Poissons marins de Saint-Pierre-et-Miquelon
256 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) | 63 | 5,95% | 63 | 51,64% | 63 | 52,07% | 63 | 52,07% |
| Simian et al. (2022) | 44 | 4,16% | 44 | 36,07% | 44 | 36,36% | 44 | 36,36% |
| Linnaeus (1758) | 27 | 2,55% | 12 | 9,84% | 12 | 9,92% | 12 | 9,92% |
| Rafinesque Schmaltz (1810) | 16 | 1,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourt et al. (2017) | 14 | 1,32% | 14 | 11,48% | 14 | 11,57% | 14 | 11,57% |
| Fricke et al. (2011) | 14 | 1,32% | 14 | 11,48% | 14 | 11,57% | 14 | 11,57% |
| Fricke et al. (2009) | 12 | 1,13% | 11 | 9,02% | 11 | 9,09% | 11 | 9,09% |
| Schnakenbeck (1931) | 12 | 1,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walbaum (1792) | 12 | 1,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel & Jamon (2010) | 12 | 1,13% | 11 | 9,02% | 11 | 9,09% | 11 | 9,09% |
| Cuvier & Valenciennes (1829) | 11 | 1,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1833) | 11 | 1,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Guelpen (2016) | 11 | 1,04% | 11 | 9,02% | 11 | 9,09% | 11 | 9,09% |
| Bloch & Schneider (1801) | 10 | 0,95% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denys et al. (2022) | 9 | 0,85% | 7 | 5,74% | 7 | 5,79% | 7 | 5,79% |
| Gmelin (1789) | 9 | 0,85% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Mitchill (1815) | 9 | 0,85% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Nelson-Smith et al. (2014) | 9 | 0,85% | 7 | 5,74% | 7 | 5,79% | 7 | 5,79% |
| Reinhardt (1837) | 9 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 8 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel et al. (2005) | 8 | 0,76% | 7 | 5,74% | 7 | 5,79% | 7 | 5,79% |
| Lacepède (1803) | 8 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sellier et al. (2016) | 8 | 0,76% | 8 | 6,56% | 8 | 6,61% | 8 | 6,61% |
| Siu et al. (2017) | 8 | 0,76% | 8 | 6,56% | 8 | 6,61% | 8 | 6,61% |
| Dekay (1842) | 7 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas [1814] | 7 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1858-61) | 7 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preynat (2013) | 7 | 0,66% | 7 | 5,74% | 7 | 5,79% | 7 | 5,79% |
| Questel (2020) | 7 | 0,66% | 7 | 5,74% | 7 | 5,79% | 7 | 5,79% |
| Risso (1810) | 7 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charbonnel (1990) | 6 | 0,57% | 6 | 4,92% | 6 | 4,96% | 6 | 4,96% |
| Collette & Nauen (1983) | 6 | 0,57% | 6 | 4,92% | 6 | 4,96% | 6 | 4,96% |
| Duméril (1870) | 6 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleming (1828) | 6 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1896) | 6 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nardo (1827) | 6 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 5 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 5 | 0,47% | 5 | 4,1% | 5 | 4,13% | 5 | 4,13% |
| Ifremer (2009) | 5 | 0,47% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
| Lacepède (1800) | 5 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller & Henle (1841) | 5 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 5 | 0,47% | 5 | 4,1% | 5 | 4,13% | 5 | 4,13% |
| Bonnaterre (1788) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro et al. (2005) | 4 | 0,38% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
| Fourriére et al. (2014) | 4 | 0,38% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
| Gill (1883) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gronow (1854) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1801) | 4 | 0,38% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Malm (1877) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nakamura (1985) | 4 | 0,38% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
| Rafinesque (1810) | 4 | 0,38% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Risso (1827) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1997) | 4 | 0,38% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
| Storer (1839) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1816) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breton (2014) | 3 | 0,28% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
| Facciolà (1882) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 0,28% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Leach (1818) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1818) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1770) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Soubeyran (2008) | 3 | 0,28% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
| Ascanius (1772) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ascanius (1775) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bacchet et al. (2007) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Berry & Smith-Vaniz (1978) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Bertin (1928) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Blainville (1810) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1795) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1788) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1875) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Costa (1829-1853) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1838) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes ([1832]) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1847) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1848) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donovan (1803-08) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frenot et al. (2005) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Garman (1913) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1895) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gunnerus (1765) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Gunnerus (1765) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Howell Rivero (1936) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1862) | 2 | 0,19% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Jordan (1896) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 0,19% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Jung et al. (2024) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Keith et al. (2011) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Kulbicki (comm. pers., 2011) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Lesueur (1818) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1821) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1822) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millot et al. (2023) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Moreau (1881) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Antonelli, Venezia. 128 pp.">Nardo (1847) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nilsson (1832) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nordmann (1840-1842) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osório (1909) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Palko et al. (1982) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Pascal et al. (2006) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Perez Canto (1886) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1887) | 2 | 0,19% | 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) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Reinhardt (1825) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 2 | 0,19% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Séret & Quod (2023) | 2 | 0,19% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
| Shaw & Nodder (1792-1793) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1849) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Snodgrass & Heller (1905) | 2 | 0,19% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Storer (1858) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1839) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Temminck & Schlegel (1850) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1836-1844) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1933) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1939) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1829) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1832) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allain & Morice (1971) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Anonyme. (2004) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Anonyme. (2004) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Audige (1927) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ayres (1848) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barthélémy (1926) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1810) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1782-1784) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1784) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1787) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1788) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Bonaparte (1837) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1839[1838]) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro & Louis (1986) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Bouxin & Legendre (1952) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Jornal de Sciencias Mathematicas, Physicas e Naturaes, Academia Real das Sciencias de Lisboa 2(7): 233-238.">Brito Capello (1869) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2006) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Brünnich (1768) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chaine & Duvergier (1928) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chassaing et al. (2018) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Cornish (1885) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa (1862) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1849) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1866) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couteyen (2006) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Cuvier & Valenciennes (1830-1832) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1846) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1849) | 1 | 0,09% | 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) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Danois (1913) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin et al. (2015) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Desbrosses (1934) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Desbrosses (1935) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Desse-berset & Williot (2011) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Desse-Berset & Williot (2012) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Desse-Berset (2012) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Diaz & Cuzange (2009) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Dollfus (1960) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Fabricius (1780) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1882) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forest (1946) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Forskål (1775) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1908) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy et al. (1996) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Garman (1913) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gérard et al. (2017) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Gill & Ryder (1883) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Gill (1861) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1864) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1873-1874) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1878) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1855) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gistel (1848) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1877) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1879) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Goode & Bean (1883) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Goode (1881) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren & Galil (2015) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1864) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1866) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1878) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1888) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Günther (1889) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jensen (1905) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Evermann (1898) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Jordan & Gilbert (1881) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1892) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Joyeux (1923) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Keith & Dorson (2003) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Keith & Machino (2003) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Keith et al. (2002) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Keith et al. (2006) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Keith (2002) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Kiszka et al. (2009) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Krøyer (1845) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1845) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1852-53) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legendre (1923) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Lim et al. (2002) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Lowe et al. (2007) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Lowe (1838) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1887) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1892) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maddalena & Zuffa (2008) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Malm (1861) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marshall (1955) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Merckx (1998) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Mitchill (1814) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monti et al. (2010) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Moreau (1881) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ogilby (1911) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osbeck (1765) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1787) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1812) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1902) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Puissauve, Legros, Evanno & Acou (2015) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Quéro (2017) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Quero et al. (2013) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Richer de Forges et al. (2005) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Rignault & Chevallier (2017) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Rousseau (2010) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Sawai et al. (2018) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Scoresby (1820) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw (1804) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherborn (1895) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sigalas (1931) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Simian et al. (2008) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Steenstrup (1876) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1881) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1846) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1848) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN Comité français, OFB & MNHN (2021) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Urtizberea et al. (2021) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Vaillant (1888) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaillant (1888) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet & Agrnsm (2018) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Whitley (1944) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1948) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wood (1848) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zugmayer (1911) | 1 | 0,09% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
