Poissons cartilagineux
315 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Béarez et al. (2017) | 106 | 7,15% | 104 | 37,01% | 104 | 37,14% | 104 | 37,01% |
| Fricke et al. (2011) | 73 | 4,93% | 65 | 23,13% | 64 | 22,86% | 65 | 23,13% |
| Siu et al. (2017) | 40 | 2,7% | 37 | 13,17% | 37 | 13,21% | 37 | 13,17% |
| Fricke et al. (2009) | 39 | 2,63% | 34 | 12,1% | 34 | 12,14% | 34 | 12,1% |
| Wickel & Jamon (2010) | 39 | 2,63% | 32 | 11,39% | 32 | 11,43% | 32 | 11,39% |
| Linnaeus (1758) | 24 | 1,62% | 4 | 1,42% | 4 | 1,43% | 4 | 1,42% |
| Müller & Henle (1841) | 24 | 1,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1837) | 21 | 1,42% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Compagno (1984) | 21 | 1,42% | 21 | 7,47% | 21 | 7,5% | 21 | 7,47% |
| Fourt et al. (2017) | 20 | 1,35% | 20 | 7,12% | 20 | 7,14% | 20 | 7,12% |
| Kiszka et al. (2009) | 18 | 1,21% | 15 | 5,34% | 15 | 5,36% | 15 | 5,34% |
| Rafinesque Schmaltz (1810) | 16 | 1,08% | 4 | 1,42% | 4 | 1,43% | 4 | 1,42% |
| Séret (2014) | 16 | 1,08% | 14 | 4,98% | 13 | 4,64% | 14 | 4,98% |
| Quero et al. (2013) | 15 | 1,01% | 14 | 4,98% | 14 | 5% | 14 | 4,98% |
| Delrieu-Trottin et al. (2015) | 14 | 0,94% | 12 | 4,27% | 12 | 4,29% | 12 | 4,27% |
| Questel & Le Quellec (2012) | 14 | 0,94% | 11 | 3,91% | 11 | 3,93% | 11 | 3,91% |
| Questel (2020) | 14 | 0,94% | 13 | 4,63% | 13 | 4,64% | 13 | 4,63% |
| Bacchet et al. (2007) | 13 | 0,88% | 10 | 3,56% | 10 | 3,57% | 10 | 3,56% |
| Compagno (1984) | 13 | 0,88% | 12 | 4,27% | 12 | 4,29% | 12 | 4,27% |
| Risso (1827) | 13 | 0,88% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 10 | 0,67% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1810) | 10 | 0,67% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Chabanet & Durville (2005) | 9 | 0,61% | 4 | 1,42% | 4 | 1,43% | 4 | 1,42% |
| Duhamel et al. (2005) | 9 | 0,61% | 7 | 2,49% | 7 | 2,5% | 7 | 2,49% |
| Fricke et al. (2013) | 9 | 0,61% | 9 | 3,2% | 8 | 2,86% | 9 | 3,2% |
| Nelson-Smith et al. (2014) | 9 | 0,61% | 7 | 2,49% | 7 | 2,5% | 7 | 2,49% |
| Béarez & Séret (2009) | 8 | 0,54% | 7 | 2,49% | 7 | 2,5% | 7 | 2,49% |
| Fourriére et al. (2014) | 8 | 0,54% | 7 | 2,49% | 7 | 2,5% | 7 | 2,49% |
| Bloch & Schneider (1801) | 7 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kulbicki et al. (2000) | 7 | 0,47% | 6 | 2,14% | 6 | 2,14% | 6 | 2,14% |
| Rafinesque (1810) | 7 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret & Last (2003) | 7 | 0,47% | 7 | 2,49% | 7 | 2,5% | 7 | 2,49% |
| Blainville (1816) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril (1865) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gronow (1854) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kulbicki (comm. pers., 2011) | 6 | 0,4% | 5 | 1,78% | 5 | 1,79% | 5 | 1,78% |
| Pavan-Kumar et al. (2018) | 6 | 0,4% | 5 | 1,78% | 5 | 1,79% | 5 | 1,78% |
| Simian et al. (2022) | 6 | 0,4% | 6 | 2,14% | 6 | 2,14% | 6 | 2,14% |
| Smith (1997) | 6 | 0,4% | 4 | 1,42% | 4 | 1,43% | 4 | 1,42% |
| Vaillant (1888) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1836-1844) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barbosa du Bocage & Brito Capello (1864) | 5 | 0,34% | 4 | 1,42% | 4 | 1,43% | 4 | 1,42% |
| Borsa et al. (2013) | 5 | 0,34% | 3 | 1,07% | 2 | 0,71% | 3 | 1,07% |
| Klunzinger (1871) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perez Canto (1886) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 5 | 0,34% | 5 | 1,78% | 5 | 1,79% | 5 | 1,78% |
| Williams et al. (2006) | 5 | 0,34% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Couch (1877) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourmanoir & Rivaton (1979) | 4 | 0,27% | 4 | 1,42% | 4 | 1,43% | 4 | 1,42% |
| Geoffroy Saint-Hilaire ([1817]) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1803) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1794) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Bail et al. (2012) | 4 | 0,27% | 4 | 1,42% | 4 | 1,43% | 4 | 1,42% |
| Malm (1877) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marshall et al. (2009) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1887) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pylaie (1835) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1906) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 4 | 0,27% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Rüppell (1835) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret & Last (2007) | 4 | 0,27% | 4 | 1,42% | 4 | 1,43% | 4 | 1,42% |
| Smith (1849) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1822) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béarez & Bouffandeau (2019) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Bouchon-Navaro et al. (2005) | 3 | 0,2% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Capape et al. (1999) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Chen et al. (2024) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Collett (1904) | 3 | 0,2% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Dekay (1842) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delaroche (1809) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Faria et al. (2013) | 3 | 0,2% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Fourmanoir (1979) | 3 | 0,2% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Garman (1913) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geoffroy Saint-Hilaire (1809) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren & Galil (2015) | 3 | 0,2% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Hutchinson et al. (2019) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Jordan (1898) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Lacepède (1802) | 3 | 0,2% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Larson (2002) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Last et al. (2016) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Last et al. (2016) | 3 | 0,2% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Leach (1818) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1818) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1822) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1881) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mourier et al. (2013) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Philippi (1902) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1858-61) | 3 | 0,2% | 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 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Shaw (1804) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1839) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tamayo et al. (2021) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Vaslet & Agrnsm (2018) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Westby (1988) | 3 | 0,2% | 3 | 1,07% | 3 | 1,07% | 3 | 1,07% |
| Whitley (1931) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1944) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen (2002) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Ascanius (1772) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ayres (1843) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bellotti (1878) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1810) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1852) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1863) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cocco (1836[1834]) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1838) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le règne animal distribué d'après son organisation, pour servir de base à l'histoire naturelle des animaux et d'introduction à l'anatomie comparée. Tome 2, contenant les reptiles, les poissons, les mollusques et les annélides. Déterville, Paris. i-xviii+1-532 pp. ">Cuvier (1816) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 2 | 0,13% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Odontaspis ferox" Agassiz dans le Golf de Gascogne. Bulletin de la Société zoologique de France, 54: 233-235.">Desbrosses (1930) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Deynat (2006) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Didier & Séret (2002) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Döderlein (1884) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donovan (1803-08) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fernandez-Carvalho et al. (2013) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Fischer (1884) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleming (1828) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1910) | 2 | 0,13% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Garman (1884) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Garman (1906) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1895) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Goode & Bean (1896) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Griffith & Smith (1834) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gunnerus (1765) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1876) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1877) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoese et al. (2011) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Howell Rivero (1936) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hureau (1966) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2009) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglésias & Lévy-Hartmann (2012) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Iglesias et al. (2022) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Kyne et al. (2016) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Lacepède (1800) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lafont (1873) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Last et al. (2007) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Legendre (1942) | 2 | 0,13% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Lesueur (1817) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letourneur et al. (2004) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1841) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1843) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Luchetti et al. (2011) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Lunel (1879) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macdonald & Barron (1868) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| McEachran & Seret (1987) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Mitchill (1815) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montagu (1818) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Motomura & Causse (2011) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Nakaya & Séret (1999) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Nardo (1827) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ogilby (1911) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2022) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Reinhardt (1825) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richer de Forges et al. (2005) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Séret & Last (2012) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Séret & Quod (2023) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Seret & Shao (2011) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Seret (1990) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Smith (1912) | 2 | 0,13% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Storer (1839) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Straube et al. (2011) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Tanaka (1911) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Temminck & Schlegel (1850) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN France & MNHN (2013) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
| Viana & Carvalho (2018) | 2 | 0,13% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Whitley (1939) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Agassiz (1833-1843) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alcock (1898) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen (comm. pers., 2009) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Anonyme (1965) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Atwood (1869) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bancroft (1832) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigelow et al. (1953) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1810) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blanc (1954) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1782-1784) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1784) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1839[1838]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1846) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouxin & Legendre (1952) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Breton (2014) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Brito Capello (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brito Capello (1868) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Jornal de Sciencias Mathematicas, Physicas e Naturaes, Academia Real das Sciencias de Lisboa 2(7): 233-238.">Brito Capello (1869) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2005) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1768) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buray et al. (2009) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Capape et al. (2002) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Capape et al. (2017) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Records of the Indian Museum (Calcutta). 2(4): 391-392.">Chaudhuri (1908) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clua & Imirizaldu (2017) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Clua et al. (2021) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Compagno et al. (2005) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Cornish (1885) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa (1829-1853) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Voigt (1832) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Day (1865) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Diaz & Cuzange (2009) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Dollfus (1926) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Engelhardt (1912) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| European Nucleotide Archive (2019) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Fleming (1841) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forskål (1775) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forster (1967) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fraser-brunner (1950) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke (1999) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Fries (1839) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Froese & Pauly (2020) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Garman (1908) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrick (1961) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1861) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1862) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1878) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1883) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1855) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondot et al. (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gistel (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guichenot (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1870) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holt & Byrne (1909) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Holt (1894) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hureau & Ozouf-Costaz (1980) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Hussakof (1909) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| IUCN (2014) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Jensen (1905) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1868) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Evermann (1903) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1880) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Snyder (1902) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Snyder (1904) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Starks (1901) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1895) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1798) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lapinski & Giovos (2019) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Lassauce et al. (2020) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Last et al. (2016) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Legendre (1923) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Lesson (1830-1831) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1887) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macleay (1881) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maddalena & Zuffa (2008) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Mckenzie (2016) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Meek & Hildebrand (1923) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mourier (2012) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1884) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1887) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nakaya (2012) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Antonelli, Venezia. 128 pp.">Nardo (1847) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nilsson (1832) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noronha (1926) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Notarbartolo et al. (2020) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Osbeck (1765) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas [1814] | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parnell (1845) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin & Loppé (1914) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Pennant (1812) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Péron (1807-1816) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pietschmann (1906) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pinault et al. (2013) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Plucàr (1846) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1865) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Quéro (2017) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Rafinesque (1820) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramsay & Ogilby (1887) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramsay (1880) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Earle (2000) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ranzani (1839) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1906) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1923) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1820) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Romanov et al. (2013) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Saemundsson (1922) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (1997) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Bulletin de la Station Biologique d'Arcachon, 34: 59-63.">Sigalas & Budker (1937) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Snodgrass & Heller (1905) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer & Waller (1969) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1941) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1944) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1950) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1846) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storm (1881) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tanaka (1918) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (1985) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2017) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Vaillant (1888) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van & Kampen (1907) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet et al. (2010) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Walbaum (1792) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| White (1937) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1929) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1930) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1934) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1943) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1950) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel et al. (2014) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Wickel et al. (2023) | 1 | 0,07% | 1 | 0,36% | 1 | 0,36% | 1 | 0,36% |
| Wood (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
