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)).
608 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 | 23,02% | 760 | 82,7% | 612 | 82,26% | 669 | 81,99% |
Falkner et al. (2002) | 818 | 21,15% | 613 | 66,7% | 496 | 66,67% | 533 | 65,32% |
Welter-schultes (2012) | 416 | 10,76% | 359 | 39,06% | 359 | 48,25% | 289 | 35,42% |
Gargominy (2011-2023) | 343 | 8,87% | 331 | 36,02% | 222 | 29,84% | 328 | 40,2% |
Kerney & Cameron (1999) | 303 | 7,84% | 265 | 28,84% | 259 | 34,81% | 202 | 24,75% |
Glöer (2022) | 124 | 3,21% | 115 | 12,51% | 99 | 13,31% | 115 | 14,09% |
Prié (2017) | 101 | 2,61% | 90 | 9,79% | 82 | 11,02% | 86 | 10,54% |
Müller (1774) | 57 | 1,47% | 5 | 0,54% | 5 | 0,67% | 5 | 0,61% |
Griffiths & Florens (2006) | 50 | 1,29% | 23 | 2,5% | 23 | 3,09% | 23 | 2,82% |
Gerber (2018) | 41 | 1,06% | 40 | 4,35% | 40 | 5,38% | 36 | 4,41% |
Caziot (1903) | 39 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1801) | 36 | 0,93% | 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 | 3,31% |
Lamand & Prié (2017) | 30 | 0,78% | 29 | 3,16% | 29 | 3,9% | 27 | 3,31% |
Draparnaud (1805) | 29 | 0,75% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
Boeters & Falkner (2003) | 27 | 0,7% | 26 | 2,83% | 26 | 3,49% | 26 | 3,19% |
Dupuy (1847-1852) | 26 | 0,67% | 0 | 0% | 0 | 0% | 0 | 0% |
Caziot (1910) | 24 | 0,62% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
Servain (1880) | 21 | 0,54% | 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 | 1,61% | 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 | 0,28% | 5 | 0,54% | 3 | 0,4% | 4 | 0,49% |
Macé (1860) | 11 | 0,28% | 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% |
Locard (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% |
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% | 4 | 0,44% | 2 | 0,27% | 4 | 0,49% |
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% |
Hutchinson et al. (2022) | 5 | 0,13% | 3 | 0,33% | 3 | 0,4% | 3 | 0,37% |
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% |
Bourguignat (1866) | 4 | 0,1% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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% |
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 (1867) | 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 (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% |
Coutagne (1883) | 3 | 0,08% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
Fagot (1879) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1879) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Falkner (2000) | 3 | 0,08% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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% | 2 | 0,22% | 2 | 0,27% | 1 | 0,12% |
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 (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 (1841) | 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% |
Ahmad & Gabrion (1975) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Bourguignat (1865) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
Bruguière (1789-1792) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabaret et al. (1986) | 2 | 0,05% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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% |
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% |
Gassies (1867) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Geniez & Bertrand (2001) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain (1911) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi & Bertrand (2009) | 2 | 0,05% | 2 | 0,22% | 0 | 0% | 2 | 0,25% |
Girardi & Bertrand (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 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% |
Høpner et al. (1971) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Lopes-lima et al. (2024) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
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% |
Magnin (2023) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
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% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
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% |
Saint-simon (1848) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Saito et al. (2024) | 2 | 0,05% | 2 | 0,22% | 2 | 0,27% | 2 | 0,25% |
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% |
Westerlund (1884‑1890) | 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% | 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% |
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% | 0 | 0% | 0 | 0% | 0 | 0% |
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. (1991) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Brumpt (1944) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Buttner (1953) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
Cadevall & Orozco (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
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% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
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% |
Eichhorst (2016) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Geist et al. (2022) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
Gérard (2004) | 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% |
Huet & Cadet (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Kerckhof et al. (2017) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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% |
Lampri et al. (2024) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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% |
Leger & Leger (1974) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Locard (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Locard (1884) | 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% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Nakamura et al. (2024) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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% |
N’gore-traore (1973) | 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% |
Pezy et al. (2022) | 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% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié et al. (2012) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
Prieto & Puente (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst et al. (2003) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
Proćków et al. (2013) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
Proćków et al. (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Proćków et al. (2018) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
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% | 1 | 0,12% |
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% |
Reise et al. (2020) | 1 | 0,03% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
Requien (1848) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
Reyniés (1844) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Ryelandt et al. (2024) | 1 | 0,03% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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% | 1 | 0,11% | 1 | 0,13% | 1 | 0,12% |
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 (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% |