Mollusques continentaux de Nouvelle-Calédonie
Mollusca continentaux (sens large) de Nouvelle-Calédonie : inclut l'eau douce (habitat 2), le terrestre (habitat 3) et toutes les combinaisons incluant ces 2 milieux (eau douce / marin (habitat 4), terrestre / marin (habitat 5), eau saumâtre (habitat 6) et eau douce / terrestre (habitats 7 et 8)).
225 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Solem (1961) | 226 | 20,77% | 146 | 39,35% | 145 | 40,96% | 142 | 38,9% |
| Neubert et al. (2009) | 159 | 14,61% | 25 | 6,74% | 10 | 2,82% | 21 | 5,75% |
| Pawlowska-Banasiak (2008) | 93 | 8,55% | 88 | 23,72% | 88 | 24,86% | 88 | 24,11% |
| Haase & Bouchet (1998) | 56 | 5,15% | 51 | 13,75% | 51 | 14,41% | 51 | 13,97% |
| Griffiths & Florens (2006) | 42 | 3,86% | 23 | 6,2% | 23 | 6,5% | 23 | 6,3% |
| Richling (2009) | 36 | 3,31% | 18 | 4,85% | 18 | 5,08% | 18 | 4,93% |
| Solem (1964) | 36 | 3,31% | 23 | 6,2% | 23 | 6,5% | 23 | 6,3% |
| Starmühlner (1970) | 26 | 2,39% | 16 | 4,31% | 16 | 4,52% | 16 | 4,38% |
| Grimpe & Hoffmann (1925) | 24 | 2,21% | 15 | 4,04% | 15 | 4,24% | 15 | 4,11% |
| Cowie (2000) | 22 | 2,02% | 16 | 4,31% | 16 | 4,52% | 16 | 4,38% |
| Mary (2017) | 22 | 2,02% | 15 | 4,04% | 15 | 4,24% | 15 | 4,11% |
| Franc (1956) | 21 | 1,93% | 13 | 3,5% | 13 | 3,67% | 13 | 3,56% |
| Delannoye et al. (2015) | 20 | 1,84% | 14 | 3,77% | 14 | 3,95% | 14 | 3,84% |
| Crosse (1874) | 19 | 1,75% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Crosse (1870) | 18 | 1,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1868) | 16 | 1,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2013) | 16 | 1,47% | 10 | 2,7% | 10 | 2,82% | 10 | 2,74% |
| Tillier (1981) | 16 | 1,47% | 16 | 4,31% | 16 | 4,52% | 16 | 4,38% |
| Brook (2010) | 14 | 1,29% | 8 | 2,16% | 8 | 2,26% | 7 | 1,92% |
| Crosse (1870) | 14 | 1,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1884) | 14 | 1,29% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Hovestadt & Neckheim (2020) | 14 | 1,29% | 13 | 3,5% | 13 | 3,67% | 13 | 3,56% |
| Jourdan et al. (2014) | 13 | 1,19% | 10 | 2,7% | 10 | 2,82% | 10 | 2,74% |
| Crosse (1855) | 12 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1863) | 11 | 1,01% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| Haynes (2001) | 11 | 1,01% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Jay et al. (2009) | 11 | 1,01% | 7 | 1,89% | 7 | 1,98% | 7 | 1,92% |
| Pilsbry (1906-1907) | 11 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Marquet (1990) | 11 | 1,01% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Gassies (1871) | 10 | 0,92% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Gassies (1874) | 10 | 0,92% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Haase & Zielske (2015) | 10 | 0,92% | 10 | 2,7% | 10 | 2,82% | 10 | 2,74% |
| Mordan & Tillier (1986) | 9 | 0,83% | 9 | 2,43% | 9 | 2,54% | 9 | 2,47% |
| Tillier & Mordan (1995) | 9 | 0,83% | 5 | 1,35% | 5 | 1,41% | 5 | 1,37% |
| Bouchet & Pointier (1998) | 8 | 0,74% | 3 | 0,81% | 3 | 0,85% | 3 | 0,82% |
| Cooke (1934) | 8 | 0,74% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Crosse (1868) | 8 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner et al. (2002) | 8 | 0,74% | 6 | 1,62% | 6 | 1,69% | 6 | 1,64% |
| Gargominy et al. (2011) | 8 | 0,74% | 8 | 2,16% | 8 | 2,26% | 8 | 2,19% |
| Jourdan (2020) | 8 | 0,74% | 8 | 2,16% | 8 | 2,26% | 8 | 2,19% |
| Preston (1907) | 8 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welter-schultes (2012) | 8 | 0,74% | 5 | 1,35% | 5 | 1,41% | 5 | 1,37% |
| Abdou et al. (2004) | 7 | 0,64% | 3 | 0,81% | 3 | 0,85% | 3 | 0,82% |
| Crosse (1874) | 7 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1887) | 7 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1938) | 6 | 0,55% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| Crosse (1872) | 6 | 0,55% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| Dautzenberg (1923) | 6 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1852) | 6 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamy & Pointier (2018) | 6 | 0,55% | 3 | 0,81% | 3 | 0,85% | 3 | 0,82% |
| Massemin et al. (2009) | 6 | 0,55% | 3 | 0,81% | 3 | 0,85% | 3 | 0,82% |
| Montrouzier (1859) | 6 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1850) | 6 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souverbie (1860) | 6 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1894) | 5 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1863) | 5 | 0,46% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Gassies (1866) | 5 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1880) | 5 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan & Mille (2006) | 5 | 0,46% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Mousson (1872) | 5 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1774) | 5 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1916-1918) | 5 | 0,46% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| Questel (2020) | 5 | 0,46% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| UICN Comité français, OFB & MNHN (2021) | 5 | 0,46% | 5 | 1,35% | 5 | 1,41% | 5 | 1,37% |
| Zielske & Haase (2015) | 5 | 0,46% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| Adamson (1935) | 4 | 0,37% | 3 | 0,81% | 3 | 0,85% | 3 | 0,82% |
| Bouchet et al. (1991) | 4 | 0,37% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Coomans (1967) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1867) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcellini et al. (2012) | 4 | 0,37% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Gargominy (2016-2021) | 4 | 0,37% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| Garrett (1879) | 4 | 0,37% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Gassies (1857) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1858) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1869) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerber (2018) | 4 | 0,37% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| Gmelin (1791) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2023) | 4 | 0,37% | 4 | 1,08% | 4 | 1,13% | 4 | 1,1% |
| Pilsbry (1901-1902) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1920-1921) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1995) | 4 | 0,37% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Abdou et al. (2019) | 3 | 0,28% | 3 | 0,81% | 3 | 0,85% | 3 | 0,82% |
| Crosse (1870) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1871) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss et al. (2013) | 3 | 0,28% | 3 | 0,81% | 3 | 0,85% | 3 | 0,82% |
| Férussac (1821) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fossati & Marquet (1998) | 3 | 0,28% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Hausdorf (2007) | 3 | 0,28% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Kerney & Cameron (1999) | 3 | 0,28% | 3 | 0,81% | 3 | 0,85% | 3 | 0,82% |
| Monterosato (1892) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1998) | 3 | 0,28% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Questel (2017) | 3 | 0,28% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Solem (1959) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souverbie (1859) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Trewick et al. (2009) | 3 | 0,28% | 3 | 0,81% | 3 | 0,85% | 1 | 0,27% |
| Tröndlé & Boutet (2009) | 3 | 0,28% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Yokoyama (2013) | 3 | 0,28% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Abdou (2021) | 2 | 0,18% | 2 | 0,54% | 1 | 0,28% | 1 | 0,27% |
| Baker (1941) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Binney (1841) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Kondo (1961) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Crosse & Marie (1867) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1805) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupouy (1966) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1822) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1827) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1868) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy (2011-2023) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Gassies (1867) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1874) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gomes & Thome (2004) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Gould (1843) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1846) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gude (1900) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley (1898) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Houart (1991) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutton (1834) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hyman & Ponder (2010) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Johnson (1994) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jousseaume (1884) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1816) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 0,18% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Marie (1870) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martens (1875) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martins (1995) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Mousson (1865) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neiber & Glaubrecht (2018) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Neubert & Gosteli (2003) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pain (1958) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1865) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1869) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Pease (1869) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1871) | 2 | 0,18% | 1 | 0,27% | 1 | 0,28% | 0 | 0% |
| Pfeiffer (1846) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry & Cooke (1915-1916) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1909-1910) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (2001) | 2 | 0,18% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Questel & Le Quellec (2012) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1853) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1842) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1851-1854) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reise et al. (2011) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richling (2017) | 2 | 0,18% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Schröder et al. (2024) | 2 | 0,18% | 2 | 0,54% | 2 | 0,56% | 2 | 0,55% |
| Solem (1960) | 2 | 0,18% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Souverbie (1863) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1840) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (2003) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adams (1845) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ancey (1892) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1940) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beltramino et al. (2018) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Benoit (1881) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1850) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boettger (1880) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet et al. (2008) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1856) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1822) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Broderip (1833) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brown (1994) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruguière (1789-1792) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabaret et al. (1986) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1903) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cockerell (1901) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke (1928) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Cowie et al. (2009) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Cowie (1998) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse & Fischer (1870) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1868) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1872) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Crosse (1887) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer-piette & Bedoucha (1964) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilla et al. (2014) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Gamiette et al. (2023) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy & Fontaine (2014) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Gargominy (2007) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Garrett (1881) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Germain (1931) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1859) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulding et al. (2021) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Guiller & Madec (2010) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Héros et al. (2007) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Hervé (2010) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Houart et al. (2021) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| IUCN (2013) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1964) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Kaiser (2009) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kirch (1973) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Lamarck (1822) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1830-1831) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letacq (1924) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lounnas et al. (2017) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Lovenburg (2009) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Lydeard et al. (2016) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1883) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1869) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naudon et al. (2015) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Neubert & Gosteli (2005) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orbigny (1835) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1861) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1861) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelorce & Hoarau (comm. pers., 2012) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Pfeiffer (1850) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1860) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1868) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1927-1935) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Blanc (1985) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Pointier et al. (2007) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Questel (2014) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Reeve (1849) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1873-1874) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (2006) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Salles et al. (2018) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Say (1817) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherpa et al. (2018) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Shuttleworth (1852) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simroth (1918) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1976) | 1 | 0,09% | 1 | 0,27% | 1 | 0,28% | 1 | 0,27% |
| Tryon (1886) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1922) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
