Poissons marins de France métropolitaine
Poissons marins (sens large) de France métropolitaine : inclut les espèces strictement marines (habitat 1) ou pouvant également être retrouvées en eau douce (habitat 4 = eau douce / marin) ou en eau saumâtre (habitat 6).
946 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Béarez et al. (2017) | 729 | 12,74% | 715 | 88,05% | 715 | 88,93% | 707 | 87,94% |
| Linnaeus (1758) | 181 | 3,16% | 48 | 5,91% | 48 | 5,97% | 47 | 5,85% |
| Fourt et al. (2017) | 160 | 2,8% | 156 | 19,21% | 156 | 19,4% | 150 | 18,66% |
| Charbonnel (1990) | 118 | 2,06% | 100 | 12,32% | 100 | 12,44% | 98 | 12,19% |
| Fricke et al. (2011) | 110 | 1,92% | 106 | 13,05% | 106 | 13,18% | 105 | 13,06% |
| Nelson-Smith et al. (2014) | 107 | 1,87% | 71 | 8,74% | 71 | 8,83% | 71 | 8,83% |
| Rafinesque Schmaltz (1810) | 106 | 1,85% | 10 | 1,23% | 10 | 1,24% | 10 | 1,24% |
| Risso (1827) | 91 | 1,59% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Risso (1810) | 90 | 1,57% | 6 | 0,74% | 6 | 0,75% | 6 | 0,75% |
| Fricke et al. (2009) | 69 | 1,21% | 66 | 8,13% | 66 | 8,21% | 64 | 7,96% |
| Siu et al. (2017) | 48 | 0,84% | 47 | 5,79% | 47 | 5,85% | 47 | 5,85% |
| Poey (1858-61) | 46 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1836-1844) | 46 | 0,8% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Breton (2014) | 44 | 0,77% | 41 | 5,05% | 41 | 5,1% | 41 | 5,1% |
| Bonaparte (1837) | 43 | 0,75% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Cuvier & Valenciennes (1833) | 41 | 0,72% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Ifremer (2009) | 38 | 0,66% | 31 | 3,82% | 31 | 3,86% | 30 | 3,73% |
| Bonnaterre (1788) | 37 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 37 | 0,65% | 7 | 0,86% | 7 | 0,87% | 7 | 0,87% |
| Rafinesque (1810) | 37 | 0,65% | 5 | 0,62% | 5 | 0,62% | 5 | 0,62% |
| Walbaum (1792) | 36 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1896) | 35 | 0,61% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Pallas [1814] | 35 | 0,61% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Wickel & Jamon (2010) | 35 | 0,61% | 34 | 4,19% | 34 | 4,23% | 34 | 4,23% |
| Swainson (1839) | 34 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 33 | 0,58% | 33 | 4,06% | 33 | 4,1% | 33 | 4,1% |
| Rignault & Chevallier (2017) | 33 | 0,58% | 28 | 3,45% | 28 | 3,48% | 28 | 3,48% |
| Bloch & Schneider (1801) | 32 | 0,56% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Fourriére et al. (2014) | 29 | 0,51% | 28 | 3,45% | 28 | 3,48% | 28 | 3,48% |
| Questel (2020) | 28 | 0,49% | 27 | 3,33% | 27 | 3,36% | 26 | 3,23% |
| Simian et al. (2022) | 28 | 0,49% | 28 | 3,45% | 28 | 3,48% | 27 | 3,36% |
| Vaillant (1888) | 28 | 0,49% | 5 | 0,62% | 5 | 0,62% | 5 | 0,62% |
| Gmelin (1789) | 27 | 0,47% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Gronow (1854) | 27 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel et al. (2005) | 26 | 0,45% | 25 | 3,08% | 24 | 2,99% | 25 | 3,11% |
| Kaup (1856) | 26 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 24 | 0,42% | 24 | 2,96% | 24 | 2,99% | 24 | 2,99% |
| Collette & Nauen (1983) | 23 | 0,4% | 23 | 2,83% | 19 | 2,36% | 23 | 2,86% |
| Cuvier & Valenciennes (1830) | 23 | 0,4% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Fleming (1828) | 23 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1801) | 23 | 0,4% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lacepède (1803) | 23 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller & Henle (1841) | 23 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa (1829-1853) | 22 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delaroche (1809) | 21 | 0,37% | 5 | 0,62% | 5 | 0,62% | 5 | 0,62% |
| Lacepède (1800) | 19 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1836) | 18 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren & Galil (2015) | 17 | 0,3% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Lacepède (1802) | 17 | 0,3% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Cuvier & Valenciennes (1829) | 16 | 0,28% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Duméril (1870) | 16 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nardo (1827) | 16 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes ([1832]) | 15 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1848) | 15 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mitchill (1815) | 15 | 0,26% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Quero et al. (2013) | 15 | 0,26% | 14 | 1,72% | 14 | 1,74% | 14 | 1,74% |
| Bacchet et al. (2007) | 14 | 0,24% | 14 | 1,72% | 14 | 1,74% | 14 | 1,74% |
| Guichenot (1850) | 14 | 0,24% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 14 | 0,24% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Malm (1877) | 14 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Antonelli, Venezia. 128 pp.">Nardo (1847) | 14 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1825) | 13 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geoffroy Saint-Hilaire ([1817]) | 13 | 0,23% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cocco (1838) | 12 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1830-1832) | 12 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1835) | 12 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1899) | 12 | 0,21% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Günther (1878) | 12 | 0,21% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Nakamura (1985) | 12 | 0,21% | 12 | 1,48% | 12 | 1,49% | 12 | 1,49% |
| Reinhardt (1837) | 12 | 0,21% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Schnakenbeck (1931) | 12 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1837) | 11 | 0,19% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Cuvier & Valenciennes (1847) | 11 | 0,19% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Köhler (1896) | 11 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ascanius (1772) | 10 | 0,17% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Bloch (1785-1795) | 10 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1768) | 10 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1839) | 10 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin et al. (2015) | 10 | 0,17% | 10 | 1,23% | 10 | 1,24% | 10 | 1,24% |
| Goulletquer (2016) | 10 | 0,17% | 10 | 1,23% | 10 | 1,24% | 10 | 1,24% |
| Günther (1861) | 10 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglésias & Lorance (2016) | 10 | 0,17% | 10 | 1,23% | 10 | 1,24% | 10 | 1,24% |
| Nilsson (1832) | 10 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1820) | 10 | 0,17% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Zugmayer (1911) | 10 | 0,17% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Bloch & Schneider (1801) | 9 | 0,16% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bourcier (1988) | 9 | 0,16% | 8 | 0,99% | 8 | 1% | 7 | 0,87% |
| Cuvier & Valenciennes (1846) | 9 | 0,16% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cuvier & Valenciennes (1846) | 9 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1866) | 9 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kulbicki (comm. pers., 2011) | 9 | 0,16% | 9 | 1,11% | 9 | 1,12% | 9 | 1,12% |
| Lowe (1843) | 9 | 0,16% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Zander (1982) | 9 | 0,16% | 9 | 1,11% | 9 | 1,12% | 9 | 1,12% |
| Bartoli & Prévot (1986) | 8 | 0,14% | 7 | 0,86% | 7 | 0,87% | 7 | 0,87% |
| Bertin (1928) | 8 | 0,14% | 5 | 0,62% | 5 | 0,62% | 4 | 0,5% |
| Compagno (1984) | 8 | 0,14% | 8 | 0,99% | 8 | 1% | 8 | 1% |
| Dekay (1842) | 8 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1883) | 8 | 0,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Günther (1887) | 8 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 8 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1838) | 8 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1997) | 8 | 0,14% | 8 | 0,99% | 8 | 1% | 8 | 1% |
| Bloch (1785-1795) | 7 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 7 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1846) | 7 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 7 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forskål (1775) | 7 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke et al. (2013) | 7 | 0,12% | 7 | 0,86% | 7 | 0,87% | 7 | 0,87% |
| Iglésias et al. (2020) | 7 | 0,12% | 7 | 0,86% | 7 | 0,87% | 7 | 0,87% |
| Keith et al. (2011) | 7 | 0,12% | 6 | 0,74% | 6 | 0,75% | 6 | 0,75% |
| Lowe (1841) | 7 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1816) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1792) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Compagno (1984) | 6 | 0,1% | 6 | 0,74% | 6 | 0,75% | 6 | 0,75% |
| Cuvier & Valenciennes (1830) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denys et al. (2022) | 6 | 0,1% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Donovan (1803-08) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril (1865) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1883) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilchrist (1906) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1883) | 6 | 0,1% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Günther (1862) | 6 | 0,1% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Kiszka et al. (2009) | 6 | 0,1% | 5 | 0,62% | 5 | 0,62% | 5 | 0,62% |
| Nordmann (1840-1842) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pylaie (1835) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1835) | 6 | 0,1% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Smith (1849) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annali del Museo Civico di Storia Naturale di Genova 18: 465-590, tavv. I-III.">Vinciguerra (1883) | 6 | 0,1% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Whitley (1931) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barbosa du Bocage & Brito Capello (1864) | 5 | 0,09% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Beebe (1932) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1795) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Düben & Koren (1846) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1862) | 5 | 0,09% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Klunzinger (1871) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1818) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1834) | 5 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1843) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1874) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perez Canto (1886) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Raibaut et al. (1979) | 5 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Richer de Forges et al. (2005) | 5 | 0,09% | 5 | 0,62% | 5 | 0,62% | 5 | 0,62% |
| Soubeyran (2008) | 5 | 0,09% | 5 | 0,62% | 5 | 0,62% | 5 | 0,62% |
| Spitz et al. (2015) | 5 | 0,09% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Storer (1839) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thompson (1837) | 5 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Van Guelpen (2016) | 5 | 0,09% | 5 | 0,62% | 5 | 0,62% | 5 | 0,62% |
| Bellotti (1878) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berry & Smith-Vaniz (1978) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Bouchereau & Guelorget (1999) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Bouchon-Navaro et al. (2005) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Brisout de Barneville (1846) | 4 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Canestrini (1862) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cocco (1833) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1904) | 4 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Couch (1877) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1849) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le règne animal distribué d'après son organisation, pour servir de base à l'histoire naturelle des animaux et d'introduction à l'anatomie comparée. Tome 2, contenant les reptiles, les poissons, les mollusques et les annélides. Déterville, Paris. i-xviii+1-532 pp. ">Cuvier (1816) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Düben (1845) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Euphrasen (1786) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frenot et al. (2005) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Geoffroy Saint-Hilaire (1809) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1867) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1870) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1877) | 4 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Heckel & Kner (1858) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Henriques et al. (2002) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Heymer & Zander (1992) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 4 | 0,07% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Johnson (1863) | 4 | 0,07% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Jordan (1894) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaup (1856) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaup (1858) | 4 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Kulbicki et al. (2000) | 4 | 0,07% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Laffaille et al. (1999) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Latham (1794) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legendre (1942) | 4 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lesueur (1814) | 4 | 0,07% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Moreau (1881) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nilsson (1855) | 4 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Owen (1853) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1770) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1887) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preynat (2013) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Regan (1906) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodriguez (1996) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sawai et al. (2018) | 4 | 0,07% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Schinz (1822) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sellier et al. (2016) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Shaw (1803) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw (1804) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Snodgrass & Heller (1905) | 4 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Spitz et al. (2007) | 4 | 0,07% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Swainson (1838) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1822) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet & Agrnsm (2018) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Wagner (1828) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1933) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams et al. (2006) | 4 | 0,07% | 4 | 0,49% | 4 | 0,5% | 4 | 0,5% |
| Béarez & Séret (2009) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Bleeker (1863) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1782-1784) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1791) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brauer (1902) | 3 | 0,05% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Bruslesicard (1997) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Capape et al. (1999) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Chabanet & Durville (2005) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Chanet et al. (2024) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Cohen et al. (1990) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Couch (1832) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1838) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1829) | 3 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cuvier & Valenciennes (1839) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denys et al. (2024) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Diaz & Cuzange (2009) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Facciolà (1882) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1919) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill & Townsend (1897) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1862) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giorna (1809) | 3 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hemida et al. (2003) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglésias et al. (2021) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Jordan & Gilbert (1882) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1898) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Keith et al. (2006) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Kessler (1874) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kottelat & Freyhof (2007) | 3 | 0,05% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Kottelat (1997) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kovacic & Sanda (2016) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Lavier (1936) | 3 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Leach (1818) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1818) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1822) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louis et al. (1992) | 3 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lowe (1852) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maillard (1970) | 3 | 0,05% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Montagu (1818) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1881) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nardo (1824) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman (1930) | 3 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pampoulie et al. (2001) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Pascal et al. (2006) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Philippi (1902) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1916) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reinhardt (1825) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roule (1916) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ruchon et al. (1993) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sbaihi et al. (2001) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Sherborn (1895) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith-Vaniz & Carpenter (2007) | 3 | 0,05% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Spinola (1807) | 3 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Spix & Agassiz (1829-31) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1868) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tamayo et al. (2021) | 3 | 0,05% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Wheeler & Dunne (1975) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1944) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1948) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zugmayer (1914) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ahnelt & Dorda (2003) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Alcock (1898) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alili & Berrebi (1989) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Antipa (1904) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arnold (1956) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ascanius (1767) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Ascanius (1775) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Asso (1801) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Astruch et al. (2022) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Ayres (1843) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barthélémy (1926) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bath (1973) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Béarez & Bouffandeau (2019) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Belloc (1928) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bellotti (1888) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Benejam et al. (2008) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Bennett (1831) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bergeron (2009) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Berrebi et al. (2018) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Blainville (1810) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1852) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1784) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1787) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonelli (1820) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borsa et al. (2004) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Bouchereau & Tomasini (1989) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Bouchon-Navaro & Louis (1986) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Brito Capello (1867) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brook (1890) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2006) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Brünnich (1788) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1788) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1788) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buron & Chauvet (2003) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Caillot et al. (1999) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Cardinal et al. (2011) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Cheze (1969) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Cocco (1833) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cocco (1836[1834]) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cocco (1884-1885) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1874) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1875) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Costa (1866) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Curd et al. (2015) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Delamare-Deboutteville & Nunes-Ruivo (1955) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Odontaspis ferox" Agassiz dans le Golf de Gascogne. Bulletin de la Société zoologique de France, 54: 233-235.">Desbrosses (1930) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Desbrosses (1935) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Direac'h & Francour (1998) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Döderlein (1884) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donovan (1802-08) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eichwald (1831) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Evermann & Clark (1928) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1887) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faria et al. (2013) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Fernandez-Carvalho et al. (2013) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Fischer (1884) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1885) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1903) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1910) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Francour (2008) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Fries (1837) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Fries (1838) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1884) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Garman (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1906) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giglioli (1889) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Gilbert & Hubbs (1916) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilbert (1915) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1863) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1884) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Girard (1859) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gistel (1848) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bulletin of the Museum of Comparative Zoology at Harvard College. 12:153-170">Goode & Bean (1886) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Goode & Bean (1895) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Goode & Bean (1895) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Griffith & Smith (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guichenot (1848) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guichenot (1859) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gunnerus (1765) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gunnerus (1765) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Günther (1861) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1880) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haast (1878) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harmelin-Vivien et al. (2012) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Heckel (1836) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heckel ([1837]1840) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hildebrand (1948) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hofrichter & Patzner (1997) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Hohnbaum-hornschuch & van der Hoeven (1843) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holbrook (1855) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holt & Byrne (1908) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Howell Rivero (1936) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglésias et al. (2021) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Jordan & Snyder (1901) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Starks (1904) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Thompson (1914) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Jung et al. (2024) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Kaup (1856) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaup (1858) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Kaup (1860) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2020) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Kessler (1859) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kner & Steindachner (1867) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koeck et al. (2014) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Kovacic et al. (2022) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Krøyer (1846-53) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1798) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lafont (1873) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Bail et al. (2012) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Lesueur (1817) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1821) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letourneur et al. (2004) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Lowe et al. (2007) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Luchetti et al. (2011) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Lunel (1879) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1871) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Lütken (1878) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1878) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1892) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macdonald & Barron (1868) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malm (1861) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| McEachran & Seret (1987) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Meeus et al. (1993) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Menzies (1791) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miller (1992) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Millot et al. (2023) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Minding (1832) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morales-Nin & Aldebert (1997) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Moreau (1881) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1891) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1845) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nichols & Breder (1928) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ogilby (1911) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliver et al. (1980) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Osório (1909) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Palko et al. (1982) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Pampoulie et al. (1999) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Pampoulie et al. (1999) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Pampoulie et al. (1999) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Parenti (2021) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parnell (1831-1837) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Pennant (1776) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Petter (1970) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Plucàr (1846) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1851-1854) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero et al. (1998) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Questel (2023) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Randall & Earle (2000) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Rathke (1837) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Regan (1903) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Richardson (1846) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1848) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1820) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Risso (1820) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1840) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Roule & Angel (1933) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rousseau (2010) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sardou (1986) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Schmidt (1912) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schomburgk (1848) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schultz (1943) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret & Quod (2023) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Shaw & Nodder (1789-1790) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw & Nodder (1792-1793) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw & Nodder (1795-1796) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherborn (1925) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1912) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Spitz & Quero (2004) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Staentzel et al. (2023) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Steindachner (1868) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1870) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Steindachner (1882) | 2 | 0,03% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Storer (1858) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tanaka (1911) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Temminck & Schlegel (1850) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ternengo et al. (2005) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Troschel (1860) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN France & MNHN (2013) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Vinciguerra (1880) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weber (1913) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitehead (1985) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Whitley (1937) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1939) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel et al. (2014) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Xia & Durand (2016) | 2 | 0,03% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Yarrell (1829) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1832) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aboussouan & Rasonarivo (1986) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Acolas et al. (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Adam (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Agassiz (1833-1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ahnelt & Patzner (1995) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Alcock (1890) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Alcock (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen (comm. pers., 2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Anonyme (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Atwood (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Audige (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ayres (1848) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Ballesta et al. (1992) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bancroft (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barnard (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartoli et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartoli (1987) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bean (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bean (1890) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bean (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beaulaton et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Beebe & Tee-van (1932) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beebe (1933) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bellotti (1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beslagic et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bianco (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bigelow et al. (1953) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1810) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1782) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1788) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bloch (1790) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1794) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bodilis et al. (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bodilis et al. (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bodilis et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Boisseau & Lubet (1955) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Boisseau (1952) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bonaparte (1839[1838]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchereau (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bouchon-Navaro et al. (1992) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bourret (1971) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bouxin & Legendre (1952) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bragoni et al. (1983) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Brauer (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jena, G. Fischer. 468 pp.">Brauer (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breder & Nichols (1930) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brito Capello (1868) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Jornal de Sciencias Mathematicas, Physicas e Naturaes, Academia Real das Sciencias de Lisboa 2(7): 233-238.">Brito Capello (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brito Capello (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buen & Fage (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buen (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buron et al. (1990) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Byrne (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cadenat & Blache (1970) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Campana-Rouget & Chabaud (1956) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Canestrini (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Capape et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Caruso (1989) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Casamajor et al. (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Casamajor (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Causse & Hautecoeur (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cazio & Isnard (1920) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Chabanaud (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chaine & Duvergier (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chanet & Dettai (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Chassaing et al. (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Records of the Indian Museum (Calcutta). 2(4): 391-392.">Chaudhuri (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevaldonné et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cocco (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collet (1896) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1889) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Collett (1890) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1905) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Collette (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Compagno et al. (2005) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cormier (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cornide (1788) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cornish (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cottalorda et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Couch (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coulon & Sautet (1931) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cousins et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Couteyen (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cuvier & Valenciennes (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1828-1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Voigt (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1814) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1815) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1817) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daniel et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Danois (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Danois (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Danois (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Day (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| De Vis (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denys et al. (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Desbrosses (1934) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Desbrosses (1936) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Desse-berset & Williot (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Desse-Berset & Williot (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Desse-Berset & Williot (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Desse-Berset (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Desse-Berset (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Dettaï et al. (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Döderlein (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dollfus (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dollfus (1927) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Dollfus (1960) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Duhamel (1996) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Dulzetto (1947) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Engelhardt (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Escoubet et al. (1981) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Escoubet et al. (1981) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Esmark (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Esmark (1871) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Esposito et al. (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Euphrasen (1788) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Euphrasen (1791) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| European Nucleotide Archive (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Euzet & Marc (1963) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Faber (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1779) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1780) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faure-Fremiet & Guilcher (1948) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleming (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forest (1946) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Forster (1967) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler & Phillips (1910) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1935) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Francour & Mouine (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Fraser-brunner (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fries (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy et al. (1996) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Garman (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrick (1961) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geistdoerfer (1970) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gérard et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gergaud et al. (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gerovasileiou et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gharbi et al. (1985) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Giglioli & Issel (1884) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Giglioli (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giglioli (1882) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Giglioli (1883) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Giglioli (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilbert (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilchrist (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill & Ryder (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill & Ryder (1883) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gill (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1873-1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1878) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ginsburg (1953) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Godet et al. (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Golani et al. (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1878-1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1879) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Goode & Bean (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grey (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1874) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Günther (1876) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1889) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1889) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hankó (1920-1921) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heckel (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hector (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hermant et al. (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hilgendorf (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holt & Byrne (1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holt & Byrne (1906) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Holt & Byrne (1909) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Holt & Byrne (1910) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Holt (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holten (1802) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hussakof (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutton (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglésias (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Jensen (1905) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jenyns (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1890) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Evermann (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Fowler (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Jordan (1922) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Meek (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Snyder (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Snyder (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Starks (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan et al. (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1890) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Jordan (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1921) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdain (1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Joyeux (1923) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Keith & Machino (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Keith et al. (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Keith et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Keith (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Keith (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Report Sars North Atlantic Deep Sea Expedition, 4(2 no. 2): 1-27.">Koefoed (1952) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Annales de l'Université de Lyon, 26: 475-526, Pls. 26-27.">Koehler (1896) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kolombatović (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kolombatovic (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kotlyar (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Kovačić et al. (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Kovačić et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Kovačić (2001) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Krøyer (1838-40) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1843-45) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1845) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Krøyer (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1852-53) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Laffaille et al. (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lapinski & Giovos (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Last et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lavier (1936) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Legand (1950) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Legardere et al. (1979) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Legendre (1923) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Legendre (1924) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legendre (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1830-1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lindroth (1798) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lizé (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lizé (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lloyd (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loir (1978) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lönnberg (1905) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorance et al. (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lowe (1833) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lowe (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1846) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lowe (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lozano-rey (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1880) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Lütken (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1898) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macculloch (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macleay (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maddalena & Zuffa (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Mahé et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Maillard (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malm (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malm (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maran & Chanet (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Maréchal & Pérès (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Marshall (1955) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mather (1971) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Matsui & Rosenblatt (1979) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| M'Coy (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mead & Böhlke (1953) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mead (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meek & Hildebrand (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Merckx (1998) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Merckx (1998) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Merckx (1998) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Merrett (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miller (1972) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miller (1982) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Mitchill (1814) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morato et al. (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Moreau (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moser et al. (1976) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Müller (1776) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nafpaktitis (1975) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Nardo (1827) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Newman (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nielsen & Cohen (1986) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Noël, Meunier (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Norman (1922) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noronha (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noronha (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Notarbartolo et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Ogilby (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orsi Relini (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Osbeck (1765) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1774) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pampoulie et al. (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Parnell (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parr (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pastor & Francour (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pastor et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pellegrin & Fage (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin & Loppé (1914) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pellegrin (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Péron (1807-1816) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peters (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Petter (1969) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pietschmann (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1873) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| 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 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Puente (1988) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Puissauve & Evanno (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Puissauve, Legros & Poulet (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Puissauve, Legros, Evanno & Acou (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| PUISSAUVE Renaud & BAGLINIERE Jean-Luc (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| PUISSAUVE Renaud & BAGLINIERE Jean-Luc (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Putnam (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quéro (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Quéro & Delmas (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero & Laborde (1996) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Quero et al. (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero et al. (1997) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Quero et al. (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Quero (1986) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Quero (1998) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Questel (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Quignard et al. (1982) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Rafinesque (1814) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Rafinesque (1814) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rafinesque (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Raitt (1934) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Ramsay & Ogilby (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramsay (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ranzani (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ranzani (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1910) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Regan (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reid et al. (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Richardson (1844-48) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robins & Sylva (1963) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Romanov et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Rossignol & Blache (1961) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roule (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roule (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roule (1922) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Roule (1935) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Roule (1936) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Rüppell (1828-1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saemundsson (1922) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sardou (1980) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sardou (1980) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sardou (1981) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sasal et al. (2001) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sauvage (1824) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sauvage (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sauvage (1886) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Saville-kent (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scharff (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schinz (1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidt (1915) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Scoresby (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (1997) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Séret (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bulletin de la Station Biologique d'Arcachon, 34: 59-63.">Sigalas & Budker (1937) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sigalas & Chapheau (1931) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sigalas & Mandoul (1938) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sigalas (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sigalas (1931) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Snyder (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer & Waller (1969) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1941) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1944) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steenstrup (1876) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner & Kolombatovic (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1876) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Steindachner (1876) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1878) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1898) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storm (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tanaka (1918) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thompson (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thompson (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Torchio (1961) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tortonese (1959) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Tsadok et al. (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Urtizberea et al. (2021) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Uyeno et al. (1983) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Vachon et al. (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Vaillant (1882) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Vaillant (1886) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Vaillant (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vallot (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van & Kampen (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villarins et al. (2022) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Vincent (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Waite (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Waite (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walbaum (1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welsh (1923) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Wheeler (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| White (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1930) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1930) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1943) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Wirtz (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wood (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zilli (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
