Poissons exclusivement marins de métropole
828 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) | 706 | 14,35% | 694 | 90,01% | 694 | 90,96% | 686 | 89,91% |
Linnaeus (1758) | 165 | 3,35% | 42 | 5,45% | 42 | 5,5% | 41 | 5,37% |
Fourt et al. (2017) | 160 | 3,25% | 156 | 20,23% | 156 | 20,45% | 150 | 19,66% |
Charbonnel (1990) | 114 | 2,32% | 96 | 12,45% | 96 | 12,58% | 94 | 12,32% |
Fricke et al. (2011) | 109 | 2,21% | 105 | 13,62% | 105 | 13,76% | 104 | 13,63% |
Rafinesque Schmaltz (1810) | 106 | 2,15% | 10 | 1,3% | 10 | 1,31% | 10 | 1,31% |
Nelson-Smith et al. (2014) | 98 | 1,99% | 64 | 8,3% | 64 | 8,39% | 64 | 8,39% |
Risso (1810) | 88 | 1,79% | 5 | 0,65% | 5 | 0,66% | 5 | 0,66% |
Risso (1827) | 86 | 1,75% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Fricke et al. (2009) | 64 | 1,3% | 62 | 8,04% | 62 | 8,13% | 60 | 7,86% |
Siu et al. (2017) | 47 | 0,96% | 46 | 5,97% | 46 | 6,03% | 46 | 6,03% |
Poey (1858-61) | 45 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1836-1844) | 44 | 0,89% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cuvier & Valenciennes (1833) | 41 | 0,83% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bonaparte (1837) | 40 | 0,81% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Breton (2014) | 40 | 0,81% | 37 | 4,8% | 37 | 4,85% | 37 | 4,85% |
Ifremer (2009) | 38 | 0,77% | 31 | 4,02% | 31 | 4,06% | 30 | 3,93% |
Bonnaterre (1788) | 36 | 0,73% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1896) | 35 | 0,71% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Swainson (1839) | 34 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel & Jamon (2010) | 34 | 0,69% | 33 | 4,28% | 33 | 4,33% | 33 | 4,33% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 33 | 0,67% | 33 | 4,28% | 33 | 4,33% | 33 | 4,33% |
Rignault & Chevallier (2017) | 33 | 0,67% | 28 | 3,63% | 28 | 3,67% | 28 | 3,67% |
Rafinesque (1810) | 32 | 0,65% | 5 | 0,65% | 5 | 0,66% | 5 | 0,66% |
Bloch & Schneider (1801) | 29 | 0,59% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cuvier (1829) | 29 | 0,59% | 7 | 0,91% | 7 | 0,92% | 7 | 0,92% |
Fourriére et al. (2014) | 29 | 0,59% | 28 | 3,63% | 28 | 3,67% | 28 | 3,67% |
Vaillant (1888) | 28 | 0,57% | 5 | 0,65% | 5 | 0,66% | 5 | 0,66% |
Questel (2020) | 27 | 0,55% | 26 | 3,37% | 26 | 3,41% | 25 | 3,28% |
Simian et al. (2022) | 27 | 0,55% | 27 | 3,5% | 27 | 3,54% | 26 | 3,41% |
Walbaum (1792) | 27 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Gronow (1854) | 26 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 25 | 0,51% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Collette & Nauen (1983) | 23 | 0,47% | 23 | 2,98% | 19 | 2,49% | 23 | 3,01% |
Cuvier & Valenciennes (1830) | 23 | 0,47% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Fleming (1828) | 23 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller & Henle (1841) | 23 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 23 | 0,47% | 23 | 2,98% | 23 | 3,01% | 23 | 3,01% |
Lacepède (1801) | 22 | 0,45% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Delaroche (1809) | 21 | 0,43% | 5 | 0,65% | 5 | 0,66% | 5 | 0,66% |
Duhamel et al. (2005) | 21 | 0,43% | 20 | 2,59% | 19 | 2,49% | 20 | 2,62% |
Costa (1829-1853) | 20 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Goren & Galil (2015) | 17 | 0,35% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Lacepède (1800) | 17 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas [1814] | 17 | 0,35% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cuvier & Valenciennes ([1832]) | 15 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1802) | 15 | 0,3% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Quero et al. (2013) | 15 | 0,3% | 14 | 1,82% | 14 | 1,83% | 14 | 1,83% |
Bacchet et al. (2007) | 14 | 0,28% | 14 | 1,82% | 14 | 1,83% | 14 | 1,83% |
Lacepède (1803) | 14 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1825) | 13 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1836) | 13 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 13 | 0,26% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cocco (1838) | 12 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1830-1832) | 12 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1899) | 12 | 0,24% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Guichenot (1850) | 12 | 0,24% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Günther (1878) | 12 | 0,24% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Malm (1877) | 12 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Mitchill (1815) | 12 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Nakamura (1985) | 12 | 0,24% | 12 | 1,56% | 12 | 1,57% | 12 | 1,57% |
Nardo (1827) | 12 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Schnakenbeck (1931) | 12 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1837) | 11 | 0,22% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Geoffroy Saint-Hilaire ([1817]) | 11 | 0,22% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Köhler (1896) | 11 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Ascanius (1772) | 10 | 0,2% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Brünnich (1768) | 10 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1835) | 10 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1839) | 10 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1847) | 10 | 0,2% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Delrieu-Trottin et al. (2015) | 10 | 0,2% | 10 | 1,3% | 10 | 1,31% | 10 | 1,31% |
Goulletquer (2016) | 10 | 0,2% | 10 | 1,3% | 10 | 1,31% | 10 | 1,31% |
Iglésias & Lorance (2016) | 10 | 0,2% | 10 | 1,3% | 10 | 1,31% | 10 | 1,31% |
Risso (1820) | 10 | 0,2% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Zugmayer (1911) | 10 | 0,2% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bloch (1785-1795) | 9 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourcier (1988) | 9 | 0,18% | 8 | 1,04% | 8 | 1,05% | 7 | 0,92% |
Kulbicki (comm. pers., 2011) | 9 | 0,18% | 9 | 1,17% | 9 | 1,18% | 9 | 1,18% |
Lowe (1843) | 9 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Nilsson (1832) | 9 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Zander (1982) | 9 | 0,18% | 9 | 1,17% | 9 | 1,18% | 9 | 1,18% |
Bertin (1928) | 8 | 0,16% | 5 | 0,65% | 5 | 0,66% | 4 | 0,52% |
Compagno (1984) | 8 | 0,16% | 8 | 1,04% | 8 | 1,05% | 8 | 1,05% |
Cuvier & Valenciennes (1846) | 8 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1887) | 8 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Antonelli, Venezia. 128 pp.">Nardo (1847) | 8 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Reinhardt (1837) | 8 | 0,16% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Smith (1997) | 8 | 0,16% | 8 | 1,04% | 8 | 1,05% | 8 | 1,05% |
Bloch & Schneider (1801) | 7 | 0,14% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bloch (1793) | 7 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 7 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke et al. (2013) | 7 | 0,14% | 7 | 0,91% | 7 | 0,92% | 7 | 0,92% |
Iglésias et al. (2020) | 7 | 0,14% | 7 | 0,91% | 7 | 0,92% | 7 | 0,92% |
Kaup (1856) | 7 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 7 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1838) | 7 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1841) | 7 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Blainville (1816) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Compagno (1984) | 6 | 0,12% | 6 | 0,78% | 6 | 0,79% | 6 | 0,79% |
Cuvier & Valenciennes (1829) | 6 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cuvier & Valenciennes (1830) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1803-08) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Facciolà (1883) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Forskål (1775) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1913) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilchrist (1906) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1883) | 6 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Goode & Bean (1883) | 6 | 0,12% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Günther (1861) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al. (2009) | 6 | 0,12% | 5 | 0,65% | 5 | 0,66% | 5 | 0,66% |
Rüppell (1835) | 6 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Smith (1849) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Annali del Museo Civico di Storia Naturale di Genova 18: 465-590, tavv. I-III.">Vinciguerra (1883) | 6 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Whitley (1931) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbosa du Bocage & Brito Capello (1864) | 5 | 0,1% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Beebe (1932) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1792) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1846) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1848) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Düben & Koren (1846) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1862) | 5 | 0,1% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Johnson (1862) | 5 | 0,1% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Klunzinger (1871) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1834) | 5 | 0,1% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1843) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1874) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Perez Canto (1886) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Pylaie (1835) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer de Forges et al. (2005) | 5 | 0,1% | 5 | 0,65% | 5 | 0,66% | 5 | 0,66% |
Storer (1839) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Thompson (1837) | 5 | 0,1% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Van Guelpen (2016) | 5 | 0,1% | 5 | 0,65% | 5 | 0,66% | 5 | 0,66% |
Bartoli & Prévot (1986) | 4 | 0,08% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Bellotti (1878) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Berry & Smith-Vaniz (1978) | 4 | 0,08% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Bloch (1795) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchereau & Guelorget (1999) | 4 | 0,08% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Bouchon-Navaro et al. (2005) | 4 | 0,08% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Brisout de Barneville (1846) | 4 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Canestrini (1862) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cocco (1833) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Collett (1904) | 4 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Couch (1877) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1849) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Düben (1845) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Euphrasen (1786) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Faber (1829) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy Saint-Hilaire (1809) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1867) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1870) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1877) | 4 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Henriques et al. (2002) | 4 | 0,08% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Heymer & Zander (1992) | 4 | 0,08% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 4 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Johnson (1863) | 4 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kaup (1856) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaup (1858) | 4 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Legendre (1942) | 4 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lesueur (1814) | 4 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lesueur (1818) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Nilsson (1855) | 4 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Owen (1853) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1887) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Regan (1906) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodriguez (1996) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Sawai et al. (2018) | 4 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Schinz (1822) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Shaw (1803) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Shaw (1804) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Snodgrass & Heller (1905) | 4 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Spitz et al. (2007) | 4 | 0,08% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Spitz et al. (2015) | 4 | 0,08% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Swainson (1838) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1822) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet & Agrnsm (2018) | 4 | 0,08% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Whitley (1933) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2006) | 4 | 0,08% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Béarez & Séret (2009) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Bleeker (1863) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1791) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Brauer (1902) | 3 | 0,06% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bruslesicard (1997) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Capape et al. (1999) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Chabanet & Durville (2005) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Chanet et al. (2024) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Cohen et al. (1990) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Couch (1832) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Couch (1838) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1829) | 3 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cuvier & Valenciennes (1839) | 3 | 0,06% | 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) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Duméril (1865) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Facciolà (1882) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler (1919) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1913) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill & Townsend (1897) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1862) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Giorna (1809) | 3 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Günther (1866) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemida et al. (2003) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Iglésias et al. (2021) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Jordan (1898) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Kessler (1874) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kovacic & Sanda (2016) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Leach (1818) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1822) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1852) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Maillard (1970) | 3 | 0,06% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Montagu (1818) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1881) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Nardo (1824) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Nordmann (1840-1842) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman (1930) | 3 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pallas (1770) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1902) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Reinhardt (1825) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Roule (1916) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruchon et al. (1993) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sbaihi et al. (2001) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Sellier et al. (2016) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Smith-Vaniz & Carpenter (2007) | 3 | 0,06% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Spinola (1807) | 3 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Spix & Agassiz (1829-31) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1868) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Tamayo et al. (2021) | 3 | 0,06% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Wheeler & Dunne (1975) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1944) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1948) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Zugmayer (1914) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ahnelt & Dorda (2003) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Alcock (1898) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Alili & Berrebi (1989) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Antipa (1904) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnold (1956) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ascanius (1767) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ascanius (1775) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Asso (1801) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Astruch et al. (2022) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ayres (1843) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bath (1973) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Béarez & Bouffandeau (2019) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Belloc (1928) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellotti (1888) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bennett (1831) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bennett (1834) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bergeron (2009) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Blainville (1810) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1852) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1787) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonelli (1820) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsa et al. (2004) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bouchereau & Tomasini (1989) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bouchon-Navaro & Louis (1986) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Brito Capello (1867) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brook (1890) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2006) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Brünnich (1788) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünnich (1788) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünnich (1788) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Buron & Chauvet (2003) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cardinal et al. (2011) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cheze (1969) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cocco (1833) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cocco (1836[1834]) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cocco (1884-1885) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Collett (1874) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Collett (1875) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Costa (1866) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Couch (1877) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Curd et al. (2015) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Delamare-Deboutteville & Nunes-Ruivo (1955) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Odontaspis ferox" Agassiz dans le Golf de Gascogne. Bulletin de la Société zoologique de France, 54: 233-235.">Desbrosses (1930) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Desbrosses (1935) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Direac'h & Francour (1998) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Döderlein (1884) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1802-08) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Evermann & Clark (1928) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Facciolà (1887) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer (1885) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler (1910) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Francour (2008) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Fries (1837) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Fries (1838) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1884) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Garman (1896) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1906) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Giglioli (1889) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gilbert & Hubbs (1916) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilbert (1915) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1863) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1884) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 12:153-170">Goode & Bean (1886) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Goode & Bean (1895) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1895) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Griffith & Smith (1834) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1848) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunnerus (1765) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunnerus (1765) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Günther (1880) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Haast (1878) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Harmelin-Vivien et al. (2012) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Heckel ([1837]1840) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hildebrand (1948) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hofrichter & Patzner (1997) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Hohnbaum-hornschuch & van der Hoeven (1843) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Holbrook (1855) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Holt & Byrne (1908) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Howell Rivero (1936) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Iglésias et al. (2021) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Jordan & Gilbert (1882) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Snyder (1901) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Starks (1904) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Thompson (1914) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jung et al. (2024) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kaup (1856) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaup (1858) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kaup (1860) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kessler (1859) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kner & Steindachner (1867) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Koeck et al. (2014) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kovacic et al. (2022) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kulbicki et al. (2000) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Laffaille et al. (1999) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lafont (1873) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1817) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1821) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur et al. (2004) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Louis et al. (1992) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Luchetti et al. (2011) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lunel (1879) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lütken (1871) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lütken (1878) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lütken (1878) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lütken (1892) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
McEachran & Seret (1987) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Menzies (1791) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Miller (1992) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Millot et al. (2023) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Minding (1832) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Morales-Nin & Aldebert (1997) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Moreau (1881) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1891) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1845) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Nichols & Breder (1928) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ogilby (1911) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver et al. (1980) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Osório (1909) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Palko et al. (1982) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pampoulie et al. (1999) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Parenti (2021) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnell (1831-1837) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pennant (1776) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Petter (1970) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Plucàr (1846) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1851-1854) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Quero et al. (1998) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Questel (2023) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Randall & Earle (2000) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rathke (1837) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Regan (1903) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard et al. (1982) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Richardson (1846) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1848) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1820) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Risso (1820) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1840) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Roule & Angel (1933) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rousseau (2010) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sardou (1986) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Schmidt (1912) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Schomburgk (1848) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Schultz (1943) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret & Quod (2023) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Shaw & Nodder (1789-1790) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Shaw & Nodder (1792-1793) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn (1895) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn (1925) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1912) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Spitz & Quero (2004) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Steindachner (1868) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1870) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Steindachner (1882) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Storer (1858) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Tanaka (1911) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Temminck & Schlegel (1850) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ternengo et al. (2005) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Troschel (1860) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Vinciguerra (1880) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Weber (1913) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitehead (1985) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Whitley (1937) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1939) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2014) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Yarrell (1829) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Yarrell (1832) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Aboussouan & Rasonarivo (1986) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Agassiz (1833-1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ahnelt & Patzner (1995) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Alcock (1890) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Alcock (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (comm. pers., 2009) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Atwood (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ayres (1848) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ballesta et al. (1992) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% |
Beebe & Tee-van (1932) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beebe (1933) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bellotti (1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bennett (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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 (1782-1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1784) | 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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bloch (1790) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bodilis et al. (2011) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bodilis et al. (2012) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bodilis et al. (2013) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Boisseau & Lubet (1955) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Boisseau (1952) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bonaparte (1839[1838]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchereau (2002) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bouchon-Navaro et al. (1992) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bourret (1971) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bouxin & Legendre (1952) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Campana-Rouget & Chabaud (1956) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Canestrini (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Capape et al. (2017) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Caruso (1989) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Casamajor et al. (2000) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Casamajor (2016) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Causse & Hautecoeur (2006) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cazio & Isnard (1920) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevaldonné et al. (2008) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Collette (2003) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Compagno et al. (2005) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% |
Cousins et al. (2013) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% |
Desbrosses (1934) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Desbrosses (1936) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dettaï et al. (2011) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dollfus (1960) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Duhamel (1996) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dulzetto (1947) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichwald (1831) | 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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Escoubet et al. (1981) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Esmark (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Esmark (1871) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Euzet & Marc (1963) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 (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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Fraser-brunner (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fries (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gerovasileiou et al. (2020) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gharbi et al. (1985) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Giglioli & Issel (1884) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Giglioli (1882) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Giglioli (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Giglioli (1883) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gill & Ryder (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Gistel (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Goode & Bean (1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% |
Hector (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hermant et al. (2010) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Holt & Byrne (1909) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Holt & Byrne (1910) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Report Sars North Atlantic Deep Sea Expedition, 4(2 no. 2): 1-27.">Koefoed (1952) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kovačić et al. (2016) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kovačić et al. (2017) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kovačić (2001) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Krøyer (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1846-53) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1798) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapinski & Giovos (2019) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Last et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavier (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavier (1936) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Legand (1950) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Legardere et al. (1979) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Legendre (1923) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lizé (2018) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lowe (1833) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lowe (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1846) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lozano-rey (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lütken (1880) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% |
Macleay (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddalena & Zuffa (2008) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Mahé et al. (2013) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Malm (1861) | 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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Maréchal & Pérès (2007) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Marshall (1955) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mather (1971) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Matsui & Rosenblatt (1979) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% |
Meeus et al. (1993) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Merckx (1998) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Merckx (1998) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Merckx (1998) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Mitchill (1814) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morato et al. (2000) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Moreau (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noël, Meunier (2010) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ogilby (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Orsi Relini (2002) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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% |
Parnell (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Parr (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pastor & Francour (2010) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pastor et al. (2008) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pellegrin & Fage (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pellegrin & Loppé (1914) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Puente (1988) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Putnam (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Quéro (2017) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Quero & Laborde (1996) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Quero et al. (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Quero et al. (1997) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Quero et al. (2006) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Quero (1986) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Quero (1998) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Questel (2017) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Quignard et al. (1982) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Rafinesque (1814) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque (1814) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Raibaut et al. (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Raitt (1934) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Regan (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Reid et al. (2016) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Romanov et al. (2013) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Rossignol & Blache (1961) | 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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Roule (1935) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Roule (1936) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sardou (1980) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sardou (1981) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sasal et al. (2001) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Saville-kent (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scharff (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmidt (1915) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Scoresby (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scoresby (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret (2014) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bulletin de la Station Biologique d'Arcachon, 34: 59-63.">Sigalas & Budker (1937) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sigalas & Chapheau (1931) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sigalas & Mandoul (1938) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sigalas (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sigalas (1931) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 (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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 (1898) | 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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tsadok et al. (2015) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Uyeno et al. (1983) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vachon et al. (2007) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vaillant (1882) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vaillant (1886) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vaillant (1888) | 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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vincent (2009) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
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 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Wirtz (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (1848) | 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 (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% |