Copépodes cavernicoles de France métropolitaine
cavernicole au sens large (inclut les stygobies/stygophiles/stygoxènes)
82 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Defaye & Deharveng (2024) | 122 | 53,28% | 110 | 80,29% | 92 | 84,4% | 103 | 83,06% |
| Rouch (1970) | 15 | 6,55% | 15 | 10,95% | 15 | 13,76% | 15 | 12,1% |
| Rouch (1980) | 11 | 4,8% | 11 | 8,03% | 11 | 10,09% | 11 | 8,87% |
| Balvay (2009) | 10 | 4,37% | 10 | 7,3% | 9 | 8,26% | 6 | 4,84% |
| Chappuis & Rouch (1959) | 10 | 4,37% | 4 | 2,92% | 4 | 3,67% | 4 | 3,23% |
| Dole-Olivier et al. (2015) | 8 | 3,49% | 7 | 5,11% | 6 | 5,5% | 7 | 5,65% |
| Apostolov (1998) | 6 | 2,62% | 6 | 4,38% | 6 | 5,5% | 6 | 4,84% |
| Champeau (1967) | 6 | 2,62% | 5 | 3,65% | 5 | 4,59% | 2 | 1,61% |
| Kerhervé (1914) | 6 | 2,62% | 1 | 0,73% | 1 | 0,92% | 0 | 0% |
| Kiefer (1937) | 6 | 2,62% | 6 | 4,38% | 6 | 5,5% | 6 | 4,84% |
| Pelosse (1927) | 5 | 2,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pélosse (1930) | 5 | 2,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Apostolov (2002) | 4 | 1,75% | 4 | 2,92% | 4 | 3,67% | 4 | 3,23% |
| Apostolov (2005) | 4 | 1,75% | 4 | 2,92% | 4 | 3,67% | 4 | 3,23% |
| Cottarelli et al. (2000) | 4 | 1,75% | 4 | 2,92% | 4 | 3,67% | 4 | 3,23% |
| Kiefer (1954) | 4 | 1,75% | 4 | 2,92% | 0 | 0% | 4 | 3,23% |
| Pelosse (1925) | 4 | 1,75% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelosse (1927) | 4 | 1,75% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouch (1990) | 4 | 1,75% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Apostolov (2004) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Champeau & Thiéry (1990) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 1 | 0,81% |
| Chappuis & Rouch (1960) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Chappuis (1956) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Chappuis (1956) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Defaye & Dussart (2011) | 3 | 1,31% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Lescher-Montoue (1974) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Lescher-Moutoue (1968) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Lescher-moutoue (1968) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Lescher-moutoue (1968) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Lescher-moutoue (1969) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Lescher-Moutoue (1974) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Lescher-moutoue (1978) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Moniez (1887) | 3 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pesce & Galassi (1988) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Richard (1890) | 3 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouch & Lescher-Moutoué (1977) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Rouch (1988) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Rouch (1988) | 3 | 1,31% | 3 | 2,19% | 3 | 2,75% | 3 | 2,42% |
| Rouch (1992) | 3 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouch (1996) | 3 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roy (1922) | 3 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roy (1927) | 3 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mémoires de Biospéologie, 28(55): 1-8.">Apostolov (2002) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Apostolov (2002) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Apostolov (2003) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Chappuis & Rouch (1959) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chappuis (1928) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Cottarelli & Bruno (1993) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Dussart (1963) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 1 | 0,81% |
| Dussart (1970) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Ferreira et al. (2007) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fiers & Pandourski (2008) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Fossati & Marquet (1998) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 1 | 0,81% |
| Galassi et al. (1999) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Galassi et al. (1999) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Galassi et al. (2019) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Jakubisiak (1922) | 2 | 0,87% | 1 | 0,73% | 1 | 0,92% | 0 | 0% |
| Jurine (1820) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescher-Moutoué (1971) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monard (1925) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramage (2017) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 1 | 0,81% |
| Richard (1887) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouch (1964) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 2 | 1,61% |
| Roy (1931) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 0 | 0% |
| Russell et al. (2021) | 2 | 0,87% | 2 | 1,46% | 2 | 1,83% | 0 | 0% |
| Brady (1880) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevey (1927) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferreira (2005) | 1 | 0,44% | 1 | 0,73% | 1 | 0,92% | 1 | 0,81% |
| Galassi & De Laurentiis (2004) | 1 | 0,44% | 1 | 0,73% | 1 | 0,92% | 1 | 0,81% |
| Labbé (1926) | 1 | 0,44% | 1 | 0,73% | 1 | 0,92% | 0 | 0% |
| Lilljeborg (1901) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monard (1928) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mrázek (1894) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman & Scott (1906) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Omaly (1970) | 1 | 0,44% | 1 | 0,73% | 1 | 0,92% | 1 | 0,81% |
| Pugh et al. (2002) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1888) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1890) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1897) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmeil (1893) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiébaud (1927) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1920) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |