Poissons marins de Polynésie française
472 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Siu et al. (2017) | 1206 | 16,19% | 1173 | 77,37% | 1172 | 77,46% | 1172 | 77,41% |
| Fricke et al. (2011) | 1003 | 13,46% | 963 | 63,52% | 962 | 63,58% | 962 | 63,54% |
| Fricke et al. (2009) | 531 | 7,13% | 505 | 33,31% | 505 | 33,38% | 504 | 33,29% |
| Williams et al. (2006) | 482 | 6,47% | 457 | 30,15% | 457 | 30,2% | 456 | 30,12% |
| Delrieu-Trottin et al. (2015) | 472 | 6,33% | 445 | 29,35% | 443 | 29,28% | 445 | 29,39% |
| Kulbicki (comm. pers., 2011) | 449 | 6,03% | 413 | 27,24% | 413 | 27,3% | 413 | 27,28% |
| Wickel & Jamon (2010) | 438 | 5,88% | 420 | 27,7% | 420 | 27,76% | 419 | 27,68% |
| Bacchet et al. (2007) | 378 | 5,07% | 351 | 23,15% | 351 | 23,2% | 351 | 23,18% |
| Kulbicki et al. (2000) | 272 | 3,65% | 237 | 15,63% | 237 | 15,66% | 235 | 15,52% |
| Fricke et al. (2013) | 255 | 3,42% | 248 | 16,36% | 247 | 16,33% | 247 | 16,31% |
| Chabanet & Durville (2005) | 201 | 2,7% | 181 | 11,94% | 181 | 11,96% | 181 | 11,96% |
| Allen (comm. pers., 2009) | 136 | 1,83% | 119 | 7,85% | 119 | 7,87% | 118 | 7,79% |
| Richard et al. (1982) | 96 | 1,29% | 34 | 2,24% | 34 | 2,25% | 33 | 2,18% |
| Fourriére et al. (2014) | 68 | 0,91% | 66 | 4,35% | 66 | 4,36% | 66 | 4,36% |
| Béarez & Bouffandeau (2019) | 51 | 0,68% | 51 | 3,36% | 51 | 3,37% | 50 | 3,3% |
| Béarez et al. (2017) | 49 | 0,66% | 49 | 3,23% | 49 | 3,24% | 49 | 3,24% |
| Randall & Earle (2000) | 46 | 0,62% | 40 | 2,64% | 39 | 2,58% | 40 | 2,64% |
| Keith et al. (2013) | 44 | 0,59% | 38 | 2,51% | 38 | 2,51% | 38 | 2,51% |
| Legand (1950) | 44 | 0,59% | 24 | 1,58% | 24 | 1,59% | 24 | 1,59% |
| Béarez & Séret (2009) | 39 | 0,52% | 37 | 2,44% | 37 | 2,45% | 37 | 2,44% |
| Questel (2020) | 35 | 0,47% | 34 | 2,24% | 34 | 2,25% | 32 | 2,11% |
| Questel & Le Quellec (2012) | 33 | 0,44% | 31 | 2,04% | 31 | 2,05% | 29 | 1,92% |
| Cuvier & Valenciennes (1833) | 32 | 0,43% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Poey (1858-61) | 26 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin (2013) | 24 | 0,32% | 22 | 1,45% | 22 | 1,45% | 22 | 1,45% |
| Kronen et al. (2009) | 24 | 0,32% | 23 | 1,52% | 23 | 1,52% | 23 | 1,52% |
| Séret (1997) | 24 | 0,32% | 23 | 1,52% | 23 | 1,52% | 23 | 1,52% |
| Keith et al. (2006) | 23 | 0,31% | 15 | 0,99% | 15 | 0,99% | 15 | 0,99% |
| Collette & Nauen (1983) | 19 | 0,25% | 19 | 1,25% | 19 | 1,26% | 19 | 1,25% |
| Bouchon-Navaro et al. (2005) | 18 | 0,24% | 11 | 0,73% | 11 | 0,73% | 10 | 0,66% |
| Keith et al. (2002) | 18 | 0,24% | 14 | 0,92% | 14 | 0,93% | 14 | 0,92% |
| Linnaeus (1758) | 18 | 0,24% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Eudeline (2022) | 15 | 0,2% | 15 | 0,99% | 15 | 0,99% | 15 | 0,99% |
| Rafinesque Schmaltz (1810) | 14 | 0,19% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Schwarzhans et al. (2005) | 13 | 0,17% | 13 | 0,86% | 13 | 0,86% | 13 | 0,86% |
| Smith (1997) | 13 | 0,17% | 11 | 0,73% | 9 | 0,59% | 11 | 0,73% |
| Pearman et al. (2020) | 12 | 0,16% | 12 | 0,79% | 12 | 0,79% | 12 | 0,79% |
| Randall (1998) | 12 | 0,16% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Kiszka et al. (2009) | 11 | 0,15% | 9 | 0,59% | 9 | 0,59% | 9 | 0,59% |
| Williams & Viviani (2016) | 11 | 0,15% | 10 | 0,66% | 10 | 0,66% | 10 | 0,66% |
| Compagno (1984) | 10 | 0,13% | 10 | 0,66% | 10 | 0,66% | 10 | 0,66% |
| Justine et al. (2010) | 10 | 0,13% | 10 | 0,66% | 10 | 0,66% | 10 | 0,66% |
| Kronen et al. (2008) | 10 | 0,13% | 10 | 0,66% | 10 | 0,66% | 10 | 0,66% |
| Müller & Henle (1841) | 10 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Soubeyran (2008) | 10 | 0,13% | 10 | 0,66% | 10 | 0,66% | 10 | 0,66% |
| Pinault et al. (2013) | 9 | 0,12% | 8 | 0,53% | 8 | 0,53% | 8 | 0,53% |
| Causse et al. (2023) | 8 | 0,11% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Compagno (1984) | 8 | 0,11% | 8 | 0,53% | 8 | 0,53% | 8 | 0,53% |
| Cuvier & Valenciennes ([1832]) | 8 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letourneur et al. (2004) | 8 | 0,11% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Wickel et al. (2014) | 8 | 0,11% | 7 | 0,46% | 7 | 0,46% | 7 | 0,46% |
| Bloch & Schneider (1801) | 7 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Fricke et al. (2024) | 7 | 0,09% | 7 | 0,46% | 7 | 0,46% | 7 | 0,46% |
| Keith & Marquet (2011) | 7 | 0,09% | 7 | 0,46% | 7 | 0,46% | 7 | 0,46% |
| Lourie et al. (2016) | 7 | 0,09% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Mulochau et al. (2019) | 7 | 0,09% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Snodgrass & Heller (1905) | 7 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Wantiez (comm. pers., 2008) | 7 | 0,09% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Berry & Smith-Vaniz (1978) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Bonnaterre (1788) | 6 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charbonnel (1990) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Fourt et al. (2017) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Gronow (1854) | 6 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2009) | 6 | 0,08% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Pezold & Larson (2015) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Randall (2005) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Rousseau (2010) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Simian et al. (2022) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Tornabene et al. (2013) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Viviani et al. (2016) | 6 | 0,08% | 6 | 0,4% | 6 | 0,4% | 6 | 0,4% |
| Borsa et al. (2013) | 5 | 0,07% | 3 | 0,2% | 2 | 0,13% | 3 | 0,2% |
| Bouchon-Navaro & Louis (1986) | 5 | 0,07% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Cuvier & Valenciennes (1830) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hibino et al. (2016) | 5 | 0,07% | 5 | 0,33% | 5 | 0,33% | 5 | 0,33% |
| Klunzinger (1871) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Motomura et al. (2011) | 5 | 0,07% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Myers (1991) | 5 | 0,07% | 5 | 0,33% | 5 | 0,33% | 5 | 0,33% |
| Nakamura (1985) | 5 | 0,07% | 5 | 0,33% | 5 | 0,33% | 5 | 0,33% |
| Polanco & Acero (2016) | 5 | 0,07% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Randall & Rocha (2009) | 5 | 0,07% | 5 | 0,33% | 5 | 0,33% | 5 | 0,33% |
| Reece et al. (2010) | 5 | 0,07% | 5 | 0,33% | 5 | 0,33% | 5 | 0,33% |
| Rignault & Chevallier (2017) | 5 | 0,07% | 5 | 0,33% | 5 | 0,33% | 5 | 0,33% |
| Vaslet & Agrnsm (2018) | 5 | 0,07% | 5 | 0,33% | 5 | 0,33% | 5 | 0,33% |
| Brugneaux & Pérès (2006) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Cuvier & Valenciennes (1830-1832) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourmanoir & Rivaton (1979) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1899) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goiran & Shine (2020) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Gomon (2006) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Jordan (1894) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith (2002) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Lacepède (1801) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Pascal (2009) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Marshall et al. (2009) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| McCosker (2010) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Morris (2012) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Pinault et al. (2018) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Randall & Earle (1999) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Randall & Pyle (2001) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Randall & Wrobel (1988) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Richer de Forges et al. (2005) | 4 | 0,05% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Risso (1810) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1827) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1835) | 4 | 0,05% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Seret & Shao (2011) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Séret (2014) | 4 | 0,05% | 3 | 0,2% | 2 | 0,13% | 3 | 0,2% |
| Shepherd et al. (2020) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Uicn et al. (2019) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Walbaum (1792) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams et al. (2013) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Winterbottom & Hoese (2015) | 4 | 0,05% | 4 | 0,26% | 4 | 0,26% | 4 | 0,26% |
| Allen & Erdmann (2020) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Bloch & Schneider (1801) | 3 | 0,04% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Borsa et al. (2014) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Cohen et al. (1990) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Collet et al. (2017) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Delrieu-Trottin et al. (2014) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Diaz & Cuzange (2009) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Firmat et al. (2012) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Gargominy et al. (1996) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Goulletquer (2016) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Greenfield & Suzuki (2012) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Hemida et al. (2003) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutchinson et al. (2019) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Keith et al. (2014) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Kottelat ( 2013) | 3 | 0,04% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Larson (2002) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Linnaeus (1766) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louis et al. (1992) | 3 | 0,04% | 1 | 0,07% | 1 | 0,07% | 0 | 0% |
| Lowe et al. (2007) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| McCosker & Hibino (2015) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Motomura & Kanade (2015) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Mourier et al. (2013) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Perez Canto (1886) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1887) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1902) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero et al. (2013) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Rafinesque (1810) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schultz (1943) | 3 | 0,04% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Shao (2010) | 3 | 0,04% | 3 | 0,2% | 3 | 0,2% | 3 | 0,2% |
| Swainson (1839) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1933) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ahnelt (2020) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Amaoka & Seret (2005) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Amaoka et al. (2006) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Baird & Girard (1853) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bearez et al. (2013) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Bennett (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertin (1928) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Bleeker (1852) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1858) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1858) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785-1795) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bohlke & Randall (1981) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Bonaparte (1837) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1788) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collette (2003) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Curd et al. (2015) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Cuvier & Valenciennes (1836) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 2 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Dawson (1984) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Delventhal & Mooi (2023) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Düben & Koren (1846) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel et al. (2005) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| European Nucleotide Archive (2019) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Evermann & Clark (1928) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forskål (1775) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fraser & Randall (2003) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Fraser & Randall (2011) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Fricke (1998) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke (2004) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fritzsche (1981) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Fujiwara & Motomura (2020) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Garman (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geange (2010) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Geoffroy Saint-Hilaire ([1817]) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gon & Allen (2012) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Goode & Bean (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Griffith & Smith (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guichenot (1848) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Günther (1861) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1880) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ho (2015) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Hoban & Williams (2020) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Hoese & Larson (2005) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutchins & Randall (1982) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Ifremer (2024) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Johnson (1863) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Jordan & Starks (1904) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Karnella & Lachner (1981) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Keith & Marquet (2006) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2009) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Keith et al. (2011) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Kyne et al. (2016) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Lacepède (1800) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1803) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lecchini & Williams (2004) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Letourneur & Maggiorani (1995) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Lowe (1834) | 2 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Lowe (1838) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1843) | 2 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Macdonald & Barron (1868) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marquet et al. (2003) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Matsunuma & Motomura (2013) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Matsunuma & Motomura (2018) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| McCosker & Randall (2005) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Mccosker (1998) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| McCosker (2006) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Mennesson et al. (2019) | 2 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Menzies (1791) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millot et al. (2023) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Mitchill (1815) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Møller et al. (2004) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Monti et al. (2010) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Mooi (1998) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Morishita & Motomura (2020) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Nardo (1827) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Okamoto & Motomura (2011) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Okamoto (2016) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Palko et al. (1982) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Pallas (1770) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas [1814] | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parenti & Maciolek (1996) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Parmentier et al. (2018) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Parmentier (2004) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Pennant (1776) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1851-1854) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prokofiev (2021) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Randall & Earle (1999) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Randall & Greenfield (2004) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Randall & Lubbock (1981) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Pyle (1989) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Randall & Randall (1981) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Randall & Steene (1983) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Randall et al. (2008) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall (1988) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Randall (2004) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall (2004) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Randall (2006) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall (2011) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Richardson (1845) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1848) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Santini (2006) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Schmidt (1912) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schomburgk (1848) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw & Nodder (1792-1793) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shepherd et al. (2023) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Shibuya & Motomura (2021) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Smith-vaniz & Walsh (2019) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Snyder (1904) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Tea & Larson (2023) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Tea et al. (2020) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Teichert et al. (2013) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Victor (2017) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Weber (1913) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1931) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams & Lecchini (2004) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Williams (2018) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Winterbottom & Burridge (1989) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Winterbottom & Burridge (1993) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Winterbottom & Harold (2005) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| (2020) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
| Agassiz (1833-1843) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alcock (1890) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alcock (1894) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen & Walsh (2015) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Allen (1995) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Anonyme (1968) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Anonyme (1968) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Anonyme (1968) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Anonyme (1968) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Anonyme ([2018]) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Anonyme ([2018]) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Atwood (1869) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Audige (1927) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Australian Museum (2020) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Ayres (1848) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Barthélémy (1926) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bath (2004) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bauchot et al. (1982) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bennett (1832) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1816) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1847) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1853) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1854) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1855) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1856) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1858) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785-1795) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1790) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1792) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1794) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bodilis et al. (2011) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bohlke (1951) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bouchon-Navaro et al. (1992) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 0 | 0% |
| Bourjon & Fricke (2019) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bourjon & Fricke (2020) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bourret (1968) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bourret (1968) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bray & Cribb (2002) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Brito Capello (1868) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Brosse et al. (2021) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Buray et al. (2009) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Caillot et al. (1999) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Castle (2001) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Castle (2001) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Causse & Hautecoeur (2006) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Causse (2005) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cazio & Isnard (1920) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Chen (2013) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Clua & Imirizaldu (2017) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Clua & Planes (2019) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Clua et al. (2016) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Clua et al. (2021) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cohn et al. (2019) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Couteyen (2006) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cuvier & Valenciennes (1828-1830) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Day (1865) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Desbrosses (1935) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Downie et al. (2011) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Duncker & Mohr (1926) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Durville et al. (2009) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Durville (2020) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Euphrasen (1791) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Foata et al. (2012) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Forest (1946) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Fourmanoir (1966) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fraser-brunner (1950) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke et al. (2017) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Fricke (2002) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Fricke (2014) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Fritzsche (1980) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerovasileiou et al. (2020) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Gill (1862) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (2022) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Girard (1859) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondot et al. (2015) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren (1981) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Günther (1859) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1860) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1866) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1870) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1876) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1878) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ho (2015) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoshino & Motomura (2022) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (1990) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (1991) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (1991) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (1991) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (1997) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (1997) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (1997) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (1997) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hulley (2000) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Ifremer (2009) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Iglésias (2012) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Jordan & Evermann (1903) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Fowler (1902) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1880) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Jordan (1922) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Snyder (1904) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan et al. (1927) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1892) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kamohara (1938) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kawai & Causse (2017) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Kawai (2016) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Keith & Dorson (2003) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Keith et al. (1999) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2002) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Keith et al. (2011) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Kenaley (2006) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Klausewitz & von Hentig (1975) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1802) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Lassauce et al. (2020) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Last et al. (2016) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Lavier (1936) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Le Bail et al. (2012) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Legendre (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1830-1831) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1822) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lim et al. (2002) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Lizé (2018) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1841) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1846) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Lowe (1852) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maeda et al. (2011) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matsunuma & Motomura (2014) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Meek & Hildebrand (1923) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mochizuki & Shirakihara (1983) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Moravec & Justine (2014) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Moreau (1881) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Motomura et al. (2010) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Mourier (2012) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1884) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1887) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Antonelli, Venezia. 128 pp.">Nardo (1847) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nelson-Smith et al. (2014) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël, Meunier (2010) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Ocea & Consult' (2015) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osbeck (1765) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parenti (2021) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Pascal et al. (2006) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Pellegrin (1912) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pietsch (2004) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Pietsch (2004) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Pietsch (2006) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Pinault et al. (2014) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Plessis (1987) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Pogonoski & Gill (2021) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prokofiev (2017) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Prokofiev (2017) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Questel (2017) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Raibaut et al. (1979) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Lobel (2003) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall et al. (2015) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Randall (2013) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Ranzani (1839) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annals & Magazine of Natural History Series 9, 15: 561-567.">Regan (1925) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1846) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rigby & Adamson (1997) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Risso (1820) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saville-kent (1889) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schilling (2018) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Schultz et al. (1953) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherborn (1895) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherborn (1925) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smales et al. (2007) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Smith (1917) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Springer & Fricke (2000) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Springer & Waller (1969) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1941) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1867) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1876) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1900) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taquet (1994) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Tea & Gill (2017) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Thorp (1969) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tongboonkua et al. (2018) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Tregarot et al. (2015) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Tsadok et al. (2015) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Uyeno et al. (1983) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Vaillant (1888) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van & Kampen (1907) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wantiez (2000) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Whitley (1929) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1948) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel & Fricke (2022) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Wickel et al. (2016) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Wickel et al. (2020) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Yang et al. (2019) | 1 | 0,01% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Yarrell (1836) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
