Poissons marins de Mayotte
338 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Wickel & Jamon (2010) | 729 | 10,64% | 684 | 61,35% | 682 | 61,44% | 683 | 61,48% |
Fricke et al. (2011) | 722 | 10,54% | 690 | 61,88% | 689 | 62,07% | 689 | 62,02% |
Fricke et al. (2009) | 693 | 10,11% | 656 | 58,83% | 656 | 59,1% | 653 | 58,78% |
Siu et al. (2017) | 510 | 7,44% | 492 | 44,13% | 492 | 44,32% | 491 | 44,19% |
Fricke et al. (2013) | 355 | 5,18% | 343 | 30,76% | 342 | 30,81% | 341 | 30,69% |
Williams et al. (2006) | 354 | 5,17% | 330 | 29,6% | 330 | 29,73% | 329 | 29,61% |
Allen (comm. pers., 2009) | 283 | 4,13% | 251 | 22,51% | 251 | 22,61% | 250 | 22,5% |
Chabanet & Durville (2005) | 275 | 4,01% | 246 | 22,06% | 246 | 22,16% | 246 | 22,14% |
Delrieu-Trottin et al. (2015) | 274 | 4% | 260 | 23,32% | 259 | 23,33% | 260 | 23,4% |
Bacchet et al. (2007) | 201 | 2,93% | 185 | 16,59% | 185 | 16,67% | 185 | 16,65% |
Kulbicki et al. (2000) | 200 | 2,92% | 173 | 15,52% | 173 | 15,59% | 172 | 15,48% |
Kulbicki (comm. pers., 2011) | 151 | 2,2% | 138 | 12,38% | 138 | 12,43% | 138 | 12,42% |
Richard et al. (1982) | 84 | 1,23% | 26 | 2,33% | 26 | 2,34% | 26 | 2,34% |
Béarez & Bouffandeau (2019) | 67 | 0,98% | 65 | 5,83% | 65 | 5,86% | 64 | 5,76% |
Legand (1950) | 52 | 0,76% | 28 | 2,51% | 28 | 2,52% | 28 | 2,52% |
Fourriére et al. (2014) | 51 | 0,74% | 49 | 4,39% | 49 | 4,41% | 49 | 4,41% |
Keith et al. (2006) | 46 | 0,67% | 35 | 3,14% | 33 | 2,97% | 35 | 3,15% |
Béarez et al. (2017) | 34 | 0,5% | 34 | 3,05% | 34 | 3,06% | 34 | 3,06% |
Questel (2020) | 31 | 0,45% | 30 | 2,69% | 30 | 2,7% | 29 | 2,61% |
Béarez & Séret (2009) | 29 | 0,42% | 28 | 2,51% | 28 | 2,52% | 28 | 2,52% |
Questel & Le Quellec (2012) | 29 | 0,42% | 27 | 2,42% | 27 | 2,43% | 26 | 2,34% |
Cuvier & Valenciennes (1833) | 24 | 0,35% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Randall & Earle (2000) | 24 | 0,35% | 20 | 1,79% | 19 | 1,71% | 20 | 1,8% |
Wickel et al. (2014) | 20 | 0,29% | 17 | 1,52% | 17 | 1,53% | 17 | 1,53% |
Bouchon-Navaro et al. (2005) | 19 | 0,28% | 12 | 1,08% | 12 | 1,08% | 11 | 0,99% |
Collette & Nauen (1983) | 19 | 0,28% | 19 | 1,7% | 19 | 1,71% | 19 | 1,71% |
Eudeline (2022) | 19 | 0,28% | 19 | 1,7% | 19 | 1,71% | 19 | 1,71% |
Séret (1997) | 19 | 0,28% | 17 | 1,52% | 17 | 1,53% | 17 | 1,53% |
Mulochau et al. (2019) | 18 | 0,26% | 17 | 1,52% | 17 | 1,53% | 17 | 1,53% |
Poey (1858-61) | 18 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2013) | 17 | 0,25% | 11 | 0,99% | 11 | 0,99% | 11 | 0,99% |
Linnaeus (1758) | 16 | 0,23% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Kiszka et al. (2009) | 13 | 0,19% | 10 | 0,9% | 10 | 0,9% | 10 | 0,9% |
Rafinesque Schmaltz (1810) | 13 | 0,19% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Müller & Henle (1841) | 12 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinault et al. (2013) | 11 | 0,16% | 10 | 0,9% | 10 | 0,9% | 10 | 0,9% |
Compagno (1984) | 10 | 0,15% | 10 | 0,9% | 10 | 0,9% | 10 | 0,9% |
Smith (1997) | 10 | 0,15% | 10 | 0,9% | 8 | 0,72% | 10 | 0,9% |
Compagno (1984) | 9 | 0,13% | 8 | 0,72% | 8 | 0,72% | 8 | 0,72% |
Justine et al. (2010) | 9 | 0,13% | 9 | 0,81% | 9 | 0,81% | 9 | 0,81% |
Kronen et al. (2009) | 9 | 0,13% | 8 | 0,72% | 8 | 0,72% | 8 | 0,72% |
Letourneur et al. (2004) | 9 | 0,13% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pearman et al. (2020) | 9 | 0,13% | 9 | 0,81% | 9 | 0,81% | 9 | 0,81% |
Causse et al. (2023) | 8 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fricke et al. (2024) | 8 | 0,12% | 8 | 0,72% | 8 | 0,72% | 8 | 0,72% |
Bloch & Schneider (1801) | 7 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1788) | 7 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes ([1832]) | 7 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Kronen et al. (2008) | 7 | 0,1% | 7 | 0,63% | 7 | 0,63% | 7 | 0,63% |
Simian et al. (2022) | 7 | 0,1% | 7 | 0,63% | 7 | 0,63% | 7 | 0,63% |
Berry & Smith-Vaniz (1978) | 6 | 0,09% | 6 | 0,54% | 6 | 0,54% | 6 | 0,54% |
Charbonnel (1990) | 6 | 0,09% | 6 | 0,54% | 6 | 0,54% | 6 | 0,54% |
Fourt et al. (2017) | 6 | 0,09% | 6 | 0,54% | 6 | 0,54% | 6 | 0,54% |
Keith et al. (2002) | 6 | 0,09% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Klunzinger (1871) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lourie et al. (2016) | 6 | 0,09% | 5 | 0,45% | 5 | 0,45% | 5 | 0,45% |
Pavan-Kumar et al. (2018) | 6 | 0,09% | 5 | 0,45% | 5 | 0,45% | 5 | 0,45% |
Randall (1998) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 6 | 0,09% | 6 | 0,54% | 6 | 0,54% | 6 | 0,54% |
Bouchon-Navaro & Louis (1986) | 5 | 0,07% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Cuvier & Valenciennes (1830) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gronow (1854) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2009) | 5 | 0,07% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Lacepède (1801) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque (1810) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rousseau (2010) | 5 | 0,07% | 5 | 0,45% | 5 | 0,45% | 5 | 0,45% |
Snodgrass & Heller (1905) | 5 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Wantiez (comm. pers., 2008) | 5 | 0,07% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Wickel et al. (2016) | 5 | 0,07% | 5 | 0,45% | 5 | 0,45% | 5 | 0,45% |
Williams & Viviani (2016) | 5 | 0,07% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Brugneaux & Pérès (2006) | 4 | 0,06% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Goiran & Shine (2020) | 4 | 0,06% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Goulletquer (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Hadley & Hansen (1986) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2024) | 4 | 0,06% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Keith et al. (2014) | 4 | 0,06% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Letourneur & Maggiorani (1995) | 4 | 0,06% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Marshall et al. (2009) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Nardo (1827) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 4 | 0,06% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Risso (1810) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rüppell (1835) | 4 | 0,06% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Swainson (1839) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet & Agrnsm (2018) | 4 | 0,06% | 4 | 0,36% | 4 | 0,36% | 4 | 0,36% |
Borsa et al. (2014) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cuvier & Valenciennes (1830-1832) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1862) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (2004) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Guichenot (1847) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemida et al. (2003) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Keith & Marquet (2011) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Keith et al. (2020) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Lorvelec & Pascal (2009) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Louis et al. (1992) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Matsunuma et al. (2017) | 3 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mennesson & Keith (2017) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Mennesson & Keith (2020) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Motomura et al. (2011) | 3 | 0,04% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Mourier et al. (2013) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
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% |
Quero & Saldanha (1995) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 3 | 0,27% |
Smales et al. (2007) | 3 | 0,04% | 3 | 0,27% | 3 | 0,27% | 2 | 0,18% |
Walbaum (1792) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (2002) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
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% |
Bourjon & Fricke (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Bourjon et al. (2018) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Brünnich (1788) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Collet et al. (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
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 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Evermann & Clark (1928) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Feutry et al. (2012) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Garman (1913) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Geange (2010) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Griffith & Smith (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1848) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Günther (1880) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Holleman (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Keith & Marquet (2006) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Mennesson (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Keith & Mennesson (2023) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Klausewitz & von Hentig (1975) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Kyne et al. (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Lacepède (1800) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Last et al. (2016) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Macdonald & Barron (1868) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Marquet et al. (2003) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
McClelland (1844) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 0 | 0% |
Mennesson et al. (2019) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Millot et al. (2023) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Mitchill (1815) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1881) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nakamura (1985) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Nelson-Smith et al. (2014) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Owen (1853) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Palko et al. (1982) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Pinault et al. (2018) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
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 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Pyle (1990) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Quero et al. (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Quero (1997) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
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% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret & Quod (2023) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Séret (2014) | 2 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Shaw & Nodder (1792-1793) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1849) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tea & Larson (2023) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Teichert et al. (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Temminck & Schlegel (1850) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Weber (1913) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Winterbottom & Harold (2005) | 2 | 0,03% | 2 | 0,18% | 2 | 0,18% | 2 | 0,18% |
Agassiz (1833-1843) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (1995) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Andrews (1893) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Anonyme (2013) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Anonyme ([2018]) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Atwood (1869) | 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% |
Bennett (1831) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertin (1928) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bianconi (1895-1867) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
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 (1856) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1858) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 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 (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% |
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% |
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% |
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% |
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% |
Curd et al. (2015) | 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 (1830) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1835) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1847) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1849) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Daniel et al. (2009) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Dawson (1978) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Day (1865) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Desbrosses (1935) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Downie et al. (2011) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Duhamel (2005) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Faber (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1946) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Forsskål (1775) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir (1966) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraser-brunner (1950) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke et al. (2023) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fricke (2015) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fritzsche (1980) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1913) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
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 (1862) | 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% |
Girondot et al. (2015) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Goren (1981) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gout (1991) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Greenfield & Jewett (2011) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Günther (1859) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunther (1890) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hatooka (1984) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Haÿ et al. (2023) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hoshino & Motomura (2022) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
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% |
Jordan & Evermann (1903) | 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% |
Jufaili et al. (2022) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Kamohara (1938) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
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 et al. (1999) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Kottelat ( 2013) | 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 (1798) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1803) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lassauce et al. (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Last et al. (2016) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Legendre (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1830-1831) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1822) | 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 (2018) | 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 (1834) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
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 (1841) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddalena & Zuffa (2008) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Madi Moussa (2013) | 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% |
Matsunuma & Motomura (2018) | 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% |
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% |
Notarbartolo et al. (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ocea & Consult' (2015) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ogilby (1911) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Osbeck (1765) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pellegrin (1932) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Poey (1863) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Poss (2012) | 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 et al. (1998) | 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 (2023) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
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% |
Ranzani (1839) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Regan (1903) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer de Forges et al. (2005) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rigby & Adamson (1997) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rüppell (1828-1830) | 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% |
Schultz et al. (1953) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn (1895) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn (1925) | 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 (1957) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1966) | 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 (1848) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Subirana et al. (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
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% |
Tsadok et al. (2015) | 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% |
Van & Kampen (1907) | 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 (1931) | 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 (1944) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1948) | 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. (2020) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Wickel et al. (2023) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Wickstead (1970) | 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% |
Winterbottom & Burridge (1993) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Winterbottom & Hoese (2015) | 1 | 0,01% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Winterbottom (1989) | 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% |