Elasmobranches de métropole
244 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 | 12,18% | 97 | 89,81% | 97 | 89,81% | 97 | 89,81% |
Linnaeus (1758) | 23 | 2,83% | 3 | 2,78% | 3 | 2,78% | 3 | 2,78% |
Müller & Henle (1841) | 23 | 2,83% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1837) | 21 | 2,58% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Fourt et al. (2017) | 18 | 2,21% | 18 | 16,67% | 18 | 16,67% | 18 | 16,67% |
Fricke et al. (2009) | 17 | 2,09% | 15 | 13,89% | 15 | 13,89% | 15 | 13,89% |
Fricke et al. (2011) | 17 | 2,09% | 17 | 15,74% | 17 | 15,74% | 17 | 15,74% |
Rafinesque Schmaltz (1810) | 16 | 1,97% | 4 | 3,7% | 4 | 3,7% | 4 | 3,7% |
Quero et al. (2013) | 15 | 1,85% | 14 | 12,96% | 14 | 12,96% | 14 | 12,96% |
Risso (1827) | 12 | 1,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel & Jamon (2010) | 12 | 1,48% | 11 | 10,19% | 11 | 10,19% | 11 | 10,19% |
Siu et al. (2017) | 11 | 1,35% | 11 | 10,19% | 11 | 10,19% | 11 | 10,19% |
Bonnaterre (1788) | 10 | 1,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1810) | 10 | 1,23% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Nelson-Smith et al. (2014) | 9 | 1,11% | 7 | 6,48% | 7 | 6,48% | 7 | 6,48% |
Compagno (1984) | 8 | 0,98% | 8 | 7,41% | 8 | 7,41% | 8 | 7,41% |
Bloch & Schneider (1801) | 7 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 7 | 0,86% | 6 | 5,56% | 6 | 5,56% | 6 | 5,56% |
Rafinesque (1810) | 7 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Blainville (1816) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Compagno (1984) | 6 | 0,74% | 6 | 5,56% | 6 | 5,56% | 6 | 5,56% |
Duméril (1865) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourriére et al. (2014) | 6 | 0,74% | 5 | 4,63% | 5 | 4,63% | 5 | 4,63% |
Garman (1913) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Gronow (1854) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al. (2009) | 6 | 0,74% | 5 | 4,63% | 5 | 4,63% | 5 | 4,63% |
Questel & Le Quellec (2012) | 6 | 0,74% | 6 | 5,56% | 6 | 5,56% | 6 | 5,56% |
Vaillant (1888) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1836-1844) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Bacchet et al. (2007) | 5 | 0,62% | 5 | 4,63% | 5 | 4,63% | 5 | 4,63% |
Barbosa du Bocage & Brito Capello (1864) | 5 | 0,62% | 4 | 3,7% | 4 | 3,7% | 4 | 3,7% |
Gmelin (1789) | 5 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Klunzinger (1871) | 5 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Perez Canto (1886) | 5 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 5 | 0,62% | 5 | 4,63% | 5 | 4,63% | 5 | 4,63% |
Couch (1877) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Delrieu-Trottin et al. (2015) | 4 | 0,49% | 4 | 3,7% | 4 | 3,7% | 4 | 3,7% |
Duhamel et al. (2005) | 4 | 0,49% | 3 | 2,78% | 3 | 2,78% | 3 | 2,78% |
Fricke et al. (2013) | 4 | 0,49% | 4 | 3,7% | 4 | 3,7% | 4 | 3,7% |
Geoffroy Saint-Hilaire ([1817]) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1803) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1794) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Malm (1877) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Owen (1853) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1887) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Pylaie (1835) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Regan (1906) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Rüppell (1835) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Simian et al. (2022) | 4 | 0,49% | 4 | 3,7% | 4 | 3,7% | 4 | 3,7% |
Smith (1849) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1822) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Capape et al. (1999) | 3 | 0,37% | 3 | 2,78% | 3 | 2,78% | 3 | 2,78% |
Dekay (1842) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Delaroche (1809) | 3 | 0,37% | 3 | 2,78% | 3 | 2,78% | 3 | 2,78% |
Garman (1913) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy Saint-Hilaire (1809) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Goren & Galil (2015) | 3 | 0,37% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Hemida et al. (2003) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1898) | 3 | 0,37% | 3 | 2,78% | 3 | 2,78% | 3 | 2,78% |
Lacepède (1802) | 3 | 0,37% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Leach (1818) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1818) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1822) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Maillard (1970) | 3 | 0,37% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Moreau (1881) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1902) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1858-61) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Shaw (1804) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1839) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1931) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1944) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Ayres (1843) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Béarez & Séret (2009) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Bellotti (1878) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Blainville (1810) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1852) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1863) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Charbonnel (1990) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Cocco (1836[1834]) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Collett (1904) | 2 | 0,25% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Couch (1838) | 2 | 0,25% | 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 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 2 | 0,25% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Odontaspis ferox" Agassiz dans le Golf de Gascogne. Bulletin de la Société zoologique de France, 54: 233-235.">Desbrosses (1930) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Döderlein (1884) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1803-08) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Faber (1829) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Faria et al. (2013) | 2 | 0,25% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Fernandez-Carvalho et al. (2013) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Fischer (1884) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleming (1828) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler (1910) | 2 | 0,25% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Garman (1884) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Garman (1906) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1896) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffith & Smith (1834) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunnerus (1765) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1877) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Howell Rivero (1936) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2009) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Jung et al. (2024) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Kulbicki (comm. pers., 2011) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Lacepède (1800) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lafont (1873) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1817) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1841) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1843) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lunel (1879) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
McEachran & Seret (1987) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Mitchill (1815) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1818) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Nardo (1827) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Ogilby (1911) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Reinhardt (1825) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1912) | 2 | 0,25% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Storer (1839) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Tanaka (1911) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Temminck & Schlegel (1850) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN France & MNHN (2013) | 2 | 0,25% | 2 | 1,85% | 2 | 1,85% | 2 | 1,85% |
Whitley (1939) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1833-1843) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Alcock (1898) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (comm. pers., 2009) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Atwood (1869) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bancroft (1832) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigelow et al. (1953) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Blainville (1810) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1782-1784) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1784) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1839[1838]) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1846) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouxin & Legendre (1952) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Breton (2014) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Brito Capello (1867) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Brito Capello (1868) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Jornal de Sciencias Mathematicas, Physicas e Naturaes, Academia Real das Sciencias de Lisboa 2(7): 233-238.">Brito Capello (1869) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünnich (1768) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Capape et al. (2017) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Records of the Indian Museum (Calcutta). 2(4): 391-392.">Chaudhuri (1908) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Compagno et al. (2005) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Cornish (1885) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Costa (1829-1853) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Voigt (1832) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Day (1865) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Dollfus (1926) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Engelhardt (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleming (1841) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Forskål (1775) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Forster (1967) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraser-brunner (1950) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fries (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1908) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrick (1961) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1862) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Girard (1855) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gistel (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1870) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Holt (1894) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hussakof (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jensen (1905) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1868) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Evermann (1903) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1880) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Snyder (1902) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Snyder (1904) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Starks (1901) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1895) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Joyeux (1923) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Lacepède (1798) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapinski & Giovos (2019) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Last et al. (2016) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Legendre (1923) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Legendre (1942) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1830-1831) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lütken (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Macleay (1881) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddalena & Zuffa (2008) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Meek & Hildebrand (1923) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1884) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Antonelli, Venezia. 128 pp.">Nardo (1847) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Nilsson (1832) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Noronha (1926) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Notarbartolo et al. (2020) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Osbeck (1765) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas [1814] | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnell (1845) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pellegrin & Loppé (1914) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Pennant (1812) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Péron (1807-1816) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Petter (1969) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Pietschmann (1906) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Plucàr (1846) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1865) | 1 | 0,12% | 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 » | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Quéro (2017) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Rafinesque (1820) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramsay & Ogilby (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramsay (1880) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ranzani (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Regan (1906) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Regan (1923) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1820) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Romanov et al. (2013) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Saemundsson (1922) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Scoresby (1820) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Scoresby (1820) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret (2014) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Bulletin de la Station Biologique d'Arcachon, 34: 59-63.">Sigalas & Budker (1937) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Springer & Waller (1969) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Springer (1941) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Springer (1944) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Springer (1950) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1867) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Storer (1846) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Storer (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Storer (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Storm (1881) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Tanaka (1918) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor (1985) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaillant (1888) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Van & Kampen (1907) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet & Agrnsm (2018) | 1 | 0,12% | 1 | 0,93% | 1 | 0,93% | 1 | 0,93% |
Walbaum (1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
White (1937) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1929) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1930) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1934) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1937) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1943) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1950) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |