asignar | K. Flaccidum, Ulothrix firmbrita y Stigeoclonium helvecticum | Mitosis, Cytokinesis, and cellular organization during interphase are described. Interphase cells possess a single microbody-like organelle which occurs between, and is appressed to, the chloroplast and nucleus. The microbody-like organelle divides during |
Ficha | Microbiología marina. | García-Tello, O. | 1 A 102 | 3917 | no completo | Sin asignar | |||
Ficha | La radiación fotosintéticamente activa o PAR (photosynthetically active radiation) en la recreación ambiental del acuario marino | García-Castrillo G. and et. al. | 21 | 465-475 | NO | no completo | General | Acuarios, iluminación, extinción, MOD, gilvinas. | Los registros del PAR (photosynthetically active radiation) obtenidos en dos estaciones costeras y |
Ficha | Observaciones sobre la ecologica de las cubetas litorales en las costas de Galicia. | Gallardo, T., & Perez-Ciera, J. L. | 13 | 817-830 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | A NEW BROWN ALGAL ORDER, ISHIGEALES (PHAEOPHYCEAE), ESTABLISHED ON THE BASIS OF PLASTID PROTEIN-CODING rbcL, psaA, AND psbA REGION COMPARISONS | Ga Youn Cho and et. al. | 40 | 921-936 | NO | parcialmente completo con liga | Feofita | Ishige; Ishigeaceae; Ishigeales ord. nov.; Phaeophyceae; phylogeny; psaA; psbA; pyre- noid; rbcL; taxonomy; ultrastructure | The brown algal family Ishigeaceae currently includes a single genus, Ishige Yendo, with two spe- algal lineages is less studied in terms of their plastid ultrastructure and |
Ficha | Phylogenetic relationships within the Fucales (Phaeophyceae) assessed by the photosystem I coding psaA sequences | Ga Youn Cho and et. al. | 45 | 512-519 | NO | no completo | Feofita | Bifurcariopsis, Bifurcariopsidaceae fam. nov., Fucales, Phaeophyceae, Phylogeny, psaA, Taxonomy, Xipho- phora, Xiphophoraceae fam. nov. | Fucalean brown algae are ecologically important for maintaining intertidal to subtidal ecosystems and are currently a subject |
Ficha | The Ecology of South-East Tasmanian Phytal Animal Communities. III. Pattezrns of Species Diversity | G.J. EDGAR | 181-203 | NO | Liga perdida | Sin asignar | Diversity indices which have been widely used in ecological studies were calculated for each of 135 samples of phytal macrofauna. A comparison of the properties ofthese indices indicated that they could be grouped into those primarily in~uen~ed by dominan | ||
Ficha | Remarks on the taxouomv of Galaxaura (Nemaliales, Chaetangiaceae) | G.F. Papenfuss and Young-Meng Chiang | 6 | 303-314 | NO | parcialmente sin liga | Sin asignar | Chaetangiaceae (Nemaliales) | Galaxaura Lamouroux is a genus of tropical and subtropical calcified red algae of the family Chaetangiaceae (Nemaliales). The genus was monographed by Kjellman in 1900; he accepted 62 species, 47 of which were new. Kjellman overlooked by Butters, Børgense |
Ficha | Correction of Algal Binomial | G. ]. Hollenberg | 25 | 122 | 1740 | no completo | Sin asignar | ||
Ficha | NUTRIENT UPTAKE AND GROWTH KINETICS IN BROWN SEAWEEDS: RESPONSE TO CONTINUOUS AND SINGLE ADDITIONS OF AMMONIUM | G. ROSENBERG, T.A. PROBYN and K.H. MANN | 80 | 125-146 | No | no completo | General | The brown seaweeds Fucus distichus Linnaeus subsp. edentatus (de la Pylaie) Powell, a perennial, | |
Ficha | A revision of the genus Plocamium Lamouroux (Rhodophyta, Gigartinales) in New Zealand | G. Robin South and Nancy M. Adams | 18 | 120-132 | 1785 | no completo | Sin asignar | Nueva Zelanda; P. angllstum (J. Ag.) Hook. ajuste. et Harv .; P. cartilagineum (L.) Dixon; P. costatum (c. Ag.) Hook. fil et Harv .; P. leptophyllum Kütz .; P. hamatum J. Ag y P. microcladioides sp. nov. | Six species of Ptocamillm Lamouroux (Rhodophyta, Gigartinales) are recognized for New Zealand and the New Zealand Subantarctic Islands: P. angllstum (J. Ag.) Hook. fit. et Harv.; P. cartilagineum (L.) Dixon; P. costatum (c. Ag.) Hook. fil et Harv.; P. lep |
Ficha | Chlorella Parasitic in Bluegills | G. L. Hoffman | 27 | 175 | 83 | no completo | Sin asignar | ||
Ficha | Natural Phenomena | G. E. B uckwalter | 45-52 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Mnagement of kelp ecosystem in Japan | Fujita D. | NO | Kelp | |||||
Ficha | Metaphyton de sies lagunas de altura del departamento de Cochabamba, Bolivia. | Fuentes, M. C. | 39-62 | 3909 | no completo | Sin asignar | Metaphyton de seis lagunas de altura del departamento de Cochabamba, Bolivia. El objetivo del presente estudio es determinar la composición del metaphyton de seis lagunas ubicadas entre los 17'23'30" a 17'27'30" de latitud sud y 65'35'30" a 65'38'30" de l | ||
Ficha | Gracilaria and its epiphytes: 4. The response of two Gracilaria species to Ulva lactuca in a bacteria-limited environment | Friedlander M. , Y. Kashman, F. Weinberger & C.J. Dawes | 13 | 501-507 | NO | no completo | Cultivo | defense response, epiphytes, Gracilaria, halogenated hydrocarbons, hydrogen peroxide, Ulva | The responses of Gracilaria lemaneiformis, an easily epiphytized host, and the relatively resistant G. cornea |
Ficha | Characteristics and utility of nuclear-encoded large-subunit ribosomal gene sequences in phylogenetic studies of red algae | Freshwater D. Wilson and et. al. | 47 | 33-38 | NO | Completo | Rodofitas | Gelidiales, LSU, molecular evolution, phylogenetics, rbcL, Rhodophyta, SSU. | Primer sequences are described for amplifying and sequencing a large fragment (approximately 2500 b.p.) of the nuclear-encoded large-subunit ribosomal RNA gene (LSU) from red algae. In comparison to RuBisCo&n |
Ficha | Producción de Macroalgas en Ambiente Controlado (Hatchery) | Freres Castillo Hernán | NO | Cultivo | |||||
Ficha | Does storage time influence yield and agar properties in the tropical agarophyte Gracilaria cornea? | Freile-Pelegrín Yolanda | 12 | 153-158 | NO | no completo | Cultivo | agar, gel strength, Gracilaria cornea, storage time, yield | The agar yield and quality characteristics of Gracilaria cornea from Yucatán, Mexico, were studied during 18 |
Ficha | Phylogeny and Molecular Evolution of the Green Algae | Frederik Leliaert, David R. Smith, Herve Moreau, Matthew D. Herron, Heroen Verbruggen, Charles F. Delwiche, and Olivier De Clerck | ene-46 | NO | Liga perdida | Sin asignar | Chlorophyta, Charophyta, endosymbiosis, molecular evolution, origin of embryophytes, Prasinophyceae, phylogeny, Streptophyta | The green lineage (Viridiplantae) comprises the green algae and their descendants the land plants, and is one of the major groups of oxygenic photosynthetic eukaryotes. Current hypotheses posit the early divergence of two discrete clades from an ancest | |
Ficha | Circumscription of some Phyllophoraceae (Gigartinales, Rhodophyta) from the Cape region, South Africa, based on molecular evidence | Fredericq Suzanne and et. al. | 0 | 01-dic | NO | no completo | Rodofitas | biogeography, Gigartinales, ITS, life history, LSU rDNA, Namibia, phylogeny, Phyllophoraceae, rbcL, Rhodophyta, South Africa, molecular systematics, taxonomy | The family Phyllophoraceae is well represented in the Cape Peninsula region of South Africa with species possessing tetrasporoblasts and a bi-phasic life history placed in Gymnogongrus, and those with a heteromorphic t |
Ficha | Mesocosm Experiments Quantify the Effects of Eutrophication on Eelgrass, Zostera marina | Frederick T. Short, David M. Burdick and James E. Kaldy III | 40 | 740-749 | No | no completo | General | Outdoor mesocosm experiments were used to examine the response of eelgrass communities to excess | |
Ficha | The Chlorococcal Algal Genus Didymogenes Schmidle 1905 | Frantisek Hindák | 29 | 559-570 | 2851 | no completo | Sin asignar | Didymogenes (Chlorococcales, Chlorophyceae); taxonómica. | The taxonomical revision of the genes Didymogenes (Chlorococcales, Chlorophyceae) showed that a part from the typical species D. paiayina, also the species D. anomala (G. M. Smith) Hind and D. granulata (Hortob.) Hind. belong to the said genus. The main d |
Ficha | Seaweeeds fisheries management in France, Japan, Chile and Norway | Frangoudes K. | NO | General | |||||
Ficha | Nomenclatural Transfers Among Coccoid Algae | Francis Drouet and William A. Daily | 11 | 77-79 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Distribution and dynamics of epibiota on hard structures for coastal protection | Francesca Bacchiocchi and Laura Airoldi | 56 | 1157-1166 | NO | no completo | General | benthic organisms; community structure; spatial distribution; temporal variations; artificial habitats; coastal protection; Adriatic Sea | Hard structures for protection against erosion of shores are some of the most common human-made constructions in coastal areas. Nevertheless, little is known as to how marine organisms respond to their presence. The co |
Ficha | Comparative Ultrastructure of The Primary Nucleus in Bryopsis and Acetabularia | Frances A. Burr and John A . West | 7 | 108-113 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Characterization of the CaCO3 biomineral in coralline red algae (Corallinales) from the Pacific coast of Mexico | Fragoso D. and et. al. | 36 | 41–58 | NO | Completo | Rodofitas | Corallinales, biomineral, Rietveld method, nanostructure, scanning tunneling microscopy | Coralline red algae assimilate HCO3 – to precipitate CaCO3 in their tissues in the form of calcite or aragonite. A characterization of the biomolecular content and the crystalline structure of the biomineral |
Ficha | Diversidad e historia natural de una comunidad de Lithothamnion muelleri y Sargassum horridum en el Golfo de California | Foster M.S. and et. al. | 33 | 367-384 | NO | no completo | Feofita | comunidad, Lithothamnion, rodolito, Sargassum, especie fundamental, diversidad. | Se cuantificó la contribución relativa de la forma rodolítica de Lithothamnion muelleri, una especie fundamentales, a la |
Ficha | EPIPHYTIC CYANOBACTERIA MAINTAIN SHIFTS TO MACROALGAL DOMINANCE ON CORAL REEFS FOLLOWING ENSO DISTURBANCE | FONG PEGGY and et. al. | 87 | 1162-1168 | NO | no completo | General | alternative stable states; coral reefs; facilitation; herbivory; macroalgal bloom; nutrients; phase shifts. | Macroalgal dominance of some tropical reef communities in the Eastern Pacific |
Ficha | Harmful algae—a perspective | Fogg G.E. | 1 | 01-abr | NO | no completo | General | ||
Ficha | The importance of having two species instead of one in kelp management: the lessonia nigrescens species complex | Florence TELLIER1,2,3,4, J. M. Alonso VEGA1, Bernardo R. BROITMAN1,4, Julio A.VASQUEZ1, | 455-465 | NO | Liga perdida | Kelp | |||
Ficha | Influence of combined changes in salinity and copper modulation on growth and copper uptake in the tropical green macroalga Ulva reticulata | Florence Mamboya, Thomas J. Lyimo, Tommy Landberg, Mats Björk | 326–330 | NO | Liga perdida | Sin asignar | Ulva reticulata; copper; salinity; uptake; growth | The influence of salinity on growth and Cu uptake in the green macroalga Ulva reticulata collected from the intertidal area in the Western Indian Ocean was studied under controlled laboratory conditions. Exposure concentrations ranged from 5 to 500 mg Cu | |
Ficha | Spatial distribution and reproductive phenology of sexual and asexual Mastocarpus papillatus (Rhodophyta) | Fierst Janna L. and et. al. | 49 | 274-282 | NO | no completo | Rodofitas | Apomictic; Geographic parthenogenesis; Life cycle; Mastocarpus papillatus; Phenology; Red algae; Sexual reproduction; Spatial division; Tidal elevation | Species of the genus Mastocarpus exhibit two distinct life cycles, a sexual alternation of generations |
Ficha | Diatomeas marinas de la provincia de Chubut (República Argentina). Centrales I. | Ferrario, M. E., Sar, E. A., & Codina, R. G. | 27 | 89-106 | NO | parcialmente sin liga | Sin asignar | Marine diatoms from the Chubut Province (Argentina) Centrales I. Twenty eight species and varieties of Diatoms from Chubut (Republica Argentina), were studied using both light and scanning electron microscope. Ten of them are new for this region. Furtherm | |
Ficha | Morphological study of the marine planktonic diatom Chaetoceros castracanei Karsten (Bacillariophyceae) from Antarctic waters, with a discussion on its possible taxonomicrelationships | Ferrario Martha and et. al. | 47 | 349-355 | NO | no completo | Fitoplancton | Antarctica; Chaetoceros castracanei; diatoms; distribution; morphology. | Phytoplankton samples were collected along the north and 2000–2002. Chaetoceros castracanei Karsten, a fair- |
Ficha | Coastal urbanization leads to remarkable seaweed species loss and community shifts along the SW Atlantic | Fernando Scherner et. al. | NO | no completo | General | Phycogeographycal regions South-West Atlantic Marine biodiversity loss Urbanization metrics Macroalgae Calcareous algae | Coastal urbanization is rapidly expanding worldwide while its impacts on seaweed communities remain | ||
Ficha | Zonacion del fitobentos intermareal de la region de Cabo peñas (Asturias) | Fernandez C. and F.X. Niell | 46 | 121-141 | NO | parcialmente completo con liga | General | Fitobentos, zonación, intermareal rocoso, N. de España. | |
Ficha | Community structure and species diversity of intertidal benthic macroalgae in Fengming Island, Dalian | Fengqin Zhao, et.al. | 36 | 77-84 | NO | no completo | General | Benthic macroalgae Topic: Community structure Seasonal variation Ecological niche | We investigated the community structure, seasonal variation, species diversity, and ecological niche of the intertidal |
Ficha | Solving the coastal eutrophication problem by large scale seaweed cultivation | Fei Xiugeng | 512 | 145-151 | NO | no completo | General | environment, eutrophication, Laminaria, Gracilaria, Porphyra, red tide, seaweed cultivation, China | Eutrophication is becoming a serious problem in coastal waters in many parts of the world. It induces the phyto- cultiv |
Ficha | REDUCED GENETIC DIVERSITY AND INCREASED POPULATION DIFFERENTIATION IN PERIPHERAL AND OVERHARVESTED POPULATIONS OF GIGARTINA SKOTTSBERGII (RHODOPHYTA, GIGARTINALES) IN SOUTHERN CHILE | Faugeron Sylvain and et. al. | 40 | 454-462 | NO | Completo | Rodofitas | genetic diversity; mismatch distribution; overharvest; RAPD; Rhodophyta; seaweed; species border | This study assesses two hypotheses on the genetic diversity of populations of Gigartina skottsbergii Setchell et Gardner (Rhodophyta, Gigartinales) at the border of the species distribution: 1) peripheral populations d |
Ficha | Infectious diseases in Mazzaella laminarioides (Rhodophyta): estimating the effect of infections on host reproductive potential | Faugeron Sylvain and et. al. | 42 | 143-148 | NO | no completo | Rodofitas | Cyanobacteria · Endophyton ramosum · Endophyte infections · Fitness · Mazzaella laminarioides · Pleurocapsa | Very little is known about the potential effects of endophytic infections on the host in |
Ficha | Hierarchical spatial strucutre and discriminant analysis of genetic diversity in the red alga Mazzaella laminarioides (Gigartinales, Rhodophyta) | Faugeron S. and et. al. | NO | Rodofitas | |||||
Ficha | Long-term copper mine waste disposal in northern Chile associated with gene flow disruption of the intertidal kelp Lessonia nigrescens | Faugeron S. and et. al. | 288 | 129-140 | NO | no completo | Kelp | Kelp · Habitat disruption · Heavy metal · Gene flow · RAPD | This study tests the general hypothesis that habitat disruption caused by the release of |
Ficha | REVEALING THEMOLECULAR SECRETS OF MARINE DIATOMS | Falciatore Angela and Chris Bowler | 53 | 109-30 | NO | parcialmente completo con liga | Fitoplancton | iron, marine algae, photoperception, quorum sensing, silica | Diatoms are unicellular photosynthetic eukaryotes that contribute close world’s oceans, very little information is available at the molecular l |
Ficha | Molecular characterization of nitrate reductase gene and its expression in the marine red alga Gracilaria tenuistipitata (Rhodophyta) | Falcão Vanessa R. and et. al. | 22 | 613-622 | NO | no completo | Rodofitas | Biological rhythm . Phylogeny . Gene expression . Gracilaria tenuistipitata . Nitrate reductase | The enzyme nitrate reductase (NR) responsible rate-limiting step in nitrogen assimilation. The economical- |
Ficha | STRUCTURE AND DYNAMICS OF A POPULATION OF PALMARIA PALMATA (RHODOPHYTA) IN NORTHERN SPAIN1 | Faes Vanesa A. and Rosa M. Viejo | 39 | 1038-1049 | NO | Completo | Rodofitas | demography; epiphyte; growth; mortality; Palmaria palmata; population dynamics; population structure; Rhodophyta; state variable | Palmaria palmata (Linnaeus) O. Kuntze (Rhodophyta, Palmariaceae) is a seaweed commercially harvested for human consumption. Its population density, size structure, and frond dynamics were investigated from Ma |
Ficha | Early life stages of the South Pacific kelps Lessonia nigrescens and Lessonia trabeculata (Laminariales, Phaeophyceae) show recovery capacity following exposure to UV radiation | FADIA TALA et. al. | 46 | 467–470 | no completo | Feofita | Germination, Kelp, Lessonia, Microscopic stages, Recovery, Spores, UV radiation | This study examined the recovery capacity of early life stages of the South Pacific kelps Lessonia nigrescens and | |
Ficha | First estimates of productivity in Lessonia trabeculata and Lessonia nigrescens (Phaeophyceae, Laminariales) from the southeast Pacific | Fadia Tala and Mario Edding | 55 | 66–79 | no completo | Feofita | Chile, erosion, kelp, Lessonia, macroalgae, productivity, standing stock. | Lessonia is the main Laminariales found along the important habitat | |
Ficha | Environmental factors associted with the spatial distribution of crustose coralline algae on the Great Barrier Reef | Fabriciusw K. and G. De'ath | NO | Rodofitas | |||||
Ficha | Grazing by the sea urchins Arbacia lixula L. and Paracentrotus lividus Lam. in the Northwest Mediterranean | Fabio Bulleri, Lisandro Benedetti-Cecchi and Francesco Cinelli | 241 | 81-95 | NO | no completo | General | A. lixula; Encrusting algae; Erect algae; Grazing; Management of resources; P. lividus; Rocky reefs; Sea urchins; Subtidal | The sea urchins Arbacia lixula and Paracentrotus lividus are common on shallow subtidal reefs in the Mediterranean. Previous studies on the ecology of these species reported that P. lividus is generally more abundant on hor |
Ficha | Temperature tolerance of algae in dry soil | F.R. Trainor | 15 | 03-abr | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Problems in the Development of an Explicit Hypothetical Phylogeny of the Lower Eukaryotes | F.J.R. Taylor | 10 | 67-89 | 2856 | no completo | Sin asignar | A semi-explicit arrangement of the lower eukaryotes is provided to serve as a basis for phyletic discussions. No single character is used to determine the position of all the groups. The tree provides no ready separation of protozoa, algae and fungi, grou | |
Ficha | II. Implications and Extensions of the Serial Endosymbiosis Theory of the Origin of Eukaryotes | F.J. R. Taylor | 23 | 229-258 | 2860 | no completo | Sin asignar | In comparison to other theories put foward so far, the Serial Endosymbiosis Theory appears to be the most critically favored as an explanation for the origin of mitocondria and chloroplasts. For this reason some of its implications are drawn attention to. | |
Ficha | The taxonomy of the Chlorophyta | F.E. Round | 2 | 224-235 | no completo | General | |||
Ficha | The Sexual Male Plants of Gracilaria Cearensis (Joly et Pinheiro) Joly et Pinherio | F.C. Pinheiro and A. B. Joly | 6 | 131-134 | 1533 | no completo | Sin asignar | This paper besides transfering Tutotus cearensis Joly et Pinherio to Gracilaria cearensis (Joly et Pinheiro) Joly et Pinheiro also presents for the first time descriptions of the mal estructures of this characteristic species. | |
Ficha | A Review of Florideophycldean Life Histories and of The Culture Techniques Employed in their Investigation | F. W. Knaggs | ND | 1367 | no completo | Sin asignar | |||
Ficha | Biological Oceanography | F. W. Fri cker | 17-24 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | User-friendly guide for using benthic ecological indicators in coastal and marine quality assessment | F. Salas, et.al. | 49 | 308-331 | NO | no completo | General | Experience demonstrates that none of the available measures on biological effects of pollution | |
Ficha | Some Aspects of the Ecology of Fresh-Water Algae: (With Special Reference to Static Waters) | F. E. Fritsch | 19 | 233-272 | 2852 | no completo | Sin asignar | ||
Ficha | COROLOGÌA DE LAS ESPECIES DE ALGAS EN RELACIÓN A CIERTOS FACTORES ECOLÓGICOS EN EL LITORAL MALAGUEÑO | F. Conde and J. A. Seoane | 13 | 783-802 | NO | no completo | General | Los estudios taxonómicos, ecológicos y corológicos sobre la vegetación algal bentónica en el litoral malagueño nos han hecho detectar un límite geográfico,entre los al | |
Ficha | Marine Algae from Easter Island. | F. Börgesen | 247-309 | NO | Liga perdida | Sin asignar | |||
Ficha | Light and electron microscope observations on the vegetative and reproductive structures of Bryopsis hypnoides | F. A. Burr and J. A. West | 9 | 17-37 | NO | parcialmente sin liga | Sin asignar | Bryopsis hypnoides; fisiológico | The vegetative system of the coenocytic alga Bryopsis hypnoides has a large central vacuole which extends throughout the body of the plant. This vacuole occupies most of the volume of the thallus, leaving only a thin layer of cytoplasm appressed to the ce |
Ficha | Protein Bodies in Bryopsis hypnoides: Their Relationship to Wound-Healing and Branch Septum Development | F. A. Burr and J. A. West | 35 | 476-498 | NO | parcialmente sin liga | Sin asignar | The development of a proteinaceous substance involved in both wound-healing and the formation of basal septa in a siphonous green alga is described. The protein accumulates within swollen cisternae of the endoplasmic reticulum. In the later stages of deve | |
Ficha | Germinaçao e Desenvolvimento dos Tetrasporos de Centroceras Clavulatum (Rhodophyta-Ceramiaceae) em Cultura | Eurico Cabral de Oliveira Filho e Maria Cecilia Brinati | 2 | ND | 1281 | no completo | Sin asignar | No se alcanza a ver bien el resumen. | |
Ficha | Consideraciones Ecológicas sobre las Algas del Litoral Rocosobonaerense | Eugenia Sar, Marcela Pascual y Ana Parma | 13 | 143-147 | 2554 | no completo | Sin asignar | Mar del Plata, Buenos Aires; Hildenbrandia sp., Ralfsia expans, Enteromorpha spp., Ulva rigida. | This note deals with the intertidal zonation of the red, brown and green seaweeds in the rocky shores of Mar del Plata, Buenos Aires. The upper intertidal is characterized alternativaly by Hildenbrandia sp. or by Ralfsia expansa depending upon the type of |
Ficha | Contribucion al Conocimiento de Ulothrix Flacca (Dillwyn ) Thuret (Ulotrichales, Chlorophyta) | Eugenia Sar | 36 | 215-219 | 2552 | no completo | Sin asignar | Mar de Plata y Río Negro, Argentina; Ulothrix flacca (Dillwyn) Thuret (Ulotrichales, Chlorophyta). | Contribution to the knowledge of Ulothrix flacca (Dillwyn) Thuret (Ulotrichales, Chlorophyta).· A species of Ulothrix from the rocky shores of Mar del Plata (Prov, Buenos Aires, Rep. Argentina) was studied on fieldcollected samples and through experimenta |
Ficha | Novedades sobre la Distribucion de Thalassiosira Curviseriata Takano y T. Pacífica Gran Et Angst (Bacillariophyceae) en Argentina | Eugenia A. Sar y Marta E. Ferrario | 44 | 89-91 | 2555 | no completo | Sin asignar | Thalassiosira curviseriata, T. pacifica, Morphology, Distribution, Argentina, | Thalassiosira curviseriata Takano y T. pacifica Gran et Angst de Chubut, Argentina, fueron estudiadas utilizando microscopio óptico y electrónico de barrido. T. curviseriata es reportada por primera vez para el Océano Atlántico y T. Pacifica lo es para el |
Ficha | Carrageenan Patterns in the Phyllophoraceae | Esther L. McCandless, John A. West and Michael D. Guiry | 10 | 275-284 | NO | parcialmente sin liga | Sin asignar | Ahnfeltia; Gymnogongrus; Phyllophora; Erythrodermis, Phyllophoraceae; red algae; ?-, x -, ?-carrageenans; chemotaxonomy, gametophyte-sporophyte; life history. | Carrageenans of reproductive phases of phyllophoracean species have been shown to vary as in the Gigartinaceae - gelling ?- or x-carrageenans or their hybrids occurring in gametophytes, non-gelling ?-carrageenan in sporophytes in most instances. In Phyllo |
Ficha | Carrageenan Patterns in the Gigartinaceae | Esther L. Mccandless, John A. West and Michael D. Guiry | 11 | 175-182 | NO | parcialmente sin liga | Sin asignar | Chondrus; Gigartina; Iridaea; Petrocelis; Rhodoglossum; Gigartinaceae; red algae; carrageenans; chemotaxonomy; gametophyte; tetrasporophyte; life history. | Carrageenans of known reproductive phases of gigartinacean species are shown to differ: gelling x(?)-type carrageenan occurs in all instances in gametophytes, and viscous non-gelling ?-carrageenan or its variants ?- or ?-carrageenan in tetrasporophytes. M |
Ficha | Complex trophic interactions in kelp forest ecosystems. | Estes, J. A., Danner, E. M., Doak, D. F., Konar, B., Springer, A. M., Steinberg, P. D., ... & Williams, T. M. | 621-638 | NO | Liga perdida | Kelp | |||
Ficha | Predation, herbivory and kelp evolution | Estes James A. and P. D. Steinberg | NO | Kelp | |||||
Ficha | esquemas clorofitas | esquemas clorofitas | 0 | NO | parcialmente completo con liga | Clorofita | |||
Ficha | Annual cycle of microphytoplankton from the coasts of the tropical Mexican Pacifdic | Esqueda-Lara K. and et. al. | NO | Fitoplancton | |||||
Ficha | Algas Macroscópicas | Escuela Superior Politécnica del Litoral | NO | General | |||||
Ficha | PARMALES (CHRYSOPHYCEAE) FROM THE GULF OF TEHUANTEPEC, MEXICO, INCLUDING THE DESCRIPTION OF A NEW SPECIES, TETRAPARMA INSECTA SP. NOV., AND A PROPOSAL TO THE TAXONOMY OF THE GROUP1 | Ernesto Bravo-Sierra and David U. Hernández-Becerril | 59 | 577-583 | NO | no completo | General | Mexican Pacific Ocean; new spe- cies; Parmales; taxonomic proposal; Tetraparma; Triparma | There are few studies dedicated to species of the Order Parmales all over the world. All 12 taxa de- than 5 m). Analysis of filtered samples from the |
Ficha | Fucoidans from Brown Seaweeds Sargassum hornery,Eclonia cava, Costaria costata: Structural Characteristics and Anticancer Activity | Ermakova Svetlana and et. al. | 164 | 841-850 | NO | no completo | Feofita | Fucoidans . Structure . Anticancer activity | Fucoidans were isolated by water extraction and ion-exchange chromatography |
Ficha | Size Hierarchy and the - 3/2 "Power Law" Relationship in a Coalescent Sea Weed | Enrique Martinez and Bernabé Santelices | 28 | 259-264 | 2634 | no completo | Sin asignar | Algal size; Gini coefficient; Iridaea laminarioides; Rhodophyta; seaweed coalescence; self-thinning; size inequality. | The size structure of plant populations has been characterized by two descriptors, size-density relations and size inequality. In even aged natural or experimental populations, the logarithm of mean size is a negative function of population density, with |
Ficha | A new methodology based on littoral community cartography dominated by macroalgae for the implementation of the European Water Framework Directive | Enric Ballesteros, Xavier Torras, Susana Pinedo, María García, Luisa Mangialajo, Mariona de Torres | 172–180 | NO | Liga perdida | Sin asignar | Littoral communities; European Water Framework Directive; Bioindicators; Cartography; Macroalgae | Macroalgae is a biological key element for the assessment of the ecological status in coastal waters in the frame of the European Water Framework Directive (WFD, 2000/60/EC). Here we propose a methodology for monitoring water quality based on the cartogra | |
Ficha | Life history flexibility allows Sargassum polyceratium to persist in different environments subjected to stochastic disturbance events | Engelen A.H. and et. al. | 24 | 670-680 | NO | no completo | Feofita | Sargassum polyceratium Æ Stochastic matrix model Æ Life history strategy Æ Wave-disturbance events Æ Depth | Stochastic, stage-based matrix models were used to investigate the life history strategy of the sea- deep-water (18 m) populations. Matrix models were |
Ficha | Spatial and temporal patterns of recovery of low intertidal Laminaria digitata after experimental spring and autumn removal | Engelen A. H. and et. al. | NO | Kelp | |||||
Ficha | Fractal and multi-fractal patterns of seaweed settlement | Emmerson L.M. & A.J. Roberts | NO | no completo | General | The distribution of algae is examined at several different scales. Juve- community. Within these clumps there is a great wealth of pattern which may | |||
Ficha | The use of macroalgal species richness and composition on intertidal rocky seashores in the assessment of ecological quality under the European Water Framework Directive | Emma Wells, et. al. | 55 | 151-161 | NO | no completo | General | Macroalgae; Seaweed; Species richness; Water framework directive; Ecological quality assessment | The EC Water Framework Directive (WFD) suggests using abundance and species composition of intertidal seaweed communities for |
Ficha | The role of geomorphology in the distribution of intertidal rocky macroalgae in the NE Atlantic region | Elvira Ramos and et. al. | 179 | 90-98 | NO | no completo | General | Seaweeds Rocky shores Coastal morphology Coastal orientation Active processes Lithology | It is known that rocky macroalgae distribution depends on several abiotic factors, but little attention has |
Ficha | Is Pigmentation a Clue to Prostistan Phylogeny? | Ellsworth C. Dougherty and Mary Belle Allen | 129-144 | 27 | no completo | Sin asignar | |||
Ficha | Utilization of Nitrogen compounds by Unicellular Algae | Elizabeth C. Birdsey, Victoria H. Lynch | 763-764 | NO | parcialmente sin liga | Sin asignar | Eight Chlorophyta employ area as a sole nitrogen source; five utilize urie acid and xanthine. The Cyanophyta, Rhodophyta, and Euglenophyta studied do not grow on these three nitrogen source although Anacystis nidulans decomposes urie acid to allantoin. No | ||
Ficha | Resposta das algas perifíticas ás alteraçoes de temperatura e ao enriquecimento artificial de nutrientes em curto período de tempo | Eliza Akane Murakami e Liliana Rodrigues | 31 | 273-284 | No | no completo | General | periphytic algae, artificial enrichment, temperature, abundance, floodplain. | |
Ficha | The Growth Rings in Alaria Stipes | Egil Baardseth | 153-157 | 97 | no completo | Sin asignar | |||
Ficha | Estimating scale-dependency in disturbance impacts: El Niños and giant kelp forests in the northeast Pacific | Edwards Matthew S. | 138 | 436-447 | NO | no completo | Kelp | Disturbance . El Niño . Giant kelp . Kelp forest . Recovery | Recent discussions on scaling issues in ecology |
Ficha | The role of alternate life-history stages of a marine macroalga: A seed bank analogue? | Edwards Matthew S | 81 | 2404-2415 | NO | no completo | General | Annual alga, Carmel Bay, California (USA), Desmarestia, dormancy, gametophyte, life-history stages, alternative, marine macroalga, microscopic, overwinter, recruiment, seed bank | |
Ficha | A sustainable culture system for Gracilaria parvispora (Rhodophyta) using sporelings, reef growout and floating cages in Hawaii | Edward P. Glenn et.al. | 165 | 221–232 | no completo | General | Gracilaria; Seaweed—culture; Seaweed—spore—culture; Seaweed—cage—culture | A culture system for the edible, red seaweed, Gracilaria parÕispora Abbott long ogo , was Ž . | |
Ficha | Correlation between Gracilaria parÕispora ž / Rhodophyta biomass production and water quality factors on a tropical reef in Hawaii | Edward P. Glenn et. al. | 178 | 323–331 | NO | Liga perdida | General | Gracilaria; Coral reef ecology; Nutrient limitation; Ammonia; Growth | The factors controlling the growth of the edible, red seaweed, Gracilaria parvispora Abbott (long ogo), on the south reef of Molokai, HI, were investigated to determine where productive new plantings could be located. Exper |
Ficha | Correlation between Gracilaria parvispora khodophyta) biomass production and water quality factors on a tropical reef in Hawaii | Edward P. Glenn and et.al. | 178 | 323-331 | no completo | General | Gracilaria; Coral reef ecology; Nutrient limitation; Ammonia; Growth | The factors controlling the growth of the edible, red seaweed, Gracilaria parvispora Abbott | |
Ficha | Effects of algal canopy clearance on plant, fish and macroinvertebrate communities on eastern Tasmanian reefs | Edgar, G. J., Barrett, N. S., Morton, A. J., & Samson, C. R | 67 – 87 | NO | Liga perdida | Sin asignar | Algal canopy; Experimental clearance; Invertebrate; Marine protected area; Sublittoral; Turbo undulatus; Undaria pinnatifida; Urchin barrens | Changes in assemblages of plants, macroinvertebrates and fishes on three eastern Tasmanian reefs were monitored over 12 months in replicated control blocks and adjacent 1012-m blocks cleared of fucoid, laminarian and dictyotalean algae. Removal of canopy- | |
Ficha | The life cycle of Ralfsia clavata and R. borneti. | Edelstein, T., Chen, L. C., & McLachlan, J. | 48 | 527-531 | 3855 | no completo | Sin asignar | ||
Ficha | Lessonia | Edding M. E. and et. al. | 0 | NO | parcialmente completo con liga | Feofita | |||
Ficha | Cultures studies on the marine red alga Rhodophysema elegans (Cryptonemiales, Peysonneliacea) | E.K. Ganesan and John A. West | 14 | 161-166 | 760 | no completo | Sin asignar | Noreste del Pacífico; Rhodophysema elegans (P.L. y H.M. Crouan ex J. Ag.) Dixon (Cryptonemiales, Peysonneliaceae) | Under field conditions in the northeastern Pacific, the red alga Rhodophysema elegans (P.L. et H.M. Crouan ex J. Ag.) Dixon (Cryptonemiales, Peysonneliaceae) is known to produce only tetraspores. The life history of this species was studied under controll |
Ficha | Studies on the Morphology and Reproduction of the Articulated Coralines I | E.K. Ganesan | 4 | 43-60 | 3303 | no completo | Sin asignar | Jania, J. iyencarii | Anatomy and reproduction in a new species or Jania, J. iyencarii. are described. It has been shown that the erect axis is always attached to the crust by means of a primary or basal geniculum. Development of male, female and tetrasporic conceptacles are d |
Ficha | On the identity of Lophosiphonia bermudensis Collins and Hervey and Dipterosiphonia regens (Schousboe) Falkenberg | E.C. De Oliveira Filho and Marilza Cordeiro-Marino | 9 | 01-mar | NO | no completo | General | ||
Ficha | An Eastern Pacific Member of Yamadaia (Corallinaceae) from the San Juan Islands, Washington | E. Yale Dawson and Richard L. Steele | 8 | ND | 1503 | no completo | Sin asignar | ||
Ficha | Marine Algae from Palmyra Island with Special Reference to The Feeding Habits and Toxicology of Reef Fishes | E. Yale Dawson A. A. Aleem Bruce W. Halstead | 17 | ene-39 | 1506 | no completo | Sin asignar | Atolón Palmyra, EE.UU.; Cyanophyta, Chlorophyta, Phaeophyta y Rhodophyta; algas sésiles, dinoflagelados, diatomeas y silicoflagelado | The present work on the marine algae of Palmyra Island was indicated by the knowledge that this area harbors a large poisonous fish population and that many poisonous fishes are herbivorous. It is believed that fishes become poisonous as a direct result o |
Ficha | A New Sublittoral Gracilariopsis from Southern California | E. Yale Dawson | 10 | ND | 1504 | no completo | Sin asignar | California, EE.UU.; Gracilariopsis claviformis, G. robusta y G. andersonii. | Gracilariopsis claviformis is described from sublittoral pebble beds at Santa Cruz Island, California. Characters of male plants show near relationship to G. robusta and G. andersonii. |
Ficha | Additions to the Marine Flora of Costa Rica and Nicaragua | E. Yale Dawson | 3 | 375-395 | 2874 | no completo | Sin asignar | ||
Ficha | A Review of Yendo's Jointed Coralline Algae of Port Renfrew, Vancouver Island | E. Yale Dawson | 7 | ND | 1502 | no completo | Sin asignar | ||
Ficha | Una Clave Ilustrada de los Generos de Algas Benticas del Pacifico de la America Central | E. YALE DAWSON | 167-231 | NO | Liga perdida | Sin asignar | |||
Ficha | Notes on Some Pacific Mexican Dictyotaceae | E. Yale Dawson | 77 | 83-93 | NO | parcialmente sin liga | Sin asignar | Pacífico; Costa; Dilophus, Pachydictyon y Dictyota | The Pacific North American species of Dietyotaceae heretofore known under the name Dictyota in the older, broader sense are examined. The generic segregates Dilophus, Pachydictyon and Dictyota are recognized according to J. G. Agardh, 1894. Dilophus pinna |
Ficha | Marine Plants in the Vicinity of the Institut Océanographique de Nha Trang, Viêt Nam | E. Yale Dawson | 8 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Some Marine Algae of the Southern Marshall Islands | E. Yale Dawson | 10 | 25-66 | 1505 | no completo | Sin asignar | ||
Ficha | Marine Algae from the 1958 Cruise of the Stella Polaris to the Gulf of California | E. Yale Dawson | 27 | mar-39 | 3316 | no completo | Sin asignar | ||
Ficha | Symposium: The Biogeography of Baja California and Adjacent Seas Part II. Marine Biotas | E. Y. Dawson | 9 | 93-100 | 2516 | no completo | Sin asignar | ||
Ficha | Impact of natural ultraviolet radiation on rates of photosynthesis and on specific marine phytoplankton species | E. Walter Helbling, Virginia Villafañe, Martha Ferrario, Osmund Holm-Hansen | 80 | 89-100 | 2556 | no completo | Sin asignar | Natural phytoplankton populations from both Antarctic and tropical waters were exposed to solar radietion to determine the effects of ultraviolet radiation (UVR) on rates of photosynthesis. Radiation in the UV-A region (320 to 400 nm) was responsible for | |
Ficha | Presencia del Genero Predaea G. DeToni (Rhodophyta, Gigartinales) en Venezuela | E. K. Ganesan y A. J. Lemus | 14 | 157-163 | 3238 | no completo | Sin asignar | Venezuela y del mar Caribe; Predaea feldmannii Børgensen; morfológico. | Se reporta el alga marina roja Predaea feldmannii Børgensen (Nemastomataceae, Gigartinales) como un nueva adición a la flora marina algal de Venezuela y del mar Caribe. Este registro constituye la tercera recolección de P. feldmannii, las 2 colecciones an |
Ficha | The Gulf Stream | E. E. Watson | 76-80 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Progress of the taxonomic research on the macroalgae (Chlorophyta, Phaeophyta and Rhodophyta) along the East African coast | E. Coppejans, O. De Clerck, F. Leliaert and O. Dargent | 401-418 | NO | Liga perdida | Sin asignar | This paper discusses the phycological research and gives a historical overview of papers dealing with macroalgae from the East African coast. A review of the recent progress towards a marine algal flora of the region is presented. Additionally a limited n | ||
Ficha | The Absence Of ?-?-Diaminopimelic Acid From The Primitive Red Alga Porphyridium Cruentum | E. C. Dougherty, H. T. Gordon and Mary Belle Allen | 171-173 | 95 | no completo | Sin asignar | |||
Ficha | Implementation of a new index to assess intertidal seaweed communities as bioindicators for the European Water Framework Directory | E. Ar Gall, M. Le Duff , P.-G. Sauriau, M.-N. de Casamajor, F. Gevaert, E. Poisson, P. Hacquebart, Y. Joncourt, A.-L. Barillé, R. Buchet, M. Bréret, L. Miossec | 162-173 | NO | Liga perdida | Sin asignar | Water Framework Directory; Macroalgal communities; Intertidal seaweeds; Quality index; Coastal water bodies | An index CCO (cover, characteristic species, opportunistic species) has been developed for the implementation of the European Water Framework Directory (WFD) in coastal waters, using intertidal macroalgal communities as bio-indicator (Biological Quality E | |
Ficha | The Occurrence of Pyramimonas-Like Zoospores in the Green Alga Ecballocystis | E. A. George | 55 | 382-385 | 82 | no completo | Sin asignar | ||
Ficha | Seasonal and spatial patterns of population density in the marine macroalga Mazzaella splendens (Gigartinales, Rhodophyta) | Dyck Leonard James and Robert E. De Wreede | 54 | 21-31 | NO | parcialmente completo con liga | Rodofitas | demography, ecology, Mazzaella splendens, population, seasonality. | Insight into demographic processes that operate at larger spatial scales can be achieved through studying local populations when a particular species of interest is examined over time, by many investigators, in a variety of location |
Ficha | OfficeTrends in Bryophyte Population Dynamics | During Heinjo J. | 31 | jun-15 | NO | Completo | Rodofitas | Rapid advances in the field of bryophyte population dynamics include the de velopment of non-destructive techniques to mark and monitor individual shoots, which allowed the construction and sophisticated use of matrix model | |
Ficha | Starfish predation and the creation of mosaic patterns in a kelp-dominated community | Duggins D.O. | NO | Kelp | |||||
Ficha | Seagrass nutrient content | Duarte C.M. | 67 | 201-207 | NO | parcialmente completo con liga | General | Data on nutrient contents of 27 seagrass species at 30 locations were compiled from the | |
Ficha | Subnerged aquatic vegetation in relation to different nutrient regimes | Duarte C.M. | NO | parcialmente completo con liga | General | ||||
Ficha | A procedure for routine purification of algal cultures with antibiotics. | Droop, M. R. | 3 | 295-297 | 3750 | no completo | Sin asignar | ||
Ficha | Reproducción | Dring, M. G. | 814-840 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Sources, sinks, and fluxes of nutrients (N + P) in a small highly modified urban estuary in southern California | DR. PEGGY FONG and DR. JOY B. ZEDLER | 4 | 125–144 | No | no completo | General | nitrogen, phosphorus, macroalgae, estuary, anthropogenic | Our objective was to begin to investigate sources, sinks, and flux rates of nitrogen (N) and phosphorus |
Ficha | Changes in Macroalgal Communities in the Vicinity of a Mediterranean Sewage Outfall After the Setting Up of a Treatment Plant | DOUNIA SOLTAN and et. al. | 42 | 59-70 | NO | no completo | General | Mediterranean; wastewater treatment; macroalgae; communities; changes; pollution. | Benthic macroalgal communities of the upper rocky sublittoral were studied in 1995-1996 in the vicinity of the Marseille (Mediterranean, France) sewage outfall, 8 years after the setting up of a wastewater treatme |
Ficha | Light and Electron Microscopic Observations on Red Algal Galls | Douglas L. Mcbride, Paul Kugrens L, and John A. West | 79 | 249-264 | NO | parcialmente sin liga | Sin asignar | Polyneuropsis stolonifera (gen et sp nov.) | Lobocolax deformans Howe was found to be a bacterial gall on Prionitis Ianceolata. Rodshaped bacteria were distributed throughout the gall in intercellular locations. Algal cells in the gall area exhibited numerous proplastids and irregular cell walls. Ba |
Ficha | Investigations of New England Marine Algae VI: Distribution of Marine Algae Near Cape Cod, Massachusetts | Douglas C. Coleman and Arthur C. Mathieson | 76 | 537-563 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Investigations of New England Marine Algae VII: Seasonal Occurrence and Reproduction of Marine Algae Near Cape Cod, Massachusetts | Douglas C. Coleman and Arthur C. Mathieson | 77 | 76-104 | 1711 | no completo | Sin asignar | ||
Ficha | BIOMASS ACCUMULATION AND SHADING EFFECTS OF EPIPHYTES ON LEAVES OF THE SEAGRASS, HETEROZOSTERA TASMANICA, IN VICTORIA, AUSTRALIA | DOUGLAS A. BULTHUIS and Wm. J. WOELKERLING | 16 | 137--148 | No | no completo | General | A method is described for estimating the rate of accumulation of epiphyte biomass on | |
Ficha | SEASONAL VARIATION IN STANDING CROP, DENSITY AND LEAF GROWTH RATE OF THE SEAGRASS, HETEROZOSTERA TASMANICA, IN WESTERN PORT AND PORT PHILLIP BAY, VICTORIA, AUSTRALIA | DOUGLAS A. BULTHUIS and Wm. J. WOELKERLING | 16 | 111--136 | No | no completo | General | Standing crop, density and leaf growth rate of Heterozostera tasmanica (Martens ex Aschers.) den Hartog along with light, temperature, nutrient and sediment charac- | |
Ficha | Total and opportunistic algal cover in relation to environmental variables | Dorte Krause-Jensen, Jacob Carstensen, Karsten Dahl | 55 | 114–125 | No | no completo | General | Macroalgae; Opportunistic algae; Cover; Eutrophication; Salinity; Denmark | Based on a large data set from the national Danish monitoring program, spatial and temporal variability in total algal cover and in |
Ficha | Infestation of the Sandy Beach Amphipod Orchestoidea Corniculata by Gammaridacarus Brevisternalis (Acari: Laelaptidae) | Donna Scurlock | 74 | 05-sep | NO | parcialmente sin liga | Sin asignar | El ácaro mesostigmatid. Gammaridacariis brevisternalis | The mesostigmatid mite. Gammaridacariis brevisternalis has been found on both decomposing wrack and on the beach amphipods Orchcstoidea corniciilata and O. californiaiia. The percentage infestation of the host population increased with size of hosts and v |
Ficha | An assessment of the AFLP method for investigating population structure in the red alga Chondrus crispus Stackhouse (Gigartinales, Florideophyceae) | Donaldson Sylva L. and et. al. | 12 | 25-35 | NO | Completo | Rodofitas | AFLP, Chondrus, Florideophyceae, genetic markers, population, Rhodophyta | The appropriateness of the Amplified Fragment Length Polymorphism (AFLP) technique for investigating Chondrus crispus Stackhouse populations in the Maritime Provinces of Canada was assessed. The AFLP procedure was firs |
Ficha | Exchange of Water Through The Proposed Sea-Level Canal at Panama | Donald R. F. Harleman | 2 | 41-48 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Harmful Algal Blooms and Eutrophication Nutrient Sources, Composition, and Consequences | DONALD M, ANDERSON, PATRICIA M. GLIBERT, and JOANN M. BURKHOLDER | 25 | 704-726 | No | no completo | General | Although algal blooms, including those considered toxic or harmful, can be natural phenomena, the nature | |
Ficha | The Red Alga Polysiphonia Greville (Rhodomelaceae) from Carrie Bow Cay and Vicinity, Belize | Donald F. Kapraun and James N. Norris | 12 | 225-238 | 3260 | no completo | Sin asignar | Carrie Bow Cay y Twin Cays en la región central del arrecife de coral de Belice; Rhodomelacea; Ceramiales. | Seven taxa of the red alga Polysiphonia Greville (Rhodomelacea; Ceramiales) were found near Carrie Bow Cay and Twin Cays in the central región of the Belizean barrier reef. Polysiphonia exilis and P. flaccidissima are new records for the Caribbean marine |
Ficha | Stable isotope analysis of production and trophic relationships in a tropical marine hard-bottom community | Donald C. Behringer Æ Mark J. Butler IV | No | no completo | General | Benthic community Æ Laurencia Æ Macroalgae Æ Seagrass Æ Trophic structure | Seagrasses produce much of the organic carbon | ||
Ficha | The use of medullary unit patterns of intergenicula and genicula in the taxonomy of Amphiroa (Corallinaceae, Rhodophyta) | Dolan S. | 36 | 397-407 | NO | Liga perdida | Rodofitas | Amphiroa, anatomy, Corallinaceae, genicula, intergenicula, morphology | Branch structure and growth in Amphiroa generated by primarily dividing apical medullary cells was documented by light and scanning electron microscopy. Specific numbers of long- and short-celled tiers are formed when inter |
Ficha | Cell enlargement in relation to the development of thallus form in Florideophyceae | Dixon, P. S. | 6 | 195-205 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | The morphology, ecology and taxonomy of certain Florideae. | Dixon, P. S. | 6 | 32-33 | 3812 | no completo | Sin asignar | ||
Ficha | The occurrence of Gelidium sesquipedale (Clem.) Thur. in the british isles. | Dixon, P. S. | 6 | 47-48 | 3813 | no completo | Sin asignar | ||
Ficha | Morphological study of the genus Herposiphonia (Rhodophyta, Rhodomelaceae) on the coast of eastern Guangdong, China, with a description of H . pinnata sp. nov. | DING Lanping, and et.al. | 34 | 271-282 | NO | no completo | General | new species; morphological taxonomy; Guangdong Province; biogeography distribution | We present a taxonomic study of taxa of the red algae genus Herposiphonia (Rhodophyta, |
Ficha | Glosario de términos ficologicos | Dieguez Covarrubias, A. | 7 A 65 | 3713 | no completo | Sin asignar | |||
Ficha | Is proximity to land-based sources of coral stressors an appropriate measure of risk to coral reefs? An example from the Florida Reef Tract | Diego Lirman, Peggy Fong | 54 | 779–791 | No | no completo | General | Florida Reef Tract; Patch reefs; Coral growth; Coral population structure; Water quality gradients | Localized declines in coral condition are commonly linked to land-based sources of stressors that influence gradients of water quality, |
Ficha | Rosenvingea santae-crucis Børgesen (Scytosipho naceae, Phaeophyta) en las Islas Canarias. | Die, D., Afonso-Carrillo, J., & Gil-Rodriguez, M. C. | 1 | 269-274 | 3897 | no completo | Sin asignar | Se cita Rosenvingea santae-crucis por primera vez para las Islas Canarias y para las costas atlánticas orientales. | |
Ficha | Environmental status: Macroalgae (Seaweeds) | Diaz-Pulido Guillermo and Laurence J. McCook | NO | parcialmente completo con liga | General | ||||
Ficha | Effects of nutrient enhancement on the fecundity of a coral reef macroalga | Diaz-Pulido G. and L. J. McCook | 317 | 13-24 | NO | no completo | Feofita | Algae; Coral reef phase shifts; Fecundity; Nutrient effects; Reproduction; Sargassum | On coral reefs, there is concern that increased nutrient supply (e.g. due to eutrophication) causes increased algal growth |
Ficha | Molecular evidence for Chondrophycus poiteaui var. gemmiferus comb. et stat. nov. (Ceramiales, Rhodophyta) from the Mexican Caribbean Sea: implications for the taxonomy of the Laurencia complex | Díaz-Larrea Jhoana and et. al. | 50 | 250-256 | NO | no completo | Rodofitas | Ceramiales; Chondrophycus poiteaui; Mexican Caribbean Sea; phylogeny; rbcL. | Molecular studies were carried out on Chondrophycus gemmiferus and C. poiteaui (Rhodomelaceae) from the Mexican Caribbean Sea. These species are morphologically related, but differ mainly in the presence of the&nb |
Ficha | Systematics of Anadyomene Species (Anadyomenaceae, Chlorophyta) in the Tropical Western Atlantic | Diane S. Littler and Mark M. Littler | 101-118 | NO | Liga perdida | Sin asignar | Anadyomenaceae; Anadyomene; A. howei sp.nov; A. lacerata sp.nov.; A. linkiana sp.nov.; Cladophorales; Cystodictyon; tropical western Atlantic. | Three new species of Anadyomene are described. Anadyomene lacerata has pinnately branched vein cells.Anadyomene likiana consists of a perforate blade arising by polychotomous branching from a distinct stripe, and A.howei has an eperforate, delicate blade | |
Ficha | Modeling growth and photosynthetic response in Arthrospira platensis as function of light intensity and glucose concentration using factorial design | Dhiab Rym B. and et. al. | 22 | 745-752 | NO | no completo | General | Arthrospira platensis. Growth . Mixotrophy . Net photosynthetic rate . Response surface methodology . Spirulina | Combined effect of light intensity and glucose concentration on Arthrospira platensis growth and photosyn- This design was carried out with light levels of 50, 100, and |
Ficha | Seasonal stresses shift optimal intertidal algal habitats | Dethier M.N. and S. L. Williams | 156 | 555-567 | NO | parcialmente completo con liga | General | We studied how the growth, reproduction, and | |
Ficha | Male gametophyte fragmentation in Laminaria digitata: a life history strategy to enhance reproductive sucess | Destombe C. and L. V. Oppliger | NO | parcialmente completo con liga | Feofita | ||||
Ficha | HERBIVORE VS. NUTRIENT CONTROL OF MARINE PRIMARY PRODUCERS: CONTEXT-DEPENDENT EFFECTS | DERON E. BURKEPILE AND MARK E. HAY | 87 | 3128–3139 | No | no completo | General | benthic; bottom-up; context dependency; coral reef; eutrophication; herbivory; marine; meta-analysis; nutrient enrichment; primary producers; top-down. | Pervasive overharvesting of consumers and anthropogenic nutrient loading are |
Ficha | Enhanced production of Pacific dulse (Palmaria mollis) for co-culture with abalone in a land-based system: nitrogen, phosphorus, and trace metal nutrition | Demetropoulosa Carl L. and Chris J. Langdon | 235 | 433-455 | NO | no completo | Cultivo | Palmaria mollis; Pacific dulse; Seaweed; Nutrition; Haliotis; Recirculating systems | Pacific dulse (Palmaria mollis) is a high-quality algal feed for both red abalone (Haliotis |
Ficha | Phylogeny of the genus coleochaete (Coleochaetales, Charophyta) and related taxa inferred by analysis of the chloroplast gene rbcL | Delwiche C.F., K. G. Karol y M. T. Cimino | 38 | 394-403 | NO | parcialmente completo con liga | Clorofita | Chaetosphaeridium; Charales; Charophyte; Coleochaete; Embryophyte; Land Plant; Mesostigma; Phylogeny; rbcL; Streptophyte | The genus Coleochaete Bréb. is considered to be a key taxon in the evolution of green algae and embryophytes (land plants), but only a few of the approximately 15 species have been studied with molecular phylogenetic methods. We report here |
Ficha | Ultrastructure of cystocarp development in Gelidium robustum (Gelidiaceae: Gelidiales: Rhodophyta) | Delivopoulos S.G. | 142 | 659–667 | NO | no completo | Rodofitas | The ultrastructure of cystocarp development is described for the red alga Gelidium robustum (Gardn.) Hollenb and Abbott. The external cortical cells of the cystocarp remain uninucleate and unmodified, while t | |
Ficha | In situ photosynthetic performance of Laminaria digitata (Phaeophyceae)during spring tides in Northern Brittany | Delebecq G. and et. al. | 52 | 405-414 | NO | no completo | Feofita | Kelp l Photoinhibition l Net oxygen production l Chlorophyll fluorescence l Xanthophyll cycle | The ability of Laminaria digitata (Hudson) J.V. Lamouroux to cope with rapid and drastic changes in light was |
Ficha | Transition in nori cultivation: evolution of household contribution and gendered division of labor | Delaney A. E. | 52 | 527-533 | NO | no completo | Rodofitas | Japan l Nori l Management l Communities l Women | Consumers throughout the world have gained familiarity with the seaweed nori (porphyra spp) thanks to the |
Ficha | Zannichellia pedumculata rechb.(Zannichelliaceae) y Cladophora vadorum (Areschoug) kutzing (Chlorophyta), nuevas citas para la Isla de Tenerife (Islas Canarias). | Del Arco Aguilar, M. J., Gil-Rodríguez, M. C., & Wildpret De la Torre, W. | 15 | 117-121 | 3877 | no completo | Sin asignar | Se citan por vez primera para la isla de Tenerife Zannichellia pedun- culata Rechb. (Zannichelliaceae) y Cladophora vadorum (Areschoug) Kützing (Chlorophyta). Esta última es mencionada por vez primera para la Región Macaronésica. Ambas han sido recolectad | |
Ficha | Effects of human trampling on marine rocky shore communities | Deborah M. Brosnan, Lana L. Crumrine | 79-97 | NO | Liga perdida | Sin asignar | Alga; Barnacle; Disturbance; Epibiont; Human impact; Mussel; Rocky Shore; Trampling | The effects of human trampling on two marine intertidal communities were experimentally tested in the upper-shore algal-barnacle assemblage and mid-shore mussel bed communities. On two shores, we trampled experimental plots 250 times every month for a yea | |
Ficha | Survival of juvenil giant kelp: The effects of demographic factors, competitors and grazers | Dean T.A. and et. al. | NO | Kelp | |||||
Ficha | Growth and age class distribution of Pterygophora californica (Phaeophyta). | De Wreede, R. E. | 13 | 93-100 | NO | parcialmente sin liga | Sin asignar | Pterygophora califomica Ruprecht (Laminariales, Phaeophyta) is a perennial brown alga often found in the upper subtidal zone of oceanic coastal sites of British Columbia, Canada. The phenology and age class distribution of P. californica was studied for o | |
Ficha | The ontogenetic method for determining character polarity and its relevance to phylogenetic systematics. | De Queiroz, K. | 34 | 280-299 | NO | parcialmente sin liga | Sin asignar | In an attempt to clarify the relevance of ontogenetic transformations for system- atics, the ontogenetic method for determining character polarity (the biogenetic law of Nelson, 1978) is analyzed from the perspective of phylogenetic systematics. In phylog | |
Ficha | Culture studies on Pedobesia ryukyuensis (Derbesiales, Chlorophyta), a new record in Brazil. | De Paula, E. J., & West, J. A. | 25 | 482-493 | 3848 | no completo | Sin asignar | ||
Ficha | Propiedades antibióticas de algunas especies de algas marinas bentónicas. | De Lara-Isassi, G. | 1 | 21-28 | 3763 | no completo | Sin asignar | Se colectaron veintiocho especies de algas marinas betónicas en tres diferentes localidades, con el objeto de tener especies representativas de: zonas templadas, subtropicales y tropicales; de ellas se hicieron extractos acuosos y alcohólicos, que fueron | |
Ficha | Photosynthesis and calcification in the calcifying algae Halimeda discoideastudied with microsensors | DE BEER D.& A. W. D.LARKUM | 24 | 1209-1217 | NO | no completo | Rodofitas | Calcium; dynamics; fluxes; oxygen; pH. | With microsensors, we measured the steady-state microprofiles of O2, pH and Ca2+ on the topside of young segments of Halimeda discoidea, as well as the surface dynamics upon light–dark shifts. The effect of sever |
Ficha | Catastrophic storms, El Niño, and patch stability in a Southern California Kelp Community | DAYTON PAUL K. and M. J. Tegner | 224 | 283-285 | NO | no completo | Kelp | ||
Ficha | Temporal and spatial patterns of disturbance and recovery in a kelp forest community | DAYTON PAUL K. and et. al. | NO | Kelp | |||||
Ficha | Patch dynamics and stability of some california kelp communities | DAYTON PAUL K. and et. al. | NO | Kelp | |||||
Ficha | SLIDING BASELINES, GHOSTS, AND REDUCED EXPECTATIONS IN KELP FOREST COMMUNITIES | DAYTON PAUL K. and et. al. | 8 | 309-322 | NO | no completo | Kelp | baseline; benchmark; biodiversity; climate; elasmobranchs; fish; fishing; kelp; regime shift; trends. | The detection of trends in ecosystems depends upon (1) a good description |
Ficha | Ghost Forests in the Sea: The Use of Marine Protected Areas to Restore Biodiversity to Kelp Forest Ecosystems in Southern California | DAYTON PAUL K. | NO | Kelp | |||||
Ficha | Experimental evaluation of ecological dominance in a rocky intertidal algal community | Dayton P.K. | NO | General | |||||
Ficha | The importance of scale in community ecology: a kelp forest example with terrestrial analogs | Dayton P. K. and M. J. Tegner | NO | Kelp | |||||
Ficha | The structure and regulation of some south american kelp communities | Dayton P. K. | NO | Kelp | |||||
Ficha | Clorofíceas Marinhas Bentônicas do Município de Salvador, Bahia, Brasil | Dayse Vasques Martins, Marilza Cordeiro-Manno, Nedson Barbosa Boccanera, José Marcos de Castro Nunes. | 18 | 115-133 | 2615 | no completo | Sin asignar | Benthic marine chlorophytes, qualitative survey, Brazil. | Benthic marine chlorophvtes, Municipality of Salvador, Bahia State, Brazil. A qualitative survey of green algae was made as a contribution to the knowledge of the benthic marine algae of the State of Bahia. The coastline of this State is the longest of an |
Ficha | Response of the tropical red seaweed Gracilaria cornea to temperature,salinity and irradiance | Dawes C.J. and et. al. | 10 | 419-425 | NO | no completo | Rodofitas | Gracilaria cornea, photosynthesis, respiration, chlorophyll, phycoerythrin, Florida, salinity, tempera- ture, irradiance | The agarophyte Gracilaria cornea, collected over 2.5 y in the Florida Keys, shows adaptations to oceanic salinities |
Ficha | Cell wall structure of the agarophytes Gracilaria tikvahiae and G. cornea (Rhodophyta) and penetration by the epiphyte Ulva lactuca (Chlorophyta) | Dawes C.J. and et. al. | 12 | 567-575 | NO | no completo | Rodofitas | Gracilaria cornea, Gracilaria tikvahiae, Ulva lactuca, epiphyte attachment, red algal cell wall, algal cuticle, decklamelle | Use of light, transmission, and scanning electron microscopes revealed that the epidermal cell wall of the red algal |
Ficha | Environmental factors and commercial harvesting: exploring possible links behind the decline of the kelp Laminaria digitata in Brittany, France | Davoult D. | 52 | 429-435 | NO | no completo | Kelp | Macroalgae l Temperature increase l Fishery management l Harvesting decrease | Over the last decade, the commercially harvested quantities of the kelp Laminaria digitata have decreased along |
Ficha | Study of the morphology and distribution of two planktonic diatoms: Chaetoceros paradoxus and Ch. filiferus (Bacillariophyceae) | David Uriel Hernandez-Becerril | 3 | 169-175 | 939 | no completo | Sin asignar | Baja California y el Golfo de California; Chaetoceros Ehr., Ch. paradoxus CI. y Ch. filiferus Karst. | Two planktonic diatom species of the genus Chaetoceros Ehr., Ch. paradoxus CI. and Ch. filiferus Karst. from samples collected in coasts of Baja California and the Gulf of California were studied by light and electron microscopy. The general morphology of |
Ficha | Notes on the benthic marine algae of Puerto Rico VIII. Additions to the flora | David L. Ballantine, Hector Ruiz and Nilda E. Aponte | 47 | 335-340 | NO | no completo | General | flora; Caribbean Sea; Puerto Rico. | Ten species of benthic algae, principally associated with coral reef habitats, are newly reported for the Puerto Rican marine flora. These include eight Rhodophyta: Renouxia antillana, Lithophyllum congestum, |
Ficha | Halichrysis corallinarius sp. nov. (Rhodymeniaceae, Rhodophyta) from Puerto Rico, Caribbean Sea | David L. Ballantine, Gary W. Saunders and Hector Ruiz | 240–248 | NO | Liga perdida | Sin asignar | Caribbean, Halichrysis corallinarius, molecular systematics, Puerto Rico, Rhodophyta, Rhodymeniaceae, Rhodymeniales. | A new species, Halichrysis corallinarius sp. nov. Is described from coral reef habitats in southwest Puerto Rico as well as from Grand Cayman Island. The new species produces strap-shaped thalli supported above the substrata by abundant peg-like stipes. T | |
Ficha | An annotated checklist of deep-reef benthic marine algae from Lee Stocking Island, Bahamas (western Atlantic), I. Chlorophyta and Heterokontophyta | David L. Ballantine and Nilda E. Aponte | 113—127 | NO | Liga perdida | Sin asignar | Avrainvillea, Bahamas, coral reef algae, deep-water algae, submersible, western Altantic. | Forty two Chlorophyta and nine Heterokontophyta (Phaeophyceae) species of benthic marine algae were identified from collections made at the deep (> 27 m) fore-reef at Lee Stocking Island, Bahamas. Ten of these species represent first reports from the Baha | |
Ficha | Possible Phylogenetic Value of the Transitional Helix in Some Chromophyte Algal Classes and Some Colourless Protists | David J. Hibberd | 10 | 115-116 | 2854 | no completo | Sin asignar | ||
Ficha | Experimental Investigations into Morphogenesis in Micrasterias | David H. Tippit and Jeremy D. Pickett-Heaps | 81 | 271--296 | 1272 | no completo | Sin asignar | Micrasterias | The effect of some chemicals (cycloheximide, puromycin, actinomycin D, ribonuclease, cytochalasin B, caffeine, colchicine IPC, CIPC and glusulase) upon morphogenesis in Micrasterias was studied, and some of our results are compared to studies by other inv |
Ficha | Background for a New, Sea-Level, Panama Canal | David Challinor | 2 | 07-dic | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Sediment deposition dampens positive effects of substratum complexity on the diversity of macroalgal assemblages | David Balata, Luigi Piazzi, Fabio Bulleri | 45-51 | NO | Liga perdida | Sin asignar | Biodiversity; Rocky shore; Seaweeds; Sedimentation; Topographic complexity | A three-year experimental study was performed to evaluate the interactive effects of topographic complexity and sedimentation in determining the structure of rocky macroalgal assemblages. The following hypotheses were tested: i) the structure of macroalga | |
Ficha | Can Baptism Alone Save a Species? | David B. Kitts | 32 | 27-33 | NO | parcialmente sin liga | Sin asignar | Species names; essential properties; origin of species. | To maintain that the names of biological species are purely denotative proper names which cannot be defined is to maintain, in effect, that a biological species is confined to the actual world which is to maintain, in turn, that every property of a specie |
Ficha | HURRICANE DAMAGE TO A HAWAIIAN FOREST: NUTRIENT SUPPLY RATE AFFECTS RESISTANCE AND RESILIENCE | DARRELL A. HERBERT, JAMES H. FOWNES, AND PETER M. VITOUSEK | 80 | 908-920 | No | no completo | General | decomposition; fertilization; hurricane; Kauai, Hawaii; leaf area; montane tropical forest; nitrogen; phosphorus; productivity; resilience; resistance; roots. | Hurricane Iniki damaged a forest in which we had previously studied nutrient |
Ficha | A Mediterranean population of Spongites fruticulosus (Rhodophyta, Corallinales), the type species of Spongitesm and the taxonomic status of S. stalactitica and S. racemosa | Daniela Basso and Graziella Rodondi | 45 | 403-416 | NO | Liga perdida | General | Spongites fruticulosus, Spongites racemosa, Spongites stalactitica, Neogoniolithon, Mediterranean, nomenclature, Kützing | |
Ficha | Summary | Daniel M. Cohen | 2 | 261-266 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Controlling Eutrophication: Nitrogen and Phosphorus | Daniel J. Conley, Hans W. Paerl, Robert W. Howarth, Donald F. Boesch, Sybil P. Seitzinger, Karl E. Havens, Christiane Lancelot, Gene E. Likens | 323 | 1014-1015 | NO | no completo | General | ||
Ficha | THE MESOZOIC RADIATION OF EUKARYOTIC ALGAE: THE PORTABLE PLASTID HYPOTHESIS | Daniel Grzebyk, Oscar Schofield | 39 | 259–267 | NO | no completo | General | endosymbiosis; evolution; phytoplankton; plastid genome; RUBISCO | Although all chloroplasts appear to have been de- gave rise to red and green photoautotrophic lin- |
Ficha | THE MESOZOIC RADIATION OF EUKARYOTIC ALGAE: THE PORTABLE PLASTID HYPOTHESIS | Daniel Grzebyk, Oscar Schofield | 39 | 259–267 | NO | no completo | General | endosymbiosis; evolution; phytoplankton; plastid genome; RUBISCO | Although all chloroplasts appear to have been de- gave rise to red and green photoautotrophic lin- |
Ficha | The Theory of Diversity-stability Relationships in Ecology | Daniel Goodman | 50 | 237-260 | 2764 | no completo | Sin asignar | About twenty years ago, the belif, traditional among ecologist, that complex natural communities are more stable than simple ones was given formal expression in a way that seemed to offer promise of both precise empirical test and further theoretical deve | |
Ficha | An Exploratory Study on Soil Algae | Dan Willson and Herman S. Forest | 38 | 309-313 | 51 | no completo | Sin asignar | Norman, Oklahoma | The soil algae of the plow layer in two areas near Norman, Oklahoma, were studied through a spring season with the view of providing useful information in techniques of collecting, treatment, and examination, to use in a planned survey of soil algae in ce |
Ficha | Effects of macroalgal structural complexity on nearshore larval and post-larval crab composition | Daly B. and B. Konar | 153 | 1055–1064 | NO | parcialmente completo con liga | Fitoplancton | Larval and post-larval crab distribution was Alaska to determine temporal and spatial variability. Dis- September | |
Ficha | TECNICAS DE TINCION MODIFICADAS PARA EL ESTUDIO DE ALGAS CORALINAS NO GENICULADAS (RHODOPHYTA) | Dalila Fregoso, Judith Márquez-Guzmán, Eberto Novelo | 20 | 487-510 | NO | no completo | General | Rhodophyta, algas coralinas no geniculadas, técnicas de tinción, colorantes. | Con objeto de facilitar y mejorar la observación de características vegetativas y reproductivas de |
Ficha | Management of kelp ecosystem in Japan | Daisuke FUJITA | 52 | 499-505 | NO | no completo | General | Culture l Home sea l Kelp l Legal control l Stock enhancement l Restoration | Among the countries with kelp habitats, Japan is unique because of the highest diversity of kelp species (38 |
Ficha | Effects of Inorganic Phosphorous and Nitrogen on the Growth of an Estrùarine Cladophora in Culture | D.M. Gordon, P.B. Birch and A.J. McComb | 24 | 93-106 | No | no completo | General | ||
Ficha | Effects of Ignorganic Phosphorus and Nitrogen on the Growth of an Estuarine cladophora in Culture | D.M. Gordon, P.B. Birch and A.J. McComb | 24 | 93-106 | No | no completo | General | ||
Ficha | Composition and community structure of the coralline algal reefs from Atol das Rocas, South Atlantic, Brazil | D.F.M. Gherardi - D.W.J Bosence | 19 | 205-219 | NO | Completo | Rodofitas | ||
Ficha | A novel phytoplankton chlorophyll technique: toward automated analysis | D.A.Phinney and C.S.Yentsch | 7 | 633-642 | NO | no completo | General | Interest in the < 1 /im picoplanlcton fraction of natural waters, especially the oligotrophic oceans, The controversy concerni | |
Ficha | The Settling Behavior of Marine Algal Spores | D. A . Coon, M. Neushul, and A. C. Charters | 237-242 | 2686 | no completo | Sin asignar | The setting behavior of nonmotile marine algal spores depends in large measure upon their physical characteristic and motion in the water. A new microscopic setting-chamber tech-nique has been developed to precisely determine algal spore size and sinking | ||
Ficha | Low densities of sea urchins influence the structure of algal assemblages in the western Mediterranean | Cruz Palac?n and et. al. | 39 | 281-290 | NO | no completo | General | grazing; plant–herbivore relationship; Echinoidea; Paracentrotus lividus; western Mediterranean | Numerous studies of interactions between urchins and algae in temperate areas have shown an important structuring |
Ficha | Biotechnological bases to cultivate Chondracanthus chamissoi, an economically important seaweed of the Chilean coast | Cristian Rubén Bulboa Contador | ene-24 | NO | Liga perdida | Sin asignar | Chondracanthus chamissoi is a red algae of economic importance along the Chilean coast. Historically it has been collected for the extraction of carraghen, although in the last few years there has been a demand for direct consumption from the Asian market | ||
Ficha | First attempt to cultivate the carrageenan-producing seaweed Chondracanthus chamissoi (C. Agardh) Ku ?tzing (Rhodophyta; Gigartinales) in Northern Chile | Cristian R Bulboa, and et. al. | 36 | 1069-1074 | NO | no completo | General | carrageenophyte, Chile, Chondracan- thus chamissoi, mariculture, seaweed, vegetative propagation | Chondracanthus chamissoi is an important source of the ¢rst attempt to cultivate C. chamissoi. Experi- |
Ficha | Aspectos generales de la limnología en Venezuela. | Cressa, C., Vásquez, E., Zoppi, E., Rincón, J., & López, C. | 18 | 237-248 | 3911 | no completo | Sin asignar | El presente trabajo tiene como objetivo ofrecer una visión global de la limnología en Venezuela En contraste con la inmensidad de los recursos fluviales y lacustres del país, llama la atención la escasez de estudios sistemáticos sobre los aspectos teórico | |
Ficha | Subtidal Macroalgal Assemblages in Temperate Australian Coastal Waters | Craig S. J. | NO | no completo | General | Bioregionalization and macroalgal assemblages are considered for temperate Australian | |||
Ficha | Evolution of macrocystis spp. (Phaeophyceae) as determined by its1 and its2 sequences | Coyer J. A. and et. al. | 37 | 574-585 | NO | no completo | Feofita | Alaria; antitropical distribution; bio- geography; Costaria; evolution; ITS; kelp; Laminaria; Macrocystis; Nereocystis; Pelagophycus; species concepts | Macrocystis (Lessoniaceae) displays an antitropical along western North America in the northern hemi- We used the noncoding rDN |
Ficha | Spatial and Seasonal Distribution of Seaweeds on Coral Reefs from Southern Bahia, Brazil | Costa O. S. Jr and et. al. | 45 | 346-355 | NO | no completo | General | Macroalgae are major components of Atlantic shallow coral reef communities and potentially a major com- | |
Ficha | Estudio biológico de Pterocladia capillacea (Gmelin) Bornet in Bornet & Thuret. Crecimiento de la planta in situ. | Cos ASENSIO, C. & M. A. RIBERA SIGUAN | NO | Rodofitas | |||||
Ficha | Bioengineer effects on understory species richness, diversity, and composition change along an environmental stress gradient: Experimental and mensurative evidence | Cortney A. Watt, Ricardo A. Scrosati | oct-18 | NO | Liga perdida | Sin asignar | Atlantic; Canada; Nova Scotia; Ascophyllum; canopy; Fucus; intertidal; seaweed; understory | Canopy-forming bioengineer species are commonly assumed to increase local species richness and diversity. We tested this notion by investigating the effects of fucoid seaweed canopies on understory communities along rocky intertidal elevation gradients in | |
Ficha | Guia iluistrada de las algas encontradas en la platraforma los cobanos (diciembre 2002-mayo 2003) | Cortez Hernandez L. M. and et. al. | NO | General | |||||
Ficha | Effects of some environmental factors on growth of sporelings in two species of Gelidium (Rhodophyta). | Correa, J., Avila, M., & Santelices, B. | 44 | 221-227 | 3861 | no completo | Sin asignar | The effects of temperature, photoperiod and photon-flux density on growth of spore- lings of two species of the economically important red algal genus Gelidium were evaluated, and a basic set of abiotic conditions for growing these sporelings was defined. | |
Ficha | Experimental transplants of the large kelp Lessonia nigrescens (Phaeophyceae) in high-energy wave exposed rocky intertidal habitats of northern Chile: Experimental, restoration and management applications | Correa Juan A. and et. al. | 335 | 13-18 | NO | no completo | Feofita | Experimental ecology; Intertidal; Kelps; Lessonia nigrescens; Rocky shore; Restoration; Transplant | Potential for addressing ecological and physiological issues becomes severely limited when the organisms required to |
Ficha | INFECTIOUS DISEASES OF MAZZAELIA LAMlNARIODES (RHODOPHYTA) : CHANGES IN INFECTION PREVALENCE AND DISEASE EXPRESSION ASSOCIATED WITH SEASON,LOCALITY, AND WITHIN-SITE LOCATION | Correa J. A. and et. al. | 33 | 344-352 | NO | no completo | Rodofitas | infectious disease; Mazzaella; prevalence. | This study addresses the issues of infection prevalence |
Ficha | The prevalence and production of turf-forming algae on a temperate subtidal coast | Copertino M. and et. al. | 44 | 241-248 | NO | parcialmente completo con liga | Feofita | ||
Ficha | CULTIVO EN MAR DE MACROALGAS | Contreras Naranjo Luis | NO | Cultivo | |||||
Ficha | Mazzaella spp. XI Congreso Latinoamericano de Ciencia del Mar | Congreso | 0 | NO | Rodofitas | ||||
Ficha | Corología de las especies de algas en relación a ciertos factores ecológicos en el litoral Malagueño. | Conde, F., & Seoane Camba, J. A. | 13 | 783-802 | NO | parcialmente sin liga | Sin asignar | Los estudios taxonómicos, ecológicos y corológicos sobre la vegetación algal bentónica en el litoral malagueño nos han hecho detectar un límite geográfico,entre los alrededores de Marbella y el Faro de Calaburras (Fuen giróla), para la gran mayoría de las | |
Ficha | The genus Steinedesmus Kofoid (Scenedesmaceae, Chlorellales). | Comas, A., & Komárek, J. | 57 | 97-110 | 3776 | no completo | Sin asignar | ||
Ficha | A Working Key to the Genera of North American Algae. | Collins F.S. | 4 | ene-50 | 59 | no completo | Sin asignar | ||
Ficha | Macroalgas del sistema lagunar Nichupté, Quintana Roo | Collado-Vides, L., & González-González, J. | 752-760 | NO | parcialmente sin liga | Sin asignar | El sistema lagunar de Nichupté es una laguna costera oligotrófica. Está ubicada en el Caribe mexicano y es uno de los atractivos turísticos importantes del corredor Cancún-Tulum. El sistema lagunar de Nichupté se encuentra sujeto a las presiones ambiental | ||
Ficha | Spatio-temporal patterns and nutrient status of macroalgae in a heavily managed region of Biscayne Bay, Florida, USA | Collado-Vides Ligia and et. al. | 54 | 377–390 | NO | no completo | General | Biscayne Bay; community-level indicators; macroalgae; nutrient content. | The coastal bays of South Florida are located downstream |
Ficha | Clonal architecture in marine macroalgae: ecological and evolutionary perspectives | Collado-Vides Ligia | 15 | 531-545 | NO | no completo | General | Macroalgae, clonal, marine algae, algal architecture modules, rammets | The study of the ecological and evolutionary consequences of clonal growth in vascular |
Ficha | Una revision taxonomica del genero Udotea en el caribe mexicano y cubano | Collado-Vides L., A.M. Suarez y R. Cabrera | NO | parcialmente completo con liga | Clorofita | ||||
Ficha | Morphological Plasticity of Caulerpa prolifera (Caulerpales, Chlorophyta) inRelation to Growth Form in a Coral Reef Lagoon | Collado-Vides L. | 45 | 123-129 | NO | no completo | Clorofita | Caulerpa, a coenocytic marine macroalgae, is a genus characterized by having a prostrate indeterminate axis | |
Ficha | Variation in the strength of continental boundary currents determines continent-wide connectivity in kelp | Coleman M.A. and et. al. | 0 | NO | no completo | Kelp | dispersal, Ecklonia radiata, ecology, gene flow, marine, oceanography, seaweed | 1. Determining the extent to which coastal oceanographic processes facilitate connectivity of mar- Continental boundary currents are a dominant ph | |
Ficha | The role of recruitment in structuring patterns of small-scale spatial variability in intertidal and subtidal algal turfs | Coleman M.A. | 291 | 131-145 | NO | no completo | General | Recruitment; Algal assemblages; Variability; Scale; Turf | Recruitment is often important in structuring patterns of distribution and abundance of algal |
Ficha | Mass mortality of a dominant kelp (laminariales) at Goat Island, North-eastern New Zealand | Cole R.G. and R.C. Babcock | 47 | 907-911 | NO | no completo | Kelp | In north-eastern New Zealand, monospecific stands of the laminarian Ecklonia radiata | |
Ficha | presentacion clorophyta | Clorophyta | 0 | NO | Clorofita | ||||
Ficha | Culture Studies on Eucheuma Nudum J. Agardh, A Carrageenan Producing Red Alga From Florida | Clinton J. Dawes, John W. LaClaire and Ralph E. Moon | 7 | 01-sep | 1719 | no completo | Sin asignar | Florida, EE.UU.; Eucheuma nudum J. Agardh | Optimum growth conditions for mariculture of Eucheuma nudum J. Agardh, a Florida species of the economically important pantropical red algal genus, were investigated in laboratory culture. Manometric techniques were utilized to monitor plant responses to |
Ficha | Organisms as cooperative ecosystem engineers in intertidal flats | Claire Passarelli et.al. | 92 | 92-101 | NO | no completo | General | Tidal Flats Biogenic Structure Sediment Stability Habitat Cascade Cooperative Ecosystem Engineers | The importance of facilitative interactions and organismal ecosystem engineering for establishing the structure of |
Ficha | The impact of coastal urbanization on the structure of phytobenthic communities in southern Brazil | Cintia D.L. Martins, and et. al. | 64 | 772-778 | NO | Liga perdida | Sin asignar | Macroalgae; Rocky shore; Human impact; Sewage impact | The anthropogenic pressures on coastal areas represent important factors affecting local, regional, and even global patterns of distribution and abundance of benthic organisms. This report undertakes a comparative analysis of the community structure of |
Ficha | Using Molecular-Assisted Alpha Taxonomy to Better Understand Red Algal Biodiversity in Bermuda | Cianciola Elisabeth N. and et. al. | 2 | 946-958 | NO | no completo | General | algae; Bermuda; convergence; cryptic species; molecular-assisted alpha taxonomy (MAAT), Rhodophyta | Molecular-assisted alpha taxonomy has recently become an effective practice in |
Ficha | The Use of Feeding Noises to Determine the Algal Foods Being Consumed by Individual Intertidal Molluscs | Christopher L. Kitting | 40 | ene-17 | 1507 | no completo | Sin asignar | To study the diets of individual animals in the context of intraspecific resource partitioning, it is desirable to detect what individuals are eating without disturbing them. Animals such as slow-moving molluscs on two-dimensional algal foods would be con | |
Ficha | GENETIC VARIATION AMONG STRAINS OF THE TOXIC DINOFLAGELLATE GYMNODINIUM CATENATUM (DINOPHYCEAE) | Christopher J. S. Bolch et. al. | 35 | 356-367 | NO | no completo | General | allozyme; ballast water; dinoflagellate; DNA; genetic variation; Gymnodinium catenatum; isozyme; multidimensional scaling; popula- tion genetics | The toxic dinoflagellate Gymnodinium catenatum Graham has formed recurrent toxic blooms in southeastern Tasmanian waters since its discovery in the area in 1986. Current evidence suggests that this species might h |
Ficha | Ecological indicators for assessing and communicating seagrass status and trends in Florida Bay | Christopher J. Madden and etal | 95 | 568–582 | No | no completo | General | Florida Bay Seagrass Status Indicators Thalassia Restoration Comprehensive Everglades Restoration Plan | A suite of seagrass indicator metrics is developed to evaluate four essential measures of seagrass |
Ficha | Male gametophyte fragmentation in Laminaria digitata: a life history strategy to enhance reproductive success | Christophe DESTOMBE and L. Valeria OPPLIGER | 52 | 385-394 | no completo | General | Life history l Gametophyte l Vegetative reproduction l Sex l Resource allocation | An understanding of the life history of Laminaria digitata is crucial to implementing efficient management | |
Ficha | Algal Spores | Christine A. Maggs, Maureen E. Callow | 01-jun | NO | Liga perdida | General | |||
Ficha | Molecular Phylogeny of the Cladophoraceae (Cladophorales, Ulvophyceae), with the Resurrection of Acrocladus Nägeli and Willeella Børgesen, and the Description of Lurbica Gen. Nov. and Pseudorhizoclonium Gen. Nov. | Christian Boedeker, Frederik Leliaert and Giuseppe C. Zuccarello | 905–928 | NO | Liga perdida | Sin asignar | Chaetomorpha; Cladophora; green algae; molecular phylogenetics; polyphyly; rDNA; Rhizoclonium; taxonomy | The taxonomy of the Cladophoraceae, a large family of filamentous green algae, has been problematic for a long time due to morphological simplicity, parallel evolution, phenotypic plasticity, and unknown distribution ranges. Partial large subunit (LSU) rD | |
Ficha | Effects of Variations in Salinity and Temperature on Some Estuarine Macro-algae | Chris K. Kjeldsen and H.K. Phinney | 301-308 | 3244 | no completo | Sin asignar | |||
Ficha | PROTOCOL FOR MONITORING OF SEAWEEDS | Chopin Thierry | NO | parcialmente completo con liga | General | ||||
Ficha | Integrating seaweeds into marine aquaculture systems: A key toward sustainability | Chopin T. and et. al. | NO | Cultivo | |||||
Ficha | Calcification by crustose coralline algae on the Northern Great Barries Reef, Australia | Chisholm J.R.M. | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Vegetative development of the gametophyte of Bonnemaisonia hamifera from a filamentous state. | Chen, L. C., Edelstein, T., & McLachlan, J. | 48 | 523-525 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | A Cultural Assessment of The Taxonomic Criteria of Selected Marine Chaetopiioraceae (Chlorophyta) | Charles Yarish | 26 | ND | NO | parcialmente sin liga | Sin asignar | Chaetophoraceae | The primary objetives of this study were to examine in culture the development of epiphytic, endophytic and epizoide marine microalgae in the family Chaetophoraceae and to evaluate the taxonomic cris… corrently used for delimitation in this heterogenous f |
Ficha | Polymorphism of selected marine Chaetophoraceae (Chlorophyta) | Charles Yarish | 11 | 29-38 | NO | parcialmente sin liga | Sin asignar | The effect of variations in light-intensity and temperature on morphology, and the formation of setae as a function of nitrate and phosphate concentrations were determined for ten species of epiphytic, endozoic and epizoic marine Chaetophoraceae. Pronounc | |
Ficha | A Field and Cultural Investigation of The Seasonal and Horizontal Distribution of Estuarine Red Algae of New Jersey | Charles Yarish | 37 | ND | 1539 | no completo | Sin asignar | ||
Ficha | The Status of Herpetology in Panama | Charles W. Myers | 2 | 199-210 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Mammalogy in Panama | Charles 0. Handley, Jr | 2 | 217-227 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Food web structure of a restored macroalgal bed in the eastern Korean peninsula determined by C and N stable isotope analyses | Chang-Keun Kang and et. al. | 153 | 1181-1198 | NO | no completo | General | Loss of macroalgae habitats has been wide- peninsula, and efforts for restoration and creation of | |
Ficha | Pelamis Platurus as a Potential Colonizer of the Caribbean Seat | Chaim Kropach | 2 | 267-270 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Profiling the Transcriptome of Gracilaria changii (Rhodophyta) in Response to Light Deprivation | Chai-Ling Ho and et. al. | 11 | 513-519 | NO | no completo | Rodofitas | cDNA microarray . Irradiance . Gracilaria changii . Light deprivation . Seaweed | Light regulates photosynthesis, growth and re- starch contents in seaweeds. Despite its importance as an |
Ficha | Sur la morphologie de quelques Céramiacées | Chadefaud, M. | 2 | 71-87 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Taxonomy of postrate species of Codium (Chlorophyta) From the Canary Islands. | Chacana, M., Gil-Rodriguez, M. C. & Wildpret De la Torre, W. | 1 | 105-108 | 3905 | no completo | Sin asignar | Tres especies costrosas de Codium (Chlorophyta) han sido citadas para las Islas Canarias: C. adhuerms (Cabrera) C. Agardh, C. effusum (Rafinesque) Dclle Chiaje y C. intertextum Collíns & Hcrvey. El análisis reciente de numerosas poblaciones naturales y co | |
Ficha | A revision of the Crustaceos species of Codium from the Canary Islands at the Boergensen's Herbarium. | Chacana, M. & Gil-Rodriguez, M. C. | 159 | 143-147 | 3902 | no completo | Sin asignar | The taxonomic problems of the genus Codium STACKHOUSE from the Canary Islands have led us to review the specimens collected and reported by BOERGESEN (1925). Misidentif'ications of the erect species of Codium by BOERGESEN were already reported by SILVA (1 | |
Ficha | Algo Rythme | CEVA | ND | 3783 | no completo | Sin asignar | |||
Ficha | Nuevos registros de macroalgas para el Atlantico Mexicano y riqueza floristica del caribe mexicano | Cetz Navarro N. P. and et. al. | NO | General | |||||
Ficha | Estudio piloto sobre la industria y el comercio mundiales de algas. | Centro de Comercio Internacional. | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Chloroplast Evolution: Secondary Symbiogenesis and Multiple Losses | Cavalier-Smith T. | 12 | R62–R64 | NO | no completo | General | Chloroplasts originated from cyanobacteria only | |
Ficha | Adiciones a la Ficoflora Marina Bentónica de las Costas de Oaxaca, México | Catalina Mendoza González, Luz Elena Mateo Cid | 39-58 | NO | Liga perdida | Sin asignar | Nuevos registros, algas marinas, Oaxaca, México. | Se citan dos nuevos registros de algas marinas bentónicas para la costa del Pacífico de México: Lithophyllum farlowii Heydrich y Bornetia binderiana (Sonder) Zanardini. Se registran ocho especies adicionales en las costas de Oaxaca: Tricleocarpa cylindric | |
Ficha | Estudios ecológicos en la zona costera afectada por contaminación del Northern Breeze. Introducción general y comunidades de playas de arenas. | Castilla, J. C., Sánchez, M., & Mena, O. | 2 | 53-64 | NO | parcialmente sin liga | Sin asignar | A fin de evaluar cuantitativamente los daños ecológicos derivados del derrame de petroleo del "Northern Breeze", se estudiaron las comunidades intermareales de playas rocosas en 2 habitats ubicados cerca de Caleta Horcón, Chile Central. Estos lugares tien | |
Ficha | Evidence for the conspecificity of Palisada papillosa with P. perforata (Ceramiales, Rhodophyta) from the western and eastern Atlantic Ocean on the basis of morphological and molecular analyses | CASSANO VALERIA and et. al. | 48 | 86–100 | NO | no completo | Rodofitas | Palisada papillosa, P. perforata, Phylogeny, rbcL, Rhodomelaceae, Taxonomy | Morphological and molecular studies were carried out on Palisada papillosa and P. perforata from the Canary Islands (type locality of P. perforata), Mexico and Brazil. The two species have been distinguished by features of their external morp |
Ficha | Laurencia caduciramulosa (Ceramiales, Rhodophyta) from the Canary Islands, Spain: a new record for the eastern Atlantic Ocean | CASSANO VALERIA and et. al. | 51 | 156-158 | NO | no completo | Rodofitas | Atlantic Ocean; Canary Islands; geographical distribution; Laurencia caduciramulosa; taxonomy. | Laurencia caduciramulosa is recorded for the first time growing epilithically in the lower intertidal zone on mod- |
Ficha | Vida en grupo en algas: Selección por parentesco en Lessonia nigrescens | Casares F.A. & S. Faugeron | NO | parcialmente completo con liga | General | ||||
Ficha | LIFE HISTORY PHASES AND THE BIOMECHANICAL PROPERTIES OF THE RED ALGA CHONDRUS CRISPUS (RHODOPHYTA) | Carrington Emily, Sean Patrick Grace and Thierry Chopin | 37 | 699-704 | NO | no completo | Rodofitas | biomechanics; carrageenans; Chon- drus crispus; material properties, Rhodophyta; strength, wave exposure; water motion | Chondrus crispus Stackhouse alternates between two isomorphic life history phases that differ in cell- kappa-type carrageen |
Ficha | THE LIVING MARINE RESOURCES OF THE WESTERN CENTRAL PACIFIC | Carpenter Kent E. & Volker H. Niem | 1-686 | NO | no completo | General | This multivolume field guide covers the species of interest to fisheries of the major | ||
Ficha | ULTRASTRUCTURE OF PSEUDOCILIA IN TETRASPORA LUBRICA (ROTH) AG. | CAROLE A. LEMBI AND PATRICIA L. WALNE | 9 | 569-579 | No | no completo | General | The flagella-like, but immobile, pseudocilia of the unicellular green alga, Tetraspora lubrica, | |
Ficha | IS THERE AN ECOPHYSIOLOGICAL EXPLANATION FOR THE GAMETOPHYTE TETRASPOROPHYTE RATIO IN GELIDIUM SESQUIPEDALE (RHODOPHYTA)? | Carmona Raquel and Rui Santos | NO | Rodofitas | |||||
Ficha | Ecology and morphological characterization of gametophyte and ‘Chantransia’ stages of Sirodotia huillensis (Batrachospermales, Rhodophyta) from a stream in central Mexico | Carmona Javier and et. al. | 54 | 108-115 | NO | Completo | Rodofitas | Batrachospermales, ‘Chantransia’ stages, ecology, gametophyte, morphology, Rhodophyta, Siro- dotia huillensis, stream. | The morphology and phenology of Sirodotia huillensis was evaluated seasonally in a central Mexican firstorder calcareous stream. Water temperature was constant (24–25°C) and pH circumneutral to alkaline& |
Ficha | ESTUDIO BIOLÓGICO DE PTEROCLADIA CAPILLACEA (GMELIN) BORNET ÍV BORNET & THURET. CRECIMIENTO DE LA PLANTA IN SITU | CARMEN COS ASENSIO & Ma. ANTONIA RIBERA SIGUÁN | 46 | 47-54 | NO | Completo | Rodofitas | Rhodophyta, Peterocladia capillacea, biología. | Se ha realizado un estudio biológico de Pterocladia capillacea (Gmelin) Bornet in Bornet & Thuret en Estartit y Rosas (noreste de la Península Ibérica), en el cual se ha cuantificado el crecimiento |
Ficha | ? 15 N values of macroalgae as an indicator of the potential presence of waste disposal from land-based marine fish farms | Carlos Carballeira et. al. | 25 | 97-107 | NO | no completo | General | Fucus Codium tomentosum Pollution Monitoring Bioconcentration Aquaculture Eutrophication | The nitrogen isotope ratio (δ 15 N) in tissues of native macroalgae was evaluated as a |
Ficha | Hydrodictyon, uma Rede Aquática | Carlos Nobre Rosa | 5 | 23-26 | 88 | no completo | Sin asignar | ||
Ficha | Submerged aquatic vegetation in relation to different nutrient regimes | Carlos M. Duarte | 41 | 87-112 | 1285 | no completo | General | ||
Ficha | SYSTEMATICS OF GRACILARIOPSIS (GRACILARIALES, RHODOPHYTA) BASED ON rbcL SEQUENCE ANALYSES AND MORPHOLOGICAL EVIDENCE | Carlos Fredrerico D. Gurgel et. al. | 39 | ene-19 | NO | Liga perdida | General | Biogeography; Gracilariaceae; Gracilariales; Gracilariopsis; invasive species; phylogeny; rbcL; Rhodophyta; systematics | A phylogeny has been inferred from parsimony and likelihood analyses of plastid rbcL DNA sequences for seven recognized and six undescribed species of Gracilariopsis (Gp.) (Gracilariales, Rhodophyta). New descript |
Ficha | Algas da Lagoa das Prateleiras, Parque Nacional do Itatiaia, Brasil | Carlos Eduardo de Mattos Bicudo, Rosa Maria Teixeira Bicudo | 4 | ene-40 | NO | parcialmente sin liga | Sin asignar | Río de Janeiro, Brasil, | The present paper is a contribution to the knowledge of Brazilian alpine algalflora. It is a list of the algae (except for the diatoms) of the Prateleiras sphagnum-bog located about 7,500 feet high within the Italiaia National Park, in the State of Rio de |
Ficha | The Genus Borzia Cohn Ex Gom In S. Paulo, Brazil | Carlos Eduardo De Mattos Bicudo | 2 | 147-152 | 78 | no completo | Sin asignar | Sao Pablo, Brasil; piscinas artificiales, Borzia trilocularis COHN ex Gom | As known by the author, this is the first time that the genus Borzia COHN ex Gom. is cited for São Paulo City, Brazil, and possibly for all South America . It is reported the presence of the type species of the genus, Borzia trilocularis COHN ex Gom., fou |
Ficha | Contribution to the Knowledge of the Desminds of the State of São Paulo (Brazil) | Carlos Eduardo de Mattos Bicudo | 17 | ND | NO | parcialmente sin liga | Sin asignar | Sao Pablo, Brasil; Cosmarium, Closterium, Micrasteria, Euastrum, | The present paper is a contribution to the knowledge of the desmids (Chlorophyceae) of the State of Sao Paulo, Brazil, including a few from 2 localities in the neighbour state of Minas Gerais. From the 50 collections at my disposal I have been able to rec |
Ficha | Algas do Brejo da Lapa, Parque Nacional do Itatiaia, Brasil. | Carlos E. M. Bicudo e Maria Rosa Ventrice | ND | NO | parcialmente sin liga | Sin asignar | Minas Gerais, Brasil; Pantano; Chlorophyceae, aluvionales Cosmarium, Scenedesmus, Cosmarium microsphinctium, Netrium digitus, Staurodesmus dejectus y Tetmemorus brebissonii. | The present paper is another contribution to the knowledge of the Brazilian alpine algalflora. It is a list of 75 differen t species, 20 varieties, and 3 named formae of freshwater algae (except for the diatoms) collected from the "brejo da Lapa", a sphag | |
Ficha | Bjornbergiella, a New Genus of Cryptophyceae from Hawaiian Soil | Carlos E. M. Bicudo | 5 | 217-221 | NO | parcialmente sin liga | Sin asignar | Kaunaoa, Hawaii; Bjornbergiella hawaiiensis gen. et sp. nov. (Criptophyceae) | Bjornbergiella hawaiiensis gen. et sp. nov. (Cryptophyceae) is described from a soil sample gathered in the proximity of Kaunaoa, Hawaii. |
Ficha | Genetic variation of Meristotheca cylindrica (Solieriaceae, Rhodophyta) in Campeche, Mexico | Carlos Adán Palma Ortiz et. al. | 27 | 315-326 | NO | no completo | General | cox2-3 spacer, genetic structure, genetic diversity, haplotypes, RuBisCo spacer. | Background. Meristotheca cylindrica is a red alga distributed in the Campeche coast, usually misidentified by the morphological variation spectrum exhibited in its populations. Objectives. We proposed to evaluate the geneti |
Ficha | Do plant density, nutrient availability, and herbivore grazing interact to aVect phlorotannin plasticity in the brown seaweed Ascophyllum nodosum | Carl Johan Svensson · Henrik Pavia · Gunilla B. Toth | 151 | 2177–2181 | No | no completo | General | Plants have diVerent strategies to cope with | |
Ficha | Prospeccion del recurso Chondracanthus chamissoi "cochayuyo" en la playa de Huanchaco (trujillo), junio-julio 2005 | Carbajal W. and et. al. | NO | parcialmente completo con liga | General | ||||
Ficha | Sustained high yields of Gracilaria (Rhodophyta) grown in intensive large-scale culture | Capo Thomas R. and et. al. | 11 | 143-147 | NO | no completo | Rodofitas | Gracilaria, sustainable productivity, land-based culture | Gracilaria ferox J. Agardh was grown continuously in large, outdoor tanks under a pulse-fed nutrient regime for |
Ficha | Comparison of ITS RFLP patterns of Gracilaria (Rhodophyceae, Gracilariales) populations from Chile and New Zealand and an examination of interfertility of Chilean morphotypes | Candia Arturo and et. al. | 11 | 185-193 | NO | no completo | Rodofitas | Chile, interfertility trials, Gracilaria, ITS region, morphotypes, PCR, RFLPs, New Zealand | Restriction fragment length polymorphism (RFLP) patterns of the internal transcribed spacer (ITS) of the nuclear |
Ficha | Comunidades Algales Intermareales del Ambiente "Riscos" en Guerrero, Mexico. | Candelaria-silva, Carlos, León-Alvarez, Daniel y González-González, Jorge | ND | 2481 | no completo | Sin asignar | Guerrero, México; Rhodophyta, Phaeophyta y Chlorophyta. | Se hace la tipificación de la comunidad algal del ambiente intermareal denominado zona de riscos, considerando su composición especifica, patrones de distribución de las principales especies y asociaciones, y su caracterización fisiografico-ecológica, en | |
Ficha | Niveles de concentración de metales pesados en algas marinas bentónicas del litoral de la Isla de Tenerife (Islas Canarias). I, Cu, Zn y Fe. | Campos, M., Galindo, L. R., Gil-Rodríguez, M. C., Hardis-Son, A., & Lozano, G. | 4 | 78-81 | NO | parcialmente sin liga | Sin asignar | Se determinan el cobre. zinc y hierro en siete especies de algas marinas bentónicas pertenecientes a la división Phaeophyta (Cystoseira abies-marinas, Cystoseira compressa, Cystoseira foeniculacea, Cystoseira humilis, Fucus spiralis, Sargassum vulgare y P | |
Ficha | Temperature responses of several Cladophora species in relation to their geographic distribution. | Cambridge, M. | 19 | 190 | 3736 | no completo | Sin asignar | ||
Ficha | Utilización de biotransformados de Laminaria saccharina (L.) Lamouroux en la alimentación de la semilla de la almeja Ruditapes decussatus (L., 1758) | Camacho A. Pérez and et. al. | 18 | 321-328 | NO | no completo | Feofita | Biotransformado, células detríticas, Laminaria saccharina, alimentación, culti- vo, Ruditapes decussatus. | En este estudio se desarrolla una técnica de producción de biotransformados de Laminaria saccharina (L.) Lamouroux basada en la acción secuencial de enzimas (endoglucanasas y celula- |
Ficha | Biomass and agar assessment of three species of Gracilaria from Negros Island, central Philippines | Calumpong H.P. and et. al. | 173-182 | NO | no completo | Rodofitas | agar, biomass, Gracilaria, Philippines, seasonality, yield | Biomass, cover and agar quality of three species of Gracilaria were monitored monthly in three sites in Negros | |
Ficha | Notas sobre tres especies de Gigartinaceae (Rhodophyta) del litoral peruano | Calderón Martha and et. al. | 17 | 115-121 | NO | no completo | Rodofitas | Género, morfología, reproductivo, distribución, taxonomía | La gran variabilidad morfológica de la familia Gigartinaceae ha producido constantes cambios taxonómicos |
Ficha | Frog Spit and Pond Scum | Cain, S.A. | 53 | 292-294 | 757 | no completo | Sin asignar | ||
Ficha | CULTIVO DE MACROALGAS PERT 207031021, BAHÍA SALADO HIDROCULTIVOS S.A. CALDERA, III REGIÓN. | Cabrera Undurraga Carlos | ene-32 | NO | no completo | Cultivo | |||
Ficha | Anatomy of a red tide bloom off the southwest coast of Florida | C.S. Yentsch and etal. | 7 | 817–826 | No | no completo | General | Ataxonomic analysis Chromophoric dissolved organic matter Early warning system Eutrophication Flow cytometry Karenia brevis Particle absorbance Visible reflected light | A massive outbreak of Karenia brevis that had been ongoing for several months along the southwestern |
Ficha | Nature of Obligate Photoautotrophy | C.R. Benedict | 29 | 67-93 | 2863 | no completo | Sin asignar | ||
Ficha | The monitoring of opportunistic macroalgal blooms for the water framework directive | C.M. Scanlan and et. al. | 55 | 162-171 | NO | no completo | General | Among the various quality elements which the Water Framework Directive requires should be monitored are macroalgae. One aspect | |
Ficha | Chemical Fluctuations due to Seasonal and Cropping Effects on an Algal-Seagrass Community | C.J. Dawes, K. Bird, M. Durako, R. Goddaed, W. Hoffman and R. McIntosh | 6 | 79--86 | 1720 | no completo | Sin asignar | Tarpon Springs, Florida; Thalassia testudinum Banks ex König | Benthic algae as well as blades and short shoots of Thalassia testudinum Banks ex König (turtle grass) were collected from caged plots in February, May, and October off Tarpon Springs, Florida in 1m of water. The study was designed to determine chemical c |
Ficha | Acclimation Responses to Salinity of Three Estuarine Red Algae from New Jersey | C. Yarish, P. Edwards and S. Casey | 51 | 289-294 | 1536 | no completo | Sin asignar | Great Bay Estuary, Nueva Jersey, EE. UU.; Bostrychia radicans Mont., Caloglossa leprieurii (Mont.) J. Ag., y Polysiphonia subtilissima Mont. | The effects of salinity and acclimation time on the net photosynthetic responses of 3 estuarine red algae, Bostrychia radicans Mont., Caloglossa leprieurii (Mont.) J. Ag., and Polysiphonia subtilissima Mont., from Great Bay Estuary, New Jersey, USA, were |
Ficha | The State of Knowledge of the Coastal Fish Fauna of the Panamic Region Prior to the Construction of an Interoceanic Sea-Level Canal | C. Richard Robins | 2 | 159-166 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Algae in America Sewage stabilization ponds | C. Mervin Palmer | 9 | no completo | Sin asignar | ||||
Ficha | Nutrient Assimilation by Algae in Waste Stabilization Ponds | C. Mervin Palmer | 204-209 | 11 | no completo | Sin asignar | The natural science approach to assimilation of nutrients involves the use of aquatic microorganisms to decompose unwanted wastes and to permit the products of decomposition, after absorption and assimilation by algae, to form cell substances that tend to | ||
Ficha | Evaluation of New Algicides for Water Supply Purposes | C. Mervin Palmer | 48 | 1133-1137 | NO | parcialmente sin liga | Sin asignar | The screening tests for algicides thus far conducted serve to indicate that there are a number of chemical groups which contain compounds that are algicidal. The promising chemical groups include the inorganic salts, organic salts, rosin amine compounds, | |
Ficha | Algae in Rivers of the United States | C. Mervin Palmer | 61 | 34-38 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Algal Records for Three Indiana Sewage Stabilization Ponds | C. Mervin Palmer | 138-145 | NO | parcialmente sin liga | Sin asignar | Algal identifications have been recorded from 376 samples collected from three Indiana sewage stabilization ponds during a period from May 1962 to August 1968. Although certain genera were found frequently in all three ponds, each pond had a distinctive a | ||
Ficha | A study of Lemanea in Indiana with notes on its distribution in North America | C. M. Palmer | 5 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Zonación del fitobentos intermareal de la región de Cabo Peñas (Asturias) | C. Fernández y F.X. Niell | 46 | 121-141 | NO | no completo | General | Fitobentos, zonación, intermareal rocoso, N. de España | |
Ficha | Molecular data suggest a hybrid origin for the invasive Caulerpa racemosa (Caulerpales, Chlorophyta) in the Mediterranean Sea | C. Durand, M. Manuel, C. F. Boudouresque, A. Meinesz, M. Verlaque & Y. Le Parco | 122-133 | NO | Liga perdida | Sin asignar | Caulerpa racemosa; concerted evolution; hybrid; ITS1±ITS2; Mediterranean Sea; molecular phylogeny; polymorphism; ribosomal DNA; systematics; 18S intron. | Morphological data has provided a basis for the hypothesis that three taxa belonging to the Caulerpa racemosa complex occur in the Mediterranean Sea: var. turbinata±uvifera, var. lamourouxi, and the `invasive variety'. In order to test this hypothesis and | |
Ficha | Predator diversity strengthens trophic cascades in kepl forests by modifying herbivore behaviour | Byrnes J. and et. al. | 9 | 61-71 | NO | no completo | Kelp | Behaviourally modified interaction, biodiversity ecosystem function, kelp forest, multiple predator effects, predator diversity, trait-mediated indirect interactions, trophic cascade. | Although human-mediated extinctions disproportionately affect higher trophic levels, |
Ficha | Plant cytoplasm. Contribution of French cytologists | Buvat Roger | 80 | 143-146 | NO | Liga perdida | Sin asignar | ||
Ficha | Cultivation of Gigartina skottsbergii (Gigartinales, Rhodophyta): Recent advances and challenges for the future | Buschmann, A. H., Correa, J. A., Westermeier, R., Paredes, M. A., Aedo, D., Potin, P., ... & Hernández-González, M. C. (2001). | 13 | 255–266 | NO | Liga perdida | Cultivo | carrageenan, Chile, exploitation, Gigartina skottsbergii, indoor and outdoor cultivation, protoplasts, regeneration | This study integrates landings statistics and biological studies of the red alga Gigartina skottsbergii Setchell et |
Ficha | The effect of water movement, temperature and salinity on abundance and reproductive patterns of latitudes Macrocystis spp. (Phaeophyta) at different in Chile | Buschmann et.al. | 145 | 849–862 | NO | parcialmente completo con liga | Sin asignar | This study describes the density variation and populations from northern and southern Chile, respec- | |
Ficha | Experimental indoor cultivation of the carrageenophytic red alga Gigartina skottsbergii | Buschmann Alejandro H. and et. al. | 241 | 357-370 | NO | no completo | Cultivo | Chile; Cultivation methods; Gigartina skottsbergii; Growth; Harvesting; Indoor tanks; Irradiance; Temperature | Exploitation of carrageenophytic seaweeds in Chile has increased significantly over the past few |
Ficha | Red algal farming in Chile: a review | Buschmann Alejandro H. and et. al. | 194 | 203-220 | NO | Completo | Rodofitas | Agarophytes; Carrageenophytes; Chile; Edible seaweeds; Research advances; Seaweed cultivation | Production of seaweeds in Chile has fluctuated between 74,000 and 322,000 wet metric tonsryear during the last 14 years, involving different species of Phaeophyta and Rhodophyta. Among Rhodophyta, the most importa |
Ficha | Reproduction strategies of Macrocystis pyrifera (Phaeophyta) in Southern Chile: The importance of population dynamics | Buschmann Alejandro H. and et. al. | 18 | 575-582 | NO | no completo | Feofita | Macrocystis pyrifera, reproduction strategies, southern Chile, spore production, sporophylls | Macrocystis pyrifera is an ecologically dominant species along the temperate Northern and Southern Pacific Coast |
Ficha | Determinants of disease expression and survival ofinfected individual froonds in wild populations of Mazzaella laminarioides (Rhodophyta) in central and southern Chile | Buschmann A. H. and et. al. | NO | Rodofitas | |||||
Ficha | The effect of water movement, temperature and salinity on abundance and reproductive patterns of Macrocystis spp. (Phaeophyta) at different latitudes in Chile | Buschmann A. H. and et. al. | 145 | 849-862 | NO | no completo | Feofita | This study describes the density variation and populations from northern and southern Chile, respec- | |
Ficha | Recent advances in the understanding of the biological basis for Gigartina skottsbergii (Rhodophyta) cultivation in Chile | Buschmann A. H. and et. al. | 427-434 | NO | no completo | Rodofitas | carrageenophytes, cultivation, Gigartina skottsbergii, population dynamics | The demand in Chile for carrageenophytic algae has increased strongly during the last 3 years, with emphasis on Gigartina skottsbergii, a species representing landings of 32 438 t (wet) during 1996. Various sources of inform- | |
Ficha | Nutrient versus herbivore control of macroalgal community development and coral growth on a Caribbean reef | Burkepile Deron E. and Mark E. Hay | 389 | 71-84 | NO | parcialmente completo con liga | General | Eutrophication · Overfishing · Parrotfish · Selective grazing · Surgeonfish · Plant–herbivore interactions | Coral reefs are in global decline, with seaweeds replacing corals as spatial dominants. |
Ficha | Taxonomic Challenges and Distribution of Gracilarioid Algae (Gracilariales, Rhodophyta) in Tanzania | Buriyo A.S. and et. al. | 3 | 135-141 | NO | no completo | Rodofitas | Gracilaria, Gracilariales, taxonomy, distribution,Tanzania | This paper reviews the taxonomical literature of the gracilarioid algae from Tanzania, |
Ficha | The Effectiveness of Macroalgal Reduction and Diadema antillarum Addition in Maintaining Algal Turfs and Facilitating Coral Recovery | BURDICK David | 0 | NO | no completo | General | |||
Ficha | First attempt to cultivate the carrageenan-producing seaweed Chondracanthus chamissoi (C. Agardh) Ku¨tzing (Rhodophyta; Gigartinales) in Northern Chile | BulboaBulboa Cristian R. and et. al. | 01-jun | NO | no completo | Cultivo | carrageenophyte, Chile, Chondracanthus chamissoi, mariculture, seaweed, vegetativepropagation | Chondracanthus chamissioi is an important source of carrageenan in -Chile. Presently, all the production is harvested from wild populations. This study reports the first attempt to cultivate c. chamissoi. experiments were conducted with female gametoph | |
Ficha | First attempt to ciltivate the carrageenan-producing seaweed Chondracanthus chamissoi (c: Agardh) Kutzing (Rhodophyta; Gigartinales) in Northern Chile | Bulboa et.al. | NO | parcialmente completo con liga | Sin asignar | ||||
Ficha | First attempt to cultivate the carrageenan-producing seaweed Chondracanthus chamissoi (C. Agardh)Ku¨tzing (Rhodophyta; Gigartinales) in Northern Chile | Bulboa Cristian R and et. al. | NO | Rodofitas | |||||
Ficha | Cultivation of cystocarpic, tetrasporic and vegetative fronds of Chondracanthus chamissoi (Rhodophyta, Gigartinales) on ropes at two localities in northern Chile* | Bulboa Cristian & Juan Macchiavello | 34 | 109-112 | NO | parcialmente completo con liga | Rodofitas | algas, cultivo, Chondracanthus chamissoi, Rhodophyta, Chile. | RESUMEN. Chondracanthus chamissoi es una macroalga altamente apreciada como alimento natural en países asiá- c |
Ficha | The Effects of Light and Temperature on Different Phases of the Life Cycle in the Carrageenan Producing Alga Chondracanthus chamissoi (Rhodophyta, Gigartinales) | Bulboa C. R. and J. E. Macchiavello | 44 | 371-374 | NO | parcialmente completo con liga | Rodofitas | Growth of female gametophyte and sporophyte phases of Chondracanthus chamissoi was measured under | |
Ficha | Coccolith and Silicoflagellate Stratigraphy, Northwestern Pacific Ocean, Deep Sea Drilling Project Leg 32. | Bukry, D. | 32 | 677-701 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Silicoflagellate and Coccolith stratigraphy, northwestern Pacific Ocean, Deep Sea Drilling Project Leg 34. | Bukry, D. | 34 | 715-735 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | STABLE ISOTOPES IN ECOSYSTEM STUDIES | Bruce J. Peterson and Brian Fry | 18 | 293-320 | No | no completo | General | ||
Ficha | Viable Soil Algae From The Herbarium of The Missouri Botanical Garden | Bruce C. Parker, Noe Schanen, and Richard Renner | 56 | 112-119 | NO | parcialmente sin liga | Sin asignar | Herbario del jardín botánico de Missouri | Soil particles from herbarium sheets of aquatic, bog and terrestrial plants were used as innoculum on Bold´s modified Bristol´s medium. Forty-six of the 124 innoculations were successful, and algae were obtained from specimens up to 60 years old. Green al |
Ficha | Contributions in Phycology | Bruce C. Parker and R. Malcolm Brown | 22 | 560 | 781 | no completo | Sin asignar | ||
Ficha | Biotic Relationships between Soil Algae and Other Microorganisms | Bruce C. Parker and Harold C. Bold | 48 | 185-197 | 17 | no completo | Sin asignar | Texas; Cultivos de agua en el suelo; Bracteacoccus, Chlamydomonas, Chlamydomonas, Phormidium sp.; ecológico. | A study was conducted of biotic relationships between various algae and other microorganisms isolated from a sample of Texas soil. From 143 two-membered combinations of organisms tested in soil-water cultures, 3 were selected for detailed studies of the n |
Ficha | Community Organization in Temperate and Tropical Rocky Intertidal Habitats: Prey Refuges in Relation to Consumer Pressure Gradients | Bruce A. Menge and Jane Lubchenco | 51 | 429-450 | NO | no completo | General | algae; barnacles; bivalves; community structure; consumer pressure;fishes; gastro- pods; herbivory; predation; refugia; rocky intertidal; temperate vs. tropical; zonation. | The structure of a tropical rocky intertidal community on Taboguilla Island on the |
Ficha | Comparison of three techniques for identifying isomorphic phases of Chondrus crispus (Gigartinaceae) | Brown M. T. and et. al. | 16 | 447-450 | NO | no completo | Rodofitas | Chondrus crispus, FT-IR, Gigartinaceae, iridescence, resorcinol test | Chondrus crispus, a member of the economically important family Gigartinaceae, alternates between two free-living |
Ficha | Utility of psbA and nSSU for phylogenetic reconstruction in the Corallinales based on New Zealand taxa | Broom Judith E.S. and et. al. | 46 | 958–973 | NO | Liga perdida | Rodofitas | Corallinales; nSSU; psbA; Hapalidiaceae; Corallinaceae; Sporolithaceae; New Zealand; Mesophyllum; Spongites | A number of molecular studies of the Corallinales, a calcified order of the red algae, have used the conservative nSSU gene to investigate relationships within the order. However interspecific variation at this locus is low |
Ficha | Parsimony analysis in historical biogeography and coevolution: methodological and theoretical update. | Brooks, D. R. | 39 | 14-30 | NO | parcialmente sin liga | Sin asignar | A unified methodology for parsimony analysis in studies of the co-speciation of clades that co-occur in ecological associations is presented. It incorporates two methodological prescriptions proposed by Wiley with a third, namely duplication of areas when | |
Ficha | Unravelling the algae. The past, present and future of algal systematics | Brodie J. & J. Lewis | NO | parcialmente completo con liga | General | ||||
Ficha | Effects of red macroalgal (Gracilariopsis sp.) abundance on eelgrass Zostera marina in Tomales Bay, California, USA | Brittany E. Huntington, Katharyn E. Boyer | 367 | 133-142 | No | no completo | General | Macroalgae · Bloom · Seagrass · Zostera marina · Tomales Bay | Observations of increasing red macroalgal (Gracilariopsis sp.) abundance in Tomales |
Ficha | Nutrient Inputs from the Watershed and Coastal Eutrophication in the Florida Keys | BRIAN E. LAPOINTE, MARK W. CLARK | 15 | 465-476 | No | no completo | General | Widespread use of septic tanks in the Florida Keys increase the nutrient concentrations of limestone groundwaters that discharge into shallow nearshore waters, resulting in coastal eutrophication. This study char- | |
Ficha | Hurricanes Frances and Jeanne Remove Blooms of the Invasive Green Alga Caulerpa brachypus forma parvifolia (Harvey) Cribb From Coral Reefs Off Northern Palm Beach County, Florida | BRIAN E. LAPOINTE, BRADLEY J. BEDFORD, and REX BAUMBERGER | 29 | 966–971 | No | no completo | General | Coral reefs worldwide are under stress from a variety of anthropogenic activities that can alter or inhibit | |
Ficha | EXPERIMENTAL OUTDOOR STUDIES WITH ULVA FASCZATA Delile. 1. INTERACTION OF LIGHT AND NITROGEN ON NUTRIENT UPTAKE, GROWTH, AND BIOCHEMICAL COMPOSITION | BRIAN E. LAPOINTE and KENNETH R. TENORE | 53 | 135-152 | No | no completo | General | ||
Ficha | Macroalgal blooms on southeast Florida coral reefs I. Nutrient stoichiometry of the invasive green alga Codium isthmocladum in the wider Caribbean indicates nutrient enrichment | Brian E. Lapointe and etal. | 4 | 1092–1105 | No | no completo | General | Nitrogen; Phosphorus; Macroalgae; Coral reefs; Eutrophication | Invasive blooms of the siphonaceous green algae Codium spp. have been considered a symptom of coastal eutrophication but, |
Ficha | Nutrient thresholds for bottom-up control of macroalgal blooms on coral reefs in Jamaica and southeast Florida | Brian E. Lapointe | 42 | 1119-1131 | NO | no completo | General | During the past two decades coral reefs in the greater Caribbean area have been altered by phase shifts away | |
Ficha | Nitrogen fixation by Nostoc colonies in terrestrial environments of Aldabra Atoll, Indian Ocean | Brian A. Whitton, Alan Donaldson and Malcolm Potts | 18 | 278-287 | NO | no completo | General | The rates of acetylene reduction were compared in situ for six diffrerent types of terrestial and semu-aquatic Nostoc colonies and Aldabra as an indication of their rates of nitrogen fixation. The rates per unite chlorophyl | |
Ficha | Ecological Differences Between the Isomorphic Phases of Mazzaella lilacina (Rhodophyta, Gigartinaceae) | Brent Philips | 1-127 | NO | Completo | Rodofitas | Some of the potential factors responsible for the observed increase in the proportion of tetrasporophytes in wave exposed populations of Mazzaella lilacina (Postels et Ruprecht) Leister have been examined. By counting the n | ||
Ficha | Ecological Differences Between the Isomorphic Phases of Mazzaella lilacina (Rhodophyta, Gigartinaceae) | Brent Philips | 1-127 | NO | Completo | Rodofitas | Some of the potential factors responsible for the observed increase in the proportion of tetrasporophytes in wave exposed populations of Mazzaella lilacina (Postels et Ruprecht) Leister have been examined. By counting the n | ||
Ficha | PARMALES (CHRYSOPHYCEAE) FROM THE GULF OF TEHUANTEPEC, MEXICO INCLUDING THE DESCRIPTION OF A NEW species, Tetraparma insecta so. Nov., AND A PROPOSAL TO THE TAXONOMY OF THE GROUP | Bravo-Sierra E and D. U. Hernandez-Becerril | NO | parcialmente completo con liga | General | ||||
Ficha | Über die morphologischen Verhältnisse der Cladophora-Basis. | Brand, F. | 27 | 292-300 | 3727 | no completo | Sin asignar | ||
Ficha | DIVERSITY OF INTERTIDAL MACROALGAE INCREASES WITH NITROGEN LOADING BY INVERTEBRATES | BRACKEN MATTHEW E. S. AND KARINA J. NIELSEN | 85 | 2828-2836 | NO | no completo | General | diversity; facilitation; macroalgae; nitrogen uptake; nutrients; positive interactions; productivity; rocky intertidal; species richness; tide pools. | Many ecological phenomena are characterized by context dependency, and the relationship between diversity and productivity is no exception. We examined the re- |
Ficha | SPORES’ GERMINATION OF Gelidiun Floridanum (GELIDIALES, RHODOPHYTA): CYTOCHEMICAL AND ULTRASTRUCTURAL STUDY | Bouzon, Z. L. and et. al. | 12 | NO | no completo | Rodofitas | |||
Ficha | Ultrastructure of tetraspore germination in the agar-producing seaweed Gelidium floridanum (Gelidiales, Rhodophyta) | Bouzon Z.L. and et. al. | 44 | 409-415 | NO | Completo | Rodofitas | Spore germination is a crucial step in the dispersion and establishment of algae. Here we describe for the first time the ultrastructure of the initial stages of the tetraspore germination of Gelidium floridanum, a spe | |
Ficha | GENETIC STRUCTURE OF NATURAL POPULATIONS IN THE RED ALGAE GELIDIUM CANARIENSE (GELIDIALES, RHODOPHYTA) INVESTIGATED BY RANDOM AMPLIFIED POLYMORPHIC DNA (RAPD) MARKERS | Bouza Nieves and et. al. | 42 | 304-311 | NO | no completo | Rodofitas | Canary Islands; Gelidium canari- ense; genetic diversity; genetic structure; popula- tion genetics; RAPD; Rhodophyta | Random amplified polymorphic DNA (RAPD) marker variation was analyzed in female game- |
Ficha | Metal (Fe, Zn, Cu, Pb and Cd) concentration patterns in components of a macrophyte-based coastal lagoon ecosystem | Boubonari Theodora and et. al. | 635 | 27-36 | NO | no completo | General | Metals Sediments Macrophytes Invertebrates Fish Feeding habits | Information on the metal biological fate in development of predictive model |
Ficha | Photosynthesis and calcification in the articulated coralline red algae Amphiroa anceps and A. foliacea | Borowitzka M.A. | 62 | 17-23 | NO | Completo | Rodofitas | ||
Ficha | Effects of macroalgal mats on intertidal sandflats: an experimental study | Bolam Stefan G. and et. al. | 249 | 123-137 | NO | no completo | General | Macroalgal mats; Macrobenthic community; Sandflats; Sediment variables | The growth of green macroalgal mats is becoming increasingly common in many marine |
Ficha | Scotiellopsis, cine neue Gattung aus der gleichnamigen Unterfamilie Scotiellopsioideae (Oocystaceae, Chlorococcales}, nebst Bemerkungen zu den verwandten Gattungcn | Bohuslav Fott | 48 | 289 -298 | 2847 | no completo | Sin asignar | Scotiellopsis Fott.; Oocystaceae, Chlorococcales. | A new genus Scotiellopsis Fott has be estabilished. It involves inucellullar Chlorococcales having the habit of the genus Scotiella Fritsch, but reproducing by autospores. The cell Wall of those autospores exhibits the same structure as that of the mother |
Ficha | Dinoflagellates of the coastal waters of the western pacific. | Böhm, A. | 137 | 1 A 45 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Effect of Nitrogen and Phosphorus Supply on Growth and Tissue Composition of Ulva Fenestrata and Enteromorpha Intestinalis (Ulvales, Chlorophyta) | Bo R. Björnsäter, Patricia A. Wheeler | 603-611 | NO | Liga perdida | Sin asignar | Chlorophyta; Enteromorpha intestinals; growth rates; nutrient limitation; tissue nitrogen; tissue phosphorus; Ulva fenestrata | The chlorophyte macroalgae Ulva fenestrata (Postels and Ruprecht) and Enteromorpha intestinalis (Linnaeus) Link. were grown under various nutrient regimes in indoor semi-continuous and batch cultures. Tissue nitrogen contents ranged from 1.3–5.4% N (dry w | |
Ficha | Fucoidan: Structure and Bioactivity | Bo Li*, Fei Lu, Xinjun Wei and Ruixiang Zhao | 13 | 1671-1695 | NO | no completo | Feofita | Fucoidan, structure, bioactivity | Fucoidan refers to a type of polysaccharide which contains substantial |
Ficha | Comparison between a new application of multivariate regression and current spectroscopy methods for the determination of... | Bo Karlberg, U. Larsson | 411 | 137-143 | NO | no completo | General | Chlorophyll a; Chlorophyll b; Chlorophyll c; Pheophytin a; Pheophytin b; Pheoporphyrin c; Multivariate calibration; Partial least squares regression | A multivariate calibration model, partial least squares regression for several independent variables (PLS2), has been devel- |
Ficha | Cross-habitat impacts of species decline: response of estuarine sediment communities to changing detrital resources | Bishop M.J. and M. A. Coleman | 163 | 517-525 | NO | Liga perdida | Feofita | Detritus Extinction Macroinvertebrates Phyllospora comosa Spatial subsidy | Food webs of many ecosystems are sustained by |
Ficha | Cladophora growth in the Peel-Harvey estuarine system following blooms of the cyanobacterium Nodularia spumigena. | Birch, P. B., & Gabrielson, J. O. | 27 | 17-22 | NO | parcialmente sin liga | Sin asignar | In recent years severe blooms of the nitrogen-fixing cyanobacterium Nodularia spumigcna have occurrcd during spring and early summer in the eutrophic Peel-Harvey Estuary. Following decomposition of thesc blooms there are blooms of Cladophora and other mac | |
Ficha | The effects of temperature on producers, consumers, and plant–herbivore interactions in an intertidal community | Bionda Morelissen, Christopher D.G. Harley | 348 | 162-173 | NO | no completo | General | Herbivory; Lottia (Collisella) scabra; Macroalgae; Microalgae; Thermal stress; Top-down vs. bottom-up effects | Although global warming is acknowledged as a primary threat to populations and communities, the impact of rising temperature |
Ficha | Supraspecific taxa as terminals in cladistic analysis: implicit assumptions of monophyly and a comparison of methods | BININDA-EMONDS OLAF R. P. | NO | parcialmente completo con liga | Sin asignar | ||||
Ficha | Numerical simulations suggest that counting sums and taxonomic resolution of diatom analyses to determine IPS pollution and ACID acidity indices can be reduced | Bigler Christian, Veronika Gälman & Ingemar Renberg | 22 | 541-548 | NO | parcialmente completo con liga | Sin asignar | Epilithic diatoms. Index . Monitoring . Counting sum size . Numerical simulations | Implementation of the European Union Water |
Ficha | Algal Phylogeny and the Origin of Land Plants1 | Bhattacharya Debashish and Linda Medlin | 116 | sep-15 | NO | no completo | General | The green algae and land plants form a monophyletic | |
Ficha | Algae of the James River Basin, Virginia I. Zygnemataceae and Oedogoniaceae | Bernard Woodson and G. W. Prescott | 80 | 166-175 | 2848 | no completo | Sin asignar | Río James, Virginia, EE.UU.; Zygnemataceae y Oedogoniaceae | This report is the first of several which we propose to make from studies of the algal flora of Virginia. The initial study, made in 1956, was a survey of the Chlorophyta of the James River Basin. Field work included the taking of limnological and ecologi |
Ficha | SPORELING COALESCENCE AND INTRACLONAL VARIATION IN GRACILARIA CHILENSIS (CRACILARIALES, RHODOPHYTA)' | Bernabé Santelices et. al. | 32 | 313-322 | NO | no completo | Rodofitas | bicolor individuals; Gracilaria chilensis; intraclonal variation; RAPD; Rhodophyta; sporeling coalescence | This study n<aluates the hypothesis that spore coalescence may cause intraclonal variation. Spore coalescence might allow the occurrence of unitary thalli that in fact correspond to genetically different, coale |
Ficha | New records of marine algae from Chile and their effect on phytogeography | Bernabe Santelices and Isabella A. Abbott | 17 | 213-222 | NO | parcialmente sin liga | Sin asignar | centro y norte de Chile; Chlorophyta, Phaeophyta y Rhodophyta | Forty species of marine algae (ten Chlorophyta, nine Phaeophyta and twenty-one Rhodophyta) are newly reported from central and northern Chile. Of these, seventeen are new to Pacific South America, the remaining are range extensions from Peru and within Ch |
Ficha | Taxonomic and nomenclatural notes on some Gelidiales (Rhodophyta) | Bernabé Santelices | 15 | 165-173 | 1349 | no completo | Sin asignar | Gelidillm caerlliescens Klitzing, G. irreglliare Loomis, Pterocladia tropica Dawson y P. rigida Loomis | Examination of the description and the type specimen of five species of Gelidiales (Rhodophyta) indicates that four of them, namely Gelidillm caerlliescens Klitzing, G. irreglliare Loomis, Pterocladia tropica Dawson and P. rigida Loomis, could be included |
Ficha | A Taxonomic Review of Hawaiian Gelidiales (Rhodophyta) | Bernabé Santelices | 31 | 61-84 | 1363 | no completo | Sin asignar | Hawai, G. acerosa (Forsskal) Feldmann et Hamel, G. adnata Dawson, G. machrisiana Dawson y G. myrioclada Børgesen | The present study reviews most collections of Gelidiales known from Hawaii. Three genera, each one including four species, are recognized among nearly 350 specimens examined. The genus Gelidiefla is represented in Hawaii by G. acerosa (Forsskal) Feldmann |
Ficha | Branching coral as a macroalgal refuge in a marginal coral reef system | Bennett S. and et. al. | 29 | 471-480 | NO | Liga perdida | Feofita | Herbivory Lobophora variegata Ecosystem function Phase shift Resilience Coral reef | Marginal coral reef systems may provide alternate ecosystem state. This study investigates the pro- |
Ficha | Effects of wave exposure on the proportion of gametophytes and tetrasporophytes of Mazzaella oregona (Rhodophyta: Gigartinales) from Pacific Canada | Benita Mudge and Ricardo Scrosati | 83 | 701-704 | NO | Completo | Rodofitas | The proportion of life history phases in red seaweeds is an important descriptor of population structure. This paper describes the relative abundance of gametophytes and tetrasporophytes of Mazzaella oregona (Rhodophyta: Gi | |
Ficha | Efects of wave exposure on the proportion of gametophytes and tetrasporophytes of Mazzaella oregona (Rhodophyta: Gigartinales) from Pacific Canada | Benita Mudge and Ricardo Scrosati | 83 | 701-704 | NO | Liga perdida | Rodofitas | The proportion of life history phases in red seaweeds is an important descriptor of population structure. This paper describes the relative abundance of gametophytes and tetrasporophytes of Mazzaella oregona (Rhodophyta: Gi | |
Ficha | Microalgae biotechnology. | Benemann, J. R., Tillett, D. M., & Weissman, J. C. | 5 | 47-53 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Variation in gametophyte dominance in populations of Chondrus verrucosus (Gigartinaceae, Rhodophyta) | Bellgrove Alecia and Masakazu N. Aoki | 56 | 246-254 | NO | Completo | Rodofitas | dispersal, gametophyte, isomorphic, macroalgae, phase dominance, resorcinol-acetal test, tetrasporophyte. | We describe the abundance, including spatial and temporal variability, of phases of the isomorphic Chondrus verrucosus Mikami from Japan. Chondrus verrucosus occurred in a dense (~90% cover) and temporally stable& |
Ficha | Small-scale temporal variation in propagule supply of an intertidal red alga | Bellgrove A. & M. N. Aoki | 45 | 458-464 | NO | parcialmente completo con liga | Rodofitas | Chondrus verrucosus, Propagule supply, Spore release, Supply-side ecology, Temporal variation, Tidal rhythm | |
Ficha | Applying flow tank measurements to the surf zone: Predicting dislodgment of the Gigartinaceae | Bell Emily C. | 47 | 159-166 | NO | no completo | Rodofitas | dislodgment, drag, Gigartinaceae, hydro- dynamic force, Mastocarpus, Mazzaella, mechanical design, wave exposure. | Our understanding of how flow affects the survival of members of the Gigartinaceae has advanced consider- developed that give phycologists a powerful tool with which to pr |
Ficha | Ecology from individuals to ecosystems | Begon et.al. | NO | parcialmente completo con liga | Sin asignar | ||||
Ficha | Macroalgal canopies: distribution and diversity of associated invertebrates and effects on the recruitment and growth of mussels | Bégin Chantale and et. al. | 271 | 121-132 | NO | no completo | General | Biodiversity · Community structure · Ecosystem engineering · Kelp bed · Mytilus edulis · Positive interactions | We examined the invertebrate assemblages associated with macroalgal canopies in the |
Ficha | Assessing sewage impact in a South-West Atlantic rocky shore intertidal algal community | Becherucci Maria Eugenia, Santiago Lucerito, Benavides Hugo Rodolfo, Vallarino Eduardo Alberto | 388–394 | NO | Liga perdida | Sin asignar | Sewage outfall; Coastal pollution; Algal indicators; Mar del Plata; Argentina | The spatial and seasonal variation of the specific composition and community parameters (abundance, diversity, richness and evenness) of the intertidal algal assemblages was studied at four coastal sampling sites, distributed along an environmental gradie | |
Ficha | Nuevos Registros del Género Anadyomene J.V. Lamouroux (Anadyomenaceae, Chlorophyta) para el Mar Caribe | Beatriz Vera, César Paz y Juan Linares | 105-111. | NO | Liga perdida | Sin asignar | Anadyomene, Archipiélago Los Roques, Caribe, Chlorophyta, Venezuela | Dos nuevos registros del género Anadyomene (Anadyomenaceae, Chlorophyta) se reportan para la costa venezolana: A. pavonina y A. rhizoidifera, originalmente descritas para Florida y Brasil respectivamente. Estas algas se colectaron creciendo sobre Sargassu | |
Ficha | New coral reef boring sponges (Hadromerida: Clionaidae) from the Mexican Paci¢c Ocean | Bautista-Guerrero OP, Jose¤ Luis Carballo, Jose¤ Antonio Cruz-Barraza O and Hector H. Nava | NO | parcialmente completo con liga | Sin asignar | ||||
Ficha | The extensive development of the turf-forming red alga Womersleyella setacea (Hollenberg) R. E. Norris (Rhodophyta, Ceramiales) in the Bay of Boka Kotorska, Montenegro (southern Adriatic Sea) | BATTELLI CLAUDIO & FABIO RINDI | 142 | 120 – 125 | NO | Liga perdida | Rodofitas | Macrobenthic algae, southern Adriatic Sea, sublittoral, turf-forming, Womersleyella setacea | In August 2003, dense turfs formed by the filamentous red alga Womersleyella setacea (Hollenberg) R. E. Norris were found in the open part of the Bay of Boka Kotorska, on the shore of Montenegro (southern Adriatic Sea). The |
Ficha | A comparative study between Lithothamnion minervae and the type material of Millepora fasciculata (Corallinales, Rhodophyta) | Basso Daniela and et. al. | 43 | 215-223 | NO | Completo | Rodofitas | ||
Ficha | A Mediterranean population of Spongites fructiculosus (Rhodophyta, Corallinales) the type species of spongites, and the taxonomic status of S. stalactitica and S. racemosa | Basso D. and G. Rodondi | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Designing marine reserves for interacting species: Insights from theory | Basketta Marissa L. , Fiorenza Michelib, Simon A. Levina | NO | parcialmente completo con liga | Sin asignar | ||||
Ficha | Observations on Several Benthic Marine Algae from South Padre Island, Texas | Bart J. Baca, Elenor R. Cox and L. O. Sorensen | 21 | 459-462 | NO | parcialmente sin liga | Sin asignar | Costa sur de Texas, EE. UU.; Spatoglossum schroederi | Habit descriptions and additional ecological data are given for four benthic marine algae found on the south Texas coast. Spatoglossum schroederi is reported for the first time from South Padre Island. The collections represent the northernmost range of e |
Ficha | A developmental mutation in Enteromorpha lingulata J. Ag. (Chlorophyta, Ulvales) | Bart J. Baca and Elenor R. Cox | 18 | 369-377 | NO | parcialmente sin liga | Sin asignar | Enteromorpha lingulata | A mutation which appears only in the haploid female state and affects the early development of Enteromorpha lingulata by disorienting direction of cell division is described. The atypical spheroid thallus is the result of interaction between Mendelian and |
Ficha | A developmental mutation in Enteromorpha lingulata J. Ag. (Chlorophyta, Ulvales) | Bart J. Baca and Elenor R. Cox | 369-377 | NO | Sin asignar | A mutation which appears only in the haploid female state and affects the early development of Enteromorpha lingulata by disorienting direction of cell division is described. The atypical spheroid thallus is the result of interaction between Mendelian and | |||
Ficha | Algae Anatomy, Biochemistry,and Biotechnology | Barsanti Laura and Paolo Gualtieri | NO | parcialmente completo con liga | General | ||||
Ficha | RAPD differetiation of Grateloupia lanceola and the invasive Grateloupia turuturu (Gigartinales, Rhodophyta) in the Iberian Peninsula | Barreiro R. and et. al. | NO | Rodofitas | |||||
Ficha | Fast sporophyte replacement after removal suggests banks of latent microscopic stages of Laminaria ochroleuca (phaeophyceae) in tide pools in northern Portugal | Barradas, A., Alberto, F., Engelen, A. H., & Serrào, E. A. | 52 | 435-439 | NO | Completo | Sin asignar | Recruitment l Bank of microscopic forms l Laminaria ochroleuca l Kelp canopy l Disturbance l Life history | This study investigated the effects of a physical disturbance consisting of the removal of adult kelps (Laminaria ochroleuca Bachelot de la Pylaie) and their corresponding understorey turf assemblage in tide pools in northe |
Ficha | New species of Polycavernosa Chang & Xia (Gracilariaceae, Rhodophyta) from the western Pacific. | Bangmei, X., & Abbott, I. A. | 26 | 405-418 | NO | parcialmente sin liga | Sin asignar | Four new species of Polycavernosa (Gracilariaceae) are described from the western Pacific: P. changii from Malaysia and Thailand; P. divergens from the Philippines; P. fisheri from Thailand; P. subtilis from Malaysia. Hydropuntia urvillei Montagne, origin | |
Ficha | Raphidophyceans on the coasts of Mexico | Band-Schmidt Christine J. and et. al. | 515 | 79-89 | NO | no completo | Fitoplancton | Chattonella marina, culture, Fibrocapsa japonica, Heterosigma akashiwo, raphidophyceae, Mexico | The presence of ichthyotoxic phytoflagellates Chattonella marina, Fibrocapsa japonica, and Heterosigma |
Ficha | Catálogo de las algas bentónicas (con exclusión de las diatomeas) de la costa catalana. | Ballesteros i Sagarra, E., & Romero, J. R. M. | 13 | 723-765 | NO | parcialmente sin liga | Sin asignar | A check-list of the benthic algae of the Catalan coast (NE of Spain) is presented. A bibliographical revision as well as many samples taken all along the Catalan coast have been the sources of this check-list. The gene- ral arrangement of the work is base | |
Ficha | Nuclear 18S rRNA gene sequeence analyses indicate that the Mastophoroideae (Corallinaceae, Rhodophyta) is a polyphyletic taxon | Bailey J. C. and et. al. | 43 | 03-dic | NO | Liga perdida | Rodofitas | ||
Ficha | Nuclear 18S rRNA gene sequence analyses indicate that the Mastophoroideae (Corallinaceae, Rhodophyta) is a polyphyletic taxon | Bailey et.al. 2004 | 43 | 03-dic | NO | Liga perdida | Rodofitas | ||
Ficha | Investigaciones sobre algas marinas de importancia industrial. | Baardseth, E. | 4 | 1 A 18 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Effects of boating activities on aquatic vegetation in the Stockholm archipelago, Baltic Sea | B.K. Eriksson, A. Sandström, M. Isæus, H. Schreiber, P. Karas | 339–349 | NO | Liga perdida | Sin asignar | recreational boating; ferry traffic; brackish community composition; charophytes; multivariate analyses; t-value biplot | The aquatic vegetation in 44 similar shallow and sheltered inlets exposed to different kinds of disturbances by boating was studied in a rocky archipelago in the Baltic Sea. The results indicate that both recreational boating activities and traffic by med | |
Ficha | Taxonomy and Biology of the Fresh Water Red Alga Compsopogon in Bihar, India | B.D. Sinha and N.K. Srivastava | 71-76 | NO | parcialmente sin liga | Sin asignar | Bihar, India; Compsopogon coeruleus (Balbis) Mont. y C. aeruginosus (J. Ag.) Kútz | Algological investigations of a fish pond and a lake at Muzaffarpur in the state of Bihar, India have shown the occurrence of two species of the fresh wáter red alga viz. Compsopogon coeruleus (Balbis) Mont. and C. aeruginosus (J. Ag.) Kútz. The biology o | |
Ficha | BLUE-GREEN ALGAE (CYANOBACTERIA) OF E OCEANIC COAST OF ALDABRA | B.A. Whitton and M. Potts | 238 | No | no completo | General | An account is given of the blue-green algae of the oceanic coast | ||
Ficha | An Updated and Annotated List of Marine Brown Algae (Phaeophyceae) of the Caribbean Coast of the Republic of Panama | B. Wysor and O. De Clerck | 46 | 151-160 | NO | Liga perdida | General | Thirty-six taxa of brown macroalgae (Phaeophyceae) are reported for the Caribbean coast of the Republic of Panama including 16 new records. Most of the species diversity is restricted to two families, Dictyotaceae and Sarga | |
Ficha | A Study Of A Green Unicellular Alga of Genus Botrydium Wallroth, Xanthophyta Found in Subtropic of Brasil, South America. | B. V. SKVORTZOV | 25 | ND | 84 | no completo | Sin asignar | Sao Paulo, Brasil; Botrydium Wall., Xanthophyta | The author gives the description of econogy, morthology and life history of a green unicellular alga of genus Botrydium Wall., Xanthophyta found in Sao Paulo in 1962-1963. Genus Botrydium is of a cosmopolitan distribution and is growing of sewage fields i |
Ficha | Nomenclature and typification of Gelidiella tenuissima (Gelidiales, Rhodophyta) | B. Santellces and J.M. Rico | 41 | 436-440 | NO | Liga perdida | Sin asignar | The nomenclature and the type material of the entity presently known as Gelidiella pannosa (Feldmann) Feldmann & Hamel are considered. It is concluded that C. tenuissima Feldmann & Hamel is the correct name for the | |
Ficha | Ecological studies for harvesting and culturing Gymnogongrus furcellatus (Rhodophyta, Gigartinales) in Central Chile | B. Santelices, P. Camus & A. J. Hoffmann | 171-181 | NO | Sin asignar | harvesting methods, seaweed cultivation, Gymnogongrus, sand invasion | Every year, several hundred tonnes of dry Gymnogongrus furcellatus are exported from Chile for carrageenan production. The present study provides ecological information for rational harvesting practices, including an understanding of the effects of enviro | ||
Ficha | Ecological studies for harvesting and culturing Gymnogongrus furcellatus (Rhodophyta, Gigartinales) in Central Chile | B. Santelices, P. Camus & A. J. Hoffmann | 1 | 171-181 | NO | parcialmente sin liga | Sin asignar | Harvesting methods, seaweed cultivation, Gymnogongrus, sand invasion. | Every year, several hundred tonnes of dry Gymnogongrus furcellatus are exported from Chile for carrageenan production. The present study provides ecological information for rational harvesting practices, including an understanding of the effects of enviro |
Ficha | A Review of Gracilaria Farming | B. Santelices and M. S. Doty | 78 | 95-133 | NO | Liga perdida | General | Close to 5000 tonnes (t) of agar are processed annually from 25 000 to 30 000 t of Gracilaria, harvested mainly from the wild in Chile, Argentina, Brazil and South Africa and from fishpond culture in Taiwan, Haina | |
Ficha | DEMOGRAPHIC CONSEQUENCES OF COALESCENCE IN SPORELING POPULATIONS OF MAZZAELLA LAMINARIOIDES (GIGARTINALES, RHODOPHYTA) | B. Santelices and J. L. Alvarado | 44 | 624-636 | NO | Completo | Rodofitas | coalescence; Mazzaella; red algae; settlement; survivorship curve | Coalescing macroalgae are ecologically important members of intertidal and shallow subtidal communities. However, we still lack quantitative information on the demographic consequences of coalescence. Using demogr |
Ficha | Ecological differences among Chilean populations of commercial Gracilaria | B. Santelices & R. Ugarte | 17-26 | 2638 | Sin asignar | agronomic traits, ecological differences, epiphytes, Gracilaria cultivation, sand abrasion, sand burial | Field farming of Gracilaria is gradually replacing use of the wild crop in Chile. The most popular planting method consists of establishing underground thallus systems for patches of Gracilaria on wave-sheltered, soft-bottom habitats. Commercial cultivati | ||
Ficha | Ecological differences among Chilean populations of commercial Gracilaria | B. Santelices & R. Ugarte | 2 | 17-26 | 2638 | no completo | Sin asignar | Agronomic traits, ecological differences, epiphytes, Gracilaria cultivation, sand abrasion, sand burial | Field farming of Gracilaria is gradually replacing use of the wild crop in Chile. The most popular planting method consists of establishing underground thallus systems for patches of Gracilaria on wave-sheltered, soft-bottom habitats. Commercial cultivati |
Ficha | Taxonomy of the Palmelloid Genera Gloeocystis Nägeli and Plmogloea Kützing (Chlorophyceae) | B. Fott and M. Novárová | 113 | 322-333 | 1269 | no completo | Sin asignar | no se alcanza a leer. | |
Ficha | Phosphorus- and nitrogen-limited photosynthesis and growth of Gracilaria tikvahiae (Rhodophyceae) in the Florida Keys: an experimental field study | B. E. Lapointe | 93 | 561-568 | No | no completo | General | The relative effects of NH4 + (N) and PO~- (P) on growth | |
Ficha | The Use of Nucleic Acid Sequence Data in Phylogenetic Reconstruction | B. D. Mishler, K. Bremer, C. J. Humphries and S. P. Churchill | 37 | 391-395 | 2757 | no completo | Sin asignar | ||
Ficha | Considerações sobre a Flora Algológica Marinha da Ilha da Trindade | Aylthon B . Joly | 1532 | no completo | Sin asignar | ||||
Ficha | Origin of the Existing Panamic Molluscan Biotas in Terms of their Geologic History and Their Separation by the Isthmian Land Barrier | Axel A. Olsson | 2 | 117-124 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Biological basis for the management of luga negra (Sarcothalia crispata Gigartinales, Rhodophyta) in southern Chile | Avila, M., Otaíza, R., Norambuena, R., & Nuñez, M. | 245-252 | NO | Completo | Rodofitas | Chile, management, Rhodophyta, Sarcothalia, seaweed | ||
Ficha | Interacciones de temperatura, densidad de flujo fotónico y fotoperíodo sobre el desarrollo de etapas microscópicas de Lessonia nigrescens (Phaeophyta, Laminariales). | Avila, M., Hoffmann, A. J., & Santelices, B. | 58 | 71-82 | NO | Liga perdida | Feofita | Se estudian los efectos de distintas combinaciones de temperatura, densidades de flujo fotónico y fotoperíodos sobre el desarrollo de meiosporas de Lessonia nigrescens Bory (Laminariales), proveniente de Pelan | |
Ficha | Reproductive biology of Gigartina skottsbergii (Gigartinaceae, Rhodophyta) from Chile. | Avila, M., Candia, A., Nuñez, M., & Romo, H | 149–157 | NO | Liga perdida | Rodofitas | cystocarps, Gigartina, phenology, reproductive phases, reproductive potential, spores, tetrasporangial sori, viability | Reproductive phenology and spore viability were studied in a natural bed of Gigartina skottsbergii at the locality | |
Ficha | Economic feasibility of Sarcothalia (Gigartinales, Rhodophyta) cultivation. | Avila, M., Ask, E., Rudolph, B., Nuñez, M., & Norambuena, R | 435–442 | NO | Liga perdida | Rodofitas | Sarcothalia, cultivation, Gigartinales | Studies to develop a technology for Sarcothalia cultivation were carried out based on results of a pilot scale farm. | |
Ficha | Biological basis for the management of "luga negra" (Sarcothalia crispata Gigartinales, Rhodophyta) in southern Chile | Avila et.al. | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Interacciones de temperatura, densidad de flujo fotónico y fotoperiodo sobre el desarrollo de etapas microscopicas de Lessonia nigrescens (Phaeophyta, Laminariales) | Avila et.al. | NO | parcialmente completo con liga | Sin asignar | ||||
Ficha | Interactive effects of grazing and environmental stress on macroalgal biomass in subtropical rocky shores: Modulation of bottom-up inputs by wave action | Augusto A.V. Flores, Ronaldo A. Christofoletti, Ana Luisa F. Peres, Aurea M. Ciotti, Sergio A. Navarrete | 39-48 | NO | Liga perdida | Sin asignar | Nutrient flux; Desiccation stress; Herbivory; Ephemeral algae; Ulva; Porphyra | In contrast to what is observed in most temperate regions, perennial macroalgae are rare at the mid intertidal level of tropical and subtropical shores, and energy transfer through benthic herbivores largely relies on the consumption of periphyton and eph | |
Ficha | C:N:P Ratios of Benthic Marine Plants | Atkinson M. J. and S. V. Smith | 28 | 568-574 | NO | parcialmente completo con liga | General | The median C:N:P atomic ratio of benthic marine macroalgae and seagrasses is about 550:30:1. Benthic plants are much | |
Ficha | Contents of Trace Metals in Water and Macroalgae along the Mediterranean Coast of Tunisia | Ati–Hellal M. El and et. al. | 78 | 30-34 | NO | no completo | General | Marine macroalgae are able to accumulate trace metals 2002). Moreover, these species are sedentary, wide- | |
Ficha | The genus Mesophyllum (Melobesioideae, Corallinales, Rhodophyta) on the north | Athanasiadis Athanasios and et. al. | 43 | 126-165 | NO | Liga perdida | Rodofitas | ||
Ficha | The genus Leptophytum (Melobesioideae, Corallinales, Rhodophyta) on the Pacific coast of North America | Athanasiadis A. and W. H. Adey | 45 | 71-115 | NO | Liga perdida | Rodofitas | adeyi, Corallinales, foecundum, juliceae, lamellicola, Leptophytum, Melobedioideae, microsporum, Rhodophyta, sandrae, taxonomy, tenue | |
Ficha | Boletín de la asociación Argentina de Ficología. | Asociación Argentina de Ficología | 1 A 10 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Boletín de la asociación Argentina de Ficología | Asociación Argentina de Ficología | ND | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Comparison of ITS RFLP patterns of Gracilaria (Rhodophyceae, Gracilariales) populations from Chile and New Zealand and an examination of interfertility of Chilean morphotypes | Arturo Candia et. al. | 11 | 185-193 | no completo | General | Chile, interfertility trials, Gracilaria, ITS region, morphotypes, PCR, RFLPs, New Zealand | Restriction fragment length polymorphism (RFLP) patterns of the internal transcribed spacer (ITS) of the nuclear ribosomal cistron and crossability trials were used to characterize four morphotypes of Gracilaria from Lenga, Isla Santa María and | |
Ficha | Development of Janczewskla Morlmotol (Ceramlales) on its Host Laurencia Nipponica (Ceramiales, Rhodophyceae) | Arthur M . Nonomura | 15 | 154- 162 | 2567 | no completo | Sin asignar | Ceramiales; endophyte, Janczewskia; Laurencia; life history, Janczewskia; parasitic algae; parasite, Janczewskia; Rhodophyta | Janczewskia morimotoi Tokida was successfully cultured from spore to reproductive maturity on its host Laurencia nipponica Yamada. The spore penetrates the host without requirement for wound or abrasion sites, growing between host cortical cell, and devel |
Ficha | Result of the Tektite Program Phycological Studies During Tektite II, AT ST. John, U.S.V.I. | Arthur C. Mathieson, Richard A. Fralick, Richard Burns and William Flashive | 20 | 77-103 | NO | parcialmente sin liga | Sin asignar | St. John, Virgin Island; Phaeophyta, Chlorophyta y Rhodophyta | A stucy of the distribution and abundance of benthic plants in Grea t Lameshur Bay, St. John, Virgin Islands was conducted in June 1970 during mission 4-50 of Tektite II. A comparison of the subtidal flora of New England (i.e., Jaffrey Point. New Hampshir |
Ficha | Seasonal Studies of Florida Sublittoral Marine Algae | Arthur C. Mathieson and Clinton J. Dawes | 25 | 46-65 | NO | parcialmente sin liga | Sin asignar | Los Cayos de Florida; Rhodophyceae, Chlorophyceae, Phaeophyceae. | The seasonal occurrence and reproduction of the sublittoral seaweed populations at four Florida sites are described, A total of 180 taxa were collected, including 105 Rhodophyceae, 49 Chlorophyceae, and 26 Phaeophyceae. The two southern sites in the Flori |
Ficha | Batimetría y morfometría de los lagos “maars” de la cuenca de Oriental, Puebla, México. | Arredondo-Figueroa, J. L., Borrego-Enríquez, L. E., Castillo-Domínguez, R. M., & Valladolid-Laredo, M. A. | 8 | 37-47 | NO | parcialmente sin liga | Sin asignar | A bathymetric and morphometric study of the volcanic lakes of the cuenca de Oriental in the state of Puebla, México, was carried out. The data was obtained from aerial photographs, contour maps and field observations. Fourteen morphometric parameters were | |
Ficha | Variable responses within epiphytic and benthic microalgal communities to nutrient enrichment | Armitage Anna R. and et. al. | 569 | 423-435 | NO | parcialmente completo con liga | General | chemotaxonomy, HPLC, Florida Bay, microphytobenthos, seagrass, subtropical estuaries | We evaluated how changes in nutrient supply altered the composition of epiphytic and benthic microalgal |
Ficha | The utilization of a filamentous green alga (Clad glomerata (l) kutzin) as a protein sourse in pellet feeds for Sarotherodon (Tilapia) niloticus fingeri. | Appler, H. N., Jauncey, K. | 30 | 21 a 30 | 3730 | no completo | Sin asignar | Duplicate groups of S. niloticus fingerlings were fed each of five different d 8 weeks. The diets contained 30% crude protein supplied by varying proportion fishmeal and C. glomerata meal. The five diets were formulated to supply fishn tein: C. g | |
Ficha | Pneophyllum conicum a coralline red alga causing coral reef-death in Mauritius | Antonius A. | 19 | 418 | NO | no completo | Rodofitas | ||
Ficha | Factors influencing human visitation of southern California rocky intertidal ecosystems | Anthony Garcia, Jayson R. Smith | 44-53 | NO | Liga perdida | Sin asignar | In highly urbanized regions, rocky intertidal habitats attract a large number of visitors for recreation, education, and subsistence harvesting. The collecting, trampling, and handling activities of visitors can have detrimental impacts on intertidal flor | ||
Ficha | Experimental Nutrient Enrichment Causes Complex Changes in Seagrass, Microalgae, and Macroalgae Community Structure in Florida Bay | Anna R. Armitage, Thomas A. Frankovich, Kenneth L. Heck, Jr., and James W. Fourqurean | 422-434 | NO | Liga perdida | Sin asignar | We examined the spatial extent of nitrogen (N) and phosphorus (P) limitation of each of the major benthic primary producer groups in Florida Bay (seagrass, epiphytes, macroalgae, and benthic microalgae) and characterized the shifts in primary producer com | ||
Ficha | Long-Term Effects of Adding Nutrients to an Oligotrophic Coastal Environment | Anna R. Armitage, Thomas A. Frankovich, and James W. Fourqurean | 14 | 430–444 | No | no completo | General | aboveground and belowground biomass; epiphyte; eutrophication; macroalgae; nutrient; press; pulse; ramp disturbances; seagrass. | Management of ecological disturbances requires an |
Ficha | Stable Isotopes Reveal Complex Changes in Trophic Relationships Following Nutrient Addition in a Coastal Marine Ecosystem | Anna R. Armitage & James W. Fourqurean | 32 | 1152–1164 | No | no completo | General | Caridean . Gastropod . Palatability . Shoalgrass. Turtle grass. Epiphytes. Nutrients | Complex links between the top-down and bottom- anthropogenic alterations of natural habitats. We used relative |
Ficha | Plant Communities of the Napeague Dunes | Ann F. Johnson | 76-84 | NO | Liga perdida | Sin asignar | Napeague Dunles; Ronkonkoma terminal moraine; Montauk; succession. | Using the Braun-Blanquet relevé method, this study documents the composition and soil profiles of three of the most mesic of the eight plant communities occurring on the Napeague Dunes, east of Amagansett, (Suffolk Co.) N.Y. Differentiation, both between | |
Ficha | Does a large-scale continuous algal production system provide a stable supply of fatty acids to bivalve hatcheries? | Anita Jacobsen, Otto Grahl-Nielsen & Thorolf Magnesen | 22 | 769–777 | no completo | Cultivo | Fatty acids. Continuous algal culture . Bivalve hatchery. Isochrysis sp. . Pavlova lutheri . Chaetoceros muelleri | The variation of fatty acid (FA) content and | |
Ficha | Morphological Variation in Acrosiphonia arcta (Codiolales, Chlorophyta) from Environmentally Different Habitats in Nova Scotia, Canada | Andrea V. Sussmann and Ricardo A. Scrosati | 113 | 87-105 | NO | no completo | General | Acrosiphonia arcta, Acrosiphonia spinescens, Acrosiphonia son- deri, estuarine, morphological variability, Northwest Atlantic, open coastal, Spongomorpha | We characterized the morphological variation and algal species |
Ficha | Plankton functional type modelling: running before we can walk? | ANDERSON THOMAS R. | 27 | 1073-1081 | NO | no completo | Fitoplancton | Biogeochemical cycling in marine systems is intimately linked to the activity of specific plankton focus for contemporary modelling studies. | |
Ficha | Survival of sand-burial by seaweeds with crustose bases or life-history stages structures the biotic community on an intertidal rocky shore | Anderson Robert J. and et. al. | 51 | 10–20 | NO | Liga perdida | Rodofitas | crusts; disturbance; Gymnogongrus; Mazzaella; sand-burial. | Responses of a rocky intertidal community to seasonal sand-inundation were investigated on the cool-temperate west coast of South Africa by experimentally testing the hypothesis that the crustose components i |
Ficha | Eighteenth International Seaweed Symposium | Anderson Robert and et. al. | 0 | NO | General | ||||
Ficha | Patterns in subtidal seaweed communities on coral-dominated reefs at Sodwana Bay on the KwaZulu-Natal coast, South Africa | Anderson RJ , C McKune, JJ Bolton, O DeClerck and E Tronchin | 27 | 529-537 | NO | parcialmente completo con liga | Sin asignar | coral reef algae, seaweed communities, seaweed diversity, Sodwana Bay, South Africa, turf algae | Subtidal seaweed communities of the northern coast of |
Ficha | Upwelling and fish-factory waste as nitrogen sources for suspended cultivation of Gracilaria gracilis in Saldanha Bay, South Africa | Anderson R. J. and et. al. | 455-462 | NO | no completo | Rodofitas | nitrogen, Gracilaria gracilis, cultivation, stable isotopes, ?15N | In Small Bay, Saldanha, the water becomes highly stratified in summer. The cold bottom layer (of upwelling | |
Ficha | Biology and systematics of heterokont and haptophyte algae | Andersen R. A. | 91 | 1508-1522 | NO | no completo | Feofita | chromalveolate; chromist; chromophyte; flagella; phylogeny; stramenopile; tree of life. | In this paper, I review what is currently known of phylogenetic relationships of heterokont and haptophyte algae. Heterokont algae |
Ficha | Spatial and temporal variations in sediment accumulation in an algal turf and their impact on associated fauna | Anchana Prathep - R.H. Marrs - T.A. Norton | 142 | 381-390 | NO | no completo | General | The relationships between the fauna inhabiting | |
Ficha | Clave para el Reconocimiento de los Generos de Algas Macrofitas del Intermareal Rocoso Bonaerense | Ana Parma, Marcela Pascual y Eugenia Sar | 15 | ene-29 | 2528 | no completo | Sin asignar | ||
Ficha | Variación de epifitismo en Stypopodium zonale (Lamouroux) Papenfuss a lo largo de un año. | Ana M. Suárez, Lucinio Gil y Reinaldo Posek. | 10 | ND | 2619 | no completo | Sin asignar | Fitobentos, epífitos, variaciones estacionales. | Se presentan las variaciones de la diversidad del epifitismo en el alga parda Stypopodium zonale (Lamouroux) Papenfuss (Dictyotales, Isogenerate) en el año. Se obtuvieron los índices de diversidad por Shannon-Weaver, el Índice de Riqueza de Margalef y el |
Ficha | Observaciones Preliminares de la flora algológica de la región de Tuxtepec Oaxaca | Amelia Samano Bishop | ND | 43 | no completo | Sin asignar | |||
Ficha | Pediastrum Acantostephanos Samano | Amelia Samano Bishop | ND | 90 | no completo | Sin asignar | |||
Ficha | Chara Tehuacanesis. Samano Adinterim | Amelia Samano Bishop | 233-234 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Estructura de los mantos de rodolitos de 4 a 55 metros de profundidad en la costa sur del estado de Espírito Santo, Brasil | Amado-Filho GM and et. al. | 33 | 399-410 | NO | no completo | Kelp | rodolitos, plataforma continental, distribución, comunidad epibéntica. | Los mantos de rodolitos son de las comunidades bentónicas más extensas de la plataforma continental brasileña, pero su |
Ficha | Biodiversidad en macroalgas marinas. Factores a considerar para su uso sustentable | Alveal V. K. | NO | parcialmente completo con liga | General | ||||
Ficha | Mass cultivation of the agar-producing alga Gracilaria chilensis (Rhodophyta) from spores | Alveal K. and et. al. | 148 | 77-83 | NO | no completo | Rodofitas | Grcrciluriu chilensis; Farming; Culture methods; Management; Mariculture | Grucifuria chifensis has been extensively cultivated in Chile by means of vegetative propaga- to muddy or sandy substrata at densities of abou |
Ficha | Effect of salinity and pH on growth and agar yield of Gracilaria tenuistipitata var. liui in laboratory and outdoor cultivation | Alvaro Israel and et. al. | 11 | 543-549 | NO | no completo | Cultivo | agar, Gracilaria tenuistipitata, growth, salinity, seawater pH | Acclimation responses of the red alga Gracilaria tenuistipitata var. liui collected on the northwest coast of Philip- conditi |
Ficha | Population biology of the subtidal kelps Macrocystis integrifolia and Lessonia trabeculata (Laminariales, Phaeophyceae) in an upwelling ecosystem of northern Chile: interannual variability and El Niño 1997-1998 | Alonso-Vega J.M. and et. al. | 78 | 33-50 | NO | no completo | Kelp | hábitat submareales, ecología de poblaciones y comunidades, procesos de extinción y recolonización, interacción planta-herbívoro, El Niño, La Niña. | Este trabajo describe la biología poblacional de Macrocystis integrifolia y Lessonia trabeculata durante |
Ficha | Plankton diatoms of the Gulf of California obtained by the G. Allan Hancock Expedition of 1936. | Allen, W. E. Plankton diatoms of the Gulf of California obtained by the G. Allan Hancock Expedition of 1936. University of Southern California Press. | 3 | 47-59 | 3851 | no completo | Sin asignar | ||
Ficha | A special effect of light on the Growyh of Chlorella Vulgaris | Allen Killam and Jack Myers | 43 | 569-572 | NO | parcialmente sin liga | Sin asignar | Emerson de Chlorella vulgaris | There is a special effect of light observable on growth of the Emerson strain of Chlorella vulgaris but not in the growth of other related algae. In darkness glucose supports only a very low rate of cell proliferation accompanied by formation of larger ce |
Ficha | Redefinición de Cediopsylla Jordan y Hoplopsyllus | Alfredo Barrera | 27 | 67-83 | 2752 | no completo | Sin asignar | D. F. y Volcán Popocateptl, México; Cediopsylla tepolita nov sp. y Hoplopsyllus (Hoplopsyllus) pectinatus nov sp. | Cediopsylla tepolita nov sp. and Hoplopsyllus (Hoplopsyllus) pectinatus nov sp. are described from near El Guarda, D. F., and Popocateptl Volcano, Mexico at latitudes higher than 2800m above sea level, ex Romerolagus diazi, a Paleolaginae rabbit, endemic |
Ficha | The Birds of the Isthmus of Panama | Alexander Wetmore | 2 | 211-216 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Effects of physical and biological disturbances on algal turfs in Kaneohe Bay, Hawaii | Alexander G. Cheroske, Susan L. Williams, Robert C. Carpenter | ene-34 | NO | Liga perdida | Sin asignar | Algal turfs; Coral reef; Disturbance; Hawaii; Herbivores; Hydrodynamics; Macroalgae | Disturbance in coral reef environments commonly results in an algal community dominated by highly productive, small filamentous forms and cyanobacteria, collectively known as algal turf. Research on the types of disturbance responsible for this community | |
Ficha | Macroalgas marinas del Estado Falcón (Venezuela). I. | Albornoz, O. | 17 | 1 A 34 | 3790 | no completo | Sin asignar | Se estudiaron las algas colectadas entre los años 1971 y 1979 en las localidades de Punta Varadero, Ad1cora, Tumatei (Piedras Negras), Puerto Escondido y Cabo San Román, pertenecientes a la costa del Estado Falcón. Se identificaron 20 especies correspondi | |
Ficha | Effects of different light conditions on Lyngbya sp. in culture. | Albertano, P., & Grilli Caiola, M. Effects of different light conditions on Lyngbya sp. in culture. Algological Studies/Archiv für Hydrobiologie, Supplement Volumes, 47-54. | 47-54 | NO | parcialmente sin liga | Sin asignar | Unialgal cultures of a red pigmented Lyngbya sp. which grows on frescoes at very low ligh intensity, are studied under illumination provided by lamps with differcnt spectrai composition at various light intensities. Incandescent or fluorescent lamp effect | ||
Ficha | Kelp harvesting fleet dynamics and the fleet's dependence on Laminaria forests in the Iroise Sea (North Finistere, France) | Alban F. and et. al. | NO | Kelp | |||||
Ficha | The life history of a monoecious species of Callithamnion (Rhodophyta, Ceramiaceae) in culture | Alan Whittick and John A. West | 18 | 30-37 | NO | parcialmente sin liga | Sin asignar | Massachusetts, EE. UU. Y Terranova, Canadá; Callithamnion baileyi Harv. | The life history of an alga, tentatively referred to Callithamnion baileyi Harv., has been examined in cultured isolates from Massachusetts, U.S.A. and Newfoundland, Canada. A sequence of monoecious gametophytes, carposporophytes and tetrasporophytes is d |
Ficha | Marine benthic algae of North East Herald Cay, Coral Sea, South Pacific | Alan J. K. Millar | 398/399 | 65-74 | NO | no completo | General | Australia, Coral Sea, marine algae, taxonomy, biogeography. | The marine benthic algae from North East Herald Cay, Coral Sea, South Pacific, are listed with taxonomic, bibliographic and biogeographic details. The checklist includes 66 species of which 23 are green, 2 are brown, and 41 |
Ficha | Rocky shore turfs dominated by Corallina (Corallinales, Rhodophyta) in northern Japan | Akioka H. and et. al. | 47 | 199–206 | NO | parcialmente completo con liga | General | algal turfs, Corallina, coralline algae, inter- tidal ecology, Japan, Rhodophyta. | Three intertidal sites dominated by Corallina turfs were investigated in Hokkaido, Japan. The sites (A, B and C) differed in slope, wave exposure and length of time exposed to air during tidal cycles. Monthly |
Ficha | Species of the Genus Thalassiosira (Bacillariophyceae) from the Gulf of Tehuantepec, Mexico | Ake´-Castillo J. A. and et. al. | 42 | 487-503 | NO | no completo | Fitoplancton | Species of the diatom genus Thalassiosira are an important component of the marine phytoplankton all over | |
Ficha | Male organs of Gelidium amansii LMX., Gelidium pacifium Okam., and Gelidium pusillum (Stackh.) Le Jol. | Akatsuka, I. | 18 | 112-115 | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Responses of turf-forming algae to spatial variations in the deposition of sediments | Airoldi L. and Massimiliano Virgilio | NO | parcialmente completo con liga | General | ||||
Ficha | Microdictyon (Chlorophyta, Anadyomenaceae) do Estado da Bahia, Brasil | Aigara Miranda Alves et. al. | 11 | 57-61 | NO | no completo | General | macroalgae, Northeast Brazil, phycology, taxonomy. | Abstract (Microdictyon (Chlorophyta, Anadyomenaceae) from the State of Bahia, Brazil) –A morpho-taxonomic study of |
Ficha | A fast algal bioassay for assessment of copper toxicity in water using Euglena gracilis | Ahmed Hoda& Donat-Peter Häder | 22 | 785-792 | NO | parcialmente completo con liga | Cultivo | Euglena gracilis. Copper. PAM . Motility. Bioassay | A rapid, sensitive algal bioassay was investigated |
Ficha | Liquenes. | Ahmadjian, V. | 1 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Marine algae from the Gulf of Santa Clara, Sonora, M´exico | Aguilar-Rosas L.E. and et. al. | NO | General | |||||
Ficha | El género Colpomenia (Scytosiphonaceae, Phaeophycota) de las costas de México | Aguilar- Rosas L.E. and et. al. | 3 | NO | parcialmente completo con liga | Feofita | |||
Ficha | Nya alger Fran Mexico | Agardh | 0 | may-17 | NO | General | |||
Ficha | THE IMPACT OF SPECIES CONCEPT ON BIODIVERSITY STUDIES | Agapow et. al. | NO | parcialmente completo con liga | Sin asignar | ||||
Ficha | An endophytic Streblonema (Phaeophyta) associated with galls in Fucus spiralis (Phaeophyta) from the Canary Islands. | Afonso-Carrillo, J., Sanson, M., Gil-Rodríguez, M. C., Chacana, M., & Reyes, J. | 1 | 73-76 | 3907 | no completo | Sin asignar | Un Streblonema (Phneophvta) endofítico asociado con agallas en el Fucus spiralis en las Islas Canarias. Se observaron agallas verrucosas de 1-7 mm de diámetro en el engrosamiento central de las plantas de Fucus spiralis. Las agallas presentan una estructu | |
Ficha | Adiciones y correlaciones al catálogo de algas marinas bentónicas para el Archipiélago Canario. | Afonso-Carrillo, J., Gil-Rodríguez, M. C., Hauroum T., R., Villena B., M. & Wildpret De la Torre, W. | 13 | 27 - 49 | NO | parcialmente sin liga | Sin asignar | The catalogue of benthic algae in the Canarian Archipelago is exten- ded to include thirteen new species; two Chlorophyta : Caulerpa sertula- rioides (Gmelin) Howe and Gayralia oxysperma (Kützing) Vinogradova; three Phaeophyta :Dictyota ciliolata Kützing | |
Ficha | Sobre la presencia de un fondo de" Maerl" en las Islas Canarias. | Afonso-Carrillo, J., & Gil-Rodríguez, M. C. | 13 | 703-708 | NO | parcialmente sin liga | Sin asignar | The presence of the vegetal formation "maerl", well known on the european coasts, has been detected of the E. coast of Tenerife on the sea bed at a depth of between 20 t o 60 m. It is composed principally of the accumulation of arbuscular stems of Lith | |
Ficha | Datos para la flora marina de la Isla de Fuerteventura. | Afonso-Carrillo, J. & Gil-Rodriguez, M. C. | 10 | 147-170 | NO | parcialmente sin liga | Sin asignar | This paper presents the results of a study of the marine flora of island of Fuerteventura, the least know in the Canary Archipelago from a ficological point of view. A catalogue comprising 139 species has been prepared, and data is presented that demostra | |
Ficha | Sobre el límite meridional de Sauvageaugloia Chordariaeformis (Crouan) Kylin (Chordariaceae, Phaeophyta). | Afonso-Carrillo, J. & Gil-Rodriguez, M. C. | 45 | 297-300 | 3899 | no completo | Sin asignar | Sauvageaugloia chordariaeformis fue encontrada en las Islas Canarias en el verano de 1976. La localidad en que fueron recolectados dos ejemplares adultos y fructificados representa el nuevo límite meridional de su distribución geográfica, que estaba fijad | |
Ficha | Estudios en las algas Corallinaceae (Rhodophyta) de las Islas Canarias. II. Notas taxonomicas. | Afonso-Carrillo, J. | 13 | 127-144 | NO | parcialmente sin liga | Sin asignar | The study of the type material according to modern systemtic has revealed a new taxonomic position of some crustose coralline algae of Canary Island. In this paper the following new combinations are proposed: Neogoniolithon hirtum (Lemoine) Afonso-Carrill | |
Ficha | Algunas observaciones sobre la distribución vertical de las algas en la isla del Hierro (Canarias). | Afonso-Carrillo, J. | 10 | 3 A 16 | NO | parcialmente sin liga | Sin asignar | On several locality at Hierro the vertical distribution of the algae is studied. The ecological notes pointed to analogy with the south of Tenerife littoral vegetation. Thuretella schousboei (Thuret) Schmitz y Dudresnaya verticillata (With.) Le Jol. Repre | |
Ficha | Nota sobre algunas corallinaceae (Rhodophyta) nuevas para la flora ficológica de las Islas Canarias. | Afonso-Carrillo, J. | 10 | 53-58 | NO | parcialmente sin liga | Sin asignar | Four species of Corallinaceae, Amphiroa fragilissima (L. ) L amx., Jania adhaerens Lamx. , Schmitziella endophlaea Borne t et Batters y Cho- reonema thuretii (Bornet) Schmitz, have been recorded on the cast ofthe Canary Islands for the first time. Ecologi | |
Ficha | Estudios en las algas Corallinaceae (Rhodophyta) de las Islas Canarias. I. Aspectos metodológicos. | Afonso-Carillo, J., Gil-Rodriguez, M. C., & Wildpret De la Torre, W. | 13 | 113-125 | NO | parcialmente sin liga | Sin asignar | The metodology for study of species of the Corallinaceae family is described in this paper. Plants of Corallinaceae were collected and fixed immediately in 4% formalin-seawater. After morphologycal study, selected parts of the fixed material were decalcif | |
Ficha | The diversity of harmful algal blooms: a challenge for science and management | Adriana Zingonea, Henrik Oksfeldt Enevoldsen | 43 | 725-748 | No | no completo | General | A broad spectrum of events come under the category of harmful algal blooms (HABs), the | |
Ficha | Macroalgal Responses to Nitrogen Source and Availability: Amino Acid Metabolic Profiling as a Bioindicator Using Gracilaria Edulis (Rhodophyta) | Adrian B. Jones, William C. Dennison, and George R. Stewart | 757-766 | NO | Liga perdida | Sin asignar | amino acids; bioindicator; Gracilaria edulis; macroalgae; metabolic profiling; nutrients; pigments; Rhodophsta; tissue nitrogen; water quality | The use of macroalgae as biological indicators of dissolved nutrient source and availability in the water column was investigated. Total tissue nitrogen (N) content, pigments, and amino acids of the red alga Gracilaria edulis (Gmelin) Silva were compared | |
Ficha | The genus Amphiroa (Lithophylloideae, Corallinaceae, Rhodophyta) from the temperate coasts of the Australian continent, including the newly described A. klochkovana | Adele S. Harvey, William J. Woelkerling And Alan J.K. Millar | 258–290 | NO | Liga perdida | Sin asignar | Studies of Amphiroa (Lithophylloideae, Corallinaceae, Rhodophyta) from the temperate coasts of Australia provide new evidence that differences in tetrasporangial conceptacle pore canal anatomy are diagnostically significant in delimiting species within th | ||
Ficha | Zygnemataceae (Conjugales, Chlorophyceae) of the river Segura basin, southeastern Spain. | Aboal, M. | 47 | 389-402 | NO | parcialmente sin liga | Sin asignar | Dentro de un estudio que abarca algunas localidades del sureste español, en especial de la cuenca de río Segura, se presentan los datos referentes a las Zignrmatáceas. Se recopilan un total de 25 especies de las que se aportan descripciones morfológicas, | |
Ficha | Algas | Aboal Sanjurjo Marina | NO | General | |||||
Ficha | EPIZOIC ALGAE OF NESTING SEA TURTLES CARETTA CARETTA (L.) AND CHELONIA MYDAS (L.) FROM THE MEXICAN CARIBBEAN | Abel Sentíes G., J. Espinoza-Avalos and J. C. Zurita | 64 | 185-188 | NO | no completo | General | The epizoan and commensal organisms of marine turtles have been documented in several investigations (Ernst and Barbour, 1972; Frazier et al., 1985; Caine, 1986; Dodd, 1988; Monhanty-Hejamdi et al., 1989; Frazier | |
Ficha | RELATIONSHIP OF WALL BIOCHEMISTRY TO ENVIRONMENTALLY INDUCED MORPHOLOGICAL CHANGES IN THE DIATOM, PHAEODACTYLUM TRICORNUTUM (BACILLARIOPHYCEAE). | Abdullahi Abass S. and et. al. | NO | Fitoplancton | |||||
Ficha | Observations on Liagorophila endophytica, a rare species in the Acrochaetiaceae (Rhodophyceae). | Abbott, I. A. | 2 | 147-150 | 3828 | no completo | Sin asignar | ||
Ficha | Some new species and new combinations of marine red algae from the central Pacific | Abbott Isabella A. | 46 | 97-109 | NO | no completo | General | Ceramium, Chondracanthus, Dasya, Haiymenia, Poiyopes, Prionitis. | Six new species in five genera of Rhodophyta are de- is also proposed. These taxa were encountered while Islands. Am |
Ficha | Taxomomic of economic seaweeds with reference to the Pacific and other locations | Abbott I.A. and K. J. McDermid | NO | parcialmente completo con liga | General | ||||
Ficha | Taxonomy of Economic Seaweeds: With Reference to Some Pacific Species | Abbot I. A. and K. McDermid | 15 | 91 | NO | no completo | General | ||
Ficha | The stable isotope of nitrogen in an experimental culture of Ulva spp. and its assimilation in the nutrition of white shrimp Litopenaeus vannamei, Baja California Sur, Mexico | A.Sánchez, I. Sánchez-Rodríguez, M. Casas-Valdez | 24 | 507-511 | NO | no completo | General | Stable nitrogen isotope . Seaweeds . Shrimp . Ulva spp. . Commercial food | Stable nitrogen isotope ratios have been used to |
Ficha | A guide to nongeniculate coralline red algal (Corallinales, Rhodophyta) rhodolith identification | A.S. Harvey and W.J. Woelkerling | 33 | 411-426 | NO | Liga perdida | Rodofitas | rhodolith, coralline algae, identification, Corallinales. | Rhodoliths are free-living structures composed mostly of nongeniculate coralline red algae. Species that form rhodoliths usually cannot be identified with certainty using only growth form or other external morphologica |
Ficha | Some additional figures of the desmind Staurostrum paradoxum | A.J.Brook | 3 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Taxonomic sufficiency and the increasing insufficiency of taxonomic expertise | A. Terlizzi, et. al. | 46 | 556-561 | NO | no completo | General | Taxonomic sufficiency; Taxonomy; Environmental impact assessment; Biological conservation | Taxonomic sufficiency (TS) involves the identification of taxa only to a level of taxonomic resolution sufficient to permit the |
Ficha | Is benthic food web structure related to diversity of marine macrobenthic communities? | A. Soko1owski et. al. | 108 | 76-86 | NO | no completo | General | macrobenthic communities biodiversity food web structure diversity-structure interactions European waters | Numerical structure and the organisation of food webs within macrozoobenthic communities has been |
Ficha | Testing taxonomic resolution, data transformation and selection of species for monitoring macroalgae communities | A. Puente, J.A. Juanes | 78 | 327-340 | NO | no completo | General | taxonomic resolution; macroalgae; monitoring; multivariate analysis; transformation; cost-effectiveness; Water Framework Directive; Habitat Directive; coastal waters; Spain | The Water Framework and Habitats Directives require the evaluation of both the conservation and ecological status of macroalgae commu- |
Ficha | Quality Index of Subtidal Macroalgae (QISubMac): A suitable tool for ecological quality status assessment under the scope of the European Water Framework Directive | A. Le Gal, S. Derrien-Courtel | 334-348 | NO | Liga perdida | Sin asignar | Ecological quality status; Indicators; Subtidal macroalgae; Rocky bottom; QISubMac; Water Framework Directive | Despite their representativeness and importance in coastal waters, subtidal rocky bottom habitats have been under-studied. This has resulted in a lack of available indicators for subtidal hard substrate communities. However, a few indicators using subtida | |
Ficha | Pilot Studies for Designs of Surveys of Human Disturbance of Intertidal Habitats in New South Wales | A. J. Underwood and S. J. Kennelly | 41 | 165-173 | NO | parcialmente sin liga | Sin asignar | Data are presented from pilot studies as the first step in the design of large-scale surveys of the effects of human recreational activities on intertidal habitats in New South Wales. People visiting the seashore were counted and interviewed. Numbers of o | |
Ficha | Sinking rates and viability of spores from benthic algae in central Chile | A. J. Hoffmann and P. Camus | 126 | 281-291 | NO | Liga perdida | General | Dispersal; Germination; Intertidal; Seaweed; Sinking rate; Spore | Spore-sinking rates and viability were studied in 12 species of benthic macroalgae from the intertidal zone in central Chile: two Chlorophyta, Enteromorpha intestinalis (L.) Link and UIva rigida C. Ag.; one Phaeophyta, Less |
Ficha | How Uniform is the Thallus of the Alga, Ulva? | A. J. Bernatowlcz | 18 | ND | NO | parcialmente sin liga | Sin asignar | ||
Ficha | Oceanography and the Mariner | A. J. Barther | 01-ago | NO | parcialmente sin liga | Sin asignar | Oceanography can be properly defined as a combination of sciences which deals with physical, chemical, biological, and dynamic propieties, as well as other phenomena found in, on, and around the earth´s hydrosphere exclusive of strictly freswater bodies. | ||
Ficha | Aspects of Spore Production in the Red Alga Ceramium | A. H. L. Chamberlain and L. V. Evans | 76 | 139--159 | 1386 | no completo | Sin asignar | Tetraspore development from the post-meiotic to the mature stage has been studied using light and electron microscopy and histochemistry. The structure of the mature carpospore is identical to that of the tetraspore suggesting a similar developmental sequ | |
Ficha | Determinants of disease expression and survival of infected individual fronds in wild populations of Mazzaella laminarioides (Rhodophyta) in central and southern Chile | A. H. Buschmann et. al. | 154 | 269-280 | NO | Completo | Rodofitas | Endophytes . Mazzaella . Transplant experiment Survivorship . Herbivore preference . Chile | study provides evidence that the expression of a deformative disease in wild populations of the red algal host Mazzaella laminarioides is strongly influenced by exogenous factors. This was particularly the case for a p |
Ficha | Checklist of Mediterranean Seaweeds. III. Rhodophyceae Rabenh. 1. Ceramiales Oltm. | A. Gómez Garreta et. al. | 44 | 425-460 | NO | Liga perdida | General | An annotated checklist of the Ceramiales (Rhodophyceae; red algae) of the Mediterranean, based on literature records, is given. The distribution of each taxon in the area (which is divided into 16 regions) is reported. The | |
Ficha | Use of δ15N signatures of different functional forms of macroalgae and filter-feeders to reveal temporal and spatial patterns in sewage dispersal | A. Gartner, P. Lavery, A. J. Smit | 235 | 63–73 | No | no completo | General | Stable isotopes · δ15N · Nitrogen · Sewage · Marine macroalgae · Reefs · Western Australia | We examined whether δ15N levels of marine biota with different nutrient uptake character- whether they can reveal the dispersal |
Ficha | Zoospore Structure and Colony Formation in Pediastrum Spp. and Hydrodictyon reticulatum (L.) Langerheim | A. F. Hawkins and G. F. Leedale | 35 | 201-211 | 1421 | no completo | Sin asignar | Meyen, P. tetras (Ehren- berg) Ralfs, P. duplex Meyen, y reticulatum Hydrodictyon (L.) Lagerheim | The process of daughter colony formation in Pediastrum biradiatum Meyen, P. tetras (Ehren- berg) Ralfs, P. duplex Meyen, and Hydrodictyon reticulatum (L.) Lagerheim has been investi- gated using light microscopy and electron microscopy of thin sections. T |
Ficha | Premiere contribution a l'etude des phytocenoses de la Manche orientale (du cap Levy à la bale de Veys) | A. Duglet | 22 | 206-217 | 1723 | no completo | Sin asignar | Various factors account for the qualitative and quantitative distribution of benthic macroalgal species. Study of the phytocoerioses in the baie des Veys during a complete seasonal cycle and comparisons with different samplings areas allow to establish a | |
Ficha | Algas marinas poco comunes de la flora mexicana. IX-Colacodasya califomica Hollenberg (Rhodophycophyta-Dasyaceae). | A. Catalina Mendoza-González y Luz Elena Mateo-Cid | 35 | 23-28 | 2811 | no completo | Sin asignar | San José del Cabo, Baja California, Méx.; Colacodasya califonica Hollenberg | En este trabajo se describen los talos tetraspóricos, gametofíticos masculinos y feme- ninos de la especie "parásita" Colacodasya califonica Hollenberg colectada en San Jose del Cabo, Baja California Sur, se trata de un nuevo registro para las costas mexi |
Ficha | Avances de un Estudio sobre las Macroalgas Marinas de Guerrero y Oaxaca, México | A. Catalina Mendonza-González, Luz Elena Mateo-Cid | 15-29 | NO | Liga perdida | Sin asignar | FOTO | ||
Ficha | Spyridiocolax and Heterodasya two new genera of the Rhodophyceae | A. B. Joly and E. Cabral De Oliveira Filho | 18 | 115-125 | 1540 | no completo | Sin asignar | The present paper gives the descriptlons or two ne w genera or marine Rhodophyta, namely Spyridloeolax and Heterodasya found along the Brazlllan shores. The first one Is based on Spyridiocolax capixaba, also a new species here described, that is a parasit | |
Ficha | The Titanic 50 Years Later | 0. L. Martin. Jr. | 35-44 | NO | parcialmente sin liga | Sin asignar | |||
Ficha | Culturing Techniques | 0 | 70 | no completo | Sin asignar | ||||
Ficha | Maintenance of algal cultures | 0 | 71 | no completo | Sin asignar | ||||
Ficha | Variability in per capita oogonia and sporophyte production from giant kelp gametophytes (Macrocystis pyrifera, Phaeophyceae) | MUÑOZ VERÓNICA and et. al. | 77 | 639-647 | NO | no completo | Feofita | gametofitos, Macrocystis pyrifera, nutrientes, producción de oogonios, producción de esporofitos, temperatura. | El crecimiento vegetativo y la fertilidad de gametofitos de huiros son antagónicos, de modo tal, que un |
Ficha | Mariculture of Kappaphycus alvarezii (Rhodophyta, Solieriaceae) color strains in tropical waters of Yucata´n, Me´xico | Muñoz Julieta, Yolanda Freile-Pelegr?´n, Daniel Robledo | NO | Cultivo | |||||
Ficha | Biochemical characterization of carotenoids in two species of Trentepohlia (Trentepohliales, Chlorophyta) | Mukherjee Rumila and et.al., | 22 | 569-571 | NO | no completo | Clorofita | Algae . Trentepohlia . Carotenoid . HPLC | Two species of Trentepohlia, i.e., Trentepohlia |
Ficha | Performance benefits of growth-form plasticity in a clonal red seaweed | MONRO KEYNE and ALISTAIR G. B. POORE | 97 | 80–89 | NO | Completo | Rodofitas | clonal growth – modular organism – phenotypic plasticity. | Phenotypic plasticity may be adaptive if the phenotype expressed in a focal environment performs better there relative to alternative phenotypes. Plasticity in morphology may particularly benefit modular organisms that must |
Ficha | TOTAL AMMONIA CONCENTRATIONS IN SOIL, SEDIMENTS, SURFACE WATER AND GROUNDWATER ALONG THE WESTERN SHORELINE OF BISCAYNE BAY WITH THE FOCUS ON BLACK POINT AND A REFERENCE MANGROVE SITE | Meeder John and Joseph N. Boyer | NO | General | |||||
Ficha | A direct comparison of the performance of the seaweed biofilters,Asparagopsis armata and Ulva rigida | Mata Leonardo& Andreas Schuenhoff & Rui Santos | 22 | 639-644 | NO | no completo | Clorofita | Asparagopsis armata . Seaweed biofilter. Integrated aquaculture . Ulva rigida | The tetrasporophyte of Asparagopsis armata has been previously established as a novel seaweed biofilter for integrated land-based mariculture. The species growth and biofiltration rates were much higher than the values described in |
Ficha | Potential of the seaweed Gracilaria lemaneiformis for integrated multi-trophic aquaculture with scallop Chlamys farreri in North China | Mao Yuze and et. al. | 21 | 649-656 | NO | no completo | Cultivo | Gracilaria lemaneiformis. Integrated Multi-trophic Aquaculture (IMTA) . Nutrient uptake rate . Nutrient reduction efficiency . Scallop | In this study the red alga, Gracilaria lemanei- an integrated multi-trophic aquaculture (IMTA) system for |
Ficha | Mechanical and biological consequences of repetitive loading: crack initiation and fatigue failure in the red macroalga Mazzaella | Mach K. J. | 961-976 | NO | Completo | Rodofitas | fatigue, crack initiation, crack growth, breakage, life history phases, endophytes, Mazzaella, macroalgae, seaweed, biomechanics. | On rocky shores, wave-swept macroalgae experience dramatic and repeated wave-induced hydrodynamic forces. However, previous studies of macroalgal mechanics have shown that individual waves are not forceful enough to account | |
Ficha | Production of Macrocystis pyrifera (Laminariales; Phaeophyceae) in northern Chile on spore-based culture | Macchiavello Juan and et. al. | 22 | 691-697 | NO | no completo | Feofita | Abalone . Chile . Kelps. Macrocystis. Mariculture . Seaweeds | Since the establishment of abalone farming, there |
Ficha | A comparative analysis of agarans from commercial species of Gracilaria (Gracilariales, Rhodophyta) grown in vitro | Macchiavello Juan and et. al. | 397-400 | NO | Completo | Rodofitas | agar, agarans, 3,6-anhydrogalactopyranose, Gracilaria, seaweed, Brazil | The agaran yield, 3,6-anhydrogalactopyranose (3,6-AG) and sulphate content were compared in four commercial species of Gracilaria grown under parallel conditions in vitro. Gracilaria chilensis Bird, McLachlan et Oliveira fr | |
Ficha | Biodiesel production from algal oil using cassava (Manihot esculenta Crantz) as feedstock | Lu Yue and et. al. | 22 | 573–578 | NO | no completo | General | Biodiesel . Cassava (Manihot esculenta Crantz) . Chlorella protothecoides. Fermentation | As a potential source of biomass supplies, |
Ficha | Responses of the macroalga Gracilaria tenuistipitata var. liui (Rhodophyta) to iron stress | Liu Jingwen and et. al. | 12 | 605-612 | NO | no completo | Rodofitas | carbon fixation, Gracilaria tenuistipitata var. liui, iron stress, iron uptake | Chlorophyll (Chl), phycoerythrin (PE), total nitrogen (TN% dw) and Fe in tissues were measured in Fe-deficient |
Ficha | Unusual linear arrays of the coral reef macrophyte Halimeda incrassata in the Bahamas | Littler M. M. and et. al. | 26 | 817-818 | NO | no completo | Clorofita | ||
Ficha | Spatial and temporal variation in distribution of Gelidium canariensis (Rhodophyta) from natural populations of the Canary Islands | Lindgren A. and et. al. | 10 | 273-278 | NO | no completo | Rodofitas | Canary Islands, Gelidium canariensis, hierarchical sampling, spatial variation, temporal variation | This study was designed to investigate spatial and temporal variation in Gelidium canariensis populations at two |
Ficha | A MORPHOLOGICAL STUDY AND TAXONOMIC REASSESSMENT OF THE GENERITYPE SPECIES IN THE GRACILARIACEAE1 | Liao Lawrence M. and Max H. Hommersand | 39 | 1207-1232 | NO | no completo | Rodofitas | cystocarp; Gracilariaceae; Graci- lariales; marine algae; morphology; Rhodophyta; taxonomy | We investigated the reproductive morphology of |
Ficha | GREEN ALGAE AND THE ORIGIN OF LAND PLANTS | LEWIS LOUISE A. AND RICHARD M. MCCOURT | NO | Clorofita | |||||
Ficha | Management of natural Ulva spp. blooms in San Quintin Bay, Baja California: Is it justified? | Jorgensen Pablo & et. al. | 22 | 549-558 | NO | no completo | Clorofita | Zostera marina . Ulva bloom . Grazer control . Oyster culture . Seagrass management | According to Zertuche-González et al. (2009), Ulva spp. blooms, favored by oyster cultivation, are likely |
Ficha | Evaluation of the toxicity of Arthrospira (Spirulina) platensis extract | Hutadilok-Towatana Nongporn & et. al. | 22 | 599-605 | NO | no completo | Clorofita | Acute toxicity. Arthrospira platensis. Blue-green algae . Methanol extract . Spirulina . Subchronic toxicity | In this study, the methanol extract of Arthrospira |
Ficha | Use of Acadian marine plant extract powder from Ascophyllum nodosum in tissue culture of Kappaphycus varieties | Hurtado Anicia Q. and et. al. | 21 | 633-639 | NO | no completo | Cultivo | Soluble seaweed extract powder. Tissue culture . Shoot growth . Kappaphycus | Three varieties of Kappaphycus alvarezii |
Ficha | Biogeography of the marine red algae of the South African West Coast: a molecular approach | Hommersand Max H & Suzanne Fredericq | 0 | 01-nov | NO | parcialmente completo con liga | Rodofitas | red algae, South Africa, Namibia, biogeography, distribution, phylogeny, species clusters | This study investigates the hypothesis that a major portion of the present red algal flora of the South African |
Ficha | Species of the planktonic diatom genus Pseudo-nitzschia of the Pacific coasts of Mexico | Hernandez-Becerril David U. | 379 | 77-84 | NO | no completo | Fitoplancton | planktonic diatoms, Pseudo-nitzschia, distribution, Mexican Pacific, Domoic acid | Species of the diatom genus Pseudo-nitzschia are common in the marine phytoplankton world-wide. Some species |
Ficha | Biofiltering efficiency in removal of dissolved nutrients by three species of estuarine macroalgae cultivated with sea bass (Dicentrarchus labrax) waste waters 2. Ammoniumbass | Hernández I. and et. al | 14 | 375-384 | NO | no completo | Cultivo | Aquaculture, Ecological engineering, Enteromorpha, Gracilaria, Nitrogen, Ulva | Three estuarine macroalgae (Ulva rotundata, Enteromorpha intestinalis, Gracilaria gracilis) of economic poten- a sea bass (D |
Ficha | Linnaeus was right all along: Ulva and Enteromorpha are not distinct genera | HAYDEN HILLARY S. and et. al. | 38 | 277-294 | NO | no completo | Clorofita | Chloropelta, Enteromorpha, nuclear ribosomal internal transcribed spacer DNA (ITS nrDNA), rbcL, Ulva, Umbraulva | Ulva, one of the first Linnaean genera, was later circumscribed to consist of green seaweeds with distromatic blades, and |
Ficha | MOLECULAR SYSTEMATICS OF THE FLORIDEOPHYCEAE (RHODOPHYTA) USING NUCLEAR LARGE AND SMALL SUBUNIT rDNA SEQUENCE DATA | Harper James T. and Gary W. Saunders | 37 | 1073-1082 | NO | parcialmente completo con liga | Rodofitas | Florideophyceae; group I intron; large subunit rDNA; molecular phylogeny; red algae; Rhodo- phyta; small subunit rDNA; systematics; taxonomy | Sequence data are presented for approximately for one member of the Bangiophyceae and 47 mem- all but one of the currently rec |
Ficha | Comparative phosphate acquisition in giant-celled rhizophytic algae (Bryopsidales, Chlorophyta): Fleshy vs. calcified forms | Demes, Kyle W. a, Mark M. Littler b, Diane S. Littler | 92 | 157-160 | NO | no completo | Clorofita | Bryopsidales; Calcification; Nutrient uptake; Phosphate; Rhizoids | Phosphate uptake through above-ground thalli vs. subterranean rhizoids has been compared in |
Ficha | SEAWEEDS AND THEIR MARICULTURE | Chopin T. and M. Sawhney | 0 | 4477-4486 | NO | parcialmente completo con liga | Cultivo | ||
Ficha | PATRÓN DE DISTRIBUCIÓN DE MACROALGAS EN UN CANAL DE CORRIENTES | Candelaria Silva Carlos F. and et. al. | 9 | 65-72 | NO | no completo | General | Comunidades de macroalgas marinas, distribución ecológica, ecología intermareal, patrones de zonación. | Los canales de corrientes son uno de los ambientes rocosos intermareales reconocidos en el Pacífico Tropical |
Ficha | Macroalgas y pasto marino, ´utiles bioindicadores de contaminacion por hidrocarburos f´osiles en sistemas acu´aticos | Calva B. L. G. y R. Torres Alvarado | NO | General | |||||
Ficha | Seaweed future cultivation in Chile: perspectives and challenges | Buschmann Alejandro H. & et. al. | 33 | 432-456 | NO | no completo | Cultivo | Chile; Phaeophyta; research developments; Rhodophyta; seaweed cultivation. | Production of seaweeds in Chile has fluctuated between 120,000 and |
Ficha | Elevated nutrient content of tropical macroalgae increases rates of herbivory in coral, seagrass, and mangrove habitats | Boyer K. E. and et. al. | 23 | 530-538 | NO | no completo | General | Acanthophora Æ Herbivory Æ Honduras Æ Macroalgae Æ Nutrients | We explored the role of food quality in herbi- elevated tissue nitrogen and phosphorus concentrations. |
Ficha | Sarcothalia crispata | Boraso Alicia & Juan Manuel Zaixso | NO | parcialmente completo con liga | Rodofitas | ||||
Ficha | Microhabitat and morphological variation in fresh water Blennothrix ganeshii (Oscillatoriaceae, Cyanophyceae) populations in streams of central Mexico | BELTRAN-MAGOS YENNY and et. al. | 133-146 | NO | no completo | General | Blennothrix, central Mexico, Cyanobacteria, Cyanophyceae, ionic com- position, current velocity, irradiance, microhabitat, morphometric varia- tion, streams. | Microhabitat was investigated in four populations of B. ganeshii in calcareous | |
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | General | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 354 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 1284 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 18 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 62 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3835 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3872 | no completo | Sin asignar | ||||||
Ficha | Sin asignar | ||||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3743 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3748 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3773 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3271 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3782 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3323 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3321 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3827 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3773 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 759 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | Carregeenan in Cooked Ham | ene-27 | NO | parcialmente sin liga | Sin asignar | ||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | Liga perdida | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | Liga perdida | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | Algae brasiliensis a cl. Glazione collectae | 1070-1071 | NO | parcialmente sin liga | Sin asignar | ||||
Ficha | Toothpaste | ene-44 | NO | parcialmente sin liga | Sin asignar | ||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | Phycological Resources of the Herbarium of the University of California at Berkeley | ene-15 | 876 | no completo | Sin asignar | ||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | Occurrence of Vaucheria adela, V Iii, and V. nasuta (Xanthophyceae) in Brackish Marshes of the Northern Gulf of Mexico | 2 | 137-140 | 1493 | no completo | Sin asignar | |||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | 3223 | no completo | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente sin liga | Sin asignar | Es un boletín y directorio | |||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente sin liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente sin liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente sin liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente sin liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | 3920 | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | NO | parcialmente completo con liga | Sin asignar | ||||||
Ficha | |||||||||
Ficha | No | no completo | Sin asignar |