Gastéropodes continentaux de métropole
Gastropoda continentaux de France métropolitaine : inclut les espèces d'eau douce (habitat 2), terrestres (habitat 3) ou à l'interface entre ces 2 milieux (habitats 7 et 8).
526 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) | 803 | 23,44% | 710 | 84,22% | 565 | 83,83% | 621 | 83,58% |
Falkner et al. (2002) | 728 | 21,25% | 582 | 69,04% | 468 | 69,44% | 503 | 67,7% |
Welter-schultes (2012) | 403 | 11,76% | 353 | 41,87% | 353 | 52,37% | 283 | 38,09% |
Gargominy (2011-2023) | 341 | 9,95% | 334 | 39,62% | 224 | 33,23% | 331 | 44,55% |
Kerney & Cameron (1999) | 301 | 8,79% | 268 | 31,79% | 262 | 38,87% | 204 | 27,46% |
Glöer (2022) | 124 | 3,62% | 115 | 13,64% | 99 | 14,69% | 115 | 15,48% |
Müller (1774) | 52 | 1,52% | 5 | 0,59% | 5 | 0,74% | 5 | 0,67% |
Griffiths & Florens (2006) | 49 | 1,43% | 25 | 2,97% | 25 | 3,71% | 25 | 3,36% |
Gerber (2018) | 41 | 1,2% | 40 | 4,74% | 40 | 5,93% | 36 | 4,85% |
Caziot (1903) | 40 | 1,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1801) | 35 | 1,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy & Ripken (2006) | 34 | 0,99% | 28 | 3,32% | 13 | 1,93% | 27 | 3,63% |
Paladilhe (1869) | 31 | 0,9% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Draparnaud (1805) | 29 | 0,85% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Boeters & Falkner (2003) | 27 | 0,79% | 26 | 3,08% | 26 | 3,86% | 26 | 3,5% |
Dupuy (1847-1852) | 26 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Caziot (1910) | 24 | 0,7% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Germain (1931) | 20 | 0,58% | 5 | 0,59% | 5 | 0,74% | 4 | 0,54% |
Monterosato (1892) | 20 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Servain (1880) | 20 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters et al. (1989) | 19 | 0,55% | 13 | 1,54% | 13 | 1,93% | 10 | 1,35% |
Moquin-Tandon (1855-1856) | 17 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 15 | 0,44% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Risso (1826) | 15 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters & Falkner (2008) | 14 | 0,41% | 12 | 1,42% | 12 | 1,78% | 12 | 1,62% |
Pollonera (1885) | 14 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Hagenmüller (1888) | 13 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas (1891) | 12 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Gittenberger (1993) | 11 | 0,32% | 5 | 0,59% | 3 | 0,45% | 4 | 0,54% |
Letacq (1924) | 11 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Moutier & Moutier (1920) | 11 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Delannoye et al. (2015) | 10 | 0,29% | 6 | 0,71% | 6 | 0,89% | 6 | 0,81% |
Groenenberg et al. (2016) | 10 | 0,29% | 9 | 1,07% | 6 | 0,89% | 7 | 0,94% |
Locard (1893) | 10 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaud (1831) | 10 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters (2019) | 9 | 0,26% | 6 | 0,71% | 2 | 0,3% | 5 | 0,67% |
Bourguignat (1864) | 9 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamy & Pointier (2018) | 9 | 0,26% | 5 | 0,59% | 5 | 0,74% | 5 | 0,67% |
Lessona (1880) | 9 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Bichain et al. (2007) | 8 | 0,23% | 2 | 0,24% | 2 | 0,3% | 1 | 0,13% |
Boeters (2000) | 8 | 0,23% | 6 | 0,71% | 4 | 0,59% | 6 | 0,81% |
Caziot (1908) | 8 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
de Winter (1986) | 8 | 0,23% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Girardi (2009) | 8 | 0,23% | 6 | 0,71% | 0 | 0% | 6 | 0,81% |
Bernasconi (2000) | 7 | 0,2% | 5 | 0,59% | 5 | 0,74% | 5 | 0,67% |
Bourguignat (1869) | 7 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Cowie (2000) | 7 | 0,2% | 5 | 0,59% | 5 | 0,74% | 5 | 0,67% |
Dupuy (1849) | 7 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Lessona & Pollonera (1882) | 7 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Mabille (1869) | 7 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Marquet (1990) | 7 | 0,2% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Zallot et al. (2014) | 7 | 0,2% | 7 | 0,83% | 7 | 1,04% | 6 | 0,81% |
Bernasconi (1985) | 6 | 0,18% | 3 | 0,36% | 3 | 0,45% | 2 | 0,27% |
Bernasconi (1989) | 6 | 0,18% | 4 | 0,47% | 2 | 0,3% | 4 | 0,54% |
Boeters & Falkner (2009) | 6 | 0,18% | 6 | 0,71% | 6 | 0,89% | 6 | 0,81% |
Boeters (1981) | 6 | 0,18% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Boeters (2022) | 6 | 0,18% | 6 | 0,71% | 6 | 0,89% | 6 | 0,81% |
Callot-Girardi (2015) | 6 | 0,18% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Clerx & Gittenberger (1977) | 6 | 0,18% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
de Cristofori & Jan (1832) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Folin & Bérillon (1877) | 6 | 0,18% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2009) | 6 | 0,18% | 6 | 0,71% | 6 | 0,89% | 6 | 0,81% |
Locard (1882) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Macé (1860) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Mary (2017) | 6 | 0,18% | 6 | 0,71% | 6 | 0,89% | 6 | 0,81% |
Michaud (1829) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelet (1845) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Mousson (1872) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollonera (1905) | 6 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié et al. (2024) | 6 | 0,18% | 6 | 0,71% | 6 | 0,89% | 6 | 0,81% |
Boeters & Bertrand (2001) | 5 | 0,15% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Boeters & Falkner (2017) | 5 | 0,15% | 5 | 0,59% | 3 | 0,45% | 5 | 0,67% |
Boeters (2000) | 5 | 0,15% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Bourguignat (1861-1862) | 5 | 0,15% | 1 | 0,12% | 1 | 0,15% | 0 | 0% |
Bourguignat (1862) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1868) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1877) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcellini et al. (2012) | 5 | 0,15% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Haase (2000) | 5 | 0,15% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Hausdorf (2023) | 5 | 0,15% | 5 | 0,59% | 5 | 0,74% | 5 | 0,67% |
Haynes (2001) | 5 | 0,15% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Horsáková et al. (2022) | 5 | 0,15% | 5 | 0,59% | 5 | 0,74% | 5 | 0,67% |
Locard (1883) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Mabille (1881) | 5 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Reise et al. (2011) | 5 | 0,15% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Shuttleworth (1843) | 5 | 0,15% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Solem (1964) | 5 | 0,15% | 4 | 0,47% | 4 | 0,59% | 4 | 0,54% |
Aksenova et al. (2018) | 4 | 0,12% | 4 | 0,47% | 4 | 0,59% | 4 | 0,54% |
Alder (1830) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Benoit (1857) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters & Falkner (2003) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters (2008) | 4 | 0,12% | 4 | 0,47% | 4 | 0,59% | 4 | 0,54% |
Bouchet & Pointier (1998) | 4 | 0,12% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Bourguignat (1860) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot-Girardi (2015) | 4 | 0,12% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-Girardi (2015) | 4 | 0,12% | 4 | 0,47% | 4 | 0,59% | 4 | 0,54% |
Caziot (1909) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Coutagne (1882) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse & Debeaux (1869) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
De Stefani (1883) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dutailly (1867) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1821) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer (1885) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi et al. (2002) | 4 | 0,12% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2009) | 4 | 0,12% | 4 | 0,47% | 0 | 0% | 4 | 0,54% |
Girardi (2009) | 4 | 0,12% | 4 | 0,47% | 4 | 0,59% | 4 | 0,54% |
Girardi (2009) | 4 | 0,12% | 4 | 0,47% | 4 | 0,59% | 4 | 0,54% |
Gittenberger (2002) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gómez et al. (2023) | 4 | 0,12% | 2 | 0,24% | 0 | 0% | 2 | 0,27% |
Horsáková et al. (2020) | 4 | 0,12% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Hutchinson et al. (2022) | 4 | 0,12% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Mabille (1877) | 4 | 0,12% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Martínez-Ortí & Borredà (2012) | 4 | 0,12% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Neubert & Gosteli (2003) | 4 | 0,12% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Paladilhe (1874) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollonera (1889) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossmässler (1854) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Vallot (1801) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Zallot et al. (2024) | 4 | 0,12% | 4 | 0,47% | 4 | 0,59% | 2 | 0,27% |
Bichain et al. (2021) | 3 | 0,09% | 3 | 0,36% | 3 | 0,45% | 2 | 0,27% |
Boeters (1969) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters (2009) | 3 | 0,09% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Boettger (1949) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1864) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1864) | 3 | 0,09% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Bourguignat (1866) | 3 | 0,09% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Bourguignat (1876) | 3 | 0,09% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Callot-Girardi (2017) | 3 | 0,09% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Callot-girardi (2017) | 3 | 0,09% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Caziot (1903) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Caziot (1905) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1879) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1879) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain (1931) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Gittenberger (1973) | 3 | 0,09% | 1 | 0,12% | 0 | 0% | 1 | 0,13% |
Gmelin (1791) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hatteland et al. (2015) | 3 | 0,09% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Hovestadt & Neckheim (2020) | 3 | 0,09% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Jeffreys (1830) | 3 | 0,09% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Locard (1894) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Mabille (1880) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Manganelli et al. (2019) | 3 | 0,09% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Montagu (1803) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Moquin-Tandon (1855-1856) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Nevill (1879) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Paladilhe (1866) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Paladilhe (1867) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Paladilhe (1876) | 3 | 0,09% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Pointier (2001) | 3 | 0,09% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Rambur (1869) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Récluz (1852) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1851-1854) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Reygrobellet (1963) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ripken & Bouchet (1998) | 3 | 0,09% | 3 | 0,36% | 3 | 0,45% | 2 | 0,27% |
Schallenberg et al. (2022) | 3 | 0,09% | 3 | 0,36% | 3 | 0,45% | 3 | 0,4% |
Solem (1961) | 3 | 0,09% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Vandel (1922) | 3 | 0,09% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Zilch (1947) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamcová et al. (2024) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Badie (1977) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Benoit (1881) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bérenguier (1883) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bérenguier (1900-1902) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Bernasconi (1968) | 2 | 0,06% | 2 | 0,24% | 0 | 0% | 2 | 0,27% |
Bernasconi (1985) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Berthier (1884) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (2001) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Bertrand (2004) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Bertrand (2004) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (2015) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (2017) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Bertrand (2022) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Bichain & Bertrand (2022) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Binney (1841) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters & Gittenberger (1980) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Boeters et al. (2015) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters (1983) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters (1999) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Boubée (1833-1834) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boubée (1836) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchet et al. (1997) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Bourguignat (1856) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1856) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruguière (1789-1792) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot-Girardi & Boeters (2015) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-Girardi & Boeters (2015) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-Girardi & Boeters (2017) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-girardi et al. (2017) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-Girardi (2012) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-Girardi (2013) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-Girardi (2015) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-Girardi (2015) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Callot-Girardi (2017) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Caziot (1911) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Christensen (2016) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Debeaux (1867) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Delicado et al. (2015) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Delicado et al. (2024) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Des Moulins (1827) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Fagot (1881) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Fagot (1882) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1884) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1884) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1885) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1888) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Falkner (2000) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fert� et al. (2004) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Férussac (1827) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcart (1946) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fossati & Marquet (1998) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Gargominy et al. (2008) | 2 | 0,06% | 2 | 0,24% | 1 | 0,15% | 1 | 0,13% |
Geniez & Bertrand (2001) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi & Bertrand (2009) | 2 | 0,06% | 2 | 0,24% | 0 | 0% | 2 | 0,27% |
Girardi & Bertrand (2009) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2001) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi (2002) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi (2004) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2004) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi (2004) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2009) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2009) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2009) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2009) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Girardi (2009) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Gittenberger & de Winter (1985) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gittenberger et al. (2016) | 2 | 0,06% | 2 | 0,24% | 1 | 0,15% | 1 | 0,13% |
Giusti & Manganelli (1987) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Giusti & Manganelli (1989) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Giusti (1976) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1852) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gras (1840) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Grimpe & Hoffmann (1925) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartmann (1821) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Holyoak & Holyoak (2012) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Horsák et al. (2022) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Jay et al. (2009) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Jourdan et al. (2014) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Klemm (1939) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kobelt (1875-1880) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Lemaire & Gerriet (2014) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Lorencová et al. (2021) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mabille (1875) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Magnin et al. (2012) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 0 | 0% |
Massemin et al. (2009) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Nekola et al. (2015) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Nordsieck (2003) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 0 | 0% |
Paladilhe (1870) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulucci (1882) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Payraudeau (1826) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1828) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pieńkowska et al. (2018) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Pieńkowska et al. (2022) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Pilsbry (1889) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1906-1907) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1918-1920) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1922-1926) | 2 | 0,06% | 2 | 0,24% | 0 | 0% | 2 | 0,27% |
Pini (1883) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pintér (1983) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Poliński (1929) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollonera (1887) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Prie & Bichain (2009) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié & Cucherat (2021) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 2 | 0,06% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Rambur (1868) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rang (1831) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Récluz (1841) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Reynès (1870) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Richling et al. (2016) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossmässler & Kobelt (1906) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossmässler (1838) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossmässler (1880) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rowson et al. (2014) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sayn (1889) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schikov (2017) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Taylor (2003) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Vial (1979) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Westerlund (1876) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wetherby (1879) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiktor (1998) | 2 | 0,06% | 2 | 0,24% | 2 | 0,3% | 2 | 0,27% |
Abdou et al. (2004) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Andreae (1879) | 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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Anonyme. (2004) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Anonyme. (2004) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Anonyme. (2004) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Audibert & Paillet (2014) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Aureglia et al. (2023) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Badie et al. (1992) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Baker (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1941) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Bertrand (2004) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Betta (1852) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bichain & Ryelandt (2023) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Boeters & Falkner (2000) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters (1967) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Boettger (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bofill & Poch (1897) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bößneck (2000) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Bouaziz-Yahiatene et al. (2017) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Bouchet et al. (1998) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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% |
Breton (2014) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Brown (1994) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugel (2016) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Callot-Girardi (2015) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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% |
Coomans (1967) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Correa et al. (2010) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Cuénot & Mercier (1914) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dance et al. (1986) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
De Winter (1990) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Dewarumez et al. (2011) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Doby et al. (1966) | 1 | 0,03% | 1 | 0,12% | 0 | 0% | 1 | 0,13% |
Dommergues & Gargominy (2024) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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% |
Falkner (2008) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Fitzinger (1833) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Gargominy et al. (2022) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Germain (1928) | 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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Gittenberger (1973) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gittenberger (1978) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 0 | 0% |
Gittenberger (1978) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 0 | 0% |
Gittenberger (2004) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Gittenberger (2005) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Giusti et al. (2011) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Giusti (1970) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Glöer & Zettler (2009) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Glöer (2019) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Gould (1846) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Gourdon (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gregorio (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Grossu & Lupu (1965) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Guiller & Madec (2010) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Hausdorf (2022) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Held (1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hobbs et al. (2021) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Holyoak & Holyoak (2012) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Holyoak & Holyoak (2018) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Holyoak et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Holyoak et al. (2020) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Jesse et al. (2011) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Johnson (1964) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan & Mille (2006) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Jourdan (2020) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Kadolsky (2012) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Kokshoorn & Gittenberger (2010) | 1 | 0,03% | 1 | 0,12% | 0 | 0% | 1 | 0,13% |
Kosicka et al. (2022) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Kruger et al. (2019) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Küster (1852) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1822) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lecaplain (2013) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Locard (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Locard (1901) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Locard (1903) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Lounnas et al. (2017) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Lowe et al. (2007) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Manganelli (2018) | 1 | 0,03% | 1 | 0,12% | 0 | 0% | 1 | 0,13% |
Martínez-Ortí (2021) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Miller et al. (2022) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Miller et al. (2023) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Mousson (1847) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mousson (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Naudon et al. (2015) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Neiber & Hausdorf (2015) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Neiber et al. (2017) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 0 | 0% |
Neiber et al. (2021) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Nitz et al. (2010) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Odhner (1950) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Oueslati & Duvivier (2016) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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% |
Paris (1918) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Pascal (1873) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1852-1860) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Pfeiffer (1853) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfenninger et al. (2003) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Philippi (1836) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1844) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pieńkowska et al. (2024) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Pointier et al. (2007) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Poiret (1801) | 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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Prévot et al. (2014) | 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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Pugh & Scott (2002) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Puissauve, Cohen & Cucherat (2015) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Questel & Le Quellec (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Questel (2017) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Quintana (2010) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Razkin et al. (2016) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Riedel (1979) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Rossmässler et al. (1835) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossmässler (1839) | 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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Salvador et al. (2023) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 0 | 0% |
Saulcy (1852) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1817) | 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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Servain (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherpa et al. (2018) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Soyer (1958) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Stévanovich (1994) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Stévanovitch (1991) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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% |
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 | 0,12% | 1 | 0,15% | 1 | 0,13% |
von Proschwitz et al. (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wagner (2021) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
Waldén (1966) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |
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% |
Yokoyama (2013) | 1 | 0,03% | 1 | 0,12% | 1 | 0,15% | 1 | 0,13% |