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Seasonal dynamics of all major protozoan groups were investigated in the plankton of the River Danube, upstream of Budapest (Hungary), by bi-weekly sampling over a 1-year long period. Sixty-one heterotrophic flagellate, 14 naked amoeba, 50 testate amoeba, 4 heliozoan and 83 ciliate morphospecies were identified. The estimated abundance ranges of major groups throughout the year were as follows: heterotrophic flagellates, 0.27-7.8 x 10(6)ind.l(-1); naked amoebae, max. 3300ind.l(-1); testaceans, max. 1600ind.l(-1); heliozoans, max. 8500ind.l(-1); ciliates, 132-34,000ind.l(-1). In terms of biovolume, heterotrophic flagellates dominated throughout the year (max. 0.58mm(3)l(-1)), and ciliates only exceeded their biovolume in summer (max. 0.76mm(3)l(-1)). Naked amoeba and heliozoan biovolume was about one, and testacean biovolume 1-3, orders of magnitude lower than that of ciliates. In winter, flagellates, mainly chrysomonads, had the highest biomass, whilst ciliates were dominated by peritrichs. In 2005 from April to July a long spring/summer peak occurred for all protozoan groups. Beside chrysomonads typical flagellates were choanoflagellates, bicosoecids and abundant microflagellates (large chrysomonads and Collodictyon). Most abundant ciliates were oligotrichs, while Phascolodon, Urotricha, Vorticella, haptorids, Suctoria, Climacostomum and Stokesia also contributed significantly to biovolume during rapid succession processes. In October and November a second high protozoan peak occurred, with flagellate dominance, and slightly different taxonomic composition.
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http://dx.doi.org/10.1016/j.ejop.2008.08.002 | DOI Listing |
Biology (Basel)
July 2025
Department of Hydrobiology and Protection of Ecosystems, University of Life Sciences, Dobrzańskiego 37, 20-262 Lublin, Poland.
Climate change can have a direct impact on the decomposition of organic matter, as well as indirect effects on peatland vegetation (including carnivorous plants) and the microbial communities associated with this environment. The activity of microbes varies depending on the type of peatland they inhabit. Because some microorganisms are highly sensitive, they can be used as indicators of climate change.
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July 2025
Department of Biology, Institute of Biology and Biotechnology, Faculty of Natural Sciences, University of Ss. Cyril and Methodius in Trnava, Nám. J. Herdu 2, Trnava, SK-917 01, Slovakia.
Euglena gracilis is a flagellate photosynthetic microalga that, thanks to its metabolic adaptability, can grow under both autotrophic and heterotrophic conditions. This adaptability makes euglena an interesting species for applied biotechnology. We focused on the proteome of E.
View Article and Find Full Text PDFOpen Biol
June 2025
Institute of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki Prefecture, Japan.
Culturing protists offers a powerful approach to exploring eukaryotic diversity, especially for deep-branching lineages. In this study, we cultured and described a novel protist species, named n sp. within the poorly studied and unclassified genus .
View Article and Find Full Text PDFEur J Protistol
June 2025
Department of Botany, Faculty of Science, University of South Bohemia in České Budějovice, České Budějovice, Czech Republic; Třeboň Experimental Garden and Gene Pool Collections, Institute of Botany of the Czech Academy of Sciences, Třeboň, Czech Republic.
This study brings the first information about the autecological traits of heterotrophic euglenoids at eighteen localities in South Bohemia (Czech Republic). A number of environmental and landscape parameters including water chemistry and diversity of algae as well as of heterotrophic protists were analyzed over two years in order to assess the effect of environmental parameters on heterotrophic euglenoids. The major diversity of osmotrophs was found in acidic wetlands (i.
View Article and Find Full Text PDFISME Commun
January 2025
Department Biodiversity, University of Duisburg-Essen, Essen, NRW 45141, Germany.
Microbial predator-prey interactions play a crucial role in aquatic food webs. Bacterivorous protists not only regulate the quantity and biomass of bacterial populations but also profoundly influence the structure of bacterial communities. Consequently, alterations in both the quantity and quality of protist bacterivory can influence the overall structure of aquatic food webs.
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