Crustacés Isopodes Oniscidea
134 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) | 299 | 43,21% | 213 | 49,53% | 142 | 42,64% | 190 | 48,97% |
| Verhoeff (1926) | 102 | 14,74% | 79 | 18,37% | 69 | 20,72% | 69 | 17,78% |
| Racovitza (1908) | 38 | 5,49% | 17 | 3,95% | 17 | 5,11% | 9 | 2,32% |
| Legrand (1950) | 37 | 5,35% | 26 | 6,05% | 26 | 7,81% | 16 | 4,12% |
| Legrand (1953) | 33 | 4,77% | 19 | 4,42% | 18 | 5,41% | 14 | 3,61% |
| Taiti & Ferrara (1996) | 32 | 4,62% | 30 | 6,98% | 30 | 9,01% | 30 | 7,73% |
| Delsalle & Sechet (2014) | 31 | 4,48% | 31 | 7,21% | 31 | 9,31% | 22 | 5,67% |
| Jackson (1933) | 29 | 4,19% | 18 | 4,19% | 18 | 5,41% | 18 | 4,64% |
| Ramage (2017) | 29 | 4,19% | 26 | 6,05% | 26 | 7,81% | 25 | 6,44% |
| Legrand (1949) | 26 | 3,76% | 20 | 4,65% | 20 | 6,01% | 14 | 3,61% |
| Jackson (1941) | 25 | 3,61% | 22 | 5,12% | 22 | 6,61% | 21 | 5,41% |
| Schmalfuss (2003) | 25 | 3,61% | 20 | 4,65% | 20 | 6,01% | 19 | 4,9% |
| Vandel (1946) | 22 | 3,18% | 22 | 5,12% | 8 | 2,4% | 21 | 5,41% |
| Paulian & Félice (1941) | 21 | 3,03% | 14 | 3,26% | 14 | 4,2% | 12 | 3,09% |
| Jackson (1938) | 18 | 2,6% | 15 | 3,49% | 15 | 4,5% | 14 | 3,61% |
| Vandel (1947) | 18 | 2,6% | 18 | 4,19% | 13 | 3,9% | 16 | 4,12% |
| Budde-Lund (1885) | 13 | 1,88% | 8 | 1,86% | 8 | 2,4% | 5 | 1,29% |
| Miers (1878) | 12 | 1,73% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Leistikow & Wägele (1999) | 11 | 1,59% | 11 | 2,56% | 11 | 3,3% | 10 | 2,58% |
| Dalens (1993) | 10 | 1,45% | 10 | 2,33% | 10 | 3% | 10 | 2,58% |
| Jackson (1933) | 10 | 1,45% | 5 | 1,16% | 5 | 1,5% | 5 | 1,29% |
| Legrand (1943) | 10 | 1,45% | 5 | 1,16% | 0 | 0% | 5 | 1,29% |
| Vandel (1957) | 10 | 1,45% | 8 | 1,86% | 2 | 0,6% | 8 | 2,06% |
| Carl (1909) | 9 | 1,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carl (1908) | 8 | 1,16% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Stebbing (1900) | 8 | 1,16% | 4 | 0,93% | 4 | 1,2% | 4 | 1,03% |
| Vandel (1943) | 8 | 1,16% | 5 | 1,16% | 5 | 1,5% | 4 | 1,03% |
| Dalens et al. (1996) | 7 | 1,01% | 6 | 1,4% | 6 | 1,8% | 4 | 1,03% |
| Taiti & Ferrara (1983) | 7 | 1,01% | 6 | 1,4% | 6 | 1,8% | 6 | 1,55% |
| Brandt (1833) | 6 | 0,87% | 4 | 0,93% | 4 | 1,2% | 4 | 1,03% |
| Legrand (1942) | 6 | 0,87% | 6 | 1,4% | 3 | 0,9% | 3 | 0,77% |
| Richardson (1914) | 6 | 0,87% | 6 | 1,4% | 6 | 1,8% | 6 | 1,55% |
| Séchet et al. (2014) | 6 | 0,87% | 6 | 1,4% | 6 | 1,8% | 6 | 1,55% |
| Taiti & Ferrara (1989) | 6 | 0,87% | 6 | 1,4% | 6 | 1,8% | 6 | 1,55% |
| Dalens et al. (1997) | 5 | 0,72% | 5 | 1,16% | 5 | 1,5% | 5 | 1,29% |
| Dollfus (1884) | 5 | 0,72% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lillemets & Wilson (2002) | 5 | 0,72% | 2 | 0,47% | 0 | 0% | 2 | 0,52% |
| Racovitza (1907) | 5 | 0,72% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Taiti & Ferrara (1996) | 5 | 0,72% | 5 | 1,16% | 2 | 0,6% | 5 | 1,29% |
| Vandel (1954) | 5 | 0,72% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Verhoeff (1928) | 5 | 0,72% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnefoy (1945) | 4 | 0,58% | 4 | 0,93% | 4 | 1,2% | 4 | 1,03% |
| Cuvier (1792) | 4 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dollfus (1895) | 4 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2010) | 4 | 0,58% | 3 | 0,7% | 3 | 0,9% | 3 | 0,77% |
| Nelson-Smith et al. (2014) | 4 | 0,58% | 3 | 0,7% | 3 | 0,9% | 3 | 0,77% |
| Paulian & Felice (1944) | 4 | 0,58% | 4 | 0,93% | 4 | 1,2% | 4 | 1,03% |
| Vandel (1946) | 4 | 0,58% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Ferrara & Taiti (1983) | 3 | 0,43% | 3 | 0,7% | 3 | 0,9% | 3 | 0,77% |
| 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 | 0,43% | 3 | 0,7% | 0 | 0% | 3 | 0,77% |
| Legrand (1953) | 3 | 0,43% | 3 | 0,7% | 3 | 0,9% | 3 | 0,77% |
| Legrand (1954) | 3 | 0,43% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Meurgey (2011) | 3 | 0,43% | 3 | 0,7% | 3 | 0,9% | 3 | 0,77% |
| Questel (2014) | 3 | 0,43% | 3 | 0,7% | 3 | 0,9% | 3 | 0,77% |
| Questel (2020) | 3 | 0,43% | 3 | 0,7% | 3 | 0,9% | 3 | 0,77% |
| Vandel (1924) | 3 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1938) | 3 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1981) | 3 | 0,43% | 3 | 0,7% | 3 | 0,9% | 3 | 0,77% |
| Carl (1908) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cochard et al. (2010) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Coulis (2017) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Dalens (1998) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Dalens (1998) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Dollfus (1887) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Frankenberger (1938) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garcia & Robla (2022) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Herold (1923) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Legrand (1956) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meinert (1880) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Mocquard (1974) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Moniez (1887) | 2 | 0,29% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Pavon et al. (2021) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Pugh et al. (2002) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Sars (1899) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Séchet et al. (2014) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Séchet (2014) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Taiti & Wynne (2015) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Taiti et al. (1995) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Thomas (2015) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Verhoeff (1908) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verhoeff (1917) | 2 | 0,29% | 2 | 0,47% | 2 | 0,6% | 2 | 0,52% |
| Adelski (2023) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Allspach & Brandt (2020) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Bagnall (1908) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Besse et al. (1975) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Bilton (1994) | 1 | 0,14% | 1 | 0,23% | 0 | 0% | 1 | 0,26% |
| Brandt (1833) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Budde-Lund (1879) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 0 | 0% |
| Budde-lund (1913) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Campos-Filho et al. (2017) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Cochereau (1974) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Dalens (1966) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Dalens (1966) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| De Geer (1778) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deblock et al. (1960) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Desmots (2016) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Dollfus (1889) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Dollfus (1893) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 0 | 0% |
| Fabricius (1798) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Ferrara & Taiti (1979) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Hullé et al. (2018) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Kilpert & Podsiadlowski (2006) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Kinahan (1857) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1838) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latreille (1804) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Latreille (1804) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legendre (1966) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Lemaire (2011) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 0 | 0% |
| Linnaeus (1758) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 0 | 0% |
| Linnaeus (1767) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lohmander (1924) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Magne (1969) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 0 | 0% |
| Mary (2017) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Michel-Salzat & Bouchon (2000) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Noël & Séchet (2007) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Noël et al. (2022) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Noël et al. (2023) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Perrier (1929) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Raupach et al. (2014) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Sardet et al. (2015) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmalfuss (2004) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Schotte et al. (1995 onwards) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Schultz (1974) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Scopoli (1763) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taiti (2014) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Touroult et al. (2020) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Vandel (1960) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Verhoeff (1908) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 0 | 0% |
| Verhoeff (1910) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Waga (1857) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Willmer et al. (1989) | 1 | 0,14% | 1 | 0,23% | 1 | 0,3% | 1 | 0,26% |
| Zaddach (1844) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
