Gastéropodes continentaux
Gastropoda continentaux (sens strict)
971 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) | 804 | 12,31% | 702 | 32,61% | 557 | 30,45% | 614 | 30,93% |
| Falkner et al. (2002) | 731 | 11,19% | 579 | 26,89% | 465 | 25,42% | 501 | 25,24% |
| Welter-schultes (2012) | 403 | 6,17% | 349 | 16,21% | 349 | 19,08% | 279 | 14,06% |
| Gargominy (2011-2023) | 341 | 5,22% | 329 | 15,28% | 220 | 12,03% | 326 | 16,42% |
| Kerney & Cameron (1999) | 301 | 4,61% | 263 | 12,22% | 257 | 14,05% | 200 | 10,08% |
| Solem (1976) | 260 | 3,98% | 256 | 11,89% | 212 | 11,59% | 242 | 12,19% |
| Garrett (1884) | 259 | 3,97% | 73 | 3,39% | 73 | 3,99% | 66 | 3,32% |
| Solem (1961) | 222 | 3,4% | 143 | 6,64% | 142 | 7,76% | 138 | 6,95% |
| Griffiths & Florens (2006) | 208 | 3,18% | 151 | 7,01% | 151 | 8,26% | 151 | 7,61% |
| Delannoye et al. (2015) | 178 | 2,73% | 118 | 5,48% | 112 | 6,12% | 116 | 5,84% |
| Cooke & Kondo (1961) | 167 | 2,56% | 153 | 7,11% | 91 | 4,98% | 135 | 6,8% |
| Neubert et al. (2009) | 159 | 2,43% | 25 | 1,16% | 10 | 0,55% | 21 | 1,06% |
| Gerlach (2016) | 141 | 2,16% | 104 | 4,83% | 79 | 4,32% | 95 | 4,79% |
| Glöer (2022) | 124 | 1,9% | 115 | 5,34% | 99 | 5,41% | 115 | 5,79% |
| Baker (1938) | 117 | 1,79% | 111 | 5,16% | 86 | 4,7% | 98 | 4,94% |
| Pawlowska-Banasiak (2008) | 93 | 1,42% | 88 | 4,09% | 88 | 4,81% | 88 | 4,43% |
| Massemin et al. (2009) | 87 | 1,33% | 61 | 2,83% | 60 | 3,28% | 61 | 3,07% |
| Abdou et al. (2004) | 81 | 1,24% | 63 | 2,93% | 61 | 3,34% | 63 | 3,17% |
| Baker (1940) | 77 | 1,18% | 74 | 3,44% | 56 | 3,06% | 66 | 3,32% |
| Hovestadt & Neckheim (2020) | 76 | 1,16% | 62 | 2,88% | 56 | 3,06% | 57 | 2,87% |
| Bouchet & Pointier (1998) | 68 | 1,04% | 43 | 2% | 43 | 2,35% | 40 | 2,02% |
| Gargominy (2016-2021) | 65 | 1% | 57 | 2,65% | 55 | 3,01% | 57 | 2,87% |
| Sartori et al. (2014) | 62 | 0,95% | 62 | 2,88% | 62 | 3,39% | 62 | 3,12% |
| Coote & Loeve (2003) | 60 | 0,92% | 40 | 1,86% | 40 | 2,19% | 32 | 1,61% |
| Pilsbry (1909-1910) | 59 | 0,9% | 20 | 0,93% | 18 | 0,98% | 17 | 0,86% |
| Haase & Bouchet (1998) | 56 | 0,86% | 51 | 2,37% | 51 | 2,79% | 51 | 2,57% |
| Müller (1774) | 56 | 0,86% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Gould (1852) | 52 | 0,8% | 12 | 0,56% | 12 | 0,66% | 12 | 0,6% |
| Lamy & Pointier (2018) | 52 | 0,8% | 42 | 1,95% | 42 | 2,3% | 42 | 2,12% |
| Wagner (1907-1911) | 50 | 0,77% | 11 | 0,51% | 11 | 0,6% | 11 | 0,55% |
| Garrett (1887) | 49 | 0,75% | 8 | 0,37% | 8 | 0,44% | 8 | 0,4% |
| Abdou & Bouchet (2000) | 47 | 0,72% | 47 | 2,18% | 45 | 2,46% | 46 | 2,32% |
| Wagner (1905) | 45 | 0,69% | 8 | 0,37% | 8 | 0,44% | 8 | 0,4% |
| Coomans (1967) | 44 | 0,67% | 16 | 0,74% | 13 | 0,71% | 13 | 0,65% |
| Gerber (2018) | 41 | 0,63% | 40 | 1,86% | 40 | 2,19% | 36 | 1,81% |
| Kondo (1962) | 41 | 0,63% | 40 | 1,86% | 17 | 0,93% | 38 | 1,91% |
| Caziot (1903) | 39 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richling (2009) | 37 | 0,57% | 19 | 0,88% | 19 | 1,04% | 19 | 0,96% |
| Solem (1964) | 36 | 0,55% | 23 | 1,07% | 23 | 1,26% | 22 | 1,11% |
| Draparnaud (1801) | 35 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy & Fontaine (2014) | 34 | 0,52% | 34 | 1,58% | 31 | 1,69% | 33 | 1,66% |
| Gargominy & Ripken (2006) | 34 | 0,52% | 28 | 1,3% | 13 | 0,71% | 27 | 1,36% |
| Cowie (2000) | 33 | 0,51% | 24 | 1,11% | 24 | 1,31% | 23 | 1,16% |
| Richling & Bouchet (2013) | 33 | 0,51% | 32 | 1,49% | 32 | 1,75% | 31 | 1,56% |
| Paladilhe (1869) | 31 | 0,47% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Pease (1865) | 30 | 0,46% | 6 | 0,28% | 6 | 0,33% | 4 | 0,2% |
| Pease (1869) | 30 | 0,46% | 20 | 0,93% | 20 | 1,09% | 20 | 1,01% |
| Draparnaud (1805) | 29 | 0,44% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Boeters & Falkner (2003) | 27 | 0,41% | 26 | 1,21% | 26 | 1,42% | 26 | 1,31% |
| Partula. The species inhabiting Tahiti. Carnegie Institute of Washington Publication, 228: 1-313.">Crampton (1917) | 27 | 0,41% | 7 | 0,33% | 5 | 0,27% | 6 | 0,3% |
| Jourdan et al. (2014) | 27 | 0,41% | 17 | 0,79% | 17 | 0,93% | 17 | 0,86% |
| Pease (1871) | 27 | 0,41% | 5 | 0,23% | 5 | 0,27% | 4 | 0,2% |
| Dupuy (1847-1852) | 26 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brook (2010) | 25 | 0,38% | 17 | 0,79% | 17 | 0,93% | 14 | 0,71% |
| Pilsbry (1906-1907) | 25 | 0,38% | 4 | 0,19% | 4 | 0,22% | 2 | 0,1% |
| Caziot (1910) | 24 | 0,37% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Drouët (1859) | 24 | 0,37% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Grimpe & Hoffmann (1925) | 24 | 0,37% | 15 | 0,7% | 15 | 0,82% | 15 | 0,76% |
| Pease (1867) | 24 | 0,37% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Sartori et al. (2013) | 24 | 0,37% | 24 | 1,11% | 24 | 1,31% | 24 | 1,21% |
| Tryon (1886) | 24 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1994) | 23 | 0,35% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Pfeiffer (1852-1860) | 23 | 0,35% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Reeve (1873-1874) | 23 | 0,35% | 5 | 0,23% | 5 | 0,27% | 4 | 0,2% |
| Pilsbry & Cooke (1915-1916) | 22 | 0,34% | 7 | 0,33% | 7 | 0,38% | 7 | 0,35% |
| Reeve (1849-1851) | 22 | 0,34% | 10 | 0,46% | 10 | 0,55% | 6 | 0,3% |
| Cooke (1934) | 21 | 0,32% | 7 | 0,33% | 7 | 0,38% | 7 | 0,35% |
| Deshayes (1863) | 21 | 0,32% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Garrett (1879) | 21 | 0,32% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Crampton & Cooke (1953) | 20 | 0,31% | 10 | 0,46% | 10 | 0,55% | 10 | 0,5% |
| Crampton (1956) | 20 | 0,31% | 14 | 0,65% | 14 | 0,77% | 14 | 0,71% |
| Germain (1931) | 20 | 0,31% | 5 | 0,23% | 5 | 0,27% | 4 | 0,2% |
| Monterosato (1892) | 20 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Servain (1880) | 20 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters et al. (1989) | 19 | 0,29% | 13 | 0,6% | 13 | 0,71% | 10 | 0,5% |
| Bouchet et al. (1991) | 19 | 0,29% | 7 | 0,33% | 7 | 0,38% | 7 | 0,35% |
| Crosse (1874) | 19 | 0,29% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Mary (2017) | 19 | 0,29% | 12 | 0,56% | 12 | 0,66% | 12 | 0,6% |
| Pointier & Marquet (1990) | 19 | 0,29% | 8 | 0,37% | 8 | 0,44% | 8 | 0,4% |
| Crosse (1870) | 18 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haase et al. (2005) | 18 | 0,28% | 16 | 0,74% | 16 | 0,87% | 16 | 0,81% |
| Lee et al. (2009) | 18 | 0,28% | 11 | 0,51% | 10 | 0,55% | 9 | 0,45% |
| Linnaeus (1758) | 18 | 0,28% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pease (1866) | 18 | 0,28% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Haynes (2001) | 17 | 0,26% | 12 | 0,56% | 12 | 0,66% | 12 | 0,6% |
| Moquin-Tandon (1855-1856) | 17 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muratov et al. (2005) | 17 | 0,26% | 17 | 0,79% | 17 | 0,93% | 17 | 0,86% |
| Pfeiffer (1850-1853) | 17 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 17 | 0,26% | 8 | 0,37% | 8 | 0,44% | 8 | 0,4% |
| Crosse (1868) | 16 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2013) | 16 | 0,24% | 10 | 0,46% | 10 | 0,55% | 10 | 0,5% |
| Pease (1868) | 16 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1918-1920) | 16 | 0,24% | 13 | 0,6% | 13 | 0,71% | 13 | 0,65% |
| Preece (1995) | 16 | 0,24% | 10 | 0,46% | 8 | 0,44% | 10 | 0,5% |
| Solem (1983) | 16 | 0,24% | 16 | 0,74% | 15 | 0,82% | 15 | 0,76% |
| Tillier (1981) | 16 | 0,24% | 16 | 0,74% | 16 | 0,87% | 16 | 0,81% |
| Questel (2020) | 15 | 0,23% | 9 | 0,42% | 9 | 0,49% | 9 | 0,45% |
| Risso (1826) | 15 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN Comité français, OFB & MNHN (2021) | 15 | 0,23% | 12 | 0,56% | 12 | 0,66% | 12 | 0,6% |
| Baker (1941) | 14 | 0,21% | 13 | 0,6% | 13 | 0,71% | 13 | 0,65% |
| Boeters & Falkner (2008) | 14 | 0,21% | 12 | 0,56% | 12 | 0,66% | 12 | 0,6% |
| Crosse (1870) | 14 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kondo (1968) | 14 | 0,21% | 9 | 0,42% | 9 | 0,49% | 9 | 0,45% |
| Pease (1868) | 14 | 0,21% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Pollonera (1885) | 14 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2017) | 14 | 0,21% | 6 | 0,28% | 6 | 0,33% | 6 | 0,3% |
| Gould (1846) | 13 | 0,2% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Hagenmüller (1888) | 13 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1851-1854) | 13 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet & Abdou (2003) | 12 | 0,18% | 7 | 0,33% | 7 | 0,38% | 7 | 0,35% |
| Crosse (1855) | 12 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcellini et al. (2012) | 12 | 0,18% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Gargominy (2008) | 12 | 0,18% | 12 | 0,56% | 12 | 0,66% | 12 | 0,6% |
| Hausdorf (2023) | 12 | 0,18% | 12 | 0,56% | 12 | 0,66% | 12 | 0,6% |
| Hombron & Jacquinot (1842-1853) | 12 | 0,18% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Nicolas (1891) | 12 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rousseau (1854) | 12 | 0,18% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Sowerby (1842) | 12 | 0,18% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Zimmermann et al. (2009) | 12 | 0,18% | 12 | 0,56% | 12 | 0,66% | 12 | 0,6% |
| Anton (1838) | 11 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boettger (1880) | 11 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1865) | 11 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger (1993) | 11 | 0,17% | 5 | 0,23% | 3 | 0,16% | 4 | 0,2% |
| Letacq (1924) | 11 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moutier & Moutier (1920) | 11 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Burch (2007) | 10 | 0,15% | 10 | 0,46% | 10 | 0,55% | 8 | 0,4% |
| Cooke & Clench (1943) | 10 | 0,15% | 10 | 0,46% | 6 | 0,33% | 8 | 0,4% |
| Gassies (1874) | 10 | 0,15% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Groenenberg et al. (2016) | 10 | 0,15% | 9 | 0,42% | 6 | 0,33% | 7 | 0,35% |
| Haase & Zielske (2015) | 10 | 0,15% | 10 | 0,46% | 10 | 0,55% | 10 | 0,5% |
| Locard (1893) | 10 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Michaud (1831) | 10 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1840-1850) | 10 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1998) | 10 | 0,15% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Reeve (1842) | 10 | 0,15% | 5 | 0,23% | 5 | 0,27% | 3 | 0,15% |
| Abdou et al. (2008) | 9 | 0,14% | 9 | 0,42% | 9 | 0,49% | 9 | 0,45% |
| Boeters (2019) | 9 | 0,14% | 6 | 0,28% | 2 | 0,11% | 5 | 0,25% |
| Bourguignat (1864) | 9 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crampton (1932) | 9 | 0,14% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Férussac (1821) | 9 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Franc (1956) | 9 | 0,14% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Gargominy & Muratov (2012) | 9 | 0,14% | 9 | 0,42% | 9 | 0,49% | 9 | 0,45% |
| Gassies (1863) | 9 | 0,14% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Jay et al. (2009) | 9 | 0,14% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Lesson (1830-1831) | 9 | 0,14% | 5 | 0,23% | 5 | 0,27% | 3 | 0,15% |
| Lessona (1880) | 9 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mordan & Tillier (1986) | 9 | 0,14% | 9 | 0,42% | 9 | 0,49% | 9 | 0,45% |
| Murray & Clarke (1980) | 9 | 0,14% | 6 | 0,28% | 6 | 0,33% | 4 | 0,2% |
| Pfeiffer (1852) | 9 | 0,14% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Tillier & Mordan (1995) | 9 | 0,14% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Tillier (1980) | 9 | 0,14% | 2 | 0,09% | 1 | 0,05% | 2 | 0,1% |
| Bichain et al. (2007) | 8 | 0,12% | 2 | 0,09% | 2 | 0,11% | 1 | 0,05% |
| Boeters (2000) | 8 | 0,12% | 6 | 0,28% | 4 | 0,22% | 6 | 0,3% |
| Caziot (1908) | 8 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen et al. (2018) | 8 | 0,12% | 8 | 0,37% | 8 | 0,44% | 8 | 0,4% |
| Crampton (1924) | 8 | 0,12% | 4 | 0,19% | 4 | 0,22% | 2 | 0,1% |
| Crosse (1868) | 8 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| de Winter (1986) | 8 | 0,12% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Fischer-piette & Vukadinovic (1970) | 8 | 0,12% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Gassies (1871) | 8 | 0,12% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi (2009) | 8 | 0,12% | 6 | 0,28% | 0 | 0% | 6 | 0,3% |
| Gould (1847) | 8 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson et al. (2000) | 8 | 0,12% | 7 | 0,33% | 7 | 0,38% | 6 | 0,3% |
| Jourdan (2020) | 8 | 0,12% | 8 | 0,37% | 8 | 0,44% | 8 | 0,4% |
| Pilsbry (1920-1921) | 8 | 0,12% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Preston (1907) | 8 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (2000) | 7 | 0,11% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Bourguignat (1869) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1874) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupuy (1849) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lessona & Pollonera (1882) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1882) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1869) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1871) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neubert & Gosteli (2003) | 7 | 0,11% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pease (1869) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1858) | 7 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1916-1918) | 7 | 0,11% | 6 | 0,28% | 6 | 0,33% | 4 | 0,2% |
| Yokoyama (2013) | 7 | 0,11% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Zallot et al. (2014) | 7 | 0,11% | 7 | 0,33% | 7 | 0,38% | 6 | 0,3% |
| Beck (1837) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (1985) | 6 | 0,09% | 3 | 0,14% | 3 | 0,16% | 2 | 0,1% |
| Bernasconi (1989) | 6 | 0,09% | 4 | 0,19% | 2 | 0,11% | 4 | 0,2% |
| Boeters & Falkner (2009) | 6 | 0,09% | 6 | 0,28% | 6 | 0,33% | 6 | 0,3% |
| Boeters (1981) | 6 | 0,09% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Boeters (2022) | 6 | 0,09% | 6 | 0,28% | 6 | 0,33% | 6 | 0,3% |
| Bouchet & Abdou (2001) | 6 | 0,09% | 6 | 0,28% | 6 | 0,33% | 6 | 0,3% |
| Callot-Girardi (2015) | 6 | 0,09% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Clerx & Gittenberger (1977) | 6 | 0,09% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Cooke & Clench (1945) | 6 | 0,09% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Dautzenberg (1923) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| de Cristofori & Jan (1832) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer-piette & Bedoucha (1964) | 6 | 0,09% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Folin & Bérillon (1877) | 6 | 0,09% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Fossati & Marquet (1998) | 6 | 0,09% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Girardi (2009) | 6 | 0,09% | 6 | 0,28% | 6 | 0,33% | 6 | 0,3% |
| Gray (1839) | 6 | 0,09% | 2 | 0,09% | 2 | 0,11% | 0 | 0% |
| Hartman (1890) | 6 | 0,09% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Hyman & Ponder (2010) | 6 | 0,09% | 6 | 0,28% | 6 | 0,33% | 6 | 0,3% |
| Kondo (1944) | 6 | 0,09% | 6 | 0,28% | 6 | 0,33% | 4 | 0,2% |
| Macé (1860) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1883) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Michaud (1829) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montrouzier (1859) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1845) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1869) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1872) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1871) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1843-1850) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1857) | 6 | 0,09% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pfeiffer (1872) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (2001) | 6 | 0,09% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Pollonera (1905) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié et al. (2024) | 6 | 0,09% | 6 | 0,28% | 6 | 0,33% | 6 | 0,3% |
| Récluz (1850) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souverbie (1860) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abdou et al. (2019) | 5 | 0,08% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Adamson (1935) | 5 | 0,08% | 4 | 0,19% | 4 | 0,22% | 3 | 0,15% |
| Boeters & Bertrand (2001) | 5 | 0,08% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Boeters & Falkner (2017) | 5 | 0,08% | 4 | 0,19% | 2 | 0,11% | 4 | 0,2% |
| Boeters (2000) | 5 | 0,08% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Bourguignat (1861-1862) | 5 | 0,08% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Bourguignat (1862) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1868) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1877) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruguière (1789-1792) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1894) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1880) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haase (2000) | 5 | 0,08% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Horsáková et al. (2022) | 5 | 0,08% | 5 | 0,23% | 5 | 0,27% | 5 | 0,25% |
| Hutchinson et al. (2022) | 5 | 0,08% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Jourdan & Mille (2006) | 5 | 0,08% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Locard (1883) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1881) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1861) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1855) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1876) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1927-1935) | 5 | 0,08% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Potiez & Michaud (1835-1838) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 5 | 0,08% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Reise et al. (2011) | 5 | 0,08% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Shuttleworth (1843) | 5 | 0,08% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Solem (1959) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tröndlé & Boutet (2009) | 5 | 0,08% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Zielske & Haase (2015) | 5 | 0,08% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Abdou (2021) | 4 | 0,06% | 4 | 0,19% | 2 | 0,11% | 3 | 0,15% |
| Aksenova et al. (2018) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Alder (1830) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benoit (1857) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters & Falkner (2003) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (2008) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Bourguignat (1860) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1866) | 4 | 0,06% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Callot-Girardi (2015) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Callot-Girardi (2015) | 4 | 0,06% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Caziot (1909) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clench & Turner (1948) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Coutagne (1882) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse & Debeaux (1869) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1867) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1872) | 4 | 0,06% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| De Stefani (1883) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1830-1832) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss et al. (2013) | 4 | 0,06% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Dutailly (1867) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eichhorst (2016) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Férussac (1822) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1885) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1874) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1857) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi et al. (2002) | 4 | 0,06% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi (2009) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Girardi (2009) | 4 | 0,06% | 4 | 0,19% | 0 | 0% | 4 | 0,2% |
| Girardi (2009) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Gittenberger (2002) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1791) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gómez et al. (2023) | 4 | 0,06% | 2 | 0,09% | 0 | 0% | 2 | 0,1% |
| Guppy (1878) | 4 | 0,06% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Hartman (1885) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1886) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2007) | 4 | 0,06% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Haynes (2001) | 4 | 0,06% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Horsáková et al. (2020) | 4 | 0,06% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Hubendick (1952) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutton (1834) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1822) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1877) | 4 | 0,06% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Martínez-Ortí & Borredà (2012) | 4 | 0,06% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Morelet (1853) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1881) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1867) | 4 | 0,06% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Paladilhe (1874) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 4 | 0,06% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pfeiffer (1850) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1851) | 4 | 0,06% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Pfeiffer (1854-1860) | 4 | 0,06% | 2 | 0,09% | 2 | 0,11% | 0 | 0% |
| Pfeiffer (1855) | 4 | 0,06% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Pilsbry (1901-1902) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pollonera (1889) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1831) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1841) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1854) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vallot (1801) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zallot et al. (2024) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 2 | 0,1% |
| Zilch (1967) | 4 | 0,06% | 4 | 0,19% | 4 | 0,22% | 4 | 0,2% |
| Altena et al. (1975) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Baker (1927) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bichain et al. (2021) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 2 | 0,1% |
| Boeters (1969) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (2009) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Boettger (1949) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1864) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1864) | 3 | 0,05% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Bourguignat (1876) | 3 | 0,05% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Breure (2016) | 3 | 0,05% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Broderip (1832) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Callot-Girardi (2017) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Callot-girardi (2017) | 3 | 0,05% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Caziot (1903) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1905) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charles (2016) | 3 | 0,05% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Coutagne (1883) | 3 | 0,05% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Crosse (1870) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1871) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1874) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupouy (1966) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Fagot (1879) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1879) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner (2000) | 3 | 0,05% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Férussac (1827) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1858) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1866) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Germain (1931) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger (1973) | 3 | 0,05% | 1 | 0,05% | 0 | 0% | 1 | 0,05% |
| Gray (1824) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Hatteland et al. (2015) | 3 | 0,05% | 2 | 0,09% | 2 | 0,11% | 1 | 0,05% |
| IUCN (2012) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jeffreys (1830) | 3 | 0,05% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Jousseaume (1872) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Kondo (1973) | 3 | 0,05% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Locard (1894) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 3 | 0,05% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Mabille (1880) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Manganelli et al. (2019) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Montagu (1803) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moquin-Tandon (1855-1856) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1869) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muratov & Gargominy (2011) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nevill (1879) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1866) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1876) | 3 | 0,05% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pease (1861) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1841) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1848) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 3 | 0,05% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pfeiffer (1868) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry & Cooke (1933) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Pilsbry (1899) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rambur (1869) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1852) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1849) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reygrobellet (1963) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ripken & Bouchet (1998) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 2 | 0,1% |
| Rowson & Tattersfield (2013) | 3 | 0,05% | 3 | 0,14% | 1 | 0,05% | 2 | 0,1% |
| Schallenberg et al. (2022) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Smith (1902) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souverbie (1859) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1842-1887) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1976) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 3 | 0,15% |
| Trewick et al. (2009) | 3 | 0,05% | 3 | 0,14% | 3 | 0,16% | 1 | 0,05% |
| Vandel (1922) | 3 | 0,05% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Vernhout (1914) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zilch (1947) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adamcová et al. (2024) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Ahmad & Gabrion (1975) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Altena (1974) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ancey (1889) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ancey (1889) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Badie (1977) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baird (1850) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Baker (1923) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1926) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartsch (1942) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Benoit (1881) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bérenguier (1883) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bérenguier (1900-1902) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bernasconi (1968) | 2 | 0,03% | 2 | 0,09% | 0 | 0% | 2 | 0,1% |
| Bernasconi (1985) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berthier (1884) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertrand (2001) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Bertrand (2004) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertrand (2004) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Bertrand (2015) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertrand (2017) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bertrand (2022) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Bichain & Bertrand (2022) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Binney (1841) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters & Gittenberger (1980) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Boeters et al. (2015) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (1983) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (1999) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Boettger (1891) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boettger (1916) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Boubée (1833-1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boubée (1836) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet et al. (1997) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bourguignat (1856) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1856) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1865) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Breure et al. (2020) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Antidrymaeus L. Germain, 1907 (Mollusca: Gastropoda: Bulimulidae), with notes on miscellaneous species of Drymaeus Albers, 1850 and Mesembrinus Albers, 1850. Archiv für Molluskenkunde, 153(2): 135-162.">Breure et al. (2024) | 2 | 0,03% | 2 | 0,09% | 0 | 0% | 2 | 0,1% |
| Breure (1976) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabaret et al. (1986) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Callot-Girardi & Boeters (2015) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Callot-Girardi & Boeters (2015) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Callot-Girardi & Boeters (2017) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Callot-girardi et al. (2017) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Callot-Girardi (2012) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Callot-Girardi (2013) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Callot-Girardi (2015) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Callot-Girardi (2015) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Callot-Girardi (2017) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Caziot (1911) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Charles (2014) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Christensen (2016) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Clapp (1918) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clench (1964) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Crampton (1930) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Cooke & Kondo (1943) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Crosse & Marie (1867) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Debeaux (1867) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delicado et al. (2015) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Delicado et al. (2024) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Des Moulins (1827) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1831) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dézallier et al. (1780) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dohrn (1859) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Fagot (1881) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Fagot (1882) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1884) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1884) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1885) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1888) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fert� et al. (2004) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Férussac & Deshayes (1820-51) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1868) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcart (1946) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frauenfeld (1863) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy & Fontaine (2015) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Gargominy et al. (2008) | 2 | 0,03% | 2 | 0,09% | 1 | 0,05% | 1 | 0,05% |
| Garrett (1872) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1881) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1867) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1867) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1874) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geniez & Bertrand (2001) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Germain (1911) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi & Bertrand (2009) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi & Bertrand (2009) | 2 | 0,03% | 2 | 0,09% | 0 | 0% | 2 | 0,1% |
| Girardi (2001) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2002) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2004) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2004) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi (2004) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi (2009) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi (2009) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi (2009) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi (2009) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Girardi (2009) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Gittenberger & de Winter (1985) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger et al. (2016) | 2 | 0,03% | 2 | 0,09% | 1 | 0,05% | 1 | 0,05% |
| Giusti & Manganelli (1987) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Giusti & Manganelli (1989) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Giusti (1976) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gomes & Thome (2004) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Gould (1843) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulding et al. (2023) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gras (1840) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Griffiths & Florens (2004) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Gude (1900) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1866) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Hartmann (1821) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley (1898) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hertlein & Allison (1968) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Higgins (1872) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Holyoak & Holyoak (2012) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Horsák et al. (2022) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Hupé (1857) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jousseaume (1889) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kirch (1973) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Klemm (1939) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kobelt (1875-1880) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Kondo (1981) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Küster & Pfeiffer (1845-1855) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lee et al. (2007) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Lemaire & Gerriet (2014) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Liardet (1876) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lightfoot (1786) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorencová et al. (2021) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1875) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Magnin et al. (2012) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Magnin (2023) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Marie (1870) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martens & Langkavel (1871) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martens (1881) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martyn (1845) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mayer (1902) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mörch (1850) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moricand (1837) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1865) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1870) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neiber & Glaubrecht (2018) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Nekola et al. (2015) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neubert & Gosteli (2005) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nordsieck (2003) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 0 | 0% |
| Odhner (1921) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Pain (1958) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1870) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulucci (1882) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Payraudeau (1826) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Petit de la Saussaye (1840) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Petit de la Saussaye (1843) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1828) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1842) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1845) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1847) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Pfeiffer (1854) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Pieńkowska et al. (2018) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Pieńkowska et al. (2022) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pilsbry (1889) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1889-1890) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pilsbry (1922-1926) | 2 | 0,03% | 2 | 0,09% | 0 | 0% | 2 | 0,1% |
| Pini (1883) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pintér (1983) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Pointier et al. (1977) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Poliński (1929) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pollonera (1887) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potiez & Michaud (1844) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prie & Bichain (2009) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Cucherat (2021) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pugh & Scott (2002) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Rambur (1868) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ravalo et al. (2023) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Récluz (1842) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1852) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Reeve (1843) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1846-1860) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Reynès (1870) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richling et al. (2016) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richling (2017) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Robinson et al. (2009) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Rossmässler & Kobelt (1906) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1838) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1880) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rowson et al. (2014) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saint-simon (1848) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saito et al. (2024) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Salvador et al. (2023) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 1 | 0,05% |
| Say (1817) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sayn (1889) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schikov (2017) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Schröder et al. (2024) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Shuttleworth (1852) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Solem (1960) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Souverbie (1863) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1825) | 2 | 0,03% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Sowerby (1843) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1843) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1840) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (2003) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tryon (1866) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vial (1979) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1876) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1884‑1890) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wetherby (1879) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiktor (1998) | 2 | 0,03% | 2 | 0,09% | 2 | 0,11% | 2 | 0,1% |
| Abbott (1958) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Adams (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adams (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Altena Regteren Van (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Altena (1961) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Altena (1973) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Ancey (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Andreae (1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anistratenko et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anistratenko et al. (2019) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Anonyme. (2004) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Arruda et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Audibert & Paillet (2014) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Aureglia et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Badie et al. (1992) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Baker (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1961) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bank et al. (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bank (1978) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bank (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barré et al. (1982) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Beltramino et al. (2018) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Benke et al. (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1850) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1854) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bérenguier (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (1988) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bernasconi (1994) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernasconi (2002) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bertrand (2004) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bertrand (2017) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Betta (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bichain & Ryelandt (2023) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bland & Binney (1872) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters & Falkner (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeters (1967) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Boettger (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bofill & Poch (1897) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bößneck (2000) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bouaziz-Yahiatene et al. (2017) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bouchet et al. (1998) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bourguignat (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1864) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bourguignat (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1870) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1870) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1822) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breton (2014) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Breure & Ablett (2014) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Breure & Ablett (2015) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Breure et al. (2018) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Breure (2011) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Broderip (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Broderip (1832) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Brown (1994) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugel (2016) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bruguière et al. (1789-1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brumpt (1944) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buttner (1953) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Cadevall & Orozco (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Callot-Girardi (2015) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Camus et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1910) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1916) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charrier et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen & Kahn (2017) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Christensen & Kirch (1986) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Christensen (2013) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Chueca et al. (2017) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Clanzig (1995) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clarke et al. (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clavier et al. (2010) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Clessin (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clessin (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clessin (1911) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cockerell (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Neal (1928) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Cooke (1928) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Correa et al. (2010) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Cowie et al. (2009) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Cowie (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse & Fischer (1870) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1872) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Crosse (1876) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cucherat & Demuynck (2004) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Cuénot & Mercier (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cunningham & Daszak (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dall (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dance et al. (1986) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| D'Ávila et al. (2020) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| De Winter (1990) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Delannoye & Massemin (2010) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Dell (1954) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Des Moulins (1827) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewarumez et al. (2011) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Dillwyn (1817) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Doby et al. (1966) | 1 | 0,02% | 1 | 0,05% | 0 | 0% | 1 | 0,05% |
| Dommergues & Gargominy (2024) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Drouët (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dunker (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| European Nucleotide Archive (2019) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Fagot (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fagot (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner (2008) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Férussac (1807) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fiorentino et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1925) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Fischer-piette et al. (1993) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Fitzinger (1833) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilla et al. (2014) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Frenot et al. (2005) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gamiette et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy & Meyer (2012) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gargominy et al. (2020) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gargominy et al. (2022) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gargominy et al. (2025) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gargominy (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy (2007) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Garrett & Smith (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geist et al. (2022) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gérard (2004) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Germain (1921) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Germain (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger & Ripken (1993) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger et al. (2006) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gittenberger (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gittenberger (1978) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Gittenberger (1978) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Gittenberger (2004) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gittenberger (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giusti et al. (2011) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Giusti (1970) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Glöer & Zettler (2009) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Glöer (2019) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gould (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Gourdon (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1825) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gregorio (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grossu & Lupu (1965) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Guilding (1824) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guilding (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guiller & Madec (2010) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Haas (1938) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1880) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Hartmann (1840-1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartmann (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf & Bermúdez (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf & Solvery (2021) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Hausdorf (2006) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Hausdorf (2022) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Held (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hobbs et al. (2021) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Holyoak & Holyoak (2012) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Holyoak & Holyoak (2018) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Holyoak et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holyoak et al. (2020) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Huet & Cadet (2024) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huet (2023) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Hullé et al. (2018) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Jay (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jesse et al. (2011) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Johnson et al. (1986) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Johnson (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourde et al. (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Julvez et al. (1990) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Kaiser (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kennard & Woodward (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Klemm (1943) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kneubühler et al. (2021) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Kokshoorn & Gittenberger (2010) | 1 | 0,02% | 1 | 0,05% | 0 | 0% | 1 | 0,05% |
| Kondo & Burch (1983) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kondo & Burch (1989) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Kosicka et al. (2022) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Kruger et al. (2019) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Küster (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1816) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lampri et al. (2024) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Lecaplain (2013) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Leger & Leger (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lenoble et al. (2018) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Lenoble et al. (2018) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Lenoble (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1892) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Locard (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Locard (1903) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Lounnas et al. (2017) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Lovenburg (2009) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Lowe (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lydeard et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maassen (1987) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Mabille (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1871) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| MacMillan (1946) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Madec & Bellido (2007) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Magnin et al. (2008) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Manganelli (2018) | 1 | 0,02% | 1 | 0,05% | 0 | 0% | 1 | 0,05% |
| Martínez-Ortí (2021) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Massot (1872) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menke & Pfeiffer (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menke (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mienis (2008) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Miller et al. (2022) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Miller et al. (2023) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Millet (1813) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mittre (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Möllendorf (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Möllendorf (1897) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Monod & Dollfus (1932) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montfort (1810) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moquin-Tandon (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moquin-Tandon (1850) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mörch (1864) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Morelet (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naggs (1989) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Naggs (1994) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Naudon et al. (2015) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Neiber & Hausdorf (2015) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Neiber et al. (2017) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Neiber et al. (2021) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| N’gore-traore (1973) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Nitz et al. (2010) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Odhner (1950) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Orbigny (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oueslati & Duvivier (2016) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Paget (1854) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paladilhe (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paris (1918) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pascal (1873) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Patterson (1989) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Paulay & Brown (2019) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pease (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer & Zelebor (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1848) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pfeiffer (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1854) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pfeiffer (1854) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1858) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfenninger et al. (2003) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Philippi (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pieńkowska et al. (2024) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pilsbry & Hirase (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pini (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pini (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Blanc (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pointier & Théron (2006) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pointier et al. (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier et al. (2007) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pointier (1976) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (1996) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Pointier (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poiret (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Porro (1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pouchard & Bichain (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prévot et al. (2013) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Prévot et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prieto & Puente (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst et al. (2003) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Proćków et al. (2013) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Proćków et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proćków et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Puissauve, Cohen & Cucherat (2015) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Questel (2014) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Questel (2023) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Quintana (2010) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Rang (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Razkin et al. (2016) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Razoumowsky (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Navicelle. Revue Zoologique, par la Société Cuvierienne, 4: 369-382.">Récluz (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1856) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reischütz (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reise et al. (2020) | 1 | 0,02% | 1 | 0,05% | 0 | 0% | 1 | 0,05% |
| Requien (1848) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Reyniés (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard et al. (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Riedel (1979) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Rocha & D'ávila (2019) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Roosen & Breure (2024) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Rossmässler et al. (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ryelandt et al. (2024) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Saito et al. (2023) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Salles et al. (2018) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Salvador et al. (2020) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Salvador et al. (2023) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 0 | 0% |
| Saulcy (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scacchi (1833) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schröter (1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sei et al. (2017) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Histoire malacologique du lac Balaton en Hongrie. Poissy (S. Lejay). 125 pp.">Servain (1882) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Servain (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherpa et al. (2018) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Shuttleworth (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simroth (1918) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Singh et al. (2022) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Smith (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Solem (1968) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Sowerby (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1833) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Soyer (1958) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Stabile (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stévanovich (1994) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Stévanovitch (1991) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Strobel (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Strøm (1765) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson ([1820-1821]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Talenti et al. (2020) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Bullettino Malacologico Italiano, 2: 33-36, 65-73, 113-123.">Tiberi (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tillier (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turton & Gray (1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van & Bruggen (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vareille-Morel (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vermeulen & Raven (1998) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Vernhout (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vernhout (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidigal et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villa (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vinarski (2017) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| von Proschwitz et al. (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wagner (2021) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Waldén (1966) | 1 | 0,02% | 1 | 0,05% | 1 | 0,05% | 1 | 0,05% |
| Wallenberg (1858) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Watters (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westerlund (1889) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
