Araignées de la Réunion
119 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Cazanove (2022) | 130 | 27,78% | 127 | 94,07% | 127 | 94,07% | 127 | 94,07% |
| Nentwig et al. (2019) | 32 | 6,84% | 31 | 22,96% | 31 | 22,96% | 31 | 22,96% |
| Ramage (2017) | 23 | 4,91% | 21 | 15,56% | 21 | 15,56% | 21 | 15,56% |
| Berland (1933) | 22 | 4,7% | 10 | 7,41% | 10 | 7,41% | 10 | 7,41% |
| Ledoux (2007) | 21 | 4,49% | 19 | 14,07% | 19 | 14,07% | 19 | 14,07% |
| Dierkens & Charlat (2011) | 18 | 3,85% | 15 | 11,11% | 15 | 11,11% | 15 | 11,11% |
| Ledoux (2004) | 18 | 3,85% | 13 | 9,63% | 13 | 9,63% | 13 | 9,63% |
| Berland (1934) | 15 | 3,21% | 5 | 3,7% | 5 | 3,7% | 5 | 3,7% |
| Berland (1934) | 15 | 3,21% | 9 | 6,67% | 9 | 6,67% | 9 | 6,67% |
| Dierkens & Ramage (2016) | 15 | 3,21% | 14 | 10,37% | 14 | 10,37% | 14 | 10,37% |
| Berland (1942) | 14 | 2,99% | 7 | 5,19% | 7 | 5,19% | 7 | 5,19% |
| Ledoux & Hallé (1995) | 14 | 2,99% | 10 | 7,41% | 10 | 7,41% | 10 | 7,41% |
| Berland (1924) | 13 | 2,78% | 5 | 3,7% | 5 | 3,7% | 5 | 3,7% |
| Platnick (1993) | 13 | 2,78% | 8 | 5,93% | 8 | 5,93% | 8 | 5,93% |
| Souza et al. (2019) | 12 | 2,56% | 5 | 3,7% | 5 | 3,7% | 5 | 3,7% |
| Vedel et al. (2013) | 12 | 2,56% | 12 | 8,89% | 12 | 8,89% | 12 | 8,89% |
| Vayssières et al. (2001) | 11 | 2,35% | 8 | 5,93% | 8 | 5,93% | 8 | 5,93% |
| Berland (1935) | 10 | 2,14% | 5 | 3,7% | 5 | 3,7% | 5 | 3,7% |
| Dierkens (2021) | 10 | 2,14% | 10 | 7,41% | 10 | 7,41% | 10 | 7,41% |
| Lopez (1990) | 8 | 1,71% | 8 | 5,93% | 8 | 5,93% | 8 | 5,93% |
| Bonaldo & Brescovit (1992) | 7 | 1,5% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Hervé & Garrouste (2009) | 7 | 1,5% | 7 | 5,19% | 7 | 5,19% | 7 | 5,19% |
| Jacquot et al. (2016) | 7 | 1,5% | 7 | 5,19% | 7 | 5,19% | 7 | 5,19% |
| Jourdan & Mille (2006) | 7 | 1,5% | 6 | 4,44% | 6 | 4,44% | 6 | 4,44% |
| Questel (2020) | 7 | 1,5% | 7 | 5,19% | 7 | 5,19% | 7 | 5,19% |
| Roger (2018) | 7 | 1,5% | 7 | 5,19% | 7 | 5,19% | 7 | 5,19% |
| Taczanowski (1874) | 7 | 1,5% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Aharon et al. (2017) | 6 | 1,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berland (1929) | 6 | 1,28% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Hullé et al. (2018) | 6 | 1,28% | 6 | 4,44% | 6 | 4,44% | 6 | 4,44% |
| Jourdan (2020) | 6 | 1,28% | 5 | 3,7% | 5 | 3,7% | 5 | 3,7% |
| Schmidt & Jocqué (1983) | 6 | 1,28% | 3 | 2,22% | 3 | 2,22% | 3 | 2,22% |
| Yokoyama (2013) | 6 | 1,28% | 6 | 4,44% | 6 | 4,44% | 6 | 4,44% |
| Dupérré (2023) | 5 | 1,07% | 4 | 2,96% | 4 | 2,96% | 4 | 2,96% |
| Huber et al. (2023) | 5 | 1,07% | 5 | 3,7% | 5 | 3,7% | 5 | 3,7% |
| UICN Comité français, OFB, MNHN & AsFrA (2023) | 5 | 1,07% | 4 | 2,96% | 4 | 2,96% | 4 | 2,96% |
| Bigot (1992) | 4 | 0,85% | 3 | 2,22% | 3 | 2,22% | 3 | 2,22% |
| Marples (1957) | 4 | 0,85% | 3 | 2,22% | 3 | 2,22% | 3 | 2,22% |
| Questel & Le Quellec (2012) | 4 | 0,85% | 4 | 2,96% | 4 | 2,96% | 4 | 2,96% |
| Vinson (1863) | 4 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1802) | 4 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beatty et al. (2008) | 3 | 0,64% | 3 | 2,22% | 3 | 2,22% | 3 | 2,22% |
| Berland (1927) | 3 | 0,64% | 3 | 2,22% | 3 | 2,22% | 3 | 2,22% |
| Berry et al. (1998) | 3 | 0,64% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Cazanove et al. (2022) | 3 | 0,64% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Duhamel (2018) | 3 | 0,64% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Gasnier et al. (2015) | 3 | 0,64% | 3 | 2,22% | 3 | 2,22% | 3 | 2,22% |
| Hullé & Vernon (2021) | 3 | 0,64% | 3 | 2,22% | 3 | 2,22% | 3 | 2,22% |
| Simon (1897) | 3 | 0,64% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Taczanowski (1871) | 3 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal & Vansteene (2021) | 3 | 0,64% | 3 | 2,22% | 3 | 2,22% | 3 | 2,22% |
| Baehr et al. (2013) | 2 | 0,43% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Berry et al. (1997) | 2 | 0,43% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Brignoli (1981) | 2 | 0,43% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Bryant (1942) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caporiacco & Denis (1954) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cochereau (1966) | 2 | 0,43% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Courtial (2023) | 2 | 0,43% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Doleschall (1857) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kemal (2008) | 2 | 0,43% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Odin (2014) | 2 | 0,43% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Odin (2017) | 2 | 0,43% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Raven (2015) | 2 | 0,43% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Roberts (2014) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taczanowski (1872) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taczanowski (1874) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult et al. (2020) | 2 | 0,43% | 2 | 1,48% | 2 | 1,48% | 2 | 1,48% |
| Walckenaer ([1841]) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yaginuma (1972) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Audouin (1826) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Banks (1909) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beatty et al. (1991) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Bosmans & Hervé (2021) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambridge (1879) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cazanove (2019) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Couteyen (2021) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Déjean et al. (2023) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Déjean (2015) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Dierkens (2011) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Dierkens (2012) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Dufour (1831) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Emerit & Ledoux (2008) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Forskål (1775) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Frenot et al. (2005) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Gillespie (2003) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Gillespie (2003) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Huber (2012) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Jäger (2002) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1836) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuntner et al. (2018) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Lecigne et al. (2021) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Luo (2023) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Mammola & Milano (2019) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Maréchal & Iinuma (2013) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Marie & Vetter (2015) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Mello-leitao (1942) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mello-Leitão (1945) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nardi et al. (2023) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Nentwig & Kobelt (2010) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Nibouche et al. (202X) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Pavesi (1883) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Platnick et al. (2011) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Ponel et al. (2017) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Rivière (1979) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Rossi & Godoy (2006) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Seurat (1934) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Simon (1864) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1873) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1892) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1893) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1909) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1983) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thorell (1875) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Thorell (1887) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valerio (1981) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal (2012) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
| Walckenaer (1805) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1837) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1837) | 1 | 0,21% | 1 | 0,74% | 1 | 0,74% | 1 | 0,74% |
