Bivalves
Bivalvia
476 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Lamy & Pointier (2018) | 582 | 7,84% | 541 | 31,04% | 541 | 31,24% | 541 | 31,18% |
| Héros et al. (2007) | 327 | 4,4% | 247 | 14,17% | 247 | 14,26% | 246 | 14,18% |
| Jay et al. (2009) | 307 | 4,13% | 183 | 10,5% | 183 | 10,57% | 183 | 10,55% |
| Martin (2011) | 242 | 3,26% | 202 | 11,59% | 202 | 11,66% | 202 | 11,64% |
| Tröndlé & Boutet (2009) | 196 | 2,64% | 132 | 7,57% | 132 | 7,62% | 132 | 7,61% |
| Linnaeus (1758) | 152 | 2,05% | 18 | 1,03% | 18 | 1,04% | 18 | 1,04% |
| Nelson-Smith et al. (2014) | 146 | 1,97% | 111 | 6,37% | 111 | 6,41% | 111 | 6,4% |
| Massemin et al. (2009) | 131 | 1,76% | 90 | 5,16% | 90 | 5,2% | 90 | 5,19% |
| Ifremer (2009) | 130 | 1,75% | 91 | 5,22% | 91 | 5,25% | 89 | 5,13% |
| Deshayes (1863) | 107 | 1,44% | 16 | 0,92% | 16 | 0,92% | 16 | 0,92% |
| Prié (2017) | 101 | 1,36% | 96 | 5,51% | 82 | 4,73% | 88 | 5,07% |
| Deuss et al. (2013) | 98 | 1,32% | 55 | 3,16% | 55 | 3,18% | 55 | 3,17% |
| Godet et al. (2010) | 97 | 1,31% | 75 | 4,3% | 75 | 4,33% | 75 | 4,32% |
| Bouchet et al. (2008) | 83 | 1,12% | 72 | 4,13% | 72 | 4,16% | 72 | 4,15% |
| Falkner et al. (2002) | 66 | 0,89% | 26 | 1,49% | 21 | 1,21% | 23 | 1,33% |
| Gargominy et al. (2011) | 63 | 0,85% | 42 | 2,41% | 37 | 2,14% | 39 | 2,25% |
| Krylova & Janssen (2019) | 63 | 0,85% | 63 | 3,61% | 62 | 3,58% | 62 | 3,57% |
| Bourcier (1988) | 55 | 0,74% | 28 | 1,61% | 28 | 1,62% | 28 | 1,61% |
| Gmelin (1791) | 50 | 0,67% | 4 | 0,23% | 4 | 0,23% | 4 | 0,23% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 50 | 0,67% | 4 | 0,23% | 4 | 0,23% | 4 | 0,23% |
| Questel (2020) | 42 | 0,57% | 39 | 2,24% | 39 | 2,25% | 39 | 2,25% |
| Iredale (1939) | 41 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 40 | 0,54% | 31 | 1,78% | 31 | 1,79% | 31 | 1,79% |
| Glover & Taylor (2007) | 39 | 0,53% | 37 | 2,12% | 37 | 2,14% | 37 | 2,13% |
| Taylor & Glover (2016) | 37 | 0,5% | 37 | 2,12% | 37 | 2,14% | 37 | 2,13% |
| Dall et al. (1938) | 35 | 0,47% | 9 | 0,52% | 9 | 0,52% | 9 | 0,52% |
| Powell (1960) | 33 | 0,44% | 15 | 0,86% | 15 | 0,87% | 15 | 0,86% |
| Dijkstra (1995) | 29 | 0,39% | 25 | 1,43% | 25 | 1,44% | 25 | 1,44% |
| Kaiser (2009) | 28 | 0,38% | 21 | 1,2% | 21 | 1,21% | 21 | 1,21% |
| Richard (2006) | 26 | 0,35% | 22 | 1,26% | 22 | 1,27% | 22 | 1,27% |
| Breton (2014) | 25 | 0,34% | 21 | 1,2% | 21 | 1,21% | 20 | 1,15% |
| Dijkstra (2001) | 25 | 0,34% | 25 | 1,43% | 25 | 1,44% | 25 | 1,44% |
| Lamprell & Stanisic (1996) | 25 | 0,34% | 15 | 0,86% | 15 | 0,87% | 15 | 0,86% |
| Bucquoy et al. (1892) | 24 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 24 | 0,32% | 18 | 1,03% | 18 | 1,04% | 18 | 1,04% |
| Smith (1885) | 20 | 0,27% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Arnaud (1974) | 19 | 0,26% | 13 | 0,75% | 13 | 0,75% | 13 | 0,75% |
| Lamprell & Healy (2001) | 19 | 0,26% | 11 | 0,63% | 11 | 0,64% | 11 | 0,63% |
| Arnaud (1974) | 18 | 0,24% | 12 | 0,69% | 12 | 0,69% | 12 | 0,69% |
| Chabanet et al. (2007) | 18 | 0,24% | 14 | 0,8% | 14 | 0,81% | 14 | 0,81% |
| Dijkstra & Maestrati (2010) | 18 | 0,24% | 16 | 0,92% | 16 | 0,92% | 16 | 0,92% |
| Huber et al. (2015) | 18 | 0,24% | 17 | 0,98% | 17 | 0,98% | 17 | 0,98% |
| Kleemann & Maestrati (2012) | 17 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal (1999) | 17 | 0,23% | 17 | 0,98% | 15 | 0,87% | 17 | 0,98% |
| Goulletquer (2016) | 16 | 0,22% | 13 | 0,75% | 13 | 0,75% | 13 | 0,75% |
| Poutiers (1984) | 16 | 0,22% | 7 | 0,4% | 7 | 0,4% | 7 | 0,4% |
| Vidal (1994) | 16 | 0,22% | 9 | 0,52% | 9 | 0,52% | 9 | 0,52% |
| Taylor et al. (2016) | 14 | 0,19% | 13 | 0,75% | 13 | 0,75% | 13 | 0,75% |
| Fourt et al. (2017) | 13 | 0,18% | 13 | 0,75% | 13 | 0,75% | 13 | 0,75% |
| Héros (comm. pers., 2011) | 13 | 0,18% | 10 | 0,57% | 10 | 0,58% | 10 | 0,58% |
| Lamarck (1818) | 13 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 13 | 0,18% | 7 | 0,4% | 7 | 0,4% | 7 | 0,4% |
| Vidal & Kirkendale (2007) | 13 | 0,18% | 6 | 0,34% | 6 | 0,35% | 6 | 0,35% |
| Dijkstra (1991) | 12 | 0,16% | 11 | 0,63% | 11 | 0,64% | 11 | 0,63% |
| Lopes-Lima et al. (2016) | 12 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mulochau et al. (2020) | 12 | 0,16% | 11 | 0,63% | 11 | 0,64% | 11 | 0,63% |
| Turton (1932) | 12 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Australian Museum (2020) | 11 | 0,15% | 10 | 0,57% | 10 | 0,58% | 10 | 0,58% |
| Dewarumez et al. (2011) | 11 | 0,15% | 9 | 0,52% | 9 | 0,52% | 9 | 0,52% |
| Dijkstra & Maestrati (2013) | 11 | 0,15% | 10 | 0,57% | 10 | 0,58% | 10 | 0,58% |
| Pearman et al. (2020) | 11 | 0,15% | 7 | 0,4% | 7 | 0,4% | 7 | 0,4% |
| Prié (2020) | 11 | 0,15% | 9 | 0,52% | 9 | 0,52% | 9 | 0,52% |
| Pelorce & Hoarau (comm. pers., 2012) | 10 | 0,13% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Uicn et al. (2019) | 10 | 0,13% | 8 | 0,46% | 8 | 0,46% | 8 | 0,46% |
| Verrill & Bush (1898) | 10 | 0,13% | 5 | 0,29% | 5 | 0,29% | 5 | 0,29% |
| Bergmans (1991) | 9 | 0,12% | 6 | 0,34% | 6 | 0,35% | 6 | 0,35% |
| Poutiers & Bernard (1995) | 9 | 0,12% | 6 | 0,34% | 6 | 0,35% | 6 | 0,35% |
| Arnaud (1965) | 8 | 0,11% | 5 | 0,29% | 5 | 0,29% | 5 | 0,29% |
| Goud et al. (2020) | 8 | 0,11% | 8 | 0,46% | 8 | 0,46% | 8 | 0,46% |
| Huber (2010) | 8 | 0,11% | 4 | 0,23% | 4 | 0,23% | 4 | 0,23% |
| Souverbie (1863) | 8 | 0,11% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Vélain (1877) | 8 | 0,11% | 8 | 0,46% | 8 | 0,46% | 8 | 0,46% |
| Delannoye et al. (2015) | 7 | 0,09% | 6 | 0,34% | 6 | 0,35% | 6 | 0,35% |
| Huber (2015) | 7 | 0,09% | 6 | 0,34% | 6 | 0,35% | 6 | 0,35% |
| Prashad (1932) | 7 | 0,09% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Thiele & Jaeckel (1931) | 7 | 0,09% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Viader (1951) | 7 | 0,09% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Bartsch (1947) | 6 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambert et al. (2011) | 6 | 0,08% | 4 | 0,23% | 4 | 0,23% | 4 | 0,23% |
| Dall (1916) | 6 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dautzenberg & Fischer (1897) | 6 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gaillard (1954) | 6 | 0,08% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Gout (1991) | 6 | 0,08% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Kronen et al. (2008) | 6 | 0,08% | 5 | 0,29% | 5 | 0,29% | 5 | 0,29% |
| Willan (1993) | 6 | 0,08% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Etcheberry & Abraham (2009) | 5 | 0,07% | 5 | 0,29% | 5 | 0,29% | 5 | 0,29% |
| Gaillard (1954) | 5 | 0,07% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Langeveld et al. (2020) | 5 | 0,07% | 5 | 0,29% | 5 | 0,29% | 5 | 0,29% |
| Macé (1860) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| MGnify (2017) | 5 | 0,07% | 5 | 0,29% | 5 | 0,29% | 5 | 0,29% |
| Müller (1774) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poutiers (2006) | 5 | 0,07% | 5 | 0,29% | 5 | 0,29% | 5 | 0,29% |
| Wang (1983) | 5 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet et al. (2022) | 4 | 0,05% | 4 | 0,23% | 4 | 0,23% | 4 | 0,23% |
| Cépède (1914) | 4 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dall & Simpson (1901) | 4 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra & Maestrati (2013) | 4 | 0,05% | 4 | 0,23% | 4 | 0,23% | 4 | 0,23% |
| Drivas & Jay (1990) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer-Piette (1977) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fulton (1915) | 4 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Hedley (1916) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1929) | 4 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Krylova (2001) | 4 | 0,05% | 4 | 0,23% | 4 | 0,23% | 4 | 0,23% |
| Melvill (1909) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nicet & Denis (2011) | 4 | 0,05% | 4 | 0,23% | 4 | 0,23% | 4 | 0,23% |
| Odhner (1919) | 4 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Olsson (1961) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poulicek (2020) | 4 | 0,05% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Poutiers (1981) | 4 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Powell (1933) | 4 | 0,05% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Preston (1908) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié et al. (2012) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rehder (1943) | 4 | 0,05% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Smith (1875) | 4 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen & Hannah (1989) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Barnard (1964) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Born (1778) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boshoff (1965) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coan (1988) | 3 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Cosel (1995) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa (1778) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cox (1927) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dautzenberg (1900) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupuy (1849) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Memoirs of the Australian Museum, iv: 287-324.">Hedley (1902) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huber (2010) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Ifremer (2020) | 3 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Iredale (1927) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1931) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1936) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kotaka (1977) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuriakose et al. (1976) | 3 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Linnaeus (1767) | 3 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Lucas (1984) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matsukuma (1996) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Melvill (1898) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orton (1928) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulmier (2018) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Payraudeau (1826) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelseneer (1903) | 3 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Pilsbry & Lowe (1932) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1921) | 3 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Poorten & Ter (2019) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Poutiers (1982) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Pulteney (1799) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roch & Moll (1931) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sakurai & Habe (1966) | 3 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Salas & Gofas (1998) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Salisbury (1934) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taki & Habe (1945) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor & Glover (2013) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vergonzanne (1977) | 3 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Vidal (2005) | 3 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vierna et al. (2012) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Wantiez (2001) | 3 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Welter-schultes (2012) | 3 | 0,04% | 3 | 0,17% | 3 | 0,17% | 3 | 0,17% |
| Arnaud (1964) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Azuma (1960) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartsch & Rehder (1939) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Bernard (1983) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boisseau & Lubet (1955) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boss (1964) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boss (1969) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Bouchet & Pointier (1998) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Bourcier & Zibrowius (1969) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bozzetti (1996) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cossignani & Allary (2018) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Dall (1901) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dall (1908) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dell (1956) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra & Marshall (2008) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Dijkstra (1986) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra (1988) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra (1990) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Dijkstra (1990) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra (2011) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Fischer (1859) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Garrard (1966) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Grau (1960) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Griffiths & Florens (2006) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Habe & Kosuge (1966) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Habe (1958) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Habe (1976) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Posidonia oceanica Delile. Recueil des Travaux de la Station Marine d'Endoume, 35(51): 43-105.">Harmelin (1964) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harry (1985) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harte & Lamprell (1999) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Harte (1993) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hertlein & Grant (1972) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hertlein & Strong (1949) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hidalgo (1903) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Høpner et al. (1971) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourde et al. (2017) | 2 | 0,03% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Kaltenbach (1943) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaltenbach (1949) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kleemann (1980) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kleemann (2008) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kronen et al. (2009) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Kuronuma (1931) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamprell & Healy (1997) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamprell & Kilburn (1999) | 2 | 0,03% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Lamy (1907) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Laseron (1953) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Mao et al. (2020) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Letacq (1924) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 1 | 0,06% |
| Lucas et al. (1991) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas (1984) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mars (1965) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Massemin et al. (2011) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Menzel (1974) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montrouzier (1860) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Moore (1977) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Narchi (1975) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nielsen (1986) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Nolf (2022) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Oliver & Holmes (2004) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oyama (1951) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulmier (1997) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelorce & Poutiers (2009) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Pennant (1777) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Petit (1964) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Petuch (1995) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poutiers (1985) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Powell (1967) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preston (1904) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Petit (2022) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Prié & Puillandre (2014) | 2 | 0,03% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
| Rehder & Abbott (1951) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robert et al. (1991) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Schultz & Huber (2013) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Shikama (1964) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1884) | 2 | 0,03% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Smith (1910) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souverbie (1860) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Ter Poorten (2012) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Ter Poorten (2013) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| ter Poorten (2023) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Thang & Tsi (1960) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiele (1930) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal (1993) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Von & Cosel (2009) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Voskuil & Onverwagt (1991) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walier (1972) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wang (1984) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wisshak et al. (2009) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Zinke et al. (2005) | 2 | 0,03% | 2 | 0,11% | 2 | 0,12% | 2 | 0,12% |
| Zorina (1978) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allain & Morice (1971) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen (2015) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Allen (2015) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Andrefouet et al. (2014) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Andrusov (1897) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Anonyme. (2004) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 0 | 0% |
| Arzul et al. (2011) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Arzul et al. (2013) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Barnard (1962) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartsch (1921) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartsch (1931) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bayer (1941) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1914) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berry (1947) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bespalaya et al. (2017) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Beu (2004) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot (2006) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| bij de Vaate & Beisel (2011) | 1 | 0,01% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
| Bogi (2015) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Bonhomme (1840) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boubée (1833-1834) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet (2002) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Canu (1891) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevaldonné et al. (2015) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Clapp (1923) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Clapp (1924) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cockerell (1929) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coen (1915) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coen (1933) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coen (1941) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Combrisson (2023) | 1 | 0,01% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
| Comfort (1938) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conrad (1831) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coomans (1967) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Costa (1830) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1798) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dall (1915) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dall (1924) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dautzenberg (1891) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dautzenberg (1900) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dautzenberg (1923) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dauvin et al. (2022) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Davoult et al. (1999) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Davoult (1990) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| de Folin & Périer (1875) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekker (2006) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delongueville & Scaillet (2007) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Delsaerdt (1986) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Desgué (2020) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra & Beu (2018) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra & Maestrati (2008) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra & Maestrati (2012) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra (1993) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra (1998) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra (2005) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra (2008) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra (2008) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra (2008) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Dijkstra (2011) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Duchêne (1984) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Faillettaz et al. (2020) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Franc (1956) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fruget & Beisel (2016) | 1 | 0,01% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
| Galea et al. (2012) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Garrard (1963) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2003) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girscher (1938) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gouillieux (2018) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Grabau & King (1928) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grizel et al. (1983) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Groh et al. (2020) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1867) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1882) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gutt et al. (2007) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Haas (1969) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Habe & Tokioka (1953) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Habe (1958) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Habe (1961) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley & Petterd (1906) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley (1909) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley (1921) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hendrickx (1980) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Hertlein & Strong (1946) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Hertlein (1968) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoagland (1986) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Hoenselaar & Hoenselaar (1989) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Hovestadt & Neckheim (2020) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Huber & Schultz (2005) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Ifremer (2019) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Ifremer (2022) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Ifremer (2023) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Iredale (1924) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1929) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jameson (1901) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jeffreys (1860) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keen (1962) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kilburn (1973) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kilburn (1975) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kira (1959) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kleemann (2015) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Knop (2007) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Koch (1953) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuroda (1945) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ladd (1934) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Lamarck (1801) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1819) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamy (1918) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lea (1834) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1759) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1882) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lopes-lima et al. (2018) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Lorion (2005) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Lorion (2005) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Lucas (1978) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lynge (1909) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macsotay et al. (2001) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marescaux et al. (2012) | 1 | 0,01% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
| Mars (1951) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Journal of Conchology Leeds, 14: 182-190; 200-213.">Marshall (1914) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mary (2017) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Massé et al. (2022) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Matsukuma (1989) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Maury (1917) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| McGill (1964) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Melvill (1896) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Melvill (1906) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mohr (1786) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monod & Dollfus (1932) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Monterosato (1899) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morris & Morris (1993) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mouthon & Forcellini (2017) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Mouthon & Loiseau (2000) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mouthon et al. (2017) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Mouthon et al. (2021) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nair (1956) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nair (1958) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neuthiec (1991) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Nicolay (1981) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noda (1966) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nolf & Hubrecht (2022) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Nolf (1993) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Nolf (2010) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Normand (1844) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noseworthy et al. (2007) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ohno et al. (1995) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Okutani & Kawaguchi (1991) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliver et al. (2004) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olivi (1792) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Otuka (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1771) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pasco et al. (2023) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Pereira et al. (2013) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Perna & D'Abramo (2009) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Phillips (1928) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pigneur et al. (2011) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Pilsbry (1901) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1904) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poli (1791) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poli (1791) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Porta et al. (2009) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poutiers (1993) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Preston (1906) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preston (1910) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preston (1913) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preston (1915) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Fruget (2017) | 1 | 0,01% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
| Prié et al. (2012) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié et al. (2012) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Prime (1865) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Puissauve, Barthelemy & Lamand (2015) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 0 | 0% |
| Puissauve, Cohen, Barthelemy & Reygnaud (2015) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Quayle (1938) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quayle (1939) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2022) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Quiñonero-salgado & López-soriano (2017) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Quod et al. (1995) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1850-1851) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rehder (1980) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richards (1955) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rosewater (1984) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1842) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sartori (1993) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Sartori (1999) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Say (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schepman (1907) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Severijns (2000) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Severijns (2004) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sheppard (1823) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simone (1998) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Skarlato (1981) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annals of Natural History, xvi: 1-19.">Smith (1895) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1903) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1903) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smriglio & Buzzurro (1999) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Spengler (1793) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stepien et al. (2013) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1838) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denkschriften der Kaiserlichen Akademie der Wissenschaften, Mathematische-Naturwissenschaftlischen Classe. 63: 1-36.">Sturany (1896) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sykes (1903) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Takeda (1953) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ter Poorten (2000) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Ter Poorten (2008) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tiavouane & Fauvelot (2017) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Journal of Conchology London, 18: 307-310.">Tomlin (1929) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| van Aartsen & Giannuzzi-Savelli (1991) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| van Aartsen et al. (1984) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Van Guelpen (2016) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Van et al. (2004) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Van Rooijet al. (2010) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Vernhout (1914) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Vidal (1997) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Warén (1978) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Watson (1897) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Winckworth (1931) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Wolowicz (1992) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Wood-Mason & Alcock (1891) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Woodring (1925) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (1920) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama 1922 | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zenetos et al. (2005) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zetek & Mclean (1936) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius & Arnaud (1995) | 1 | 0,01% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
| Zilli (2021) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
