Vertébrés des TAAF (hors îles Eparses)
610 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) | 191 | 10,37% | 180 | 37,34% | 174 | 38,24% | 154 | 33,55% |
| Duhamel et al. (2005) | 130 | 7,06% | 125 | 25,93% | 122 | 26,81% | 125 | 27,23% |
| Rinaldi (2016) | 108 | 5,87% | 96 | 19,92% | 96 | 21,1% | 72 | 15,69% |
| Carzon et al. (2016) | 81 | 4,4% | 72 | 14,94% | 72 | 15,82% | 54 | 11,76% |
| Estrade et al. (2016) | 81 | 4,4% | 72 | 14,94% | 72 | 15,82% | 54 | 11,76% |
| Dettaï et al. (2011) | 64 | 3,48% | 61 | 12,66% | 61 | 13,41% | 61 | 13,29% |
| Linnaeus (1758) | 40 | 2,17% | 14 | 2,9% | 14 | 3,08% | 13 | 2,83% |
| Béarez et al. (2017) | 31 | 1,68% | 30 | 6,22% | 30 | 6,59% | 28 | 6,1% |
| Uicn et al. (2017) | 30 | 1,63% | 30 | 6,22% | 30 | 6,59% | 26 | 5,66% |
| Jarrett & Shirihai (2014) | 28 | 1,52% | 25 | 5,19% | 25 | 5,49% | 19 | 4,14% |
| Charrassin (2016) | 27 | 1,47% | 24 | 4,98% | 24 | 5,27% | 18 | 3,92% |
| Charrassin (2016) | 27 | 1,47% | 24 | 4,98% | 24 | 5,27% | 18 | 3,92% |
| Moutou (2016) | 27 | 1,47% | 24 | 4,98% | 24 | 5,27% | 18 | 3,92% |
| Spitz et al. (2016) | 27 | 1,47% | 24 | 4,98% | 24 | 5,27% | 18 | 3,92% |
| Thoisy & Bordin (2016) | 27 | 1,47% | 24 | 4,98% | 24 | 5,27% | 18 | 3,92% |
| Urtizberea (2016) | 27 | 1,47% | 24 | 4,98% | 24 | 5,27% | 18 | 3,92% |
| Barau et al. (2005) | 20 | 1,09% | 16 | 3,32% | 16 | 3,52% | 16 | 3,49% |
| Fricke et al. (2011) | 20 | 1,09% | 20 | 4,15% | 20 | 4,4% | 19 | 4,14% |
| UICN Comité français, OFB & MNHN (2021) | 20 | 1,09% | 20 | 4,15% | 20 | 4,4% | 20 | 4,36% |
| Questel (2020) | 19 | 1,03% | 18 | 3,73% | 18 | 3,96% | 17 | 3,7% |
| Shirihai (2003) | 19 | 1,03% | 15 | 3,11% | 14 | 3,08% | 11 | 2,4% |
| Uicn et al. (2015) | 19 | 1,03% | 17 | 3,53% | 17 | 3,74% | 16 | 3,49% |
| Ausilio & Zotier (1989) | 17 | 0,92% | 16 | 3,32% | 16 | 3,52% | 15 | 3,27% |
| Prévost & Mougin (1970) | 17 | 0,92% | 15 | 3,11% | 14 | 3,08% | 13 | 2,83% |
| Aulagnier (2009) | 16 | 0,87% | 14 | 2,9% | 14 | 3,08% | 8 | 1,74% |
| Perrin et al. (2002) | 16 | 0,87% | 13 | 2,7% | 12 | 2,64% | 9 | 1,96% |
| Questel & Le Quellec (2012) | 16 | 0,87% | 15 | 3,11% | 15 | 3,3% | 14 | 3,05% |
| Levesque & Delcroix (2018) | 15 | 0,81% | 15 | 3,11% | 15 | 3,3% | 15 | 3,27% |
| Yokoyama (2013) | 15 | 0,81% | 15 | 3,11% | 15 | 3,3% | 15 | 3,27% |
| Arnaud (1974) | 14 | 0,76% | 9 | 1,87% | 9 | 1,98% | 9 | 1,96% |
| Lorvelec et al. (2007) | 14 | 0,76% | 14 | 2,9% | 14 | 3,08% | 14 | 3,05% |
| Frenot et al. (2005) | 12 | 0,65% | 11 | 2,28% | 11 | 2,42% | 10 | 2,18% |
| Remsen et al. (2013) | 12 | 0,65% | 11 | 2,28% | 11 | 2,42% | 11 | 2,4% |
| Samaran & Guinet (2009) | 12 | 0,65% | 10 | 2,07% | 8 | 1,76% | 6 | 1,31% |
| Walbaum (1792) | 12 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1848) | 11 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robineau & Duhamel (2006) | 11 | 0,6% | 9 | 1,87% | 8 | 1,76% | 5 | 1,09% |
| Aulagnier et al. (2017) | 10 | 0,54% | 9 | 1,87% | 9 | 1,98% | 8 | 1,74% |
| Boer et al. (1999) | 10 | 0,54% | 9 | 1,87% | 8 | 1,76% | 8 | 1,74% |
| Boer (2000) | 10 | 0,54% | 8 | 1,66% | 7 | 1,54% | 5 | 1,09% |
| Chastel & Beaucournu (1992) | 10 | 0,54% | 10 | 2,07% | 10 | 2,2% | 8 | 1,74% |
| Rocamora (2004) | 10 | 0,54% | 9 | 1,87% | 9 | 1,98% | 9 | 1,96% |
| Shandikov (2011) | 10 | 0,54% | 10 | 2,07% | 10 | 2,2% | 10 | 2,18% |
| Tostain et al. (2013) | 10 | 0,54% | 10 | 2,07% | 10 | 2,2% | 9 | 1,96% |
| Chernova & Duhamel (2003) | 9 | 0,49% | 9 | 1,87% | 7 | 1,54% | 9 | 1,96% |
| Duhamel & King (2007) | 9 | 0,49% | 9 | 1,87% | 9 | 1,98% | 9 | 1,96% |
| Ifremer (2009) | 9 | 0,49% | 7 | 1,45% | 7 | 1,54% | 6 | 1,31% |
| Lacepède (1803) | 9 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robineau (1989) | 9 | 0,49% | 5 | 1,04% | 4 | 0,88% | 4 | 0,87% |
| Soubeyran et al. (2011) | 9 | 0,49% | 9 | 1,87% | 9 | 1,98% | 9 | 1,96% |
| Barré (2021) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 8 | 1,74% |
| Bordin et al. (2021) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 4 | 0,87% |
| Deblock et al. (1960) | 8 | 0,43% | 6 | 1,24% | 6 | 1,32% | 6 | 1,31% |
| Etcheberry & Abraham (2009) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 8 | 1,74% |
| Fourt et al. (2017) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 6 | 1,31% |
| Gannier (2001) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 5 | 1,09% |
| Gargominy et al. (1996) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 8 | 1,74% |
| Garrigue (2007) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 5 | 1,09% |
| G.E.M.M. (2012) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 5 | 1,09% |
| Moreau & Duhamel (1997) | 8 | 0,43% | 8 | 1,66% | 8 | 1,76% | 8 | 1,74% |
| Siu et al. (2017) | 8 | 0,43% | 7 | 1,45% | 7 | 1,54% | 7 | 1,53% |
| Belfan & Conde (2016) | 7 | 0,38% | 7 | 1,45% | 7 | 1,54% | 7 | 1,53% |
| Catzeflis (2012) | 7 | 0,38% | 7 | 1,45% | 7 | 1,54% | 3 | 0,65% |
| Jourdan (2020) | 7 | 0,38% | 6 | 1,24% | 6 | 1,32% | 6 | 1,31% |
| Moller & King (2007) | 7 | 0,38% | 7 | 1,45% | 7 | 1,54% | 7 | 1,53% |
| Safford & Hawkins (2013) | 7 | 0,38% | 7 | 1,45% | 6 | 1,32% | 7 | 1,53% |
| Soubeyran (2008) | 7 | 0,38% | 6 | 1,24% | 6 | 1,32% | 6 | 1,31% |
| Blanc (1954) | 6 | 0,33% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Desbrosses & Etcheberry (1987) | 6 | 0,33% | 5 | 1,04% | 5 | 1,1% | 2 | 0,44% |
| Günther (1866) | 6 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 6 | 0,33% | 6 | 1,24% | 6 | 1,32% | 6 | 1,31% |
| Pallas [1814] | 6 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potin (2013) | 6 | 0,33% | 6 | 1,24% | 6 | 1,32% | 6 | 1,31% |
| Rafinesque Schmaltz (1810) | 6 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossi-santos et al. (2007) | 6 | 0,33% | 4 | 0,83% | 4 | 0,88% | 2 | 0,44% |
| Shandikov (1995) | 6 | 0,33% | 6 | 1,24% | 6 | 1,32% | 6 | 1,31% |
| Theuerkauf et al. (2010) | 6 | 0,33% | 6 | 1,24% | 6 | 1,32% | 6 | 1,31% |
| Banks et al. (2006) | 5 | 0,27% | 4 | 0,83% | 4 | 0,88% | 1 | 0,22% |
| Borsa (1997) | 5 | 0,27% | 4 | 0,83% | 3 | 0,66% | 3 | 0,65% |
| Del Hoyo & Collar (2014) | 5 | 0,27% | 2 | 0,41% | 1 | 0,22% | 2 | 0,44% |
| Dewynter et al. (2021) | 5 | 0,27% | 5 | 1,04% | 5 | 1,1% | 4 | 0,87% |
| Fricke et al. (2009) | 5 | 0,27% | 5 | 1,04% | 5 | 1,1% | 5 | 1,09% |
| Gannier (2009) | 5 | 0,27% | 5 | 1,04% | 5 | 1,1% | 4 | 0,87% |
| Gill (1995) | 5 | 0,27% | 5 | 1,04% | 5 | 1,1% | 5 | 1,09% |
| Gmelin (1789) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 5 | 0,27% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Günther (1878) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kasamatsu & Joyce (1995) | 5 | 0,27% | 4 | 0,83% | 3 | 0,66% | 4 | 0,87% |
| UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 5 | 0,27% | 5 | 1,04% | 5 | 1,1% | 4 | 0,87% |
| Weimerskirch et al. (2009) | 5 | 0,27% | 5 | 1,04% | 5 | 1,1% | 5 | 1,09% |
| Barbraud et al. (2009) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Barre et al. (2009) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 3 | 0,65% |
| Boer & Simmonds (2000) | 4 | 0,22% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Bost et al. (2022) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 2 | 0,44% |
| Clements et al. (2015) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 3 | 0,65% |
| Clements (2012) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 3 | 0,65% |
| Delord et al. (2005) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Delord et al. (2008) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Des et al. (2021) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Forster (1781) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gannier (2000) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 3 | 0,65% |
| Gannier (2002) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 3 | 0,65% |
| Gentry et al. (2004) | 4 | 0,22% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Gilchrist (1906) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Isenmann et al. (1971) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Jaeger et al. (2020) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Jordan (1894) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kenaley (2007) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Kojadinovic et al. (2007) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Macleod et al. (2006) | 4 | 0,22% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Matsuoka et al. (2005) | 4 | 0,22% | 4 | 0,83% | 3 | 0,66% | 2 | 0,44% |
| Nielsen et al. (2008) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Nilsson (1832) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1997) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 3 | 0,65% |
| Riccialdelli et al. (2010) | 4 | 0,22% | 2 | 0,41% | 2 | 0,44% | 1 | 0,22% |
| Risso (1827) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiele et al. (1999) | 4 | 0,22% | 3 | 0,62% | 2 | 0,44% | 3 | 0,65% |
| Uicn et al. (2020) | 4 | 0,22% | 4 | 0,83% | 4 | 0,88% | 4 | 0,87% |
| Vaillant (1888) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abeyrama et al. (2021) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Ainley et al. (2007) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 2 | 0,44% |
| Andriashev (1982) | 3 | 0,16% | 3 | 0,62% | 2 | 0,44% | 3 | 0,65% |
| Aulagnier (2021) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 2 | 0,44% |
| Barbosa du Bocage & Brito Capello (1864) | 3 | 0,16% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Barbraud et al. (2021) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Bloch & Schneider (1801) | 3 | 0,16% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Bochaton et al. (2021) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Burneleau (1983) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Butaud (2021) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Carravieri et al. (2016) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Catzeflis (2018) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Cohen et al. (1990) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Cousins et al. (2013) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Cuvier (1829) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter (2021) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Duhamel (1986) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Dulau-Drouot et al. (2008) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 2 | 0,44% |
| Gill & Townsend (1897) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren & Galil (2015) | 3 | 0,16% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Guth (1971) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Hureau (1966) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglesias et al. (2012) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| IUCN (2013) | 3 | 0,16% | 2 | 0,41% | 2 | 0,44% | 1 | 0,22% |
| Jouventin et al. (1989) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kawamura (1994) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 1 | 0,22% |
| Keith et al. (2011) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Kiszka et al.(2007) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 2 | 0,44% |
| Kock et al. (2006) | 3 | 0,16% | 3 | 0,62% | 2 | 0,44% | 3 | 0,65% |
| Laran et al. (2011) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Leach (1818) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leaper et al. (2008) | 3 | 0,16% | 3 | 0,62% | 2 | 0,44% | 3 | 0,65% |
| Lescroel et al. (2009) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Pascal et al. (2006) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Ponchon et al. (2021) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Robineau (2005) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 1 | 0,22% |
| Sagar (1991) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 0 | 0% |
| Thibault et al. (2014) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Thiebot et al. (2011) | 3 | 0,16% | 3 | 0,62% | 3 | 0,66% | 3 | 0,65% |
| Thiele et al. (2004) | 3 | 0,16% | 3 | 0,62% | 2 | 0,44% | 2 | 0,44% |
| Tremblay & Cherel (2005) | 3 | 0,16% | 3 | 0,62% | 0 | 0% | 3 | 0,65% |
| AAMP (2012) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Balushkin (1996) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barthélémy (1926) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benedetti et al. (2021) | 2 | 0,11% | 2 | 0,41% | 1 | 0,22% | 1 | 0,22% |
| Berrebi et al. (2018) | 2 | 0,11% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Berta & Churchill (2012) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2013) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Bloch (1795) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bretagnolle & Attie (1991) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Brodier et al. (2011) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Cabanis (1875) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Chapuis et al. (2004) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Chartier et al. (2007) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Cherel et al. (2014) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Cherel et al. (2022) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Couch (1877) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| D'Amico (2001) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Daniel et al. (2020) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Denys et al. (2022) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Diaz & Cuzange (2009) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Dickinson & Remsen (2013) | 2 | 0,11% | 2 | 0,41% | 1 | 0,22% | 2 | 0,44% |
| Dronneau & Wassmer (2008) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Dubois et al. (2008) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Duhamel (2019) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Fort & Barrière (2021) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Frugone et al. (2021) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Garman (1896) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1906) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilbert (1915) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill & Thiele (1997) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Gill (1883) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilot et al. (1992) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Gomez & Voisin (2002) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Goode & Bean (1895) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1896) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Gould (1844) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Green (1996) | 2 | 0,11% | 2 | 0,41% | 0 | 0% | 2 | 0,44% |
| Grosser et al. (2021) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Günther (1876) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hall (1900) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Heckel & Kner (1858) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Howell Rivero (1936) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Humeau et al. (2020) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Hureau (1966) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglésias et al. (2020) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Iglesias et al. (2022) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Impact-mer (2011) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| IUCN (2012) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 1 | 0,22% |
| Proceedings of the California Academy of Sciences, 55(10): 190-207.">Iwamoto et al. (2004) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Jiguet (2002) | 2 | 0,11% | 2 | 0,41% | 0 | 0% | 2 | 0,44% |
| Jordan & Thompson (1914) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1896) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jung et al. (2024) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Karadjian et al. (2022) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Kasamatsu et al. (2000) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 1 | 0,22% |
| Kuhl (1820) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacoste (de) (2020) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Leaper et al. (2008) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 1 | 0,22% |
| Lescroel et al. (2004) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Lesueur (1821) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mahé et al. (2016) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Mas-Coma et al. (1989) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Mathews (1912) | 2 | 0,11% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mays et al. (2006) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Olson & Jouventin (1996) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Osório (1909) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1831) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. 2006 | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Pontoppidan (1763) | 2 | 0,11% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Poss & Duhamel (1991) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Preynat (2013) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Prirodina (2004) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Raust & Sanford (2007) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Reichenow (1904) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reinhardt (1837) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Revilliod (1914) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1844-48) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Richer de Forges et al. (2005) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Ridoux (1989) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Risso (1810) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robineau et al. (2007) | 2 | 0,11% | 2 | 0,41% | 0 | 0% | 2 | 0,44% |
| Routtier et al. (2023) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roux & Martinez (1987) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Roux et al. (1983) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sabine (1819) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saint et al. (1978) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Salvin (1896) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Samaran (2008) | 2 | 0,11% | 2 | 0,41% | 1 | 0,22% | 1 | 0,22% |
| Savouré-Soubelet et al. (in prep.) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Searby & Jouventin (2005) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Shandikov (2008) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Simian et al. (2022) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 1 | 0,22% |
| Stahl et al. (1985) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Storer (1839) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Straube et al. (2011) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Temminck et al. (1838) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tennyson et al. (2022) | 2 | 0,11% | 2 | 0,41% | 0 | 0% | 2 | 0,44% |
| Tostain & Dujardin (1988) | 2 | 0,11% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Tremblay & Cherel (2003) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 0 | 0% |
| Van Canneytet al. (2008) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 2 | 0,44% |
| Voisin (1971) | 2 | 0,11% | 2 | 0,41% | 0 | 0% | 2 | 0,44% |
| Vollmer et al. (2019) | 2 | 0,11% | 2 | 0,41% | 2 | 0,44% | 1 | 0,22% |
| Waugh & Weimerskirch (2003) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aboussouan & Rasonarivo (1986) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Andrew et al. (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme (1996) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2004) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Aubouin et al. (2016) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Audige (1927) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bacchet et al. (2007) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Bailenger et al. (1965) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Baker (1977) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1985) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Barre et al. (1977) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Beaucournu (1968) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bénito-espinal (1990) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Bennett (1831) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertin (1928) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Bertrand (1982) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beslagic et al. (2013) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Best & Scott (1993) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Best et al. (1995) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Bester & Roux (1986) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Bigelow et al. (1953) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Bloch (1782-1784) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1784) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1788) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Blyth (1841) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Blyth (1860) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Body (2021) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Boie (1835) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1837) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouteiller & Borsa (2022) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Branch et al. (2007) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Branch (2010) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Brandt (1837) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brownell & Cipriano (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brownell et al. (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruyn et al. (2006) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Budylenko (1977) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Buffrenil et al. (1989) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Caceres & Salamolard (2021) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Callou (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Carzon (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Causse et al. (2011) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Cerchio et al. (2009) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Chapuis et al. (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cherel & Boxshall (2004) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Cherel et al. (2004) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Cheylan et al. (2022) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Cibois et al. (2015) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Clapham et al. (1999) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Collectif (2009) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Collett (1889) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Collett (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collier et al. (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Commission de l’Avifaune Française (2016) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Condamin (1979) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Costa (1862) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cottarel et al. (2013) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Cotte et al. (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Counihan et al. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Couteyen (2006) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Crespo et al. (1997) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1829) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Cuvier & Valenciennes (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1849) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dalebout et al. (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Danel et al. (2023) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Daudin (1802) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Debout (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Dekay (1842) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delord et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin et al. (2015) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Demay et al. (2014) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Deméré (2014) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Dieme et al. (2015) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Dollfus (1966) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dorleans (2022) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Ducatez & Devore (2023) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel & Pruvost (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel & Pruvost (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel & Pruvost (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel & Pruvost (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel & Pruvost (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel & Pruvost (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel & Pruvost (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1989) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1996) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1996) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel (1997) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (2004) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Duhamel (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Ebels (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Elkins & Yesou (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ersts & Rosenbaum (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Faber (1829) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1780) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fain & Beaucournu (1984) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Falla (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Finsch (1876) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Fleming & Jackson (2011) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Fleming (1828) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flood et al. (2021) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Fordyce & Marx (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Forster (1844) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fraser-brunner (1949) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Friedlaender et al. (2010) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Garman (1899) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| GARNOT (1826) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gauthier-clerc & Lambert (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Géné (1839) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Genevois (1991) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Gill et al. (2000) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1861) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gillespie (1997) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Girard (1855) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gistel (1848) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2021) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Goodall et al. (1997) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1878-1879) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1883) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode (1881) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1838) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Gray (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1872) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Groves & Grubb (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guiguen et al. (1984) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Guinet (1991) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Guinet (2004) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Gunnerus (1767) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1862) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Günther (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1877) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1887) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harrison (1981) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Hector (1875) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley et al. (2007) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Hombron & Jacquinot (1841) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hulley (1988) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Hureau & Ozouf-Costaz (1980) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Ingels et al. (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| IUCN (2015) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Jaeger et al. (2018) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Jefferson et al. (1993) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Jehl et al. (1980) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Johnson & Wolman (1984) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Jordan & Gilbert (1881) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Snyder (1902) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1892) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bulweria baraui. Bulletin du Muséum National d'Histoire Naturelle, 35(6): 593-597.">Jouanin (1964) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouventin & Roux (1984) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouventin (1994) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Kasamatsu et al. (1995) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Kasamatsu et al. (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Keith & Dorson (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Keith & Machino (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Keith et al. (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Keith et al. (2006) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Keith (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Keith (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Kiszka et al. (2009) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Kiszka et al. (2010) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Lancastre et al. (1976) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Laran et al. (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Le Corre & Jouventin (1999) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Legendre (1942) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescroel & Bost (2006) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Lesson (1825) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Lesson (1828) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Lesueur (1818) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letacq (1924) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letourneur et al. (2004) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Levesque & Mathurin (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Lönnberg (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorance et al. (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Lorvelec & Vigne (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Loury & Puissauve (2016) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Lowe (1834) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Lowe (1843) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1846) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Lütken (1892) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Machino (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Malm (1877) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marchandeau & Letty (2021) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Marchandeau et al. (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Marion & Clergeau (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Marion & Marion (1982) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mathews & Iredale (1921) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathews (1912) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matsuoka et al. (1996) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Matsuoka et al. (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Medway (2009) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Ménard et al. (2000) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mey (2010) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Miskelly (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Monod & Dollfus (1932) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Moreau (1881) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morel (1959) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Morrison (2006) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mougin (1984) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Murase et al. (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Murphy & Harper (1916) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Murphy (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nassi et al. (1975) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Naumann (1819) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naurois (1978) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Nelson-Smith et al. (2014) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Nicol et al. (2000) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Noël (2017) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Okamura & Kitakado (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| O'reilly (1818) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oremus (2009) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| pallas (1764) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Pascal et al. (2003) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Pearman et al. (2016) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Pennant (1787) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1812) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perez Canto (1886) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perry et al. (1999) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Peters (1875) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierpoint et al. (1997) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Pinaud et al. (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Pitman & Ensor (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Prevost (1970) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Puissauve, Legros & Poulet (2015) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Rafinesque (1810) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randi et al. (2001) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Renaud et al. (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ribic et al. (1991) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Richards (2009) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Richardson (1843) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1844) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Rignault & Chevallier (2017) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Robert et al. (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Robertson (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Roche & Guinet (2007) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Rogers & Brown (1999) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Rosenbaum & Collins (2006) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Rotschikd (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rotschild (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roule (1916) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Russell et al. (2015) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Ruys & Coord (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Samaran & Guinet (2010) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Samaran et al. (2010) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Sardou (1980) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Schiebel (1910) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schramm et al. (2014) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Scopoli (1769) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sekiguchi et al. (1992) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Sekiguchi et al. (1993) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Sekiguchi et al. (2006) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw (1804) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siciliano & Santos (2003) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Sirovic et al. (2009) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Smith et al. (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Smith (1849) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spitz et al. (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stahl & Weimerskirch (1982) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Stahl et al. (1984) | 1 | 0,05% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Steadman & Bollt (2010) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Storer (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sueur (2018) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Széles et al. (2018) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Terrasse & Terrasse (1969) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Thévenot (2014) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Thiebot et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiebot et al. (2015) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Tougaard (2010) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tunstall (1880) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Vaillant (1888) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1836-1844) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Guelpen (2016) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Vanderwerf et al. (2006) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Vanwaerebeek et al. (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1819) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Waite (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wang & Liu (2016) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Warham et al. (1977) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Watson et al. (1975) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Weerdt (2023) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Weimerskirch & Jouventin (1998) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Weimerskirch et al. (2018) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Whitley (1934) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1939) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1948) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams et al. (2006) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Williams et al. (2009) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Wink et al. (1979) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Wood (1848) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wursig & Wursig (1980) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wursig et al. (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1839) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhukov (2020) | 1 | 0,05% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Zugmayer (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
