Oiseaux marins de Guadeloupe
170 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) | 88 | 34,38% | 84 | 74,34% | 74 | 75,51% | 82 | 82% |
Uicn et al. (2017) | 76 | 29,69% | 73 | 64,6% | 66 | 67,35% | 63 | 63% |
UICN Comité français, OFB & MNHN (2021) | 65 | 25,39% | 65 | 57,52% | 65 | 66,33% | 54 | 54% |
Remsen et al. (2013) | 47 | 18,36% | 44 | 38,94% | 44 | 44,9% | 35 | 35% |
Yokoyama (2013) | 47 | 18,36% | 43 | 38,05% | 42 | 42,86% | 35 | 35% |
Belfan & Conde (2016) | 41 | 16,02% | 38 | 33,63% | 33 | 33,67% | 36 | 36% |
Questel & Le Quellec (2012) | 40 | 15,62% | 38 | 33,63% | 34 | 34,69% | 33 | 33% |
Questel (2020) | 40 | 15,62% | 37 | 32,74% | 31 | 31,63% | 35 | 35% |
Etcheberry & Abraham (2009) | 35 | 13,67% | 31 | 27,43% | 31 | 31,63% | 28 | 28% |
Uicn et al. (2015) | 30 | 11,72% | 28 | 24,78% | 28 | 28,57% | 23 | 23% |
Linnaeus (1758) | 27 | 10,55% | 7 | 6,19% | 7 | 7,14% | 5 | 5% |
Clements (2012) | 21 | 8,2% | 21 | 18,58% | 19 | 19,39% | 15 | 15% |
Dewynter (2021) | 19 | 7,42% | 19 | 16,81% | 19 | 19,39% | 17 | 17% |
Tostain et al. (2013) | 17 | 6,64% | 15 | 13,27% | 15 | 15,31% | 14 | 14% |
Uicn et al. (2015) | 13 | 5,08% | 11 | 9,73% | 11 | 11,22% | 10 | 10% |
Barau et al. (2005) | 12 | 4,69% | 10 | 8,85% | 10 | 10,2% | 8 | 8% |
Uicn et al. (2020) | 12 | 4,69% | 12 | 10,62% | 12 | 12,24% | 10 | 10% |
Dickinson & Remsen (2013) | 11 | 4,3% | 10 | 8,85% | 7 | 7,14% | 8 | 8% |
Weimerskirch et al. (2009) | 11 | 4,3% | 10 | 8,85% | 10 | 10,2% | 8 | 8% |
Deblock et al. (1960) | 10 | 3,91% | 4 | 3,54% | 4 | 4,08% | 3 | 3% |
Gill (1995) | 8 | 3,12% | 8 | 7,08% | 8 | 8,16% | 5 | 5% |
Rocamora (2004) | 8 | 3,12% | 8 | 7,08% | 8 | 8,16% | 6 | 6% |
Linnaeus (1766) | 7 | 2,73% | 2 | 1,77% | 1 | 1,02% | 1 | 1% |
Thibault et al. (2014) | 7 | 2,73% | 7 | 6,19% | 7 | 7,14% | 4 | 4% |
Clements et al. (2015) | 6 | 2,34% | 6 | 5,31% | 1 | 1,02% | 6 | 6% |
Del Hoyo & Collar (2014) | 6 | 2,34% | 4 | 3,54% | 3 | 3,06% | 4 | 4% |
Gmelin (1789) | 6 | 2,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Lee & Walsh-McGehee (2000) | 5 | 1,95% | 5 | 4,42% | 0 | 0% | 5 | 5% |
Collier et al. (2002) | 4 | 1,56% | 4 | 3,54% | 3 | 3,06% | 2 | 2% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 4 | 1,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Tostain & Dujardin (1988) | 4 | 1,56% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 4 | 1,56% | 4 | 3,54% | 4 | 4,08% | 4 | 4% |
Vieillot (1819) | 4 | 1,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Ausilio & Zotier (1989) | 3 | 1,17% | 3 | 2,65% | 3 | 3,06% | 2 | 2% |
Bartoli (1972) | 3 | 1,17% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Bénito-espinal (1990) | 3 | 1,17% | 3 | 2,65% | 2 | 2,04% | 3 | 3% |
Furminieux (2019) | 3 | 1,17% | 3 | 2,65% | 3 | 3,06% | 3 | 3% |
Karadjian et al. (2022) | 3 | 1,17% | 3 | 2,65% | 3 | 3,06% | 3 | 3% |
Levesque & Delcroix (2013) | 3 | 1,17% | 3 | 2,65% | 0 | 0% | 3 | 3% |
Levesque & Delcroix (2016) | 3 | 1,17% | 2 | 1,77% | 0 | 0% | 2 | 2% |
Pontoppidan (1763) | 3 | 1,17% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Safford & Hawkins (2013) | 3 | 1,17% | 3 | 2,65% | 3 | 3,06% | 3 | 3% |
Tostain (1980) | 3 | 1,17% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Boddaert & Daubenton (1783) | 2 | 0,78% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Commission de l’Avifaune Française (2016) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 1 | 1% |
dal Molin (2009) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Davant (1967) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibson & Baker (2012) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Gourreau et al. (1998) | 2 | 0,78% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Humeau et al. (2020) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 0 | 0% |
Ingels et al. (2003) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Jardine & Selby (1826-1835) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Kojadinovic et al. (2007) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 0 | 0% |
Lepechin (1769) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1831) | 2 | 0,78% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Lorvelec et al. (2004) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Mathews (1914) | 2 | 0,78% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Mays et al. (2006) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Pezy et al. (2022) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Pons et al. (2005) | 2 | 0,78% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Vanderwerf et al. (2006) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Vieillot (1819) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 2 | 2% |
Weimerskirch et al. (2009) | 2 | 0,78% | 2 | 1,77% | 2 | 2,04% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Anonyme. (2012) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Attié et al. (1997) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Baird (1865) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Barre et al. (2009) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Beaufils (1999) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Bertrand (1982) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Birdlife International (2016) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Boie (1835) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Boschert & Dronneau (1998) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Bougeard & Siblet (2000) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Brandt (1838) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünnich (1764) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Carte (1866) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Chastel et al. (1987) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Cheke & Hume (2008) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
CHN (2017) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Clergeau & Pascal (2003) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Coues (1861) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1862) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Crouzier (2009) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
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 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Daudin (1802) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Deblock (1966) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Deflorenne et al. (2012) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Deniau & Provost (2020) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Dollfus (1966) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois et al. (2008) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Ducatez & Devore (2023) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Efe et al. (2009) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Gallien (2011) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Gauthier-clerc & Lambert (2002) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Gernigon (2008) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Giglioli & Salvadori (1868) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Golvan (1956) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Guermeur (1987) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiguen et al. (1984) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Guth (1971) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Impact-mer (2011) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Isenmann et al. (1971) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
IUCN (2014) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Johnson (1973) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin (1994) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Kuhl (1820) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1787) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Jouventin (1999) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Lesage et al. (2024) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Lesson (1839) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Levesque & Yesou (2018) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Lorvelec & Vigne (2003) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Louette & Cousin (1999) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Loury & Puissauve (2016) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Martinet et al. (1765) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1813) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Morrison (2006) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Naumann (1819) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Nuttall (1834) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
O'reilly (1818) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
pallas (1764) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1769) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearson & Prévot (1971) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Peters (1930) | 1 | 0,39% | 1 | 0,88% | 0 | 0% | 1 | 1% |
Pinaud et al. (2005) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Pinchon (1976) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Prevot (1971) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Probst (1997) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Reeber (2015) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Roques (1991) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez et al. (2004) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Scopoli (1769) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Siorat & Rocamora (1995) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Siorat et al. (2003) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Steadman & Bollt (2010) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Vanderwerf et al. (2004) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 0 | 0% |
Weimerskirch & Jouventin (1998) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Yésou (2003) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Yésou (2003) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Yésou (2003) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |
Yésou (2003) | 1 | 0,39% | 1 | 0,88% | 1 | 1,02% | 1 | 1% |