Alcidae, Stercorariidae, Laridae, Pelecanidae, Suloidea, Procellariiformes, Phaethontiformes et Sphenisciformes
357 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. (2015) | 109 | 18,96% | 103 | 37,05% | 99 | 47,14% | 76 | 32,07% |
| Uicn et al. (2017) | 57 | 9,91% | 53 | 19,06% | 47 | 22,38% | 38 | 16,03% |
| Levesque & Delcroix (2018) | 50 | 8,7% | 47 | 16,91% | 41 | 19,52% | 38 | 16,03% |
| UICN Comité français, OFB & MNHN (2021) | 38 | 6,61% | 38 | 13,67% | 38 | 18,1% | 23 | 9,7% |
| Remsen et al. (2013) | 29 | 5,04% | 26 | 9,35% | 26 | 12,38% | 15 | 6,33% |
| Uicn et al. (2015) | 27 | 4,7% | 24 | 8,63% | 24 | 11,43% | 23 | 9,7% |
| Linnaeus (1758) | 25 | 4,35% | 9 | 3,24% | 9 | 4,29% | 6 | 2,53% |
| Clements (2012) | 24 | 4,17% | 23 | 8,27% | 19 | 9,05% | 18 | 7,59% |
| Yokoyama (2013) | 23 | 4% | 22 | 7,91% | 21 | 10% | 10 | 4,22% |
| Questel & Le Quellec (2012) | 22 | 3,83% | 20 | 7,19% | 17 | 8,1% | 11 | 4,64% |
| Belfan & Conde (2016) | 20 | 3,48% | 16 | 5,76% | 14 | 6,67% | 14 | 5,91% |
| Etcheberry & Abraham (2009) | 18 | 3,13% | 14 | 5,04% | 14 | 6,67% | 12 | 5,06% |
| Questel (2020) | 18 | 3,13% | 16 | 5,76% | 12 | 5,71% | 13 | 5,49% |
| Tostain et al. (2013) | 18 | 3,13% | 17 | 6,12% | 17 | 8,1% | 13 | 5,49% |
| Barau et al. (2005) | 17 | 2,96% | 12 | 4,32% | 12 | 5,71% | 7 | 2,95% |
| Dickinson & Remsen (2013) | 17 | 2,96% | 15 | 5,4% | 9 | 4,29% | 13 | 5,49% |
| Gmelin (1789) | 16 | 2,78% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Weimerskirch et al. (2009) | 14 | 2,43% | 12 | 4,32% | 11 | 5,24% | 5 | 2,11% |
| Gill (1995) | 12 | 2,09% | 11 | 3,96% | 11 | 5,24% | 3 | 1,27% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 11 | 1,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thibault et al. (2014) | 11 | 1,91% | 11 | 3,96% | 11 | 5,24% | 3 | 1,27% |
| Ausilio & Zotier (1989) | 10 | 1,74% | 9 | 3,24% | 9 | 4,29% | 8 | 3,38% |
| Chastel & Beaucournu (1992) | 10 | 1,74% | 10 | 3,6% | 10 | 4,76% | 8 | 3,38% |
| Rocamora (2004) | 10 | 1,74% | 8 | 2,88% | 7 | 3,33% | 4 | 1,69% |
| Safford & Hawkins (2013) | 10 | 1,74% | 10 | 3,6% | 7 | 3,33% | 7 | 2,95% |
| Clements et al. (2015) | 9 | 1,57% | 9 | 3,24% | 4 | 1,9% | 8 | 3,38% |
| Probst (1997) | 9 | 1,57% | 5 | 1,8% | 5 | 2,38% | 4 | 1,69% |
| Barre et al. (2009) | 8 | 1,39% | 8 | 2,88% | 8 | 3,81% | 7 | 2,95% |
| Del Hoyo & Collar (2014) | 8 | 1,39% | 5 | 1,8% | 2 | 0,95% | 5 | 2,11% |
| Potin (2013) | 8 | 1,39% | 7 | 2,52% | 6 | 2,86% | 6 | 2,53% |
| UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 7 | 1,22% | 7 | 2,52% | 6 | 2,86% | 6 | 2,53% |
| Kojadinovic et al. (2007) | 6 | 1,04% | 4 | 1,44% | 4 | 1,9% | 2 | 0,84% |
| Uicn et al. (2020) | 6 | 1,04% | 6 | 2,16% | 6 | 2,86% | 4 | 1,69% |
| Banks et al. (2006) | 5 | 0,87% | 4 | 1,44% | 4 | 1,9% | 1 | 0,42% |
| Bénito-espinal (1990) | 5 | 0,87% | 5 | 1,8% | 2 | 0,95% | 4 | 1,69% |
| Furminieux (2019) | 5 | 0,87% | 5 | 1,8% | 5 | 2,38% | 4 | 1,69% |
| Lee & Walsh-McGehee (2000) | 5 | 0,87% | 5 | 1,8% | 0 | 0% | 5 | 2,11% |
| Linnaeus (1766) | 5 | 0,87% | 2 | 0,72% | 1 | 0,48% | 1 | 0,42% |
| Barbraud et al. (2009) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 4 | 1,69% |
| Bost et al. (2022) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 2 | 0,84% |
| CHN (2017) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 3 | 1,27% |
| Collier et al. (2002) | 4 | 0,7% | 4 | 1,44% | 3 | 1,43% | 1 | 0,42% |
| Commission de l’Avifaune Française (2016) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 1 | 0,42% |
| Deblock et al. (1960) | 4 | 0,7% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Delord et al. (2005) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 4 | 1,69% |
| Delord et al. (2008) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 4 | 1,69% |
| Forster (1781) | 4 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Humeau et al. (2020) | 4 | 0,7% | 4 | 1,44% | 2 | 0,95% | 2 | 0,84% |
| Isenmann et al. (1971) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 4 | 1,69% |
| Jaeger et al. (2020) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 4 | 1,69% |
| Karadjian et al. (2022) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 3 | 1,27% |
| Tostain & Dujardin (1988) | 4 | 0,7% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Vanderwerf et al. (2006) | 4 | 0,7% | 4 | 1,44% | 4 | 1,9% | 1 | 0,42% |
| Abeyrama et al. (2021) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Barbraud et al. (2021) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Bretagnolle et al. (2021) | 3 | 0,52% | 3 | 1,08% | 0 | 0% | 3 | 1,27% |
| Bretagnolle et al. (2022) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Cadiou et al. (2010) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 0 | 0% |
| Carravieri et al. (2016) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Dodson & Fitzgerald (1980) | 3 | 0,52% | 2 | 0,72% | 0 | 0% | 2 | 0,84% |
| Dubois et al. (2008) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Ehrhardt (1971) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faggio et al. (2022) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Gould (1844) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| IUCN (2013) | 3 | 0,52% | 2 | 0,72% | 2 | 0,95% | 1 | 0,42% |
| Jiguet (2002) | 3 | 0,52% | 3 | 1,08% | 0 | 0% | 3 | 1,27% |
| Jouventin et al. (1989) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Corre & Jouventin (1999) | 3 | 0,52% | 3 | 1,08% | 1 | 0,48% | 2 | 0,84% |
| Lescroel et al. (2009) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Levesque & Delcroix (2013) | 3 | 0,52% | 3 | 1,08% | 0 | 0% | 3 | 1,27% |
| Mathews (1912) | 3 | 0,52% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Mathews (1914) | 3 | 0,52% | 2 | 0,72% | 1 | 0,48% | 2 | 0,84% |
| Medway (2009) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Naurois (1978) | 3 | 0,52% | 3 | 1,08% | 1 | 0,48% | 3 | 1,27% |
| Ponchon et al. (2021) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Pons et al. (2005) | 3 | 0,52% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Pontoppidan (1763) | 3 | 0,52% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Sagar (1991) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 0 | 0% |
| Thiebot et al. (2011) | 3 | 0,52% | 3 | 1,08% | 3 | 1,43% | 3 | 1,27% |
| Tremblay & Cherel (2005) | 3 | 0,52% | 3 | 1,08% | 0 | 0% | 3 | 1,27% |
| Villard et al. (2006) | 3 | 0,52% | 3 | 1,08% | 2 | 0,95% | 1 | 0,42% |
| Beaubrun (2004) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Birdlife International (2013) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Blumenbach (1810) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boddaert & Daubenton (1783) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Bourne (1959) | 2 | 0,35% | 2 | 0,72% | 0 | 0% | 2 | 0,84% |
| Bouteiller & Borsa (2022) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 1 | 0,42% |
| Bretagnolle & Attie (1991) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Brodier et al. (2011) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Cabanis (1875) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Chappuis et al. (1974) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Cherel et al. (2014) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Cherel et al. (2022) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Collinson et al. (2017) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Condamin (1979) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| dal Molin (2009) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Davant (1967) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois (2006) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Flood et al. (2021) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Forster (1844) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frugone et al. (2021) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Gomez & Voisin (2002) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Gourreau et al. (1998) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Grosser et al. (2021) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Guiguen et al. (1984) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 1 | 0,42% |
| Hall (1900) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Hervé & François (1995) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jardine & Selby (1826-1835) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuhl (1820) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lepechin (1769) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesage et al. (2024) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Lescroel et al. (2004) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Lesson (1831) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Lichtenstein (1823) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louette & Cousin (1999) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Mays et al. (2006) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Pallas (1773) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1831) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Palma & Tennyson (2005) | 2 | 0,35% | 2 | 0,72% | 0 | 0% | 2 | 0,84% |
| Pezy et al. (2022) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Raust & Sanford (2007) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Ridoux (1989) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Ringler et al. (2015) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Roux et al. (1983) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sabine (1819) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salvin (1888) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Salvin (1896) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Searby & Jouventin (2005) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Shirihai et al. (2017) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stahl et al. (1985) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Steadman (2002) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 2 | 0,84% |
| Tatin et al. (2003) | 2 | 0,35% | 2 | 0,72% | 0 | 0% | 2 | 0,84% |
| Temminck et al. (1838) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Temminck (1818-1838) | 2 | 0,35% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Tennyson et al. (2022) | 2 | 0,35% | 2 | 0,72% | 0 | 0% | 2 | 0,84% |
| Tremblay & Cherel (2003) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Trotignon et al. (1994) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Voisin (1971) | 2 | 0,35% | 2 | 0,72% | 0 | 0% | 2 | 0,84% |
| Waugh & Weimerskirch (2003) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weimerskirch et al. (2009) | 2 | 0,35% | 2 | 0,72% | 2 | 0,95% | 0 | 0% |
| Zilli (2021) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Acerbi (1827) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Anonyme. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Attié et al. (1997) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Austin et al. (2004) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Baling et al. (2009) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barré & Géraux (2004) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Barre et al. (1977) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Bartoli & Prévot (1986) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartoli (1972) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson et al. (1975) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Benson (1967) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Bertrand (1982) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Birdlife International (2013) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Blyth (1860) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boie (1835) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1857) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boschert & Dronneau (1998) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Bougeard (2007) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourne (2008) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brandt (1837) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brandt (1838) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brème (1839) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bretagnolle et al. (2000) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Bruch (1832) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Brünnich (1764) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carte (1866) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Champeau et al. (2011) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Chastel et al. (1987) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Cheke & Hume (2008) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Cherel & Boxshall (2004) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Cibois et al. (2015) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Claessens et al. (2014) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clements et al. (2017) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Commecy et al. (2013) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Corre & Jouventin (1997) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Cory (1881) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coues (1862) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Danel et al. (2023) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| 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 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Daudin (1802) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Deblock (1966) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Debout & Desmares (1996) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Debout (1992) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Debout (2017) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Deflorenne et al. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Delord et al. (2011) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Demay et al. (2014) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Deniau & Provost (2020) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Ducatez & Devore (2023) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Dufour & Veyrunes (2019) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Ebels (2001) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Efe et al. (2009) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Elkins & Yesou (1998) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fain & Beaucournu (1984) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Falla (1933) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Finsch (1876) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Flitti & Rocha (2014) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Flood et al. (2017) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Gallien (2011) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Gangloff et al. (2009) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| GARNOT (1826) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gauthier-clerc & Lambert (2002) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Genevois (1991) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Gernigon & Lacaze (2009) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Gernigon (2008) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giglioli & Salvadori (1868) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Golvan (1956) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1838) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Gould (1842) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Gould (1844) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guermeur (1987) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gunnerus (1767) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Harcourt (1851) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harrison (1981) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Heller & Snodgrass (1901) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hombron & Jacquinot (1841) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Homeyer (1853) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglesias-vasquez et al. (2017) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Jaeger et al. (2018) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Jornvall et al. (2006) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Bulweria baraui. Bulletin du Muséum National d'Histoire Naturelle, 35(6): 593-597.">Jouanin (1964) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouventin & Roux (1984) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouventin (1994) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| King (1828) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Lacan & Mougin (1974) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1787) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Corre (1996) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Leblond (2003) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Legros & Puissauve (2015) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Leopold (1965) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Lescroel & Bost (2006) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Lesson (1825) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Lesson (1839) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Lethuillier (1999) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Levesque & Yesou (2018) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Lorvelec et al. (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Lorvelec et al. (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Louette & Herremans (1985) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Lowe (1920) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macgillivray (1824) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Magaud & D'aubusson (1906) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Marion (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Martinet et al. (1765) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathews & Iredale (1921) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathews & Serventy (1941) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Mathews (1912) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathews (1913) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Mey (2010) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Milne-edwards (1882) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Miskelly (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Montagu (1813) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Mougin (1984) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Murphy & Harper (1916) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Murphy (1929) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murphy (1949) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Naumann (1819) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naumann (1840) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Nuttall (1834) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Olson & Warheit (1988) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| O'reilly (1818) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| pallas (1764) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1776) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Payraudeau (1826) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peale (1848) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearson & Prévot (1971) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Peters (1930) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Petit (1976) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Phipps (1774) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pinaud et al. (2005) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Plestan et al. (2009) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Portelli (2016) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Prevost (1970) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Prevot (1971) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Ramírez et al. (2013) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Reeber et al. (1996) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ridgway (1893) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Riethmuller et al. (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Robertson (2002) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Roques (1991) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rothschild (1902) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Rotschikd (1903) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rotschild (1893) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Russell et al. (2015) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Salvadori (1899) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sanchez et al. (2004) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Schlegel (1863) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schramm et al. (2014) | 1 | 0,17% | 1 | 0,36% | 0 | 0% | 1 | 0,42% |
| Scopoli (1769) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1786) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siorat & Rocamora (1995) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Siorat et al. (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Siorat et al. (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Smith (1849) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stahl & Weimerskirch (1982) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Steadman & Bollt (2010) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Streets (1877) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Temminck et al. ([1820-1840]) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Texier (1914) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Thibault & Cibois (2017) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiebot et al. (2011) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiebot et al. (2015) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Tostain (1980) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Townsend (1890) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Uicn et al. (2014) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vanderwerf et al. (2004) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1817) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1819) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Vincent (1990) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Wang & Liu (2016) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Warham et al. (1977) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Watson et al. (1975) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Weimerskirch & Jouventin (1998) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Weimerskirch et al. (2018) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Wetmore (1939) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yesou & Thebault (2012) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Yésou (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Yésou (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Yésou (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Yésou (2003) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yésou (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Yésou (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 1 | 0,42% |
| Yésou (2003) | 1 | 0,17% | 1 | 0,36% | 1 | 0,48% | 0 | 0% |
| Yésou (2003) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yeung et al. (2009) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
