Gastéropodes continentaux de Guyane
144 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Massemin et al. (2009) | 87 | 21,91% | 61 | 57,55% | 60 | 57,69% | 61 | 58,65% |
Gargominy (2016-2021) | 65 | 16,37% | 57 | 53,77% | 55 | 52,88% | 57 | 54,81% |
Delannoye et al. (2015) | 62 | 15,62% | 37 | 34,91% | 37 | 35,58% | 37 | 35,58% |
Lamy & Pointier (2018) | 32 | 8,06% | 26 | 24,53% | 26 | 25% | 26 | 25% |
Hovestadt & Neckheim (2020) | 25 | 6,3% | 20 | 18,87% | 20 | 19,23% | 20 | 19,23% |
Bouchet & Pointier (1998) | 24 | 6,05% | 14 | 13,21% | 14 | 13,46% | 14 | 13,46% |
Griffiths & Florens (2006) | 22 | 5,54% | 8 | 7,55% | 8 | 7,69% | 8 | 7,69% |
Pilsbry (1906-1907) | 20 | 5,04% | 4 | 3,77% | 4 | 3,85% | 2 | 1,92% |
Drouët (1859) | 16 | 4,03% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Coomans (1967) | 13 | 3,27% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Cowie (2000) | 9 | 2,27% | 6 | 5,66% | 6 | 5,77% | 6 | 5,77% |
Gargominy & Muratov (2012) | 9 | 2,27% | 9 | 8,49% | 9 | 8,65% | 9 | 8,65% |
Tillier (1980) | 9 | 2,27% | 2 | 1,89% | 1 | 0,96% | 2 | 1,92% |
Bouchet et al. (1991) | 8 | 2,02% | 3 | 2,83% | 3 | 2,88% | 3 | 2,88% |
Jourdan et al. (2014) | 8 | 2,02% | 5 | 4,72% | 5 | 4,81% | 5 | 4,81% |
Abdou et al. (2004) | 6 | 1,51% | 5 | 4,72% | 5 | 4,81% | 5 | 4,81% |
Brook (2010) | 6 | 1,51% | 5 | 4,72% | 5 | 4,81% | 5 | 4,81% |
Pfeiffer (1872) | 6 | 1,51% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1995) | 6 | 1,51% | 3 | 2,83% | 3 | 2,88% | 3 | 2,88% |
UICN Comité français, OFB & MNHN (2021) | 6 | 1,51% | 5 | 4,72% | 5 | 4,81% | 5 | 4,81% |
Mousson (1872) | 5 | 1,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 5 | 1,26% | 3 | 2,83% | 3 | 2,88% | 3 | 2,88% |
Solem (1961) | 5 | 1,26% | 4 | 3,77% | 4 | 3,85% | 4 | 3,85% |
Cooke (1934) | 4 | 1,01% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Deshayes (1830-1832) | 4 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1852) | 4 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Guppy (1878) | 4 | 1,01% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Haynes (2001) | 4 | 1,01% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Hutton (1834) | 4 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Mary (2017) | 4 | 1,01% | 4 | 3,77% | 4 | 3,85% | 4 | 3,85% |
Pilsbry (1916-1918) | 4 | 1,01% | 4 | 3,77% | 4 | 3,85% | 4 | 3,85% |
Pilsbry (1920-1921) | 4 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1927-1935) | 4 | 1,01% | 3 | 2,83% | 3 | 2,88% | 3 | 2,88% |
Pointier & Marquet (1990) | 4 | 1,01% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Rang (1831) | 4 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1851-1854) | 4 | 1,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Solem (1964) | 4 | 1,01% | 4 | 3,77% | 4 | 3,85% | 4 | 3,85% |
Altena et al. (1975) | 3 | 0,76% | 3 | 2,83% | 3 | 2,88% | 3 | 2,88% |
Baker (1927) | 3 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Deshayes (1863) | 3 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf (2007) | 3 | 0,76% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Hausdorf (2023) | 3 | 0,76% | 3 | 2,83% | 3 | 2,88% | 3 | 2,88% |
Mazé (1883) | 3 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 3 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Muratov & Gargominy (2011) | 3 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier (2001) | 3 | 0,76% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Potiez & Michaud (1835-1838) | 3 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 3 | 0,76% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Reeve (1849) | 3 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Vernhout (1914) | 3 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1935) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Altena (1974) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1923) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure et al. (2020) | 2 | 0,5% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Breure (1976) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Clench (1964) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Deshayes (1831) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Dézallier et al. (1780) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Falkner et al. (2002) | 2 | 0,5% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Férussac & Deshayes (1820-51) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1822) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1827) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcellini et al. (2012) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Fossati & Marquet (1998) | 2 | 0,5% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Gargominy & Fontaine (2015) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Gargominy et al. (2011) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Gerber (2018) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Gould (1843) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Guppy (1866) | 2 | 0,5% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Higgins (1872) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Hupé (1857) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Hyman & Ponder (2010) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Jay et al. (2009) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Jousseaume (1889) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Küster & Pfeiffer (1845-1855) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1822) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Lightfoot (1786) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit de la Saussaye (1840) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1899) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier et al. (1977) | 2 | 0,5% | 2 | 1,89% | 2 | 1,92% | 2 | 1,92% |
Potiez & Michaud (1844) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Sowerby (1842) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor (2003) | 2 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Welter-schultes (2012) | 2 | 0,5% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Yokoyama (2013) | 2 | 0,5% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Adams (1845) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Ancey (1892) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Arruda et al. (2016) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1961) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Benoit (1881) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Benson (1850) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1856) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure & Ablett (2015) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Brown (1994) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruguière (1789-1792) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Christensen & Kahn (2017) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Clavier et al. (2010) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Cooke (1928) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Crosse (1864) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1876) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall (1885) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
D'Ávila et al. (2020) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Deuss et al. (2013) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Dillwyn (1817) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (2022) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Gargominy et al. (2025) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Gargominy (2001) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrett (1879) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1866) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1859) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilding (1828) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf & Bermúdez (2003) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf (2006) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Johnson (1964) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourde et al. (2017) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Kadolsky (2012) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Lemaire & Gerriet (2014) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1838) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lydeard et al. (2016) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1890) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelet (1860) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Naggs (1989) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Orbigny (1835) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1840) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1846) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1855) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Delay (1995) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Pointier & Théron (2006) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Pointier (1976) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1998) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Reeve (1873-1874) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Roosen & Breure (2024) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Salvador et al. (2020) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Say (1817) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1970) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1976) | 1 | 0,25% | 1 | 0,94% | 1 | 0,96% | 1 | 0,96% |
Tillier (1981) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1922) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Vernhout (1914) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidigal et al. (2018) | 1 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |