Poissons de Martinique
254 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) | 286 | 9,43% | 284 | 53,69% | 284 | 54,51% | 280 | 53,64% |
| Questel & Le Quellec (2012) | 259 | 8,54% | 248 | 46,88% | 248 | 47,6% | 246 | 47,13% |
| Smith (1997) | 252 | 8,31% | 232 | 43,86% | 226 | 43,38% | 232 | 44,44% |
| Bouchon-Navaro et al. (2005) | 224 | 7,39% | 184 | 34,78% | 184 | 35,32% | 183 | 35,06% |
| Bouchon-Navaro & Louis (1986) | 119 | 3,92% | 102 | 19,28% | 102 | 19,58% | 102 | 19,54% |
| Diaz & Cuzange (2009) | 104 | 3,43% | 96 | 18,15% | 96 | 18,43% | 95 | 18,2% |
| Brugneaux & Pérès (2006) | 85 | 2,8% | 76 | 14,37% | 76 | 14,59% | 76 | 14,56% |
| Louis et al. (1992) | 60 | 1,98% | 49 | 9,26% | 49 | 9,4% | 47 | 9% |
| Fricke et al. (2011) | 56 | 1,85% | 54 | 10,21% | 54 | 10,36% | 52 | 9,96% |
| Fricke et al. (2009) | 52 | 1,71% | 50 | 9,45% | 50 | 9,6% | 47 | 9% |
| Rousseau (2010) | 48 | 1,58% | 46 | 8,7% | 46 | 8,83% | 46 | 8,81% |
| Siu et al. (2017) | 46 | 1,52% | 43 | 8,13% | 43 | 8,25% | 41 | 7,85% |
| Béarez et al. (2017) | 40 | 1,32% | 40 | 7,56% | 40 | 7,68% | 38 | 7,28% |
| Wickel & Jamon (2010) | 36 | 1,19% | 35 | 6,62% | 35 | 6,72% | 34 | 6,51% |
| Poey (1858-61) | 35 | 1,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collette & Nauen (1983) | 30 | 0,99% | 30 | 5,67% | 26 | 4,99% | 30 | 5,75% |
| Bouchon-Navaro et al. (1992) | 25 | 0,82% | 22 | 4,16% | 22 | 4,22% | 21 | 4,02% |
| Questel (2017) | 23 | 0,76% | 23 | 4,35% | 23 | 4,41% | 23 | 4,41% |
| Fourriére et al. (2014) | 22 | 0,73% | 22 | 4,16% | 22 | 4,22% | 22 | 4,21% |
| Compagno (1984) | 21 | 0,69% | 21 | 3,97% | 21 | 4,03% | 21 | 4,02% |
| Delrieu-Trottin et al. (2015) | 20 | 0,66% | 20 | 3,78% | 19 | 3,65% | 20 | 3,83% |
| Le Bail et al. (2012) | 20 | 0,66% | 20 | 3,78% | 20 | 3,84% | 20 | 3,83% |
| Lim et al. (2002) | 20 | 0,66% | 16 | 3,02% | 16 | 3,07% | 16 | 3,07% |
| Bacchet et al. (2007) | 19 | 0,63% | 18 | 3,4% | 18 | 3,45% | 18 | 3,45% |
| Linnaeus (1758) | 18 | 0,59% | 3 | 0,57% | 3 | 0,58% | 3 | 0,57% |
| Rafinesque Schmaltz (1810) | 18 | 0,59% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Cuvier & Valenciennes (1833) | 16 | 0,53% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Monti et al. (2010) | 16 | 0,53% | 14 | 2,65% | 14 | 2,69% | 14 | 2,68% |
| Whitehead et al. (1988) | 16 | 0,53% | 16 | 3,02% | 16 | 3,07% | 16 | 3,07% |
| Heemstra & Randall (1993) | 15 | 0,49% | 15 | 2,84% | 15 | 2,88% | 15 | 2,87% |
| Allen (1985) | 13 | 0,43% | 13 | 2,46% | 13 | 2,5% | 13 | 2,49% |
| Deynat (2011) | 13 | 0,43% | 12 | 2,27% | 12 | 2,3% | 12 | 2,3% |
| Berry & Smith-Vaniz (1978) | 12 | 0,4% | 12 | 2,27% | 12 | 2,3% | 12 | 2,3% |
| Compagno (1984) | 12 | 0,4% | 12 | 2,27% | 12 | 2,3% | 12 | 2,3% |
| Nakamura (1985) | 12 | 0,4% | 12 | 2,27% | 12 | 2,3% | 12 | 2,3% |
| UICN Comité français, OFB & MNHN (2021) | 12 | 0,4% | 12 | 2,27% | 12 | 2,3% | 12 | 2,3% |
| Kulbicki (comm. pers., 2011) | 11 | 0,36% | 9 | 1,7% | 9 | 1,73% | 9 | 1,72% |
| Cohen et al. (1990) | 10 | 0,33% | 10 | 1,89% | 10 | 1,92% | 10 | 1,92% |
| Cuvier & Valenciennes ([1832]) | 10 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke et al. (2013) | 10 | 0,33% | 10 | 1,89% | 10 | 1,92% | 9 | 1,72% |
| Kulbicki et al. (2000) | 10 | 0,33% | 9 | 1,7% | 9 | 1,73% | 8 | 1,53% |
| Béarez & Séret (2009) | 9 | 0,3% | 9 | 1,7% | 9 | 1,73% | 9 | 1,72% |
| Soubeyran (2008) | 9 | 0,3% | 9 | 1,7% | 9 | 1,73% | 9 | 1,72% |
| Béarez & Bouffandeau (2019) | 8 | 0,26% | 8 | 1,51% | 8 | 1,54% | 7 | 1,34% |
| Charbonnel (1990) | 8 | 0,26% | 6 | 1,13% | 6 | 1,15% | 4 | 0,77% |
| Gronow (1854) | 8 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 8 | 0,26% | 4 | 0,76% | 4 | 0,77% | 4 | 0,77% |
| Whitehead (1985) | 8 | 0,26% | 8 | 1,51% | 8 | 1,54% | 8 | 1,53% |
| Bloch & Schneider (1801) | 7 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller & Henle (1841) | 7 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Vergara (1978) | 7 | 0,23% | 7 | 1,32% | 5 | 0,96% | 7 | 1,34% |
| Simian et al. (2022) | 7 | 0,23% | 7 | 1,32% | 7 | 1,34% | 7 | 1,34% |
| Uicn et al. (2019) | 7 | 0,23% | 7 | 1,32% | 7 | 1,34% | 7 | 1,34% |
| Williams et al. (2006) | 7 | 0,23% | 6 | 1,13% | 6 | 1,15% | 5 | 0,96% |
| Chabanaud (1927) | 6 | 0,2% | 5 | 0,95% | 5 | 0,96% | 5 | 0,96% |
| Cuvier & Valenciennes (1846) | 6 | 0,2% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Nardo (1827) | 6 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1810) | 6 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1827) | 6 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet & Agrnsm (2018) | 6 | 0,2% | 6 | 1,13% | 6 | 1,15% | 6 | 1,15% |
| Allen (comm. pers., 2009) | 5 | 0,16% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Chabanet & Durville (2005) | 5 | 0,16% | 5 | 0,95% | 5 | 0,96% | 5 | 0,96% |
| Cuvier & Valenciennes (1830) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1830-1832) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 5 | 0,16% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Keith et al. (2013) | 5 | 0,16% | 5 | 0,95% | 5 | 0,96% | 5 | 0,96% |
| Lacepède (1800) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1801) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Trégarot (2012) | 5 | 0,16% | 4 | 0,76% | 4 | 0,77% | 4 | 0,77% |
| Polanco & Acero (2016) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2023) | 5 | 0,16% | 5 | 0,95% | 5 | 0,96% | 5 | 0,96% |
| Séret (1997) | 5 | 0,16% | 5 | 0,95% | 5 | 0,96% | 5 | 0,96% |
| Snodgrass & Heller (1905) | 5 | 0,16% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Swainson (1839) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1836-1844) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1847) | 4 | 0,13% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Fourt et al. (2017) | 4 | 0,13% | 4 | 0,76% | 4 | 0,77% | 4 | 0,77% |
| Keith et al. (2002) | 4 | 0,13% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Keith et al. (2006) | 4 | 0,13% | 4 | 0,76% | 4 | 0,77% | 4 | 0,77% |
| Klunzinger (1871) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marceniuk et al. (2020) | 4 | 0,13% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Mitchill (1815) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Møller et al. (2005) | 4 | 0,13% | 4 | 0,76% | 4 | 0,77% | 4 | 0,77% |
| Morris (2012) | 4 | 0,13% | 4 | 0,76% | 4 | 0,77% | 4 | 0,77% |
| Pezold et al. (2015) | 4 | 0,13% | 4 | 0,76% | 4 | 0,77% | 4 | 0,77% |
| Walbaum (1792) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1839) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Firmat et al. (2012) | 3 | 0,1% | 3 | 0,57% | 3 | 0,58% | 3 | 0,57% |
| Hutchinson et al. (2019) | 3 | 0,1% | 3 | 0,57% | 3 | 0,58% | 3 | 0,57% |
| Kottelat ( 2013) | 3 | 0,1% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Legand (1950) | 3 | 0,1% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Maréchal et al. (2006) | 3 | 0,1% | 3 | 0,57% | 3 | 0,58% | 3 | 0,57% |
| Randall & Earle (2000) | 3 | 0,1% | 3 | 0,57% | 2 | 0,38% | 3 | 0,57% |
| Rignault & Chevallier (2017) | 3 | 0,1% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Swainson (1838) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1933) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertin (1928) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Bleeker (1852) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1825) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brosse et al. (2021) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Brugneaux & Pérès (2005) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Costa (2011) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Durand (2016) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Evermann & Clark (1928) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontan (2019) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Fowler (1919) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy et al. (1996) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Geoffroy Saint-Hilaire ([1817]) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harrison et al. (2007) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Hildebrand (1948) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (1999) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Keith (2002) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Lacepède (1802) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Macdonald & Barron (1868) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Pérès (2007) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Marquet et al. (2003) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Millot et al. (2023) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Monti et al. (2018) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Nichols & Breder (1928) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Palko et al. (1982) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Pallas (1770) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parenti (2021) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Pearman et al. (2020) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Pennant (1776) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2022) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Rafinesque (1810) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seegers & Huber (1981) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spix & Agassiz (1829-31) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tavera et al. (2018) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Temminck & Schlegel (1850) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2020) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Victor (2020) | 2 | 0,07% | 2 | 0,38% | 2 | 0,38% | 2 | 0,38% |
| Yokoyama (2013) | 2 | 0,07% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Agassiz (1833-1843) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alley et al. (2023) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Capape et al. (2002) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collette (2003) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 0 | 0% |
| Conway et al. (2017) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Cuvier & Valenciennes (1828-1830) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denys et al. (2022) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Desbrosses (1934) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Desbrosses (1935) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Etcheberry & Abraham (2009) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Faber (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forest (1946) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Garman (1899) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerovasileiou et al. (2020) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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% |
| Goode & Bean (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Günther (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Ifremer (2009) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Iglésias et al. (2021) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| IUCN (2014) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Jamonneau et al. (2025) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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 (1884) | 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Kaup (1856) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith & Marquet (2011) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Kiszka et al. (2009) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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% |
| Letourneur et al. (2004) | 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Lorvelec & Pascal (2009) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Lourie et al. (2016) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Lowe et al. (2007) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Lowe (1838) | 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Malm (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meek & Hildebrand (1923) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1884) | 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% |
| Owen (1853) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1887) | 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Quéro & Delmas (1982) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero & Laborde (1996) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Quero et al. (1998) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Quero et al. (2006) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Quero et al. (2013) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Quero (1998) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Questel (2014) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Questel (2017) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Ranzani (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ranzani (1842) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reis et al. (2003) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Richardson (1846) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robins & Sylva (1963) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Rosen (1911) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1835) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sawai et al. (2018) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Schinz (1822) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sellier et al. (2016) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Sigalas (1931) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Smith-Vaniz & Carpenter (2007) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Smith-vaniz & Jelks (2014) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| Van & Kampen (1907) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vernoux (1988) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
| 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% |
| Wickel et al. (2014) | 1 | 0,03% | 1 | 0,19% | 1 | 0,19% | 1 | 0,19% |
