Crustacés Isopodes terrestres de France métropolitaine
Crustacés Isopoda terrestres de France métropolitaine : correspond au sous-ordre des Oniscidea (= cloportes).
127 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Séchet & Noël (2015) | 293 | 56,45% | 210 | 67,52% | 141 | 62,11% | 187 | 68% |
Racovitza (1908) | 38 | 7,32% | 17 | 5,47% | 17 | 7,49% | 9 | 3,27% |
Legrand (1950) | 37 | 7,13% | 26 | 8,36% | 26 | 11,45% | 16 | 5,82% |
Legrand (1953) | 33 | 6,36% | 19 | 6,11% | 18 | 7,93% | 14 | 5,09% |
Taiti & Ferrara (1996) | 32 | 6,17% | 30 | 9,65% | 30 | 13,22% | 30 | 10,91% |
Delsalle & Sechet (2014) | 31 | 5,97% | 31 | 9,97% | 31 | 13,66% | 22 | 8% |
Legrand (1949) | 26 | 5,01% | 20 | 6,43% | 20 | 8,81% | 14 | 5,09% |
Paulian & Félice (1941) | 21 | 4,05% | 14 | 4,5% | 14 | 6,17% | 12 | 4,36% |
Vandel (1946) | 19 | 3,66% | 19 | 6,11% | 8 | 3,52% | 18 | 6,55% |
Vandel (1947) | 18 | 3,47% | 18 | 5,79% | 13 | 5,73% | 16 | 5,82% |
Noël (2024) | 14 | 2,7% | 14 | 4,5% | 14 | 6,17% | 12 | 4,36% |
Budde-Lund (1885) | 13 | 2,5% | 8 | 2,57% | 8 | 3,52% | 5 | 1,82% |
Legrand (1943) | 10 | 1,93% | 5 | 1,61% | 0 | 0% | 5 | 1,82% |
Vandel (1957) | 10 | 1,93% | 8 | 2,57% | 2 | 0,88% | 8 | 2,91% |
Carl (1909) | 9 | 1,73% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1878) | 9 | 1,73% | 0 | 0% | 0 | 0% | 0 | 0% |
Carl (1908) | 8 | 1,54% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Vandel (1943) | 8 | 1,54% | 5 | 1,61% | 5 | 2,2% | 4 | 1,45% |
Dalens et al. (1996) | 7 | 1,35% | 6 | 1,93% | 6 | 2,64% | 4 | 1,45% |
Legrand (1942) | 6 | 1,16% | 6 | 1,93% | 3 | 1,32% | 3 | 1,09% |
Séchet et al. (2014) | 6 | 1,16% | 6 | 1,93% | 6 | 2,64% | 6 | 2,18% |
Brandt (1833) | 5 | 0,96% | 3 | 0,96% | 3 | 1,32% | 3 | 1,09% |
Dalens et al. (1997) | 5 | 0,96% | 5 | 1,61% | 5 | 2,2% | 5 | 1,82% |
Dollfus (1884) | 5 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
Racovitza (1907) | 5 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
Taiti & Ferrara (1996) | 5 | 0,96% | 5 | 1,61% | 2 | 0,88% | 5 | 1,82% |
Vandel (1954) | 5 | 0,96% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Verhoeff (1928) | 5 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnefoy (1945) | 4 | 0,77% | 4 | 1,29% | 4 | 1,76% | 4 | 1,45% |
Cuvier (1792) | 4 | 0,77% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 4 | 0,77% | 3 | 0,96% | 3 | 1,32% | 3 | 1,09% |
Nelson-Smith et al. (2014) | 4 | 0,77% | 3 | 0,96% | 3 | 1,32% | 3 | 1,09% |
Rigaud et al. (1997) | 4 | 0,77% | 4 | 1,29% | 4 | 1,76% | 4 | 1,45% |
Vandel (1946) | 4 | 0,77% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Ferrara & Taiti (1983) | 3 | 0,58% | 3 | 0,96% | 3 | 1,32% | 3 | 1,09% |
Jackson (1933) | 3 | 0,58% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Jackson (1941) | 3 | 0,58% | 3 | 0,96% | 3 | 1,32% | 2 | 0,73% |
petiti Vandel de Porcellio dilatatus Brandt recoltée à l'Ile Saint-Honorat (Alpes-Maritimes) critères morphologiques, génétiques et physiologiques. Bulletin de la Société Zoologique de France, 99: 461-471.">Legrand et al. (1974) | 3 | 0,58% | 3 | 0,96% | 0 | 0% | 3 | 1,09% |
Legrand (1953) | 3 | 0,58% | 3 | 0,96% | 3 | 1,32% | 3 | 1,09% |
Legrand (1954) | 3 | 0,58% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Ramage (2017) | 3 | 0,58% | 3 | 0,96% | 3 | 1,32% | 2 | 0,73% |
Schmalfuss (2003) | 3 | 0,58% | 1 | 0,32% | 1 | 0,44% | 0 | 0% |
Vandel (1924) | 3 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1938) | 3 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnefoy & Marchal (1942) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 0 | 0% |
Carl (1908) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochard et al. (2010) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Dalens (1998) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Dollfus (1887) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Dollfus (1897) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Frankenberger (1938) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Garcia & Robla (2022) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Herold (1923) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Jackson (1938) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 1 | 0,36% |
Jourdan (2020) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Juchault et al. (1981) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1956) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Leistikow & Wägele (1999) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 1 | 0,36% |
Meinert (1880) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Mocquard (1974) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Moniez (1887) | 2 | 0,39% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Pavon et al. (2021) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Questel (2014) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Questel (2020) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Racovitza (1919) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Racovitza (1922) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Remy (1928) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 1 | 0,36% |
Richardson (1914) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Sars (1899) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Séchet et al. (2014) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Séchet (2014) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Taiti & Ferrara (1983) | 2 | 0,39% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Thomas (2015) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Vandel (1981) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Verhoeff (1908) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1917) | 2 | 0,39% | 2 | 0,64% | 2 | 0,88% | 2 | 0,73% |
Verhoeff (1926) | 2 | 0,39% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Adelski (2023) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Arcangeli (1938) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Besse et al. (1975) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Bilton (1994) | 1 | 0,19% | 1 | 0,32% | 0 | 0% | 1 | 0,36% |
Brandt (1833) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Budde-Lund (1879) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 0 | 0% |
Dalens (1966) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Dalens (1966) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
De Geer (1778) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock et al. (1960) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Desmots (2016) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Dollfus & Dalens (1960) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Dollfus (1889) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Dollfus (1895) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 0 | 0% |
Fabricius (1798) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Henry (1974) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Hubart (1982) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Hullé et al. (2018) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Kilpert & Podsiadlowski (2006) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Kinahan (1857) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1838) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1804) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Latreille (1804) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaire (2011) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 0 | 0% |
Linnaeus (1758) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 0 | 0% |
Linnaeus (1767) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Lohmander (1924) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Magne (1969) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 0 | 0% |
Maury (1931) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 0 | 0% |
Meurgey (2011) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Noël & Séchet (2007) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Noël et al. (2022) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Noël et al. (2023) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Noël et al. (2024) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Notenboom et al. (2006) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Perrier (1929) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Raupach et al. (2014) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Remy (1948) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Robert (2010) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Sardet et al. (2015) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1922) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1960) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Verhoeff (1908) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Verhoeff (1908) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 0 | 0% |
Verhoeff (1910) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Waga (1857) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Willmer et al. (1989) | 1 | 0,19% | 1 | 0,32% | 1 | 0,44% | 1 | 0,36% |
Zaddach (1844) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |