Scorpions et pseudoscorpions
141 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Heurtault (1986) | 46 | 10,45% | 42 | 15,44% | 42 | 17,14% | 38 | 15,2% |
| Ythier (2018) | 34 | 7,73% | 34 | 12,5% | 33 | 13,47% | 34 | 13,6% |
| Ythier et al. (2020) | 20 | 4,55% | 20 | 7,35% | 20 | 8,16% | 20 | 8% |
| Lourenço (1983) | 18 | 4,09% | 12 | 4,41% | 12 | 4,9% | 12 | 4,8% |
| Meurgey (2011) | 13 | 2,95% | 12 | 4,41% | 12 | 4,9% | 12 | 4,8% |
| Leclerc (1981) | 12 | 2,73% | 12 | 4,41% | 8 | 3,27% | 9 | 3,6% |
| Mahnert (1975) | 12 | 2,73% | 12 | 4,41% | 9 | 3,67% | 12 | 4,8% |
| Vitali-di & Castri (1984) | 12 | 2,73% | 10 | 3,68% | 10 | 4,08% | 10 | 4% |
| Ythier (2019) | 11 | 2,5% | 11 | 4,04% | 11 | 4,49% | 11 | 4,4% |
| Beier (1966) | 10 | 2,27% | 10 | 3,68% | 10 | 4,08% | 10 | 4% |
| Beron (2017) | 10 | 2,27% | 9 | 3,31% | 9 | 3,67% | 9 | 3,6% |
| Lourenço (2018) | 10 | 2,27% | 10 | 3,68% | 10 | 4,08% | 10 | 4% |
| Beier (1964) | 9 | 2,05% | 6 | 2,21% | 6 | 2,45% | 6 | 2,4% |
| Lourenço (1987) | 9 | 2,05% | 8 | 2,94% | 8 | 3,27% | 8 | 3,2% |
| Krajčovičová et al. (2024) | 8 | 1,82% | 8 | 2,94% | 8 | 3,27% | 8 | 3,2% |
| Lourenço et al. (2020) | 8 | 1,82% | 8 | 2,94% | 8 | 3,27% | 8 | 3,2% |
| Chevalier & Dewynter (2020) | 7 | 1,59% | 6 | 2,21% | 6 | 2,45% | 6 | 2,4% |
| Gardini (2022) | 7 | 1,59% | 7 | 2,57% | 7 | 2,86% | 7 | 2,8% |
| Lourenço (2021) | 7 | 1,59% | 7 | 2,57% | 7 | 2,86% | 7 | 2,8% |
| Rageau (1958) | 6 | 1,36% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Ramage (2017) | 6 | 1,36% | 6 | 2,21% | 6 | 2,45% | 6 | 2,4% |
| Vachon (1937) | 6 | 1,36% | 6 | 2,21% | 6 | 2,45% | 4 | 1,6% |
| Beier (1934) | 5 | 1,14% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Cosgrove et al. (2016) | 5 | 1,14% | 5 | 1,84% | 5 | 2,04% | 5 | 2% |
| Lourenço & Leguin (2008) | 5 | 1,14% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Lourenço (1997) | 5 | 1,14% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Tropea & Parmakelis (2022) | 5 | 1,14% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Callaini (1981) | 4 | 0,91% | 4 | 1,47% | 4 | 1,63% | 4 | 1,6% |
| Heurtault (1980) | 4 | 0,91% | 4 | 1,47% | 4 | 1,63% | 2 | 0,8% |
| Kraepelin (1914) | 4 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lourenco (1984) | 4 | 0,91% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Ćurčić et al. (2010) | 4 | 0,91% | 4 | 1,47% | 4 | 1,63% | 4 | 1,6% |
| Beier (1968) | 3 | 0,68% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Chamberlin (1939) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Gardini et al. (2017) | 3 | 0,68% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Heurtault (1968) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Heurtault (1969) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Heurtault (1978) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Iorio (2023) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Leclerc (1983) | 3 | 0,68% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lourenco (2001) | 3 | 0,68% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço (2008) | 3 | 0,68% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lourenço (2013) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Mahnert (1974) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Monod (2011) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Pocock (1897) | 3 | 0,68% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Questel & Le Quellec (2012) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Questel (2020) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Sissom & Francke (1983) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Teruel & Questel (2020) | 3 | 0,68% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Teruel (2008) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Ythier & Chevalier (2020) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Ythier et al. (2022) | 3 | 0,68% | 3 | 1,1% | 3 | 1,22% | 3 | 1,2% |
| Zaragoza (2017) | 3 | 0,68% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Adamson (1935) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Beier (1954) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Beier (1965) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beier (1979) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Coulis (2017) | 2 | 0,45% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Courtial (2014) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Curcic (2013) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Ellingsen (1908) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellingsen (1909) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fet & Braunwalder (2000) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardini (2009) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardini (2021) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Gardini (2023) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Harvey (1989) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Harvey (2009) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Harvey (2020) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Heurtault (1968) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heurtault-Rossi (1963) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Heurtault-Rossi (1968) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Hullé et al. (2018) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Klein et al. (1982) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Koch (1841) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lourenço & Chevalier (2022) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço & Goodman (2009) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço & Monod (1999) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço & Ythier (2011) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço et al. (2022) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço (1981) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço (1995) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenco (2003) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço (2003) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço (2012) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço (2012) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço (2016) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Lourenço (2016) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Mahnert (1978) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Rageau (1956) | 2 | 0,45% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Simon (1872) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1876) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1879) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1879) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1881) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Teruel & Chazal (2010) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Vachon & Heurtault-rossi (1964) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Vachon (1947) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Vachon (1954) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Vachon (1963) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Vachon (1976) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Walckenaer & Gervais (1844) | 2 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ythier & Laborieux (2022) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Ythier (2015) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Ythier (2021) | 2 | 0,45% | 2 | 0,74% | 2 | 0,82% | 2 | 0,8% |
| Bigot (1992) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Chamberlin (1939) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Christophoryova et al. (2011) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cochereau (1966) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Buthus occitanus (Amoreux, 1789) (Scorpiones, Buthidae). Sa répartition en France. Arachnides, 54(Supplément): 1-33.">Dupré et al. (2008) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| Esposito et al. (2017) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| European Nucleotide Archive (2019) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harvey et al. (2007) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Heurtault (1990) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Hullé & Vernon (2021) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Iorio (2003) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan & Mille (2006) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Juberthie (1995) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Kew (1916) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Koch (1873) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kovařík (2003) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Leach (1817) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemaire & Raffaldi (2016) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Linnaeus (1758) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Livory & Santais (2022) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Lourenço (1998) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Lourenço (2015) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Lourenço (2019) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Lourenço (2023) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Mahnert (2011) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Mahnert (2014) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Navás (1925) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Oger (2016) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Preyssler (1790) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rivière (1979) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Seurat (1934) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Taylor et al. (1977) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vachon (1941) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annals of Natural History, (7)(xv): 94-143.">With (1905) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
| Yokoyama (2013) | 1 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,4% |
