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1.
Braz J Biol ; 74(1): 191-8, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25055101

RESUMO

This study reports the occurrence and the effect of the environmental factors on the spatial and temporal distribution of the dinoflagellate Akashiwo sanguinea (Hirasaka) Hansen & Moestrup in estuarine waters of northeastern Brazil. Samples were collected at seven stations from March 2007 to February 2008 during high tide and low tide, using Van Dorn bottles. The samples were immediately fixed with Lugol and analyzed with the Utermöhl method. Water samples were also collected for the identification of the hydrological characteristics of the area. Akashiwo sanguinea occurred throughout the annual cycle and at all sampling sites with densities ranging between 5 and 410 x 103 cells.L-1. The highest densities were recorded at low tide, especially during the months of the rainy season (July: 210 x 103 cells.L-1; August: 410 x 103 cells.L-1). Density values were within the normal range and blooms were not detected. Despite being common in the area, the species showed preference for sites with high concentrations of orthophosphate and total dissolved phosphorus and with salinity in the mesohaline regime.


Assuntos
Dinoflagellida/classificação , Brasil , Monitoramento Ambiental/métodos , Estuários , Densidade Demográfica , Dinâmica Populacional , Estações do Ano
2.
Braz. j. biol ; Braz. j. biol;74(1): 191-198, 2/2014. tab, graf
Artigo em Inglês | LILACS | ID: lil-715578

RESUMO

This study reports the occurrence and the effect of the environmental factors on the spatial and temporal distribution of the dinoflagellate Akashiwo sanguinea (Hirasaka) Hansen & Moestrup in estuarine waters of northeastern Brazil. Samples were collected at seven stations from March 2007 to February 2008 during high tide and low tide, using Van Dorn bottles. The samples were immediately fixed with Lugol and analyzed with the Utermöhl method. Water samples were also collected for the identification of the hydrological characteristics of the area. Akashiwo sanguinea occurred throughout the annual cycle and at all sampling sites with densities ranging between 5 and 410 x 103 cells.L–1. The highest densities were recorded at low tide, especially during the months of the rainy season (July: 210 x 103 cells.L–1; August: 410 x 103 cells.L–1). Density values were within the normal range and blooms were not detected. Despite being common in the area, the species showed preference for sites with high concentrations of orthophosphate and total dissolved phosphorus and with salinity in the mesohaline regime.


Este estudo relata a ocorrência e o efeito dos fatores ambientais na distribuição espacial e temporal do dinoflagelado Akashiwo sanguinea (Hirasaka) Hansen et Moestrup em águas estuarinas do Nordeste do Brasil. As amostras foram coletadas em sete estações, durante o período de março 2007 a fevereiro 2008 durante os regimes de preamar e baixa-mar, com o auxílio de garrafas tipo Van Dorn. As amostras foram imediatamente fixadas com lugol e analisadas pelo método de Utermöhl. Amostras de água foram também coletadas para a identificação das características hidrológicas da área. Akashiwo sanguinea ocorreu em todo o ciclo anual e em todos os locais de coleta com densidade variando de 5 a 410 cells.L–1 x 103, sendo as maiores densidades registradas na baixa-mar, principalmente, durante os meses do período chuvoso (julho 210 cells.L–1 x 103, agosto 410 cells.L–1 x 103). Os valores quantitativos estiveram dentro dos padrões normais, não tendo sido detectados florescimentos com conotações de blooms. Apesar de ser frequente na área, a espécie mostrou preferência pelos locais com maiores concentrações de ortofosfato dissolvido e fósforo total dissolvido e salinidade compreendida no regime mesoalino.


Assuntos
Dinoflagellida/classificação , Brasil , Estuários , Monitoramento Ambiental/métodos , Densidade Demográfica , Dinâmica Populacional , Estações do Ano
3.
J Eukaryot Microbiol ; 58(4): 284-309, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21535293

RESUMO

The heterotrophic dinoflagellate Gyrodiniellum shiwhaense n. gen., n. sp. is described from live cells and from cells prepared for light, scanning electron, and transmission electron microscopy. Also, sequences of the small subunit (SSU) and large subunit (LSU) of rDNA have been analyzed. The episome is conical, while the hyposome is ellipsoid. Cells are covered with polygonal amphiesmal vesicles arranged in 16 horizontal rows. Unlike other Gyrodinium-like dinoflagellates, the apical end of the cell shows a loop-shaped row of five elongate amphiesmal vesicles. The cingulum is displaced by 0.3-0.5 × cell length. Cells that were feeding on the dinoflagellate Amphidinium carterae Hulburt were 9.1-21.6 µm long and 6.6-15.7 µm wide. Cells of G. shiwhaense contain nematocysts, trichocysts, a peduncle, and pusule systems, but they lack chloroplasts. The SSU rDNA sequence is >3% different from that of the six most closely related species: Warnowia sp. (FJ947040), Lepidodinium viride Watanabe, Suda, Inouye, Sawaguchi & Chihara, Gymnodinium aureolum (Hulburt) Hansen, Gymnodinium catenatum Graham, Nematodinium sp. (FJ947039), and Gymnodinium sp. MUCC284 (AF022196), while the LSU rDNA is 11-12% different from that of Warnowia sp., G. aureolum, and Nematodinium sp. (FJ947041). The phylogenetic trees show that the species belongs in the Gymnodinium sensu stricto clade. However, in contrast to Gymnodinium spp., cells lack nuclear envelope chambers and a nuclear fibrous connective. Unlike Polykrikos spp., cells of which possess a taeniocyst-nematocyst complex, G. shiwhaense has nematocysts but lacks taeniocysts. It differs from Paragymnodinium shiwhaense Kang, Jeong, Moestrup & Shin by possessing nematocysts with stylets and filaments. Gyrodiniellum shiwhaense n. gen., n. sp. furthermore lacks ocelloids, in contrast to Warnowia spp., Nematodinium spp., and Proterythropsis spp. Based on morphological and molecular data, we suggest that the taxon represents a new species within a new genus.


Assuntos
DNA de Protozoário/genética , Dinoflagellida/classificação , Dinoflagellida/isolamento & purificação , Sequência de Bases , DNA Ribossômico/genética , Dinoflagellida/genética , Dinoflagellida/ultraestrutura , Coreia (Geográfico) , Microscopia Eletrônica , Dados de Sequência Molecular , Membrana Nuclear/ultraestrutura , Organelas/ultraestrutura , Plâncton , Análise de Sequência de DNA
4.
J Eukaryot Microbiol ; 55(2): 91-9, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18318861

RESUMO

Cultures of four strains of the dinoflagellate Gymnodinium aureolum (Hulburt) G. Hansen were established from the Elizabeth River, a tidal tributary of the Chesapeake Bay, USA. Light microscopy, scanning electron microscopy, nuclear-encoded large sub-unit rDNA sequencing, and culturing observations were conducted to further characterize this species. Observations of morphology included: a multiple structured apical groove; a peduncle located between the emerging points of the two flagella; pentagonal and hexagonal vesicles on the amphiesma; production and germination of resting cysts; variation in the location of the nucleus within the center of the cell; a longitudinal ventral concavity; and considerable variation in cell width/length and overall cell size. A fish bioassay using juvenile sheepshead minnows detected no ichthyotoxicity from any of the strains over a 48-h period. Molecular analysis confirmed the dinoflagellate was conspecific with G. aureolum strains from around the world, and formed a cluster along with several other Gymnodinium species. Morphological evidence suggests that further research is necessary to examine the relationship between G. aureolum and a possibly closely related species Gymnodinium maguelonnense.


Assuntos
Dinoflagellida/classificação , Dinoflagellida/genética , Água Doce/parasitologia , Animais , Cyprinidae/parasitologia , DNA de Protozoário/química , DNA de Protozoário/genética , DNA Ribossômico/química , DNA Ribossômico/genética , Dinoflagellida/ultraestrutura , Doenças dos Peixes/parasitologia , Microscopia , Microscopia Eletrônica de Varredura , Dados de Sequência Molecular , Organelas/ultraestrutura , Doenças Parasitárias em Animais , Filogenia , Análise de Sequência de DNA , Homologia de Sequência do Ácido Nucleico , Estados Unidos
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