Crustacés Branchiopodes Phyllopodes de France
Crustacés Branchiopoda Phyllopoda de France (métropole et outre-mer)
100 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Balvay (2009) | 93 | 27,03% | 78 | 44,57% | 78 | 46,15% | 77 | 45,29% |
Monnier (2014) | 61 | 17,73% | 53 | 30,29% | 53 | 31,36% | 50 | 29,41% |
Moniez (1887) | 47 | 13,66% | 30 | 17,14% | 30 | 17,75% | 30 | 17,65% |
Paris (1919) | 26 | 7,56% | 22 | 12,57% | 22 | 13,02% | 22 | 12,94% |
Richard (1887) | 24 | 6,98% | 8 | 4,57% | 8 | 4,73% | 8 | 4,71% |
Chevey (1927) | 17 | 4,94% | 15 | 8,57% | 15 | 8,88% | 15 | 8,82% |
Monard (1928) | 17 | 4,94% | 14 | 8% | 14 | 8,28% | 14 | 8,24% |
Richard (1890) | 16 | 4,65% | 10 | 5,71% | 10 | 5,92% | 10 | 5,88% |
Sars (1862) | 14 | 4,07% | 9 | 5,14% | 9 | 5,33% | 9 | 5,29% |
Timms (1985) | 14 | 4,07% | 10 | 5,71% | 7 | 4,14% | 10 | 5,88% |
Pélosse (1930) | 12 | 3,49% | 11 | 6,29% | 11 | 6,51% | 11 | 6,47% |
Müller (1776) | 11 | 3,2% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Roy (1931) | 11 | 3,2% | 11 | 6,29% | 11 | 6,51% | 11 | 6,47% |
Richard (1897) | 10 | 2,91% | 5 | 2,86% | 5 | 2,96% | 5 | 2,94% |
Paris (1916) | 9 | 2,62% | 7 | 4% | 7 | 4,14% | 7 | 4,12% |
Pelosse (1925) | 9 | 2,62% | 8 | 4,57% | 8 | 4,73% | 8 | 4,71% |
Pelosse (1927) | 8 | 2,33% | 8 | 4,57% | 8 | 4,73% | 8 | 4,71% |
Pelosse (1927) | 8 | 2,33% | 7 | 4% | 7 | 4,14% | 7 | 4,12% |
Richard (1888) | 8 | 2,33% | 2 | 1,14% | 2 | 1,18% | 2 | 1,18% |
Stingelin (1915) | 8 | 2,33% | 4 | 2,29% | 2 | 1,18% | 4 | 2,35% |
Studer (1878) | 8 | 2,33% | 4 | 2,29% | 4 | 2,37% | 4 | 2,35% |
Horeau et al. (2005) | 7 | 2,03% | 7 | 4% | 7 | 4,14% | 7 | 4,12% |
Richard (1890) | 7 | 2,03% | 4 | 2,29% | 4 | 2,37% | 4 | 2,35% |
Guerne & Richard (1891) | 6 | 1,74% | 5 | 2,86% | 5 | 2,96% | 5 | 2,94% |
Nourisson & Thiéry (1988) | 6 | 1,74% | 6 | 3,43% | 6 | 3,55% | 6 | 3,53% |
Paris (1918) | 6 | 1,74% | 5 | 2,86% | 5 | 2,96% | 5 | 2,94% |
Dumont (1983) | 5 | 1,45% | 3 | 1,71% | 3 | 1,78% | 3 | 1,76% |
Stifter (1988) | 5 | 1,45% | 5 | 2,86% | 5 | 2,96% | 5 | 2,94% |
Aguesse (1960) | 4 | 1,16% | 4 | 2,29% | 4 | 2,37% | 4 | 2,35% |
Crosetti & Margaritora (1985) | 4 | 1,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Kotov (2007) | 4 | 1,16% | 4 | 2,29% | 4 | 2,37% | 4 | 2,35% |
Rabet et al. (2005) | 4 | 1,16% | 4 | 2,29% | 4 | 2,37% | 4 | 2,35% |
Rogers et al. (2020) | 4 | 1,16% | 4 | 2,29% | 4 | 2,37% | 4 | 2,35% |
Van Damme et al. (2009) | 4 | 1,16% | 4 | 2,29% | 4 | 2,37% | 4 | 2,35% |
Amoros (1980) | 3 | 0,87% | 3 | 1,71% | 3 | 1,78% | 3 | 1,76% |
Durr & Thiery (2020) | 3 | 0,87% | 3 | 1,71% | 3 | 1,78% | 3 | 1,76% |
Olesen et al. (2016) | 3 | 0,87% | 3 | 1,71% | 3 | 1,78% | 3 | 1,76% |
Sinev & Dumont (2016) | 3 | 0,87% | 3 | 1,71% | 3 | 1,78% | 3 | 1,76% |
Sinev (2015) | 3 | 0,87% | 3 | 1,71% | 3 | 1,78% | 3 | 1,76% |
Baird (1836) | 2 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer (1848) | 2 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenzel & Alonso (1988) | 2 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Frey (1980) | 2 | 0,58% | 2 | 1,14% | 2 | 1,18% | 2 | 1,18% |
Furnestin (1960) | 2 | 0,58% | 2 | 1,14% | 2 | 1,18% | 2 | 1,18% |
Hertzog (1935) | 2 | 0,58% | 2 | 1,14% | 2 | 1,18% | 2 | 1,18% |
Jurine (1820) | 2 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Longurst (1955) | 2 | 0,58% | 2 | 1,14% | 0 | 0% | 2 | 1,18% |
Margaritora (1971) | 2 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 2 | 0,58% | 2 | 1,14% | 2 | 1,18% | 2 | 1,18% |
Questel & Le Quellec (2012) | 2 | 0,58% | 2 | 1,14% | 2 | 1,18% | 1 | 0,59% |
Questel (2020) | 2 | 0,58% | 2 | 1,14% | 2 | 1,18% | 1 | 0,59% |
Rabet et al. (2014) | 2 | 0,58% | 2 | 1,14% | 2 | 1,18% | 2 | 1,18% |
Schabetsberger et al. (2009) | 2 | 0,58% | 2 | 1,14% | 2 | 1,18% | 2 | 1,18% |
Sinev (2020) | 2 | 0,58% | 1 | 0,57% | 1 | 0,59% | 0 | 0% |
Van et al. (2011) | 2 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Australian Museum (2020) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Baird (1843) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Baird (1859) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Balsamo-Crivelli (1859) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1928) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Belk (1989) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Benzie (2005) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Bosc (1801-1802) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Brtek & Thiery (1995) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Cépède (1914) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Chien (1970) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Daday (1884) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1778) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumont & Silva-Briano (2000) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Frescheville de (1958) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Goulletquer (2016) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
King (1853) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1844) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Korovchinsky (2000) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Krynicki (1830) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Kurz (1875) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
LeConte (1846) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Leveau (1965) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Liévin (1848) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Upsala, Druck der Akademischen buchdruckerei E. Berling. 701 pp.">Lilljeborg (1900) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Marková et al. (2007) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Masson (1979) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Müller (1785) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Negrea (1984) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Noël (2016) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Omaly (1970) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Pugh et al. (2002) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Rey (1966) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Richard (1895) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Scourfield (1947) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Sinev et al. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Sinev et al. (2023) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Thiery & Pont (1987) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Uicn et al. (2014) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Van Damme & Dumont (2008) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Vandel (1922) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Vannier et al. (2003) | 1 | 0,29% | 1 | 0,57% | 1 | 0,59% | 1 | 0,59% |
Zilli (2021) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |