Poissons des Antilles françaises
293 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Questel (2020) | 338 | 9,96% | 336 | 52,17% | 336 | 52,91% | 331 | 52,04% |
| Questel & Le Quellec (2012) | 307 | 9,04% | 291 | 45,19% | 291 | 45,83% | 288 | 45,28% |
| Smith (1997) | 252 | 7,42% | 232 | 36,02% | 226 | 35,59% | 232 | 36,48% |
| Bouchon-Navaro et al. (2005) | 228 | 6,72% | 188 | 29,19% | 188 | 29,61% | 187 | 29,4% |
| Bouchon-Navaro & Louis (1986) | 119 | 3,51% | 102 | 15,84% | 102 | 16,06% | 102 | 16,04% |
| Diaz & Cuzange (2009) | 104 | 3,06% | 96 | 14,91% | 96 | 15,12% | 95 | 14,94% |
| Brugneaux & Pérès (2006) | 85 | 2,5% | 76 | 11,8% | 76 | 11,97% | 76 | 11,95% |
| Fricke et al. (2011) | 64 | 1,89% | 62 | 9,63% | 62 | 9,76% | 60 | 9,43% |
| Fricke et al. (2009) | 60 | 1,77% | 56 | 8,7% | 56 | 8,82% | 53 | 8,33% |
| Louis et al. (1992) | 60 | 1,77% | 49 | 7,61% | 49 | 7,72% | 47 | 7,39% |
| Siu et al. (2017) | 53 | 1,56% | 49 | 7,61% | 49 | 7,72% | 47 | 7,39% |
| Rousseau (2010) | 48 | 1,41% | 46 | 7,14% | 46 | 7,24% | 46 | 7,23% |
| Béarez et al. (2017) | 45 | 1,33% | 45 | 6,99% | 45 | 7,09% | 43 | 6,76% |
| Wickel & Jamon (2010) | 43 | 1,27% | 41 | 6,37% | 41 | 6,46% | 40 | 6,29% |
| Poey (1858-61) | 36 | 1,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collette & Nauen (1983) | 30 | 0,88% | 30 | 4,66% | 26 | 4,09% | 30 | 4,72% |
| Questel (2017) | 30 | 0,88% | 30 | 4,66% | 30 | 4,72% | 30 | 4,72% |
| Bouchon-Navaro et al. (1992) | 25 | 0,74% | 22 | 3,42% | 22 | 3,46% | 21 | 3,3% |
| Fourriére et al. (2014) | 25 | 0,74% | 25 | 3,88% | 25 | 3,94% | 25 | 3,93% |
| Delrieu-Trottin et al. (2015) | 23 | 0,68% | 23 | 3,57% | 22 | 3,46% | 23 | 3,62% |
| Bacchet et al. (2007) | 22 | 0,65% | 21 | 3,26% | 21 | 3,31% | 21 | 3,3% |
| Le Bail et al. (2012) | 22 | 0,65% | 22 | 3,42% | 22 | 3,46% | 22 | 3,46% |
| Compagno (1984) | 21 | 0,62% | 21 | 3,26% | 21 | 3,31% | 21 | 3,3% |
| Lim et al. (2002) | 20 | 0,59% | 16 | 2,48% | 16 | 2,52% | 16 | 2,52% |
| Linnaeus (1758) | 19 | 0,56% | 3 | 0,47% | 3 | 0,47% | 3 | 0,47% |
| Deynat (2011) | 18 | 0,53% | 17 | 2,64% | 17 | 2,68% | 17 | 2,67% |
| Rafinesque Schmaltz (1810) | 18 | 0,53% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Monti et al. (2010) | 17 | 0,5% | 15 | 2,33% | 15 | 2,36% | 15 | 2,36% |
| Cuvier & Valenciennes (1833) | 16 | 0,47% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Whitehead et al. (1988) | 16 | 0,47% | 16 | 2,48% | 16 | 2,52% | 16 | 2,52% |
| Heemstra & Randall (1993) | 15 | 0,44% | 15 | 2,33% | 15 | 2,36% | 15 | 2,36% |
| Allen (1985) | 13 | 0,38% | 13 | 2,02% | 13 | 2,05% | 13 | 2,04% |
| Fricke et al. (2013) | 13 | 0,38% | 13 | 2,02% | 13 | 2,05% | 12 | 1,89% |
| UICN Comité français, OFB & MNHN (2021) | 13 | 0,38% | 13 | 2,02% | 13 | 2,05% | 13 | 2,04% |
| Berry & Smith-Vaniz (1978) | 12 | 0,35% | 12 | 1,86% | 12 | 1,89% | 12 | 1,89% |
| Compagno (1984) | 12 | 0,35% | 12 | 1,86% | 12 | 1,89% | 12 | 1,89% |
| Kulbicki et al. (2000) | 12 | 0,35% | 10 | 1,55% | 10 | 1,57% | 8 | 1,26% |
| Nakamura (1985) | 12 | 0,35% | 12 | 1,86% | 12 | 1,89% | 12 | 1,89% |
| Béarez & Séret (2009) | 11 | 0,32% | 10 | 1,55% | 10 | 1,57% | 10 | 1,57% |
| Cuvier & Valenciennes ([1832]) | 11 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kulbicki (comm. pers., 2011) | 11 | 0,32% | 9 | 1,4% | 9 | 1,42% | 9 | 1,42% |
| Cohen et al. (1990) | 10 | 0,29% | 10 | 1,55% | 10 | 1,57% | 10 | 1,57% |
| Müller & Henle (1841) | 10 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 10 | 0,29% | 5 | 0,78% | 5 | 0,79% | 4 | 0,63% |
| Soubeyran (2008) | 10 | 0,29% | 10 | 1,55% | 10 | 1,57% | 10 | 1,57% |
| Béarez & Bouffandeau (2019) | 9 | 0,27% | 9 | 1,4% | 9 | 1,42% | 8 | 1,26% |
| Bloch & Schneider (1801) | 8 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charbonnel (1990) | 8 | 0,24% | 6 | 0,93% | 6 | 0,94% | 4 | 0,63% |
| Gronow (1854) | 8 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simian et al. (2022) | 8 | 0,24% | 8 | 1,24% | 8 | 1,26% | 8 | 1,26% |
| Uicn et al. (2019) | 8 | 0,24% | 8 | 1,24% | 8 | 1,26% | 8 | 1,26% |
| Whitehead (1985) | 8 | 0,24% | 8 | 1,24% | 8 | 1,26% | 8 | 1,26% |
| Allen (comm. pers., 2009) | 7 | 0,21% | 4 | 0,62% | 4 | 0,63% | 3 | 0,47% |
| Chabanet & Durville (2005) | 7 | 0,21% | 6 | 0,93% | 6 | 0,94% | 6 | 0,94% |
| Pezold et al. (2015) | 7 | 0,21% | 7 | 1,09% | 7 | 1,1% | 7 | 1,1% |
| Randall & Vergara (1978) | 7 | 0,21% | 7 | 1,09% | 5 | 0,79% | 7 | 1,1% |
| Risso (1810) | 7 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet & Agrnsm (2018) | 7 | 0,21% | 7 | 1,09% | 7 | 1,1% | 7 | 1,1% |
| Williams et al. (2006) | 7 | 0,21% | 6 | 0,93% | 6 | 0,94% | 5 | 0,79% |
| Chabanaud (1927) | 6 | 0,18% | 5 | 0,78% | 5 | 0,79% | 5 | 0,79% |
| Cuvier & Valenciennes (1830-1832) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1846) | 6 | 0,18% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Nardo (1827) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2022) | 6 | 0,18% | 6 | 0,93% | 6 | 0,94% | 6 | 0,94% |
| Risso (1827) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1830) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 5 | 0,15% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Keith et al. (2006) | 5 | 0,15% | 5 | 0,78% | 5 | 0,79% | 5 | 0,79% |
| Keith et al. (2013) | 5 | 0,15% | 5 | 0,78% | 5 | 0,79% | 5 | 0,79% |
| Klunzinger (1871) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1800) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1801) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Trégarot (2012) | 5 | 0,15% | 4 | 0,62% | 4 | 0,63% | 4 | 0,63% |
| Polanco & Acero (2016) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2023) | 5 | 0,15% | 5 | 0,78% | 5 | 0,79% | 5 | 0,79% |
| Randall & Earle (2000) | 5 | 0,15% | 5 | 0,78% | 4 | 0,63% | 5 | 0,79% |
| Séret (1997) | 5 | 0,15% | 5 | 0,78% | 5 | 0,79% | 5 | 0,79% |
| Snodgrass & Heller (1905) | 5 | 0,15% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Swainson (1839) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1836-1844) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1847) | 4 | 0,12% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Fourt et al. (2017) | 4 | 0,12% | 4 | 0,62% | 4 | 0,63% | 4 | 0,63% |
| Keith et al. (2002) | 4 | 0,12% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Marceniuk et al. (2020) | 4 | 0,12% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Mitchill (1815) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Møller et al. (2005) | 4 | 0,12% | 4 | 0,62% | 4 | 0,63% | 4 | 0,63% |
| Morris (2012) | 4 | 0,12% | 4 | 0,62% | 4 | 0,63% | 4 | 0,63% |
| Rignault & Chevallier (2017) | 4 | 0,12% | 3 | 0,47% | 3 | 0,47% | 3 | 0,47% |
| Walbaum (1792) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1839) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Firmat et al. (2012) | 3 | 0,09% | 3 | 0,47% | 3 | 0,47% | 3 | 0,47% |
| Gargominy et al. (1996) | 3 | 0,09% | 3 | 0,47% | 3 | 0,47% | 3 | 0,47% |
| Gill (1862) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutchinson et al. (2019) | 3 | 0,09% | 3 | 0,47% | 3 | 0,47% | 3 | 0,47% |
| Kiszka et al. (2009) | 3 | 0,09% | 3 | 0,47% | 3 | 0,47% | 3 | 0,47% |
| Kottelat ( 2013) | 3 | 0,09% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Legand (1950) | 3 | 0,09% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Maréchal et al. (2006) | 3 | 0,09% | 3 | 0,47% | 3 | 0,47% | 3 | 0,47% |
| Philippi (1887) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1835) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1838) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1933) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2013) | 3 | 0,09% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Alley et al. (2023) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Anonyme (2016) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Bertin (1928) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Bleeker (1852) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1825) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brosse et al. (2021) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Brugneaux & Pérès (2005) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Costa (2011) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Durand (2016) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Evermann & Clark (1928) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontan (2019) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Fowler (1919) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geoffroy Saint-Hilaire ([1817]) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1896) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Griffith & Smith (1834) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harrison et al. (2007) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Hildebrand (1948) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holbrook (1855) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (1999) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Keith (2002) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Lacepède (1802) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Letourneur et al. (2004) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lowe (1838) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macdonald & Barron (1868) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Pérès (2007) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Marquet et al. (2003) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Marshall et al. (2009) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millot et al. (2023) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Monti et al. (2018) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Moreau (1881) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nichols & Breder (1928) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Palko et al. (1982) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Pallas (1770) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parenti (2021) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Pearman et al. (2020) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Pennant (1776) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1851-1854) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Quero et al. (2013) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Rafinesque (1810) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reis et al. (2003) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Seegers & Huber (1981) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spix & Agassiz (1829-31) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tavera et al. (2018) | 2 | 0,06% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Temminck & Schlegel (1850) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2020) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Victor (2020) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Weber (1913) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel et al. (2014) | 2 | 0,06% | 2 | 0,31% | 2 | 0,31% | 2 | 0,31% |
| Agassiz (1833-1843) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Atwood (1869) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bancroft (1832) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bean (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béarez & Dauba (1996) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Bennett (1831) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernal & Rocha (2011) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Blache ([2018]) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Blainville (1816) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1865) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1865) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785-1795) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785-1795) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1790) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon & Lemoine (2003) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Breder & Nichols (1930) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brito Capello (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2005) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Capape et al. (2002) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Causse & Hautecoeur (2006) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Cervigon (1966) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Collette (2003) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
| Conway et al. (2017) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Cuvier & Valenciennes (1828-1830) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1849) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Day (1865) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denys et al. (2022) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Desbrosses (1934) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Desbrosses (1935) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Etcheberry & Abraham (2009) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Faber (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forest (1946) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Forskål (1775) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1900) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Francour & Mouine (2008) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Fraser-brunner (1950) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1899) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerovasileiou et al. (2020) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Gill (1862) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1863) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondot et al. (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Günther (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hein et al. (2010) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Ifremer (2009) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Iglésias et al. (2021) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| IUCN (2014) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Jamonneau et al. (2025) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Jordan & Evermann (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Jordan (1922) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan et al. (1927) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourde et al. (2017) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Kaup (1856) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith & Marquet (2011) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Keith et al. (2014) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lacepède (1803) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legendre (1937) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1830-1831) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1822) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lizé (2018) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lorvelec & Pascal (2009) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lourie et al. (2016) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lowe et al. (2007) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lowe (1833) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lowe (1834) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1841) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1843) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mahé et al. (2013) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Malm (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mcbride et al. (2010) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Mckenzie (2016) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Meek & Hildebrand (1923) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mourier (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1887) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Antonelli, Venezia. 128 pp.">Nardo (1847) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nelson-Smith et al. (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ogilby (1911) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osbeck (1765) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perez Canto (1886) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1902) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pieters & Dickinson (2005) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1863) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1868) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preynat (2013) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Quéro & Delmas (1982) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero & Laborde (1996) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Quero et al. (1998) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Quero et al. (2006) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Quero (1998) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Questel (2014) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Questel (2017) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Questel (2020) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Ranzani (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ranzani (1842) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1846) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robins & Sylva (1963) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Rosen (1911) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Runde (2016) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Sawai et al. (2018) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Schinz (1822) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sellier et al. (2016) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Séret (1993) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Séret (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sigalas (1931) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Smith-Vaniz & Carpenter (2007) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Smith-vaniz & Jelks (2014) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Springer (1941) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1861) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tregarot et al. (2015) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Van & Kampen (1907) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet et al. (2010) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Vernoux (1988) | 1 | 0,03% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Whitley (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1944) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1948) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
