Oiseaux marins de Clipperton
52 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Weimerskirch et al. (2009) | 17 | 42,5% | 15 | 78,95% | 14 | 82,35% | 14 | 77,78% |
| Uicn et al. (2015) | 14 | 35% | 14 | 73,68% | 14 | 82,35% | 13 | 72,22% |
| UICN Comité français, OFB & MNHN (2021) | 10 | 25% | 10 | 52,63% | 10 | 58,82% | 9 | 50% |
| Uicn et al. (2017) | 9 | 22,5% | 9 | 47,37% | 9 | 52,94% | 8 | 44,44% |
| Gill (1995) | 8 | 20% | 8 | 42,11% | 8 | 47,06% | 7 | 38,89% |
| Questel & Le Quellec (2012) | 8 | 20% | 8 | 42,11% | 8 | 47,06% | 7 | 38,89% |
| Yokoyama (2013) | 8 | 20% | 8 | 42,11% | 8 | 47,06% | 7 | 38,89% |
| Levesque & Delcroix (2018) | 7 | 17,5% | 7 | 36,84% | 7 | 41,18% | 6 | 33,33% |
| Remsen et al. (2013) | 7 | 17,5% | 7 | 36,84% | 7 | 41,18% | 6 | 33,33% |
| Barau et al. (2005) | 6 | 15% | 4 | 21,05% | 4 | 23,53% | 4 | 22,22% |
| Thibault et al. (2014) | 6 | 15% | 6 | 31,58% | 6 | 35,29% | 5 | 27,78% |
| Rocamora (2004) | 5 | 12,5% | 5 | 26,32% | 5 | 29,41% | 5 | 27,78% |
| Linnaeus (1758) | 4 | 10% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clements (2012) | 3 | 7,5% | 3 | 15,79% | 3 | 17,65% | 2 | 11,11% |
| Dodson & Fitzgerald (1980) | 3 | 7,5% | 2 | 10,53% | 0 | 0% | 2 | 11,11% |
| Ehrhardt (1971) | 3 | 7,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 3 | 7,5% | 2 | 10,53% | 2 | 11,76% | 2 | 11,11% |
| Gmelin (1789) | 3 | 7,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vanderwerf et al. (2006) | 3 | 7,5% | 3 | 15,79% | 3 | 17,65% | 3 | 16,67% |
| Bénito-espinal (1990) | 2 | 5% | 2 | 10,53% | 2 | 11,76% | 2 | 11,11% |
| Commission de l’Avifaune Française (2016) | 2 | 5% | 2 | 10,53% | 2 | 11,76% | 2 | 11,11% |
| Deblock et al. (1960) | 2 | 5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Dewynter (2021) | 2 | 5% | 2 | 10,53% | 2 | 11,76% | 2 | 11,11% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 2 | 5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathews (1914) | 2 | 5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Questel (2020) | 2 | 5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Ringler et al. (2015) | 2 | 5% | 2 | 10,53% | 2 | 11,76% | 2 | 11,11% |
| Tostain et al. (2013) | 2 | 5% | 2 | 10,53% | 2 | 11,76% | 2 | 11,11% |
| Uicn et al. (2015) | 2 | 5% | 2 | 10,53% | 2 | 11,76% | 2 | 11,11% |
| Weimerskirch et al. (2009) | 2 | 5% | 2 | 10,53% | 2 | 11,76% | 2 | 11,11% |
| Anonyme. (2012) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Anonyme. (2012) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Ausilio & Zotier (1989) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Belfan & Conde (2016) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Bertrand (1982) | 1 | 2,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2013) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Boddaert & Daubenton (1783) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Bougeard & Siblet (2000) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Cheke & Hume (2008) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Condamin (1979) | 1 | 2,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deblock (1966) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Deniau & Provost (2020) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 0 | 0% |
| Dickinson & Remsen (2013) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Ducatez & Devore (2023) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Flitti & Rocha (2014) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Heller & Snodgrass (1901) | 1 | 2,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacan & Mougin (1974) | 1 | 2,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1831) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Rothschild (1902) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Safford & Hawkins (2013) | 1 | 2,5% | 1 | 5,26% | 1 | 5,88% | 1 | 5,56% |
| Vanderwerf et al. (2004) | 1 | 2,5% | 0 | 0% | 0 | 0% | 0 | 0% |
