Pleuronectiformes
Pleuronectiformes
115 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) | 56 | 8,95% | 56 | 30,27% | 56 | 30,27% | 56 | 30,27% |
| Béarez et al. (2017) | 37 | 5,91% | 35 | 18,92% | 35 | 18,92% | 35 | 18,92% |
| Siu et al. (2017) | 23 | 3,67% | 23 | 12,43% | 23 | 12,43% | 23 | 12,43% |
| Linnaeus (1758) | 12 | 1,92% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Fricke et al. (2009) | 10 | 1,6% | 9 | 4,86% | 9 | 4,86% | 9 | 4,86% |
| Smith (1997) | 10 | 1,6% | 10 | 5,41% | 10 | 5,41% | 10 | 5,41% |
| Mihara & Amaoka (2004) | 8 | 1,28% | 8 | 4,32% | 8 | 4,32% | 8 | 4,32% |
| Randall (2005) | 8 | 1,28% | 8 | 4,32% | 8 | 4,32% | 8 | 4,32% |
| Breton (2014) | 7 | 1,12% | 6 | 3,24% | 6 | 3,24% | 6 | 3,24% |
| Allen (comm. pers., 2009) | 6 | 0,96% | 6 | 3,24% | 6 | 3,24% | 6 | 3,24% |
| Bonaparte (1837) | 6 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chabanaud (1927) | 6 | 0,96% | 5 | 2,7% | 5 | 2,7% | 5 | 2,7% |
| Quero (1997) | 6 | 0,96% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Risso (1810) | 6 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin et al. (2015) | 5 | 0,8% | 5 | 2,7% | 5 | 2,7% | 5 | 2,7% |
| Questel (2020) | 5 | 0,8% | 5 | 2,7% | 5 | 2,7% | 5 | 2,7% |
| Spitz et al. (2015) | 5 | 0,8% | 4 | 2,16% | 4 | 2,16% | 4 | 2,16% |
| Amaoka & Mihara (2000) | 4 | 0,64% | 4 | 2,16% | 4 | 2,16% | 4 | 2,16% |
| Duhamel et al. (2005) | 4 | 0,64% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Fourt et al. (2017) | 4 | 0,64% | 4 | 2,16% | 4 | 2,16% | 4 | 2,16% |
| Günther (1862) | 4 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaup (1858) | 4 | 0,64% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Questel & Le Quellec (2012) | 4 | 0,64% | 4 | 2,16% | 4 | 2,16% | 4 | 2,16% |
| Rafinesque (1810) | 4 | 0,64% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Richer de Forges et al. (2005) | 4 | 0,64% | 4 | 2,16% | 4 | 2,16% | 4 | 2,16% |
| Rodriguez (1996) | 4 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1836-1844) | 4 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bacchet et al. (2007) | 3 | 0,48% | 3 | 1,62% | 3 | 1,62% | 3 | 1,62% |
| Bouchon-Navaro et al. (2005) | 3 | 0,48% | 3 | 1,62% | 3 | 1,62% | 3 | 1,62% |
| Chanet et al. (2024) | 3 | 0,48% | 3 | 1,62% | 3 | 1,62% | 3 | 1,62% |
| Duhamel (1986) | 3 | 0,48% | 3 | 1,62% | 3 | 1,62% | 3 | 1,62% |
| Le Bail et al. (2012) | 3 | 0,48% | 3 | 1,62% | 3 | 1,62% | 3 | 1,62% |
| Louis et al. (1992) | 3 | 0,48% | 3 | 1,62% | 3 | 1,62% | 3 | 1,62% |
| Nelson-Smith et al. (2014) | 3 | 0,48% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Quero & Mauge (1989) | 3 | 0,48% | 3 | 1,62% | 3 | 1,62% | 3 | 1,62% |
| Rignault & Chevallier (2017) | 3 | 0,48% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Risso (1827) | 3 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walbaum (1792) | 3 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel & Jamon (2010) | 3 | 0,48% | 3 | 1,62% | 3 | 1,62% | 3 | 1,62% |
| Alili & Berrebi (1989) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Amaoka & Rivaton (1991) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Amaoka & Seret (2005) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Amaoka et al. (2006) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Bloch (1787) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delaroche (1809) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donovan (1802-08) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilchrist (1906) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kawai & Amaoka (2006) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Kawai et al. (2010) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Kawai et al. (2011) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Kulbicki (comm. pers., 2011) | 2 | 0,32% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Kulbicki et al. (2000) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Meeus et al. (1993) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Moreau (1874) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1881) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sardou (1986) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Shaw & Nodder (1795-1796) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1868) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams et al. (2006) | 2 | 0,32% | 2 | 1,08% | 2 | 1,08% | 2 | 1,08% |
| Alcock (1890) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Astarloa (2015) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Astarloa (2015) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Bartoli et al. (2001) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béarez & Causse (2002) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Béarez & Séret (2009) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Bennett (1831) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro & Louis (1986) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Brito Capello (1867) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chabanaud (1926) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chabanet & Durville (2005) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Collet et al. (2017) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Dollfus (1927) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Dollfus (1960) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Fabricius (1780) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1885) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleming (1828) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke et al. (2013) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Gill (1864) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1873-1874) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Golani et al. (2002) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1889) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hermant et al. (2010) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Kawai (2008) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Lacepède (1802) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legand (1950) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Legardere et al. (1979) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Lowe (1834) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malm (1877) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Minding (1832) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nilsson (1855) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman (1939) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Pallas [1814] | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pinault et al. (2018) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Quignard et al. (1982) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Rafinesque Schmaltz (1810) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rafinesque (1814) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Randall & Earle (2000) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Richard et al. (1982) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Rousseau (2010) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Schmidt (1915) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Sellier et al. (2016) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Sherborn (1895) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sigalas & Mandoul (1938) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Simian et al. (2022) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Steindachner (1868) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1839) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tongboonkua et al. (2018) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Torchio (1961) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vachon et al. (2007) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Vaillant (1888) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Voronina (2012) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
| Voronina (2012) | 1 | 0,16% | 1 | 0,54% | 1 | 0,54% | 1 | 0,54% |
