Espèces marines de Saint-Pierre et Miquelon
903 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Nelson-Smith et al. (2014) | 111 | 2,54% | 82 | 16,8% | 82 | 17,34% | 81 | 17,09% |
| Etcheberry & Abraham (2009) | 92 | 2,11% | 77 | 15,78% | 77 | 16,28% | 77 | 16,24% |
| Linnaeus (1758) | 89 | 2,04% | 26 | 5,33% | 26 | 5,5% | 24 | 5,06% |
| Rinaldi (2016) | 88 | 2,02% | 84 | 17,21% | 84 | 17,76% | 48 | 10,13% |
| Carzon et al. (2016) | 66 | 1,51% | 63 | 12,91% | 63 | 13,32% | 36 | 7,59% |
| Estrade et al. (2016) | 66 | 1,51% | 63 | 12,91% | 63 | 13,32% | 36 | 7,59% |
| Béarez et al. (2017) | 63 | 1,44% | 63 | 12,91% | 63 | 13,32% | 63 | 13,29% |
| Uicn et al. (2017) | 58 | 1,33% | 54 | 11,07% | 54 | 11,42% | 50 | 10,55% |
| Le Gallo (1949) | 56 | 1,28% | 32 | 6,56% | 32 | 6,77% | 30 | 6,33% |
| Burel et al. (2019) | 53 | 1,21% | 53 | 10,86% | 53 | 11,21% | 50 | 10,55% |
| Levesque & Delcroix (2018) | 53 | 1,21% | 51 | 10,45% | 51 | 10,78% | 51 | 10,76% |
| Simian et al. (2022) | 49 | 1,12% | 49 | 10,04% | 49 | 10,36% | 49 | 10,34% |
| Uicn et al. (2015) | 49 | 1,12% | 47 | 9,63% | 47 | 9,94% | 36 | 7,59% |
| UICN Comité français, OFB & MNHN (2021) | 46 | 1,05% | 46 | 9,43% | 46 | 9,73% | 46 | 9,7% |
| Questel (2020) | 40 | 0,92% | 38 | 7,79% | 38 | 8,03% | 37 | 7,81% |
| Cabioc'h & Floc'h (2014) | 38 | 0,87% | 31 | 6,35% | 31 | 6,55% | 29 | 6,12% |
| Collectif & Bebest (2019) | 37 | 0,85% | 37 | 7,58% | 37 | 7,82% | 37 | 7,81% |
| Questel & Le Quellec (2012) | 35 | 0,8% | 34 | 6,97% | 34 | 7,19% | 33 | 6,96% |
| Martin (2011) | 32 | 0,73% | 28 | 5,74% | 28 | 5,92% | 28 | 5,91% |
| Remsen et al. (2013) | 31 | 0,71% | 28 | 5,74% | 28 | 5,92% | 28 | 5,91% |
| Breton (2014) | 30 | 0,69% | 28 | 5,74% | 28 | 5,92% | 27 | 5,7% |
| Godet et al. (2010) | 30 | 0,69% | 29 | 5,94% | 29 | 6,13% | 29 | 6,12% |
| Belfan & Conde (2016) | 28 | 0,64% | 26 | 5,33% | 26 | 5,5% | 26 | 5,49% |
| Yokoyama (2013) | 28 | 0,64% | 25 | 5,12% | 25 | 5,29% | 25 | 5,27% |
| Mertens & Wermuth (1960) | 25 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charrassin (2016) | 22 | 0,5% | 21 | 4,3% | 21 | 4,44% | 12 | 2,53% |
| Charrassin (2016) | 22 | 0,5% | 21 | 4,3% | 21 | 4,44% | 12 | 2,53% |
| Jarrett & Shirihai (2014) | 22 | 0,5% | 21 | 4,3% | 21 | 4,44% | 12 | 2,53% |
| Moutou (2016) | 22 | 0,5% | 21 | 4,3% | 21 | 4,44% | 12 | 2,53% |
| Thoisy & Bordin (2016) | 22 | 0,5% | 21 | 4,3% | 21 | 4,44% | 12 | 2,53% |
| Urtizberea (2016) | 22 | 0,5% | 21 | 4,3% | 21 | 4,44% | 12 | 2,53% |
| Spitz et al. (2016) | 21 | 0,48% | 20 | 4,1% | 20 | 4,23% | 11 | 2,32% |
| Aulagnier (2009) | 20 | 0,46% | 19 | 3,89% | 19 | 4,02% | 10 | 2,11% |
| Sellier et al. (2016) | 20 | 0,46% | 20 | 4,1% | 20 | 4,23% | 19 | 4,01% |
| Goulletquer (2016) | 17 | 0,39% | 16 | 3,28% | 16 | 3,38% | 15 | 3,16% |
| Van Guelpen (2016) | 17 | 0,39% | 16 | 3,28% | 16 | 3,38% | 16 | 3,38% |
| Rafinesque Schmaltz (1810) | 16 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter (2021) | 15 | 0,34% | 15 | 3,07% | 15 | 3,17% | 15 | 3,16% |
| Giard (1872) | 15 | 0,34% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Fourt et al. (2017) | 14 | 0,32% | 14 | 2,87% | 14 | 2,96% | 14 | 2,95% |
| Fricke et al. (2011) | 14 | 0,32% | 14 | 2,87% | 14 | 2,96% | 14 | 2,95% |
| Uicn et al. (2020) | 14 | 0,32% | 14 | 2,87% | 14 | 2,96% | 13 | 2,74% |
| Dauvin et al. (2003) | 13 | 0,3% | 11 | 2,25% | 11 | 2,33% | 11 | 2,32% |
| Desbrosses & Etcheberry (1987) | 13 | 0,3% | 10 | 2,05% | 10 | 2,11% | 4 | 0,84% |
| Uicn et al. (2015) | 13 | 0,3% | 11 | 2,25% | 11 | 2,33% | 11 | 2,32% |
| Fricke et al. (2009) | 12 | 0,28% | 11 | 2,25% | 11 | 2,33% | 11 | 2,32% |
| Schnakenbeck (1931) | 12 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walbaum (1792) | 12 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel & Jamon (2010) | 12 | 0,28% | 11 | 2,25% | 11 | 2,33% | 11 | 2,32% |
| Clements (2012) | 11 | 0,25% | 11 | 2,25% | 11 | 2,33% | 11 | 2,32% |
| Cuvier & Valenciennes (1829) | 11 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1833) | 11 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deblock et al. (1960) | 11 | 0,25% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Roux (2012) | 11 | 0,25% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Tostain et al. (2013) | 11 | 0,25% | 10 | 2,05% | 10 | 2,11% | 10 | 2,11% |
| Bay-nouailhat & Bay-nouailhat (2020) | 10 | 0,23% | 10 | 2,05% | 10 | 2,11% | 10 | 2,11% |
| Bloch & Schneider (1801) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bordin et al. (2021) | 10 | 0,23% | 10 | 2,05% | 10 | 2,11% | 4 | 0,84% |
| Milne-Edwards (1841) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tison et al. (2014) | 10 | 0,23% | 6 | 1,23% | 6 | 1,27% | 6 | 1,27% |
| Uicn et al. (2019) | 10 | 0,23% | 8 | 1,64% | 8 | 1,69% | 8 | 1,69% |
| Denys et al. (2022) | 9 | 0,21% | 7 | 1,43% | 7 | 1,48% | 7 | 1,48% |
| Gannier (2001) | 9 | 0,21% | 9 | 1,84% | 9 | 1,9% | 4 | 0,84% |
| Garrigue (2007) | 9 | 0,21% | 9 | 1,84% | 9 | 1,9% | 4 | 0,84% |
| G.E.M.M. (2012) | 9 | 0,21% | 9 | 1,84% | 9 | 1,9% | 4 | 0,84% |
| Gmelin (1789) | 9 | 0,21% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Mitchill (1815) | 9 | 0,21% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Reinhardt (1837) | 9 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Dijk et al. (2012) | 9 | 0,21% | 8 | 1,64% | 8 | 1,69% | 8 | 1,69% |
| Catzeflis (2012) | 8 | 0,18% | 8 | 1,64% | 8 | 1,69% | 3 | 0,63% |
| Dekay (1842) | 8 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel et al. (2005) | 8 | 0,18% | 7 | 1,43% | 7 | 1,48% | 7 | 1,48% |
| Lacepède (1803) | 8 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 8 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siu et al. (2017) | 8 | 0,18% | 8 | 1,64% | 8 | 1,69% | 8 | 1,69% |
| Barau et al. (2005) | 7 | 0,16% | 7 | 1,43% | 7 | 1,48% | 7 | 1,48% |
| Dekay (1842) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewarumez et al. (2011) | 7 | 0,16% | 6 | 1,23% | 5 | 1,06% | 6 | 1,27% |
| Dewynter et al. (2021) | 7 | 0,16% | 7 | 1,43% | 7 | 1,48% | 5 | 1,05% |
| Ifremer (2009) | 7 | 0,16% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Pallas [1814] | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1858-61) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preynat (2013) | 7 | 0,16% | 7 | 1,43% | 7 | 1,48% | 7 | 1,48% |
| Risso (1810) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charbonnel (1990) | 6 | 0,14% | 6 | 1,23% | 6 | 1,27% | 6 | 1,27% |
| Collette & Nauen (1983) | 6 | 0,14% | 6 | 1,23% | 6 | 1,27% | 6 | 1,27% |
| Cuvier (1829) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril (1870) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleming (1828) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1896) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 6 | 0,14% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Nardo (1827) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shirihai (2003) | 6 | 0,14% | 6 | 1,23% | 6 | 1,27% | 2 | 0,42% |
| Bocquet (1953) | 5 | 0,11% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Camiñas et al. (2021) | 5 | 0,11% | 5 | 1,02% | 5 | 1,06% | 5 | 1,05% |
| Delnatte & Wynne (2016) | 5 | 0,11% | 5 | 1,02% | 5 | 1,06% | 4 | 0,84% |
| Lacepède (1800) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller & Henle (1841) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Payri & N'yeurt (1997) | 5 | 0,11% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Payri (2007) | 5 | 0,11% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Perrin et al. (2002) | 5 | 0,11% | 5 | 1,02% | 5 | 1,06% | 1 | 0,21% |
| Pontoppidan (1763) | 5 | 0,11% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Rignault & Chevallier (2017) | 5 | 0,11% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Robineau & Duhamel (2006) | 5 | 0,11% | 5 | 1,02% | 5 | 1,06% | 2 | 0,42% |
| Robineau (2005) | 5 | 0,11% | 5 | 1,02% | 5 | 1,06% | 1 | 0,21% |
| Rocamora (2004) | 5 | 0,11% | 5 | 1,02% | 5 | 1,06% | 5 | 1,05% |
| Samaran & Guinet (2009) | 5 | 0,11% | 5 | 1,02% | 5 | 1,06% | 2 | 0,42% |
| Vroman (1968) | 5 | 0,11% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Zelhuber (2009) | 5 | 0,11% | 5 | 1,02% | 4 | 0,85% | 4 | 0,84% |
| Zilli (2021) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allain & Morice (1971) | 4 | 0,09% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Aulagnier et al. (2017) | 4 | 0,09% | 3 | 0,61% | 3 | 0,63% | 2 | 0,42% |
| Barrioz & Morinière (2007) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Bedot (1910) | 4 | 0,09% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Boer et al. (1999) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 2 | 0,42% |
| Boer (2000) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 1 | 0,21% |
| Bonnaterre (1788) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro et al. (2005) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Bour et al. (2008) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Breton et al. (2003) | 4 | 0,09% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Casale et al. (2021) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| CHN (2017) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Del Hoyo & Collar (2014) | 4 | 0,09% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Dickinson & Remsen (2013) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Duguy (1988) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Duguy (1994) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Duguy (1997) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Dulau-Drouot et al. (2008) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 3 | 0,63% |
| Fournet (2002) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Fourriére et al. (2014) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Fretey & Triplet (2022) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Furminieux (2019) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Gadeau de Kerville (1900) | 4 | 0,09% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gannier (2002) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 3 | 0,63% |
| Gannier (2009) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 2 | 0,42% |
| Gill (1883) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gronow (1854) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jay et al. (2009) | 4 | 0,09% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Jordan (1894) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1801) | 4 | 0,09% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lescure et al. (2012) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Linnaeus (1766) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malm (1877) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary et al. (2019) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Morinière & Dell'amico (2011) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Muratet (2015) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Nakamura (1985) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Pearman et al. (2020) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Rafinesque (1810) | 4 | 0,09% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Risso (1827) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodríguez-Prieto et al. (1999) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 3 | 0,63% |
| Smith (1997) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Storer (1839) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tostain & Dujardin (1988) | 4 | 0,09% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 4 | 0,09% | 4 | 0,82% | 4 | 0,85% | 4 | 0,84% |
| Vieillot (1819) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weimerskirch et al. (2009) | 4 | 0,09% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Arnold & Ovenden (2014) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Ausilio & Zotier (1989) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Bartoli (1972) | 3 | 0,07% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Bioinsight/diren & Guyane (2006) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Blainville (1816) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borsa (1997) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 1 | 0,21% |
| Bourcier (1988) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Brunet et al. (2017) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1764) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chatton & Brément (1909) | 3 | 0,07% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Chevalier (2006) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Ciccione et al. (2011) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Crillon & Cuzange (2020) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Deméré (2014) | 3 | 0,07% | 3 | 0,61% | 0 | 0% | 3 | 0,63% |
| Dewynter et al. (2019) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Dewynter et al. (2019) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Dewynter et al. (2022) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Dewynter et al. (2023) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Dewynter et al. (2023) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Diaz & Cuzange (2009) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 1 | 0,21% |
| Duffaut et al. (2011) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Duguy et al. (1998) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Duguy et al. (1999) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Duguy et al. (2000) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Duguy et al. (2002) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Duguy et al. (2006) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Duguy et al. (2007) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Duguy (1990) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Duguy (1996) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Entraygues (2014) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Étaix-bonnin et al. (2011) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Facciolà (1882) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gannier (2000) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 1 | 0,21% |
| Girondot (2011) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Karadjian et al. (2022) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Kawamura (1994) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 0 | 0% |
| Kienberger et al. (2016) | 3 | 0,07% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Kiszka et al.(2007) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 2 | 0,42% |
| Knoepffler et al. (1990) | 3 | 0,07% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Koehler (1921) | 3 | 0,07% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Le Scao et al. (2011) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Leach (1818) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1818) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary et al. (2017) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Massary et al. (2018) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Massary et al. (2020) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Massary et al. (2021) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Mcdevit & Saunders (2017) | 3 | 0,07% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Méheust et al. (2018) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Morat et al. (2012) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Munzinger et al. (2016) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| N'Yeurt & Payri (2004) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| N'Yeurt & Payri (2007) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Pallas (1770) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pérez (1920) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poupin et al. (1999) | 3 | 0,07% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Probst et al. (2022) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Probst (2001) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Questel et al. (2023) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Questel et al. (2023) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Read & Farman (2018) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Read et al. (2023) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Rossi-santos et al. (2007) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 1 | 0,21% |
| Salazar-Vallejo (2014) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Sauvignet et al. (2000) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Séguy (1944) | 3 | 0,07% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Silva et al. (1996) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Soubeyran (2008) | 3 | 0,07% | 3 | 0,61% | 3 | 0,63% | 3 | 0,63% |
| Tostain (1980) | 3 | 0,07% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| AAMP (2012) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 0 | 0% |
| Abraham (2010) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Ainley et al. (2007) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 1 | 0,21% |
| Ascanius (1772) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ascanius (1775) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bacchet et al. (2007) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Baldi et al. (2022) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Bauer & Sadlier (2000) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Beauchamp (1914) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Berry & Smith-Vaniz (1978) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Bertin (1928) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Bijmoer et al. (2021) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blainville (1810) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blanc (1909) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1795) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boddaert & Daubenton (1783) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boisseau & Lubet (1955) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Boissel & Urtizberea (2024) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Bonnet et al. (2012) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Bourmaud (2003) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Brünnich (1788) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bush (1905) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cépède (1814) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cépède (1914) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chamberlin (1919) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chappuis et al. (1974) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Chassard-Bouchaud et al. (1985) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Chevallier et al. (2023) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Claparède (1863) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collett (1875) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Combescot-Lang (1976) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Costa (1829-1853) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1838) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couté & Garrouste (2009) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Cuvier & Valenciennes ([1832]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1847) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1848) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| dal Molin (2009) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Dauvin et al. (1991) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Davant (1967) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Davis & Davis (2009) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Delcroix et al. (2011) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Deshayes (1863) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss et al. (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dilman (2014) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Donovan (1803-08) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubief & Gallais (2011) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Duguy et al. (1997) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Duguy et al. (2003) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Duguy et al. (2004) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Duguy (1986) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Duguy (1987) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Duguy (1992) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Duguy (1993) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Duguy (1995) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Faber (1829) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frenot et al. (2005) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Funk et al. (2007) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Garman (1913) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gibson & Baker (2012) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Gill & Thiele (1997) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 1 | 0,21% |
| Gill (1995) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Gillandt (1979) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondo (2023) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Gmelin (1789) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1791) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1895) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gourreau et al. (1998) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gunnerus (1765) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Gunnerus (1765) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Héros et al. (2007) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoff & Daszkiewicz (2001) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Howell Rivero (1936) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ingels et al. (2003) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| IUCN (2012) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 1 | 0,21% |
| Johnson (1862) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Jordan (1896) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Julien (1881) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Jung et al. (2024) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Kasamatsu & Joyce (1995) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Kasamatsu et al. (2000) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 0 | 0% |
| Keith et al. (2011) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Kilgallen & Lowry (2014) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Kiszka et al. (2010) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Kock et al. (2006) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Koechlin (1977) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Kulbicki (comm. pers., 2011) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Lagourgue et al. (2022) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Lamy & Pointier (2018) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Laran et al. (2011) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Leach (1815-1875) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leaper et al. (2008) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Lemée (1955) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Lepechin (1769) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1818) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1821) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1822) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levring (1944) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Linnaeus (1753) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Linnaeus (1767) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Martinet et al. (1765) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathews (1914) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Matsuoka et al. (2005) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 0 | 0% |
| Mays et al. (2006) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Merrem (1820) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millot et al. (2023) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Miranda et al. (2009) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Montagu (1808) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monteiro et al. (2020) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Moreau (1881) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Antonelli, Venezia. 128 pp.">Nardo (1847) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nilsson (1832) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nordmann (1840-1842) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliver (2011) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Orrell (2019) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Osório (1909) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Palko et al. (1982) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Pallas (1766) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1776) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. (2006) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Péres (1925) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Perez Canto (1886) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peron (2014) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Pezy et al. (2022) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Philippi (1887) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poisson (1999) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Pons et al. (2005) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Probst (1997) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Probst (1998) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Read & Jean (2021) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Reinhardt (1825) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Revel et al. (2024) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Rhodin et al. (2017) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Richard et al. (1982) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Risso (1816) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robineau (1989) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 1 | 0,21% |
| Robineau (2004) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 1 | 0,21% |
| Ronot (2007) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Sabine (1819) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Safford & Hawkins (2013) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Saint-Joseph (1888) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidt (1875) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sentz‐Braconnot (1966) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Séret & Quod (2023) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Shaw & Nodder (1792-1793) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simian et al. (2008) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Smith (1849) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1910) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Snodgrass & Heller (1905) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Spitz et al. (2015) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 0 | 0% |
| Stewart (2014) | 2 | 0,05% | 2 | 0,41% | 0 | 0% | 2 | 0,42% |
| Storer (1858) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1839) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Temminck & Schlegel (1850) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thibault et al. (2014) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Thiele et al. (1999) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Thiele et al. (2004) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 1 | 0,21% |
| Thunberg (1787) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Toll (1985) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turton (1932) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2017) | 2 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Valenciennes (1836-1844) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Canneytet al. (2008) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Vasselon et al. (2019) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Vénec-Peyré (1985) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1819) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Whitley (1933) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1939) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wright (1856) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Yarrell (1829) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1832) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zardi et al. (2011) | 2 | 0,05% | 2 | 0,41% | 2 | 0,42% | 2 | 0,42% |
| Abhaya & Probst (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Abril et al. (1986) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Akhani et al. (2014) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Andouche et al. (2020) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Andrew et al. (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Andrieux et al. (1981) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anisimova & Cochrane (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Anonyme. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Arnaud (1974) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Aublet (1775) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Audige (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Augener (1918) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ayres (1848) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Baldi et al. (2023) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Barbancey (2001) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Barbancey (2001) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barré & Géraux (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Barthélémy (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartoli (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beaufils (1999) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Beauvieux et al. (2024) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bellan-Santini & Ledoyer (1974) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bellan-Santini (1972) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bellan-Santini (1972) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bénito-espinal (1990) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Best et al. (1995) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Birdlife International (2016) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Blainville (1810) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1782-1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1788) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bocquet & Stock (1958) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Boie (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1839[1838]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boschert & Dronneau (1998) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Boubert et al. (2019) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bouchon-Navaro & Louis (1986) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bourgade (2013) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bourgade (2021) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Bouxin & Legendre (1952) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Branch (2010) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Brattey et al. (1990) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brehm (1831) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| 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% |
| Brugneaux & Pérès (2006) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Brünnich (1768) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Budylenko (1977) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Campana-rouget & Biocca (1955) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Canu (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caut et al. (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Cerchio et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Chaine & Duvergier (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chambault et al. (2020) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Chamberlin (1919) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Champagne et al. (1997) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Chassaing et al. (2018) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Chastel et al. (1987) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Chatton & Lwoff (1930) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Chatton & Séguéla (1936) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Cheke (1987) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Chevallier et al. (2024) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Chevreux & de Guerne (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevreux (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevreux (1908) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Ciavatti et al. (1993) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Ciccione (2001) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Ciccione (2001) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Clark & Harrison (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clements et al. (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Clergeau & Pascal (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Clergeau et al. (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Clergeau et al. (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Cocco (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collectif (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Collinge (1917) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Comfort (1938) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Contejean (2018) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Cornish (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coste & Ricard (1990) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Coste et al. (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Costrel & Corainville (1929) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Cotte et al. (2001) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Couch (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coues (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Counihan et al. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Couté et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Couteyen (2006) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Crouzier (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Cunha et al. (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Cuvier & Valenciennes (1830-1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le règne animal distribué d'après son organisation, pour servir de base à l'histoire naturelle des animaux et d'introduction à l'anatomie comparée. Tome 2, contenant les reptiles, les poissons, les mollusques et les annélides. Déterville, Paris. i-xviii+1-532 pp. ">Cuvier (1816) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dall et al. (1938) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dalleau et al. (2014) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Danois (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dauphin (1999) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Dauvin et al. (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dauvin (1990) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Davis & Davis (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Davoult et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Davoult (1990) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Dean (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Debenay & Cabioch (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Debenay (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deblock (1966) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Debout (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Deflandre (1960) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Deflorenne et al. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Dehorne (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delcroix et al. (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| delle Chiaje (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin et al. (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Den et al. (2020) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Desbrosses (1934) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Desbrosses (1935) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Desse-berset & Williot (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Desse-Berset & Williot (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Desse-Berset (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Dollfus (1960) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Dollfus (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Düben et al. (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois et al. (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy & Duron (1981) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy & Duron (1982) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy & Duron (1983) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy & Duron (1984) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy & Duron (1985) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy et al. (1980) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy et al. (2000) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy (1983) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy (1988) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Duguy (1989) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Dupont et al. (2007) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Efe et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Elkins & Yesou (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ersts & Rosenbaum (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Esmark (1866) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Fabricius (1780) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Facciolà (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1925) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Fleming & Jackson (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Forest (1946) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Forskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fretey & Bour (1980) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Fretey et al. (2023) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Fretey (1980) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Fretey (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Frétey (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gallien (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gargominy et al. (1996) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Garman (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gérard et al. (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gérigny et al. (2020) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gernigon & Lacaze (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gernigon (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill & Ryder (1883) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gill (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1873-1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1878) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gillespie (1997) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Girard (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gistel (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Golvan (1956) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| González‐Elizondo & Peterson (1997) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Goode & Bean (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1879) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Goode & Bean (1883) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Goode (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren & Galil (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gravier (1922) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gravier-Bonnet (2007) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gray (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guermeur (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guiguen et al. (1984) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Guilcher et al. (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinet (1991) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Guinet (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Gunnerus (1767) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Günther (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1878) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1888) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Günther (1889) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hentschel (1914) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Hequet & Le Corre (2010) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Hequet et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Herdman (1882) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Herzberg (2018) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Hipeau-Jacquotte & Coste (1989) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Holthuis (1977) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Homeyer (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huber (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Hughes (1983) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hynes (1959) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Ices (2022) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Impact-mer (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Isenmann et al. (1971) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| IUCN (2014) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Jaquemet et al. (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Jefferson & & Van Waerebeek (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jehl et al. (1980) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Jensen (1905) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson & Wolman (1984) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Johnson (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Evermann (1898) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Jordan & Gilbert (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouan (1863) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Joyeux (1923) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Judkins & Kensley (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Karaa et al. (2016) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Kasamatsu et al. (1995) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Kasamatsu et al. (1998) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Keith & Machino (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Keith et al. (2002) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Keith et al. (2006) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Keith (2002) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Kilburn (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Krøyer (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1852-53) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krøyer (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuhl (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lage-Yusty et al. (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lamarck (1779) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lambert (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lambert (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Laran et al. (2012) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Latham (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bulletin de la Société Zoologique de France, 38: 282-288, 304-315.">Le Danois (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Gallo (1952) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leaper et al. (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Legendre (1923) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lesage et al. (2024) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lescure et al. (2016) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lesson (1828) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Lesson (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lethuillier (1999) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Liardet & d'Auzon (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Liardet (2004) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lichtenstein (1823) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Liebart et al. (2021) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lim et al. (2002) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Linné (1771) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lizé (2019) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Loisier et al. (2021) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lorvelec & Pascal (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lorvelec & Vigne (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louette & Cousin (1999) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Louisin & Probst (1996) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Loury & Puissauve (2016) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lovén (1845) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lowe (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 1 | 0,02% | 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 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loxton (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Lütken (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lütken (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| MacKee (1994) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Maddalena & Zuffa (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Magaud & D'aubusson (1906) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Mahé et al. (2024) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Maillard (1978) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Malm (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mancino et al. (2022) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Marenzeller & Von (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marion (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Marshall (1955) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martin et al. (2021) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Medetian & Miaud (2024) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Merckx (1998) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| MGnify (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Mitchill (1814) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moench (1794) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mohr (1786) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot & Monniot (1983) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Monniot et al. (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Monniot (1978) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Monod & Dollfus (1932) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Montagu (1813) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Monti et al. (2010) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Moreau (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morrison (2006) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Moussa et al. (1989) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Müller (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Hawaiian Entomological Society, 9(1): 69-70.">Mumford (1935) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Murase et al. (2002) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Naumann (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nicol et al. (2000) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Niort (1950) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Noël (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Noël (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Noël (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Nuttall (1834) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| N'Yeurt & Payri (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ogilby (1911) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ooishi (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| O'reilly (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ortmann (1890) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Osbeck (1765) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1835) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Owen (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| pallas (1764) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parelius (1768) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Payri et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Pearson & Prévot (1971) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Pennant (1777) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peralta & Fautin (2013) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Perry et al. (1999) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Petter (1970) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Philippi (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Phipps (1774) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierpoint et al. (1997) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Piscart et al. (2019) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Pitman & Ensor (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Pleijel (2007) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Poisson & Legueux (1926) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Poisson (1924) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Prato et al. (2022) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Preston (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prévost & Mougin (1970) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Prevot (1971) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Probst et al. (2000) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Probst et al. (2001) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Probst (1997) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Probst (1997) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Probst (2007) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Prosch (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Provan et al. (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Puissauve, Legros, Evanno & Acou (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Quatrefages (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quéro (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Quero et al. (2013) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Ramage (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Read et al. (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Redier (1971) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Reeber et al. (1996) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeber (2015) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Ribic et al. (1991) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Richard (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richer de Forges et al. (2005) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Rimblot et al. (1985) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Rinaldi et al. (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Roalson et al. (2010) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Roche & Guinet (2007) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Roos (2000) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Rosa (1908) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Rosenbaum & Collins (2006) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Rousseau et al. (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Rousseau (2010) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Roux (1913) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Annals & Magazine of Natural History, 3: 446-455.">Russell (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salisbury (1796) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Samaran (2008) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Sara et al. (1992) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Sawai et al. (2018) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Schneider (1783) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schweigger (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Servan (1976) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Severijns (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Severijns (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaver et al. (2019) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Shaw (1804) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherborn (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sigalas (1931) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Siorat & Rocamora (1995) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Siorat et al. (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Siorat et al. (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Sirovic et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Smirnov et al. (2014) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Smith et al. (2005) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Sonsino (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steenstrup (1876) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stephensen (1935) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Storer (1838) | 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% |
| Suckow (1798) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Svoboda & Cornelius (1991) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Takeda (1953) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tapolczai et al. (2017) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Theodor (1965) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Thibault et al. (2023) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Thomassin et al. (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tinturier-Hamelin (1960) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tirvengadum & Bour (1985) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Topsent (1896) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Traustedt (1881) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Tresset et al. (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Tröndlé & Boutet (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Urtizberea et al. (2021) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Vaillant (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaillant (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van de Vijver et al. (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Vandelli (1761) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vanderwerf et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Varela et al. (2007) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Vaslet & Agrnsm (2018) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Verlaque (2001) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Verrill (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Viale & Frontier (1989) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Vieillot (1817) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vincent (1987) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Vincent (1990) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Vivares & Sprague (1979) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Vollmer et al. (2019) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Waayers et al. (2011) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Weerdt (2023) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Whitley (1944) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1948) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams et al. (2009) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
| Wood (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yésou (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Yésou (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Yésou (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Yésou (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Yésou (2003) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
| Yokoyama (1920) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zdzitowiecki & Ozouf-Costaz (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zdzitowiecki et al. (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zdzitowiecki (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zugmayer (1911) | 1 | 0,02% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
