Arachnides de la Réunion
258 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 | 15,17% | 127 | 41,78% | 127 | 41,91% | 127 | 41,91% |
| Kreiter et al. (2020) | 81 | 9,45% | 41 | 13,49% | 41 | 13,53% | 41 | 13,53% |
| Mahunka (1978) | 55 | 6,42% | 28 | 9,21% | 28 | 9,24% | 28 | 9,24% |
| Kreiter et al. (2002) | 44 | 5,13% | 33 | 10,86% | 33 | 10,89% | 33 | 10,89% |
| Ramage (2017) | 43 | 5,02% | 40 | 13,16% | 40 | 13,2% | 40 | 13,2% |
| Migeon (2015) | 32 | 3,73% | 32 | 10,53% | 32 | 10,56% | 32 | 10,56% |
| Nentwig et al. (2019) | 32 | 3,73% | 31 | 10,2% | 31 | 10,23% | 31 | 10,23% |
| Mahunka (1988) | 27 | 3,15% | 8 | 2,63% | 8 | 2,64% | 8 | 2,64% |
| Quilici et al. (2000) | 24 | 2,8% | 20 | 6,58% | 20 | 6,6% | 20 | 6,6% |
| Berland (1933) | 22 | 2,57% | 10 | 3,29% | 10 | 3,3% | 10 | 3,3% |
| Jourdan & Mille (2006) | 22 | 2,57% | 19 | 6,25% | 19 | 6,27% | 19 | 6,27% |
| Vayssières et al. (2001) | 22 | 2,57% | 17 | 5,59% | 17 | 5,61% | 17 | 5,61% |
| Ledoux (2007) | 21 | 2,45% | 19 | 6,25% | 19 | 6,27% | 19 | 6,27% |
| Meurgey (2011) | 20 | 2,33% | 16 | 5,26% | 16 | 5,28% | 16 | 5,28% |
| Dierkens & Charlat (2011) | 18 | 2,1% | 15 | 4,93% | 15 | 4,95% | 15 | 4,95% |
| Ledoux (2004) | 18 | 2,1% | 13 | 4,28% | 13 | 4,29% | 13 | 4,29% |
| Berland (1934) | 15 | 1,75% | 9 | 2,96% | 9 | 2,97% | 9 | 2,97% |
| Berland (1934) | 15 | 1,75% | 5 | 1,64% | 5 | 1,65% | 5 | 1,65% |
| Dierkens & Ramage (2016) | 15 | 1,75% | 14 | 4,61% | 14 | 4,62% | 14 | 4,62% |
| Gutierrez & Etienne (1986) | 15 | 1,75% | 14 | 4,61% | 14 | 4,62% | 14 | 4,62% |
| Berland (1942) | 14 | 1,63% | 7 | 2,3% | 7 | 2,31% | 7 | 2,31% |
| Ledoux & Hallé (1995) | 14 | 1,63% | 10 | 3,29% | 10 | 3,3% | 10 | 3,3% |
| Berland (1924) | 13 | 1,52% | 5 | 1,64% | 5 | 1,65% | 5 | 1,65% |
| Niedbała (2017) | 13 | 1,52% | 12 | 3,95% | 12 | 3,96% | 12 | 3,96% |
| Platnick (1993) | 13 | 1,52% | 8 | 2,63% | 8 | 2,64% | 8 | 2,64% |
| Quilici et al. (1997) | 13 | 1,52% | 13 | 4,28% | 13 | 4,29% | 13 | 4,29% |
| Mahnert (1975) | 12 | 1,4% | 12 | 3,95% | 9 | 2,97% | 12 | 3,96% |
| Souza et al. (2019) | 12 | 1,4% | 5 | 1,64% | 5 | 1,65% | 5 | 1,65% |
| Vedel et al. (2013) | 12 | 1,4% | 12 | 3,95% | 12 | 3,96% | 12 | 3,96% |
| Hammes & Putoa (1986) | 11 | 1,28% | 11 | 3,62% | 11 | 3,63% | 11 | 3,63% |
| Jourdan (2020) | 11 | 1,28% | 10 | 3,29% | 10 | 3,3% | 10 | 3,3% |
| Kreiter et al. (2013) | 11 | 1,28% | 11 | 3,62% | 11 | 3,63% | 11 | 3,63% |
| Berland (1935) | 10 | 1,17% | 5 | 1,64% | 5 | 1,65% | 5 | 1,65% |
| Dierkens (2021) | 10 | 1,17% | 10 | 3,29% | 10 | 3,3% | 10 | 3,3% |
| Flechtmann et al. (2000) | 10 | 1,17% | 10 | 3,29% | 10 | 3,3% | 10 | 3,3% |
| Guglielmone et al. (2023) | 10 | 1,17% | 10 | 3,29% | 10 | 3,3% | 10 | 3,3% |
| Kreiter et al. (2018) | 9 | 1,05% | 9 | 2,96% | 9 | 2,97% | 9 | 2,97% |
| Kreiter et al. (2020) | 9 | 1,05% | 9 | 2,96% | 9 | 2,97% | 9 | 2,97% |
| Gutierrez (1968) | 8 | 0,93% | 8 | 2,63% | 8 | 2,64% | 8 | 2,64% |
| Lopez (1990) | 8 | 0,93% | 8 | 2,63% | 8 | 2,64% | 8 | 2,64% |
| Questel (2020) | 8 | 0,93% | 8 | 2,63% | 8 | 2,64% | 8 | 2,64% |
| Bonaldo & Brescovit (1992) | 7 | 0,82% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Flechtmann et al. (1999) | 7 | 0,82% | 7 | 2,3% | 7 | 2,31% | 7 | 2,31% |
| Hervé & Garrouste (2009) | 7 | 0,82% | 7 | 2,3% | 7 | 2,31% | 7 | 2,31% |
| Jacquot et al. (2016) | 7 | 0,82% | 7 | 2,3% | 7 | 2,31% | 7 | 2,31% |
| Pritchard & Baker (1962) | 7 | 0,82% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Roger (2018) | 7 | 0,82% | 7 | 2,3% | 7 | 2,31% | 7 | 2,31% |
| Taczanowski (1874) | 7 | 0,82% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Aharon et al. (2017) | 6 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berland (1929) | 6 | 0,7% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Hullé et al. (2018) | 6 | 0,7% | 6 | 1,97% | 6 | 1,98% | 6 | 1,98% |
| Schmidt & Jocqué (1983) | 6 | 0,7% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Yokoyama (2013) | 6 | 0,7% | 6 | 1,97% | 6 | 1,98% | 6 | 1,98% |
| Delfosse (2017) | 5 | 0,58% | 5 | 1,64% | 5 | 1,65% | 5 | 1,65% |
| Dupérré (2023) | 5 | 0,58% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Etienne & Vilardebó (1978) | 5 | 0,58% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Gutierrez (1981) | 5 | 0,58% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Hammer (1972) | 5 | 0,58% | 5 | 1,64% | 5 | 1,65% | 5 | 1,65% |
| Harvey (2011) | 5 | 0,58% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Huber et al. (2023) | 5 | 0,58% | 5 | 1,64% | 5 | 1,65% | 5 | 1,65% |
| Nibouche et al. (202X) | 5 | 0,58% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Niedbała & Liu (2023) | 5 | 0,58% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Questel & Le Quellec (2012) | 5 | 0,58% | 5 | 1,64% | 5 | 1,65% | 5 | 1,65% |
| UICN Comité français, OFB, MNHN & AsFrA (2023) | 5 | 0,58% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Bigot (1992) | 4 | 0,47% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Etienne & Flechtmann (2006) | 4 | 0,47% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Kreiter & Moraes (1997) | 4 | 0,47% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Mahunka (1978) | 4 | 0,47% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Mahunka (1985) | 4 | 0,47% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Marples (1957) | 4 | 0,47% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Niedbała & Penttinen (2007) | 4 | 0,47% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Niedbała & Starý (2015) | 4 | 0,47% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Rémy (1950) | 4 | 0,47% | 4 | 1,32% | 4 | 1,32% | 4 | 1,32% |
| Vinson (1863) | 4 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1802) | 4 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adamson (1935) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Baker & Pritchard (1960) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Beatty et al. (2008) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Berland (1927) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Berry et al. (1998) | 3 | 0,35% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Bonnet (1924) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Brun et al. (1983) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Cazanove et al. (2022) | 3 | 0,35% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Cochereau (1966) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Duhamel (2018) | 3 | 0,35% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Gasnier et al. (2015) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Gutierrez (1982) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Hullé & Vernon (2021) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Maquart et al. (2018) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Parola & Barré (2004) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Rageau (1958) | 3 | 0,35% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Simon (1897) | 3 | 0,35% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Smit et al. (2023) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| Taczanowski (1871) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal & Vansteene (2021) | 3 | 0,35% | 3 | 0,99% | 3 | 0,99% | 3 | 0,99% |
| (2022) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adamson (1936) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anderson & Trueman (2000) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Anonyme (2018) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Baehr et al. (2013) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Balogh (1961) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Barre et al. (1988) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Bartsch (1986) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Beron (2020) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Berry et al. (1997) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Blommers (1974) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Brignoli (1981) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Bryant (1942) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caporiacco & Denis (1954) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Channabasavanna (1966) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Chevalier & Dewynter (2020) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Courtial (2023) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Dadant & Etienne (1973) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Doleschall (1857) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flechtmann & Etienne (2000) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Flechtmann & Etienne (2001) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Flechtmann & Etienne (2005) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Flechtmann & Etienne (2006) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Flechtmann & Moraes (2013) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Flechtmann et al. (1999) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Gaud & Atyeo (1986) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Gaud & Atyeo (1987) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Grandjean (1933) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Hammer (1961) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Hammer (1979) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Kemal (2008) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Klein et al. (1982) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Kreiter & Douin (2021) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Lawrence (1969) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lourenço (1987) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Migeon et al. (2019) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Moraes et al. (2006) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Muñoz-Leal et al. (2017) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Narita et al. (2013) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Niedbała (1994) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Niedbała (1998) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Odin (2014) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Odin (2017) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Oudemans (1912) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pritchard & Baker (1955) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Rageau (1956) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Raven (2015) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Remy (1952) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Roberts (2014) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schicha & Gutierrez (1985) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Smith et al. (1989) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taczanowski (1872) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taczanowski (1874) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult et al. (2020) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Ueckermann & Loots (1985) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vitzthum (1935) | 2 | 0,23% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Walckenaer ([1841]) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walzer et al. (2007) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| Yaginuma (1972) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zaher & Shehata (1966) | 2 | 0,23% | 2 | 0,66% | 2 | 0,66% | 2 | 0,66% |
| André (1932) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Audouin (1826) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Auger et al. (2023) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Balogh (1958) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Banks (1905) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Banks (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barré & Camus (1983) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beatty et al. (1991) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Binetruy et al. (2019) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Blommers (1976) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bosmans & Hervé (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambridge (1879) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cazanove (2019) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Chinniah & Mohanasundaram (2001) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Cicculli et al. (2019) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Cohic (1959) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Conte et al. (2007) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Coulis (2017) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Couteyen (2021) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Dandeu et al. (1991) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Déjean et al. (2023) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Déjean (2015) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Dierkens (2011) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Dierkens (2012) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Dönitz (1910) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Dosse (1958) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dufour (1831) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eldin et al. (2011) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Emerit & Ledoux (2008) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Esnault et al. (2019) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Fabricius (1798) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flechtmann & Etienne (2004) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Forskål (1775) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Fourcroy (1785) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frenot et al. (2005) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Gaud & Atyeo (1976) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Gaud (1953) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Geijskes (1939) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gillespie (2003) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Gillespie (2003) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Gonzalez-rodriguez (1963) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Grandjean (1936) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gupta (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huber (2012) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Jäger (2002) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1836) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kreiter et al. (2000) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Kreiter et al. (2016) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Kuntner et al. (2018) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Le Conte et al. (2015) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Lecigne et al. (2021) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Leon (1965) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Lourenço (1983) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Luo (2023) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Mahunka (1973) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Mahunka (1982) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Mahunka (1992) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Mammola & Milano (2019) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Maréchal & Iinuma (2013) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Marie & Vetter (2015) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Mello-leitao (1942) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mello-Leitão (1945) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moraes et al. (2000) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Nardi et al. (2023) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Navajas et al. (2010) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Nentwig & Kobelt (2010) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Neumann (1901) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neumann (1907) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Pavesi (1883) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Platnick et al. (2011) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Plénet (1965) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Ponel et al. (2017) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Rivière (1979) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Rossi & Godoy (2006) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Schicha (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schrank (1781) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seurat (1934) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Simon (1864) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1873) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1892) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1983) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smit (2002) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Smit (2009) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Staręga (1989) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Tentcheva et al. (2004) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Thorell (1875) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Thorell (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tixier et al. (2013) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Travé (1982) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ueckermann & Loots (1988) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Ueckermann (1992) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Valerio (1981) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal (2012) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Vitzthum (1935) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Walckenaer (1805) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1837) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1837) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Walter (1915) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ythier (2018) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Zannou et al. (2007) | 1 | 0,12% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
