Mollusques continentaux de Polynésie française
Mollusca continentaux (sens large) de Polynésie française
351 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Garrett (1884) | 264 | 18,92% | 74 | 11,09% | 74 | 13,5% | 67 | 10,82% |
| Solem (1976) | 260 | 18,64% | 256 | 38,38% | 212 | 38,69% | 242 | 39,1% |
| Cooke & Kondo (1961) | 167 | 11,97% | 153 | 22,94% | 91 | 16,61% | 135 | 21,81% |
| Gerlach (2016) | 139 | 9,96% | 103 | 15,44% | 78 | 14,23% | 94 | 15,19% |
| Baker (1938) | 117 | 8,39% | 111 | 16,64% | 86 | 15,69% | 98 | 15,83% |
| Baker (1940) | 77 | 5,52% | 74 | 11,09% | 56 | 10,22% | 66 | 10,66% |
| Sartori et al. (2014) | 62 | 4,44% | 62 | 9,3% | 62 | 11,31% | 62 | 10,02% |
| Coote & Loeve (2003) | 60 | 4,3% | 40 | 6% | 40 | 7,3% | 32 | 5,17% |
| Pilsbry (1909-1910) | 59 | 4,23% | 20 | 3% | 18 | 3,28% | 17 | 2,75% |
| Gould (1852) | 52 | 3,73% | 12 | 1,8% | 12 | 2,19% | 12 | 1,94% |
| Garrett (1887) | 50 | 3,58% | 8 | 1,2% | 8 | 1,46% | 8 | 1,29% |
| Wagner (1907-1911) | 50 | 3,58% | 13 | 1,95% | 11 | 2,01% | 11 | 1,78% |
| Abdou & Bouchet (2000) | 47 | 3,37% | 47 | 7,05% | 45 | 8,21% | 46 | 7,43% |
| Wagner (1905) | 45 | 3,23% | 10 | 1,5% | 8 | 1,46% | 8 | 1,29% |
| Griffiths & Florens (2006) | 42 | 3,01% | 24 | 3,6% | 24 | 4,38% | 24 | 3,88% |
| Kondo (1962) | 41 | 2,94% | 40 | 6% | 17 | 3,1% | 38 | 6,14% |
| Gargominy & Fontaine (2014) | 34 | 2,44% | 34 | 5,1% | 31 | 5,66% | 33 | 5,33% |
| Delannoye et al. (2015) | 33 | 2,37% | 19 | 2,85% | 19 | 3,47% | 19 | 3,07% |
| Richling & Bouchet (2013) | 33 | 2,37% | 32 | 4,8% | 32 | 5,84% | 31 | 5,01% |
| Cowie (2000) | 30 | 2,15% | 23 | 3,45% | 23 | 4,2% | 23 | 3,72% |
| Pease (1865) | 30 | 2,15% | 6 | 0,9% | 6 | 1,09% | 4 | 0,65% |
| Pease (1871) | 28 | 2,01% | 6 | 0,9% | 6 | 1,09% | 6 | 0,97% |
| Brook (2010) | 27 | 1,94% | 20 | 3% | 20 | 3,65% | 19 | 3,07% |
| Partula. The species inhabiting Tahiti. Carnegie Institute of Washington Publication, 228: 1-313.">Crampton (1917) | 27 | 1,94% | 7 | 1,05% | 5 | 0,91% | 6 | 0,97% |
| Pointier & Marquet (1990) | 27 | 1,94% | 8 | 1,2% | 8 | 1,46% | 8 | 1,29% |
| Pease (1869) | 26 | 1,86% | 16 | 2,4% | 16 | 2,92% | 16 | 2,58% |
| Pease (1867) | 24 | 1,72% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Sartori et al. (2013) | 24 | 1,72% | 24 | 3,6% | 24 | 4,38% | 24 | 3,88% |
| Tryon (1886) | 24 | 1,72% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1879) | 23 | 1,65% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Haynes (2001) | 23 | 1,65% | 12 | 1,8% | 12 | 2,19% | 12 | 1,94% |
| Johnson (1994) | 23 | 1,65% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Solem (1964) | 23 | 1,65% | 16 | 2,4% | 16 | 2,92% | 16 | 2,58% |
| Pfeiffer (1852-1860) | 22 | 1,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry & Cooke (1915-1916) | 22 | 1,58% | 7 | 1,05% | 7 | 1,28% | 7 | 1,13% |
| Reeve (1849-1851) | 22 | 1,58% | 10 | 1,5% | 10 | 1,82% | 6 | 0,97% |
| Cooke (1934) | 21 | 1,51% | 7 | 1,05% | 7 | 1,28% | 7 | 1,13% |
| Crampton & Cooke (1953) | 20 | 1,43% | 10 | 1,5% | 10 | 1,82% | 10 | 1,62% |
| Crampton (1956) | 20 | 1,43% | 14 | 2,1% | 14 | 2,55% | 14 | 2,26% |
| Jourdan et al. (2014) | 20 | 1,43% | 13 | 1,95% | 13 | 2,37% | 13 | 2,1% |
| Hovestadt & Neckheim (2020) | 19 | 1,36% | 16 | 2,4% | 16 | 2,92% | 16 | 2,58% |
| Solem (1961) | 19 | 1,36% | 14 | 2,1% | 14 | 2,55% | 14 | 2,26% |
| Haase et al. (2005) | 18 | 1,29% | 16 | 2,4% | 16 | 2,92% | 16 | 2,58% |
| Lee et al. (2009) | 18 | 1,29% | 11 | 1,65% | 10 | 1,82% | 9 | 1,45% |
| Pease (1866) | 18 | 1,29% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Pfeiffer (1850-1853) | 17 | 1,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1906-1907) | 17 | 1,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1868) | 16 | 1,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1873-1874) | 16 | 1,15% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Preece (1995) | 15 | 1,08% | 10 | 1,5% | 8 | 1,46% | 10 | 1,62% |
| Kondo (1968) | 14 | 1% | 9 | 1,35% | 9 | 1,64% | 9 | 1,45% |
| Pilsbry (1918-1920) | 14 | 1% | 13 | 1,95% | 13 | 2,37% | 13 | 2,1% |
| Solem (1983) | 14 | 1% | 14 | 2,1% | 14 | 2,55% | 14 | 2,26% |
| Gould (1846) | 13 | 0,93% | 5 | 0,75% | 5 | 0,91% | 5 | 0,81% |
| Bouchet & Abdou (2003) | 12 | 0,86% | 7 | 1,05% | 7 | 1,28% | 7 | 1,13% |
| Bouchet & Pointier (1998) | 12 | 0,86% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Gargominy (2008) | 12 | 0,86% | 12 | 1,8% | 12 | 2,19% | 12 | 1,94% |
| Hombron & Jacquinot (1842-1853) | 12 | 0,86% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pease (1868) | 12 | 0,86% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Rousseau (1854) | 12 | 0,86% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Tröndlé & Boutet (2009) | 12 | 0,86% | 6 | 0,9% | 6 | 1,09% | 6 | 0,97% |
| Zimmermann et al. (2009) | 12 | 0,86% | 12 | 1,8% | 12 | 2,19% | 12 | 1,94% |
| Anton (1838) | 11 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boettger (1880) | 11 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1865) | 11 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jay et al. (2009) | 11 | 0,79% | 7 | 1,05% | 7 | 1,28% | 7 | 1,13% |
| Lesson (1830-1831) | 11 | 0,79% | 5 | 0,75% | 5 | 0,91% | 3 | 0,48% |
| Massemin et al. (2009) | 11 | 0,79% | 6 | 0,9% | 6 | 1,09% | 6 | 0,97% |
| Baker (1941) | 10 | 0,72% | 10 | 1,5% | 10 | 1,82% | 10 | 1,62% |
| Burch (2007) | 10 | 0,72% | 10 | 1,5% | 10 | 1,82% | 8 | 1,29% |
| Cooke & Clench (1943) | 10 | 0,72% | 10 | 1,5% | 6 | 1,09% | 8 | 1,29% |
| Lamy & Pointier (2018) | 10 | 0,72% | 6 | 0,9% | 6 | 1,09% | 6 | 0,97% |
| Pfeiffer (1840-1850) | 10 | 0,72% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1998) | 10 | 0,72% | 7 | 1,05% | 7 | 1,28% | 7 | 1,13% |
| Reeve (1842) | 10 | 0,72% | 5 | 0,75% | 5 | 0,91% | 3 | 0,48% |
| Bouchet et al. (1991) | 9 | 0,65% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Crampton (1932) | 9 | 0,65% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Gargominy (2016-2021) | 9 | 0,65% | 9 | 1,35% | 9 | 1,64% | 9 | 1,45% |
| Murray & Clarke (1980) | 9 | 0,65% | 6 | 0,9% | 6 | 1,09% | 4 | 0,65% |
| Abdou et al. (2004) | 8 | 0,57% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Christensen et al. (2018) | 8 | 0,57% | 8 | 1,2% | 8 | 1,46% | 8 | 1,29% |
| Crampton (1924) | 8 | 0,57% | 4 | 0,6% | 4 | 0,73% | 2 | 0,32% |
| Gould (1847) | 8 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson et al. (2000) | 8 | 0,57% | 7 | 1,05% | 7 | 1,28% | 6 | 0,97% |
| Pfeiffer (1852) | 8 | 0,57% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Sowerby (1842) | 8 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1863) | 7 | 0,5% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Fossati & Marquet (1998) | 7 | 0,5% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Hausdorf (2023) | 7 | 0,5% | 7 | 1,05% | 7 | 1,28% | 7 | 1,13% |
| Pease (1869) | 7 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1858) | 7 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1920-1921) | 7 | 0,5% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Questel (2020) | 7 | 0,5% | 5 | 0,75% | 5 | 0,91% | 5 | 0,81% |
| UICN Comité français, OFB & MNHN (2021) | 7 | 0,5% | 7 | 1,05% | 7 | 1,28% | 7 | 1,13% |
| Bouchet & Abdou (2001) | 6 | 0,43% | 6 | 0,9% | 6 | 1,09% | 6 | 0,97% |
| Cooke & Clench (1945) | 6 | 0,43% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Deuss et al. (2013) | 6 | 0,43% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Gargominy et al. (2011) | 6 | 0,43% | 6 | 0,9% | 6 | 1,09% | 6 | 0,97% |
| Gray (1839) | 6 | 0,43% | 2 | 0,3% | 2 | 0,36% | 0 | 0% |
| Grimpe & Hoffmann (1925) | 6 | 0,43% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Hartman (1890) | 6 | 0,43% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Kondo (1944) | 6 | 0,43% | 6 | 0,9% | 6 | 1,09% | 4 | 0,65% |
| Mary (2017) | 6 | 0,43% | 6 | 0,9% | 6 | 1,09% | 6 | 0,97% |
| Mousson (1869) | 6 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1871) | 6 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1843-1850) | 6 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welter-schultes (2012) | 6 | 0,43% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Adamson (1935) | 5 | 0,36% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Coomans (1967) | 5 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner et al. (2002) | 5 | 0,36% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Forcellini et al. (2012) | 5 | 0,36% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Franc (1956) | 5 | 0,36% | 5 | 0,75% | 5 | 0,91% | 5 | 0,81% |
| Jourdan (2020) | 5 | 0,36% | 5 | 0,75% | 5 | 0,91% | 5 | 0,81% |
| Mousson (1872) | 5 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1861) | 5 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1855) | 5 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1857) | 5 | 0,36% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pfeiffer (1876) | 5 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1916-1918) | 5 | 0,36% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Beck (1837) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clench & Turner (1948) | 4 | 0,29% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Férussac (1821) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1874) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1791) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1885) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1886) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haynes (2001) | 4 | 0,29% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Hubendick (1952) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutton (1834) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martens (1875) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1853) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 4 | 0,29% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pfeiffer (1851) | 4 | 0,29% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Pfeiffer (1854-1860) | 4 | 0,29% | 2 | 0,3% | 2 | 0,36% | 0 | 0% |
| Pfeiffer (1855) | 4 | 0,29% | 1 | 0,15% | 1 | 0,18% | 0 | 0% |
| Pointier (2001) | 4 | 0,29% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Questel (2017) | 4 | 0,29% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Solem (1959) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2013) | 4 | 0,29% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Zilch (1967) | 4 | 0,29% | 4 | 0,6% | 4 | 0,73% | 4 | 0,65% |
| Baker (1927) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Broderip (1832) | 3 | 0,22% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Eichhorst (2016) | 3 | 0,22% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Hausdorf (2007) | 3 | 0,22% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| IUCN (2012) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kondo (1973) | 3 | 0,22% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Lamarck (1816) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1869) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neubert & Gosteli (2003) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1861) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1848) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 3 | 0,22% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pfeiffer (1868) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry & Cooke (1933) | 3 | 0,22% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Reeve (1849) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rubio & Rolán (2017) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1902) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 3 | 0,22% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Starmühlner (1976) | 3 | 0,22% | 3 | 0,45% | 3 | 0,55% | 3 | 0,48% |
| Abdou et al. (2019) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Ancey (1889) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ancey (1889) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baird (1850) | 2 | 0,14% | 1 | 0,15% | 1 | 0,18% | 0 | 0% |
| Baker (1923) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Binney (1841) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boettger (1891) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boettger (1916) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Breure et al. (2020) | 2 | 0,14% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Broderip (1833) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruguière (1789-1792) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clench (1964) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Crampton (1930) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Cooke & Kondo (1943) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Crosse (1867) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1868) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1872) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1834) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dohrn (1859) | 2 | 0,14% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Draparnaud (1805) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupouy (1966) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1822) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1827) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frauenfeld (1863) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1872) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1881) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerber (2018) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Giusti (1976) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gomes & Thome (2004) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Gould (1843) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gude (1900) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guillou (1841) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hyman & Ponder (2010) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Jousseaume (1889) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kirch (1973) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Kondo (1981) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Küster & Pfeiffer (1845-1855) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lee et al. (2007) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Liardet (1876) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 0,14% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Martens & Langkavel (1871) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martens (1881) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martyn (1845) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mayer (1902) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montrouzier (1859) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mörch (1850) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1865) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1870) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1871) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1774) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Odhner (1921) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Petit de la Saussaye (1843) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1842) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1845) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1847) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Pfeiffer (1854) | 2 | 0,14% | 1 | 0,15% | 1 | 0,18% | 0 | 0% |
| Pilsbry (1927-1935) | 2 | 0,14% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Rang (1831) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1852) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Reeve (1843) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1846-1860) | 2 | 0,14% | 2 | 0,3% | 2 | 0,36% | 2 | 0,32% |
| Reeve (1851-1854) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reise et al. (2011) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rubio & Rolán (2019) | 2 | 0,14% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Shuttleworth (1852) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1825) | 2 | 0,14% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Swainson (1840) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (2003) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tryon (1866) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wetherby (1879) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abbott (1958) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Abdou (2021) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Adams (1845) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ancey (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1961) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Beltramino et al. (2018) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Benoit (1881) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1850) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bland & Binney (1872) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1856) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1822) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Broderip (1832) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Broderip (1832) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Brown (1994) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen & Kahn (2017) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Christensen & Kirch (1986) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Christensen (2013) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Clarke et al. (1984) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cockerell (1901) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Neal (1928) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Cooke (1928) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Cowie et al. (2009) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Cowie (1998) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1871) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cunningham & Daszak (1998) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dell (1954) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Fischer (1868) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer-piette & Bedoucha (1964) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilla et al. (2014) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Gargominy & Meyer (2012) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Gargominy et al. (2020) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Gargominy (2007) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Gargominy (2011-2023) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Garrett & Smith (1902) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1866) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1859) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1825) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1880) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Hausdorf & Bermúdez (2003) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huet (2023) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Johnson et al. (1986) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Johnson (1964) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Kaiser (2009) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kerney & Cameron (1999) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Kobelt (1897-1901) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Kondo & Burch (1983) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kondo & Burch (1989) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Lamarck (1819) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1822) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letacq (1924) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lounnas et al. (2017) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Lovenburg (2009) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Lydeard et al. (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| MacMillan (1946) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Mazé (1883) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menke & Pfeiffer (1847) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Möllendorf (1888) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Möllendorf (1897) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Morelet (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1860) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naggs (1989) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Naggs (1994) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Naudon et al. (2015) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Orbigny (1835) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Patterson (1989) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pearman et al. (2020) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pease (1865) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1865) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelorce & Hoarau (comm. pers., 2012) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pfeiffer & Zelebor (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1840) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1841) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1847) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1848) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pfeiffer (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1849) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1854) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1854) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pfeiffer (1857) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1857) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1862) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1865) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry & Hirase (1904) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Blanc (1985) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Pointier et al. (1998) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier et al. (2007) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Potiez & Michaud (1835-1838) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potiez & Michaud (1844) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2014) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Navicelle. Revue Zoologique, par la Société Cuvierienne, 4: 369-382.">Récluz (1842) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1842) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1856) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salles et al. (2018) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Say (1817) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schikov (2017) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
| Simroth (1918) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1832) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1833) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1842) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turton (1932) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1922) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vermeulen & Raven (1998) | 1 | 0,07% | 1 | 0,15% | 1 | 0,18% | 1 | 0,16% |
