Arachnides des îles subantarctiques
87 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Hullé et al. (2018) | 40 | 18,35% | 38 | 34,23% | 36 | 34,62% | 36 | 34,29% |
Lohmann (1907) | 33 | 15,14% | 14 | 12,61% | 14 | 13,46% | 14 | 13,33% |
Starý & Block (1998) | 26 | 11,93% | 24 | 21,62% | 21 | 20,19% | 22 | 20,95% |
Newell (1984) | 25 | 11,47% | 20 | 18,02% | 20 | 19,23% | 20 | 19,05% |
Ledoux (1991) | 23 | 10,55% | 23 | 20,72% | 19 | 18,27% | 23 | 21,9% |
Hullé & Vernon (2021) | 19 | 8,72% | 19 | 17,12% | 17 | 16,35% | 18 | 17,14% |
Fain (1974) | 16 | 7,34% | 16 | 14,41% | 12 | 11,54% | 14 | 13,33% |
Travé (1982) | 11 | 5,05% | 9 | 8,11% | 7 | 6,73% | 9 | 8,57% |
Wallwork (1972) | 11 | 5,05% | 10 | 9,01% | 9 | 8,65% | 8 | 7,62% |
Bartsch (2009) | 10 | 4,59% | 7 | 6,31% | 7 | 6,73% | 7 | 6,67% |
Pickard-Cambridge (1876) | 10 | 4,59% | 4 | 3,6% | 4 | 3,85% | 2 | 1,9% |
Pugh (2004) | 10 | 4,59% | 10 | 9,01% | 8 | 7,69% | 9 | 8,57% |
Travé (2021) | 10 | 4,59% | 10 | 9,01% | 10 | 9,62% | 10 | 9,52% |
Subías (2004) | 9 | 4,13% | 9 | 8,11% | 8 | 7,69% | 9 | 8,57% |
Frenot et al. (2005) | 6 | 2,75% | 3 | 2,7% | 3 | 2,88% | 3 | 2,86% |
Ysnel & Ledoux (1988) | 6 | 2,75% | 6 | 5,41% | 6 | 5,77% | 5 | 4,76% |
André (1933) | 5 | 2,29% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Dalenius & Wilson (1958) | 5 | 2,29% | 3 | 2,7% | 0 | 0% | 3 | 2,86% |
Castilho et al. (2016) | 4 | 1,83% | 4 | 3,6% | 4 | 3,85% | 4 | 3,81% |
Cazanove (2022) | 4 | 1,83% | 3 | 2,7% | 3 | 2,88% | 3 | 2,86% |
Gaud (1952) | 4 | 1,83% | 4 | 3,6% | 4 | 3,85% | 4 | 3,81% |
Hammer (1958) | 4 | 1,83% | 3 | 2,7% | 3 | 2,88% | 3 | 2,86% |
Klompen & Johnson (2018) | 4 | 1,83% | 4 | 3,6% | 4 | 3,85% | 4 | 3,81% |
Pletzen van et Kok (1971) | 4 | 1,83% | 4 | 3,6% | 4 | 3,85% | 4 | 3,81% |
Arnaud (1974) | 3 | 1,38% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Bellido et al. (1987) | 3 | 1,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Beron (2021) | 3 | 1,38% | 3 | 2,7% | 3 | 2,88% | 3 | 2,86% |
Beron (2022) | 3 | 1,38% | 3 | 2,7% | 3 | 2,88% | 3 | 2,86% |
Grandjean (1955) | 3 | 1,38% | 3 | 2,7% | 3 | 2,88% | 3 | 2,86% |
Lee (1970) | 3 | 1,38% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Strandtmann & Davies (1972) | 3 | 1,38% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Vidal (2012) | 3 | 1,38% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Wallwork (1963) | 3 | 1,38% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
André & Colas-belcour (1942) | 2 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartsch (1992) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Bovée et al. (1973) | 2 | 0,92% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Cazanove et al. (2022) | 2 | 0,92% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Covarrubias (1968) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Enderlein (1909) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Forsslund (1964) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Grandjean (1957) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Hirschmann & Wisniewski (1988) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Hunter (1967) | 2 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2009) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Karg (1997) | 2 | 0,92% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Lions (1966) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 1 | 0,95% |
Nentwig & Kobelt (2010) | 2 | 0,92% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Ramage (2017) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Richters (1908) | 2 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Roberts (2014) | 2 | 0,92% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Saaristo & Tanasevitch (1996) | 2 | 0,92% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Schenker (1986) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 0 | 0% |
Trouessart (1898) | 2 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal & Vansteene (2021) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Wainstein (1956) | 2 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer (1802) | 2 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallwork (1970) | 2 | 0,92% | 2 | 1,8% | 2 | 1,92% | 2 | 1,9% |
Bartsch (2016) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Beatty et al. (1991) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Bellido & Dafonseca (1988) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Berland (1942) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Blackwall (1852) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Cambridge (1879) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Déjan (2012) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Delfosse (2017) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Fueßlin (1775) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Grandjean (1936) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Guglielmone et al. (2023) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Guiguen et al. (1987) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Hammer (1972) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Hughes & Goodman (1969) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 0 | 0% |
Hughes (1955) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 0 | 0% |
Hunter (1970) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Jourdan (2020) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Ledoux & Hallé (1995) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Mahunka (1978) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Mahunka (1985) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Mammola & Milano (2019) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Nentwig et al. (2019) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Porto & Pérez-gonzález (2020) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Trouessart (1889) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Trouessart (1902) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 1 | 0,46% | 1 | 0,9% | 1 | 0,96% | 1 | 0,95% |
Vinson (1863) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallwork (1962) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Zumpt & Till (1956) | 1 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |