Poissons cartilagineux
313 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 | 7,14% | 104 | 36,88% | 104 | 37,01% | 104 | 36,88% |
Fricke et al. (2011) | 73 | 4,92% | 65 | 23,05% | 64 | 22,78% | 65 | 23,05% |
Siu et al. (2017) | 40 | 2,7% | 37 | 13,12% | 37 | 13,17% | 37 | 13,12% |
Fricke et al. (2009) | 39 | 2,63% | 34 | 12,06% | 34 | 12,1% | 34 | 12,06% |
Wickel & Jamon (2010) | 39 | 2,63% | 32 | 11,35% | 32 | 11,39% | 32 | 11,35% |
Linnaeus (1758) | 24 | 1,62% | 4 | 1,42% | 4 | 1,42% | 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 | 7,45% | 21 | 7,47% | 21 | 7,45% |
Fourt et al. (2017) | 20 | 1,35% | 20 | 7,09% | 20 | 7,12% | 20 | 7,09% |
Kiszka et al. (2009) | 18 | 1,21% | 15 | 5,32% | 15 | 5,34% | 15 | 5,32% |
Rafinesque Schmaltz (1810) | 16 | 1,08% | 4 | 1,42% | 4 | 1,42% | 4 | 1,42% |
Séret (2014) | 16 | 1,08% | 14 | 4,96% | 13 | 4,63% | 14 | 4,96% |
Quero et al. (2013) | 15 | 1,01% | 14 | 4,96% | 14 | 4,98% | 14 | 4,96% |
Delrieu-Trottin et al. (2015) | 14 | 0,94% | 12 | 4,26% | 12 | 4,27% | 12 | 4,26% |
Questel & Le Quellec (2012) | 14 | 0,94% | 11 | 3,9% | 11 | 3,91% | 11 | 3,9% |
Questel (2020) | 14 | 0,94% | 13 | 4,61% | 13 | 4,63% | 13 | 4,61% |
Bacchet et al. (2007) | 13 | 0,88% | 10 | 3,55% | 10 | 3,56% | 10 | 3,55% |
Compagno (1984) | 13 | 0,88% | 12 | 4,26% | 12 | 4,27% | 12 | 4,26% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Chabanet & Durville (2005) | 9 | 0,61% | 4 | 1,42% | 4 | 1,42% | 4 | 1,42% |
Duhamel et al. (2005) | 9 | 0,61% | 7 | 2,48% | 7 | 2,49% | 7 | 2,48% |
Fricke et al. (2013) | 9 | 0,61% | 9 | 3,19% | 8 | 2,85% | 9 | 3,19% |
Nelson-Smith et al. (2014) | 9 | 0,61% | 7 | 2,48% | 7 | 2,49% | 7 | 2,48% |
Béarez & Séret (2009) | 8 | 0,54% | 7 | 2,48% | 7 | 2,49% | 7 | 2,48% |
Fourriére et al. (2014) | 8 | 0,54% | 7 | 2,48% | 7 | 2,49% | 7 | 2,48% |
Bloch & Schneider (1801) | 7 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Kulbicki et al. (2000) | 7 | 0,47% | 6 | 2,13% | 6 | 2,14% | 6 | 2,13% |
Rafinesque (1810) | 7 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret & Last (2003) | 7 | 0,47% | 7 | 2,48% | 7 | 2,49% | 7 | 2,48% |
Simian et al. (2022) | 7 | 0,47% | 7 | 2,48% | 7 | 2,49% | 7 | 2,48% |
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 | 1,77% | 5 | 1,78% | 5 | 1,77% |
Pavan-Kumar et al. (2018) | 6 | 0,4% | 5 | 1,77% | 5 | 1,78% | 5 | 1,77% |
Smith (1997) | 6 | 0,4% | 4 | 1,42% | 4 | 1,42% | 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 | 1,42% | 4 | 1,42% |
Borsa et al. (2013) | 5 | 0,34% | 3 | 1,06% | 2 | 0,71% | 3 | 1,06% |
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 | 1,77% | 5 | 1,78% | 5 | 1,77% |
Williams et al. (2006) | 5 | 0,34% | 3 | 1,06% | 3 | 1,07% | 3 | 1,06% |
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 | 1,42% | 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 | 1,42% | 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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Rüppell (1835) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret & Last (2007) | 4 | 0,27% | 4 | 1,42% | 4 | 1,42% | 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 | 1,06% | 3 | 1,07% | 3 | 1,06% |
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 | 1,06% | 3 | 1,07% | 3 | 1,06% |
Collett (1904) | 3 | 0,2% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Dekay (1842) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Delaroche (1809) | 3 | 0,2% | 3 | 1,06% | 3 | 1,07% | 3 | 1,06% |
Faria et al. (2013) | 3 | 0,2% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
Fourmanoir (1979) | 3 | 0,2% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Hemida et al. (2003) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,2% | 3 | 1,06% | 3 | 1,07% | 3 | 1,06% |
Jordan (1898) | 3 | 0,2% | 3 | 1,06% | 3 | 1,07% | 3 | 1,06% |
Lacepède (1802) | 3 | 0,2% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Last et al. (2016) | 3 | 0,2% | 3 | 1,06% | 3 | 1,07% | 3 | 1,06% |
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% |
Maillard (1970) | 3 | 0,2% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
Moreau (1881) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Mourier et al. (2013) | 3 | 0,2% | 3 | 1,06% | 3 | 1,07% | 3 | 1,06% |
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 | 1,06% | 3 | 1,07% | 3 | 1,06% |
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 | 1,06% | 3 | 1,07% | 3 | 1,06% |
Vaslet & Agrnsm (2018) | 3 | 0,2% | 3 | 1,06% | 3 | 1,07% | 3 | 1,06% |
Whitley (1931) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1944) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Charbonnel (1990) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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% |
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% |
Jung et al. (2024) | 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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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% |
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 (1990) | 2 | 0,13% | 2 | 0,71% | 2 | 0,71% | 2 | 0,71% |
Smith (1912) | 2 | 0,13% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Anonyme (1965) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Breton (2014) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Brito Capello (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brito Capello (1868) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Capape et al. (2002) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Capape et al. (2017) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Clua et al. (2021) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Compagno et al. (2005) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Fries (1839) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Froese & Pauly (2020) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Hussakof (1909) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2014) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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% |
Joyeux (1923) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Lacepède (1798) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapinski & Giovos (2019) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Lassauce et al. (2020) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Last et al. (2016) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Legendre (1923) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Mckenzie (2016) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Pennant (1812) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Péron (1807-1816) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Petter (1969) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Pietschmann (1906) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinault et al. (2013) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Quéro (2017) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Bulletin de la Station Biologique d'Arcachon, 34: 59-63.">Sigalas & Budker (1937) | 1 | 0,07% | 1 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
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 | 0,35% | 1 | 0,36% | 1 | 0,35% |
Wood (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |