Scorpaeniformes
Scorpaeniformes
136 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) | 126 | 15% | 123 | 42,71% | 123 | 43,31% | 123 | 43,01% |
| Siu et al. (2017) | 47 | 5,6% | 47 | 16,32% | 47 | 16,55% | 47 | 16,43% |
| Fricke et al. (2009) | 36 | 4,29% | 34 | 11,81% | 34 | 11,97% | 34 | 11,89% |
| Béarez et al. (2017) | 30 | 3,57% | 29 | 10,07% | 29 | 10,21% | 28 | 9,79% |
| Delrieu-Trottin et al. (2015) | 25 | 2,98% | 23 | 7,99% | 23 | 8,1% | 23 | 8,04% |
| Kulbicki (comm. pers., 2011) | 25 | 2,98% | 22 | 7,64% | 22 | 7,75% | 22 | 7,69% |
| Wickel & Jamon (2010) | 20 | 2,38% | 20 | 6,94% | 20 | 7,04% | 20 | 6,99% |
| Fourt et al. (2017) | 18 | 2,14% | 16 | 5,56% | 16 | 5,63% | 14 | 4,9% |
| Williams et al. (2006) | 17 | 2,02% | 16 | 5,56% | 16 | 5,63% | 16 | 5,59% |
| Bacchet et al. (2007) | 16 | 1,9% | 15 | 5,21% | 15 | 5,28% | 15 | 5,24% |
| Linnaeus (1758) | 14 | 1,67% | 4 | 1,39% | 4 | 1,41% | 4 | 1,4% |
| Motomura et al. (2011) | 13 | 1,55% | 12 | 4,17% | 12 | 4,23% | 12 | 4,2% |
| Allen (comm. pers., 2009) | 12 | 1,43% | 10 | 3,47% | 10 | 3,52% | 10 | 3,5% |
| Del et al. (1997) | 12 | 1,43% | 10 | 3,47% | 10 | 3,52% | 10 | 3,5% |
| Duhamel et al. (2005) | 10 | 1,19% | 10 | 3,47% | 8 | 2,82% | 10 | 3,5% |
| Smith (1997) | 10 | 1,19% | 10 | 3,47% | 10 | 3,52% | 10 | 3,5% |
| Chernova & Duhamel (2003) | 9 | 1,07% | 9 | 3,12% | 7 | 2,46% | 9 | 3,15% |
| Duhamel & King (2007) | 9 | 1,07% | 9 | 3,12% | 9 | 3,17% | 9 | 3,15% |
| Freyhof et al. (2005) | 9 | 1,07% | 8 | 2,78% | 8 | 2,82% | 8 | 2,8% |
| Dettaï et al. (2011) | 8 | 0,95% | 7 | 2,43% | 7 | 2,46% | 7 | 2,45% |
| Nelson-Smith et al. (2014) | 8 | 0,95% | 6 | 2,08% | 6 | 2,11% | 6 | 2,1% |
| Cuvier & Valenciennes (1829) | 6 | 0,71% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1801) | 6 | 0,71% | 0 | 0% | 0 | 0% | 0 | 0% |
| Motomura & Kanade (2015) | 6 | 0,71% | 6 | 2,08% | 6 | 2,11% | 6 | 2,1% |
| Fricke et al. (2013) | 5 | 0,6% | 5 | 1,74% | 5 | 1,76% | 5 | 1,75% |
| Matsunuma et al. (2017) | 5 | 0,6% | 3 | 1,04% | 3 | 1,06% | 3 | 1,05% |
| Questel (2020) | 5 | 0,6% | 5 | 1,74% | 5 | 1,76% | 5 | 1,75% |
| Rafinesque Schmaltz (1810) | 5 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Earle (2000) | 5 | 0,6% | 4 | 1,39% | 4 | 1,41% | 4 | 1,4% |
| Richer de Forges et al. (2005) | 5 | 0,6% | 5 | 1,74% | 5 | 1,76% | 5 | 1,75% |
| Breton (2014) | 4 | 0,48% | 4 | 1,39% | 4 | 1,41% | 4 | 1,4% |
| Chabanet & Durville (2005) | 4 | 0,48% | 4 | 1,39% | 4 | 1,41% | 4 | 1,4% |
| Fourmanoir & Rivaton (1979) | 4 | 0,48% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Morris (2012) | 4 | 0,48% | 4 | 1,39% | 4 | 1,41% | 4 | 1,4% |
| Questel & Le Quellec (2012) | 4 | 0,48% | 4 | 1,39% | 4 | 1,41% | 4 | 1,4% |
| Simian et al. (2022) | 4 | 0,48% | 4 | 1,39% | 4 | 1,41% | 4 | 1,4% |
| Swainson (1839) | 4 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2019) | 4 | 0,48% | 4 | 1,39% | 4 | 1,41% | 4 | 1,4% |
| Andriashev (1982) | 3 | 0,36% | 3 | 1,04% | 2 | 0,7% | 3 | 1,05% |
| Băcescu & Băcescu-Meşter (1964) | 3 | 0,36% | 3 | 1,04% | 3 | 1,06% | 3 | 1,05% |
| Bloch & Schneider (1801) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1896) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louis et al. (1992) | 3 | 0,36% | 3 | 1,04% | 3 | 1,06% | 3 | 1,05% |
| Randall & Greenfield (2004) | 3 | 0,36% | 3 | 1,04% | 3 | 1,06% | 3 | 1,05% |
| Rignault & Chevallier (2017) | 3 | 0,36% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Van Guelpen (2016) | 3 | 0,36% | 3 | 1,04% | 3 | 1,06% | 3 | 1,05% |
| Ascanius (1772) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Astruch et al. (2022) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Bloch & Schneider (1801) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1837) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chungthanawong & Motomura (2022) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Collett (1875) | 2 | 0,24% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Cuvier (1829) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delaroche (1809) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donovan (1803-08) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Euphrasen (1786) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1885) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourriére et al. (2014) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Fricke et al. (2013) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Fricke (2004) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Köhler (1896) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kulbicki et al. (2000) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Lizé (2018) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Matsunuma & Motomura (2013) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Matsunuma & Motomura (2018) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Motomura & Causse (2011) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Motomura et al. (2012) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Poss & Duhamel (1991) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Richard et al. (1982) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sideleva (2009) | 2 | 0,24% | 2 | 0,69% | 2 | 0,7% | 2 | 0,7% |
| Anonyme. (2004) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Anonyme. (2004) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Béarez & Séret (2009) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Bleeker (1855) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785-1795) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro et al. (1992) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Bouchon-Navaro et al. (2005) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Bravničar et al. (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Causse (2005) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Couch (1838) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1833) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Fleming (1828) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourmanoir (1970) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke et al. (2023) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Frickel (2020) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Ginsburg (1953) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gronow (1854) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1882) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1888) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Ho (2015) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Ho (2015) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Ho (2015) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoshino & Motomura (2022) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Ifremer (2009) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Jordan & Evermann (1898) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Kawai (2016) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Keith et al. (2011) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Annales de l'Université de Lyon, 26: 475-526, Pls. 26-27.">Koehler (1896) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1845) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lefèbvre et al. (2019) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Linnaeus (1766) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1841) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mahé et al. (2013) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Matsunuma & Motomura (2014) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Matsunuma & Motomura (2018) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Mitchill (1815) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Motomura & Causse (2010) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Motomura et al. (2010) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Motomura (2002) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Müller (1776) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naranji et al. (2022) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Nilsson (1832) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Pinault et al. (2013) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Poss (1982) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Poss (2012) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Poss (2012) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Questel (2017) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Rafinesque (1810) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richards et al. (1999) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Romanov et al. (2021) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Rousseau (2010) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Sellier et al. (2016) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Tortonese (1959) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Tregarot et al. (2015) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Walbaum (1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wantiez (comm. pers., 2008) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
| Zhukov (2020) | 1 | 0,12% | 1 | 0,35% | 1 | 0,35% | 1 | 0,35% |
