Araignées de Nouvelle-Calédonie
132 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Platnick (1993) | 191 | 31,89% | 155 | 47,26% | 153 | 46,93% | 155 | 47,55% |
| Berland (1924) | 157 | 26,21% | 98 | 29,88% | 98 | 30,06% | 97 | 29,75% |
| Raven (1994) | 49 | 8,18% | 49 | 14,94% | 49 | 15,03% | 49 | 15,03% |
| Raven & Churchill (1991) | 43 | 7,18% | 43 | 13,11% | 43 | 13,19% | 43 | 13,19% |
| Berland (1929) | 35 | 5,84% | 19 | 5,79% | 19 | 5,83% | 18 | 5,52% |
| Berland (1933) | 32 | 5,34% | 14 | 4,27% | 14 | 4,29% | 13 | 3,99% |
| Baehr et al. (2013) | 28 | 4,67% | 28 | 8,54% | 28 | 8,59% | 28 | 8,59% |
| Berland (1934) | 27 | 4,51% | 13 | 3,96% | 13 | 3,99% | 11 | 3,37% |
| Raven (1991) | 26 | 4,34% | 26 | 7,93% | 26 | 7,98% | 26 | 7,98% |
| Ramage (2017) | 25 | 4,17% | 21 | 6,4% | 21 | 6,44% | 19 | 5,83% |
| Berland (1934) | 24 | 4,01% | 13 | 3,96% | 13 | 3,99% | 11 | 3,37% |
| Bigot (1992) | 21 | 3,51% | 14 | 4,27% | 14 | 4,29% | 12 | 3,68% |
| Dierkens & Charlat (2011) | 20 | 3,34% | 15 | 4,57% | 15 | 4,6% | 14 | 4,29% |
| Jourdan (2020) | 19 | 3,17% | 17 | 5,18% | 17 | 5,21% | 17 | 5,21% |
| Berland (1942) | 16 | 2,67% | 9 | 2,74% | 9 | 2,76% | 7 | 2,15% |
| Cazanove (2022) | 16 | 2,67% | 14 | 4,27% | 14 | 4,29% | 13 | 3,99% |
| Patoleta et al. (2017) | 16 | 2,67% | 16 | 4,88% | 16 | 4,91% | 16 | 4,91% |
| Simon (1897) | 15 | 2,5% | 6 | 1,83% | 6 | 1,84% | 5 | 1,53% |
| Dierkens & Ramage (2016) | 14 | 2,34% | 12 | 3,66% | 12 | 3,68% | 10 | 3,07% |
| Ledoux & Hallé (1995) | 14 | 2,34% | 8 | 2,44% | 8 | 2,45% | 8 | 2,45% |
| Berland (1935) | 13 | 2,17% | 7 | 2,13% | 7 | 2,15% | 7 | 2,15% |
| Dierkens (2021) | 12 | 2% | 12 | 3,66% | 12 | 3,68% | 10 | 3,07% |
| Patoleta (2016) | 12 | 2% | 11 | 3,35% | 11 | 3,37% | 11 | 3,37% |
| Platnick & Forster (1993) | 11 | 1,84% | 11 | 3,35% | 11 | 3,37% | 11 | 3,37% |
| Gray (1992) | 10 | 1,67% | 10 | 3,05% | 10 | 3,07% | 10 | 3,07% |
| Jourdan & Mille (2006) | 10 | 1,67% | 9 | 2,74% | 9 | 2,76% | 9 | 2,76% |
| Patoleta (2014) | 10 | 1,67% | 10 | 3,05% | 10 | 3,07% | 10 | 3,07% |
| Berry et al. (1997) | 9 | 1,5% | 9 | 2,74% | 9 | 2,76% | 9 | 2,76% |
| Vedel et al. (2013) | 9 | 1,5% | 9 | 2,74% | 9 | 2,76% | 8 | 2,45% |
| Patoleta & Żabka (2019) | 8 | 1,34% | 8 | 2,44% | 8 | 2,45% | 8 | 2,45% |
| Berry et al. (1996) | 7 | 1,17% | 6 | 1,83% | 6 | 1,84% | 6 | 1,84% |
| Platnick (2002) | 7 | 1,17% | 7 | 2,13% | 7 | 2,15% | 7 | 2,15% |
| Pocock (1898) | 7 | 1,17% | 5 | 1,52% | 5 | 1,53% | 4 | 1,23% |
| Souza et al. (2019) | 7 | 1,17% | 3 | 0,91% | 3 | 0,92% | 3 | 0,92% |
| Baehr & Harvey (2013) | 6 | 1% | 6 | 1,83% | 6 | 1,84% | 6 | 1,84% |
| Marples (1957) | 6 | 1% | 4 | 1,22% | 4 | 1,23% | 3 | 0,92% |
| Nentwig et al. (2019) | 6 | 1% | 5 | 1,52% | 5 | 1,53% | 4 | 1,23% |
| Questel (2020) | 6 | 1% | 6 | 1,83% | 6 | 1,84% | 6 | 1,84% |
| Simon (1880) | 6 | 1% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN Comité français, OFB, MNHN & AsFrA (2023) | 6 | 1% | 5 | 1,52% | 5 | 1,53% | 5 | 1,53% |
| Dupérré (2023) | 5 | 0,83% | 5 | 1,52% | 5 | 1,53% | 5 | 1,53% |
| Kallal & Hormiga (2018) | 5 | 0,83% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Taczanowski (1874) | 5 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2013) | 5 | 0,83% | 5 | 1,52% | 5 | 1,53% | 5 | 1,53% |
| Cochereau (1966) | 4 | 0,67% | 4 | 1,22% | 4 | 1,23% | 3 | 0,92% |
| Magalhaes et al. (2022) | 4 | 0,67% | 4 | 1,22% | 4 | 1,23% | 4 | 1,23% |
| Questel & Le Quellec (2012) | 4 | 0,67% | 4 | 1,22% | 4 | 1,23% | 4 | 1,23% |
| Raven (2015) | 4 | 0,67% | 3 | 0,91% | 3 | 0,92% | 3 | 0,92% |
| Balogh (1978) | 3 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beatty et al. (2008) | 3 | 0,5% | 3 | 0,91% | 3 | 0,92% | 3 | 0,92% |
| Berland (1927) | 3 | 0,5% | 3 | 0,91% | 3 | 0,92% | 2 | 0,61% |
| Berry et al. (1998) | 3 | 0,5% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Brignoli (1981) | 3 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1865) | 3 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1867) | 3 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Patoleta (2009) | 3 | 0,5% | 3 | 0,91% | 3 | 0,92% | 3 | 0,92% |
| Rix & Harvey (2010) | 3 | 0,5% | 3 | 0,91% | 3 | 0,92% | 3 | 0,92% |
| Roger (2018) | 3 | 0,5% | 3 | 0,91% | 3 | 0,92% | 3 | 0,92% |
| Simon (1906) | 3 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Szuts (2002) | 3 | 0,5% | 3 | 0,91% | 3 | 0,92% | 3 | 0,92% |
| Taczanowski (1871) | 3 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alvarez-padilla et al. (2020) | 2 | 0,33% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Brignoli (1980) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chrysanthus et al. (1929) | 2 | 0,33% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Churchill & Raven (1992) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Courtial (2023) | 2 | 0,33% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Esyunin & Zamani (2020) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Harvey et al. (2007) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hervé & Garrouste (2009) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Huber (2000) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Hullé et al. (2018) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Koch (1871) | 2 | 0,33% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Kuntner et al. (2018) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Ledoux (2007) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas et al. (208-212) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Patoleta & Gardzińska (2013) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Patrick (2015) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Platnick & Baehr, 2006 | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Platnick & Dupérré (2009) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Platnick et al. (2012) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Smith (2006) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Taczanowski (1872) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taczanowski (1874) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thorell (1875) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thorell (1887) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vayssières et al. (2001) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Walckenaer ([1841]) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zabka (1992) | 2 | 0,33% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
| Audouin (1826) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cazanove (2019) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Déjean & Danflous (2017) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Déjean et al. (2023) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Doleschall (1857) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dufour (1831) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1793) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frenot et al. (2005) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fueßlin (1775) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gasnier et al. (2015) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Hentz (1847) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Hullé & Vernon (2021) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Jacquot et al. (2016) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Jäger (2002) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keyserling (1865) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keyserling (1887) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1836) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1872) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kritscher (1966) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levi (1983) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Mammola & Milano (2019) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Iinuma (2013) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Marie & Vetter (2015) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Marples (1964) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nentwig & Kobelt (2010) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pickard-cambridge (1877) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Ponel et al. (2017) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Rageau (1958) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Raven (1981) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rivière (1979) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 0 | 0% |
| Robson (1878) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossi & Godoy (2006) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Seurat (1934) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Sherwood (2022) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Simon (1864) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1889) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1983) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith et al. (2017) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Thorell (1870) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thorell (1897) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult et al. (2020) | 1 | 0,17% | 1 | 0,3% | 1 | 0,31% | 1 | 0,31% |
| Vinson (1863) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1837) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
