Anguilles et murènes
Anguilliformes, Elopiformes, Notacanthiformes, Saccopharyngiformes et Albuliformes
182 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fricke et al. (2011) | 144 | 10,62% | 140 | 40,82% | 140 | 41,06% | 140 | 41,06% |
Siu et al. (2017) | 126 | 9,29% | 124 | 36,15% | 124 | 36,36% | 124 | 36,36% |
Fricke et al. (2009) | 73 | 5,38% | 71 | 20,7% | 70 | 20,53% | 70 | 20,53% |
Kulbicki (comm. pers., 2011) | 70 | 5,16% | 67 | 19,53% | 67 | 19,65% | 67 | 19,65% |
Delrieu-Trottin et al. (2015) | 65 | 4,79% | 64 | 18,66% | 64 | 18,77% | 64 | 18,77% |
Williams et al. (2006) | 51 | 3,76% | 47 | 13,7% | 47 | 13,78% | 47 | 13,78% |
Bacchet et al. (2007) | 38 | 2,8% | 37 | 10,79% | 37 | 10,85% | 37 | 10,85% |
Béarez et al. (2017) | 29 | 2,14% | 28 | 8,16% | 28 | 8,21% | 28 | 8,21% |
Allen (comm. pers., 2009) | 27 | 1,99% | 26 | 7,58% | 26 | 7,62% | 26 | 7,62% |
Kaup (1856) | 26 | 1,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel & Jamon (2010) | 23 | 1,7% | 23 | 6,71% | 22 | 6,45% | 23 | 6,74% |
Eudeline (2022) | 19 | 1,4% | 19 | 5,54% | 19 | 5,57% | 19 | 5,57% |
Rafinesque Schmaltz (1810) | 16 | 1,18% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Fricke et al. (2013) | 14 | 1,03% | 13 | 3,79% | 13 | 3,81% | 13 | 3,81% |
Questel (2020) | 14 | 1,03% | 14 | 4,08% | 14 | 4,11% | 14 | 4,11% |
Smith (1997) | 13 | 0,96% | 13 | 3,79% | 13 | 3,81% | 13 | 3,81% |
Fourriére et al. (2014) | 12 | 0,88% | 12 | 3,5% | 12 | 3,52% | 12 | 3,52% |
Questel & Le Quellec (2012) | 12 | 0,88% | 12 | 3,5% | 12 | 3,52% | 12 | 3,52% |
Bouchon-Navaro et al. (2005) | 11 | 0,81% | 10 | 2,92% | 10 | 2,93% | 10 | 2,93% |
Randall & Earle (2000) | 11 | 0,81% | 11 | 3,21% | 11 | 3,23% | 11 | 3,23% |
Séret (1997) | 9 | 0,66% | 9 | 2,62% | 9 | 2,64% | 9 | 2,64% |
Delaroche (1809) | 8 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2006) | 8 | 0,59% | 8 | 2,33% | 6 | 1,76% | 7 | 2,05% |
Keith et al. (2013) | 8 | 0,59% | 8 | 2,33% | 8 | 2,35% | 8 | 2,35% |
McCosker (2010) | 8 | 0,59% | 8 | 2,33% | 8 | 2,35% | 8 | 2,35% |
Risso (1810) | 7 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Béarez & Séret (2009) | 6 | 0,44% | 6 | 1,75% | 6 | 1,76% | 6 | 1,76% |
Chabanet & Durville (2005) | 6 | 0,44% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Facciolà (1883) | 6 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 6 | 0,44% | 6 | 1,75% | 6 | 1,76% | 6 | 1,76% |
Linnaeus (1758) | 6 | 0,44% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Louis et al. (1992) | 6 | 0,44% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Rafinesque (1810) | 6 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer de Forges et al. (2005) | 6 | 0,44% | 6 | 1,75% | 6 | 1,76% | 6 | 1,76% |
Risso (1827) | 6 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Costa (1829-1853) | 5 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel et al. (2005) | 5 | 0,37% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Hibino et al. (2016) | 5 | 0,37% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Reece et al. (2010) | 5 | 0,37% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Rousseau (2010) | 5 | 0,37% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Bouchon-Navaro & Louis (1986) | 4 | 0,29% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Charbonnel (1990) | 4 | 0,29% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Ifremer (2009) | 4 | 0,29% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Kulbicki et al. (2000) | 4 | 0,29% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Swainson (1839) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Bohlke & Randall (1981) | 3 | 0,22% | 3 | 0,87% | 3 | 0,88% | 3 | 0,88% |
Keith & Marquet (2011) | 3 | 0,22% | 3 | 0,87% | 3 | 0,88% | 3 | 0,88% |
Keith et al. (2002) | 3 | 0,22% | 3 | 0,87% | 3 | 0,88% | 3 | 0,88% |
Legand (1950) | 3 | 0,22% | 3 | 0,87% | 3 | 0,88% | 3 | 0,88% |
McCosker & Hibino (2015) | 3 | 0,22% | 3 | 0,87% | 3 | 0,88% | 3 | 0,88% |
Nelson-Smith et al. (2014) | 3 | 0,22% | 3 | 0,87% | 3 | 0,88% | 3 | 0,88% |
Poey (1858-61) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Quero & Saldanha (1995) | 3 | 0,22% | 3 | 0,87% | 3 | 0,88% | 3 | 0,88% |
Sbaihi et al. (2001) | 3 | 0,22% | 3 | 0,87% | 3 | 0,88% | 3 | 0,88% |
Bertin (1928) | 2 | 0,15% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bleeker (1854) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1795) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1846) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1788) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Castle & Bearez (1995) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Couch (1877) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir & Rivaton (1979) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1899) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilchrist (1906) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill & Ryder (1883) | 2 | 0,15% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Gill & Townsend (1897) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1883) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1895) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Goren & Galil (2015) | 2 | 0,15% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Guichenot (1850) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Heckel & Kner (1858) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Hibino & Kimura (2016) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Hibino et al. (2019) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Johnson (1862) | 2 | 0,15% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Karmovskaya (2003) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Kaup (1856) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Klausewitz & von Hentig (1975) | 2 | 0,15% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Letourneur et al. (2004) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Marquet et al. (2003) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
McCosker & Randall (2005) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Mccosker (1998) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
McCosker (2006) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Mulochau et al. (2019) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Osório (1909) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Quéro (2001) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Reinhardt (1837) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1845) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1848) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1840) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Saldanha & Quero (1994) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Schmidt (1912) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Simian et al. (2022) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Smith et al. (1981) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Smith et al. (2019) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Snyder (1904) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Vaillant (1888) | 2 | 0,15% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Valenciennes (1836-1844) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2014) | 2 | 0,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Alcock (1894) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (1971) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Anonyme (1971) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Anonyme ([2018]) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bartoli & Prévot (1986) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bauchot & Desoutter (1992) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bauchot et al. (1982) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Béarez & Bouffandeau (2019) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Béarez & Causse (2003) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Blache ([2018]) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bleeker (1853) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1858) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1788) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bodilis et al. (2012) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bohlke (1951) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Brauer (1902) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2005) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Brugneaux & Pérès (2006) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Caillot et al. (1999) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Castle (2001) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Castle (2001) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Causse (2005) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cazio & Isnard (1920) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Cormier (1984) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Couch (1832) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cousins et al. (2013) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Cuvier & Valenciennes (1846) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
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) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Denys et al. (2022) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Diaz & Cuzange (2009) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Duhamel (1998) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Ebner et al. (2016) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Escoubet et al. (1981) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Esposito et al. (2023) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Etcheberry & Abraham (2009) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Facciolà (1893) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Giglioli (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilbert (1891) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill & Ryder (1883) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1884) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Girard (1859) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1879) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode (1881) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Gronow (1854) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1878) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hatooka (1984) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Heckel (1847) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2022) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Iglésias et al. (2020) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Kamohara (1938) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1846-53) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1800) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Bail et al. (2012) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Lim et al. (2002) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Lowe (1852) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal & Trégarot (2012) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Mcbride et al. (2010) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Monti et al. (2010) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Myers (1991) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Norman (1930) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Peters (1852) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1877) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinault et al. (2013) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Preynat (2013) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Quéro & Delmas (1982) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Quero et al. (1997) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Richardson (1844-48) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Roule (1919) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Schultz et al. (1953) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Seret & Dingerkus (1992) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Séret (1993) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
UICN Comité français, OFB & MNHN (2021) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Vaillant (1882) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Van Guelpen (2016) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Wantiez (comm. pers., 2008) | 1 | 0,07% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Weber & Beaufort (1916) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |