Gastéropodes continentaux de Saint-Martin
126 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Hovestadt & Neckheim (2020) | 72 | 25% | 58 | 87,88% | 52 | 89,66% | 50 | 86,21% |
| Delannoye et al. (2015) | 62 | 21,53% | 39 | 59,09% | 37 | 63,79% | 35 | 60,34% |
| Coomans (1967) | 43 | 14,93% | 16 | 24,24% | 13 | 22,41% | 14 | 24,14% |
| Bouchet & Pointier (1998) | 38 | 13,19% | 21 | 31,82% | 21 | 36,21% | 19 | 32,76% |
| Lamy & Pointier (2018) | 19 | 6,6% | 17 | 25,76% | 17 | 29,31% | 17 | 29,31% |
| Massemin et al. (2009) | 18 | 6,25% | 12 | 18,18% | 12 | 20,69% | 12 | 20,69% |
| Bouchet et al. (1991) | 17 | 5,9% | 4 | 6,06% | 4 | 6,9% | 4 | 6,9% |
| Griffiths & Florens (2006) | 15 | 5,21% | 7 | 10,61% | 7 | 12,07% | 7 | 12,07% |
| Questel (2017) | 13 | 4,51% | 7 | 10,61% | 5 | 8,62% | 7 | 12,07% |
| Questel (2020) | 13 | 4,51% | 7 | 10,61% | 6 | 10,34% | 7 | 12,07% |
| Gargominy (2016-2021) | 12 | 4,17% | 11 | 16,67% | 11 | 18,97% | 11 | 18,97% |
| Pilsbry (1906-1907) | 12 | 4,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cowie (2000) | 10 | 3,47% | 6 | 9,09% | 6 | 10,34% | 5 | 8,62% |
| Jourdan et al. (2014) | 8 | 2,78% | 5 | 7,58% | 5 | 8,62% | 5 | 8,62% |
| Brook (2010) | 7 | 2,43% | 4 | 6,06% | 4 | 6,9% | 3 | 5,17% |
| Solem (1961) | 7 | 2,43% | 5 | 7,58% | 5 | 8,62% | 4 | 6,9% |
| Solem (1964) | 7 | 2,43% | 5 | 7,58% | 5 | 8,62% | 4 | 6,9% |
| Yokoyama (2013) | 7 | 2,43% | 4 | 6,06% | 4 | 6,9% | 4 | 6,9% |
| Drouët (1859) | 6 | 2,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN Comité français, OFB & MNHN (2021) | 6 | 2,08% | 5 | 7,58% | 5 | 8,62% | 5 | 8,62% |
| Mousson (1872) | 5 | 1,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abdou et al. (2004) | 4 | 1,39% | 3 | 4,55% | 3 | 5,17% | 3 | 5,17% |
| Gould (1852) | 4 | 1,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haynes (2001) | 4 | 1,39% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Hutton (1834) | 4 | 1,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mary (2017) | 4 | 1,39% | 4 | 6,06% | 4 | 6,9% | 4 | 6,9% |
| Mazé (1883) | 4 | 1,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Marquet (1990) | 4 | 1,39% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Questel & Le Quellec (2012) | 4 | 1,39% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Baker (1927) | 3 | 1,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breure (2016) | 3 | 1,04% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Cooke (1934) | 3 | 1,04% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Deshayes (1863) | 3 | 1,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1827) | 3 | 1,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grimpe & Hoffmann (1925) | 3 | 1,04% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Hausdorf (2023) | 3 | 1,04% | 3 | 4,55% | 3 | 5,17% | 3 | 5,17% |
| Jay et al. (2009) | 3 | 1,04% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Pointier (2001) | 3 | 1,04% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Potiez & Michaud (1835-1838) | 3 | 1,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1995) | 3 | 1,04% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Reeve (1849) | 3 | 1,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adamson (1935) | 2 | 0,69% | 2 | 3,03% | 2 | 3,45% | 1 | 1,72% |
| Baker (1923) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breure et al. (2020) | 2 | 0,69% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Bruguière (1789-1792) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clapp (1918) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clench (1964) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1867) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1805) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner et al. (2002) | 2 | 0,69% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Forcellini et al. (2012) | 2 | 0,69% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Fossati & Marquet (1998) | 2 | 0,69% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Gargominy et al. (2011) | 2 | 0,69% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Gerber (2018) | 2 | 0,69% | 2 | 3,03% | 2 | 3,45% | 2 | 3,45% |
| Gould (1843) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1846) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1878) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jousseaume (1889) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Küster & Pfeiffer (1845-1855) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1774) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1899) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1909-1910) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1916-1918) | 2 | 0,69% | 2 | 3,03% | 2 | 3,45% | 0 | 0% |
| Rang (1831) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1873-1874) | 2 | 0,69% | 1 | 1,52% | 1 | 1,72% | 0 | 0% |
| Swainson (1840) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (2003) | 2 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welter-schultes (2012) | 2 | 0,69% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Ancey (1892) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arruda et al. (2016) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1961) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Benoit (1881) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1856) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1822) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brown (1994) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charles (2016) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen & Kahn (2017) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Clavier et al. (2010) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Cockerell (1901) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke (1928) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Crosse (1874) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss et al. (2013) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Férussac (1821) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1868) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer-piette & Bedoucha (1964) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilla et al. (2014) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Gargominy & Fontaine (2014) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Garrett (1879) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1866) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gomes & Thome (2004) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Gould (1859) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guilding (1825) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2007) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Johnson (1964) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Lenoble (2021) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lydeard et al. (2016) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naggs (1989) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Orbigny (1835) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulay & Brown (2019) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Pfeiffer (1840) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1849) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1852) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1858) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Blanc (1985) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Pointier & Théron (2006) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Potiez & Michaud (1844) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2014) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Rang (1834) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salvador et al. (2023) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Say (1817) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simroth (1918) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Solem (1959) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1976) | 1 | 0,35% | 1 | 1,52% | 1 | 1,72% | 1 | 1,72% |
| Tillier (1980) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1922) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vernhout (1914) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidigal et al. (2018) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Watters (2014) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
