Poissons de la Réunion
476 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fricke et al. (2009) | 973 | 13,13% | 923 | 78,55% | 922 | 79,07% | 918 | 78,66% |
Fricke et al. (2011) | 717 | 9,67% | 688 | 58,55% | 687 | 58,92% | 686 | 58,78% |
Wickel & Jamon (2010) | 579 | 7,81% | 550 | 46,81% | 548 | 47% | 549 | 47,04% |
Siu et al. (2017) | 508 | 6,85% | 488 | 41,53% | 487 | 41,77% | 486 | 41,65% |
Fricke et al. (2013) | 329 | 4,44% | 318 | 27,06% | 317 | 27,19% | 316 | 27,08% |
Williams et al. (2006) | 305 | 4,12% | 289 | 24,6% | 289 | 24,79% | 287 | 24,59% |
Delrieu-Trottin et al. (2015) | 273 | 3,68% | 256 | 21,79% | 254 | 21,78% | 256 | 21,94% |
Chabanet & Durville (2005) | 251 | 3,39% | 224 | 19,06% | 224 | 19,21% | 224 | 19,19% |
Bacchet et al. (2007) | 193 | 2,6% | 179 | 15,23% | 179 | 15,35% | 179 | 15,34% |
Kulbicki et al. (2000) | 181 | 2,44% | 159 | 13,53% | 159 | 13,64% | 157 | 13,45% |
Allen (comm. pers., 2009) | 150 | 2,02% | 128 | 10,89% | 128 | 10,98% | 125 | 10,71% |
Kulbicki (comm. pers., 2011) | 144 | 1,94% | 128 | 10,89% | 128 | 10,98% | 128 | 10,97% |
Richard et al. (1982) | 79 | 1,07% | 28 | 2,38% | 28 | 2,4% | 27 | 2,31% |
Béarez et al. (2017) | 73 | 0,99% | 73 | 6,21% | 73 | 6,26% | 71 | 6,08% |
Béarez & Bouffandeau (2019) | 67 | 0,9% | 65 | 5,53% | 65 | 5,57% | 64 | 5,48% |
Keith et al. (2006) | 59 | 0,8% | 43 | 3,66% | 41 | 3,52% | 42 | 3,6% |
Fourriére et al. (2014) | 58 | 0,78% | 56 | 4,77% | 56 | 4,8% | 55 | 4,71% |
Legand (1950) | 48 | 0,65% | 23 | 1,96% | 23 | 1,97% | 23 | 1,97% |
Questel (2020) | 36 | 0,49% | 35 | 2,98% | 35 | 3% | 32 | 2,74% |
Questel & Le Quellec (2012) | 33 | 0,45% | 31 | 2,64% | 31 | 2,66% | 29 | 2,49% |
Béarez & Séret (2009) | 31 | 0,42% | 30 | 2,55% | 30 | 2,57% | 30 | 2,57% |
Cuvier & Valenciennes (1833) | 31 | 0,42% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Randall & Earle (2000) | 25 | 0,34% | 23 | 1,96% | 22 | 1,89% | 23 | 1,97% |
Collette & Nauen (1983) | 23 | 0,31% | 23 | 1,96% | 19 | 1,63% | 23 | 1,97% |
Poey (1858-61) | 23 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2013) | 22 | 0,3% | 16 | 1,36% | 16 | 1,37% | 16 | 1,37% |
Linnaeus (1758) | 22 | 0,3% | 7 | 0,6% | 7 | 0,6% | 7 | 0,6% |
Letourneur et al. (2004) | 20 | 0,27% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Séret (1997) | 20 | 0,27% | 19 | 1,62% | 19 | 1,63% | 19 | 1,63% |
Bouchon-Navaro et al. (2005) | 19 | 0,26% | 12 | 1,02% | 12 | 1,03% | 11 | 0,94% |
Soubeyran (2008) | 19 | 0,26% | 17 | 1,45% | 17 | 1,46% | 17 | 1,46% |
Rafinesque Schmaltz (1810) | 16 | 0,22% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Pinault et al. (2013) | 14 | 0,19% | 13 | 1,11% | 13 | 1,11% | 13 | 1,11% |
Müller & Henle (1841) | 13 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1997) | 13 | 0,18% | 13 | 1,11% | 11 | 0,94% | 13 | 1,11% |
Keith et al. (2002) | 12 | 0,16% | 8 | 0,68% | 8 | 0,69% | 8 | 0,69% |
Kiszka et al. (2009) | 12 | 0,16% | 10 | 0,85% | 10 | 0,86% | 10 | 0,86% |
Mulochau et al. (2019) | 12 | 0,16% | 12 | 1,02% | 12 | 1,03% | 12 | 1,03% |
Bloch & Schneider (1801) | 10 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Compagno (1984) | 10 | 0,13% | 10 | 0,85% | 10 | 0,86% | 10 | 0,86% |
Cuvier & Valenciennes ([1832]) | 10 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Eudeline (2022) | 10 | 0,13% | 10 | 0,85% | 10 | 0,86% | 10 | 0,86% |
Kronen et al. (2009) | 10 | 0,13% | 9 | 0,77% | 9 | 0,77% | 9 | 0,77% |
Compagno (1984) | 9 | 0,12% | 8 | 0,68% | 8 | 0,69% | 8 | 0,69% |
Lourie et al. (2016) | 9 | 0,12% | 7 | 0,6% | 7 | 0,6% | 7 | 0,6% |
Wickel et al. (2014) | 9 | 0,12% | 9 | 0,77% | 9 | 0,77% | 9 | 0,77% |
Causse et al. (2023) | 8 | 0,11% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fourt et al. (2017) | 8 | 0,11% | 8 | 0,68% | 8 | 0,69% | 8 | 0,69% |
Kronen et al. (2008) | 8 | 0,11% | 8 | 0,68% | 8 | 0,69% | 8 | 0,69% |
Bonnaterre (1788) | 7 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Gronow (1854) | 7 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Justine et al. (2010) | 7 | 0,09% | 7 | 0,6% | 7 | 0,6% | 7 | 0,6% |
Gargominy et al. (1996) | 6 | 0,08% | 6 | 0,51% | 6 | 0,51% | 6 | 0,51% |
Keith et al. (2011) | 6 | 0,08% | 6 | 0,51% | 6 | 0,51% | 6 | 0,51% |
Keith et al. (2014) | 6 | 0,08% | 6 | 0,51% | 6 | 0,51% | 6 | 0,51% |
Klunzinger (1871) | 6 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 6 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Motomura et al. (2011) | 6 | 0,08% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Nardo (1827) | 6 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Pavan-Kumar et al. (2018) | 6 | 0,08% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Quero (1997) | 6 | 0,08% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Rignault & Chevallier (2017) | 6 | 0,08% | 6 | 0,51% | 6 | 0,51% | 6 | 0,51% |
Rousseau (2010) | 6 | 0,08% | 6 | 0,51% | 6 | 0,51% | 6 | 0,51% |
Séret (2014) | 6 | 0,08% | 5 | 0,43% | 4 | 0,34% | 5 | 0,43% |
Simian et al. (2022) | 6 | 0,08% | 6 | 0,51% | 6 | 0,51% | 6 | 0,51% |
Snodgrass & Heller (1905) | 6 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Uicn et al. (2019) | 6 | 0,08% | 6 | 0,51% | 6 | 0,51% | 6 | 0,51% |
Wantiez (comm. pers., 2008) | 6 | 0,08% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Bouchon-Navaro & Louis (1986) | 5 | 0,07% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Cuvier & Valenciennes (1830) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1830-1832) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Ifremer (2009) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Ifremer (2020) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Keith et al. (1999) | 5 | 0,07% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Keith et al. (2009) | 5 | 0,07% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Keith (2002) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Lacepède (1801) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nakamura (1985) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Nielsen & Quero (1991) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Pascal et al. (2006) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Pinault et al. (2018) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Randall et al. (2015) | 5 | 0,07% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Risso (1827) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet & Agrnsm (2018) | 5 | 0,07% | 5 | 0,43% | 5 | 0,43% | 5 | 0,43% |
Walbaum (1792) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams & Viviani (2016) | 5 | 0,07% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Berry & Smith-Vaniz (1978) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Brugneaux & Pérès (2006) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Chen et al. (2024) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Collet et al. (2017) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Duhamel et al. (2005) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Hadley & Hansen (1986) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2011) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Kenaley (2007) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Latham (1794) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Monti et al. (2010) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Rafinesque (1810) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall (1998) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer de Forges et al. (2005) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Rüppell (1835) | 4 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Smith (1849) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1839) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2020) | 4 | 0,05% | 4 | 0,34% | 4 | 0,34% | 4 | 0,34% |
Bloch & Schneider (1801) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsa et al. (2014) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Brosse et al. (2021) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Cuvier & Valenciennes (1846) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril (1865) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir (1966) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1899) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1913) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1862) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1847) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Ifremer (2022) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Johnson (1863) | 3 | 0,04% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Jourdan (2020) | 3 | 0,04% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Kaup (1856) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kottelat ( 2013) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lacepède (1800) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur & Maggiorani (1995) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Lorvelec & Pascal (2009) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Louis et al. (1992) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Lowe (1834) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Marquet et al. (2003) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Matsunuma et al. (2017) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mennesson & Keith (2017) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Mitchill (1815) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1874) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Mourier et al. (2013) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Nelson-Smith et al. (2014) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pallas (1770) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Perez Canto (1886) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1887) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1902) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Postel (1965) | 3 | 0,04% | 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) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Quero & Mauge (1989) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Quero & Saldanha (1995) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Quero et al. (2009) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Quéro et al. (2009) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Randall & Victor (2015) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Risso (1810) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Tea et al. (2020) | 3 | 0,04% | 3 | 0,26% | 3 | 0,26% | 3 | 0,26% |
Vaillant (1888) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1931) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Alley et al. (2023) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Ayres (1843) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bearez et al. (2013) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Bellotti (1878) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bennett (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1852) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1837) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsa et al. (2013) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Bourjon & Fricke (2016) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Bourjon et al. (2018) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Brünnich (1788) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Curd et al. (2015) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Cuvier & Valenciennes (1849) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Düben & Koren (1846) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Evermann & Clark (1928) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Faria et al. (2013) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fernandez-Carvalho et al. (2013) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Feutry et al. (2012) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Fischer (1884) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraser (2013) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fricke & Durville (2020) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Fricke & Durville (2021) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Fricke et al. (2013) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Fricke et al. (2021) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Fricke (1999) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fricke (2004) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Froese & Pauly (2020) | 2 | 0,03% | 2 | 0,17% | 1 | 0,09% | 2 | 0,17% |
Geange (2010) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Gill & Fricke (2001) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Goode & Bean (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Greenfield & Smith (2004) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Griffith & Smith (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1848) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Günther (1870) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1877) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1880) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hibino & Kimura (2016) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Ho & Wa (2016) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Howell Rivero (1936) | 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% |
Keith & Marquet (2006) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Mennesson (2023) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Koeck et al. (2014) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Kotlyar (1979) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kyne et al. (2016) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Lacepède (1803) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lim et al. (2002) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Lowe (1838) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1841) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Marshall et al. (2009) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Melendez & Markle (1997) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Mennesson et al. (2019) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Millot et al. (2023) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Mooi & Randall (2014) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Moreau (1881) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Myers (1991) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Nichols & Breder (1928) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ogilby (1911) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Okamoto & Motomura (2012) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Owen (1853) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Palko et al. (1982) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Pallas [1814] | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pennant (1776) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Persat & Keith (1997) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Poey (1851-1854) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Pyle (1990) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Quero et al. (2009) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Quero et al. (2013) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Randall & Dibattista (2013) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall et al. (2008) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Randall (2004) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Saldanha & Quero (1994) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Schomburgk (1848) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schwarzhans & Prokofiev (2017) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Séret & Quod (2023) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Shaw & Nodder (1792-1793) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Springer & Fricke (2000) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Tea & Larson (2023) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Teichert et al. (2013) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Temminck & Schlegel (1850) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN France & MNHN (2013) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Weber (1913) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1944) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2020) | 2 | 0,03% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Aboussouan & Rasonarivo (1986) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Agassiz (1833-1843) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Alcock (1890) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Alcock (1898) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (1995) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Allen (2018) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Anderson (2018) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Atwood (1869) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Audige (1927) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauchot & Mauge ([2018]) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bennett (1832) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bennett (1860) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertin (1928) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Blainville (1816) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1847) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1854) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1855) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1858) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1790) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1791) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1792) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1793) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bodilis et al. (2011) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bohlke & Randall (1981) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bohlke (1951) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bonaparte (1839[1838]) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsa et al. (2013) | 1 | 0,01% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Bouchon-Navaro et al. (1992) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Boulenger (1912) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourjon & Fricke (2019) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bourjon & Fricke (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bourjon et al. (2019) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Brauer (1902) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bray & Cribb (2002) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bray et al. (2010) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Breder & Nichols (1930) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Brünnich (1768) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Buray et al. (2009) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Causse & Hautecoeur (2006) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Records of the Indian Museum (Calcutta). 2(4): 391-392.">Chaudhuri (1908) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Clua & Imirizaldu (2017) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Clua & Planes (2019) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Clua et al. (2016) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Costa (1829-1853) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cottalorda et al. (2009) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Couteyen (2006) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cuvier & Valenciennes (1828-1830) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1835) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Daniel et al. (2009) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Day (1865) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Denys et al. (2014) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Denys (2008) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Desbrosses (1935) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Durville et al. (2009) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Durville (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Esmark (1871) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
European Nucleotide Archive (2019) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Faber (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Firmat & Alibert (2011) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1946) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Forskål (1775) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Forsskål (1775) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir (1970) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraser-brunner (1950) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke (2015) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Frickel (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gadenne et al. (2021) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Garman (1913) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gentry et al. (2004) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Geoffroy Saint-Hilaire ([1817]) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerovasileiou et al. (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gill & Ryder (1883) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gill (1862) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1863) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1878) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1883) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (2022) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Giorna (1809) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Girard (1855) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Girard (1859) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Girard (1859) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Girondot et al. (2015) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gistel (1848) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1879) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gozlan et al. (2010) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Günther (1859) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1860) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1878) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunther (1890) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Haÿ et al. (2023) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hibino et al. (2016) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2023) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Iglésias et al. (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Johnson (1890) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Evermann (1903) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Fowler (1902) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1880) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Jordan (1922) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Starks (1901) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan et al. (1927) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1892) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1895) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kamohara (1938) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Dorson (2003) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Keith & Dorson (2003) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Keith & Dorson (2003) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Keith & Dorson (2003) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Keith & Mennesson (2021) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Mennesson (2023) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Keith (2003) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Keith (2003) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Kishimoto (1986) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Klausewitz & von Hentig (1975) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Laboute & Grandperrin (2002) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lacepède (1802) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Le Bail et al. (2012) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Leach (1818) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Legendre (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1830-1831) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1818) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1822) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Liénard (1840) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2018) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lizé (2018) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lizé (2019) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Loiselle & Stiassny (2007) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lowe (1833) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lowe (1838) | 1 | 0,01% | 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 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1843) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Maddalena & Zuffa (2008) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Maeda et al. (2011) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Malm (1877) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsunuma & Motomura (2018) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Matsuzaki et al. (2009) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Meek & Hildebrand (1923) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Mennesson & Keith (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Merker (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mourier (2012) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1884) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1887) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Antonelli, Venezia. 128 pp.">Nardo (1847) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël, Meunier (2010) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Norman (1939) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Noronha (1926) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ocea & Consult' (2015) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Osbeck (1765) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pellegrin (1912) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelosse (1927) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Peters (1852) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pezold & Larson (2015) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pinault et al. (2014) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pinault et al. (2015) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Poey (1863) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1865) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1868) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Poss (1982) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Puissauve & Poulet (2015) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Quero & Laborde (1996) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Quero & Spitz (2012) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Quero et al. (1998) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Quero et al. (2006) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Quero (1998) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Questel (2022) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rafinesque (1814) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque (1820) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramsay (1880) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Earle (2004) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Randall & Kulbicki (2006) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Lubbock (1981) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Victor (2013) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Randall & Wrobel (1988) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Randall_1980 | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Randall_2011 | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ranzani (1839) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ranzani (1842) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Regan (1903) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Reid et al. (2016) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Richardson (1846) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rigby & Adamson (1997) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Risso (1820) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Romanov et al. (2013) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Romanov et al. (2021) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rüppell (1828-1830) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Saemundsson (1922) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sawai et al. (2018) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Sherborn (1895) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn (1925) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith & Smith (1963) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith et al. (2019) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Smith (1960) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Smith (1966) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Springer & Waller (1969) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Springer (1941) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1867) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Storer (1839) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Storer (1846) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Storer (1848) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Taquet (1994) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tea et al. (2019) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
The International Barcode of Life Consortium (2016) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tornabene et al. (2016) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tsadok et al. (2015) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
UICN Comité français, OFB & MNHN (2021) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Uyeno et al. (1983) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Vaillant (1888) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1836-1844) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Van & Kampen (1907) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Guelpen (2016) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Waite (1904) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wantiez (2000) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Whitley (1929) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1939) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1943) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel & Fricke (2022) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Wickel et al. (2016) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Williams (2018) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Yang et al. (2019) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Yokoyama (2013) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |