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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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Acanthonchus Cobb, 1920 (additional source)
Achromadora Cobb, 1913 (additional source)
Alaimus de Man, 1880 (additional source)
Amphidelus Thorne, 1939 (additional source)
Anaplectus De Coninck & Schuurmans Stekhoven, 1933 (additional source)
Anonchus Cobb, 1913 (additional source)
Anoplostoma Bütschli, 1874 (additional source)
Antomicron Cobb, 1920 (additional source)
Aphanolaimus de Man, 1880 (additional source)
Aporcelaimus Thorne & Swanger, 1936 (additional source)
Cervonema Wieser, 1954 (additional source)
Chromadorella Filipjev, 1918 (additional source)
Chromadorina Filipjev, 1918 (additional source)
Chromadorita Filipjev, 1922 (additional source)
Chronogaster Cobb, 1913 (additional source)
Comesa Gerlach, 1956 accepted as Neotonchus Cobb, 1933 (additional source)
Criconemoides Taylor, 1936 (additional source)
Cylindrolaimus de Man, 1880 (additional source)
Daptonema Cobb, 1920 (additional source)
Desmodora de Man, 1889 (additional source)
Dichromadora Kreis, 1929 (additional source)
Diplolaimelloides Meyl, 1954 (additional source)
Enoploides Ssaweljev, 1912 (additional source)
Eudorylaimus Andrássy, 1959 (additional source)
Eumonhystera Andrássy, 1981 (additional source)
Gammarinema Kinne & Gerlach, 1953 (additional source)
Geomonhystera Andrássy, 1981 (additional source)
Hypodontolaimus de Man, 1886 (additional source)
Ironus Bastian, 1865 (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)
Monhystrella Cobb, 1918 (additional source)
Mononchus Bastian, 1865 (additional source)
Oncholaimellus de Man, 1890 (additional source)
Oncholaimus Dujardin, 1845 (additional source)
Oxystomina Filipjev, 1918 (additional source)
Panagrolaimus Fuchs, 1930 (additional source)
Paracyatholaimus Micoletzky, 1922 (additional source)
Paradesmodora Schuurmans Stekhoven, 1950 (additional source)
Paramonohystera Steiner, 1916 (additional source)
Paraplectonema Strand, 1934 (additional source)
Parodontophora Timm, 1963 (additional source)
Plectus Bastian, 1865 (additional source)
Polygastrophora de Man, 1922 (additional source)
Prismatolaimus de Man, 1880 (additional source)
Prodesmodora Micoletzky, 1923 (additional source)
Punctodora Filipjev, 1928 (additional source)
Rhabdocoma Cobb, 1920 (additional source)
Rhabdolaimus de Man, 1880 (additional source)
Sabatieria Rouville, 1903 (additional source)
Spirinia Gerlach, 1963 (additional source)
Symplocostoma Bastian, 1865 (additional source)
Terschellingia de Man, 1888 (additional source)
Thalassomonhystera Jacobs, 1987 (additional source)
Theristus Bastian, 1865 (additional source)
Tobrilus (Andrássy, 1959) (additional source)
Trefusia de Man, 1893 (additional source)
Tripyloides de Man, 1886 (additional source)
Trischistoma Cobb, 1913 (additional source)
Tylocephalus Crossman, 1933 (additional source)
Udonchus Cobb, 1913 (additional source)
Viscosia de Man, 1890 (additional source)
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