Vertébrés de Clipperton
507 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Fourriére et al. (2014) | 132 | 6,49% | 128 | 45,39% | 127 | 46,52% | 128 | 46,72% |
| Fricke et al. (2011) | 111 | 5,46% | 107 | 37,94% | 107 | 39,19% | 107 | 39,05% |
| Siu et al. (2017) | 106 | 5,21% | 103 | 36,52% | 103 | 37,73% | 103 | 37,59% |
| Fricke et al. (2009) | 94 | 4,62% | 90 | 31,91% | 90 | 32,97% | 90 | 32,85% |
| Wickel & Jamon (2010) | 76 | 3,74% | 71 | 25,18% | 71 | 26,01% | 71 | 25,91% |
| Delrieu-Trottin et al. (2015) | 67 | 3,29% | 63 | 22,34% | 63 | 23,08% | 63 | 22,99% |
| Béarez & Séret (2009) | 63 | 3,1% | 60 | 21,28% | 60 | 21,98% | 60 | 21,9% |
| Questel (2020) | 53 | 2,61% | 51 | 18,09% | 51 | 18,68% | 47 | 17,15% |
| Questel & Le Quellec (2012) | 52 | 2,56% | 48 | 17,02% | 48 | 17,58% | 43 | 15,69% |
| Rinaldi (2016) | 48 | 2,36% | 48 | 17,02% | 48 | 17,58% | 32 | 11,68% |
| Williams et al. (2006) | 47 | 2,31% | 46 | 16,31% | 46 | 16,85% | 46 | 16,79% |
| Bacchet et al. (2007) | 46 | 2,26% | 40 | 14,18% | 40 | 14,65% | 40 | 14,6% |
| Uicn et al. (2015) | 39 | 1,92% | 39 | 13,83% | 39 | 14,29% | 35 | 12,77% |
| Uicn et al. (2017) | 39 | 1,92% | 36 | 12,77% | 36 | 13,19% | 31 | 11,31% |
| Fricke et al. (2013) | 38 | 1,87% | 38 | 13,48% | 38 | 13,92% | 38 | 13,87% |
| Kulbicki et al. (2000) | 38 | 1,87% | 33 | 11,7% | 33 | 12,09% | 32 | 11,68% |
| Weimerskirch et al. (2009) | 37 | 1,82% | 30 | 10,64% | 29 | 10,62% | 29 | 10,58% |
| Carzon et al. (2016) | 36 | 1,77% | 36 | 12,77% | 36 | 13,19% | 24 | 8,76% |
| Estrade et al. (2016) | 36 | 1,77% | 36 | 12,77% | 36 | 13,19% | 24 | 8,76% |
| Béarez et al. (2017) | 34 | 1,67% | 34 | 12,06% | 34 | 12,45% | 34 | 12,41% |
| Linnaeus (1758) | 31 | 1,52% | 11 | 3,9% | 11 | 4,03% | 10 | 3,65% |
| Chabanet & Durville (2005) | 30 | 1,47% | 25 | 8,87% | 25 | 9,16% | 25 | 9,12% |
| UICN Comité français, OFB & MNHN (2021) | 30 | 1,47% | 30 | 10,64% | 30 | 10,99% | 29 | 10,58% |
| Yokoyama (2013) | 27 | 1,33% | 23 | 8,16% | 23 | 8,42% | 22 | 8,03% |
| Cuvier & Valenciennes (1833) | 26 | 1,28% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Kulbicki (comm. pers., 2011) | 26 | 1,28% | 20 | 7,09% | 20 | 7,33% | 20 | 7,3% |
| Levesque & Delcroix (2018) | 21 | 1,03% | 20 | 7,09% | 20 | 7,33% | 19 | 6,93% |
| Poey (1858-61) | 21 | 1,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collette & Nauen (1983) | 19 | 0,93% | 19 | 6,74% | 19 | 6,96% | 19 | 6,93% |
| Richard et al. (1982) | 19 | 0,93% | 7 | 2,48% | 7 | 2,56% | 6 | 2,19% |
| Remsen et al. (2013) | 18 | 0,88% | 17 | 6,03% | 17 | 6,23% | 16 | 5,84% |
| Béarez & Bouffandeau (2019) | 16 | 0,79% | 16 | 5,67% | 16 | 5,86% | 16 | 5,84% |
| Etcheberry & Abraham (2009) | 16 | 0,79% | 13 | 4,61% | 13 | 4,76% | 13 | 4,74% |
| Rafinesque Schmaltz (1810) | 14 | 0,69% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Bouchon-Navaro et al. (2005) | 13 | 0,64% | 10 | 3,55% | 10 | 3,66% | 10 | 3,65% |
| Bordin et al. (2021) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Charrassin (2016) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Charrassin (2016) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Garrigue (2007) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| G.E.M.M. (2012) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Jarrett & Shirihai (2014) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Moutou (2016) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Smith (1997) | 12 | 0,59% | 10 | 3,55% | 10 | 3,66% | 10 | 3,65% |
| Snodgrass & Heller (1905) | 12 | 0,59% | 5 | 1,77% | 5 | 1,83% | 5 | 1,82% |
| Spitz et al. (2016) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Thoisy & Bordin (2016) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Urtizberea (2016) | 12 | 0,59% | 12 | 4,26% | 12 | 4,4% | 8 | 2,92% |
| Allen (comm. pers., 2009) | 11 | 0,54% | 8 | 2,84% | 8 | 2,93% | 7 | 2,55% |
| Gannier (2001) | 11 | 0,54% | 11 | 3,9% | 11 | 4,03% | 7 | 2,55% |
| Gannier (2002) | 11 | 0,54% | 11 | 3,9% | 11 | 4,03% | 8 | 2,92% |
| Aulagnier (2009) | 10 | 0,49% | 10 | 3,55% | 10 | 3,66% | 8 | 2,92% |
| Dewynter et al. (2021) | 10 | 0,49% | 10 | 3,55% | 10 | 3,66% | 8 | 2,92% |
| Gannier (2009) | 10 | 0,49% | 10 | 3,55% | 10 | 3,66% | 7 | 2,55% |
| Catzeflis (2012) | 9 | 0,44% | 9 | 3,19% | 9 | 3,3% | 6 | 2,19% |
| Gill (1995) | 9 | 0,44% | 9 | 3,19% | 9 | 3,3% | 8 | 2,92% |
| Müller & Henle (1841) | 9 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Compagno (1984) | 8 | 0,39% | 8 | 2,84% | 8 | 2,93% | 8 | 2,92% |
| Compagno (1984) | 8 | 0,39% | 8 | 2,84% | 8 | 2,93% | 8 | 2,92% |
| Ehrhardt (1971) | 8 | 0,39% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Gannier (2000) | 8 | 0,39% | 8 | 2,84% | 8 | 2,93% | 5 | 1,82% |
| Gmelin (1789) | 8 | 0,39% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Kiszka et al.(2007) | 8 | 0,39% | 8 | 2,84% | 8 | 2,93% | 5 | 1,82% |
| Laran et al. (2011) | 8 | 0,39% | 8 | 2,84% | 8 | 2,93% | 5 | 1,82% |
| Barau et al. (2005) | 7 | 0,34% | 5 | 1,77% | 5 | 1,83% | 5 | 1,82% |
| Gronow (1854) | 7 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 7 | 0,34% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Legand (1950) | 7 | 0,34% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 7 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1827) | 7 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thibault et al. (2014) | 7 | 0,34% | 6 | 2,13% | 6 | 2,2% | 5 | 1,82% |
| Belfan & Conde (2016) | 6 | 0,29% | 6 | 2,13% | 6 | 2,2% | 6 | 2,19% |
| Bloch & Schneider (1801) | 6 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes ([1832]) | 6 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter (2021) | 6 | 0,29% | 6 | 2,13% | 6 | 2,2% | 6 | 2,19% |
| Kiszka et al. (2010) | 6 | 0,29% | 6 | 2,13% | 6 | 2,2% | 3 | 1,09% |
| Nardo (1827) | 6 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Earle (2000) | 6 | 0,29% | 5 | 1,77% | 5 | 1,83% | 5 | 1,82% |
| Tostain et al. (2013) | 6 | 0,29% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Uicn et al. (2015) | 6 | 0,29% | 5 | 1,77% | 5 | 1,83% | 5 | 1,82% |
| Van Dijk et al. (2012) | 6 | 0,29% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Clements (2012) | 5 | 0,25% | 5 | 1,77% | 5 | 1,83% | 4 | 1,46% |
| Cuvier & Valenciennes (1846) | 5 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dulau-Drouot et al. (2008) | 5 | 0,25% | 5 | 1,77% | 5 | 1,83% | 2 | 0,73% |
| Klunzinger (1871) | 5 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mertens & Wermuth (1960) | 5 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rocamora (2004) | 5 | 0,25% | 5 | 1,77% | 5 | 1,83% | 5 | 1,82% |
| Rousseau (2010) | 5 | 0,25% | 5 | 1,77% | 5 | 1,83% | 5 | 1,82% |
| Uicn et al. (2020) | 5 | 0,25% | 5 | 1,77% | 5 | 1,83% | 4 | 1,46% |
| Barré (2021) | 4 | 0,2% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Bonaparte (1837) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro & Louis (1986) | 4 | 0,2% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Charbonnel (1990) | 4 | 0,2% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Fourt et al. (2017) | 4 | 0,2% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Fretey & Lescure (1999) | 4 | 0,2% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Linnaeus (1766) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Pascal (2009) | 4 | 0,2% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Lorvelec et al. (2007) | 4 | 0,2% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Rafinesque (1810) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1835) | 4 | 0,2% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Samaran & Guinet (2009) | 4 | 0,2% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Swainson (1839) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet & Agrnsm (2018) | 4 | 0,2% | 4 | 1,42% | 4 | 1,47% | 4 | 1,46% |
| Allen & Robertson (1995) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Allen & Robertson (1995) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Allen & Robertson (1999) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Allen (1995) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Bonnaterre (1788) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2006) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Commission de l’Avifaune Française (2016) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Cuvier & Valenciennes (1830-1832) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Del Hoyo & Collar (2014) | 3 | 0,15% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Dodson & Fitzgerald (1980) | 3 | 0,15% | 2 | 0,71% | 0 | 0% | 2 | 0,73% |
| Fowler (1919) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gonzalez et al. (2009) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guth (1971) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Hemida et al. (2003) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutchinson et al. (2019) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Kiszka et al. (2009) | 3 | 0,15% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Lacepède (1801) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1803) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ohler et al. (2021) | 3 | 0,15% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Perrin et al. (2002) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Philippi (1887) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1902) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Robineau (2005) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 1 | 0,36% |
| Schaefer (1987) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Shirihai (2003) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Springer (1962) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vanderwerf et al. (2006) | 3 | 0,15% | 3 | 1,06% | 3 | 1,1% | 3 | 1,09% |
| Bauer & Sadlier (2000) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 1 | 0,36% |
| Bénito-espinal (1990) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Berry & Smith-Vaniz (1978) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Bioinsight/diren & Guyane (2006) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Blanc et al. (1993) | 2 | 0,1% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Bleeker (1852) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boer et al. (1999) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Camiñas et al. (2021) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Casale et al. (2021) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Chartier et al. (2007) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Chevalier (2006) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Ciccione et al. (2011) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Clua & Planes (2019) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Clua et al. (2019) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Collette (2003) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Craig et al. (2006) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Crillon & Cuzange (2020) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Cuvier (1829) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daniel et al. (2020) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Deblock et al. (1960) | 2 | 0,1% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Dewynter et al. (2019) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Dewynter et al. (2019) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Dewynter et al. (2022) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Dewynter et al. (2023) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Dewynter et al. (2023) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Diaz & Cuzange (2009) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Duffaut et al. (2011) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Entraygues (2014) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Étaix-bonnin et al. (2011) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Evermann & Clark (1928) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fretey & Triplet (2022) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Fricke et al. (2024) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Gannier & Petiau (2006) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 0 | 0% |
| Garman (1913) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gentry et al. (2004) | 2 | 0,1% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Gmelin (1789) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Greenfield (1965) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Griffith & Smith (1834) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1880) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ineich (2016) | 2 | 0,1% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Keith et al. (2013) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Kner & Steindachner (1867) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Scao et al. (2011) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Letourneur et al. (2004) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macdonald & Barron (1868) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marshall et al. (2009) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary et al. (2018) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Massary et al. (2019) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Massary et al. (2020) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Massary et al. (2021) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Mathews (1914) | 2 | 0,1% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| McNair & Cramer-Burke (2006) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menzies (1791) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millot et al. (2023) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Muss et al. (2001) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Nakamura (1985) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Palko et al. (1982) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Pallas (1770) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Pennant (1776) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perez Canto (1886) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1851-1854) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst et al. (2022) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Quero et al. (2013) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Questel et al. (2023) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Questel et al. (2023) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Questel (2023) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Read & Farman (2018) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Read et al. (2023) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Reilly et al. (2014) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Rhodin et al. (2017) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Rignault & Chevallier (2017) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Ringler et al. (2015) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Risso (1810) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robineau & Duhamel (2006) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Roux (1913) | 2 | 0,1% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Safford & Hawkins (2013) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Sauvignet et al. (2000) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Schultz (1943) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simian et al. (2022) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Smith (1849) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thunberg (1787) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annali del Museo Civico di Storia Naturale di Genova 18: 465-590, tavv. I-III.">Vinciguerra (1883) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walbaum (1792) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weber (1913) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weimerskirch et al. (2009) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Whitley (1937) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel et al. (2014) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Wilson (1813) | 2 | 0,1% | 2 | 0,71% | 2 | 0,73% | 2 | 0,73% |
| Zdunek (2022) | 2 | 0,1% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| AAMP (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Abril et al. (1986) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Agassiz (1833-1843) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ainley et al. (2007) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Al-hasson & Ali (2020) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Allen (1997) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Andrew et al. (2008) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Angel (1935) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Anonyme (2008) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Aquarium de La Rochelle (2017) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Arnold & Ovenden (2014) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Atwood (1869) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aulagnier et al. (2017) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Ausilio & Zotier (1989) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Baldwin (1963) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Barbancey (2001) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Barbancey (2001) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Barrioz & Morinière (2007) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Bartoli (1972) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Beauvieux et al. (2024) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Beebe & Tee-van (1932) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1831) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertin (1928) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Bertrand (1982) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2013) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Blainville (1816) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blanc (1909) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785-1795) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bochaton et al. (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Boddaert & Daubenton (1783) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Bodilis et al. (2011) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Boer & Simmonds (2000) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Borsa (1997) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Bouchon-Navaro et al. (1992) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Bougeard & Siblet (2000) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Bour et al. (2008) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Bourgade (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Brun (1958) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Brünnich (1768) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butaud (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Caceres & Salamolard (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Calenge et al. (2010) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Catzeflis (2018) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Caut et al. (2008) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Chambault et al. (2020) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Champagne et al. (1997) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Cheke & Hume (2008) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Cheke (1987) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Chesser et al. (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevallier et al. (2023) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| CHN (2017) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Ciccione (2001) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Ciccione (2001) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Clements et al. (2015) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Clements (1992) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Clua et al. (2016) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Collet & Duguy (1981) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collet et al. (2017) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Condamin (1979) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooper (1863) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cottarel et al. (2013) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Crochet et al. (2022) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Csabaï (2020) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Cunha et al. (2015) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Curd et al. (2015) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Dalebout et al. (2005) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Day (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deblock (1966) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Deflandre (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delcroix et al. (2008) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Delcroix et al. (2011) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Deniau & Provost (2020) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Desbrosses & Etcheberry (1987) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Desbrosses (1935) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dickinson & Remsen (2013) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Dieme et al. (2015) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Dollfus (1966) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dreff & Delliere (1994) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubief & Gallais (2011) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Dubois & Louvet (2014) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Ducatez & Devore (2023) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Duguy et al. (1998) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Duguy et al. (2007) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Duguy (1987) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Duguy (1988) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Duguy (1994) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Duguy (1997) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Eschscholtz (1829) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eudeline (2022) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Euphrasen (1791) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eyton (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flitti & Rocha (2014) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Forest (1946) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Fort & Barrière (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Fraser-brunner (1950) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fremont (2002) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Frenot et al. (2005) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Fretey et al. (2023) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Fritz & Havaš (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fritzsche (1980) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Furminieux (2019) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Gargominy et al. (1996) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Garman (1899) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrigue & Poupon (2013) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Gilbert (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill & Thiele (1997) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Gill (1862) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1863) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1863) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1995) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Ginsburg (1947) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Girard (1858) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondo (2023) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Girondot et al. (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondot (2011) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Gmelin (1788) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goodall et al. (1997) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Goulletquer (2016) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Gray (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinet (1991) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Guinet (2004) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Günther (1866) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Havery et al. (2018) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Heimlich-boran (1993) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Heller & Snodgrass (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ineich et al. (2007) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| In: Charpy, L. (coord.) 2009. Clipperton, environnement et biodiversité d'un microcosme océanique. Muséum national d'Histoire naturelle, Paris; IRD, Marseille: 347-380. (Patrimoines naturels; 68).">Ineich et al. (2009) | 1 | 0,05% | 1 | 0,35% | 0 | 0% | 1 | 0,36% |
| Ineich (1987) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| IUCN (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Jaquemet et al. (2004) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Jefferson & & Van Waerebeek (2002) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jehl et al. (1980) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Jordan & Evermann (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Jordan (1922) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Meek (1885) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1884) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouan (1863) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Kasamatsu & Joyce (1995) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Keith et al. (2002) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Keith et al. (2006) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Kishinouye (1920) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Klein et al. (2016) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Kock et al. (2006) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Labach et al. (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Lacan & Mougin (1974) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1798) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1800) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacoste (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Lacoste (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Lambert (1988) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Laran et al. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Last et al. (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leaper et al. (2008) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Leatherwood et al. (1979) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Legendre (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescure et al. (2012) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Lescure et al. (2016) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Lesson (1826-1830) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1830-1831) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1831) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Lesueur (1822) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letacq (1924) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Liardet & d'Auzon (2004) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Liardet (2004) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Liebart et al. (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Liénard (1840) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linné (1766) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loison (1989) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Lorvelec & Pascal (2009) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 0 | 0% |
| Lorvelec et al. (2009) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Louis et al. (1992) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louisin & Probst (1996) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Lowe et al. (2007) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Lowe (1834) | 1 | 0,05% | 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) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1841) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1843) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macleod et al. (2006) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Malm (1877) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marion & Clergeau (2003) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Marion & Marion (1982) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Marion (2003) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Mas-Coma et al. (1989) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Massary et al. (2017) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Meek & Hildebrand (1923) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Méheust et al. (2018) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Merrem (1820) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1881) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morinière & Dell'amico (2011) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Mourier (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muratet (2015) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Murray (1884) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1887) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nadal & Tariel (2008) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Nelson-Smith et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël, Meunier (2010) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Noël (2017) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Noronha (1926) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Notarbartolo et al. (2020) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Ogilby (1908) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oremus (2009) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Osbeck (1765) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osburn & Nichols (1816) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal & Clergeau (2003) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Pearman et al. (2016) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Pellegrin (1912) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peron (2014) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Pitman & Ensor (2003) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Poisson (1999) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Prévost & Mougin (1970) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Probst et al. (2000) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Probst et al. (2001) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Probst (1997) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Probst (1997) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst (1998) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Probst (2001) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Ranzani (1839) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Read & Jean (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Read et al. (2015) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Revilliod (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Revuelta et al. (2015) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Riccialdelli et al. (2010) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Richardson (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richer de Forges et al. (2005) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Rinaldi et al. (2011) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Robineau (1989) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Ronot (2007) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Roos (2000) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Rossi-santos et al. (2007) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Rothschild (1902) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Sawai et al. (2018) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Schneider (1783) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schweigger (1812) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1769) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (1997) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Séret (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Servan (1976) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Shaver et al. (2019) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Snyder (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1941) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1867) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stelfox et al. (2020) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Storer (1839) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tchékémian & Leleu (2024) | 1 | 0,05% | 1 | 0,35% | 0 | 0% | 1 | 0,36% |
| Theuerkauf et al. (2010) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Thiele et al. (1999) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Tirvengadum & Bour (1985) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Uicn et al. (2016) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Uyeno et al. (1983) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Van & Kampen (1907) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vanderwerf et al. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verreaux & Des Murs (1860) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Viale & Frontier (1989) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Victor et al. (2001) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Viel (2021) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Waayers et al. (2011) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Wahl & Barbraud (2005) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
| Waite (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1931) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wursig & Wursig (1980) | 1 | 0,05% | 1 | 0,35% | 1 | 0,37% | 1 | 0,36% |
