Oiseaux marins de Guyane
162 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Uicn et al. (2017) | 90 | 37,5% | 84 | 82,35% | 73 | 82,95% | 72 | 80% |
| Levesque & Delcroix (2018) | 67 | 27,92% | 65 | 63,73% | 58 | 65,91% | 61 | 67,78% |
| UICN Comité français, OFB & MNHN (2021) | 57 | 23,75% | 57 | 55,88% | 57 | 64,77% | 45 | 50% |
| Remsen et al. (2013) | 50 | 20,83% | 46 | 45,1% | 46 | 52,27% | 36 | 40% |
| Yokoyama (2013) | 41 | 17,08% | 38 | 37,25% | 37 | 42,05% | 29 | 32,22% |
| Questel & Le Quellec (2012) | 37 | 15,42% | 36 | 35,29% | 33 | 37,5% | 29 | 32,22% |
| Questel (2020) | 36 | 15% | 33 | 32,35% | 28 | 31,82% | 28 | 31,11% |
| Uicn et al. (2015) | 31 | 12,92% | 29 | 28,43% | 29 | 32,95% | 26 | 28,89% |
| Belfan & Conde (2016) | 29 | 12,08% | 26 | 25,49% | 25 | 28,41% | 23 | 25,56% |
| Etcheberry & Abraham (2009) | 28 | 11,67% | 24 | 23,53% | 24 | 27,27% | 22 | 24,44% |
| Clements (2012) | 24 | 10% | 23 | 22,55% | 21 | 23,86% | 21 | 23,33% |
| Linnaeus (1758) | 23 | 9,58% | 8 | 7,84% | 8 | 9,09% | 5 | 5,56% |
| Tostain et al. (2013) | 21 | 8,75% | 19 | 18,63% | 19 | 21,59% | 17 | 18,89% |
| Dewynter (2021) | 19 | 7,92% | 19 | 18,63% | 19 | 21,59% | 16 | 17,78% |
| Dickinson & Remsen (2013) | 15 | 6,25% | 12 | 11,76% | 9 | 10,23% | 10 | 11,11% |
| Uicn et al. (2015) | 14 | 5,83% | 12 | 11,76% | 12 | 13,64% | 11 | 12,22% |
| Uicn et al. (2020) | 12 | 5% | 12 | 11,76% | 12 | 13,64% | 9 | 10% |
| Barau et al. (2005) | 11 | 4,58% | 9 | 8,82% | 9 | 10,23% | 8 | 8,89% |
| Deblock et al. (1960) | 10 | 4,17% | 4 | 3,92% | 4 | 4,55% | 3 | 3,33% |
| Weimerskirch et al. (2009) | 9 | 3,75% | 8 | 7,84% | 8 | 9,09% | 6 | 6,67% |
| Linnaeus (1766) | 7 | 2,92% | 2 | 1,96% | 1 | 1,14% | 1 | 1,11% |
| Clements et al. (2015) | 6 | 2,5% | 6 | 5,88% | 1 | 1,14% | 6 | 6,67% |
| Del Hoyo & Collar (2014) | 6 | 2,5% | 4 | 3,92% | 4 | 4,55% | 4 | 4,44% |
| Gill (1995) | 6 | 2,5% | 6 | 5,88% | 6 | 6,82% | 5 | 5,56% |
| Rocamora (2004) | 6 | 2,5% | 6 | 5,88% | 6 | 6,82% | 5 | 5,56% |
| Thibault et al. (2014) | 5 | 2,08% | 5 | 4,9% | 5 | 5,68% | 4 | 4,44% |
| UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 5 | 2,08% | 5 | 4,9% | 5 | 5,68% | 5 | 5,56% |
| Furminieux (2019) | 4 | 1,67% | 4 | 3,92% | 4 | 4,55% | 3 | 3,33% |
| Gmelin (1789) | 4 | 1,67% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tostain & Dujardin (1988) | 4 | 1,67% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Vieillot (1819) | 4 | 1,67% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ausilio & Zotier (1989) | 3 | 1,25% | 3 | 2,94% | 3 | 3,41% | 2 | 2,22% |
| Bartoli (1972) | 3 | 1,25% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Collier et al. (2002) | 3 | 1,25% | 3 | 2,94% | 2 | 2,27% | 2 | 2,22% |
| Commission de l’Avifaune Française (2016) | 3 | 1,25% | 3 | 2,94% | 3 | 3,41% | 2 | 2,22% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 1,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Karadjian et al. (2022) | 3 | 1,25% | 3 | 2,94% | 3 | 3,41% | 2 | 2,22% |
| Pontoppidan (1763) | 3 | 1,25% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Safford & Hawkins (2013) | 3 | 1,25% | 3 | 2,94% | 3 | 3,41% | 3 | 3,33% |
| Tostain (1980) | 3 | 1,25% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Bénito-espinal (1990) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Boddaert & Daubenton (1783) | 2 | 0,83% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| dal Molin (2009) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Davant (1967) | 2 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gibson & Baker (2012) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Gourreau et al. (1998) | 2 | 0,83% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Ingels et al. (2003) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Jardine & Selby (1826-1835) | 2 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lee & Walsh-McGehee (2000) | 2 | 0,83% | 2 | 1,96% | 0 | 0% | 2 | 2,22% |
| Lepechin (1769) | 2 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levesque & Delcroix (2013) | 2 | 0,83% | 2 | 1,96% | 0 | 0% | 2 | 2,22% |
| Levesque & Delcroix (2016) | 2 | 0,83% | 1 | 0,98% | 0 | 0% | 1 | 1,11% |
| Lorvelec et al. (2004) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Mathews (1914) | 2 | 0,83% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Mays et al. (2006) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Pezy et al. (2022) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Pons et al. (2005) | 2 | 0,83% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Sabine (1819) | 2 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vanderwerf et al. (2006) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 2 | 2,22% |
| Weimerskirch et al. (2009) | 2 | 0,83% | 2 | 1,96% | 2 | 2,27% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Anonyme. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Attié et al. (1997) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Barre et al. (2009) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Beaufils (1999) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Bertrand (1982) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Birdlife International (2016) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Boie (1835) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boschert & Dronneau (1998) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Brünnich (1764) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chastel et al. (1987) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Cheke & Hume (2008) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Claessens et al. (2014) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clergeau & Pascal (2003) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Coues (1861) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coues (1862) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Crouzier (2009) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| 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 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Deblock (1966) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Deflorenne et al. (2012) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Deniau & Provost (2020) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Dollfus (1966) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ducatez & Devore (2023) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Efe et al. (2009) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Elkins & Yesou (1998) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flitti & Rocha (2014) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Flood et al. (2017) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Gallien (2011) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Gauthier-clerc & Lambert (2002) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Gernigon (2008) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Golvan (1956) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1838) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Guiguen et al. (1984) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Guth (1971) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Harcourt (1851) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Homeyer (1853) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Impact-mer (2011) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Isenmann et al. (1971) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| IUCN (2014) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Jouventin (1994) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Kuhl (1820) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1787) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesage et al. (2024) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Lesson (1831) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Lesson (1839) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Lorvelec & Vigne (2003) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louette & Cousin (1999) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Loury & Puissauve (2016) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Martinet et al. (1765) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montagu (1813) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Morrison (2006) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Naumann (1819) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| O'reilly (1818) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| pallas (1764) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1776) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearson & Prévot (1971) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Peters (1930) | 1 | 0,42% | 1 | 0,98% | 0 | 0% | 1 | 1,11% |
| Pinaud et al. (2005) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Prevot (1971) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Probst (1997) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Ramírez et al. (2013) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Reeber et al. (1996) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeber (2015) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Roques (1991) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salvadori (1899) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sanchez et al. (2004) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Scopoli (1769) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1786) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vanderwerf et al. (2004) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1817) | 1 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1819) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Weimerskirch & Jouventin (1998) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Yésou (2003) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 0 | 0% |
| Yésou (2003) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Yésou (2003) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Yésou (2003) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
| Yésou (2003) | 1 | 0,42% | 1 | 0,98% | 1 | 1,14% | 1 | 1,11% |
