Faune cavernicole de France
Faune cavernicole au sens large (inclut les troglobies/troglophiles/trogloxènes et les stygobies/stygophiles/stygoxènes) de France, tous territoires confondus. ATTENTION : liens espèces-habitats (intérieurs des grottes) non encore pris en compte !
331 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Defaye & Deharveng (2024) | 121 | 10,49% | 107 | 19,28% | 89 | 20,84% | 100 | 20,04% |
| Gargominy et al. (2011) | 104 | 9,01% | 98 | 17,66% | 81 | 18,97% | 91 | 18,24% |
| Glöer (2022) | 78 | 6,76% | 75 | 13,51% | 61 | 14,29% | 75 | 15,03% |
| Tronquet (2014) | 65 | 5,63% | 61 | 10,99% | 34 | 7,96% | 57 | 11,42% |
| Faille et al. (2023) | 58 | 5,03% | 58 | 10,45% | 58 | 13,58% | 42 | 8,42% |
| Falkner et al. (2002) | 58 | 5,03% | 53 | 9,55% | 46 | 10,77% | 46 | 9,22% |
| Santamaria & Faille (2007) | 48 | 4,16% | 20 | 3,6% | 14 | 3,28% | 16 | 3,21% |
| Boeters & Falkner (2003) | 20 | 1,73% | 19 | 3,42% | 19 | 4,45% | 19 | 3,81% |
| Rouch (1970) | 15 | 1,3% | 15 | 2,7% | 15 | 3,51% | 15 | 3,01% |
| Faille et al. (2010) | 13 | 1,13% | 11 | 1,98% | 11 | 2,58% | 7 | 1,4% |
| Bonadona & Giordan (1988) | 12 | 1,04% | 12 | 2,16% | 9 | 2,11% | 12 | 2,4% |
| Genest (1983) | 12 | 1,04% | 6 | 1,08% | 6 | 1,41% | 6 | 1,2% |
| Kime & Enghoff (2017) | 12 | 1,04% | 12 | 2,16% | 12 | 2,81% | 11 | 2,2% |
| Rouch (1980) | 11 | 0,95% | 11 | 1,98% | 11 | 2,58% | 11 | 2,2% |
| Chappuis & Rouch (1959) | 10 | 0,87% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Ferreira et al. (2007) | 10 | 0,87% | 7 | 1,26% | 6 | 1,41% | 7 | 1,4% |
| Nicolas (1891) | 10 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Balvay (2009) | 9 | 0,78% | 9 | 1,62% | 8 | 1,87% | 5 | 1% |
| Girardi (2009) | 8 | 0,69% | 6 | 1,08% | 0 | 0% | 6 | 1,2% |
| Lemaire (2016) | 8 | 0,69% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Dole-Olivier et al. (2015) | 7 | 0,61% | 6 | 1,08% | 5 | 1,17% | 6 | 1,2% |
| Magniez (1978) | 7 | 0,61% | 7 | 1,26% | 4 | 0,94% | 6 | 1,2% |
| Apostolov (1998) | 6 | 0,52% | 6 | 1,08% | 6 | 1,41% | 6 | 1,2% |
| Beauchamp (1956) | 6 | 0,52% | 6 | 1,08% | 6 | 1,41% | 6 | 1,2% |
| Bernasconi (1985) | 6 | 0,52% | 3 | 0,54% | 3 | 0,7% | 2 | 0,4% |
| Boeters (1981) | 6 | 0,52% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Boeters (2000) | 6 | 0,52% | 6 | 1,08% | 4 | 0,94% | 6 | 1,2% |
| Callot-Girardi (2015) | 6 | 0,52% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Champeau (1967) | 6 | 0,52% | 5 | 0,9% | 5 | 1,17% | 2 | 0,4% |
| Coiffait (1969) | 6 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2009) | 6 | 0,52% | 6 | 1,08% | 6 | 1,41% | 6 | 1,2% |
| Hondt (1967) | 6 | 0,52% | 6 | 1,08% | 6 | 1,41% | 6 | 1,2% |
| Jeannel (1938) | 6 | 0,52% | 3 | 0,54% | 3 | 0,7% | 0 | 0% |
| Kerhervé (1914) | 6 | 0,52% | 1 | 0,18% | 1 | 0,23% | 0 | 0% |
| Kiefer (1937) | 6 | 0,52% | 6 | 1,08% | 6 | 1,41% | 6 | 1,2% |
| Lindner (1859) | 6 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Magniez (1968) | 6 | 0,52% | 6 | 1,08% | 0 | 0% | 6 | 1,2% |
| Paladilhe (1869) | 6 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié et al. (2024) | 6 | 0,52% | 6 | 1,08% | 6 | 1,41% | 6 | 1,2% |
| Weygoldt (2006) | 6 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1931) | 5 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters & Bertrand (2001) | 5 | 0,43% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Brölemann (1921) | 5 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Condé (1980) | 5 | 0,43% | 5 | 0,9% | 5 | 1,17% | 5 | 1% |
| Fourès (1954) | 5 | 0,43% | 5 | 0,9% | 4 | 0,94% | 4 | 0,8% |
| Locard (1883) | 5 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1893) | 5 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochs (1938) | 5 | 0,43% | 1 | 0,18% | 1 | 0,23% | 0 | 0% |
| Pelosse (1927) | 5 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pélosse (1930) | 5 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Route et al. (2004) | 5 | 0,43% | 5 | 0,9% | 5 | 1,17% | 5 | 1% |
| Achurra et al. (2012) | 4 | 0,35% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Apostolov (2002) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Apostolov (2005) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Beauchamp (1919) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beruete et al. (2021) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Boeters & Falkner (2003) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters & Falkner (2009) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Cottarelli et al. (2000) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Faille & Bourdeau (2022) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Fischer (1885) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fresneda et al. (2010) | 4 | 0,35% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Fresneda, Perreau & Vanderbergh (2010) | 4 | 0,35% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Giani & Lafont (1982) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Girardi et al. (2002) | 4 | 0,35% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Girardi (2009) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Girardi (2009) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 4 | 0,8% |
| Girardi (2009) | 4 | 0,35% | 4 | 0,72% | 0 | 0% | 4 | 0,8% |
| Jeannel (1913) | 4 | 0,35% | 4 | 0,72% | 4 | 0,94% | 3 | 0,6% |
| Jeannel (1916) | 4 | 0,35% | 3 | 0,54% | 2 | 0,47% | 2 | 0,4% |
| Jeannel (1919) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kiefer (1954) | 4 | 0,35% | 4 | 0,72% | 0 | 0% | 4 | 0,8% |
| Latella (2015) | 4 | 0,35% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Löbl & Smetana (2004) | 4 | 0,35% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Normand (1907) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelosse (1925) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelosse (1927) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perreau & Queinnec (1987) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Racovitza (1922) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouch (1990) | 4 | 0,35% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Vandel (1920) | 4 | 0,35% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Apostolov (2004) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Argod-vallon (1913) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Avon (1994) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Beauchamp (1926) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Beauchamp (1929) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Beauchamp (1937) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1950) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Beauchamp (1955) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Boeters (1969) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1864) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Brölemann (1900) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Cabidoche (1961) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Callot-Girardi (2017) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Callot-girardi (2017) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Champeau & Thiéry (1990) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 1 | 0,2% |
| Chappuis & Rouch (1960) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Chappuis (1956) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Chappuis (1956) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Chevreux (1901) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Coiffait (1976) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coutagne (1883) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Delay (1972) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dieck (1869) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupre (1991) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faille et al. (2010) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourès (1961) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fresneda et al. (2009) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Gaudin (1938) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Gaudin (1947) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Genest (1977) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giachino (1988) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giani et al. (1990) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Gourbault (1965) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Gourbault (1969) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoch et al. (2003) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Jeannel (1938) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 1 | 0,2% |
| Juget (1967) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Juget (1987) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Kerney & Cameron (1999) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 1 | 0,2% |
| Lemaire (2021) | 3 | 0,26% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Lescher-Montoue (1974) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Lescher-Moutoue (1968) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Lescher-moutoue (1968) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Lescher-moutoue (1968) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Lescher-moutoue (1969) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Lescher-Moutoue (1974) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Lescher-moutoue (1978) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Miranda et al. (2021) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Moniez (1887) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1867) | 3 | 0,26% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Pesce & Galassi (1988) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Ribaut (1947) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Richard (1890) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodriguez & Giani (1987) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Rouch & Lescher-Moutoué (1977) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Rouch (1988) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Rouch (1988) | 3 | 0,26% | 3 | 0,54% | 3 | 0,7% | 3 | 0,6% |
| Rouch (1992) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouch (1996) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roy (1922) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roy (1927) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abrahamsen (1969) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Apostolov (2002) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Mémoires de Biospéologie, 28(55): 1-8.">Apostolov (2002) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Apostolov (2003) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Avon (2007) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Beauchamp & Gourbault (1964) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Beauchamp (1932) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Bernasconi (1968) | 2 | 0,17% | 2 | 0,36% | 0 | 0% | 2 | 0,4% |
| Bernasconi (1989) | 2 | 0,17% | 2 | 0,36% | 0 | 0% | 2 | 0,4% |
| Bertrand (2001) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Bertrand (2004) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Besuchet (1981) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Boeters & Gittenberger (1980) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Boeters (1983) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (1999) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Bourguignat (1865) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Brolemann (1894) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabidoche (1965) | 2 | 0,17% | 2 | 0,36% | 0 | 0% | 2 | 0,4% |
| Cabidoche (1968) | 2 | 0,17% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Callot-Girardi & Boeters (2017) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Callot-girardi et al. (2017) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Callot-Girardi (2012) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Callot-Girardi (2013) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Callot-Girardi (2015) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Callot-Girardi (2015) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Callot-Girardi (2015) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Callot-Girardi (2017) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Caziot (1908) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cesne et al. (2022) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Chappuis & Rouch (1959) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chappuis (1928) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Condé (1981) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Condé (1989) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Cottarelli & Bruno (1993) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Deharveng & Gouze (1984) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delarouzée (1857) | 2 | 0,17% | 1 | 0,18% | 0 | 0% | 1 | 0,2% |
| Delfosse (2024) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Denis (1924) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dollfus (1897) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 0 | 0% |
| Dugès (1830) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dussart (1963) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 1 | 0,2% |
| Dussart (1970) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Fagniez (1923) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faille & Bourdeau (2008) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Faille et al. (2013) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fairmaire ([1857]) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fennah (1980) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Ferreira (2005) | 2 | 0,17% | 2 | 0,36% | 1 | 0,23% | 2 | 0,4% |
| Fiers & Pandourski (2008) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Fossati & Marquet (1998) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 1 | 0,2% |
| Fresneda & Bourdeau (2012) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Fresneda & Salgado-Costas (2006) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Fresneda et al. (2010) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Galassi et al. (1999) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Galassi et al. (1999) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Galassi et al. (2019) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Gargominy (2011-2023) | 2 | 0,17% | 2 | 0,36% | 1 | 0,23% | 2 | 0,4% |
| Gaudin (1925) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 0 | 0% |
| Gaudin (1939) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Genest & Juberthie (1983) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geoffroy & Mauriès (2017) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Germain (1911) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi & Bertrand (2009) | 2 | 0,17% | 2 | 0,36% | 0 | 0% | 2 | 0,4% |
| Girardi & Bertrand (2009) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Girardi (2001) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2002) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2004) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Girardi (2004) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2004) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Girardi (2009) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Girardi (2009) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Girardi (2009) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Girardi (2009) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Gourbault et al. (1976) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Gourbault (1969) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gourbault (1971) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Gouze (1983) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haase (2000) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hallez (1910) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heurtault (1986) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Hrabe (1937) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Iorio (2009) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Isaia et al. (2023) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Jakubisiak (1922) | 2 | 0,17% | 1 | 0,18% | 1 | 0,23% | 0 | 0% |
| Joubin (1894) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Juget & Des Chatelliers (2001) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Juget (1959) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Jurine (1820) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kosel (1980) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Lecaplain (2021) | 2 | 0,17% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Lescher-Moutoué (1971) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lopez (1996) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Martinsson et al. (2013) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Michaud (1831) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mihelčič (1960) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monard (1925) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pagès (1978) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Papp (1978) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Prie & Bichain (2009) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramage (2017) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 1 | 0,2% |
| Rémy (1949) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Richard (1887) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richling et al. (2016) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodriguez & Giani (1989) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roewer (1935) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouch (1964) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Roy (1931) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 0 | 0% |
| Russell et al. (2021) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 0 | 0% |
| Sainte-Claire Deville (1922) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 0 | 0% |
| Sayn (1889) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Secq (2013) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Sendra et al. (2017) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Thibaud (2017) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Vachon & Heurtault-rossi (1964) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Vandel (1920) | 2 | 0,17% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Vejdovský (1876) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 2 | 0,4% |
| Vuillefroy-Cassini (1893) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welter-schultes (2012) | 2 | 0,17% | 2 | 0,36% | 2 | 0,47% | 1 | 0,2% |
| Abeille & Perrin (1905) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1926) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (1988) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Bernasconi (1994) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (1999) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (1967) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Boeters (2022) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Brady (1880) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bretscher (1902) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Callot-Girardi (2015) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Casale (1988) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevey (1927) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clessin (1882) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coutagne (1882) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuénot & Mercier (1914) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Defaye & Dussart (2011) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delachaux (1921) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Delfosse (2003) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Delfosse (2004) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delfosse (2017) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| d'Hondt & Ben Ahmed (2009) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1801) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1805) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupuy (1847-1852) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evenhuis (2018) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Fagniez (1913) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 0 | 0% |
| Faille et al. (2007) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Galassi & De Laurentiis (2004) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Geoffroy & Iorio (2009) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Giani (1976) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Girardi (2009) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2009) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gisin (1963) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger (1973) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grosser (2015) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Hrabe (1963) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Hrabe (1963) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Iorio et al. (2023) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Jouin (1973) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Juberthie (1972) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Juberthie (1983) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Kneubühler et al. (2021) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Labbé (1926) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 0 | 0% |
| Lemaire (2011) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Lilljeborg (1901) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Löbl & Smetana (2003) | 1 | 0,09% | 1 | 0,18% | 0 | 0% | 1 | 0,2% |
| Locard (1883) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1901) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1903) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Monard (1928) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mrázek (1894) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman & Scott (1906) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Omaly (1970) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Paladilhe (1874) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Piguet (1906) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointner (1914) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pollonera (1887) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prieto (2008) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Pugh et al. (2002) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1888) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1890) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1897) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saint-simon (1848) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmeil (1893) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steinman (1910) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiébaud (1927) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1922) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vedel et al. (2013) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
| Vejdovský (1883) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1884‑1890) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zapparoli & Iorio (2012) | 1 | 0,09% | 1 | 0,18% | 1 | 0,23% | 1 | 0,2% |
