Poissons marins de Guyane
Poissons marins de Guyane au sens large, c'est-à-dire marins ou marins et d'eau douce ou d'eau saumâtre.
282 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) | 167 | 5,39% | 165 | 27,45% | 165 | 27,92% | 160 | 27,03% |
| Questel & Le Quellec (2012) | 148 | 4,78% | 144 | 23,96% | 144 | 24,37% | 141 | 23,82% |
| Bouchon-Navaro et al. (2005) | 126 | 4,07% | 109 | 18,14% | 109 | 18,44% | 108 | 18,24% |
| Fricke et al. (2011) | 72 | 2,32% | 69 | 11,48% | 69 | 11,68% | 66 | 11,15% |
| Bouchon-Navaro & Louis (1986) | 68 | 2,19% | 60 | 9,98% | 60 | 10,15% | 60 | 10,14% |
| Smith (1997) | 67 | 2,16% | 57 | 9,48% | 51 | 8,63% | 57 | 9,63% |
| Le Bail et al. (2012) | 64 | 2,07% | 62 | 10,32% | 62 | 10,49% | 62 | 10,47% |
| Diaz & Cuzange (2009) | 62 | 2% | 56 | 9,32% | 56 | 9,48% | 55 | 9,29% |
| Siu et al. (2017) | 52 | 1,68% | 48 | 7,99% | 48 | 8,12% | 45 | 7,6% |
| Fricke et al. (2009) | 51 | 1,65% | 46 | 7,65% | 46 | 7,78% | 43 | 7,26% |
| Béarez et al. (2017) | 50 | 1,61% | 50 | 8,32% | 50 | 8,46% | 47 | 7,94% |
| Brugneaux & Pérès (2006) | 46 | 1,48% | 41 | 6,82% | 41 | 6,94% | 41 | 6,93% |
| Louis et al. (1992) | 43 | 1,39% | 34 | 5,66% | 34 | 5,75% | 33 | 5,57% |
| Wickel & Jamon (2010) | 34 | 1,1% | 32 | 5,32% | 32 | 5,41% | 31 | 5,24% |
| Collette & Nauen (1983) | 30 | 0,97% | 30 | 4,99% | 26 | 4,4% | 30 | 5,07% |
| Rousseau (2010) | 29 | 0,94% | 28 | 4,66% | 28 | 4,74% | 28 | 4,73% |
| Poey (1858-61) | 26 | 0,84% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourriére et al. (2014) | 20 | 0,65% | 20 | 3,33% | 20 | 3,38% | 20 | 3,38% |
| Bouchon-Navaro et al. (1992) | 18 | 0,58% | 15 | 2,5% | 15 | 2,54% | 14 | 2,36% |
| Delrieu-Trottin et al. (2015) | 17 | 0,55% | 17 | 2,83% | 16 | 2,71% | 17 | 2,87% |
| Bacchet et al. (2007) | 16 | 0,52% | 15 | 2,5% | 15 | 2,54% | 15 | 2,53% |
| Compagno (1984) | 13 | 0,42% | 13 | 2,16% | 13 | 2,2% | 13 | 2,2% |
| Heemstra & Randall (1993) | 13 | 0,42% | 13 | 2,16% | 13 | 2,2% | 13 | 2,2% |
| Linnaeus (1758) | 13 | 0,42% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Marceniuk & Menezes (2007) | 13 | 0,42% | 12 | 2% | 12 | 2,03% | 12 | 2,03% |
| Berry & Smith-Vaniz (1978) | 12 | 0,39% | 12 | 2% | 12 | 2,03% | 12 | 2,03% |
| Compagno (1984) | 12 | 0,39% | 12 | 2% | 12 | 2,03% | 12 | 2,03% |
| Allen (1985) | 11 | 0,36% | 11 | 1,83% | 11 | 1,86% | 11 | 1,86% |
| Cuvier & Valenciennes ([1832]) | 11 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kulbicki et al. (2000) | 10 | 0,32% | 8 | 1,33% | 8 | 1,35% | 6 | 1,01% |
| Rafinesque Schmaltz (1810) | 10 | 0,32% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Whitehead et al. (1988) | 10 | 0,32% | 10 | 1,66% | 10 | 1,69% | 10 | 1,69% |
| Béarez & Séret (2009) | 9 | 0,29% | 8 | 1,33% | 8 | 1,35% | 8 | 1,35% |
| Cohen et al. (1990) | 8 | 0,26% | 8 | 1,33% | 8 | 1,35% | 8 | 1,35% |
| Cuvier & Valenciennes (1833) | 8 | 0,26% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Fricke et al. (2013) | 8 | 0,26% | 8 | 1,33% | 8 | 1,35% | 7 | 1,18% |
| Kulbicki (comm. pers., 2011) | 8 | 0,26% | 7 | 1,16% | 7 | 1,18% | 7 | 1,18% |
| Nakamura (1985) | 8 | 0,26% | 8 | 1,33% | 8 | 1,35% | 8 | 1,35% |
| Richard et al. (1982) | 8 | 0,26% | 4 | 0,67% | 4 | 0,68% | 3 | 0,51% |
| Whitehead (1985) | 8 | 0,26% | 8 | 1,33% | 8 | 1,35% | 8 | 1,35% |
| Béarez & Bouffandeau (2019) | 7 | 0,23% | 7 | 1,16% | 7 | 1,18% | 6 | 1,01% |
| Bloch & Schneider (1801) | 7 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Vergara (1978) | 7 | 0,23% | 7 | 1,16% | 5 | 0,85% | 7 | 1,18% |
| Simian et al. (2022) | 7 | 0,23% | 7 | 1,16% | 7 | 1,18% | 7 | 1,18% |
| Chabanaud (1927) | 6 | 0,19% | 5 | 0,83% | 5 | 0,85% | 5 | 0,84% |
| Chabanet & Durville (2005) | 6 | 0,19% | 5 | 0,83% | 5 | 0,85% | 5 | 0,84% |
| Cuvier & Valenciennes (1830-1832) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1846) | 6 | 0,19% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Duméril (1870) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourt et al. (2017) | 6 | 0,19% | 6 | 1% | 6 | 1,02% | 4 | 0,68% |
| Marceniuk et al. (2020) | 6 | 0,19% | 4 | 0,67% | 4 | 0,68% | 4 | 0,68% |
| Monti et al. (2010) | 6 | 0,19% | 6 | 1% | 6 | 1,02% | 6 | 1,01% |
| Müller & Henle (1841) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet & Agrnsm (2018) | 6 | 0,19% | 6 | 1% | 6 | 1,02% | 6 | 1,01% |
| Williams et al. (2006) | 6 | 0,19% | 5 | 0,83% | 5 | 0,85% | 4 | 0,68% |
| Allen (comm. pers., 2009) | 5 | 0,16% | 3 | 0,5% | 3 | 0,51% | 2 | 0,34% |
| Cuvier & Valenciennes (1830) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1847) | 5 | 0,16% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Klunzinger (1871) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lim et al. (2002) | 5 | 0,16% | 5 | 0,83% | 5 | 0,85% | 5 | 0,84% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Polanco & Acero (2016) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Earle (2000) | 5 | 0,16% | 5 | 0,83% | 4 | 0,68% | 5 | 0,84% |
| Soubeyran (2008) | 5 | 0,16% | 5 | 0,83% | 5 | 0,85% | 5 | 0,84% |
| Swainson (1839) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villarins et al. (2022) | 5 | 0,16% | 5 | 0,83% | 5 | 0,85% | 5 | 0,84% |
| Bloch & Schneider (1801) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1800) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1801) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1794) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 4 | 0,13% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Rivas (1986) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Betancur-r et al. (2008) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 3 | 0,1% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Duméril (1865) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faria et al. (2013) | 3 | 0,1% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Garman (1899) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1896) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gronow (1854) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutchinson et al. (2019) | 3 | 0,1% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Jordan (1898) | 3 | 0,1% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Keith et al. (2002) | 3 | 0,1% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Keith et al. (2013) | 3 | 0,1% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Kottelat ( 2013) | 3 | 0,1% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Legand (1950) | 3 | 0,1% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Maréchal & Trégarot (2012) | 3 | 0,1% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Mitchill (1815) | 3 | 0,1% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Risso (1810) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1827) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (1997) | 3 | 0,1% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Snodgrass & Heller (1905) | 3 | 0,1% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| UICN Comité français, OFB & MNHN (2021) | 3 | 0,1% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Vaillant (1888) | 3 | 0,1% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Whitley (1933) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1852) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2005) | 2 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Chao et al. (2021) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Curd et al. (2015) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Delaroche (1809) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Düben & Koren (1846) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eigenmann (1912) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evermann & Clark (1928) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fernandez-Carvalho et al. (2013) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Fischer (1884) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontan (2019) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Fowler (1919) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1883) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Griffith & Smith (1834) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1878) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harrison et al. (2007) | 2 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kiszka et al. (2009) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Lacepède (1802) | 2 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Lacepède (1803) | 2 | 0,06% | 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) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macdonald & Barron (1868) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marshall et al. (2009) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| McEachran & Seret (1987) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Millot et al. (2023) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Nelson-Smith et al. (2014) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nichols & Breder (1928) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliveira et al. (2020) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Poey (1851-1854) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Puyo (1936) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rafinesque (1810) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1846) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tavera et al. (2018) | 2 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| UICN France & MNHN (2013) | 2 | 0,06% | 2 | 0,33% | 2 | 0,34% | 2 | 0,34% |
| Vaillant (1899) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1822) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weber (1913) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Agassiz (1833-1843) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alcock (1898) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (1965) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Anonyme (1971) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Anonyme (1971) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Atwood (1869) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ayres (1848) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Bancroft (1832) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bean (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béarez & Causse (2002) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Béarez & Causse (2003) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Bennett (1831) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertin (1928) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| 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 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Jena, G. Fischer. 468 pp.">Brauer (1906) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breder & Nichols (1930) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brito Capello (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brosse et al. (2021) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Capape et al. (2002) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carvalho-Filho et al. (2023) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Causse & Hautecoeur (2006) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Causse (2005) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Causse (2005) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Chassaing et al. (2018) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Records of the Indian Museum (Calcutta). 2(4): 391-392.">Chaudhuri (1908) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collet et al. (2017) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Collette (2003) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 0 | 0% |
| Conway et al. (2017) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Costa (2011) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Cuvier & Valenciennes (1828-1830) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Day (1865) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Desbrosses (1935) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Desse-berset & Williot (2011) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Desse-Berset & Williot (2012) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Desse-Berset (2012) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Dewarumez et al. (2011) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Engelhardt (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forskål (1775) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Francour & Mouine (2008) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Gargominy et al. (1996) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Garman (1913) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geoffroy Saint-Hilaire ([1817]) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerovasileiou et al. (2020) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Gill (1862) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1863) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giorna (1809) | 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 (1880) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren & Galil (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1870) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hein et al. (2010) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Hussakof (1909) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2009) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Iglésias (2012) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Iglésias et al. (2021) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| IUCN (2014) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Jégu (2000) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| 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 & 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 (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourde et al. (2017) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Kaup (1856) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2006) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Keith (2000) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Keith (2002) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Krøyer (1852-53) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Last et al. (2016) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Legendre (1937) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legendre (1942) | 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% |
| Lourie et al. (2016) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Lowe et al. (2007) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Lowe (1834) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Malm (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Pérès (2007) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Maréchal et al. (2006) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Meek & Hildebrand (1923) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Melendez & Markle (1997) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Moser et al. (1976) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Mourier (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin (1923) | 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% |
| 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 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Quéro & Delmas (1982) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero & Laborde (1996) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Quero et al. (1997) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Quero et al. (1998) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Quero et al. (2006) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Quero et al. (2013) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Quero (1998) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Questel (2020) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Questel (2022) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Rafinesque (1820) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Rüppell (1835) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schomburgk (1848) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith-Vaniz & Carpenter (2007) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Springer (1941) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1944) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tongboonkua et al. (2018) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Uicn et al. (2017) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Uicn et al. (2020) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Uyeno et al. (1983) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Van & Kampen (1907) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet et al. (2010) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Vernoux (1988) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Walbaum (1792) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welsh (1923) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| White (1937) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1929) | 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 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Wickel et al. (2020) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Yokoyama (2013) | 1 | 0,03% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Zugmayer (1911) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
