Accipitriformes et Falconiformes
Accipitriformes et Falconiformes
176 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) | 66 | 23,24% | 66 | 45,21% | 54 | 45,76% | 54 | 42,52% |
Remsen et al. (2013) | 50 | 17,61% | 50 | 34,25% | 50 | 42,37% | 40 | 31,5% |
Linnaeus (1758) | 25 | 8,8% | 5 | 3,42% | 5 | 4,24% | 4 | 3,15% |
Gmelin (1788) | 14 | 4,93% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Delcroix (2018) | 12 | 4,23% | 12 | 8,22% | 9 | 7,63% | 8 | 6,3% |
Dickinson & Remsen (2013) | 10 | 3,52% | 7 | 4,79% | 7 | 5,93% | 6 | 4,72% |
Clements (2012) | 9 | 3,17% | 9 | 6,16% | 6 | 5,08% | 8 | 6,3% |
Dewynter & Claessens (2020) | 9 | 3,17% | 9 | 6,16% | 9 | 7,63% | 5 | 3,94% |
Etcheberry & Abraham (2009) | 9 | 3,17% | 9 | 6,16% | 9 | 7,63% | 6 | 4,72% |
Karadjian et al. (2022) | 7 | 2,46% | 7 | 4,79% | 7 | 5,93% | 4 | 3,15% |
Questel & Le Quellec (2012) | 5 | 1,76% | 5 | 3,42% | 3 | 2,54% | 4 | 3,15% |
Questel (2020) | 5 | 1,76% | 5 | 3,42% | 3 | 2,54% | 4 | 3,15% |
Rocamora (2004) | 5 | 1,76% | 5 | 3,42% | 3 | 2,54% | 5 | 3,94% |
Thiollay (2007) | 5 | 1,76% | 5 | 3,42% | 5 | 4,24% | 5 | 3,94% |
Yokoyama (2013) | 5 | 1,76% | 5 | 3,42% | 4 | 3,39% | 3 | 2,36% |
CHN (2017) | 4 | 1,41% | 4 | 2,74% | 4 | 3,39% | 4 | 3,15% |
Dewynter (2020) | 4 | 1,41% | 4 | 2,74% | 4 | 3,39% | 1 | 0,79% |
Temminck et al. (1838) | 4 | 1,41% | 4 | 2,74% | 4 | 3,39% | 4 | 3,15% |
Tostain (1980) | 4 | 1,41% | 3 | 2,05% | 3 | 2,54% | 2 | 1,57% |
UICN Comité français, OFB & MNHN (2021) | 4 | 1,41% | 4 | 2,74% | 4 | 3,39% | 1 | 0,79% |
Verreaux & Des Murs (1860) | 4 | 1,41% | 4 | 2,74% | 4 | 3,39% | 3 | 2,36% |
Barau et al. (2005) | 3 | 1,06% | 3 | 2,05% | 3 | 2,54% | 2 | 1,57% |
Belfan & Conde (2016) | 3 | 1,06% | 3 | 2,05% | 1 | 0,85% | 2 | 1,57% |
Birdlife International (2014) | 3 | 1,06% | 3 | 2,05% | 3 | 2,54% | 3 | 2,36% |
Linnaeus (1766) | 3 | 1,06% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Naurois (1985) | 3 | 1,06% | 3 | 2,05% | 3 | 2,54% | 2 | 1,57% |
Oatleya et al. (2015) | 3 | 1,06% | 3 | 2,05% | 3 | 2,54% | 3 | 2,36% |
Thiollay (1993) | 3 | 1,06% | 3 | 2,05% | 3 | 2,54% | 3 | 2,36% |
Uicn et al. (2015) | 3 | 1,06% | 3 | 2,05% | 3 | 2,54% | 2 | 1,57% |
Uicn et al. (2020) | 3 | 1,06% | 3 | 2,05% | 3 | 2,54% | 3 | 2,36% |
Une et al. (1816) | 3 | 1,06% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Voisin & Voisin (2001) | 3 | 1,06% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Arroyo et al. (2020) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Balouet & Olson (1989) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Boudarel & Scher (2022) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Bretagnolle et al. (2000) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Burger et al. (2013) | 2 | 0,7% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Commecy et al. (2013) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Cowles (1994) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Desfontaines (1787) | 2 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Dronneau & Wassmer (2008) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Gmelin (1770) | 2 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Leopold (1965) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Pallas (1831) | 2 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Safford & Hawkins (2013) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Santos et al. (2019) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Sclater (1859) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Tostain et al. (2013) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 0 | 0% |
Tunstall (1880) | 2 | 0,7% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Voisin & Voisin (2001) | 2 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Weimerskirch et al. (2009) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 1 | 0,79% |
Wells & Inskipp (2012) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Wilcox & Spotswood (2011) | 2 | 0,7% | 2 | 1,37% | 2 | 1,69% | 2 | 1,57% |
Albesa (2010) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme (1999) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2002) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme (2004) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2008) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Anonyme (2011) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 0 | 0% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme. (2012) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Anonyme (2013) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Arrigoni Degli Oddi (1903) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Arthur et al. (2010) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Baker-gabb (1979) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Bangs & Penard (1918) | 1 | 0,35% | 1 | 0,68% | 0 | 0% | 1 | 0,79% |
Barre et al. (2009) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Birdlife International (2014) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Boddaert & Daubenton (1783) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1838) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Brehm (1831) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünnich (1764) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Cassin (1845) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Claessens et al. (2014) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Clouet (1978) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Coatmeur (1999) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Commission de l’Avifaune Française (2016) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Commission des sciences et arts d'Egypte. France. (1809) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Constantin et al. (2015) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Cormier (1984) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Coton et al. (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Coton et al. (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Cox (1970) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Csabaï (2020) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
David et al. (2017) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Debout (2001) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Del Hoyo & Collar (2014) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Bulletin de la Société zooogique de France, 26: 113.">D'hHmonville (1901) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorleans (2022) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Dubois et al. (2008) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Gallardo & Penteriani (2002) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Ghestemme & Salamolard (2003) | 1 | 0,35% | 1 | 0,68% | 0 | 0% | 1 | 0,79% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Ingels et al. (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Keith & Cense (2015) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Kleinschmidt (1903) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Labouyrie & Lacassin (2022) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lang & Lecocq (2015) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Latham (1790) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1790) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Ledreff & Raynaud (1993) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lesson (1831) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Linossier et al. (2017) | 1 | 0,35% | 1 | 0,68% | 0 | 0% | 1 | 0,79% |
Lloret (1996) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Loison (1989) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lorvelec & Vigne (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lorvelec & Vigne (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lorvelec & Vigne (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lorvelec et al. (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lorvelec et al. (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lorvelec et al. (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Lydekker (1890) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Marco (2007) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Martinet et al. (1765) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Millsap et al. (2011) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Nadal & Tariel (2008) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Newton (1863) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Olson (2006) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Peale (1848) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Pilard et al. (2021) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Pilard (2010) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Pons (2018) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Pontoppidan (1763) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Poudré et al. (2016) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Puissauve & Legros (2015) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Rand (1960) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Robert et al. (2002) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Savigny (1809) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Sclater (1866) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Silva et al. (2023) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1834) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Thibault et al. (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Thibault et al. (2014) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Thiollay (1980) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Tostain et al. (1992) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Tresset et al. (2003) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
UNEP-WCMC (2005) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Vieillot (1807) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Vieillot (1817) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1818) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1823[1822]) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Vigors (1825) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Vittorio et al. (2016) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Vuilleumier & Gochfeld (1976) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
Wahl & Barbraud (2005) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 0 | 0% |
Wetmore (1964) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |
(2021) | 1 | 0,35% | 1 | 0,68% | 1 | 0,85% | 1 | 0,79% |