Gastéropodes continentaux de Martinique
170 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Delannoye et al. (2015) | 173 | 47,53% | 118 | 140,48% | 112 | 138,27% | 118 | 143,9% |
| Hovestadt & Neckheim (2020) | 43 | 11,81% | 34 | 40,48% | 33 | 40,74% | 34 | 41,46% |
| Lamy & Pointier (2018) | 41 | 11,26% | 34 | 40,48% | 34 | 41,98% | 34 | 41,46% |
| Bouchet & Pointier (1998) | 39 | 10,71% | 18 | 21,43% | 18 | 22,22% | 17 | 20,73% |
| Griffiths & Florens (2006) | 25 | 6,87% | 11 | 13,1% | 11 | 13,58% | 11 | 13,41% |
| Massemin et al. (2009) | 25 | 6,87% | 16 | 19,05% | 16 | 19,75% | 16 | 19,51% |
| Coomans (1967) | 17 | 4,67% | 4 | 4,76% | 4 | 4,94% | 3 | 3,66% |
| Gargominy (2016-2021) | 14 | 3,85% | 14 | 16,67% | 14 | 17,28% | 14 | 17,07% |
| Cowie (2000) | 13 | 3,57% | 7 | 8,33% | 7 | 8,64% | 7 | 8,54% |
| Drouët (1859) | 12 | 3,3% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Pilsbry (1906-1907) | 12 | 3,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet et al. (1991) | 9 | 2,47% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Jourdan et al. (2014) | 9 | 2,47% | 5 | 5,95% | 5 | 6,17% | 5 | 6,1% |
| Brook (2010) | 8 | 2,2% | 4 | 4,76% | 4 | 4,94% | 4 | 4,88% |
| Pointier & Marquet (1990) | 8 | 2,2% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Solem (1961) | 8 | 2,2% | 6 | 7,14% | 6 | 7,41% | 6 | 7,32% |
| Solem (1964) | 8 | 2,2% | 6 | 7,14% | 6 | 7,41% | 6 | 7,32% |
| Questel (2020) | 7 | 1,92% | 5 | 5,95% | 5 | 6,17% | 5 | 6,1% |
| UICN Comité français, OFB & MNHN (2021) | 7 | 1,92% | 7 | 8,33% | 7 | 8,64% | 7 | 8,54% |
| Abdou et al. (2004) | 6 | 1,65% | 4 | 4,76% | 4 | 4,94% | 4 | 4,88% |
| Haynes (2001) | 6 | 1,65% | 4 | 4,76% | 4 | 4,94% | 4 | 4,88% |
| Pointier (2001) | 6 | 1,65% | 4 | 4,76% | 4 | 4,94% | 4 | 4,88% |
| Preece (1995) | 6 | 1,65% | 3 | 3,57% | 3 | 3,7% | 3 | 3,66% |
| Falkner et al. (2002) | 5 | 1,37% | 4 | 4,76% | 4 | 4,94% | 4 | 4,88% |
| Gargominy et al. (2011) | 5 | 1,37% | 5 | 5,95% | 5 | 6,17% | 5 | 6,1% |
| Grimpe & Hoffmann (1925) | 5 | 1,37% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Mousson (1872) | 5 | 1,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2017) | 5 | 1,37% | 3 | 3,57% | 3 | 3,7% | 3 | 3,66% |
| Reeve (1873-1874) | 5 | 1,37% | 4 | 4,76% | 4 | 4,94% | 3 | 3,66% |
| Welter-schultes (2012) | 5 | 1,37% | 3 | 3,57% | 3 | 3,7% | 3 | 3,66% |
| Yokoyama (2013) | 5 | 1,37% | 3 | 3,57% | 3 | 3,7% | 3 | 3,66% |
| Gould (1852) | 4 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutton (1834) | 4 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mary (2017) | 4 | 1,1% | 4 | 4,76% | 4 | 4,94% | 4 | 4,88% |
| Mazé (1883) | 4 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1920-1921) | 4 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potiez & Michaud (1835-1838) | 4 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1927) | 3 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke (1934) | 3 | 0,82% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Crosse (1874) | 3 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1863) | 3 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1827) | 3 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcellini et al. (2012) | 3 | 0,82% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Hausdorf (2007) | 3 | 0,82% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Hausdorf (2023) | 3 | 0,82% | 3 | 3,57% | 3 | 3,7% | 3 | 3,66% |
| Jay et al. (2009) | 3 | 0,82% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Reeve (1849) | 3 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1923) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breure et al. (2020) | 2 | 0,55% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Bruguière (1789-1792) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charles (2016) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clench (1964) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1867) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1805) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac & Deshayes (1820-51) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1821) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1822) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fossati & Marquet (1998) | 2 | 0,55% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Gerber (2018) | 2 | 0,55% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Gould (1846) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1878) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 0,55% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Jousseaume (1889) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Küster & Pfeiffer (1845-1855) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moricand (1837) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1774) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1909-1910) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potiez & Michaud (1844) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 2 | 0,55% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Rang (1831) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ravalo et al. (2023) | 2 | 0,55% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Reise et al. (2011) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robinson et al. (2009) | 2 | 0,55% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Sowerby (1842) | 2 | 0,55% | 2 | 2,38% | 2 | 2,47% | 2 | 2,44% |
| Swainson (1840) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (2003) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tillier (1980) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wetherby (1879) | 2 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adams (1845) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adams (1861) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adamson (1935) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Arruda et al. (2016) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1961) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Beck (1837) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benoit (1881) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1850) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertrand (2017) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Bourguignat (1856) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1822) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breure & Ablett (2014) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Breure (2011) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Breure (2016) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Brown (1994) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruguière et al. (1789-1792) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen & Kahn (2017) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Clavier et al. (2010) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Cockerell (1901) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke (1928) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Crosse (1864) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delannoye & Massemin (2010) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Deuss et al. (2013) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Dunker (1848) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1868) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer-piette & Bedoucha (1964) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilla et al. (2014) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Gargominy & Fontaine (2014) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Garrett (1879) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1884) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1866) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gomes & Thome (2004) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Gould (1859) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guilding (1825) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf & Bermúdez (2003) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huet (2023) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Jay (1839) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1964) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Kerney & Cameron (1999) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Lamarck (1792) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1816) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1819) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1822) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letacq (1924) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lydeard et al. (2016) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1874) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1851) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1860) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naggs (1989) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Neubert & Gosteli (2005) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orbigny (1835) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1839) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1840) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1847) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1849) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1852) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Pfeiffer (1852) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1927-1935) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Blanc (1985) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Pointier & Théron (2006) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Pointier et al. (1998) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (1996) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Pointier (2008) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1998) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2014) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Rang (1834) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1834) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1834) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1841) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saito et al. (2023) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Salvador et al. (2023) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Say (1817) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shuttleworth (1857) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simroth (1918) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Singh et al. (2022) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Solem (1959) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1843) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1976) | 1 | 0,27% | 1 | 1,19% | 1 | 1,23% | 1 | 1,22% |
| Swainson ([1820-1821]) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1922) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vernhout (1914) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidigal et al. (2018) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Watters (2014) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
