Oiseaux de Guyane
Aves de Guyane
417 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) | 885 | 44,72% | 860 | 88,21% | 701 | 87,3% | 706 | 86,41% |
Remsen et al. (2013) | 599 | 30,27% | 565 | 57,95% | 565 | 70,36% | 443 | 54,22% |
Levesque & Delcroix (2018) | 147 | 7,43% | 143 | 14,67% | 124 | 15,44% | 130 | 15,91% |
UICN Comité français, OFB & MNHN (2021) | 120 | 6,06% | 120 | 12,31% | 120 | 14,94% | 89 | 10,89% |
Clements (2012) | 97 | 4,9% | 84 | 8,62% | 74 | 9,22% | 73 | 8,94% |
Tostain et al. (2013) | 91 | 4,6% | 76 | 7,79% | 74 | 9,22% | 61 | 7,47% |
Linnaeus (1758) | 89 | 4,5% | 22 | 2,26% | 22 | 2,74% | 16 | 1,96% |
Yokoyama (2013) | 84 | 4,24% | 76 | 7,79% | 75 | 9,34% | 55 | 6,73% |
Questel (2020) | 83 | 4,19% | 80 | 8,21% | 70 | 8,72% | 68 | 8,32% |
Dewynter & Claessens (2020) | 74 | 3,74% | 72 | 7,38% | 70 | 8,72% | 56 | 6,85% |
Questel & Le Quellec (2012) | 72 | 3,64% | 68 | 6,97% | 63 | 7,85% | 55 | 6,73% |
Dickinson & Remsen (2013) | 69 | 3,49% | 55 | 5,64% | 44 | 5,48% | 49 | 6% |
Gmelin (1789) | 66 | 3,34% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Belfan & Conde (2016) | 56 | 2,83% | 53 | 5,44% | 50 | 6,23% | 42 | 5,14% |
Etcheberry & Abraham (2009) | 49 | 2,48% | 42 | 4,31% | 42 | 5,23% | 32 | 3,92% |
Gmelin (1788) | 47 | 2,37% | 8 | 0,82% | 8 | 1% | 8 | 0,98% |
Uicn et al. (2015) | 46 | 2,32% | 44 | 4,51% | 44 | 5,48% | 30 | 3,67% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 36 | 1,82% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Dewynter (2021) | 26 | 1,31% | 26 | 2,67% | 25 | 3,11% | 21 | 2,57% |
Uicn et al. (2020) | 25 | 1,26% | 25 | 2,56% | 25 | 3,11% | 19 | 2,33% |
Linnaeus (1766) | 24 | 1,21% | 6 | 0,62% | 5 | 0,62% | 5 | 0,61% |
Weimerskirch et al. (2009) | 24 | 1,21% | 18 | 1,85% | 18 | 2,24% | 10 | 1,22% |
Ingels et al. (2003) | 22 | 1,11% | 20 | 2,05% | 20 | 2,49% | 17 | 2,08% |
Linné (1766) | 20 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2015) | 19 | 0,96% | 16 | 1,64% | 16 | 1,99% | 14 | 1,71% |
Clements et al. (2015) | 18 | 0,91% | 18 | 1,85% | 10 | 1,25% | 13 | 1,59% |
Barau et al. (2005) | 16 | 0,81% | 13 | 1,33% | 13 | 1,62% | 10 | 1,22% |
Tostain (1980) | 14 | 0,71% | 10 | 1,03% | 10 | 1,25% | 8 | 0,98% |
Deblock et al. (1960) | 12 | 0,61% | 6 | 0,62% | 6 | 0,75% | 5 | 0,61% |
Rocamora (2004) | 12 | 0,61% | 11 | 1,13% | 10 | 1,25% | 9 | 1,1% |
Todd (1920) | 11 | 0,56% | 6 | 0,62% | 2 | 0,25% | 6 | 0,73% |
Del Hoyo & Collar (2014) | 10 | 0,51% | 6 | 0,62% | 6 | 0,75% | 6 | 0,73% |
Guth (1971) | 9 | 0,45% | 9 | 0,92% | 9 | 1,12% | 6 | 0,73% |
Gill (1995) | 8 | 0,4% | 8 | 0,82% | 8 | 1% | 5 | 0,61% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 8 | 0,4% | 8 | 0,82% | 8 | 1% | 7 | 0,86% |
Boddaert & Daubenton (1783) | 7 | 0,35% | 3 | 0,31% | 3 | 0,37% | 3 | 0,37% |
Claessens et al. (2014) | 7 | 0,35% | 6 | 0,62% | 6 | 0,75% | 5 | 0,61% |
Karadjian et al. (2022) | 7 | 0,35% | 7 | 0,72% | 7 | 0,87% | 4 | 0,49% |
Thibault et al. (2014) | 7 | 0,35% | 7 | 0,72% | 7 | 0,87% | 6 | 0,73% |
Commission de l’Avifaune Française (2016) | 6 | 0,3% | 6 | 0,62% | 6 | 0,75% | 5 | 0,61% |
Isler et al. (2013) | 6 | 0,3% | 3 | 0,31% | 3 | 0,37% | 3 | 0,37% |
Lichtenstein (1823) | 6 | 0,3% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Safford & Hawkins (2013) | 6 | 0,3% | 6 | 0,62% | 6 | 0,75% | 5 | 0,61% |
Furminieux (2019) | 5 | 0,25% | 5 | 0,51% | 5 | 0,62% | 4 | 0,49% |
Pelzeln (1868) | 5 | 0,25% | 4 | 0,41% | 4 | 0,5% | 3 | 0,37% |
Temminck (1818-1838) | 5 | 0,25% | 5 | 0,51% | 5 | 0,62% | 2 | 0,24% |
Thiollay (2007) | 5 | 0,25% | 5 | 0,51% | 5 | 0,62% | 5 | 0,61% |
Vieillot (1819) | 5 | 0,25% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Ausilio & Zotier (1989) | 4 | 0,2% | 4 | 0,41% | 4 | 0,5% | 3 | 0,37% |
Bangs & Penard (1921) | 4 | 0,2% | 4 | 0,41% | 0 | 0% | 4 | 0,49% |
Bravo et al. (2012) | 4 | 0,2% | 2 | 0,21% | 2 | 0,25% | 1 | 0,12% |
Claessens (2016) | 4 | 0,2% | 4 | 0,41% | 4 | 0,5% | 4 | 0,49% |
Del Hoyo & Collar (2016) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter (2020) | 4 | 0,2% | 4 | 0,41% | 4 | 0,5% | 1 | 0,12% |
Ehrhardt (1971) | 4 | 0,2% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Erard et al. (1991) | 4 | 0,2% | 4 | 0,41% | 4 | 0,5% | 4 | 0,49% |
Müller (1776) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Pontoppidan (1763) | 4 | 0,2% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Tostain & Dujardin (1988) | 4 | 0,2% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Tostain (1986) | 4 | 0,2% | 4 | 0,41% | 4 | 0,5% | 2 | 0,24% |
Bartoli (1972) | 3 | 0,15% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Berv & Prum (2014) | 3 | 0,15% | 3 | 0,31% | 3 | 0,37% | 0 | 0% |
Bonaccorso et al. (2011) | 3 | 0,15% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Capurucho et al. (2013) | 3 | 0,15% | 3 | 0,31% | 3 | 0,37% | 3 | 0,37% |
Collier et al. (2002) | 3 | 0,15% | 3 | 0,31% | 2 | 0,25% | 2 | 0,24% |
Durant et al. (2013) | 3 | 0,15% | 3 | 0,31% | 3 | 0,37% | 0 | 0% |
Gonzalez et al. (2009) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Han et al. (2010) | 3 | 0,15% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Humphries et al. (2019) | 3 | 0,15% | 3 | 0,31% | 3 | 0,37% | 0 | 0% |
Latham (1790) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Delcroix (2016) | 3 | 0,15% | 2 | 0,21% | 0 | 0% | 2 | 0,24% |
Zootaxa, 2013: 1-16.">Nemesio & Rasmussen (2009) | 3 | 0,15% | 3 | 0,31% | 3 | 0,37% | 3 | 0,37% |
Pascal & Touroult (2015) | 3 | 0,15% | 2 | 0,21% | 1 | 0,12% | 1 | 0,12% |
Perrin et al. (2021) | 3 | 0,15% | 3 | 0,31% | 3 | 0,37% | 3 | 0,37% |
Bénito-espinal (1990) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Birdlife International (2016) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Brooks (2015) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Cabanis (1847) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Caparella & Lanyon (1985) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Chartier et al. (2007) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Claramunt (2014) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
dal Molin (2009) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Daniel et al. (2020) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Davant (1967) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Derryberry et al. (2010) | 2 | 0,1% | 2 | 0,21% | 1 | 0,12% | 1 | 0,12% |
Donegan (2013) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Donovan (1816) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois et al. (2008) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 1 | 0,12% |
Eberhard et al. (2001) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Erard & Sabatier (1988) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Figueira et al. (2015) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Gibson & Baker (2012) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Gourreau et al. (1998) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Hosner (2005) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Imfeld et al. (2021) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Impact-mer (2011) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 1 | 0,12% |
Ingels et al. (2011) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
International Commission on Zoological Nomenclature (1992) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Jardine & Selby (1826-1835) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson et al. (1988) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Jullien & Cariveau (2001) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Laverde-r et al. (2014) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Lee & Walsh-McGehee (2000) | 2 | 0,1% | 2 | 0,21% | 0 | 0% | 2 | 0,24% |
Lepechin (1769) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1831) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Levesque & Clergeau (2002) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Levesque & Delcroix (2013) | 2 | 0,1% | 2 | 0,21% | 0 | 0% | 2 | 0,24% |
Lopes & Gonzaga (2016) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Lopes et al. (2018) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Lorvelec et al. (2004) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Mann et al. (2006) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 1 | 0,12% |
Mathews (1914) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Mays et al. (2006) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Mckitrick (1985) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Mees (1987) | 2 | 0,1% | 2 | 0,21% | 0 | 0% | 2 | 0,24% |
Pezy et al. (2022) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Pons et al. (2005) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Potin (2013) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Powell et al. (2008) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Powell (2012) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Probst (1997) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Remsen et al. (2013) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Renaudier et al. (2010) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Rheindt et al. (2015) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Sabine (1819) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
SACC (2014) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 1 | 0,12% |
Santos et al. (2019) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Sclater (1866) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Scopoli (1769) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sheldon et al. (2005) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Slager & Klicka (2014) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 1 | 0,12% |
Stopiglia et al. (2022) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Swainson (1838) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 1 | 0,12% |
Tello et al. (2014) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 1 | 0,12% |
Todd (1925) | 2 | 0,1% | 2 | 0,21% | 0 | 0% | 2 | 0,24% |
Todd (1931) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Todd (1937) | 2 | 0,1% | 2 | 0,21% | 0 | 0% | 2 | 0,24% |
Tostain (1980) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Tostain (1987) | 2 | 0,1% | 1 | 0,1% | 0 | 0% | 1 | 0,12% |
Tostain (1988) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Tunstall (1880) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Une et al. (1816) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
UNEP-WCMC (2005) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Vanderwerf et al. (2006) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Vieillot (1817) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Voisin & Voisin (2001) | 2 | 0,1% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Voisin & Voisin (2001) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Weimerskirch et al. (2009) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Weller (2000) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Wenner et al. (2012) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Westcott & Smith (1994) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 2 | 0,24% |
Wilson (1813) | 2 | 0,1% | 2 | 0,21% | 2 | 0,25% | 0 | 0% |
Anonyme (2008) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme (2008) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Araripe et al. (2007) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Attié et al. (1997) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Baird (1865) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Balouet & Olson (1989) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Bangs & Penard (1918) | 1 | 0,05% | 1 | 0,1% | 0 | 0% | 1 | 0,12% |
Barre et al. (1991) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Barre et al. (2009) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Beaufils (1999) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Berlepsch & Leverkuhn (1890) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Bertrand (1982) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Birdlife International (2016) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Birdlife International (2016) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Birdlife International (2017) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Boie (1835) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1855° | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Boschert & Dronneau (1998) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Bravo et al. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Brewster (1895) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brun (1958) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Brünnich (1764) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Burmeister (1856) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Calenge et al. (2010) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Campagna et al. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Cassin (1845) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Chapman (1914) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Chastel et al. (1987) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Chastel et al. (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Cheke & Hume (2008) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Chesser et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chesser et al. (2016) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
CHN (2017) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Chubb (1919) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Claessens et al. (2005) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Claessens et al. (2011) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Claessens et al. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Claramunt et al. (2013) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Clements (1992) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Clergeau & Pascal (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Coatmeur (1999) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Commecy et al. (2013) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Coues (1861) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1862) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Crochet et al. (2022) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Crouzier (2009) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Csabaï (2020) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Le règne animal distribué d'après son organisation, pour servir de base à l'histoire naturelle des animaux et d'introduction à l'anatomie comparée. Tome 2, contenant les reptiles, les poissons, les mollusques et les annélides. Déterville, Paris. i-xviii+1-532 pp. ">Cuvier (1816) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Daszkiewicz, P. & Massary, J.-C. de 2006. Overlooked historical testimony as to the presence of Red-billed Tropicbird Phaeton aethereus in French Guiana. Bulletin of the British Ornithologists'Club, 126(1): 71-73.">Daszkiewicz & Massary (2006) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
De Bus de Gisignies (1855) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Deblock (1966) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Debout (2001) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Dechelle & Ingels (2007) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Deflandre (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Deflorenne et al. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Deniau & Provost (2020) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Zoological Bibliography, 1(4): 151-166.">Dickinson (2011) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Dollfus (1934) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Dollfus (1966) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorleans (2022) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Dreff & Delliere (1994) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Louvet (2014) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Ducatez & Devore (2023) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
D'horta et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Efe et al. (2009) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Elkins & Yesou (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Eyton (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Flood et al. (2017) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Fremont (2002) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Gallien (2011) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Garcia et al. (2016) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Gargominy et al. (1996) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Gauthier-clerc & Lambert (2002) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Gernigon (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Giraud-Audine et al. (2007) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Golvan (1956) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gorleri & Areta (2022) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Gould (1838) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Grantsau et al. (1990) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Grau et al. (2005) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Gray (1859) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Guermeur (1987) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Guiguen et al. (1984) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Gunnerus (1767) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Harcourt (1851) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Haverschmidt (1956) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Hermann (1783) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Homeyer (1853) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ingels & Dechelle (2011) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Ingels & Tauleigne (2011) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Ingels et al. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Isaac (2020) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Isenmann et al. (1971) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
IUCN (2013) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
IUCN (2014) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Jouventin (1994) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Kayser & Wilhelm (1991) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Kinnear (1927) | 1 | 0,05% | 1 | 0,1% | 0 | 0% | 1 | 0,12% |
Kuhl (1820) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1787) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1790) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Lawrence (1863) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Lawrence (1865) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Ledreff & Raynaud (1993) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Lenrumé (2023) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Lesson (1839) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Linné (1771) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Loison (1989) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Lorvelec & Vigne (2003) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Louette & Cousin (1999) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Loury & Puissauve (2016) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Lovette et al. (2010) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Machado & Silveira (2011) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Marion & Clergeau (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Marion (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Marion (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Martinet et al. (1765) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mctavish (2002) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Millsap et al. (2011) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Montagu (1813) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Morel (1959) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Morrison (2006) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Nadal & Tariel (2008) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Naumann (1819) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Olson (2006) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
O'reilly (1818) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ottema (2002) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
pallas (1764) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1769) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1776) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2016) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Pearson & Prévot (1971) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Pelzeln (1854) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelzeln (1863) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1930) | 1 | 0,05% | 1 | 0,1% | 0 | 0% | 1 | 0,12% |
Phillips (1994) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Piacentini et al. (2015) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Pinaud et al. (2005) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Prevot (1971) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Puissauve (2016) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Ramírez et al. (2013) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Rand (1960) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Reeber et al. (1996) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeber (2015) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Ritter et al. (2021) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Robert et al. (2002) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Romagnano et al. (1995) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Roques (1991) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Coll. (2017) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvadori (1899) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvin & Godman (1882) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Salvin & Godman (1884) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvin (1863) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvin (1885) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Salvin (1897) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Sanchez et al. (2004) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Scater & Salvin (1867) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Schomburgk et al. (1847-1848) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Sclater & Salvin (1868) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sclater & Salvin (1869) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Sclater & Salvin (1877) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Sclater (1864) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Sclater (1866) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Scopoli (1786) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Seguigne et al. (2022) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Shaw (1792 | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Silva et al. (2023) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Slager et al. (2014) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Zootaxa, 4942(1): 118-126.">Smith & Clay (2021) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Socolovschi et al. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Spiroux (1996) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Sueur (2018) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Sundevall (1866) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Swainson ([1820-1821]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Taberlet (1983) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Tavares et al. (2004) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Temminck (1815) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Terrasse & Terrasse (1969) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Theuerkauf et al. (2010) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Thiollay (1980) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Todd (1925) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Todd (1927) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Todd (1948) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tostain et al. (1992) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Uicn et al. (2016) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Le Kiskidi, septembre 2015: 28-40. ">Uriot (2015) |
1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Van et al. (2019) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Vanderwerf et al. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verreaux & Des Murs (1860) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Vieillot (1807) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Vieillot (1816) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Vieillot (1818) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1818) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1819) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Vigors (1825) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Wagler (1827) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wahl & Barbraud (2005) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Weimerskirch & Jouventin (1998) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Wetmore (1939) | 1 | 0,05% | 1 | 0,1% | 0 | 0% | 1 | 0,12% |
Wetmore (1964) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Willis et al. (1983) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Wink et al. (2009) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Yésou (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 0 | 0% |
Yésou (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Yésou (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Yésou (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Yésou (2003) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Zimmer & Phelps (1948) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |
Zimmer (1945) | 1 | 0,05% | 1 | 0,1% | 1 | 0,12% | 1 | 0,12% |