Oiseaux occasionnels en France
Oiseaux occasionnels en France (métropole et outre-mer)
558 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) | 209 | 16,92% | 201 | 36,48% | 187 | 36,59% | 193 | 37,19% |
Uicn et al. (2017) | 167 | 13,52% | 157 | 28,49% | 149 | 29,16% | 139 | 26,78% |
UICN Comité français, OFB & MNHN (2021) | 137 | 11,09% | 137 | 24,86% | 137 | 26,81% | 120 | 23,12% |
Uicn et al. (2015) | 134 | 10,85% | 130 | 23,59% | 130 | 25,44% | 115 | 22,16% |
Linnaeus (1758) | 121 | 9,8% | 36 | 6,53% | 36 | 7,05% | 31 | 5,97% |
Questel (2020) | 102 | 8,26% | 98 | 17,79% | 94 | 18,4% | 91 | 17,53% |
Yokoyama (2013) | 101 | 8,18% | 85 | 15,43% | 84 | 16,44% | 75 | 14,45% |
Remsen et al. (2013) | 91 | 7,37% | 85 | 15,43% | 85 | 16,63% | 71 | 13,68% |
Belfan & Conde (2016) | 80 | 6,48% | 75 | 13,61% | 67 | 13,11% | 70 | 13,49% |
Questel & Le Quellec (2012) | 72 | 5,83% | 68 | 12,34% | 67 | 13,11% | 58 | 11,18% |
Etcheberry & Abraham (2009) | 68 | 5,51% | 60 | 10,89% | 60 | 11,74% | 50 | 9,63% |
Tostain et al. (2013) | 51 | 4,13% | 45 | 8,17% | 44 | 8,61% | 42 | 8,09% |
Clements (2012) | 48 | 3,89% | 47 | 8,53% | 38 | 7,44% | 39 | 7,51% |
CHN (2017) | 47 | 3,81% | 47 | 8,53% | 47 | 9,2% | 46 | 8,86% |
Uicn et al. (2020) | 40 | 3,24% | 40 | 7,26% | 40 | 7,83% | 35 | 6,74% |
Rocamora (2004) | 38 | 3,08% | 34 | 6,17% | 30 | 5,87% | 31 | 5,97% |
Uicn et al. (2015) | 37 | 3% | 32 | 5,81% | 32 | 6,26% | 30 | 5,78% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 36 | 2,91% | 36 | 6,53% | 33 | 6,46% | 33 | 6,36% |
Barau et al. (2005) | 35 | 2,83% | 29 | 5,26% | 28 | 5,48% | 22 | 4,24% |
Gmelin (1789) | 35 | 2,83% | 8 | 1,45% | 8 | 1,57% | 7 | 1,35% |
Weimerskirch et al. (2009) | 33 | 2,67% | 26 | 4,72% | 26 | 5,09% | 20 | 3,85% |
Dewynter (2021) | 26 | 2,11% | 26 | 4,72% | 25 | 4,89% | 24 | 4,62% |
Dickinson & Remsen (2013) | 23 | 1,86% | 20 | 3,63% | 12 | 2,35% | 18 | 3,47% |
Commission de l’Avifaune Française (2016) | 22 | 1,78% | 21 | 3,81% | 20 | 3,91% | 19 | 3,66% |
Linnaeus (1766) | 22 | 1,78% | 3 | 0,54% | 2 | 0,39% | 2 | 0,39% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 19 | 1,54% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Gill (1995) | 18 | 1,46% | 17 | 3,09% | 17 | 3,33% | 13 | 2,5% |
Deblock et al. (1960) | 17 | 1,38% | 10 | 1,81% | 10 | 1,96% | 10 | 1,93% |
Ausilio & Zotier (1989) | 15 | 1,21% | 14 | 2,54% | 14 | 2,74% | 13 | 2,5% |
Del Hoyo & Collar (2014) | 15 | 1,21% | 11 | 2% | 10 | 1,96% | 11 | 2,12% |
Thibault et al. (2014) | 15 | 1,21% | 14 | 2,54% | 14 | 2,74% | 13 | 2,5% |
Safford & Hawkins (2013) | 14 | 1,13% | 14 | 2,54% | 12 | 2,35% | 13 | 2,5% |
Karadjian et al. (2022) | 11 | 0,89% | 11 | 2% | 11 | 2,15% | 8 | 1,54% |
Louette & Cousin (1999) | 11 | 0,89% | 10 | 1,81% | 9 | 1,76% | 9 | 1,73% |
Pallas (1776) | 11 | 0,89% | 7 | 1,27% | 7 | 1,37% | 7 | 1,35% |
Potin (2013) | 11 | 0,89% | 10 | 1,81% | 8 | 1,57% | 10 | 1,93% |
Probst (1997) | 11 | 0,89% | 8 | 1,45% | 8 | 1,57% | 7 | 1,35% |
Uicn et al. (2011) | 10 | 0,81% | 10 | 1,81% | 10 | 1,96% | 10 | 1,93% |
Clements et al. (2015) | 9 | 0,73% | 8 | 1,45% | 2 | 0,39% | 7 | 1,35% |
Guth (1971) | 8 | 0,65% | 7 | 1,27% | 7 | 1,37% | 6 | 1,16% |
Chastel & Beaucournu (1992) | 7 | 0,57% | 7 | 1,27% | 7 | 1,37% | 7 | 1,35% |
Furminieux (2019) | 7 | 0,57% | 7 | 1,27% | 7 | 1,37% | 7 | 1,35% |
Barre et al. (2009) | 6 | 0,49% | 6 | 1,09% | 6 | 1,17% | 5 | 0,96% |
Bartoli (1972) | 6 | 0,49% | 5 | 0,91% | 5 | 0,98% | 5 | 0,96% |
Pallas (1773) | 6 | 0,49% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Temminck et al. (1838) | 6 | 0,49% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Boddaert & Daubenton (1783) | 5 | 0,4% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Dubois et al. (2008) | 5 | 0,4% | 5 | 0,91% | 5 | 0,98% | 5 | 0,96% |
Ehrhardt (1971) | 5 | 0,4% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Gonzalez et al. (2009) | 5 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Guermeur (1987) | 5 | 0,4% | 4 | 0,73% | 4 | 0,78% | 4 | 0,77% |
Levesque & Delcroix (2016) | 5 | 0,4% | 4 | 0,73% | 2 | 0,39% | 4 | 0,77% |
Scopoli (1769) | 5 | 0,4% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Barbraud et al. (2009) | 4 | 0,32% | 4 | 0,73% | 4 | 0,78% | 4 | 0,77% |
Collier et al. (2002) | 4 | 0,32% | 4 | 0,73% | 3 | 0,59% | 3 | 0,58% |
Del Hoyo & Collar (2016) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Delord et al. (2005) | 4 | 0,32% | 4 | 0,73% | 4 | 0,78% | 4 | 0,77% |
Delord et al. (2008) | 4 | 0,32% | 4 | 0,73% | 4 | 0,78% | 4 | 0,77% |
Gmelin (1788) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2013) | 4 | 0,32% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Jaeger et al. (2020) | 4 | 0,32% | 4 | 0,73% | 4 | 0,78% | 4 | 0,77% |
Kojadinovic et al. (2007) | 4 | 0,32% | 4 | 0,73% | 4 | 0,78% | 4 | 0,77% |
Lepechin (1769) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Temminck et al. (1838) | 4 | 0,32% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Tostain & Dujardin (1988) | 4 | 0,32% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Vieillot (1819) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Abeyrama et al. (2021) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Banks et al. (2006) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Birdlife International (2014) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Carravieri et al. (2016) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Claessens et al. (2014) | 3 | 0,24% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Dewynter & Claessens (2020) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Durant et al. (2013) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Forster (1781) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Ingels et al. (2003) | 3 | 0,24% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Isenmann et al. (1971) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Joyeux & Baer (1955) | 3 | 0,24% | 2 | 0,36% | 2 | 0,39% | 1 | 0,19% |
Latham (1787) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews (1912) | 3 | 0,24% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Mathews (1914) | 3 | 0,24% | 2 | 0,36% | 1 | 0,2% | 2 | 0,39% |
pallas (1764) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1769) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Ponchon et al. (2021) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Pons et al. (2005) | 3 | 0,24% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pontoppidan (1763) | 3 | 0,24% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Tostain (1980) | 3 | 0,24% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Vanderwerf et al. (2006) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 2 | 0,39% |
Vieillot (1807) | 3 | 0,24% | 3 | 0,54% | 3 | 0,59% | 3 | 0,58% |
Bénito-espinal (1990) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 1 | 0,19% |
Birdlife International (2013) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Birdlife International (2016) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Birdlife International (2016) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Bosc (1792) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bretagnolle & Attie (1991) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Chartier et al. (2007) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 0 | 0% |
Cherel et al. (2022) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Cicero & Johnson (1998) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Claramunt (2014) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Collinson et al. (2017) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Condamin (1979) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
dal Molin (2009) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
D'Amico (2001) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Daniel et al. (2020) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 0 | 0% |
Davant (1967) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1816) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorleans (2022) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Dronneau & Wassmer (2008) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Duquet (2012) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Frugone et al. (2021) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Gibson & Baker (2012) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Gmelin (1770) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Gould (1844) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourreau et al. (1998) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Humeau et al. (2020) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Impact-mer (2011) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Jardine & Selby (1826-1835) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Knox et al. (2002) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Leopold (1965) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Lesage et al. (2024) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Lesson (1831) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Lichtenstein (1823) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Linné (1766) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2004) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Mays et al. (2006) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Oatleya et al. (2015) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Pallas (1831) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1831) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pezy et al. (2022) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Purenne (2016) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Questel (2023) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Raust & Sanford (2007) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Ridoux (1989) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Ringler et al. (2015) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Sabine (1819) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Searby & Jouventin (2005) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Stahl et al. (1985) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Temminck et al. (1838) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Temminck et al. (1838) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Tremblay & Cherel (2003) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Trotignon et al. (1994) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Tunstall (1880) | 2 | 0,16% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Verreaux & Des Murs (1860) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 1 | 0,19% |
Vieillot (1816) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1819) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Weimerskirch et al. (2009) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 0 | 0% |
Wilcox & Spotswood (2011) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Wilson (1813) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
Wilson-aggarwal et al. (2016) | 2 | 0,16% | 2 | 0,36% | 2 | 0,39% | 2 | 0,39% |
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Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Anonyme. (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Arrigoni Degli Oddi (1903) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Attié et al. (1997) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Austin et al. (2004) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Baird (1858) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Baird (1865) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Baker-gabb (1979) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Balouet & Olson (1989) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Barbraud et al. (2021) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Barbraud (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Barre et al. (1977) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Bassin (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Beaufils (1999) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Bechstein (1803) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertault (1988) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (1982) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Birdlife International (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Birdlife International (2013) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Birdlife International (2014) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Birdlife International (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Birdlife International (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Birdlife International (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Birdlife International (2017) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Birdlife International (2017) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Boie (1835) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaccorsi (1999) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaccorsi (1999) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Bonaparte (1850) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1857) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonfils (2024) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Boschert & Dronneau (1998) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Bougeard & Siblet (2000) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Bougeard (2007) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Boussemart & Gavory (2017) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Bouteiller & Borsa (2022) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Brandt (1837) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Brehm (1824) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Brewster (1895) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Brewster (1902) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Brilland (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Brooke (1971) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Brun (1958) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Brünnich (1764) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Calenge et al. (2010) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Cantera (2007) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Catil (2013) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Champion (2017) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Chastel et al. (1987) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Cheke & Hume (2008) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Cherel & Boxshall (2004) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Cibois et al. (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Claessens et al. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Clamens (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Clements (1992) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Clergeau & Pascal (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Clergeau & Pascal (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Clergeau & Pascal (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Clergeau et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Clergeau et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Commission des sciences et arts d'Egypte. France. (1809) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Cormier (1984) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Corre & Jouventin (1997) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Cory (1881) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1861) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1862) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Cox (1970) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Creau (1996) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Crepeau (1973) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Crochet et al. (2022) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Crofton et al. (2002) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Crouzier (2009) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Csabaï (2020) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Danjon (2011) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
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 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Daudin (1802) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Deblock & Rose (1964) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Deblock (1966) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Deblock (1966) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Debout & Desmares (1996) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Debout (2001) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Debout (2009) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Dechelle & Ingels (2007) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Deflandre (2007) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Deflorenne et al. (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Demay et al. (2014) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Deniau & Provost (2020) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Derozier (2020) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Dickinson & Christidis (2014) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dollfus (1966) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreff & Delliere (1994) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Cugnasse (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Dubois & Louvet (2014) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Dubois et al. (1991) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Dubois et al. (2000) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Ducatez & Devore (2023) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Efe et al. (2009) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Elkins & Yesou (1998) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Eyton (1838) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Faggio et al. (2001) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Fain & Beaucournu (1984) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Falla (1933) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrand et al. (2007) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Finsch (1876) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Flitti & Rocha (2014) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Flood et al. (2017) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Flood et al. (2021) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Fonteneau et al. (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Forster (1844) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fouquet (1996) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Frémont et al. (2007) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Fremont (2002) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Gallien (2011) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Gargominy et al. (1996) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
GARNOT (1826) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Gauthier-clerc & Lambert (2002) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Géné (1839) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Genevois (1991) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Gernigon (2008) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ghestemme & Salamolard (2003) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Giglioli & Salvadori (1868) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2021) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Golvan (1956) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Graber & Euzeby (1976) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Grantham (2005) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Gray (1831) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Guérin-Méneville (1843) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiguen et al. (1984) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Guille (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Gunnerus (1767) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Harcourt (1851) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Harrison (1981) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Hartert (1914) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Hennique et al. (2013) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Hombron & Jacquinot (1841) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Homeyer (1853) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Horsfield (1824) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ingels & Dechelle (2011) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Ingels et al. (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Isaac (2020) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Issa & Reveillaud (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
IUCN (2014) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Jackson (2011) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Jaeger et al. (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Jeanne et al. (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Jiguet et al. (2009) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Jiguet (2002) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Johnson (1973) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Jornvall et al. (2006) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Bulweria baraui. Bulletin du Muséum National d'Histoire Naturelle, 35(6): 593-597.">Jouanin (1964) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin (1994) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Kayser & Wilhelm (1991) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Kayser et al. (2004) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Kayser et al. (2019) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Kempen (1888) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Kuhl (1820) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lafresnaye (1848) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambottin (2014) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Latham (1790) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1790) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubin et al. (2019) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Lawrence (1879) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Le Corre & Jouventin (1999) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Le Corre & Probst (1997) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Le Corre (1996) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Ledreff & Raynaud (1993) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Legrand & Demongin (1999) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Legros & Puissauve (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Leisler (1812-1813) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemarinel (2019) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Lesson (1825) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Lesson (1839) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Levesque (2001) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Levesque (2013) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Lloret (1996) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Loison (1989) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Lorvelec & Clergeau (2003) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Lorvelec & Vigne (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Lorvelec et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Lorvelec et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Louette & Herremans (1985) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Loury & Puissauve (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Loury & Puissauve (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Loury & Puissauve (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Loury & Puissauve (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Lukanov & Pavlova (2022) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Maksimova (1976) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Maout (2019) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Marchal & Fluhr (2017) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Marion & Clergeau (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Marion & Clergeau (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Marion & Marion (1982) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Marion (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Martinet et al. (1765) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinet et al. (1765) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews (1912) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Mctavish (2002) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Medway (2009) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Menegaux (1909) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Miskelly (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Montagu (1813) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Morel (1959) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Morrison (2006) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Mougin (1984) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Müller (1776) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Murphy (1929) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Nadal & Tariel (2008) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Naurois (1978) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Noel et al. (2004) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Nuttall (1834) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Olioso (1996) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
O'reilly (1818) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1769) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Parkin et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Pascal & Clergeau (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pascal et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pascal et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Peale (1848) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pearman et al. (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Pearson & Prévot (1971) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pelzeln (1854) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit (1976) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinaud et al. (2005) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pons (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pratt (2011) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Prevost (1970) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Prevot (1971) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Pueschel & Stark (2017) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Puigcerver et al. (2001) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Puissauve & Legros (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Puissauve (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Radde (1862-1863) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Raitiere et al. (2013) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Ramírez et al. (2013) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Reeber et al. (1996) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeber et al. (2008) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Reeber (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Renaudier et al. (2010) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Riddiford & Ellis (1988) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Ridgway (1880) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Robert et al. (2002) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Robertson (2002) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
ROGEON & SORDELLO (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Roques (1991) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rotschikd (1903) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rotschild (1893) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Coll. (2017) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Martinez (1987) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Cormoran, 15(4): 218.">Rundle & Rundle (2007) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Russell et al. (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Salvadori (1899) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez et al. (2004) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Sangster et al. (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Savigny (1809) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Schiebel (1910) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Seriot et al. (1988) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Siorat & Rocamora (1995) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Siorat et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Smith (1849) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Société Calédonienne d'Ornithologie (2023) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
SORDELLO (2012) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Steadman & Bollt (2010) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Sueur & Wroza (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Sueur (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Swainson & Richardson (1831) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Swinhoe (1863) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Taberlet (1983) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Temminck & Schlegel (1849) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Temminck et al. (1820-1840) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Temminck et al. (1840) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Temminck (1818-1838) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Terrasse & Terrasse (1969) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Thiebot et al. (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Thomson (1842) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Trevous & Trevoux (2007) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Trevoux & Trevoux (2007) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Trevoux (2002) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Uicn et al. (2014) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Une et al. (1816) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
UNEP-WCMC (2005) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Vanderwerf et al. (2004) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Vian (1888) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Vieillot et al. ([1820-30]) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Vieillot (1818) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Viganò & Corso (2015) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Vigne et al. (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Vigors & Children (1826) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Vigors (1825) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Vincent (2012) | 1 | 0,08% | 1 | 0,18% | 0 | 0% | 1 | 0,19% |
Voisin & Voisin (2001) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Vorimore et al. (2021) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Wahl & Barbraud (2005) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Warham et al. (1977) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Weimerskirch & Jouventin (1998) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Weimerskirch et al. (2018) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Wink et al. (1979) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Wroza (2020) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Yésou (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Yésou (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Yésou (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Yésou (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Yésou (2003) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |
Zink et al. (2009) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
(1994) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
(2021) | 1 | 0,08% | 1 | 0,18% | 1 | 0,2% | 1 | 0,19% |