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De Oliveira Pinto, T.K.,Netto, S.A., Esteves, A.M., De Castro, F.J.V., Neres, P.F. and Da Silva, M.C. (2021). Free-living freshwater nematodes from Brazil: checklist of genera and regional patterns of diversity. Nematology. 0 (2021) 1-14.
404311
De Oliveira Pinto, T.K.,Netto, S.A., Esteves, A.M., De Castro, F.J.V., Neres, P.F. and Da Silva, M.C.
2021
Free-living freshwater nematodes from Brazil: checklist of genera and regional patterns of diversity
Nematology
0 (2021) 1-14
Publication
Available for editors  PDF available
Brazil has one of the largest varieties of aquatic ecosystems and rich freshwater biodiversity, but these components have constantly been damaged by the expansion of unsustainable activities. Free-living nematodes are an abundant and ubiquitous component of continental benthic communities, occurring in all freshwater habitats, including extreme environments. Despite this, hardly any studies have examined the generic composition of nematodes in different latitudes and the geographic overlap of assemblages. We provide data on nematode genera from six regions in Brazil, over a north-south gradient spanning about 4000 km, encompassing rivers, coastal lakes, and reservoirs with different levels of human impact. Interpolation/extrapolation curves were generated and the zeta diversity was used to assess the overlap of nematode assemblages. Freshwater nematode assemblages comprised 54 families and 132 genera. Mononchidae, Monhysteridae, Chromadoridae, Tobrilidae and Dorylaimidae were the most diverse families. Differences in diversity and high turnover of genera were found among regions, probably related to stochastic processes. Mononchus was the only widely distributed genus. Our results revealed a high biodiversity of free-living freshwater nematodes among the regions. The limited spatial coverage of the data reveals an enormous knowledge gap in a country with 12% of the world’s freshwater resources. The lack of spatial patterns, e.g., latitudinal variation, suggests that freshwater nematode assemblages are primarily structured by the intrinsic properties of habitats. This reinforces the uniqueness of freshwater ecosystems and suggests that the nematode assemblages may be sensitive to environmental disturbances, since the limited distributions of taxa may lead to lower resilience.
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2021-04-13 13:48:02Z
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Amphidelus Thorne, 1939 (additional source)
Anoplostoma Bütschli, 1874 (additional source)
Aporcelaimellus Heyns, 1965 (additional source)
Chromadorella Filipjev, 1918 (additional source)
Chromadorita Filipjev, 1922 (additional source)
Coomansus Jairajpuri & Khan, 1977 (additional source)
Daptonema Cobb, 1920 (additional source)
Desmodora de Man, 1889 (additional source)
Dichromadora Kreis, 1929 (additional source)
Dorylaimus Dujardin, 1845 (additional source)
Enoploides Ssaweljev, 1912 (additional source)
Eudorylaimus Andrássy, 1959 (additional source)
Eumonhystera Andrássy, 1981 (additional source)
Eutobrilus Tsalolikhin, 1981 (additional source)
Geomonhystera Andrássy, 1981 (additional source)
Hypodontolaimus de Man, 1886 (additional source)
Leptolaimus de Man, 1876 (additional source)
Linhomoeus Bastian, 1865 (additional source)
Mesodorylaimus Andrássy, 1959 (additional source)
Metoncholaimus Filipjev, 1918 (additional source)
Microlaimus de Man, 1880 (additional source)
Monhystera Bastian, 1865 (additional source)
Mononchus Bastian, 1865 (additional source)
Oncholaimus Dujardin, 1845 (additional source)
Oscheius Andrássy, 1976 (additional source)
Oxystomina Filipjev, 1918 (additional source)
Panagrolaimus Fuchs, 1930 (additional source)
Plectus Bastian, 1865 (additional source)
Sabatieria de Rouville, 1903 (additional source)
Spirinia Gerlach, 1963 (additional source)
Teratocephalus de Man, 1876 (additional source)
Terschellingia de Man, 1888 (additional source)
Thalassomonhystera Jacobs, 1987 (additional source)
Theristus Bastian, 1865 (additional source)
Viscosia de Man, 1890 (additional source)
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