Accipitriformes, Falconiformes et Strigiformes
207 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 | 22,02% | 84 | 44,44% | 66 | 44% | 66 | 40,49% |
Remsen et al. (2013) | 62 | 16,06% | 61 | 32,28% | 61 | 40,67% | 46 | 28,22% |
Linnaeus (1758) | 34 | 8,81% | 6 | 3,17% | 6 | 4% | 5 | 3,07% |
Gmelin (1788) | 17 | 4,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Clements (2012) | 16 | 4,15% | 12 | 6,35% | 7 | 4,67% | 11 | 6,75% |
Dickinson & Remsen (2013) | 16 | 4,15% | 11 | 5,82% | 10 | 6,67% | 10 | 6,13% |
Levesque & Delcroix (2018) | 14 | 3,63% | 14 | 7,41% | 10 | 6,67% | 9 | 5,52% |
Karadjian et al. (2022) | 12 | 3,11% | 12 | 6,35% | 12 | 8% | 7 | 4,29% |
Etcheberry & Abraham (2009) | 11 | 2,85% | 11 | 5,82% | 11 | 7,33% | 8 | 4,91% |
Dewynter & Claessens (2020) | 9 | 2,33% | 9 | 4,76% | 9 | 6% | 5 | 3,07% |
Rocamora (2004) | 6 | 1,55% | 5 | 2,65% | 3 | 2% | 5 | 3,07% |
Tostain (1980) | 6 | 1,55% | 4 | 2,12% | 4 | 2,67% | 2 | 1,23% |
Belfan & Conde (2016) | 5 | 1,3% | 5 | 2,65% | 2 | 1,33% | 3 | 1,84% |
Questel & Le Quellec (2012) | 5 | 1,3% | 5 | 2,65% | 3 | 2% | 4 | 2,45% |
Questel (2020) | 5 | 1,3% | 5 | 2,65% | 3 | 2% | 4 | 2,45% |
Thiollay (2007) | 5 | 1,3% | 5 | 2,65% | 5 | 3,33% | 5 | 3,07% |
Verreaux & Des Murs (1860) | 5 | 1,3% | 4 | 2,12% | 4 | 2,67% | 3 | 1,84% |
Yokoyama (2013) | 5 | 1,3% | 5 | 2,65% | 4 | 2,67% | 3 | 1,84% |
Balouet & Olson (1989) | 4 | 1,04% | 4 | 2,12% | 4 | 2,67% | 3 | 1,84% |
CHN (2017) | 4 | 1,04% | 4 | 2,12% | 4 | 2,67% | 4 | 2,45% |
Del Hoyo & Collar (2014) | 4 | 1,04% | 3 | 1,59% | 2 | 1,33% | 3 | 1,84% |
Dewynter (2020) | 4 | 1,04% | 4 | 2,12% | 4 | 2,67% | 1 | 0,61% |
Temminck et al. (1838) | 4 | 1,04% | 4 | 2,12% | 4 | 2,67% | 4 | 2,45% |
UICN Comité français, OFB & MNHN (2021) | 4 | 1,04% | 4 | 2,12% | 4 | 2,67% | 1 | 0,61% |
Uicn et al. (2015) | 4 | 1,04% | 4 | 2,12% | 4 | 2,67% | 2 | 1,23% |
Barau et al. (2005) | 3 | 0,78% | 3 | 1,59% | 3 | 2% | 2 | 1,23% |
Birdlife International (2014) | 3 | 0,78% | 3 | 1,59% | 3 | 2% | 3 | 1,84% |
Durant et al. (2013) | 3 | 0,78% | 3 | 1,59% | 3 | 2% | 0 | 0% |
Linnaeus (1766) | 3 | 0,78% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Naurois (1985) | 3 | 0,78% | 3 | 1,59% | 3 | 2% | 2 | 1,23% |
Oatleya et al. (2015) | 3 | 0,78% | 3 | 1,59% | 3 | 2% | 3 | 1,84% |
Thiollay (1993) | 3 | 0,78% | 3 | 1,59% | 3 | 2% | 3 | 1,84% |
Tostain et al. (2013) | 3 | 0,78% | 3 | 1,59% | 3 | 2% | 1 | 0,61% |
Uicn et al. (2020) | 3 | 0,78% | 3 | 1,59% | 3 | 2% | 3 | 1,84% |
Une et al. (1816) | 3 | 0,78% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Voisin & Voisin (2001) | 3 | 0,78% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Arroyo et al. (2020) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Boudarel & Scher (2022) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Bretagnolle et al. (2000) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Burger et al. (2013) | 2 | 0,52% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Commecy et al. (2013) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Cowles (1994) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Desfontaines (1787) | 2 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Dronneau & Wassmer (2008) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Gmelin (1770) | 2 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayser et al. (2019) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Leboulenger (1989) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Leopold (1965) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Louchart et al. (2018) | 2 | 0,52% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Pallas (1831) | 2 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Pontoppidan (1763) | 2 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Safford & Hawkins (2013) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Santos et al. (2019) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Sclater (1859) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Scopoli (1769) | 2 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibault et al. (2014) | 2 | 0,52% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Tunstall (1880) | 2 | 0,52% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Voisin & Voisin (2001) | 2 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Weimerskirch et al. (2009) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 1 | 0,61% |
Wells & Inskipp (2012) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Wilcox & Spotswood (2011) | 2 | 0,52% | 2 | 1,06% | 2 | 1,33% | 2 | 1,23% |
Albesa (2010) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme (1999) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2002) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme (2004) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2008) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Anonyme (2011) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 0 | 0% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Anonyme. (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Anonyme (2013) | 1 | 0,26% | 1 | 0,53% | 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 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Baker-gabb (1979) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Bangs & Penard (1918) | 1 | 0,26% | 1 | 0,53% | 0 | 0% | 1 | 0,61% |
Barre et al. (2009) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Birdlife International (2014) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Boddaert & Daubenton (1783) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1838) | 1 | 0,26% | 1 | 0,53% | 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 | 0,53% | 1 | 0,67% | 0 | 0% |
Claessens et al. (2014) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Clech (2001) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Clergeau & Vigne (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Clouet (1978) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Coatmeur (1999) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Commission de l’Avifaune Française (2016) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Commission des sciences et arts d'Egypte. France. (1809) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Constantin et al. (2015) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Cormier (1984) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Coton et al. (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Coton et al. (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Cox (1970) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Creau (1996) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Csabaï (2020) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
David et al. (2017) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Debout (2001) | 1 | 0,26% | 1 | 0,53% | 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 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Dubois et al. (2008) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Fuchs et al. (2008) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Gallardo & Penteriani (2002) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Genot et al. (2001) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Ghestemme & Salamolard (2003) | 1 | 0,26% | 1 | 0,53% | 0 | 0% | 1 | 0,61% |
Gill (1995) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Giraud-Audine et al. (2007) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
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 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Kayser & Wilhelm (1991) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Keith & Cense (2015) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Kleinschmidt (1903) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Labouyrie & Lacassin (2022) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Lang & Lecocq (2015) | 1 | 0,26% | 1 | 0,53% | 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 | 0,53% | 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 | 0,53% | 0 | 0% | 1 | 0,61% |
Lloret (1996) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Loison (1989) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Lorvelec & Vigne (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Lorvelec & Vigne (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Lorvelec & Vigne (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Lorvelec et al. (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Lorvelec et al. (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Lorvelec et al. (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Lydekker (1890) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Marco (2007) | 1 | 0,26% | 1 | 0,53% | 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 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Mourer-chauviré (1975) | 1 | 0,26% | 1 | 0,53% | 0 | 0% | 1 | 0,61% |
Nadal & Tariel (2008) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Newton (1863) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Olson (2006) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Peale (1848) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Pilard et al. (2021) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Pilard (2010) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Poirier (2020) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Pons (2018) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Poudré et al. (2016) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Pueschel & Stark (2017) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Puissauve & Legros (2015) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Puissauve (2016) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Rand (1960) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Robert et al. (2002) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Rothschild & Hartert (1910) | 1 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Savigny (1809) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Sclater (1866) | 1 | 0,26% | 1 | 0,53% | 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 | 0,53% | 1 | 0,67% | 0 | 0% |
SORDELLO (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
SORDELLO (2012) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Taberlet (1983) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Thibault et al. (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Thiollay (1980) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Tostain et al. (1992) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Tresset et al. (2003) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
UNEP-WCMC (2005) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Vieillot (1807) | 1 | 0,26% | 1 | 0,53% | 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 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Vigors (1825) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Vittorio et al. (2016) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Vuilleumier & Gochfeld (1976) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Wahl & Barbraud (2005) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 0 | 0% |
Wetmore (1964) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
Wink et al. (2009) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |
(2021) | 1 | 0,26% | 1 | 0,53% | 1 | 0,67% | 1 | 0,61% |