Espèces marines strictes avec un statut affecté au territoire métropolitain
Groupe créé pour compléter l'ABDSM pour les espèces marines avec un statut
721 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Rinaldi (2016) | 212 | 4,94% | 200 | 24,88% | 200 | 25,67% | 152 | 19,26% |
| Carzon et al. (2016) | 159 | 3,71% | 150 | 18,66% | 150 | 19,26% | 114 | 14,45% |
| Estrade et al. (2016) | 159 | 3,71% | 150 | 18,66% | 150 | 19,26% | 114 | 14,45% |
| Pichon (2007) | 158 | 3,68% | 128 | 15,92% | 128 | 16,43% | 128 | 16,22% |
| Fricke et al. (2011) | 115 | 2,68% | 104 | 12,94% | 104 | 13,35% | 104 | 13,18% |
| Béarez et al. (2017) | 108 | 2,52% | 107 | 13,31% | 107 | 13,74% | 107 | 13,56% |
| Fricke et al. (2009) | 104 | 2,42% | 99 | 12,31% | 99 | 12,71% | 99 | 12,55% |
| Pichon & Thomassin (2005) | 100 | 2,33% | 80 | 9,95% | 80 | 10,27% | 80 | 10,14% |
| Wickel & Jamon (2010) | 97 | 2,26% | 89 | 11,07% | 89 | 11,42% | 89 | 11,28% |
| Questel (2020) | 81 | 1,89% | 77 | 9,58% | 77 | 9,88% | 73 | 9,25% |
| Faure et al. (2008) | 74 | 1,72% | 62 | 7,71% | 62 | 7,96% | 62 | 7,86% |
| Pichon et al. (2007) | 74 | 1,72% | 64 | 7,96% | 64 | 8,22% | 64 | 8,11% |
| Siu et al. (2017) | 74 | 1,72% | 71 | 8,83% | 71 | 9,11% | 71 | 9% |
| Questel & Le Quellec (2012) | 71 | 1,66% | 61 | 7,59% | 61 | 7,83% | 57 | 7,22% |
| Tricart & Foubert (2000) | 65 | 1,52% | 54 | 6,72% | 54 | 6,93% | 54 | 6,84% |
| Glynn et al. (2007) | 60 | 1,4% | 52 | 6,47% | 52 | 6,68% | 52 | 6,59% |
| Linnaeus (1758) | 59 | 1,38% | 16 | 1,99% | 16 | 2,05% | 15 | 1,9% |
| Uicn et al. (2015) | 58 | 1,35% | 54 | 6,72% | 49 | 6,29% | 39 | 4,94% |
| Charrassin (2016) | 53 | 1,24% | 50 | 6,22% | 50 | 6,42% | 38 | 4,82% |
| Charrassin (2016) | 53 | 1,24% | 50 | 6,22% | 50 | 6,42% | 38 | 4,82% |
| Jarrett & Shirihai (2014) | 53 | 1,24% | 49 | 6,09% | 49 | 6,29% | 37 | 4,69% |
| Moutou (2016) | 53 | 1,24% | 50 | 6,22% | 50 | 6,42% | 38 | 4,82% |
| Spitz et al. (2016) | 53 | 1,24% | 50 | 6,22% | 50 | 6,42% | 38 | 4,82% |
| Thoisy & Bordin (2016) | 53 | 1,24% | 50 | 6,22% | 50 | 6,42% | 38 | 4,82% |
| Urtizberea (2016) | 53 | 1,24% | 50 | 6,22% | 50 | 6,42% | 38 | 4,82% |
| Fricke et al. (2013) | 46 | 1,07% | 45 | 5,6% | 45 | 5,78% | 45 | 5,7% |
| Fourt et al. (2017) | 42 | 0,98% | 40 | 4,98% | 40 | 5,13% | 40 | 5,07% |
| Pichon (comm. pers., 2012) | 41 | 0,96% | 36 | 4,48% | 36 | 4,62% | 36 | 4,56% |
| Chabanet & Durville (2005) | 40 | 0,93% | 33 | 4,1% | 33 | 4,24% | 33 | 4,18% |
| Nelson-Smith et al. (2014) | 40 | 0,93% | 32 | 3,98% | 32 | 4,11% | 31 | 3,93% |
| Uicn et al. (2020) | 39 | 0,91% | 36 | 4,48% | 36 | 4,62% | 36 | 4,56% |
| Delrieu-Trottin et al. (2015) | 34 | 0,79% | 32 | 3,98% | 32 | 4,11% | 32 | 4,06% |
| Diaz & Cuzange (2009) | 33 | 0,77% | 27 | 3,36% | 27 | 3,47% | 25 | 3,17% |
| Williams et al. (2006) | 31 | 0,72% | 28 | 3,48% | 28 | 3,59% | 28 | 3,55% |
| Garrigue (2007) | 30 | 0,7% | 30 | 3,73% | 29 | 3,72% | 22 | 2,79% |
| Bordin et al. (2021) | 29 | 0,68% | 29 | 3,61% | 29 | 3,72% | 20 | 2,53% |
| Kulbicki et al. (2000) | 27 | 0,63% | 25 | 3,11% | 25 | 3,21% | 25 | 3,17% |
| Bacchet et al. (2007) | 26 | 0,61% | 23 | 2,86% | 23 | 2,95% | 23 | 2,92% |
| Aulagnier (2009) | 25 | 0,58% | 23 | 2,86% | 23 | 2,95% | 14 | 1,77% |
| Fenner & Muir (2008) | 25 | 0,58% | 20 | 2,49% | 20 | 2,57% | 20 | 2,53% |
| G.E.M.M. (2012) | 25 | 0,58% | 25 | 3,11% | 25 | 3,21% | 17 | 2,15% |
| Dana (1846-1849) | 24 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot (comm. pers., 2018) | 23 | 0,54% | 22 | 2,74% | 22 | 2,82% | 22 | 2,79% |
| Catzeflis (2012) | 23 | 0,54% | 22 | 2,74% | 22 | 2,82% | 14 | 1,77% |
| Gannier (2001) | 23 | 0,54% | 23 | 2,86% | 23 | 2,95% | 15 | 1,9% |
| Müller & Henle (1841) | 23 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter et al. (2021) | 22 | 0,51% | 22 | 2,74% | 22 | 2,82% | 18 | 2,28% |
| Ducarme (2023) | 22 | 0,51% | 22 | 2,74% | 22 | 2,82% | 22 | 2,79% |
| Bouchon-Navaro et al. (2005) | 21 | 0,49% | 16 | 1,99% | 16 | 2,05% | 16 | 2,03% |
| Chevalier & Kuhlmann (1983) | 21 | 0,49% | 12 | 1,49% | 12 | 1,54% | 12 | 1,52% |
| Perrin et al. (2002) | 21 | 0,49% | 18 | 2,24% | 16 | 2,05% | 13 | 1,65% |
| Rafinesque Schmaltz (1810) | 20 | 0,47% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Shirihai (2003) | 20 | 0,47% | 16 | 1,99% | 15 | 1,93% | 11 | 1,39% |
| Fourriére et al. (2014) | 18 | 0,42% | 17 | 2,11% | 17 | 2,18% | 17 | 2,15% |
| Gannier (2002) | 18 | 0,42% | 18 | 2,24% | 18 | 2,31% | 14 | 1,77% |
| Gannier (2009) | 18 | 0,42% | 18 | 2,24% | 18 | 2,31% | 13 | 1,65% |
| Kiszka et al.(2007) | 18 | 0,42% | 16 | 1,99% | 16 | 2,05% | 12 | 1,52% |
| Risso (1827) | 17 | 0,4% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Uicn et al. (2017) | 17 | 0,4% | 17 | 2,11% | 17 | 2,18% | 10 | 1,27% |
| Bonaparte (1837) | 16 | 0,37% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Gannier (2000) | 16 | 0,37% | 16 | 1,99% | 16 | 2,05% | 11 | 1,39% |
| Kiszka et al. (2010) | 16 | 0,37% | 15 | 1,87% | 15 | 1,93% | 12 | 1,52% |
| Samaran & Guinet (2009) | 16 | 0,37% | 14 | 1,74% | 12 | 1,54% | 10 | 1,27% |
| Béarez & Bouffandeau (2019) | 15 | 0,35% | 15 | 1,87% | 15 | 1,93% | 15 | 1,9% |
| Lamy & Pointier (2018) | 15 | 0,35% | 10 | 1,24% | 10 | 1,28% | 10 | 1,27% |
| Charbonnel (1990) | 14 | 0,33% | 12 | 1,49% | 12 | 1,54% | 12 | 1,52% |
| Dulau-Drouot et al. (2008) | 14 | 0,33% | 14 | 1,74% | 14 | 1,8% | 10 | 1,27% |
| IUCN (2013) | 14 | 0,33% | 11 | 1,37% | 11 | 1,41% | 11 | 1,39% |
| Kiszka et al. (2009) | 14 | 0,33% | 12 | 1,49% | 12 | 1,54% | 12 | 1,52% |
| Kulbicki (comm. pers., 2011) | 14 | 0,33% | 14 | 1,74% | 14 | 1,8% | 14 | 1,77% |
| Martin (2011) | 14 | 0,33% | 14 | 1,74% | 14 | 1,8% | 14 | 1,77% |
| Sheppard (1987) | 14 | 0,33% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Compagno (1984) | 13 | 0,3% | 12 | 1,49% | 12 | 1,54% | 12 | 1,52% |
| Compagno (1984) | 13 | 0,3% | 13 | 1,62% | 13 | 1,67% | 13 | 1,65% |
| Laran et al. (2011) | 13 | 0,3% | 13 | 1,62% | 13 | 1,67% | 10 | 1,27% |
| Lourie et al. (2016) | 13 | 0,3% | 9 | 1,12% | 9 | 1,16% | 9 | 1,14% |
| Béarez & Séret (2009) | 12 | 0,28% | 10 | 1,24% | 10 | 1,28% | 10 | 1,27% |
| Fournet (2002) | 12 | 0,28% | 12 | 1,49% | 12 | 1,54% | 12 | 1,52% |
| Uthicke et al. (2004) | 12 | 0,28% | 11 | 1,37% | 11 | 1,41% | 11 | 1,39% |
| Boer et al. (1999) | 11 | 0,26% | 10 | 1,24% | 9 | 1,16% | 8 | 1,01% |
| Gronow (1854) | 11 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robineau & Duhamel (2006) | 11 | 0,26% | 9 | 1,12% | 8 | 1,03% | 5 | 0,63% |
| Améziane (2007) | 10 | 0,23% | 9 | 1,12% | 9 | 1,16% | 9 | 1,14% |
| Bloch & Schneider (1801) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boer (2000) | 10 | 0,23% | 8 | 1% | 7 | 0,9% | 4 | 0,51% |
| Bonnaterre (1788) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duchassaing et al. (1864) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1810) | 10 | 0,23% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Tison et al. (2014) | 10 | 0,23% | 5 | 0,62% | 3 | 0,39% | 4 | 0,51% |
| Desbrosses & Etcheberry (1987) | 9 | 0,21% | 7 | 0,87% | 7 | 0,9% | 2 | 0,25% |
| Eriksson et al. (2010) | 9 | 0,21% | 9 | 1,12% | 9 | 1,16% | 9 | 1,14% |
| Gmelin (1789) | 9 | 0,21% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Guille et al. (1986) | 9 | 0,21% | 9 | 1,12% | 9 | 1,16% | 9 | 1,14% |
| Rafinesque (1810) | 9 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 9 | 0,21% | 7 | 0,87% | 7 | 0,9% | 7 | 0,89% |
| Robineau (1989) | 9 | 0,21% | 5 | 0,62% | 4 | 0,51% | 3 | 0,38% |
| Smith (1997) | 9 | 0,21% | 7 | 0,87% | 7 | 0,9% | 7 | 0,89% |
| Bosserelle et al. (2014) | 8 | 0,19% | 8 | 1% | 8 | 1,03% | 8 | 1,01% |
| Breton (2014) | 8 | 0,19% | 7 | 0,87% | 7 | 0,9% | 7 | 0,89% |
| Cabioc'h & Floc'h (2014) | 8 | 0,19% | 5 | 0,62% | 5 | 0,64% | 5 | 0,63% |
| Collette & Nauen (1983) | 8 | 0,19% | 8 | 1% | 8 | 1,03% | 8 | 1,01% |
| Godet et al. (2010) | 8 | 0,19% | 8 | 1% | 8 | 1,03% | 8 | 1,01% |
| Heemstra & Randall (1993) | 8 | 0,19% | 8 | 1% | 8 | 1,03% | 8 | 1,01% |
| Kronen et al. (2008) | 8 | 0,19% | 8 | 1% | 8 | 1,03% | 8 | 1,01% |
| Payri et al. (2002) | 8 | 0,19% | 7 | 0,87% | 7 | 0,9% | 7 | 0,89% |
| Quero et al. (2013) | 8 | 0,19% | 7 | 0,87% | 7 | 0,9% | 7 | 0,89% |
| Simian et al. (2022) | 8 | 0,19% | 8 | 1% | 8 | 1,03% | 8 | 1,01% |
| Valenciennes (1836-1844) | 8 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro & Louis (1986) | 7 | 0,16% | 7 | 0,87% | 7 | 0,9% | 7 | 0,89% |
| Lacepède (1802) | 7 | 0,16% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Malm (1877) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pezold et al. (2015) | 7 | 0,16% | 7 | 0,87% | 7 | 0,9% | 7 | 0,89% |
| Poey (1858-61) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 7 | 0,16% | 7 | 0,87% | 7 | 0,9% | 7 | 0,89% |
| Rossi-santos et al. (2007) | 7 | 0,16% | 5 | 0,62% | 5 | 0,64% | 3 | 0,38% |
| Brugneaux & Pérès (2006) | 6 | 0,14% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Conand et al. (2010) | 6 | 0,14% | 6 | 0,75% | 6 | 0,77% | 6 | 0,76% |
| Dekay (1842) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel et al. (2005) | 6 | 0,14% | 5 | 0,62% | 5 | 0,64% | 5 | 0,63% |
| Fleming (1828) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1803) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas [1814] | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quelch (1886) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1816) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet & Agrnsm (2018) | 6 | 0,14% | 6 | 0,75% | 6 | 0,77% | 6 | 0,76% |
| Walbaum (1792) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1816) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boer & Simmonds (2000) | 5 | 0,12% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Borsa (1997) | 5 | 0,12% | 4 | 0,5% | 3 | 0,39% | 2 | 0,25% |
| Burel et al. (2019) | 5 | 0,12% | 5 | 0,62% | 5 | 0,64% | 5 | 0,63% |
| Dekay (1842) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delaroche (1809) | 5 | 0,12% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Geoffroy Saint-Hilaire ([1817]) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Héros et al. (2007) | 5 | 0,12% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| IUCN (2012) | 5 | 0,12% | 5 | 0,62% | 5 | 0,64% | 3 | 0,38% |
| Jay et al. (2009) | 5 | 0,12% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Kasamatsu & Joyce (1995) | 5 | 0,12% | 4 | 0,5% | 3 | 0,39% | 4 | 0,51% |
| Klunzinger (1871) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koehler (1921) | 5 | 0,12% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Mitchill (1815) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nakamura (1985) | 5 | 0,12% | 5 | 0,62% | 5 | 0,64% | 5 | 0,63% |
| Perez Canto (1886) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Riccialdelli et al. (2010) | 5 | 0,12% | 3 | 0,37% | 3 | 0,39% | 2 | 0,25% |
| Robineau (2005) | 5 | 0,12% | 5 | 0,62% | 5 | 0,64% | 1 | 0,13% |
| Swainson (1839) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| . Rapport GIS "Lag-May" / Conseil Général de Mayotte / Centre d'Océanologie de Marseille. 61 pp.">Thomassin et al. (1998) | 5 | 0,12% | 5 | 0,62% | 5 | 0,64% | 5 | 0,63% |
| Uicn et al. (2020) | 5 | 0,12% | 5 | 0,62% | 5 | 0,64% | 3 | 0,38% |
| Adjeroud et al. (2012) | 4 | 0,09% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Allen (1985) | 4 | 0,09% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Ascanius (1772) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barbosa du Bocage & Brito Capello (1864) | 4 | 0,09% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Conand et al. (2016) | 4 | 0,09% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Couch (1877) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1830-1832) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes ([1832]) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 4 | 0,09% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Delnatte & Wynne (2016) | 4 | 0,09% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Deméré (2014) | 4 | 0,09% | 4 | 0,5% | 0 | 0% | 4 | 0,51% |
| Etcheberry & Abraham (2009) | 4 | 0,09% | 3 | 0,37% | 3 | 0,39% | 2 | 0,25% |
| Flot & Adjeroud (2009) | 4 | 0,09% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Hily et al. (2010) | 4 | 0,09% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Legand (1950) | 4 | 0,09% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Letourneur et al. (2004) | 4 | 0,09% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Macleod et al. (2006) | 4 | 0,09% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Marshall et al. (2009) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matsuoka et al. (2005) | 4 | 0,09% | 4 | 0,5% | 3 | 0,39% | 2 | 0,25% |
| Nardo (1827) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Antonelli, Venezia. 128 pp.">Nardo (1847) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 4 | 0,09% | 4 | 0,5% | 4 | 0,51% | 4 | 0,51% |
| Philippi (1887) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pylaie (1835) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1835) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (2014) | 4 | 0,09% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Smith (1849) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiele et al. (1999) | 4 | 0,09% | 3 | 0,37% | 2 | 0,26% | 3 | 0,38% |
| Valenciennes (1822) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaughan (1906) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wells (1968) | 4 | 0,09% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Whitley (1931) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zelhuber (2009) | 4 | 0,09% | 4 | 0,5% | 3 | 0,39% | 3 | 0,38% |
| AAMP (2012) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 0 | 0% |
| Ainley et al. (2007) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 2 | 0,25% |
| Allen & Robertson (1995) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Allen & Robertson (1995) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Allen (1995) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Arrigoni et al. (2016) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Borsa et al. (2014) | 3 | 0,07% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Brünnich (1768) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Capape et al. (1999) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Costa (1829-1853) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cottarel et al. (2013) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Couch (1838) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1830) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2008) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2014) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril (1865) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gallissian (1982) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Garman (1913) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrigue & Poupon (2013) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Geoffroy Saint-Hilaire (1809) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holthuis (1977) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 0,07% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Hutchinson et al. (2019) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Jefferson & Rosenbaum (2014) | 3 | 0,07% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Kawamura (1994) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 0 | 0% |
| Kock et al. (2006) | 3 | 0,07% | 3 | 0,37% | 2 | 0,26% | 3 | 0,38% |
| Lacepède (1800) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1801) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Laran et al. (2012) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 2 | 0,25% |
| Leach (1818) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leaper et al. (2008) | 3 | 0,07% | 3 | 0,37% | 2 | 0,26% | 3 | 0,38% |
| Lecchini et al. (2002) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Lesueur (1818) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1822) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morat et al. (2012) | 3 | 0,07% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Moreau (1881) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mourier et al. (2013) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Munzinger et al. (2016) | 3 | 0,07% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Orrell (2019) | 3 | 0,07% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Philippi (1902) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Postel (1965) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prévost & Mougin (1970) | 3 | 0,07% | 2 | 0,25% | 2 | 0,26% | 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 » | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Questel (2017) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Reinhardt (1825) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rousseau (2010) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Samaran (2008) | 3 | 0,07% | 3 | 0,37% | 1 | 0,13% | 2 | 0,25% |
| Sellier et al. (2016) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Shaw (1804) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Snodgrass & Heller (1905) | 3 | 0,07% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Springer (1962) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1839) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tamayo et al. (2021) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Thiele et al. (2004) | 3 | 0,07% | 3 | 0,37% | 2 | 0,26% | 2 | 0,25% |
| Tröndlé & Boutet (2009) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| UICN (2009) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Vacelet & Boury-Esnault (1996) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vacelet & Levi (1958) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Vollmer et al. (2019) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 2 | 0,25% |
| Volpi & Benvenuti (2003) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wantiez (2001) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Whitley (1944) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zarrouk et al. (2013) | 3 | 0,07% | 3 | 0,37% | 3 | 0,39% | 3 | 0,38% |
| Allen (comm. pers., 2009) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Anthony (1925) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Ayres (1843) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bellotti (1878) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1810) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1852) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1863) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785-1795) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bocquet (1953) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bourjon & Fricke (2016) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Branch et al. (2007) | 2 | 0,05% | 2 | 0,25% | 0 | 0% | 2 | 0,25% |
| Chevaldonné et al. (2015) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Clua et al. (2019) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Cocco (1836[1834]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conand et al. (2014) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Cunha et al. (2015) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Cuvier & Valenciennes (1830) | 2 | 0,05% | 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) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Odontaspis ferox" Agassiz dans le Golf de Gascogne. Bulletin de la Société zoologique de France, 54: 233-235.">Desbrosses (1930) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Döderlein (1884) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donovan (1803-08) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Düben & Koren (1846) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontan (2019) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Forskål (1775) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1910) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Fricke (2004) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gannier & Petiau (2006) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 0 | 0% |
| Gardiner (1899) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrigue et al. (2022) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Gautret (1986) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Gilis et al. (2011) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Gilis et al. (2012) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Gill & Thiele (1997) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 1 | 0,13% |
| Goodall et al. (1997) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Greenfield (1965) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Griffith & Smith (1834) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guérin-Méneville (1855) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gunnerus (1765) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gunnerus (1765) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Günther (1870) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harold & Winterbottom (1999) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Hermans et al. (2010) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Holbrook (1855) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Howell Rivero (1936) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2009) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Ifremer (2020) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglésias & Lorance (2016) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Impact-Mer et al. (2011) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Jung et al. (2024) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Kasamatsu et al. (2000) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 0 | 0% |
| Koeck et al. (2014) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Kyne et al. (2016) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Lafont (1873) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Last et al. (2016) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Leaper et al. (2008) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 1 | 0,13% |
| Lesueur (1817) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levesque & Delcroix (2018) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Li et al. (2022) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Linnaeus (1767) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linsley et al. (1999) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Lowe (1834) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1841) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas et al. (1991) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lunel (1879) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macdonald & Barron (1868) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macleod et al. (2024) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Maillard (1970) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Manconi et al. (2009) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| McEachran & Seret (1987) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Millot et al. (2023) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Montagu (1818) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1891) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mulochau & Conand (2008) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| National Institute of Water and Atmospheric Research (2016) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nilsson (1832) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ogilby (1911) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oremus (2009) | 2 | 0,05% | 2 | 0,25% | 1 | 0,13% | 2 | 0,25% |
| Pallas (1766) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potin (2013) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Questel (2022) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Randall & Earle (2000) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Raybaudi & Massilia (1992) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Regan (1906) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reilly et al. (2014) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Richard (2006) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Robert et al. (1991) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Robineau et al. (2007) | 2 | 0,05% | 2 | 0,25% | 0 | 0% | 2 | 0,25% |
| Roule (1900) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Samaran & Guinet (2010) | 2 | 0,05% | 2 | 0,25% | 0 | 0% | 2 | 0,25% |
| Samaran et al. (2010) | 2 | 0,05% | 2 | 0,25% | 0 | 0% | 2 | 0,25% |
| Schinz (1822) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (1997) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Sheppard et al. (2008) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Temminck & Schlegel (1850) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turak et al. (2008) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Turak et al. (2014) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Uicn et al. (2015) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Uicn et al. (2017) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Vacelet (1961) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Vacelet (1964) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Vacelet (1969) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Van Canneytet al. (2008) | 2 | 0,05% | 2 | 0,25% | 2 | 0,26% | 2 | 0,25% |
| Wells (1961) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1939) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wursig & Wursig (1980) | 2 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Abril et al. (1986) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Agassiz (1833-1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alcock (1898) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Amade et al. (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Andouche et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Andrefouet et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Andrew et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Anonyme (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Antipa (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aronson et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Aronson et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Aronson et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Aronson et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Aronson et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Aronson et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Aronson et al. (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arzul et al. (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Atwood (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aublet (1775) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Baker (1977) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1985) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Baldwin (1963) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bancroft (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartoli & Prévot (1986) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Belfan & Conde (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Benson et al. (1975) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Benson (1967) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bernard (1897) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bertin (1928) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Best & Scott (1993) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Best et al. (1995) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 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 (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 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 (1785-1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1791) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1839[1838]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boubert et al. (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bouchet et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bouchon-Navaro et al. (1992) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bourcier (1988) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bourjon et al. (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bourmaud (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bouvier (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouxin & Legendre (1952) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Branch (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Brito Capello (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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% |
| Brook (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brownell & Cipriano (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brownell et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruyn et al. (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Budylenko (1977) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Buffrenil et al. (1989) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Buray et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Buron & Chauvet (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Buron et al. (1990) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caballero et al. (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Capape et al. (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Capape et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Carzon (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Casamajor de et al. (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Caziot (1921) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cerchio et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Cervigon (1966) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Chabanet et al. (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Clapham et al. (1999) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Clua & Imirizaldu (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Collectif (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Collet & Duguy (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1889) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Compagno et al. (2005) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Conand et al. (2013) | 1 | 0,02% | 1 | 0,12% | 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% |
| Cottalorda et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Cotte et al. (2001) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Couch (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Counihan et al. (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Couté & Garrouste (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crespo et al. (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuif et al. (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Cuvier & Valenciennes (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1833) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Voigt (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dalebout et al. (2005) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Day (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Del Hoyo & Collar (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delongueville & Scaillet (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Desbrosses (1934) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Desbrosses (1935) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Deshayes (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Devantier et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Devantier et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| deVantier et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Devantier et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| deVantier et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| deVantier et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| deVantier et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Dollfus (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dollfus (1960) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Eichwald (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ersts & Rosenbaum (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Fabricius (1780) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faure (1982) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Fenaux (1965) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Féral et al. (2021) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Fleming & Jackson (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Fleming (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fordyce & Marx (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Forsskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fraser-brunner (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke (1999) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Friedlaender et al. (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Fries (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Froese & Pauly (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Funk et al. (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Gall (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gharbi et al. (1985) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Gill et al. (2000) | 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% |
| Gillespie (1997) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Girard (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondot et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gistel (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren & Galil (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Goud et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gravier (1910) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Gray (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1850) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gregory (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinet (1991) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Guinet (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Günther (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley et al. (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Hedley (1921) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heimlich-boran (1993) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Hoeksema et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Hoeksema et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holt (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hureau & Ozouf-Costaz (1980) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Hynes (1959) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Jaquemet et al. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Jefferson & & Van Waerebeek (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jefferson & Barros (1997) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Jefferson et al. (1993) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Jehl et al. (1980) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Johnson & Wolman (1984) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Johnson (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Evermann (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1880) | 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 (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Starks (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Joyeux (1923) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Kasamatsu et al. (1995) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Kasamatsu et al. (1998) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Kaup (1856) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kiszka et al. (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Knop (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Krajewsky (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Kronen et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Krøyer (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Labach et al. (2021) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Lacepède (1798) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ladd (1934) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Lamarck (1813) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1816) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1816) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lapinski & Giovos (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Lassauce et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Last et al. (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Last et al. (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Latreille ([1802]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Bail et al. (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Leatherwood et al. (1979) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Legendre (1923) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Legendre (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legendre (1942) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Lemée (1955) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Lesage et al. (2024) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Lesson (1828) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Lesson (1830-1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letourneur & Maggiorani (1995) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Linnaeus (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Liu et al. (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Lorance et al. (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Lorvelec et al. (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louis et al. (1992) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Lowe (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macleay (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maddalena & Zuffa (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Mahé et al. (2024) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Maréchal et al. (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Marryat (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matsuoka et al. (1996) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Matsuoka et al. (2005) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Mckenna et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Meek & Hildebrand (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| MGnify (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Micael et al. (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Milne & Edwards (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne et al. (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Minding (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mourier (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mulochau et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Murase et al. (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Murray (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nemenzo (1976) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Nicol et al. (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Niort (1950) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Noël (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Noël (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Notarbartolo et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| N'Yeurt & Payri (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Obura et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Ocana & Brito (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Okamura & Kitakado (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Okutani & Kawaguchi (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olson & Warheit (1988) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Orton (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osbeck (1765) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1770) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1776) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parnell (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Payri & N'yeurt (1997) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Pennant (1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Père, & Noël (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Pérez (1931) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Péron (1807-1816) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrin et al. (1994) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Perry et al. (1999) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Petuch (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierpoint et al. (1997) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Pinault et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Pitman & Ensor (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Plucàr (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poisson (1924) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Praderi et al. (1992) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Probst (1997) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Purcell et al. (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Pusineri & Caceres (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Pusineri et al. (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Quéro (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Questel (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Rabiller & Richard (2019) | 1 | 0,02% | 1 | 0,12% | 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% |
| Randall & Earle (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Ranzani (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1910) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Régis (1979) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Reid et al. (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Ribic et al. (1991) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Richards et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Richards et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Richards (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Richer de Forges et al. (2005) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Ridgway (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roche & Guinet (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Rodríguez-Prieto et al. (1999) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Rogers & Brown (1999) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Rosenbaum & Collins (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Roule (1916) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saemundsson (1922) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sauvage (1886) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Sawai et al. (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Schleyer & Benayahu (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Schmidt (1862) | 1 | 0,02% | 1 | 0,12% | 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% |
| Sekiguchi et al. (1992) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Sekiguchi et al. (1993) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Sekiguchi et al. (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sheppard et al. (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siciliano & Santos (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Bulletin de la Station Biologique d'Arcachon, 34: 59-63.">Sigalas & Budker (1937) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Sigalas (1931) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Sirovic et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Slater et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Smith et al. (2005) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Smith (1912) | 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 (1867) | 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% |
| Thibaut et al. (2016) | 1 | 0,02% | 1 | 0,12% | 0 | 0% | 1 | 0,13% |
| Tiavouane & Fauvelot (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Tougaard (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turak et al. (2008) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| UICN Comité français, OFB & MNHN (2021) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Uicn et al. (2019) | 1 | 0,02% | 1 | 0,12% | 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% |
| Van Ofwegen (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Vanwaerebeek et al. (1995) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet et al. (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Vaughan (1907) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Verlaque et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Veron et al. (1977) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Veron (1985) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Veron (1985) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Viale & Frontier (1989) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Victor et al. (2001) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Vroman (1968) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Wada et al. (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Wallace & Wolstenholme (1998) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Wallace (1994) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Wallace (1999) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Wang et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wantiez (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Weber (1913) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Weerdt (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 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 (1933) | 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. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Williams et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 0 | 0% |
| Wood (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wursig et al. (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yabe & Sugiyama (1937) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
| Zibrowius (1968) | 1 | 0,02% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
