Oiseaux de Guadeloupe
Aves de Guadeloupe
339 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) | 305 | 35,51% | 294 | 76,17% | 249 | 75,23% | 290 | 86,05% |
| UICN Comité français, OFB & MNHN (2021) | 178 | 20,72% | 178 | 46,11% | 178 | 53,78% | 136 | 40,36% |
| Uicn et al. (2017) | 175 | 20,37% | 169 | 43,78% | 152 | 45,92% | 136 | 40,36% |
| Questel (2020) | 135 | 15,72% | 130 | 33,68% | 108 | 32,63% | 122 | 36,2% |
| Yokoyama (2013) | 126 | 14,67% | 110 | 28,5% | 104 | 31,42% | 88 | 26,11% |
| Remsen et al. (2013) | 110 | 12,81% | 105 | 27,2% | 105 | 31,72% | 75 | 22,26% |
| Belfan & Conde (2016) | 105 | 12,22% | 102 | 26,42% | 75 | 22,66% | 98 | 29,08% |
| Questel & Le Quellec (2012) | 105 | 12,22% | 100 | 25,91% | 86 | 25,98% | 86 | 25,52% |
| Linnaeus (1758) | 99 | 11,53% | 25 | 6,48% | 25 | 7,55% | 19 | 5,64% |
| Etcheberry & Abraham (2009) | 63 | 7,33% | 55 | 14,25% | 55 | 16,62% | 45 | 13,35% |
| Uicn et al. (2015) | 46 | 5,36% | 44 | 11,4% | 44 | 13,29% | 30 | 8,9% |
| Uicn et al. (2020) | 39 | 4,54% | 39 | 10,1% | 39 | 11,78% | 32 | 9,5% |
| Tostain et al. (2013) | 35 | 4,07% | 29 | 7,51% | 28 | 8,46% | 28 | 8,31% |
| Clements (2012) | 30 | 3,49% | 30 | 7,77% | 25 | 7,55% | 22 | 6,53% |
| Weimerskirch et al. (2009) | 29 | 3,38% | 23 | 5,96% | 23 | 6,95% | 16 | 4,75% |
| Gmelin (1789) | 28 | 3,26% | 5 | 1,3% | 5 | 1,51% | 4 | 1,19% |
| Dewynter (2021) | 27 | 3,14% | 27 | 6,99% | 26 | 7,85% | 24 | 7,12% |
| Linnaeus (1766) | 25 | 2,91% | 2 | 0,52% | 1 | 0,3% | 1 | 0,3% |
| Barau et al. (2005) | 23 | 2,68% | 19 | 4,92% | 19 | 5,74% | 15 | 4,45% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 19 | 2,21% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Uicn et al. (2015) | 17 | 1,98% | 14 | 3,63% | 14 | 4,23% | 12 | 3,56% |
| Dickinson & Remsen (2013) | 16 | 1,86% | 15 | 3,89% | 8 | 2,42% | 13 | 3,86% |
| Rocamora (2004) | 15 | 1,75% | 14 | 3,63% | 13 | 3,93% | 11 | 3,26% |
| Clements et al. (2015) | 13 | 1,51% | 13 | 3,37% | 3 | 0,91% | 12 | 3,56% |
| Del Hoyo & Collar (2014) | 13 | 1,51% | 9 | 2,33% | 8 | 2,42% | 9 | 2,67% |
| Dewynter & Claessens (2020) | 13 | 1,51% | 13 | 3,37% | 13 | 3,93% | 6 | 1,78% |
| Guth (1971) | 13 | 1,51% | 12 | 3,11% | 12 | 3,63% | 7 | 2,08% |
| Deblock et al. (1960) | 12 | 1,4% | 7 | 1,81% | 7 | 2,11% | 6 | 1,78% |
| Commission de l’Avifaune Française (2016) | 9 | 1,05% | 9 | 2,33% | 9 | 2,72% | 7 | 2,08% |
| Gill (1995) | 9 | 1,05% | 9 | 2,33% | 9 | 2,72% | 5 | 1,48% |
| Gmelin (1788) | 8 | 0,93% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Karadjian et al. (2022) | 8 | 0,93% | 8 | 2,07% | 8 | 2,42% | 8 | 2,37% |
| Thibault et al. (2014) | 8 | 0,93% | 8 | 2,07% | 8 | 2,42% | 5 | 1,48% |
| Furminieux (2019) | 6 | 0,7% | 6 | 1,55% | 6 | 1,81% | 6 | 1,78% |
| Gonzalez et al. (2009) | 6 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levesque & Delcroix (2016) | 6 | 0,7% | 5 | 1,3% | 2 | 0,6% | 5 | 1,48% |
| Safford & Hawkins (2013) | 6 | 0,7% | 6 | 1,55% | 6 | 1,81% | 5 | 1,48% |
| Vieillot (1819) | 6 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ehrhardt (1971) | 5 | 0,58% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Lee & Walsh-McGehee (2000) | 5 | 0,58% | 5 | 1,3% | 0 | 0% | 5 | 1,48% |
| Scopoli (1769) | 5 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2016) | 4 | 0,47% | 4 | 1,04% | 4 | 1,21% | 0 | 0% |
| Boddaert & Daubenton (1783) | 4 | 0,47% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Collier et al. (2002) | 4 | 0,47% | 4 | 1,04% | 3 | 0,91% | 2 | 0,59% |
| Dubois et al. (2008) | 4 | 0,47% | 4 | 1,04% | 4 | 1,21% | 4 | 1,19% |
| Tostain & Dujardin (1988) | 4 | 0,47% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Ausilio & Zotier (1989) | 3 | 0,35% | 3 | 0,78% | 3 | 0,91% | 2 | 0,59% |
| Bénito-espinal (1990) | 3 | 0,35% | 3 | 0,78% | 2 | 0,6% | 3 | 0,89% |
| Birdlife International (2014) | 3 | 0,35% | 3 | 0,78% | 3 | 0,91% | 3 | 0,89% |
| Durant et al. (2013) | 3 | 0,35% | 3 | 0,78% | 3 | 0,91% | 3 | 0,89% |
| Gargominy et al. (1996) | 3 | 0,35% | 3 | 0,78% | 3 | 0,91% | 3 | 0,89% |
| Humphries et al. (2019) | 3 | 0,35% | 3 | 0,78% | 3 | 0,91% | 0 | 0% |
| Ingels et al. (2003) | 3 | 0,35% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Lawrence (1879) | 3 | 0,35% | 3 | 0,78% | 2 | 0,6% | 2 | 0,59% |
| Levesque & Delcroix (2013) | 3 | 0,35% | 3 | 0,78% | 0 | 0% | 3 | 0,89% |
| Pontoppidan (1763) | 3 | 0,35% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Potin (2013) | 3 | 0,35% | 3 | 0,78% | 3 | 0,91% | 3 | 0,89% |
| Probst (1997) | 3 | 0,35% | 3 | 0,78% | 3 | 0,91% | 3 | 0,89% |
| Tostain (1980) | 3 | 0,35% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Vieillot (1807) | 3 | 0,35% | 3 | 0,78% | 3 | 0,91% | 3 | 0,89% |
| Barre et al. (2009) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Birdlife International (2016) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Birdlife International (2016) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| Birdlife International (2016) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| Birdlife International (2016) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Bosc (1792) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chartier et al. (2007) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| CHN (2017) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 1 | 0,3% |
| Cicero & Johnson (1998) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Clements et al. (2017) | 2 | 0,23% | 2 | 0,52% | 0 | 0% | 2 | 0,59% |
| dal Molin (2009) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Danforth (1937) | 2 | 0,23% | 2 | 0,52% | 0 | 0% | 2 | 0,59% |
| Daniel et al. (2020) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| Davant (1967) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Del Hoyo & Collar (2016) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dickinson & Christidis (2014) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donovan (1816) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gibson & Baker (2012) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Gourreau et al. (1998) | 2 | 0,23% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Guermeur (1987) | 2 | 0,23% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Humeau et al. (2020) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| Impact-mer (2011) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 1 | 0,3% |
| Jardine & Selby (1826-1835) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kojadinovic et al. (2007) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| Lafresnaye (1844) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lepechin (1769) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1831) | 2 | 0,23% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Levesque & Clergeau (2002) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Linné (1766) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec et al. (2004) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Mathews (1914) | 2 | 0,23% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Mays et al. (2006) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| McNair & Cramer-Burke (2006) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oustalet (1895) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| pallas (1764) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pons et al. (2005) | 2 | 0,23% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Powell et al. (2008) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| Seutin et al. (1993) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| Theuerkauf et al. (2010) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Tunstall (1880) | 2 | 0,23% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| UNEP-WCMC (2005) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Vanderwerf et al. (2006) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Vieillot (1817) | 2 | 0,23% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Vieillot (1819) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Weimerskirch et al. (2009) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 0 | 0% |
| Wilson (1813) | 2 | 0,23% | 2 | 0,52% | 2 | 0,6% | 2 | 0,59% |
| Anonyme (2008) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Attié et al. (1997) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Baird (1858) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baird (1865) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Balouet & Olson (1989) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Bangs (1913) | 1 | 0,12% | 1 | 0,26% | 0 | 0% | 1 | 0,3% |
| Barlow (1978) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barre et al. (1991) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Beaufils (1999) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Bertault (1988) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertrand (1982) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Birdlife International (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Birdlife International (2016) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Birdlife International (2016) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Birdlife International (2017) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Birdlife International (2017) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Boie (1835) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boschert & Dronneau (1998) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Bougeard & Siblet (2000) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Brandt (1838) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brehm (1831) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brewster (1895) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brewster (1902) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brun (1958) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Brünnich (1764) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Calenge et al. (2010) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Carte (1866) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Catil (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Champion (2017) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Chastel et al. (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Cheke & Hume (2008) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Chesser et al. (2016) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clark (1905) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Clements (1992) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Clergeau et al. (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coatmeur (1999) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Commecy et al. (2013) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Cory (1886) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coues (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coues (1862) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Crochet et al. (2022) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Crouzier (2009) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Csabaï (2020) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Danforth (1935) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Daudin (1802) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Deblock & Rose (1964) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Deblock (1966) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Debout (2001) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Dechelle & Ingels (2007) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Deflandre (2007) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delacour (1963) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Deniau & Provost (2020) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Deutsche & Ornithologen-gesellschaft (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dorleans (2022) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Dreff & Delliere (1994) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois & Cugnasse (2015) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Dubois & Louvet (2014) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Ducatez & Devore (2023) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Efe et al. (2009) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Eyton (1838) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flitti & Rocha (2014) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Fremont (2002) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Gallien (2011) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Gauthier-clerc & Lambert (2002) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Gernigon (2008) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giglioli & Salvadori (1868) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giraud-Audine et al. (2007) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Gmelin (1770) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hennique et al. (2013) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Huey (1927) | 1 | 0,12% | 1 | 0,26% | 0 | 0% | 1 | 0,3% |
| Isaac (2020) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Isenmann et al. (1971) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| IUCN (2014) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Jouventin (1994) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Joyeux & Baer (1955) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kayser & Wilhelm (1991) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Kuhl (1820) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lafresnaye (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1787) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lawrence (1877) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Lawrence (1885) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Corre & Jouventin (1999) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Ledreff & Raynaud (1993) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Legros & Puissauve (2015) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Lenoble (2015) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Lesson (1839) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Levesque & Yesou (2018) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Levesque (2001) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Levesque (2013) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Loison (1989) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Lorvelec & Clergeau (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Vigne (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Lorvelec & Vigne (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Louette & Cousin (1999) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Marion & Clergeau (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Marion & Marion (1982) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Marion (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Marion (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Martinet et al. (1765) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martinet et al. (1765) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martinet et al. (1765) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mctavish (2002) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Melin et al. (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Montagu (1813) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Morrison (2006) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Nadal & Tariel (2008) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Naumann (1819) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noel et al. (2004) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Nuttall (1834) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| O'reilly (1818) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Pascal et al. (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Pascal et al. (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Pearman et al. (2016) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Pearson & Prévot (1971) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Peters (1930) | 1 | 0,12% | 1 | 0,26% | 0 | 0% | 1 | 0,3% |
| Pinaud et al. (2005) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Pinchon (1976) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Prevot (1971) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Puissauve & Legros (2015) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Purenne (2016) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Reeber (2015) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Remsen et al. (2013) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Ridgway (1880) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robert et al. (2002) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Routtier et al. (2023) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Roux & Coll. (2017) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cormoran, 15(4): 218.">Rundle & Rundle (2007) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Sanchez et al. (2004) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Schiebel (1910) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schuchmann (1981) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Sclater (1866) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1786) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seriot et al. (1988) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siorat & Rocamora (1995) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Siorat et al. (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Socolovschi et al. (2012) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Spiroux (1996) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Steadman & Bollt (2010) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Sundevall (1857) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1838) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Taberlet (1983) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Trevoux & Trevoux (2007) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Uicn et al. (2016) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Vanderwerf et al. (2004) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verreaux & Des Murs (1860) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Vieillot (1816) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1817) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1817) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wahl & Barbraud (2005) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Wang & Liu (2016) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
| Weimerskirch & Jouventin (1998) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Yésou (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Yésou (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Yésou (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
| Yésou (2003) | 1 | 0,12% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
