Espèces éteintes
Toutes les espèces éteintes en France métropolitaine et d'outre-mer (statuts X et Z)
365 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Solem (1976) | 103 | 12,68% | 102 | 23,45% | 98 | 25,86% | 100 | 25,13% |
| Gerlach (2016) | 94 | 11,58% | 76 | 17,47% | 54 | 14,25% | 68 | 17,09% |
| Garrett (1884) | 89 | 10,96% | 22 | 5,06% | 22 | 5,8% | 16 | 4,02% |
| Sartori et al. (2014) | 60 | 7,39% | 60 | 13,79% | 60 | 15,83% | 60 | 15,08% |
| Coote & Loeve (2003) | 51 | 6,28% | 32 | 7,36% | 32 | 8,44% | 24 | 6,03% |
| Abdou & Bouchet (2000) | 44 | 5,42% | 44 | 10,11% | 42 | 11,08% | 43 | 10,8% |
| Gargominy & Fontaine (2014) | 33 | 4,06% | 33 | 7,59% | 30 | 7,92% | 32 | 8,04% |
| Richling & Bouchet (2013) | 27 | 3,33% | 26 | 5,98% | 26 | 6,86% | 26 | 6,53% |
| Tison et al. (2014) | 26 | 3,2% | 21 | 4,83% | 17 | 4,49% | 18 | 4,52% |
| Sartori et al. (2013) | 24 | 2,96% | 24 | 5,52% | 24 | 6,33% | 24 | 6,03% |
| Pilsbry (1909-1910) | 23 | 2,83% | 13 | 2,99% | 11 | 2,9% | 10 | 2,51% |
| Crampton (1956) | 20 | 2,46% | 14 | 3,22% | 14 | 3,69% | 14 | 3,52% |
| Neubert et al. (2009) | 17 | 2,09% | 6 | 1,38% | 5 | 1,32% | 5 | 1,26% |
| Hedges & Conn (2012) | 16 | 1,97% | 12 | 2,76% | 12 | 3,17% | 12 | 3,02% |
| Kolibáč et al. (2020) | 15 | 1,85% | 15 | 3,45% | 15 | 3,96% | 15 | 3,77% |
| Porch et al. (2020) | 15 | 1,85% | 15 | 3,45% | 15 | 3,96% | 15 | 3,77% |
| Pease (1867) | 14 | 1,72% | 4 | 0,92% | 4 | 1,06% | 4 | 1,01% |
| Aulagnier et al. (2017) | 12 | 1,48% | 11 | 2,53% | 11 | 2,9% | 5 | 1,26% |
| Baker (1938) | 12 | 1,48% | 12 | 2,76% | 12 | 3,17% | 12 | 3,02% |
| Reeve (1849-1851) | 12 | 1,48% | 7 | 1,61% | 7 | 1,85% | 3 | 0,75% |
| Zimmermann et al. (2009) | 12 | 1,48% | 12 | 2,76% | 12 | 3,17% | 12 | 3,02% |
| Pease (1866) | 11 | 1,35% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Balouet & Olson (1989) | 10 | 1,23% | 9 | 2,07% | 9 | 2,37% | 9 | 2,26% |
| Crampton & Cooke (1953) | 10 | 1,23% | 10 | 2,3% | 10 | 2,64% | 10 | 2,51% |
| Partula. The species inhabiting Tahiti. Carnegie Institute of Washington Publication, 228: 1-313.">Crampton (1917) | 10 | 1,23% | 3 | 0,69% | 2 | 0,53% | 2 | 0,5% |
| Lee et al. (2009) | 9 | 1,11% | 6 | 1,38% | 5 | 1,32% | 4 | 1,01% |
| Solem (1961) | 9 | 1,11% | 5 | 1,15% | 5 | 1,32% | 4 | 1,01% |
| Bouchet & Abdou (2003) | 8 | 0,99% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Christensen et al. (2018) | 8 | 0,99% | 8 | 1,84% | 8 | 2,11% | 8 | 2,01% |
| Crampton (1924) | 8 | 0,99% | 4 | 0,92% | 4 | 1,06% | 2 | 0,5% |
| Griffiths & Florens (2006) | 8 | 0,99% | 8 | 1,84% | 8 | 2,11% | 8 | 2,01% |
| Henderson & Breuil (2012) | 8 | 0,99% | 4 | 0,92% | 4 | 1,06% | 4 | 1,01% |
| Massary et al. (2021) | 8 | 0,99% | 8 | 1,84% | 7 | 1,85% | 7 | 1,76% |
| Burch (2007) | 7 | 0,86% | 7 | 1,61% | 7 | 1,85% | 5 | 1,26% |
| Cibois et al. (2008) | 7 | 0,86% | 3 | 0,69% | 2 | 0,53% | 2 | 0,5% |
| Gmelin (1789) | 7 | 0,86% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Murray & Clarke (1980) | 7 | 0,86% | 5 | 1,15% | 5 | 1,32% | 3 | 0,75% |
| Pease (1865) | 7 | 0,86% | 4 | 0,92% | 4 | 1,06% | 2 | 0,5% |
| Reeve (1842) | 7 | 0,86% | 4 | 0,92% | 4 | 1,06% | 2 | 0,5% |
| Bouchet & Abdou (2001) | 6 | 0,74% | 6 | 1,38% | 6 | 1,58% | 6 | 1,51% |
| Cooke & Clench (1943) | 6 | 0,74% | 6 | 1,38% | 2 | 0,53% | 4 | 1,01% |
| Cowles (1994) | 6 | 0,74% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Kirchman & Steadman (2007) | 6 | 0,74% | 6 | 1,38% | 6 | 1,58% | 6 | 1,51% |
| Levesque & Delcroix (2018) | 6 | 0,74% | 4 | 0,92% | 3 | 0,79% | 3 | 0,75% |
| Murphy & Matthews (1928) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steadman & Zarriello (1987) | 6 | 0,74% | 6 | 1,38% | 6 | 1,58% | 6 | 1,51% |
| Cibois et al. (2004) | 5 | 0,62% | 4 | 0,92% | 3 | 0,79% | 4 | 1,01% |
| Dickinson et al. (2019) | 5 | 0,62% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Hume (2007) | 5 | 0,62% | 3 | 0,69% | 3 | 0,79% | 2 | 0,5% |
| Kirchman & Steadman (2006) | 5 | 0,62% | 5 | 1,15% | 5 | 1,32% | 5 | 1,26% |
| Linnaeus (1758) | 5 | 0,62% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Mourer-chauviré (1975) | 5 | 0,62% | 5 | 1,15% | 2 | 0,53% | 5 | 1,26% |
| Uicn et al. (2012) | 5 | 0,62% | 5 | 1,15% | 5 | 1,32% | 5 | 1,26% |
| Vinciguerra & Delahaye (2006) | 5 | 0,62% | 5 | 1,15% | 5 | 1,32% | 5 | 1,26% |
| Arnold (1979) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aulagnier (2009) | 4 | 0,49% | 4 | 0,92% | 4 | 1,06% | 0 | 0% |
| Breuil (2009) | 4 | 0,49% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Crampton (1932) | 4 | 0,49% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Crosse (1865) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter et al. (2019) | 4 | 0,49% | 4 | 0,92% | 4 | 1,06% | 4 | 1,01% |
| Garrett (1887) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1788) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goicoechea et al. (2016) | 4 | 0,49% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Gould (1852) | 4 | 0,49% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Mourer-Chauvire et al. (1999) | 4 | 0,49% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Pfeiffer (1854-1860) | 4 | 0,49% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Porch & Smith (2017) | 4 | 0,49% | 4 | 0,92% | 4 | 1,06% | 4 | 1,01% |
| Probst et al. (2022) | 4 | 0,49% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Abdou et al. (2004) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Arnold & Bour (2008) | 3 | 0,37% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Austin et al. (2009) | 3 | 0,37% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Belfan & Conde (2016) | 3 | 0,37% | 3 | 0,69% | 1 | 0,26% | 2 | 0,5% |
| Bochaton et al. (2017) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Bochaton et al. (2021) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 2 | 0,5% |
| Breuil (2002) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Broderip (1832) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 0,37% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| IUCN (2012) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1830-1831) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 1 | 0,25% |
| Pfeiffer (1855) | 3 | 0,37% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Pfeiffer (1857) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1997) | 3 | 0,37% | 1 | 0,23% | 0 | 0% | 1 | 0,25% |
| Remsen et al. (2013) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 0 | 0% |
| Rossini et al. (2021) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Sayah et al. (2023) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Smith (1902) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steadman (1989) | 3 | 0,37% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Steadman (1992) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Suessenguth (1936) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Véron et al. (2021) | 3 | 0,37% | 3 | 0,69% | 3 | 0,79% | 3 | 0,75% |
| Antonius (2016) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Aouraghe (1990) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Austin et al. (2002) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1940) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barau et al. (2005) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Barbour & Noble (1915) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartsch (1942) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Battiston et al. (2010) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Bochaton & Bailon (2018) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Bochaton et al. (2021) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Bour (1980) | 2 | 0,25% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Bour (1984) | 2 | 0,25% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| in: De Broin, F. & Jiménez-Fuentes, E. [Eds]. Studia Geologica Salmanticensia. Vol. esp. 1. Studia Palaeocheloniologica 1: 17-76. ">Bour (1985) |
2 | 0,25% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Braun et al. (2019) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Butaud & Hodel (2017) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Chaline (1980) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Crampton (1930) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Crosse (1868) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delannoye et al. (2015) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Dewynter & Claessens (2020) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Drouët (1859) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Esper & Charpentier (1789-[1804]) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Falkner et al. (2002) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Forster (1844) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy et al. (2011) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Garrett (1874) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gentry et al. (2004) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Gray (1839) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Grazziotin et al. (2012) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 1 | 0,25% |
| Guerin et al. (1981) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Holyoak & Thibault (1978) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holyoak (1973) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| ICZN (2020) | 2 | 0,25% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Jansen et al. (2021) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Johnson et al. (2000) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 1 | 0,25% |
| Jowers et al. (2013) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Knutson & Vala (2011) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Kondo (1944) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Kondo (1962) | 2 | 0,25% | 2 | 0,46% | 0 | 0% | 2 | 0,5% |
| Kondo (1981) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec et al. (2007) | 2 | 0,25% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Louchart et al. (2018) | 2 | 0,25% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Lourenço (1995) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Magnin (2023) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Martyn (1845) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mees (1991) | 2 | 0,25% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Morelet (1853) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nel & Chauliac (1983) | 2 | 0,25% | 2 | 0,46% | 0 | 0% | 2 | 0,5% |
| Ogilvie-grant (1889) | 2 | 0,25% | 2 | 0,46% | 0 | 0% | 2 | 0,5% |
| Olson & Jouventin (1996) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Pease (1868) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1871) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1843-1850) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1852-1860) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1854) | 2 | 0,25% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Pilsbry & Cooke (1915-1916) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Podsiadlowski et al. (2017) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rigal et al. (2018) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Salvador et al. (2021) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Selys-Longchamps (1848) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sharpe (1906) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Steadman (1988) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Steadman (2002) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Tirvengadum & Bour (1985) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tröndlé & Letourneux (2012) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Uicn et al. (2017) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 0 | 0% |
| Verreaux & Des Murs (1860) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wagner (1907-1911) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walters (1991) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Worthy & Bollt (2011) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Worthy et al. (2013) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 2 | 0,5% |
| Yokoyama (2013) | 2 | 0,25% | 2 | 0,46% | 2 | 0,53% | 1 | 0,25% |
| Ancey (1889) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anderson (1925) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Anonyme. (2004) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Anthony (1917) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Anton (1838) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aubouin et al. (2016) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Aulagnier (2021) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Austin & Arnold (2001) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Austin et al. (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Bailon et al. (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Baird (1850) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Bakhoum et al. (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Balouet & Buffetaut 1987 | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Barbour (1914) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barlow (1978) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berlioz (1934) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Blanchet et al. (1998) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Blumenbach (1799) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bochaton & Hanot (2021) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Boddaert & Daubenton (1783) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonelli et al. (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Bonnaterre (1789) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet & Pointier (1998) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Bour et al. (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Bour (1978) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (1979) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (1981) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brace et al. (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Brace et al. (2023) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Bregulla (1993) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Bruguière (1789-1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambecèdes et al. (2012) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Caut & Jowers (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Chaline & Laborier (1981) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Champagne et al. (1997) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cheke & Bour (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Cheke (1987) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevalier & Dewynter (2020) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Chrétien (1897) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Cibois et al. (2011) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Clark (1905) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Clark (1905) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Clech (2001) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Cochard et al. (2019) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Condamine et al. (2023) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Cooke & Kondo (1961) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Cope (1879) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cory (1886) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crampe & Barascud (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Cunningham & Daszak (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1863) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter et al. (2021) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Dewynter et al. (2023) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| DREAL Occitanie (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Duméril & Bibron (1837) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril & Bibron (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril & Bribron (1835) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril et al. (1870-1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabre & Orsini (2016) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Falconer & Cautley (1846) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Florence (2004) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Ibis, : pp. 303-307.">Forbes (1879) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Froidevaux (1899) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gagnaison (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Garrett & Smith (1902) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1872) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Genot et al. (2001) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Gilot et al. (1992) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Giraud-Audine et al. (2007) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Glöer (2022) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Gmelin (1791) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goedert et al. (2020) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Gonzalez et al. (2021) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Gray (1850) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Greenwood (1955) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Grenier & Godron (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guerin (2004) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Guillerme et al. (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Günther (1877) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haase & Bouchet (1998) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Hartman (1880) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Heppner (1981) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Hinton (1910) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holt et al. (2007) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Houard & Jaulin (2018) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Hume et al. (2021) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| IUCN (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jansen & Cheke (2020) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Jauzein (2001) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Johnson et al. (1986) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Jones et al. (2019) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Jourdane & Mas-Coma (1977) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Karadjian et al. (2022) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Kerguélen & Bock (2011) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kondo (1968) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Kratochvil (1981) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Kwet (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| La Cepède (1788) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| La Cepède (1789) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lafranchis (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Lafranchis (2016) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Lenoble et al. (2020) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Lenoble (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Lescure (2018) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Linnaeus (1766) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linné (1771) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loiseleur-deslongchamps (1807) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Vigne (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Lorvelec (2011) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Lydekker (1890) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Marco (2007) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Marquet & Seronie-vivien (2016) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| MEDDE & MAAF (2013) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Medde (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| MEEDDAT & MAP (2008) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Meisner (1804) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mey (2005) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Miller (1779) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miralles et al. (2017) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Moquin-Tandon (1855-1856) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morel (1959) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Mourer-Chauvire & Balouet (2005) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| MTES & MAA (2018) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Nesti (1825) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Newton & Gadow (1893) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Nolf & Cahuzac (2009) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Aplonis mavornata Buller. Notornis, Journal of the Ornithological Society of New Zealand, 33(4): 197-208.">Olson (1986) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paget (1854) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal & Vigne (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Pease (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1871) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pereira et al. (2001) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Pfeiffer (1845) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1854) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1857) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1858) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poplin & Mourer-chauviré (1985) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Poplin (1980) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Portis (1888) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potin (2013) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Probst & Abhaya (2009) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Probst (1996) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Questel (2011) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Questel (2023) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Ramousse & Le Berre (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Reeve (1843) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1873-1874) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reinach (1900) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Reverté et al. (2023) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Rocamora (2004) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Rothschild (1907) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Saint et al. (1978) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Sanchez & Bour (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Sanchez & Probst (2009) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Schneider (1783) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schwartz & Henderson (1991) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sclater (1866) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1769) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Slater et al. (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Smith (1892) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| SORDELLO (2012) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Sowerby (1832) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Speight (2013) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Stoetzel et al. (2016) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Strauchch (1865) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Theobald (1940) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Theuerkauf et al. (2010) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Thibault (1989) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Turpin & Probst (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turpin & Probst (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN Comité français, OFB & MNHN (2021) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| UICN France et al. (2013) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Uicn et al. (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Uicn et al. (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vaillant (1900) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Dijk et al. (2014) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vigne & Pascal (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vigne et al. (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vigne et al. (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vigne (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vigne (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vigne (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| Vigne (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vigne (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vigne (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 1 | 0,25% |
| Vinson & Vinson (1969) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wagner (1832) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zakharov et al. (2004) | 1 | 0,12% | 1 | 0,23% | 1 | 0,26% | 0 | 0% |
| (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
