Oiseaux marins de Nouvelle-Calédonie
128 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) | 53 | 26,37% | 51 | 54,26% | 50 | 66,67% | 38 | 50,67% |
| UICN Comité français, OFB & MNHN (2021) | 22 | 10,95% | 22 | 23,4% | 22 | 29,33% | 15 | 20% |
| Uicn et al. (2017) | 22 | 10,95% | 21 | 22,34% | 21 | 28% | 14 | 18,67% |
| Uicn et al. (2015) | 20 | 9,95% | 18 | 19,15% | 18 | 24% | 18 | 24% |
| Barau et al. (2005) | 18 | 8,96% | 14 | 14,89% | 14 | 18,67% | 10 | 13,33% |
| Levesque & Delcroix (2018) | 18 | 8,96% | 18 | 19,15% | 18 | 24% | 12 | 16% |
| Remsen et al. (2013) | 17 | 8,46% | 16 | 17,02% | 16 | 21,33% | 11 | 14,67% |
| Gill (1995) | 14 | 6,97% | 13 | 13,83% | 13 | 17,33% | 7 | 9,33% |
| Rocamora (2004) | 13 | 6,47% | 12 | 12,77% | 11 | 14,67% | 9 | 12% |
| Weimerskirch et al. (2009) | 13 | 6,47% | 12 | 12,77% | 12 | 16% | 5 | 6,67% |
| Yokoyama (2013) | 13 | 6,47% | 13 | 13,83% | 13 | 17,33% | 6 | 8% |
| Questel & Le Quellec (2012) | 11 | 5,47% | 11 | 11,7% | 11 | 14,67% | 4 | 5,33% |
| Thibault et al. (2014) | 11 | 5,47% | 11 | 11,7% | 11 | 14,67% | 6 | 8% |
| Clements (2012) | 10 | 4,98% | 10 | 10,64% | 9 | 12% | 8 | 10,67% |
| Linnaeus (1758) | 10 | 4,98% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Belfan & Conde (2016) | 9 | 4,48% | 8 | 8,51% | 8 | 10,67% | 7 | 9,33% |
| Gmelin (1789) | 9 | 4,48% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Barre et al. (2009) | 8 | 3,98% | 8 | 8,51% | 8 | 10,67% | 7 | 9,33% |
| Etcheberry & Abraham (2009) | 8 | 3,98% | 8 | 8,51% | 8 | 10,67% | 8 | 10,67% |
| Questel (2020) | 8 | 3,98% | 8 | 8,51% | 8 | 10,67% | 7 | 9,33% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 7 | 3,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Safford & Hawkins (2013) | 6 | 2,99% | 6 | 6,38% | 5 | 6,67% | 3 | 4% |
| Deblock et al. (1960) | 5 | 2,49% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Dewynter (2021) | 5 | 2,49% | 5 | 5,32% | 5 | 6,67% | 5 | 6,67% |
| Delord et al. (2008) | 4 | 1,99% | 4 | 4,26% | 4 | 5,33% | 4 | 5,33% |
| Probst (1997) | 4 | 1,99% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Tostain et al. (2013) | 4 | 1,99% | 4 | 4,26% | 4 | 5,33% | 2 | 2,67% |
| Ausilio & Zotier (1989) | 3 | 1,49% | 3 | 3,19% | 3 | 4% | 3 | 4% |
| Bretagnolle et al. (2021) | 3 | 1,49% | 3 | 3,19% | 0 | 0% | 3 | 4% |
| Bretagnolle et al. (2022) | 3 | 1,49% | 3 | 3,19% | 3 | 4% | 3 | 4% |
| Dickinson & Remsen (2013) | 3 | 1,49% | 3 | 3,19% | 2 | 2,67% | 3 | 4% |
| IUCN (2013) | 3 | 1,49% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Naurois (1978) | 3 | 1,49% | 3 | 3,19% | 1 | 1,33% | 3 | 4% |
| Vanderwerf et al. (2006) | 3 | 1,49% | 3 | 3,19% | 3 | 4% | 0 | 0% |
| Barbraud et al. (2009) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Bouteiller & Borsa (2022) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 1 | 1,33% |
| Collier et al. (2002) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 1 | 1,33% |
| Collinson et al. (2017) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 0 | 0% |
| Commission de l’Avifaune Française (2016) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 0 | 0% |
| Condamin (1979) | 2 | 1% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Del Hoyo & Collar (2014) | 2 | 1% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Delord et al. (2005) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Forster (1844) | 2 | 1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1844) | 2 | 1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Humeau et al. (2020) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Isenmann et al. (1971) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Kojadinovic et al. (2007) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Lichtenstein (1823) | 2 | 1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 2 | 1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathews (1912) | 2 | 1% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| pallas (1764) | 2 | 1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Palma & Tennyson (2005) | 2 | 1% | 2 | 2,13% | 0 | 0% | 2 | 2,67% |
| Potin (2013) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Raust & Sanford (2007) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Ringler et al. (2015) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Salvin (1888) | 2 | 1% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Temminck et al. (1838) | 2 | 1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Temminck (1818-1838) | 2 | 1% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Tostain & Dujardin (1988) | 2 | 1% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Trotignon et al. (1994) | 2 | 1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2020) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 2 | 2,67% |
| Villard et al. (2006) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 0 | 0% |
| Weimerskirch et al. (2009) | 2 | 1% | 2 | 2,13% | 2 | 2,67% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Anonyme. (2012) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Barré & Géraux (2004) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Bénito-espinal (1990) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Bertrand (1982) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2013) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Birdlife International (2016) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Boddaert & Daubenton (1783) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Bougeard & Siblet (2000) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Bourne (2008) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cheke & Hume (2008) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Cibois et al. (2015) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Daudin (1802) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Debout & Desmares (1996) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Debout (2017) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Demay et al. (2014) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Deniau & Provost (2020) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Dubois et al. (2008) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Ducatez & Devore (2023) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Ehrhardt (1971) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flitti & Rocha (2014) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Flood et al. (2021) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Gallien (2011) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Genevois (1991) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Giglioli & Salvadori (1868) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1838) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Gould (1844) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harcourt (1851) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harrison (1981) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Iglesias-vasquez et al. (2017) | 1 | 0,5% | 1 | 1,06% | 0 | 0% | 1 | 1,33% |
| Impact-mer (2011) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Ingels et al. (2003) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Kuhl (1820) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Corre & Jouventin (1999) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Legros & Puissauve (2015) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Leopold (1965) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Lesson (1825) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Lesson (1831) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Lesson (1839) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Marion (2003) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Mathews & Serventy (1941) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Medway (2009) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Montagu (1813) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Morrison (2006) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Pallas (1831) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peale (1848) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pontoppidan (1763) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Portelli (2016) | 1 | 0,5% | 1 | 1,06% | 0 | 0% | 1 | 1,33% |
| Reeber (2015) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Rotschild (1893) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1786) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steadman & Bollt (2010) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Tostain (1980) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 0 | 0% |
| Wang & Liu (2016) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Warham et al. (1977) | 1 | 0,5% | 1 | 1,06% | 1 | 1,33% | 1 | 1,33% |
| Wetmore (1939) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yeung et al. (2009) | 1 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
