Mollusques continentaux de France métropolitaine
Mollusca continentaux (sens large) de France métropolitaine : 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)).
579 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Gargominy et al. (2011) | 890 | 23,12% | 771 | 83,9% | 621 | 83,81% | 678 | 83,29% |
| Falkner et al. (2002) | 818 | 21,25% | 621 | 67,57% | 502 | 67,75% | 539 | 66,22% |
| Welter-schultes (2012) | 416 | 10,81% | 364 | 39,61% | 364 | 49,12% | 294 | 36,12% |
| Gargominy (2011-2023) | 343 | 8,91% | 337 | 36,67% | 227 | 30,63% | 334 | 41,03% |
| Kerney & Cameron (1999) | 303 | 7,87% | 271 | 29,49% | 265 | 35,76% | 207 | 25,43% |
| Glöer (2022) | 124 | 3,22% | 115 | 12,51% | 99 | 13,36% | 115 | 14,13% |
| Prié (2017) | 101 | 2,62% | 96 | 10,45% | 82 | 11,07% | 88 | 10,81% |
| Müller (1774) | 57 | 1,48% | 5 | 0,54% | 5 | 0,67% | 5 | 0,61% |
| Griffiths & Florens (2006) | 49 | 1,27% | 25 | 2,72% | 25 | 3,37% | 25 | 3,07% |
| Gerber (2018) | 41 | 1,07% | 40 | 4,35% | 40 | 5,4% | 36 | 4,42% |
| Caziot (1903) | 40 | 1,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1801) | 36 | 0,94% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1869) | 35 | 0,91% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Gargominy & Ripken (2006) | 34 | 0,88% | 28 | 3,05% | 13 | 1,75% | 27 | 3,32% |
| Draparnaud (1805) | 29 | 0,75% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Boeters & Falkner (2003) | 27 | 0,7% | 26 | 2,83% | 26 | 3,51% | 26 | 3,19% |
| Dupuy (1847-1852) | 26 | 0,68% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1910) | 24 | 0,62% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Servain (1880) | 21 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Germain (1931) | 20 | 0,52% | 5 | 0,54% | 5 | 0,67% | 4 | 0,49% |
| Linnaeus (1758) | 20 | 0,52% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Monterosato (1892) | 20 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters et al. (1989) | 19 | 0,49% | 13 | 1,41% | 13 | 1,75% | 10 | 1,23% |
| Moquin-Tandon (1855-1856) | 17 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1826) | 15 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters & Falkner (2008) | 14 | 0,36% | 12 | 1,31% | 12 | 1,62% | 12 | 1,47% |
| Pollonera (1885) | 14 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hagenmüller (1888) | 13 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letacq (1924) | 13 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delannoye et al. (2015) | 12 | 0,31% | 8 | 0,87% | 8 | 1,08% | 8 | 0,98% |
| Lopes-Lima et al. (2016) | 12 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moutier & Moutier (1920) | 12 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nicolas (1891) | 12 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger (1993) | 11 | 0,29% | 5 | 0,54% | 3 | 0,4% | 4 | 0,49% |
| Macé (1860) | 11 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1864) | 10 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupuy (1849) | 10 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Groenenberg et al. (2016) | 10 | 0,26% | 9 | 0,98% | 6 | 0,81% | 7 | 0,86% |
| Lamy & Pointier (2018) | 10 | 0,26% | 6 | 0,65% | 6 | 0,81% | 6 | 0,74% |
| Locard (1893) | 10 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Michaud (1831) | 10 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (2019) | 9 | 0,23% | 6 | 0,65% | 2 | 0,27% | 5 | 0,61% |
| Lessona (1880) | 9 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bichain et al. (2007) | 8 | 0,21% | 2 | 0,22% | 2 | 0,27% | 1 | 0,12% |
| Boeters (2000) | 8 | 0,21% | 6 | 0,65% | 4 | 0,54% | 6 | 0,74% |
| Caziot (1908) | 8 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| de Winter (1986) | 8 | 0,21% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Girardi (2009) | 8 | 0,21% | 6 | 0,65% | 0 | 0% | 6 | 0,74% |
| Bernasconi (2000) | 7 | 0,18% | 5 | 0,54% | 5 | 0,67% | 5 | 0,61% |
| Bourguignat (1869) | 7 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cowie (2000) | 7 | 0,18% | 5 | 0,54% | 5 | 0,67% | 5 | 0,61% |
| Lessona & Pollonera (1882) | 7 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1869) | 7 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Marquet (1990) | 7 | 0,18% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Zallot et al. (2014) | 7 | 0,18% | 7 | 0,76% | 7 | 0,94% | 6 | 0,74% |
| Bernasconi (1985) | 6 | 0,16% | 3 | 0,33% | 3 | 0,4% | 2 | 0,25% |
| Bernasconi (1989) | 6 | 0,16% | 4 | 0,44% | 2 | 0,27% | 4 | 0,49% |
| Boeters & Falkner (2009) | 6 | 0,16% | 6 | 0,65% | 6 | 0,81% | 6 | 0,74% |
| Boeters (1981) | 6 | 0,16% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Boeters (2022) | 6 | 0,16% | 6 | 0,65% | 6 | 0,81% | 6 | 0,74% |
| Callot-Girardi (2015) | 6 | 0,16% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Caziot (1909) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clerx & Gittenberger (1977) | 6 | 0,16% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| de Cristofori & Jan (1832) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Folin & Bérillon (1877) | 6 | 0,16% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi (2009) | 6 | 0,16% | 6 | 0,65% | 6 | 0,81% | 6 | 0,74% |
| Locard (1882) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mary (2017) | 6 | 0,16% | 6 | 0,65% | 6 | 0,81% | 6 | 0,74% |
| Michaud (1829) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1845) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1872) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nelson-Smith et al. (2014) | 6 | 0,16% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Pollonera (1905) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié et al. (2024) | 6 | 0,16% | 6 | 0,65% | 6 | 0,81% | 6 | 0,74% |
| Boeters & Bertrand (2001) | 5 | 0,13% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Boeters & Falkner (2017) | 5 | 0,13% | 5 | 0,54% | 3 | 0,4% | 5 | 0,61% |
| Boeters (2000) | 5 | 0,13% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Bourguignat (1861-1862) | 5 | 0,13% | 1 | 0,11% | 1 | 0,13% | 0 | 0% |
| Bourguignat (1862) | 5 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1868) | 5 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1877) | 5 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcellini et al. (2012) | 5 | 0,13% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Haase (2000) | 5 | 0,13% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Hausdorf (2023) | 5 | 0,13% | 5 | 0,54% | 5 | 0,67% | 5 | 0,61% |
| Haynes (2001) | 5 | 0,13% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Horsáková et al. (2022) | 5 | 0,13% | 5 | 0,54% | 5 | 0,67% | 5 | 0,61% |
| Locard (1883) | 5 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1881) | 5 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reise et al. (2011) | 5 | 0,13% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Shuttleworth (1843) | 5 | 0,13% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Solem (1964) | 5 | 0,13% | 4 | 0,44% | 4 | 0,54% | 4 | 0,49% |
| Aksenova et al. (2018) | 4 | 0,1% | 4 | 0,44% | 4 | 0,54% | 4 | 0,49% |
| Alder (1830) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benoit (1857) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters & Falkner (2003) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (2008) | 4 | 0,1% | 4 | 0,44% | 4 | 0,54% | 4 | 0,49% |
| Bouchet & Pointier (1998) | 4 | 0,1% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Bourguignat (1860) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Callot-Girardi (2015) | 4 | 0,1% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-Girardi (2015) | 4 | 0,1% | 4 | 0,44% | 4 | 0,54% | 4 | 0,49% |
| Caziot (1909) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coutagne (1882) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse & Debeaux (1869) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| De Stefani (1883) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewarumez et al. (2011) | 4 | 0,1% | 4 | 0,44% | 4 | 0,54% | 4 | 0,49% |
| Dutailly (1867) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1821) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1885) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi et al. (2002) | 4 | 0,1% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi (2009) | 4 | 0,1% | 4 | 0,44% | 4 | 0,54% | 4 | 0,49% |
| Girardi (2009) | 4 | 0,1% | 4 | 0,44% | 4 | 0,54% | 4 | 0,49% |
| Girardi (2009) | 4 | 0,1% | 4 | 0,44% | 0 | 0% | 4 | 0,49% |
| Gittenberger (2002) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2010) | 4 | 0,1% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Gómez et al. (2023) | 4 | 0,1% | 2 | 0,22% | 0 | 0% | 2 | 0,25% |
| Horsáková et al. (2020) | 4 | 0,1% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Hutchinson et al. (2022) | 4 | 0,1% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Mabille (1877) | 4 | 0,1% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Martínez-Ortí & Borredà (2012) | 4 | 0,1% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Massemin et al. (2009) | 4 | 0,1% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Neubert & Gosteli (2003) | 4 | 0,1% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Paladilhe (1874) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Payraudeau (1826) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pollonera (1889) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié et al. (2012) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1854) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vallot (1801) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zallot et al. (2024) | 4 | 0,1% | 4 | 0,44% | 4 | 0,54% | 2 | 0,25% |
| Bichain et al. (2021) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 2 | 0,25% |
| Boeters (1969) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (2009) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Boettger (1949) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boubée (1833-1834) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1864) | 3 | 0,08% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Bourguignat (1864) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1866) | 3 | 0,08% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bourguignat (1876) | 3 | 0,08% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Breton (2014) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 2 | 0,25% |
| Callot-Girardi (2017) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Callot-girardi (2017) | 3 | 0,08% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Caziot (1903) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1905) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1879) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1879) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Germain (1931) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger (1973) | 3 | 0,08% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Gmelin (1791) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Hatteland et al. (2015) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Hovestadt & Neckheim (2020) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Jeffreys (1830) | 3 | 0,08% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Kadolsky (2012) | 3 | 0,08% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Locard (1894) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1880) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Manganelli et al. (2019) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Montagu (1803) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moquin-Tandon (1855-1856) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nevill (1879) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1866) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1867) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1876) | 3 | 0,08% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Philippi (1844) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (2001) | 3 | 0,08% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Rambur (1869) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1852) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1851-1854) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reygrobellet (1963) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ripken & Bouchet (1998) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 2 | 0,25% |
| Schallenberg et al. (2022) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Solem (1961) | 3 | 0,08% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| van Aartsen (2008) | 3 | 0,08% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
| Vandel (1922) | 3 | 0,08% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Zilch (1947) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adamcová et al. (2024) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Badie (1977) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benoit (1881) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bérenguier (1883) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bérenguier (1900-1902) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bernasconi (1968) | 2 | 0,05% | 2 | 0,22% | 0 | 0% | 2 | 0,25% |
| Bernasconi (1985) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berthier (1884) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertrand (2001) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Bertrand (2004) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertrand (2004) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Bertrand (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertrand (2017) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bertrand (2022) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Bichain & Bertrand (2022) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Binney (1841) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters & Gittenberger (1980) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Boeters et al. (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (1983) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (1999) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Boubée (1836) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet et al. (1997) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bourguignat (1856) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1856) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruguière (1789-1792) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Callot-Girardi & Boeters (2015) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-Girardi & Boeters (2015) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-Girardi & Boeters (2017) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-girardi et al. (2017) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-Girardi (2012) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-Girardi (2013) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-Girardi (2015) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-Girardi (2015) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Callot-Girardi (2017) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Caziot (1911) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Christensen (2016) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Debeaux (1867) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delicado et al. (2015) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Delicado et al. (2024) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Des Moulins (1827) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Fagot (1881) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Fagot (1882) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1884) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1884) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1885) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1888) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner (2000) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fert� et al. (2004) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Férussac (1827) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcart (1946) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fossati & Marquet (1998) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Gargominy et al. (2008) | 2 | 0,05% | 2 | 0,22% | 1 | 0,13% | 1 | 0,12% |
| Geniez & Bertrand (2001) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi & Bertrand (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi & Bertrand (2009) | 2 | 0,05% | 2 | 0,22% | 0 | 0% | 2 | 0,25% |
| Girardi (2001) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2002) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2004) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi (2004) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi (2004) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Girardi (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Gittenberger & de Winter (1985) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger et al. (2016) | 2 | 0,05% | 2 | 0,22% | 1 | 0,13% | 1 | 0,12% |
| Giusti & Manganelli (1987) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Giusti & Manganelli (1989) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Giusti (1976) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1852) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gras (1840) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grimpe & Hoffmann (1925) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartmann (1821) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holyoak & Holyoak (2012) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Horsák et al. (2022) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Jay et al. (2009) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Jourdan et al. (2014) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Klemm (1939) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kobelt (1875-1880) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Lamarck (1818) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemaire & Gerriet (2014) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Locard (1882) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorencová et al. (2021) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 1 | 0,12% |
| Mabille (1875) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Magnin et al. (2012) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 0 | 0% |
| Nekola et al. (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nordsieck (2003) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 0 | 0% |
| Paladilhe (1870) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulucci (1882) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pfeiffer (1828) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pieńkowska et al. (2018) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Pieńkowska et al. (2022) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pilsbry (1889) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1906-1907) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1918-1920) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1922-1926) | 2 | 0,05% | 2 | 0,22% | 0 | 0% | 2 | 0,25% |
| Pini (1883) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pintér (1983) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Poliński (1929) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pollonera (1887) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prie & Bichain (2009) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Cucherat (2021) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Puillandre (2014) | 2 | 0,05% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Questel (2020) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Rambur (1868) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1831) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1841) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reynès (1870) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richling et al. (2016) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler & Kobelt (1906) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1838) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1880) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rowson et al. (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sayn (1889) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schikov (2017) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Taylor (2003) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN Comité français, OFB & MNHN (2021) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Vial (1979) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1876) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wetherby (1879) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiktor (1998) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
| Abdou et al. (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Altena Regteren Van (1958) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Altena (1961) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Altena (1973) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Andreae (1879) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Andrusov (1897) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anistratenko et al. (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anistratenko et al. (2019) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Anonyme. (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Audibert & Paillet (2014) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Aureglia et al. (2023) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Badie et al. (1992) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Baker (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1941) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bank et al. (2003) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bank (1978) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bank (2011) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bavay (1920) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beck (1837) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benke et al. (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1854) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bérenguier (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (1988) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bernasconi (1994) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (2002) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bertrand (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bespalaya et al. (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Betta (1852) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bichain & Ryelandt (2023) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| bij de Vaate & Beisel (2011) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Boeters & Falkner (2000) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (1967) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Boettger (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bofill & Poch (1897) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonhomme (1840) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bößneck (2000) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bouaziz-Yahiatene et al. (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bouchet et al. (1998) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bourguignat (1853) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1861) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1863) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1864) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bourguignat (1864) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1870) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1870) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1880) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brown (1994) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugel (2016) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Callot-Girardi (2015) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Camus et al. (2023) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1910) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1916) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charrier et al. (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chueca et al. (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Clanzig (1995) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clessin (1874) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clessin (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clessin (1911) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Combrisson (2023) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Conrad (1831) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coomans (1967) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Correa et al. (2010) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Coutagne (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1864) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cucherat & Demuynck (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Cuénot & Mercier (1914) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1798) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dance et al. (1986) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Dayrat (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| De Winter (1990) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Des Moulins (1827) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1863) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss et al. (2013) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Doby et al. (1966) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Dommergues & Gargominy (2024) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Drouët (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dunker (1848) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1891) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1904) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faillettaz et al. (2020) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Falkner (2008) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Férussac (1807) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fiorentino et al. (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1925) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Fitzinger (1833) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frenot et al. (2005) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Fruget & Beisel (2016) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Gargominy et al. (2022) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Garrett (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geist et al. (2022) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Germain (1928) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2003) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger & Ripken (1993) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger et al. (2006) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Gittenberger (1973) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger (1978) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 0 | 0% |
| Gittenberger (1978) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 0 | 0% |
| Gittenberger (2004) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Gittenberger (2005) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giusti et al. (2011) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Giusti (1970) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Glöer & Zettler (2009) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Glöer (2019) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Gould (1846) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gourdon (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gregorio (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Groh et al. (2020) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grossu & Lupu (1965) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Guiller & Madec (2010) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Haas (1969) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartmann (1840-1844) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartmann (1844) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf & Solvery (2021) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Hausdorf (2022) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Held (1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hobbs et al. (2021) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Holyoak & Holyoak (2012) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Holyoak & Holyoak (2018) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Holyoak et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holyoak et al. (2020) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Jesse et al. (2011) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Johnson (1964) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan & Mille (2006) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Jourdan (2020) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Kennard & Woodward (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Klemm (1943) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kneubühler et al. (2021) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Kokshoorn & Gittenberger (2010) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Kosicka et al. (2022) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Kroll et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kruger et al. (2019) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Küster (1852) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1822) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lea (1834) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lecaplain (2013) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Locard (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1892) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Locard (1901) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1903) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Lopes-lima et al. (2018) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Lounnas et al. (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Lowe (1855) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lydeard et al. (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maassen (1987) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Mabille (1868) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1871) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Magnin et al. (2008) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Manganelli (2018) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Marescaux et al. (2012) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Martínez-Ortí (2021) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Massot (1872) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menke (1828) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mienis (2008) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Miller et al. (2022) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Miller et al. (2023) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Millet (1813) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mittre (1842) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montfort (1810) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moquin-Tandon (1843) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moquin-Tandon (1850) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mörch (1864) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Mousson (1847) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mouthon & Forcellini (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Mouthon & Loiseau (2000) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mouthon et al. (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Mouthon et al. (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naudon et al. (2015) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Neiber & Hausdorf (2015) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Neiber et al. (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 0 | 0% |
| Neiber et al. (2021) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Nitz et al. (2010) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Normand (1844) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Odhner (1950) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Oueslati & Duvivier (2016) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Paget (1854) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1868) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1875) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1771) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paris (1918) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pascal (1873) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pasco et al. (2023) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pease (1869) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pfeiffer (1852-1860) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pfeiffer (1853) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfenninger et al. (2003) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Philippi (1836) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Phillips (1928) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pieńkowska et al. (2024) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pigneur et al. (2011) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pilsbry (1920-1921) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pini (1885) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pini (1886) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pointier et al. (2007) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Poiret (1801) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poli (1791) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Porro (1840) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potiez & Michaud (1835-1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pouchard & Bichain (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prévot et al. (2013) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Prévot et al. (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Fruget (2017) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Prié et al. (2012) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Prié et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prieto & Puente (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proćków et al. (2013) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Pugh & Scott (2002) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Puissauve, Barthelemy & Lamand (2015) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 0 | 0% |
| Puissauve, Cohen & Cucherat (2015) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Puissauve, Cohen, Barthelemy & Reygnaud (2015) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Questel & Le Quellec (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2014) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Questel (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Quintana (2010) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Quiñonero-salgado & López-soriano (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Razkin et al. (2016) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Razoumowsky (1789) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1842) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reischütz (1973) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Requien (1848) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Riedel (1979) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Rossmässler et al. (1835) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1842) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saint-simon (1848) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saito et al. (2023) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Salvador et al. (2023) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 0 | 0% |
| Saulcy (1852) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Say (1817) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Say (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scacchi (1833) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schröter (1784) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Histoire malacologique du lac Balaton en Hongrie. Poissy (S. Lejay). 125 pp.">Servain (1882) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Servain (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sheppard (1823) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherpa et al. (2018) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Soyer (1958) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Spengler (1793) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stabile (1864) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1976) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Stepien et al. (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stévanovich (1994) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Stévanovitch (1991) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Strobel (1855) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Strøm (1765) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Talenti et al. (2020) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Bullettino Malacologico Italiano, 2: 33-36, 65-73, 113-123.">Tiberi (1869) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turton & Gray (1840) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van & Bruggen (1991) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| van Aartsen et al. (1984) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vareille-Morel (1982) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villa (1841) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vinarski (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| von Proschwitz et al. (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wagner (2021) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Waldén (1966) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Wallenberg (1858) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1884‑1890) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1885) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1889) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wolowicz (1992) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
| Yokoyama (2013) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
