Oiseaux marins des îles subantarctiques
165 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) | 105 | 51,98% | 99 | 110% | 97 | 122,78% | 85 | 106,25% |
Uicn et al. (2015) | 16 | 7,92% | 14 | 15,56% | 14 | 17,72% | 13 | 16,25% |
Uicn et al. (2017) | 16 | 7,92% | 16 | 17,78% | 16 | 20,25% | 15 | 18,75% |
UICN Comité français, OFB & MNHN (2021) | 14 | 6,93% | 14 | 15,56% | 14 | 17,72% | 14 | 17,5% |
Ausilio & Zotier (1989) | 13 | 6,44% | 12 | 13,33% | 12 | 15,19% | 11 | 13,75% |
Barau et al. (2005) | 12 | 5,94% | 10 | 11,11% | 10 | 12,66% | 10 | 12,5% |
Levesque & Delcroix (2018) | 12 | 5,94% | 12 | 13,33% | 12 | 15,19% | 12 | 15% |
Chastel & Beaucournu (1992) | 10 | 4,95% | 10 | 11,11% | 10 | 12,66% | 8 | 10% |
Remsen et al. (2013) | 9 | 4,46% | 8 | 8,89% | 8 | 10,13% | 8 | 10% |
Linnaeus (1758) | 7 | 3,47% | 2 | 2,22% | 2 | 2,53% | 1 | 1,25% |
Belfan & Conde (2016) | 6 | 2,97% | 6 | 6,67% | 6 | 7,59% | 6 | 7,5% |
Tostain et al. (2013) | 6 | 2,97% | 6 | 6,67% | 6 | 7,59% | 5 | 6,25% |
Banks et al. (2006) | 5 | 2,48% | 4 | 4,44% | 4 | 5,06% | 1 | 1,25% |
Etcheberry & Abraham (2009) | 5 | 2,48% | 5 | 5,56% | 5 | 6,33% | 5 | 6,25% |
Gmelin (1789) | 5 | 2,48% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Questel & Le Quellec (2012) | 5 | 2,48% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Questel (2020) | 5 | 2,48% | 5 | 5,56% | 5 | 6,33% | 5 | 6,25% |
Rocamora (2004) | 5 | 2,48% | 5 | 5,56% | 5 | 6,33% | 5 | 6,25% |
Yokoyama (2013) | 5 | 2,48% | 5 | 5,56% | 5 | 6,33% | 5 | 6,25% |
Barbraud et al. (2009) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Barre et al. (2009) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 3 | 3,75% |
Bost et al. (2022) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 2 | 2,5% |
Deblock et al. (1960) | 4 | 1,98% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Del Hoyo & Collar (2014) | 4 | 1,98% | 1 | 1,11% | 0 | 0% | 1 | 1,25% |
Delord et al. (2005) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Delord et al. (2008) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Forster (1781) | 4 | 1,98% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1995) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Isenmann et al. (1971) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Jaeger et al. (2020) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Kojadinovic et al. (2007) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Potin (2013) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 4 | 5% |
Probst (1997) | 4 | 1,98% | 4 | 4,44% | 4 | 5,06% | 3 | 3,75% |
Safford & Hawkins (2013) | 4 | 1,98% | 4 | 4,44% | 3 | 3,8% | 4 | 5% |
Abeyrama et al. (2021) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 3 | 3,75% |
Barbraud et al. (2021) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 3 | 3,75% |
Carravieri et al. (2016) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 3 | 3,75% |
Clements et al. (2015) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 2 | 2,5% |
Clements (2012) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 2 | 2,5% |
Dewynter (2021) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 3 | 3,75% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 1,49% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2013) | 3 | 1,49% | 2 | 2,22% | 2 | 2,53% | 1 | 1,25% |
Jouventin et al. (1989) | 3 | 1,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescroel et al. (2009) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 3 | 3,75% |
Ponchon et al. (2021) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 3 | 3,75% |
Sagar (1991) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 0 | 0% |
Thiebot et al. (2011) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 3 | 3,75% |
Tremblay & Cherel (2005) | 3 | 1,49% | 3 | 3,33% | 0 | 0% | 3 | 3,75% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 2 | 2,5% |
Weimerskirch et al. (2009) | 3 | 1,49% | 3 | 3,33% | 3 | 3,8% | 3 | 3,75% |
Birdlife International (2013) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Bretagnolle & Attie (1991) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Brodier et al. (2011) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Cabanis (1875) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 0 | 0% |
Cherel et al. (2014) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 0 | 0% |
Cherel et al. (2022) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Dickinson & Remsen (2013) | 2 | 0,99% | 2 | 2,22% | 1 | 1,27% | 2 | 2,5% |
Frugone et al. (2021) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 0 | 0% |
Gomez & Voisin (2002) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 0 | 0% |
Gould (1844) | 2 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Grosser et al. (2021) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 0 | 0% |
Hall (1900) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 0 | 0% |
Humeau et al. (2020) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Jiguet (2002) | 2 | 0,99% | 2 | 2,22% | 0 | 0% | 2 | 2,5% |
Kuhl (1820) | 2 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesage et al. (2024) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Lescroel et al. (2004) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Mathews (1912) | 2 | 0,99% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Mays et al. (2006) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Pontoppidan (1763) | 2 | 0,99% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Raust & Sanford (2007) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Ridoux (1989) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Roux et al. (1983) | 2 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Sabine (1819) | 2 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvin (1896) | 2 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Searby & Jouventin (2005) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 0 | 0% |
Stahl et al. (1985) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Temminck et al. (1838) | 2 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Tennyson et al. (2022) | 2 | 0,99% | 2 | 2,22% | 0 | 0% | 2 | 2,5% |
Thibault et al. (2014) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 2 | 2,5% |
Tostain & Dujardin (1988) | 2 | 0,99% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Tremblay & Cherel (2003) | 2 | 0,99% | 2 | 2,22% | 2 | 2,53% | 0 | 0% |
Voisin (1971) | 2 | 0,99% | 2 | 2,22% | 0 | 0% | 2 | 2,5% |
Waugh & Weimerskirch (2003) | 2 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Barre et al. (1977) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Bénito-espinal (1990) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Bertrand (1982) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Blyth (1860) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Boie (1835) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouteiller & Borsa (2022) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Brandt (1837) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Cherel & Boxshall (2004) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 0 | 0% |
Cibois et al. (2015) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Collier et al. (2002) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Commission de l’Avifaune Française (2016) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 0 | 0% |
Condamin (1979) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Danel et al. (2023) | 1 | 0,5% | 1 | 1,11% | 0 | 0% | 1 | 1,25% |
Daudin (1802) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Delord et al. (2011) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Demay et al. (2014) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Dollfus (1966) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois et al. (2008) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Ducatez & Devore (2023) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Ebels (2001) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Elkins & Yesou (1998) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Fain & Beaucournu (1984) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Falla (1933) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Finsch (1876) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
GARNOT (1826) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Gauthier-clerc & Lambert (2002) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Genevois (1991) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Gould (1838) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 0 | 0% |
Guiguen et al. (1984) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Harrison (1981) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Hombron & Jacquinot (1841) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Impact-mer (2011) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Ingels et al. (2003) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Jaeger et al. (2018) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Bulweria baraui. Bulletin du Muséum National d'Histoire Naturelle, 35(6): 593-597.">Jouanin (1964) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin & Roux (1984) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin (1994) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Le Corre & Jouventin (1999) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Lescroel & Bost (2006) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Lesson (1825) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Linnaeus (1766) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews & Iredale (1921) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews (1912) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Medway (2009) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Mey (2010) | 1 | 0,5% | 1 | 1,11% | 0 | 0% | 1 | 1,25% |
Miskelly (2012) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Morrison (2006) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Mougin (1984) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Murphy & Harper (1916) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Murphy (1929) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Naumann (1819) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Naurois (1978) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
O'reilly (1818) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
pallas (1764) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinaud et al. (2005) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Prevost (1970) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Robertson (2002) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Rotschikd (1903) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Rotschild (1893) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell et al. (2015) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Schramm et al. (2014) | 1 | 0,5% | 1 | 1,11% | 0 | 0% | 1 | 1,25% |
Scopoli (1769) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1849) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Stahl & Weimerskirch (1982) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 0 | 0% |
Steadman & Bollt (2010) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Thiebot et al. (2011) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiebot et al. (2015) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Uicn et al. (2020) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Vanderwerf et al. (2006) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Vieillot (1819) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Wang & Liu (2016) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Watson et al. (1975) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Weimerskirch & Jouventin (1998) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |
Weimerskirch et al. (2018) | 1 | 0,5% | 1 | 1,11% | 1 | 1,27% | 1 | 1,25% |