Accipitriformes, Falconiformes et Strigiformes
225 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Uicn et al. (2017) | 85 | 21,68% | 84 | 43,98% | 66 | 44% | 66 | 40,24% |
| Remsen et al. (2013) | 62 | 15,82% | 61 | 31,94% | 61 | 40,67% | 46 | 28,05% |
| Linnaeus (1758) | 34 | 8,67% | 6 | 3,14% | 6 | 4% | 4 | 2,44% |
| Gmelin (1788) | 17 | 4,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clements (2012) | 16 | 4,08% | 12 | 6,28% | 7 | 4,67% | 11 | 6,71% |
| Dickinson & Remsen (2013) | 16 | 4,08% | 11 | 5,76% | 10 | 6,67% | 10 | 6,1% |
| Levesque & Delcroix (2018) | 14 | 3,57% | 14 | 7,33% | 10 | 6,67% | 9 | 5,49% |
| Karadjian et al. (2022) | 12 | 3,06% | 12 | 6,28% | 12 | 8% | 6 | 3,66% |
| Etcheberry & Abraham (2009) | 11 | 2,81% | 11 | 5,76% | 11 | 7,33% | 8 | 4,88% |
| Dewynter & Claessens (2020) | 9 | 2,3% | 9 | 4,71% | 9 | 6% | 5 | 3,05% |
| Rocamora (2004) | 6 | 1,53% | 5 | 2,62% | 3 | 2% | 5 | 3,05% |
| Tostain (1980) | 6 | 1,53% | 4 | 2,09% | 4 | 2,67% | 2 | 1,22% |
| Belfan & Conde (2016) | 5 | 1,28% | 5 | 2,62% | 2 | 1,33% | 3 | 1,83% |
| Questel & Le Quellec (2012) | 5 | 1,28% | 5 | 2,62% | 3 | 2% | 4 | 2,44% |
| Questel (2020) | 5 | 1,28% | 5 | 2,62% | 3 | 2% | 4 | 2,44% |
| Thiollay (2007) | 5 | 1,28% | 5 | 2,62% | 5 | 3,33% | 5 | 3,05% |
| Verreaux & Des Murs (1860) | 5 | 1,28% | 4 | 2,09% | 4 | 2,67% | 3 | 1,83% |
| Yokoyama (2013) | 5 | 1,28% | 5 | 2,62% | 4 | 2,67% | 3 | 1,83% |
| Balouet & Olson (1989) | 4 | 1,02% | 4 | 2,09% | 4 | 2,67% | 3 | 1,83% |
| CHN (2017) | 4 | 1,02% | 4 | 2,09% | 4 | 2,67% | 4 | 2,44% |
| Del Hoyo & Collar (2014) | 4 | 1,02% | 3 | 1,57% | 2 | 1,33% | 3 | 1,83% |
| Dewynter (2020) | 4 | 1,02% | 4 | 2,09% | 4 | 2,67% | 1 | 0,61% |
| Temminck et al. (1838) | 4 | 1,02% | 4 | 2,09% | 4 | 2,67% | 4 | 2,44% |
| UICN Comité français, OFB & MNHN (2021) | 4 | 1,02% | 4 | 2,09% | 4 | 2,67% | 1 | 0,61% |
| Uicn et al. (2015) | 4 | 1,02% | 4 | 2,09% | 4 | 2,67% | 2 | 1,22% |
| Barau et al. (2005) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 2 | 1,22% |
| Birdlife International (2014) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 3 | 1,83% |
| Blat (2013) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 3 | 1,83% |
| Durant et al. (2013) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 0 | 0% |
| Linnaeus (1766) | 3 | 0,77% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Naurois (1985) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 2 | 1,22% |
| Oatleya et al. (2015) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 3 | 1,83% |
| Thiollay (1993) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 3 | 1,83% |
| Tostain et al. (2013) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 1 | 0,61% |
| Uicn et al. (2020) | 3 | 0,77% | 3 | 1,57% | 3 | 2% | 3 | 1,83% |
| Une et al. (1816) | 3 | 0,77% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Voisin & Voisin (2001) | 3 | 0,77% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Arroyo et al. (2020) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Bavoux et al. (1993) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Boudarel & Scher (2022) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Bretagnolle et al. (2000) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Burger et al. (2013) | 2 | 0,51% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Coeurdassier et al. (2019) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Commecy et al. (2013) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Cowles (1994) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Desfontaines (1787) | 2 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dronneau & Wassmer (2008) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Gmelin (1770) | 2 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guichard (1957) | 2 | 0,51% | 2 | 1,05% | 0 | 0% | 2 | 1,22% |
| Joubert & Margerit (1986) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 0 | 0% |
| Kayser et al. (2019) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Leboulenger (1989) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Leopold (1965) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Louchart et al. (2018) | 2 | 0,51% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Pallas (1831) | 2 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pontoppidan (1763) | 2 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rathgeber & Bayle (1997) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Safford & Hawkins (2013) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Santos et al. (2019) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Sclater (1859) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Scopoli (1769) | 2 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thibault et al. (2014) | 2 | 0,51% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Tunstall (1880) | 2 | 0,51% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Voisin & Voisin (2001) | 2 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weimerskirch et al. (2009) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 1 | 0,61% |
| Wells & Inskipp (2012) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Wilcox & Spotswood (2011) | 2 | 0,51% | 2 | 1,05% | 2 | 1,33% | 2 | 1,22% |
| Albesa (2010) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme (1999) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2002) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme (2004) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2008) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Anonyme (2011) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 0 | 0% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme. (2012) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Anonyme (2013) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Arrigoni Degli Oddi (1903) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arthur et al. (2010) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Baker-gabb (1979) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Bangs & Penard (1918) | 1 | 0,26% | 1 | 0,52% | 0 | 0% | 1 | 0,61% |
| Barre et al. (2009) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Birdlife International (2014) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Boddaert & Daubenton (1783) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1838) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Brasil (1916) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brehm (1831) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1764) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cassin (1845) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Claessens et al. (2014) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Clech (2001) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Clement & Chapalain (2016) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Clergeau & Vigne (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Clouet (1978) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Coatmeur (1999) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Commission de l’Avifaune Française (2016) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Commission des sciences et arts d'Egypte. France. (1809) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Constantin et al. (2015) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Cormier (1984) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Coton et al. (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Coton et al. (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Cox (1970) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Creau (1996) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Csabaï (2020) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Daudin (1802) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| David et al. (2017) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Debout (2001) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Bulletin de la Société zooogique de France, 26: 113.">D'hHmonville (1901) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dorleans (2022) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Dubois et al. (2008) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Fournier et al. (1993) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Fuchs et al. (2008) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Gallardo & Penteriani (2002) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Géné (1839) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Genot et al. (2001) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Ghestemme & Salamolard (2003) | 1 | 0,26% | 1 | 0,52% | 0 | 0% | 1 | 0,61% |
| Gill (1995) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Giraud-Audine et al. (2007) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Grantham (2005) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ingels et al. (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Kayser & Wilhelm (1991) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Keith & Cense (2015) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Kleinschmidt (1903) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kowalski & Lesiñski (1990) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Labitte (1952) | 1 | 0,26% | 1 | 0,52% | 0 | 0% | 1 | 0,61% |
| Labouyrie & Lacassin (2022) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lang & Lecocq (2015) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Latham (1790) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1790) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ledreff & Raynaud (1993) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lesson (1831) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linossier et al. (2017) | 1 | 0,26% | 1 | 0,52% | 0 | 0% | 1 | 0,61% |
| Lloret (1996) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Loison (1989) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Lorvelec & Clergeau (2003) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Clergeau (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lorvelec & Clergeau (2003) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Vigne (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lorvelec & Vigne (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lorvelec & Vigne (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lorvelec et al. (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lorvelec et al. (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lorvelec et al. (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Lydekker (1890) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Marco (2007) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Martinet et al. (1765) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millsap et al. (2011) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Morel (1959) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Mourer-chauviré (1975) | 1 | 0,26% | 1 | 0,52% | 0 | 0% | 1 | 0,61% |
| Nadal & Tariel (2008) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Newton (1863) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Olson (2006) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Peale (1848) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Pilard et al. (2021) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Pilard (2010) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Poirier (2020) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Pons (2018) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Poudré et al. (2016) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Pueschel & Stark (2017) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Puissauve & Legros (2015) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Puissauve (2016) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Radde (1862-1863) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Rand (1960) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Robert et al. (2002) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Rothschild & Hartert (1910) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Savigny (1809) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Sclater (1866) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Silva et al. (2023) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1834) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| SORDELLO (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| SORDELLO (2012) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Taberlet (1983) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Taquet (2013) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Terrasse & Terrasse (1969) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Thibault et al. (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Thiollay (1980) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Tostain et al. (1992) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Tresset et al. (2003) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| UNEP-WCMC (2005) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Vieillot (1807) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Vieillot (1817) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1818) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1823[1822]) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Vigors (1825) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Vittorio et al. (2016) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Vuilleumier & Gochfeld (1976) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Wahl & Barbraud (2005) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 0 | 0% |
| Wetmore (1964) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Wink et al. (1979) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| Wink et al. (2009) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
| (2021) | 1 | 0,26% | 1 | 0,52% | 1 | 0,67% | 1 | 0,61% |
