Oiseaux de Martinique
Aves de Martinique
281 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Levesque & Delcroix (2018) | 192 | 30,77% | 186 | 64,81% | 164 | 65,08% | 180 | 71,15% |
UICN Comité français, OFB & MNHN (2021) | 157 | 25,16% | 157 | 54,7% | 157 | 62,3% | 127 | 50,2% |
Uicn et al. (2017) | 145 | 23,24% | 137 | 47,74% | 131 | 51,98% | 116 | 45,85% |
Belfan & Conde (2016) | 132 | 21,15% | 127 | 44,25% | 93 | 36,9% | 124 | 49,01% |
Questel (2020) | 112 | 17,95% | 108 | 37,63% | 96 | 38,1% | 102 | 40,32% |
Yokoyama (2013) | 112 | 17,95% | 99 | 34,49% | 96 | 38,1% | 87 | 34,39% |
Remsen et al. (2013) | 104 | 16,67% | 98 | 34,15% | 98 | 38,89% | 79 | 31,23% |
Questel & Le Quellec (2012) | 92 | 14,74% | 88 | 30,66% | 83 | 32,94% | 77 | 30,43% |
Linnaeus (1758) | 76 | 12,18% | 22 | 7,67% | 22 | 8,73% | 17 | 6,72% |
Etcheberry & Abraham (2009) | 51 | 8,17% | 43 | 14,98% | 43 | 17,06% | 40 | 15,81% |
Uicn et al. (2020) | 43 | 6,89% | 43 | 14,98% | 43 | 17,06% | 38 | 15,02% |
Uicn et al. (2015) | 40 | 6,41% | 38 | 13,24% | 38 | 15,08% | 29 | 11,46% |
Dewynter (2021) | 27 | 4,33% | 27 | 9,41% | 26 | 10,32% | 27 | 10,67% |
Weimerskirch et al. (2009) | 25 | 4,01% | 19 | 6,62% | 19 | 7,54% | 16 | 6,32% |
Gmelin (1789) | 24 | 3,85% | 4 | 1,39% | 4 | 1,59% | 3 | 1,19% |
Tostain et al. (2013) | 24 | 3,85% | 19 | 6,62% | 18 | 7,14% | 18 | 7,11% |
Clements (2012) | 23 | 3,69% | 23 | 8,01% | 21 | 8,33% | 22 | 8,7% |
Barau et al. (2005) | 19 | 3,04% | 16 | 5,57% | 16 | 6,35% | 13 | 5,14% |
Uicn et al. (2015) | 17 | 2,72% | 14 | 4,88% | 14 | 5,56% | 13 | 5,14% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 16 | 2,56% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Linnaeus (1766) | 16 | 2,56% | 2 | 0,7% | 1 | 0,4% | 1 | 0,4% |
Dewynter & Claessens (2020) | 15 | 2,4% | 15 | 5,23% | 15 | 5,95% | 10 | 3,95% |
Clements et al. (2015) | 14 | 2,24% | 13 | 4,53% | 3 | 1,19% | 12 | 4,74% |
Dickinson & Remsen (2013) | 13 | 2,08% | 12 | 4,18% | 8 | 3,17% | 11 | 4,35% |
Rocamora (2004) | 12 | 1,92% | 10 | 3,48% | 9 | 3,57% | 8 | 3,16% |
Del Hoyo & Collar (2014) | 11 | 1,76% | 7 | 2,44% | 7 | 2,78% | 7 | 2,77% |
Deblock et al. (1960) | 10 | 1,6% | 4 | 1,39% | 4 | 1,59% | 4 | 1,58% |
Commission de l’Avifaune Française (2016) | 9 | 1,44% | 9 | 3,14% | 9 | 3,57% | 7 | 2,77% |
Guth (1971) | 9 | 1,44% | 9 | 3,14% | 9 | 3,57% | 5 | 1,98% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 9 | 1,44% | 9 | 3,14% | 9 | 3,57% | 8 | 3,16% |
Gill (1995) | 7 | 1,12% | 7 | 2,44% | 7 | 2,78% | 5 | 1,98% |
Thibault et al. (2014) | 7 | 1,12% | 7 | 2,44% | 7 | 2,78% | 6 | 2,37% |
Gmelin (1788) | 6 | 0,96% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Safford & Hawkins (2013) | 6 | 0,96% | 6 | 2,09% | 6 | 2,38% | 5 | 1,98% |
Gonzalez et al. (2009) | 5 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Karadjian et al. (2022) | 5 | 0,8% | 5 | 1,74% | 5 | 1,98% | 5 | 1,98% |
Lee & Walsh-McGehee (2000) | 5 | 0,8% | 5 | 1,74% | 0 | 0% | 5 | 1,98% |
Birdlife International (2016) | 4 | 0,64% | 4 | 1,39% | 4 | 1,59% | 0 | 0% |
Collier et al. (2002) | 4 | 0,64% | 4 | 1,39% | 3 | 1,19% | 2 | 0,79% |
Dubois et al. (2008) | 4 | 0,64% | 4 | 1,39% | 4 | 1,59% | 4 | 1,58% |
Ehrhardt (1971) | 4 | 0,64% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Furminieux (2019) | 4 | 0,64% | 4 | 1,39% | 4 | 1,59% | 4 | 1,58% |
Levesque & Delcroix (2016) | 4 | 0,64% | 3 | 1,05% | 1 | 0,4% | 3 | 1,19% |
Vieillot (1819) | 4 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Ausilio & Zotier (1989) | 3 | 0,48% | 3 | 1,05% | 3 | 1,19% | 3 | 1,19% |
Bartoli (1972) | 3 | 0,48% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Birdlife International (2014) | 3 | 0,48% | 3 | 1,05% | 3 | 1,19% | 3 | 1,19% |
Gargominy et al. (1996) | 3 | 0,48% | 3 | 1,05% | 3 | 1,19% | 3 | 1,19% |
Humphries et al. (2019) | 3 | 0,48% | 3 | 1,05% | 3 | 1,19% | 0 | 0% |
Ingels et al. (2003) | 3 | 0,48% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Levesque & Delcroix (2013) | 3 | 0,48% | 3 | 1,05% | 0 | 0% | 3 | 1,19% |
Potin (2013) | 3 | 0,48% | 3 | 1,05% | 3 | 1,19% | 3 | 1,19% |
Probst (1997) | 3 | 0,48% | 3 | 1,05% | 3 | 1,19% | 3 | 1,19% |
Tostain & Dujardin (1988) | 3 | 0,48% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Tostain (1980) | 3 | 0,48% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Vieillot (1807) | 3 | 0,48% | 3 | 1,05% | 3 | 1,19% | 3 | 1,19% |
Bénito-espinal (1990) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Birdlife International (2016) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 0 | 0% |
Birdlife International (2016) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Birdlife International (2016) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Birdlife International (2016) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 0 | 0% |
Boddaert & Daubenton (1783) | 2 | 0,32% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Chartier et al. (2007) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 0 | 0% |
Cicero & Johnson (1998) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Dacosta et al. (2019) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
dal Molin (2009) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Daniel et al. (2020) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 0 | 0% |
Davant (1967) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Del Hoyo & Collar (2016) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Dickinson & Christidis (2014) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1816) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibson & Baker (2012) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Guermeur (1987) | 2 | 0,32% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Humeau et al. (2020) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 0 | 0% |
Impact-mer (2011) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 1 | 0,4% |
Kojadinovic et al. (2007) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 0 | 0% |
Lawrence (1879) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Lawrence (1879) | 2 | 0,32% | 2 | 0,7% | 1 | 0,4% | 1 | 0,4% |
Lepechin (1769) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2004) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Mathews (1914) | 2 | 0,32% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
McNair & Cramer-Burke (2006) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Oustalet (1895) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Pons et al. (2005) | 2 | 0,32% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Powell et al. (2008) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 0 | 0% |
Purenne (2016) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Questel (2023) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Scopoli (1786) | 2 | 0,32% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Seutin et al. (1993) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Temminck et al. (1838) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Theuerkauf et al. (2010) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Tunstall (1880) | 2 | 0,32% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
UNEP-WCMC (2005) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Vanderwerf et al. (2006) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Vieillot (1816) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 2 | 0,32% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Vieillot (1819) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Weimerskirch et al. (2009) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 0 | 0% |
Wilson (1813) | 2 | 0,32% | 2 | 0,7% | 2 | 0,79% | 2 | 0,79% |
Anonyme (2008) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Baird (1858) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Barre et al. (1991) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Bassin (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Beaufils (1999) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Bertault (1988) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (1982) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2016) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Birdlife International (2016) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Birdlife International (2016) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Birdlife International (2017) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Birdlife International (2017) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Boschert & Dronneau (1998) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Brandt (1838) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Brun (1958) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Brünnich (1764) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Calenge et al. (2010) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Cantera (2007) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Chastel et al. (1981) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Cheke & Hume (2008) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Chesser et al. (2016) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
CHN (2017) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Clark (1905) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Clark (1905) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Clements (1992) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Clergeau & Pascal (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Clergeau & Pascal (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Commecy et al. (2013) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Cory (1881) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1861) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1862) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Crochet et al. (2022) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Crouzier (2009) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Csabaï (2020) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
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 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Daudin (1802) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Deblock (1966) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Debout (2001) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Dechelle & Ingels (2007) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Deflandre (2007) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Deflorenne et al. (2012) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Delacour (1963) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Deniau & Provost (2020) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Dollfus (1966) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorleans (2022) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Dreff & Delliere (1994) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Louvet (2014) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Ducatez & Devore (2023) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Efe et al. (2009) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Eyton (1838) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Fremont (2002) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Gallien (2011) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Gernigon (2008) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Giraud-Audine et al. (2007) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Golvan (1956) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourreau et al. (1998) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Graber & Euzeby (1976) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Harcourt (1851) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Isenmann et al. (1971) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
IUCN (2014) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
IUCN (2015) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Johnson (1973) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuhl (1820) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lafresnaye (1848) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1787) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lawrence (1877) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Lawrence (1885) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Jouventin (1999) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Ledreff & Raynaud (1993) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Legros & Puissauve (2015) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Lesage et al. (2024) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Lesson (1831) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Lesson (1839) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Levesque & Yesou (2018) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Levesque (2001) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Levesque (2013) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Linné (1766) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Loison (1989) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Lorvelec & Clergeau (2003) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Lorvelec & Vigne (2003) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Lorvelec et al. (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Louette & Cousin (1999) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Loury & Puissauve (2016) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Maël Dewynter, Catherine Godefroid, Beatriz Conde, Willy Raitière, Distribution, écologie & statut de conservation du Colibri à tête bleue (Cyanophaia bicolor), Septembre (2014) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Maksimova (1976) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Marion & Clergeau (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Marion & Clergeau (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Marion & Marion (1982) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Marion (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Marion (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Martinet et al. (1765) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Mctavish (2002) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Montagu (1813) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Morel (1959) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Morrison (2006) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Nadal & Tariel (2008) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
O'reilly (1818) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
pallas (1764) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1769) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal & Melin (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Pascal et al. (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Pascal et al. (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Pearman et al. (2016) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Peters (1930) | 1 | 0,16% | 1 | 0,35% | 0 | 0% | 1 | 0,4% |
Pinchon (1976) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Pontoppidan (1763) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Reeber (2015) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Reyt (2021) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ridgway (1880) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Robert et al. (2002) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Roques (1991) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Routtier et al. (2023) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Roux & Coll. (2017) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Martinez (1987) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Sanchez et al. (2004) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Schuchmann (1981) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Sclater (1866) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Siorat & Rocamora (1995) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Siorat et al. (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Spiroux (1996) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Steadman & Bollt (2010) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Swainson (1838) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Terrasse & Terrasse (1969) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Uicn et al. (2016) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Vanderwerf et al. (2004) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Verreaux & Des Murs (1860) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Vieillot (1817) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Wahl & Barbraud (2005) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Wang & Liu (2016) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 0 | 0% |
Yésou (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Yésou (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |
Yésou (2003) | 1 | 0,16% | 1 | 0,35% | 1 | 0,4% | 1 | 0,4% |