Reptiles endémiques
Tous les reptiles (Crocodylia, Testudines et Squamates) endémiques de France (métropole et outre-mer) : inclut les endémiques actuels (E) ou éteints (Z).
373 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Bauer et al. (2022) | 69 | 16,01% | 69 | 30% | 69 | 38,12% | 69 | 32,09% |
| Bauer & Sadlier (2000) | 60 | 13,92% | 49 | 21,3% | 49 | 27,07% | 48 | 22,33% |
| Henderson & Breuil (2012) | 51 | 11,83% | 21 | 9,13% | 12 | 6,63% | 18 | 8,37% |
| Massary et al. (2021) | 42 | 9,74% | 42 | 18,26% | 16 | 8,84% | 36 | 16,74% |
| Hedges & Conn (2012) | 36 | 8,35% | 20 | 8,7% | 20 | 11,05% | 16 | 7,44% |
| Roux (1913) | 36 | 8,35% | 5 | 2,17% | 5 | 2,76% | 5 | 2,33% |
| Bernstein et al. (2021) | 33 | 7,66% | 33 | 14,35% | 33 | 18,23% | 33 | 15,35% |
| Nicholson et al. (2012) | 30 | 6,96% | 19 | 8,26% | 4 | 2,21% | 17 | 7,91% |
| Breuil (2002) | 29 | 6,73% | 11 | 4,78% | 4 | 2,21% | 7 | 3,26% |
| Uicn et al. (2015) | 19 | 4,41% | 7 | 3,04% | 7 | 3,87% | 7 | 3,26% |
| Geneva et al. (2013) | 18 | 4,18% | 16 | 6,96% | 16 | 8,84% | 16 | 7,44% |
| Bauer et al. (2006) | 16 | 3,71% | 16 | 6,96% | 16 | 8,84% | 16 | 7,44% |
| Bauer et al. (2012) | 13 | 3,02% | 11 | 4,78% | 11 | 6,08% | 11 | 5,12% |
| Dewynter et al. (2019) | 13 | 3,02% | 13 | 5,65% | 9 | 4,97% | 11 | 5,12% |
| Duval et al. (2019) | 13 | 3,02% | 13 | 5,65% | 13 | 7,18% | 13 | 6,05% |
| Sadlier et al. (2014) | 13 | 3,02% | 13 | 5,65% | 13 | 7,18% | 13 | 6,05% |
| Turpin & Probst (1998) | 12 | 2,78% | 8 | 3,48% | 6 | 3,31% | 7 | 3,26% |
| Massary et al. (2020) | 11 | 2,55% | 10 | 4,35% | 8 | 4,42% | 8 | 3,72% |
| Sadlier et al. (2009) | 11 | 2,55% | 11 | 4,78% | 11 | 6,08% | 11 | 5,12% |
| Bauer & Sadlier (1994) | 10 | 2,32% | 7 | 3,04% | 7 | 3,87% | 7 | 3,26% |
| Bavay (1869) | 10 | 2,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss & Jourdan (2022) | 10 | 2,32% | 10 | 4,35% | 10 | 5,52% | 10 | 4,65% |
| Sadlier et al. (2002) | 10 | 2,32% | 10 | 4,35% | 10 | 5,52% | 10 | 4,65% |
| Breuil (2009) | 9 | 2,09% | 5 | 2,17% | 5 | 2,76% | 3 | 1,4% |
| Probst et al. (2022) | 9 | 2,09% | 8 | 3,48% | 6 | 3,31% | 6 | 2,79% |
| Sadlier et al. (2004) | 9 | 2,09% | 9 | 3,91% | 9 | 4,97% | 9 | 4,19% |
| Astrongatt (2017) | 8 | 1,86% | 8 | 3,48% | 8 | 4,42% | 8 | 3,72% |
| Sadlier et al. (2014) | 8 | 1,86% | 8 | 3,48% | 8 | 4,42% | 8 | 3,72% |
| Bochaton et al. (2021) | 7 | 1,62% | 7 | 3,04% | 7 | 3,87% | 4 | 1,86% |
| Caut et al. (2013) | 7 | 1,62% | 6 | 2,61% | 6 | 3,31% | 6 | 2,79% |
| Goicoechea et al. (2016) | 7 | 1,62% | 4 | 1,74% | 4 | 2,21% | 2 | 0,93% |
| Lazell (1964) | 7 | 1,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muñoz et al. (2013) | 7 | 1,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sanchez et al. (2019) | 7 | 1,62% | 5 | 2,17% | 5 | 2,76% | 5 | 2,33% |
| Anonyme (2015) | 6 | 1,39% | 5 | 2,17% | 5 | 2,76% | 5 | 2,33% |
| Astrongatt (2019) | 6 | 1,39% | 6 | 2,61% | 6 | 3,31% | 6 | 2,79% |
| Dewynter et al. (2023) | 6 | 1,39% | 6 | 2,61% | 6 | 3,31% | 4 | 1,86% |
| Good et al. (1997) | 6 | 1,39% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Probst (1997) | 6 | 1,39% | 2 | 0,87% | 1 | 0,55% | 2 | 0,93% |
| Sadlier et al. (1999) | 6 | 1,39% | 6 | 2,61% | 6 | 3,31% | 6 | 2,79% |
| Sadlier (1988) | 6 | 1,39% | 3 | 1,3% | 3 | 1,66% | 3 | 1,4% |
| Thomas (1964) | 6 | 1,39% | 5 | 2,17% | 0 | 0% | 5 | 2,33% |
| Bauer & Sadlier (2000) | 5 | 1,16% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Caceres (2002) | 5 | 1,16% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Glaw & Rösler (2015) | 5 | 1,16% | 5 | 2,17% | 5 | 2,76% | 4 | 1,86% |
| Lazell (1972) | 5 | 1,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mertens & Wermuth (1960) | 5 | 1,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1997) | 5 | 1,16% | 4 | 1,74% | 3 | 1,66% | 4 | 1,86% |
| Sadlier et al. (2006) | 5 | 1,16% | 5 | 2,17% | 5 | 2,76% | 5 | 2,33% |
| Sadlier et al. (2014) | 5 | 1,16% | 5 | 2,17% | 5 | 2,76% | 5 | 2,33% |
| Sadlier et al. (2015) | 5 | 1,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sayah et al. (2023) | 5 | 1,16% | 4 | 1,74% | 4 | 2,21% | 4 | 1,86% |
| Arnold (1979) | 4 | 0,93% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barbrour (1915) | 4 | 0,93% | 2 | 0,87% | 1 | 0,55% | 1 | 0,47% |
| Bauer et al. (1998) | 4 | 0,93% | 4 | 1,74% | 4 | 2,21% | 4 | 1,86% |
| Bauer et al. (2009) | 4 | 0,93% | 4 | 1,74% | 4 | 2,21% | 4 | 1,86% |
| Bauer et al. (2012) | 4 | 0,93% | 3 | 1,3% | 3 | 1,66% | 3 | 1,4% |
| Hawlitschek et al. (2012) | 4 | 0,93% | 2 | 0,87% | 0 | 0% | 2 | 0,93% |
| Hedges et al. (2014) | 4 | 0,93% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Horner (2007) | 4 | 0,93% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Hudel et al. (2020) | 4 | 0,93% | 4 | 1,74% | 4 | 2,21% | 4 | 1,86% |
| Lescure et al. (2012) | 4 | 0,93% | 2 | 0,87% | 1 | 0,55% | 1 | 0,47% |
| Massary et al. (2017) | 4 | 0,93% | 3 | 1,3% | 3 | 1,66% | 2 | 0,93% |
| Muratet (2015) | 4 | 0,93% | 3 | 1,3% | 2 | 1,1% | 1 | 0,47% |
| Routtier et al. (2023) | 4 | 0,93% | 4 | 1,74% | 4 | 2,21% | 1 | 0,47% |
| Sadlier et al. (2004) | 4 | 0,93% | 4 | 1,74% | 4 | 2,21% | 4 | 1,86% |
| Sadlier et al. (2012) | 4 | 0,93% | 4 | 1,74% | 4 | 2,21% | 4 | 1,86% |
| Sadlier (1987) | 4 | 0,93% | 4 | 1,74% | 4 | 2,21% | 4 | 1,86% |
| Tirvengadum & Bour (1985) | 4 | 0,93% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Wright et al. (2000) | 4 | 0,93% | 4 | 1,74% | 4 | 2,21% | 4 | 1,86% |
| Arnold & Bour (2008) | 3 | 0,7% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Augros et al. (2017) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 3 | 1,4% |
| Augros et al. (2018) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 3 | 1,4% |
| Austin et al. (2004) | 3 | 0,7% | 3 | 1,3% | 1 | 0,55% | 2 | 0,93% |
| Austin et al. (2009) | 3 | 0,7% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bochaton & Hanot (2021) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 2 | 0,93% |
| Bochaton et al. (2017) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 3 | 1,4% |
| Dewynter et al. (2022) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 2 | 0,93% |
| Dewynter et al. (2023) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 2 | 0,93% |
| Duméril & Bibron (1837) | 3 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1872) | 3 | 0,7% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Hawlitschek & Glaw (2012) | 3 | 0,7% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Hawlitschek et al. (2011) | 3 | 0,7% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| La Cepède (1789) | 3 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescure et al. (2020) | 3 | 0,7% | 3 | 1,3% | 2 | 1,1% | 3 | 1,4% |
| Miralles et al. (2017) | 3 | 0,7% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Ohler et al. (2021) | 3 | 0,7% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Peters (1874) | 3 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (2001) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 1 | 0,47% |
| Ronot (2007) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 1 | 0,47% |
| Roughgarden (1995) | 3 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sadlier et al. (1997) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 3 | 1,4% |
| Sadlier et al. (2009) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 3 | 1,4% |
| Sanchez (2020) | 3 | 0,7% | 3 | 1,3% | 3 | 1,66% | 1 | 0,47% |
| Schwartz (1964) | 3 | 0,7% | 3 | 1,3% | 0 | 0% | 3 | 1,4% |
| Seipp & Obst (1994) | 3 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thorpe et al. (2008) | 3 | 0,7% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Andres et al. (2014) | 2 | 0,46% | 2 | 0,87% | 1 | 0,55% | 1 | 0,47% |
| Arnold & Ovenden (2014) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Arribas (1999) | 2 | 0,46% | 2 | 0,87% | 1 | 0,55% | 1 | 0,47% |
| Arribas (2000) | 2 | 0,46% | 2 | 0,87% | 0 | 0% | 2 | 0,93% |
| Augros (2022) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Austin et al. (2002) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bailon et al. (2015) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Barbour & Noble (1915) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barré et al. (2016) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Bauer et al. (2000) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bauer et al. (2006) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Bischoff (2020) | 2 | 0,46% | 2 | 0,87% | 1 | 0,55% | 1 | 0,47% |
| Blanc et al. (1993) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Bocage (1873) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bocage (1873) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Bochaton & Bailon (2018) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Bochaton et al. (2021) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Boettger (1913) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Böhme (1976) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Böhme (1979) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Börner (1980) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour et al. (2008) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Bour (1980) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bour (1984) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| in: De Broin, F. & Jiménez-Fuentes, E. [Eds]. Studia Geologica Salmanticensia. Vol. esp. 1. Studia Palaeocheloniologica 1: 17-76. ">Bour (1985) |
2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Cazanove et al. (2023) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Cheke (1987) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Cope (1864) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| de Massary et al. (2015) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Dubos et al. (2023) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Duméril & Bibron (1836) | 2 | 0,46% | 2 | 0,87% | 1 | 0,55% | 1 | 0,47% |
| Duméril et al. (1870-1909) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Girard (1997) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Gomés et al. (2018) | 2 | 0,46% | 2 | 0,87% | 1 | 0,55% | 2 | 0,93% |
| Gouillard (1973) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Grazziotin et al. (2012) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Guichenot (1866) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Hawlitschek et al. (2021) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Hedges et al. (2016) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Henkel & Böhme (2001) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Ineich & Sadlier (1991) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jowers et al. (2013) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Kindler et al. (2017) | 2 | 0,46% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Köhler & Vesely (2011) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| La Cepède (1788) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescure (2018) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Linnaeus (1758) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Lorvelec et al. (2021) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Massary et al. (2018) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Massary et al. (2019) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 0 | 0% |
| Meier (1984) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Meier (1995) | 2 | 0,46% | 2 | 0,87% | 0 | 0% | 2 | 0,93% |
| Mertens (1928) | 2 | 0,46% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Mertens (1966) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst et al. (2000) | 2 | 0,46% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Probst et al. (2001) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1998) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1998) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Probst (2003) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Questel et al. (2023) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Questel et al. (2023) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Questel (2011) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rasmussen & Ineich (2000) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Röll et al. (2023) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Sadlier & Bauer (2000) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Sadlier et al. (1998) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sadlier et al. (2006) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Sadlier et al. (2014) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Sadlier et al. (2019) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Sadlier et al. (2019) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Sanchez & Probst (2009) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Schmitz et al. (2022) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 0 | 0% |
| Schultze et al. (2020) | 2 | 0,46% | 2 | 0,87% | 1 | 0,55% | 1 | 0,47% |
| Schwartz & Thomas (1975) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Skipwith et al. (2014) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 2 | 0,93% |
| Thorpe et al. (2010) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turpin & Probst (1998) | 2 | 0,46% | 2 | 0,87% | 0 | 0% | 2 | 0,93% |
| UICN France et al. (2013) | 2 | 0,46% | 2 | 0,87% | 2 | 1,1% | 1 | 0,47% |
| Zdunek (2022) | 2 | 0,46% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Adalsteinsson et al. (2009) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Andersson (1908) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme [BUFO] (2023) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Anonyme (2019) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Antoniama & Probst (2010) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Asztalos et al. (2020) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Augros et al. (2017) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Augros et al. (2017) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Austin & Arnold (2001) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Austin et al. (2003) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Axelsson et al. (2020) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Baker & Allain (2020) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Barbour (1914) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bauer et al. (2008) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bauer et al. (2022) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bauer et al. (2024) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bauer (1985) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baxter-gilbert et al. (2021) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bègue et al. (2014) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Bertrand (2000) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Bischoff (1988) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Blom et al. (2019) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bochaton et al. (2017) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonanno (2016) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Bonnaterre (1789) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1790) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnet et al. (1999) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borczyk et al. (2022) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Boulenger (1878) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boulenger (1883) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boulenger (1891) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Boulenger (1900) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour & Moutou (1982) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour et al. (2014) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bour (1978) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (1979) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (1980) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (1981) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourgade (2020) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Bourgade (2020) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Breuil et al. (2010) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breuil (1999) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brocchi (1876) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Burneleau (1983) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caceres et al. (2010) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Caut & Jowers (2015) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Censky & Paulson (1992) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Champagne et al. (1997) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cheke & Bour (2014) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Choeur et al. (2022) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Claudin et al. (2022) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Clémencet et al. (2013) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Clement et al. (2022) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Coatmeur (1999) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Cochran (1938) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cope (1869) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cope (1879) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Corbett & Tamarind (1979) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Cuvier (1829) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| David et al. (2002) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delafontaine et al. (2018) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Desjardins (1831) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deso & Probst (2007) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Deso et al. (2002) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Dewynter & Rufray (2012) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Dubos (2013) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Duméril & Bibron (1839) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril & Bibron (1839) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril & Bribron (1835) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Erens et al. (2017) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Fritz & Schmidtler (2020) | 1 | 0,23% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Fritz et al. (2020) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Froidevaux (1899) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1887) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1899) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1995) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Girard (1995) | 1 | 0,23% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Girard (2007) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Glaw (2015) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Gomès & Ibéné (2013) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Graitson et al. (2012) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grant-mackie et al. (2003) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Gros-désormeaux et al. (2017) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Guiller & Vacher (2022) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Günther (1858) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1877) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hamilton (2021) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Harmon & Gibson (2006) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Hass (1991) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Havery et al. (2018) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Hawlitschek et al. (2014) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Hecht (1930) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedges et al. (2009) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedges (2008) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Henderson & Powell (2009) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Heym et al. (2013) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Hoff & Daszkiewicz (2001) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holden & Ineich (2018) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Honsterette & Probst (1999) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Hume et al. (2021) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Ineich et al. (2007) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| In: Charpy, L. (coord.) 2009. Clipperton, environnement et biodiversité d'un microcosme océanique. Muséum national d'Histoire naturelle, Paris; IRD, Marseille: 347-380. (Patrimoines naturels; 68).">Ineich et al. (2009) | 1 | 0,23% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Ineich et al. (2014) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Ineich (1987) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ineich (2009) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Ineich (2016) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johansson et al. (2013) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jowers et al. (2022) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Kharin & Dotsenko (2012) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Klaver (2008) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Klein et al. (2016) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Kwet (2013) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lambert (1988) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Lazell (1994) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1826-1830) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ljungström et al. (2015) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Lock & Griffiths (2022) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Lorvelec & Pascal (2009) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Lorvelec et al. (2013) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Lorvelec (2011) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Loveridge (1941) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meier (1981) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Mertens (1957) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau de Jonnès (1816) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Palacios & Castroviejo (1975) | 1 | 0,23% | 1 | 0,43% | 0 | 0% | 1 | 0,47% |
| Pallas [1814] | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paré & Lorvelec (2012) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Parker (1926) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parker (1936) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peters (1869) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Piteau (2016) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Polidori & Caratti (1992) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Porcel et al. (2021) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Probst & Abhaya (2009) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Probst & Deso (2001) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Probst & Deso (2001) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Probst & Turpin (1997) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Probst (1996) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1997) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1997) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Probst (2000) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Probst (2000) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (2001) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Probst (2003) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Puissauve, Cohen & De Massary (2015) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2018) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Questel (2020) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Renner (2002) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Résière et al. (2018) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Richmond (1966) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rocha et al. (2006) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roughgarden (1974) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rufz (1859 | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sadlier & Bauer (1997) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sadlier & Bauer (1999) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sadlier & Bauer (2002) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sadlier et al. (2002) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sadlier et al. (2013) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sadlier et al. (2014) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sanchez & Bour (2014) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sanchez & Caceres (2011) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sanchez & Caceres (2019) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sanchez & Gandar (2009) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sanchez & Probst (2009) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sanchez & Probst (2017) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Sanchez et al. (2009) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sanchez et al. (2010) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Sanchez (2007) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Sanchez (2010) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Sansault (2021) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Schlegel (1837) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schneider (1783) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schwartz & Henderson (1991) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seipp & Klemmer (1994) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw (1802) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stejneger (1893) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Strauchch (1865) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sulton (2020) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Surget-Groba & Thorpe (2013) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tamon et al. (2018) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Thibault et al. (2017) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thorpe & Stenson (2003) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turpin & Probst (1998) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turpin (2002) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Uicn et al. (2017) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaillant (1900) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Dijk et al. (2014) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vingadachetty et al. (2015) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Vinson & Vinson (1969) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wallach et al. (2014) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weinell et al. (2019) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Werner (1910) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wieczorek et al. (2020) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Williams et al. (2020) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 0 | 0% |
| Wüster et al. (2002) | 1 | 0,23% | 1 | 0,43% | 1 | 0,55% | 1 | 0,47% |
| Yokoyama (2013) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
