Copépodes cavernicoles de France métropolitaine
cavernicole au sens large (inclut les stygobies/stygophiles/stygoxènes)
80 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) | 120 | 54,05% | 106 | 79,7% | 88 | 83,02% | 100 | 82,64% |
Rouch (1970) | 15 | 6,76% | 15 | 11,28% | 15 | 14,15% | 15 | 12,4% |
Rouch (1980) | 11 | 4,95% | 11 | 8,27% | 11 | 10,38% | 11 | 9,09% |
Chappuis & Rouch (1959) | 10 | 4,5% | 4 | 3,01% | 4 | 3,77% | 4 | 3,31% |
Balvay (2009) | 9 | 4,05% | 9 | 6,77% | 8 | 7,55% | 5 | 4,13% |
Apostolov (1998) | 6 | 2,7% | 6 | 4,51% | 6 | 5,66% | 6 | 4,96% |
Champeau (1967) | 6 | 2,7% | 5 | 3,76% | 5 | 4,72% | 2 | 1,65% |
Dole-Olivier et al. (2015) | 6 | 2,7% | 5 | 3,76% | 4 | 3,77% | 5 | 4,13% |
Kiefer (1937) | 6 | 2,7% | 6 | 4,51% | 6 | 5,66% | 6 | 4,96% |
Kerhervé (1914) | 5 | 2,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelosse (1927) | 5 | 2,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pélosse (1930) | 5 | 2,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Apostolov (2002) | 4 | 1,8% | 4 | 3,01% | 4 | 3,77% | 4 | 3,31% |
Apostolov (2005) | 4 | 1,8% | 4 | 3,01% | 4 | 3,77% | 4 | 3,31% |
Cottarelli et al. (2000) | 4 | 1,8% | 4 | 3,01% | 4 | 3,77% | 4 | 3,31% |
Kiefer (1954) | 4 | 1,8% | 4 | 3,01% | 0 | 0% | 4 | 3,31% |
Pelosse (1925) | 4 | 1,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelosse (1927) | 4 | 1,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouch (1990) | 4 | 1,8% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Apostolov (2004) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Champeau & Thiéry (1990) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 1 | 0,83% |
Chappuis & Rouch (1960) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Chappuis (1956) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Chappuis (1956) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Lescher-Montoue (1974) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Lescher-Moutoue (1968) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Lescher-moutoue (1968) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Lescher-moutoue (1968) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Lescher-moutoue (1969) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Lescher-Moutoue (1974) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Lescher-moutoue (1978) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Moniez (1887) | 3 | 1,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Pesce & Galassi (1988) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Rouch & Lescher-Moutoué (1977) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Rouch (1988) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Rouch (1988) | 3 | 1,35% | 3 | 2,26% | 3 | 2,83% | 3 | 2,48% |
Rouch (1992) | 3 | 1,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouch (1996) | 3 | 1,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (1922) | 3 | 1,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (1927) | 3 | 1,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Mémoires de Biospéologie, 28(55): 1-8.">Apostolov (2002) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Apostolov (2002) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Apostolov (2003) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Chappuis & Rouch (1959) | 2 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Chappuis (1928) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Cottarelli & Bruno (1993) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Dussart (1963) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 1 | 0,83% |
Dussart (1970) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Ferreira et al. (2007) | 2 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Fiers & Pandourski (2008) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Fossati & Marquet (1998) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 1 | 0,83% |
Galassi et al. (1999) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Galassi et al. (1999) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Galassi et al. (2019) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Jurine (1820) | 2 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescher-Moutoué (1971) | 2 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Monard (1925) | 2 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage (2017) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 1 | 0,83% |
Richard (1887) | 2 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1890) | 2 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouch (1964) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 2 | 1,65% |
Roy (1931) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 0 | 0% |
Russell et al. (2021) | 2 | 0,9% | 2 | 1,5% | 2 | 1,89% | 0 | 0% |
Chevey (1927) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Defaye & Dussart (2011) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferreira (2005) | 1 | 0,45% | 1 | 0,75% | 1 | 0,94% | 1 | 0,83% |
Galassi & De Laurentiis (2004) | 1 | 0,45% | 1 | 0,75% | 1 | 0,94% | 1 | 0,83% |
Jakubisiak (1922) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Lilljeborg (1901) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Monard (1928) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Mrázek (1894) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman & Scott (1906) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Omaly (1970) | 1 | 0,45% | 1 | 0,75% | 1 | 0,94% | 1 | 0,83% |
Pugh et al. (2002) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1888) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1890) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1897) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmeil (1893) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiébaud (1927) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1920) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |