Elasmobranches de France
Elasmobranchii
305 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) | 99 | 6,89% | 97 | 36,74% | 97 | 36,88% | 97 | 36,74% |
Fricke et al. (2011) | 68 | 4,74% | 60 | 22,73% | 59 | 22,43% | 60 | 22,73% |
Siu et al. (2017) | 40 | 2,79% | 37 | 14,02% | 37 | 14,07% | 37 | 14,02% |
Fricke et al. (2009) | 39 | 2,72% | 34 | 12,88% | 34 | 12,93% | 34 | 12,88% |
Wickel & Jamon (2010) | 38 | 2,65% | 31 | 11,74% | 31 | 11,79% | 31 | 11,74% |
Müller & Henle (1841) | 24 | 1,67% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 23 | 1,6% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Bonaparte (1837) | 21 | 1,46% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Compagno (1984) | 21 | 1,46% | 21 | 7,95% | 21 | 7,98% | 21 | 7,95% |
Fourt et al. (2017) | 18 | 1,25% | 18 | 6,82% | 18 | 6,84% | 18 | 6,82% |
Kiszka et al. (2009) | 18 | 1,25% | 15 | 5,68% | 15 | 5,7% | 15 | 5,68% |
Rafinesque Schmaltz (1810) | 16 | 1,11% | 4 | 1,52% | 4 | 1,52% | 4 | 1,52% |
Quero et al. (2013) | 15 | 1,04% | 14 | 5,3% | 14 | 5,32% | 14 | 5,3% |
Delrieu-Trottin et al. (2015) | 14 | 0,97% | 12 | 4,55% | 12 | 4,56% | 12 | 4,55% |
Questel & Le Quellec (2012) | 14 | 0,97% | 11 | 4,17% | 11 | 4,18% | 11 | 4,17% |
Questel (2020) | 14 | 0,97% | 13 | 4,92% | 13 | 4,94% | 13 | 4,92% |
Séret (2014) | 14 | 0,97% | 12 | 4,55% | 11 | 4,18% | 12 | 4,55% |
Bacchet et al. (2007) | 13 | 0,91% | 10 | 3,79% | 10 | 3,8% | 10 | 3,79% |
Compagno (1984) | 13 | 0,91% | 12 | 4,55% | 12 | 4,56% | 12 | 4,55% |
Risso (1827) | 12 | 0,84% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1788) | 10 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1810) | 10 | 0,7% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Chabanet & Durville (2005) | 9 | 0,63% | 4 | 1,52% | 4 | 1,52% | 4 | 1,52% |
Duhamel et al. (2005) | 9 | 0,63% | 7 | 2,65% | 7 | 2,66% | 7 | 2,65% |
Fricke et al. (2013) | 9 | 0,63% | 9 | 3,41% | 8 | 3,04% | 9 | 3,41% |
Nelson-Smith et al. (2014) | 9 | 0,63% | 7 | 2,65% | 7 | 2,66% | 7 | 2,65% |
Béarez & Séret (2009) | 8 | 0,56% | 7 | 2,65% | 7 | 2,66% | 7 | 2,65% |
Fourriére et al. (2014) | 8 | 0,56% | 7 | 2,65% | 7 | 2,66% | 7 | 2,65% |
Bloch & Schneider (1801) | 7 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Kulbicki et al. (2000) | 7 | 0,49% | 6 | 2,27% | 6 | 2,28% | 6 | 2,27% |
Rafinesque (1810) | 7 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret & Last (2003) | 7 | 0,49% | 7 | 2,65% | 7 | 2,66% | 7 | 2,65% |
Blainville (1816) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril (1865) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1913) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Gronow (1854) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Kulbicki (comm. pers., 2011) | 6 | 0,42% | 5 | 1,89% | 5 | 1,9% | 5 | 1,89% |
Pavan-Kumar et al. (2018) | 6 | 0,42% | 5 | 1,89% | 5 | 1,9% | 5 | 1,89% |
Simian et al. (2022) | 6 | 0,42% | 6 | 2,27% | 6 | 2,28% | 6 | 2,27% |
Smith (1997) | 6 | 0,42% | 4 | 1,52% | 4 | 1,52% | 4 | 1,52% |
Vaillant (1888) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1836-1844) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbosa du Bocage & Brito Capello (1864) | 5 | 0,35% | 4 | 1,52% | 4 | 1,52% | 4 | 1,52% |
Borsa et al. (2013) | 5 | 0,35% | 3 | 1,14% | 2 | 0,76% | 3 | 1,14% |
Klunzinger (1871) | 5 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Perez Canto (1886) | 5 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 5 | 0,35% | 5 | 1,89% | 5 | 1,9% | 5 | 1,89% |
Williams et al. (2006) | 5 | 0,35% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Couch (1877) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir & Rivaton (1979) | 4 | 0,28% | 4 | 1,52% | 4 | 1,52% | 4 | 1,52% |
Geoffroy Saint-Hilaire ([1817]) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1803) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1794) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Bail et al. (2012) | 4 | 0,28% | 4 | 1,52% | 4 | 1,52% | 4 | 1,52% |
Malm (1877) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Marshall et al. (2009) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Owen (1853) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1887) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Pylaie (1835) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Regan (1906) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard et al. (1982) | 4 | 0,28% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Rüppell (1835) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Seguigne et al. (2022) | 4 | 0,28% | 4 | 1,52% | 4 | 1,52% | 4 | 1,52% |
Séret & Last (2007) | 4 | 0,28% | 4 | 1,52% | 4 | 1,52% | 4 | 1,52% |
Smith (1849) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1822) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Béarez & Bouffandeau (2019) | 3 | 0,21% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Bouchon-Navaro et al. (2005) | 3 | 0,21% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Capape et al. (1999) | 3 | 0,21% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Dekay (1842) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Delaroche (1809) | 3 | 0,21% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Faria et al. (2013) | 3 | 0,21% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Fourmanoir (1979) | 3 | 0,21% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Garman (1913) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy Saint-Hilaire (1809) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Goren & Galil (2015) | 3 | 0,21% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Hemida et al. (2003) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,21% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Jordan (1898) | 3 | 0,21% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Lacepède (1802) | 3 | 0,21% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Last et al. (2016) | 3 | 0,21% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Leach (1818) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1818) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1822) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Maillard (1970) | 3 | 0,21% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Moreau (1881) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Mourier et al. (2013) | 3 | 0,21% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Philippi (1902) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1858-61) | 3 | 0,21% | 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 | 0,21% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Shaw (1804) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1839) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet & Agrnsm (2018) | 3 | 0,21% | 3 | 1,14% | 3 | 1,14% | 3 | 1,14% |
Whitley (1931) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1944) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Ayres (1843) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellotti (1878) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Blainville (1810) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1852) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1863) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Charbonnel (1990) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Cocco (1836[1834]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Collett (1904) | 2 | 0,14% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Couch (1838) | 2 | 0,14% | 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 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 2 | 0,14% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Odontaspis ferox" Agassiz dans le Golf de Gascogne. Bulletin de la Société zoologique de France, 54: 233-235.">Desbrosses (1930) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Deynat (2006) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Döderlein (1884) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1803-08) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Faber (1829) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernandez-Carvalho et al. (2013) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Fischer (1884) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleming (1828) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler (1910) | 2 | 0,14% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Garman (1884) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Garman (1906) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1896) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffith & Smith (1834) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunnerus (1765) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1876) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1877) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Howell Rivero (1936) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hureau (1966) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2009) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Iglésias & Lévy-Hartmann (2012) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Jung et al. (2024) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Kyne et al. (2016) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Lacepède (1800) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lafont (1873) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Last et al. (2007) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Lesueur (1817) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur et al. (2004) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1841) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1843) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lunel (1879) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
McEachran & Seret (1987) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Mitchill (1815) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1818) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Nakaya & Séret (1999) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Nardo (1827) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ogilby (1911) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2022) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Reinhardt (1825) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer de Forges et al. (2005) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Séret & Last (2012) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Seret (1990) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Smith (1912) | 2 | 0,14% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Storer (1839) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Straube et al. (2011) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Tanaka (1911) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Temminck & Schlegel (1850) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN France & MNHN (2013) | 2 | 0,14% | 2 | 0,76% | 2 | 0,76% | 2 | 0,76% |
Viana & Carvalho (2018) | 2 | 0,14% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Whitley (1939) | 2 | 0,14% | 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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Anonyme (1965) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Breton (2014) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Brito Capello (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brito Capello (1868) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Capape et al. (2002) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Capape et al. (2017) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Clua et al. (2021) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Compagno et al. (2005) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Fries (1839) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
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 (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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Hussakof (1909) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2014) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 & Seale (1926) | 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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Lacepède (1798) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapinski & Giovos (2019) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Lassauce et al. (2020) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Last et al. (2016) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Last et al. (2016) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Legendre (1923) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Legendre (1942) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Mckenzie (2016) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Pietschmann (1906) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pietschmann (1928) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Pinault et al. (2013) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Quéro (2017) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Bulletin de la Station Biologique d'Arcachon, 34: 59-63.">Sigalas & Budker (1937) | 1 | 0,07% | 1 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
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 | 0,38% | 1 | 0,38% | 1 | 0,38% |
Wood (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |