Béloniformes
Beloniformes
85 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) | 31 | 6,55% | 28 | 33,73% | 28 | 38,89% | 27 | 35,06% |
| Siu et al. (2017) | 22 | 4,65% | 22 | 26,51% | 21 | 29,17% | 20 | 25,97% |
| Fourriére et al. (2014) | 20 | 4,23% | 18 | 21,69% | 17 | 23,61% | 18 | 23,38% |
| Fricke et al. (2009) | 15 | 3,17% | 14 | 16,87% | 14 | 19,44% | 13 | 16,88% |
| Kulbicki (comm. pers., 2011) | 12 | 2,54% | 11 | 13,25% | 10 | 13,89% | 11 | 14,29% |
| Smith (1997) | 10 | 2,11% | 8 | 9,64% | 6 | 8,33% | 8 | 10,39% |
| Béarez et al. (2017) | 9 | 1,9% | 9 | 10,84% | 9 | 12,5% | 8 | 10,39% |
| Wickel & Jamon (2010) | 9 | 1,9% | 9 | 10,84% | 9 | 12,5% | 8 | 10,39% |
| Cuvier & Valenciennes (1846) | 8 | 1,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rafinesque Schmaltz (1810) | 8 | 1,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 7 | 1,48% | 7 | 8,43% | 7 | 9,72% | 4 | 5,19% |
| Delrieu-Trottin et al. (2015) | 5 | 1,06% | 4 | 4,82% | 1 | 1,39% | 4 | 5,19% |
| Questel & Le Quellec (2012) | 5 | 1,06% | 5 | 6,02% | 5 | 6,94% | 3 | 3,9% |
| Fricke et al. (2013) | 4 | 0,85% | 4 | 4,82% | 4 | 5,56% | 3 | 3,9% |
| Lacepède (1803) | 4 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 4 | 0,85% | 3 | 3,61% | 3 | 4,17% | 2 | 2,6% |
| Collette (2003) | 3 | 0,63% | 2 | 2,41% | 2 | 2,78% | 1 | 1,3% |
| Fowler (1919) | 3 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1866) | 3 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kulbicki et al. (2000) | 3 | 0,63% | 2 | 2,41% | 2 | 2,78% | 0 | 0% |
| Louis et al. (1992) | 3 | 0,63% | 2 | 2,41% | 2 | 2,78% | 0 | 0% |
| Allen (comm. pers., 2009) | 2 | 0,42% | 2 | 2,41% | 2 | 2,78% | 1 | 1,3% |
| Bacchet et al. (2007) | 2 | 0,42% | 2 | 2,41% | 2 | 2,78% | 2 | 2,6% |
| Cocco (1833) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1846) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1847) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Diaz & Cuzange (2009) | 2 | 0,42% | 2 | 2,41% | 2 | 2,78% | 1 | 1,3% |
| Gill (1863) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hohnbaum-hornschuch & van der Hoeven (1843) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kner & Steindachner (1867) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Bail et al. (2012) | 2 | 0,42% | 2 | 2,41% | 2 | 2,78% | 2 | 2,6% |
| Lesueur (1821) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nichols & Breder (1928) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1858-61) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annali del Museo Civico di Storia Naturale di Genova 18: 465-590, tavv. I-III.">Vinciguerra (1883) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams et al. (2006) | 2 | 0,42% | 2 | 2,41% | 2 | 2,78% | 1 | 1,3% |
| Béarez & Bouffandeau (2019) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 0 | 0% |
| Béarez & Séret (2009) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 1 | 1,3% |
| Beebe & Tee-van (1932) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1831) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1832) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1860) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1858) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1865) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro et al. (1992) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 0 | 0% |
| Bouchon-Navaro et al. (2005) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 0 | 0% |
| Breder & Nichols (1930) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooper (1863) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa (1862) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1848) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleming (1828) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gronow (1854) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Meek (1885) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1884) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kronen et al. (2009) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 1 | 1,3% |
| Legand (1950) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 1 | 1,3% |
| Linnaeus (1758) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 1 | 1,3% |
| Linnaeus (1761) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malm (1877) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ogilby (1908) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osburn & Nichols (1816) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1787) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1868) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero et al. (2006) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 1 | 1,3% |
| Rafinesque (1810) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Earle (2000) | 1 | 0,21% | 1 | 1,2% | 0 | 0% | 1 | 1,3% |
| Ranzani (1842) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1843) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1846) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richer de Forges et al. (2005) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 1 | 1,3% |
| Risso (1827) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schinz (1822) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (1997) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 1 | 1,3% |
| Snodgrass & Heller (1905) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Snyder (1904) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walbaum (1792) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel et al. (2014) | 1 | 0,21% | 1 | 1,2% | 1 | 1,39% | 1 | 1,3% |
| Yarrell (1837) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zilli (2021) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
