Osmériformes et Stomiiformes
102 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) | 67 | 12,93% | 67 | 34,9% | 67 | 35,08% | 66 | 34,55% |
Fricke et al. (2011) | 60 | 11,58% | 57 | 29,69% | 57 | 29,84% | 57 | 29,84% |
Duhamel et al. (2005) | 14 | 2,7% | 14 | 7,29% | 13 | 6,81% | 14 | 7,33% |
Ifremer (2009) | 11 | 2,12% | 10 | 5,21% | 10 | 5,24% | 9 | 4,71% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 11 | 2,12% | 11 | 5,73% | 11 | 5,76% | 11 | 5,76% |
Fricke et al. (2009) | 10 | 1,93% | 10 | 5,21% | 10 | 5,24% | 10 | 5,24% |
Siu et al. (2017) | 10 | 1,93% | 10 | 5,21% | 10 | 5,24% | 10 | 5,24% |
Fourt et al. (2017) | 8 | 1,54% | 8 | 4,17% | 8 | 4,19% | 6 | 3,14% |
Goode & Bean (1896) | 8 | 1,54% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Richer de Forges et al. (2005) | 7 | 1,35% | 7 | 3,65% | 7 | 3,66% | 7 | 3,66% |
Vaillant (1888) | 7 | 1,35% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Günther (1878) | 6 | 1,16% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Garman (1899) | 5 | 0,97% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Roupsard & Caillot (2018) | 5 | 0,97% | 5 | 2,6% | 5 | 2,62% | 5 | 2,62% |
Villarins et al. (2022) | 5 | 0,97% | 5 | 2,6% | 5 | 2,62% | 5 | 2,62% |
Cocco (1838) | 4 | 0,77% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1848) | 4 | 0,77% | 0 | 0% | 0 | 0% | 0 | 0% |
Kenaley (2007) | 4 | 0,77% | 4 | 2,08% | 4 | 2,09% | 4 | 2,09% |
Köhler (1896) | 4 | 0,77% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 4 | 0,77% | 0 | 0% | 0 | 0% | 0 | 0% |
Simian et al. (2022) | 4 | 0,77% | 4 | 2,08% | 4 | 2,09% | 3 | 1,57% |
Risso (1810) | 3 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Zugmayer (1911) | 3 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Ascanius (1775) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Brauer (1902) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Costa (1829-1853) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1849) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Denys et al. (2022) | 2 | 0,39% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Dettaï et al. (2011) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Fourriére et al. (2014) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Gill (1883) | 2 | 0,39% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Iglésias et al. (2020) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Linnaeus (1758) | 2 | 0,39% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Prokofiev (2020) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Prokofiev (2020) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Quero et al. (2009) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Risso (1820) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Vourey et al. (2017) | 2 | 0,39% | 2 | 1,04% | 2 | 1,05% | 2 | 1,05% |
Alcock (1898) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (1968) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Anonyme (1996) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme ([2018]) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Ayres (1848) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Beebe (1932) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Beebe (1933) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Bertin (1928) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Bloch & Schneider (1801) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Bloch (1782) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1782-1784) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourret (1968) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Bourret (1971) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Jena, G. Fischer. 468 pp.">Brauer (1906) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Collet (1896) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel & Pruvost (2001) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Duhamel (1989) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Duhamel (1996) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel (1996) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Duhamel (1998) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Duhamel (1998) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Duhamel (2005) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Esmark (1871) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
European Nucleotide Archive (2019) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Facciolà (1887) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Giglioli (1882) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Gill (1884) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1879) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Goode & Bean (1883) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Goren & Galil (2015) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Grey (1958) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Holt & Byrne (1910) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Kenaley (2006) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Lloyd (1906) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Lönnberg (1905) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsui & Rosenblatt (1979) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Mead & Böhlke (1953) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Nilsson (1832) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman (1930) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas [1814] | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Preynat (2013) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Prokofiev (2017) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Prokofiev (2017) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Rafinesque (1810) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Roule (1916) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Sardou (1980) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Sazonov (1999) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Sazonov (1999) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Sazonov (1999) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Sazonov (1999) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Sazonov (1999) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Séret (1997) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Simian et al. (2008) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Spitz & Quero (2004) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Vaillant (1886) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Walbaum (1792) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Welsh (1923) | 1 | 0,19% | 1 | 0,52% | 1 | 0,52% | 1 | 0,52% |
Yarrell (1839) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Zugmayer (1914) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |