Mollusques continentaux de Guadeloupe
Mollusca continentaux (sens large) de Guadeloupe
188 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) | 132 | 26,77% | 86 | 74,78% | 86 | 75,44% | 86 | 75,44% |
| Bouchet & Pointier (1998) | 71 | 14,4% | 45 | 39,13% | 45 | 39,47% | 44 | 38,6% |
| Hovestadt & Neckheim (2020) | 69 | 14% | 55 | 47,83% | 55 | 48,25% | 55 | 48,25% |
| Lamy & Pointier (2018) | 65 | 13,18% | 53 | 46,09% | 53 | 46,49% | 53 | 46,49% |
| Coomans (1967) | 34 | 6,9% | 11 | 9,57% | 11 | 9,65% | 11 | 9,65% |
| Massemin et al. (2009) | 33 | 6,69% | 20 | 17,39% | 20 | 17,54% | 20 | 17,54% |
| Griffiths & Florens (2006) | 29 | 5,88% | 14 | 12,17% | 14 | 12,28% | 14 | 12,28% |
| Cowie (2000) | 16 | 3,25% | 10 | 8,7% | 10 | 8,77% | 10 | 8,77% |
| Gargominy (2016-2021) | 16 | 3,25% | 14 | 12,17% | 14 | 12,28% | 14 | 12,28% |
| Bouchet et al. (1991) | 15 | 3,04% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| UICN Comité français, OFB & MNHN (2021) | 15 | 3,04% | 13 | 11,3% | 13 | 11,4% | 13 | 11,4% |
| Questel (2020) | 14 | 2,84% | 7 | 6,09% | 7 | 6,14% | 7 | 6,14% |
| Jourdan et al. (2014) | 12 | 2,43% | 8 | 6,96% | 8 | 7,02% | 8 | 7,02% |
| Pilsbry (1906-1907) | 12 | 2,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2017) | 11 | 2,23% | 5 | 4,35% | 5 | 4,39% | 5 | 4,39% |
| Solem (1961) | 10 | 2,03% | 8 | 6,96% | 8 | 7,02% | 8 | 7,02% |
| Solem (1964) | 10 | 2,03% | 8 | 6,96% | 8 | 7,02% | 8 | 7,02% |
| Pointier & Marquet (1990) | 9 | 1,83% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Brook (2010) | 8 | 1,62% | 4 | 3,48% | 4 | 3,51% | 4 | 3,51% |
| Yokoyama (2013) | 8 | 1,62% | 4 | 3,48% | 4 | 3,51% | 4 | 3,51% |
| Gargominy et al. (2011) | 7 | 1,42% | 7 | 6,09% | 7 | 6,14% | 7 | 6,14% |
| Haynes (2001) | 7 | 1,42% | 4 | 3,48% | 4 | 3,51% | 4 | 3,51% |
| Welter-schultes (2012) | 7 | 1,42% | 5 | 4,35% | 5 | 4,39% | 5 | 4,39% |
| Drouët (1859) | 6 | 1,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner et al. (2002) | 6 | 1,22% | 5 | 4,35% | 5 | 4,39% | 5 | 4,39% |
| Hausdorf (2023) | 6 | 1,22% | 6 | 5,22% | 6 | 5,26% | 6 | 5,26% |
| Mary (2017) | 6 | 1,22% | 6 | 5,22% | 6 | 5,26% | 6 | 5,26% |
| Abdou et al. (2004) | 5 | 1,01% | 3 | 2,61% | 3 | 2,63% | 3 | 2,63% |
| Cooke (1934) | 5 | 1,01% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Forcellini et al. (2012) | 5 | 1,01% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Grimpe & Hoffmann (1925) | 5 | 1,01% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Mousson (1872) | 5 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (2001) | 5 | 1,01% | 3 | 2,61% | 3 | 2,63% | 3 | 2,63% |
| Preece (1995) | 5 | 1,01% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Reeve (1873-1874) | 5 | 1,01% | 4 | 3,48% | 4 | 3,51% | 4 | 3,51% |
| Gould (1852) | 4 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutton (1834) | 4 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1883) | 4 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1774) | 4 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1920-1921) | 4 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 4 | 0,81% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Baker (1927) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breure (2016) | 3 | 0,61% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Charles (2016) | 3 | 0,61% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Deshayes (1863) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1827) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1824) | 3 | 0,61% | 3 | 2,61% | 3 | 2,63% | 3 | 2,63% |
| Hausdorf (2007) | 3 | 0,61% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Jay et al. (2009) | 3 | 0,61% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Jourdan (2020) | 3 | 0,61% | 3 | 2,61% | 3 | 2,63% | 3 | 2,63% |
| Linnaeus (1758) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potiez & Michaud (1835-1838) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1849) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1842-1887) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adamson (1935) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Baker (1923) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1926) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartsch (1942) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Binney (1841) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breure et al. (2020) | 2 | 0,41% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Bruguière (1789-1792) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charles (2014) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Clench (1964) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1867) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1874) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1834) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1805) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac & Deshayes (1820-51) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1822) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fossati & Marquet (1998) | 2 | 0,41% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Gerber (2018) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Gould (1843) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1846) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1878) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jousseaume (1889) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Küster & Pfeiffer (1845-1855) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massemin et al. (2011) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Mazé (1890) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moricand (1837) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1841) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1889-1890) | 2 | 0,41% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Pilsbry (1899) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1909-1910) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1916-1918) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Prié (2017) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Questel (2014) | 2 | 0,41% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Rang (1831) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reise et al. (2011) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robinson et al. (2009) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Salvador et al. (2023) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Say (1817) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1842) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Starmühlner (1976) | 2 | 0,41% | 2 | 1,74% | 2 | 1,75% | 2 | 1,75% |
| Swainson (1840) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (2003) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tillier (1980) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wetherby (1879) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adams (1845) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ancey (1892) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arruda et al. (2016) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Audibert & Paillet (2014) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Baker (1941) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Baker (1961) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Benoit (1881) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1850) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1856) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1822) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brown (1994) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen & Kahn (2017) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Clavier et al. (2010) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Cockerell (1901) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conrad (1831) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke (1928) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Crosse (1864) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss et al. (2013) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Dewarumez et al. (2011) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Dunker (1848) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1821) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1868) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer-piette & Bedoucha (1964) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilla et al. (2014) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Gargominy & Fontaine (2014) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Garrett (1879) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1884) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1866) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2003) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gomes & Thome (2004) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Gould (1859) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Guilding (1825) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guilding (1828) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1867) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf & Bermúdez (2003) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huet (2023) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Johnson (1964) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourde et al. (2017) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Kerney & Cameron (1999) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Lamarck (1816) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1819) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1822) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lenoble et al. (2018) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Lenoble et al. (2018) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Lenoble (2021) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letacq (1924) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lounnas et al. (2017) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Lowe et al. (2007) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lydeard et al. (2016) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1851) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1860) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naggs (1989) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Naggs (1994) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Naudon et al. (2015) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Orbigny (1835) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1839) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1840) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1847) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1849) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1852) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Pfeiffer (1852) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1857) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1858) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1927-1935) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Blanc (1985) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Pointier & Théron (2006) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Pointier et al. (1998) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier et al. (2007) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Pointier (1976) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (2008) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potiez & Michaud (1844) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1998) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Petit (2022) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Prime (1865) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1834) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1841) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rocha & D'ávila (2019) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Saito et al. (2023) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Simroth (1918) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Singh et al. (2022) | 1 | 0,2% | 1 | 0,87% | 1 | 0,88% | 1 | 0,88% |
| Solem (1959) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1922) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vernhout (1914) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidigal et al. (2018) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Watters (2014) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
