Gastéropodes terrestres de Guyane
103 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Gargominy (2016-2021) | 65 | 25,29% | 57 | 75% | 55 | 74,32% | 57 | 77,03% |
Massemin et al. (2009) | 64 | 24,9% | 45 | 59,21% | 44 | 59,46% | 45 | 60,81% |
Delannoye et al. (2015) | 28 | 10,89% | 18 | 23,68% | 18 | 24,32% | 18 | 24,32% |
Pilsbry (1906-1907) | 20 | 7,78% | 4 | 5,26% | 4 | 5,41% | 2 | 2,7% |
Hovestadt & Neckheim (2020) | 19 | 7,39% | 16 | 21,05% | 16 | 21,62% | 16 | 21,62% |
Griffiths & Florens (2006) | 16 | 6,23% | 7 | 9,21% | 7 | 9,46% | 7 | 9,46% |
Drouët (1859) | 14 | 5,45% | 2 | 2,63% | 2 | 2,7% | 2 | 2,7% |
Bouchet & Pointier (1998) | 12 | 4,67% | 6 | 7,89% | 6 | 8,11% | 6 | 8,11% |
Gargominy & Muratov (2012) | 9 | 3,5% | 9 | 11,84% | 9 | 12,16% | 9 | 12,16% |
Bouchet et al. (1991) | 7 | 2,72% | 3 | 3,95% | 3 | 4,05% | 3 | 4,05% |
Cowie (2000) | 7 | 2,72% | 5 | 6,58% | 5 | 6,76% | 5 | 6,76% |
Jourdan et al. (2014) | 7 | 2,72% | 5 | 6,58% | 5 | 6,76% | 5 | 6,76% |
Abdou et al. (2004) | 6 | 2,33% | 5 | 6,58% | 5 | 6,76% | 5 | 6,76% |
Brook (2010) | 6 | 2,33% | 5 | 6,58% | 5 | 6,76% | 5 | 6,76% |
Coomans (1967) | 6 | 2,33% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Pfeiffer (1872) | 6 | 2,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1995) | 6 | 2,33% | 3 | 3,95% | 3 | 4,05% | 3 | 4,05% |
Tillier (1980) | 6 | 2,33% | 2 | 2,63% | 1 | 1,35% | 2 | 2,7% |
UICN Comité français, OFB & MNHN (2021) | 6 | 2,33% | 5 | 6,58% | 5 | 6,76% | 5 | 6,76% |
Solem (1961) | 5 | 1,95% | 4 | 5,26% | 4 | 5,41% | 4 | 5,41% |
Cooke (1934) | 4 | 1,56% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Guppy (1878) | 4 | 1,56% | 2 | 2,63% | 2 | 2,7% | 2 | 2,7% |
Hutton (1834) | 4 | 1,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1916-1918) | 4 | 1,56% | 4 | 5,26% | 4 | 5,41% | 4 | 5,41% |
Pilsbry (1920-1921) | 4 | 1,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1927-1935) | 4 | 1,56% | 3 | 3,95% | 3 | 4,05% | 3 | 4,05% |
Rang (1831) | 4 | 1,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1851-1854) | 4 | 1,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Solem (1964) | 4 | 1,56% | 4 | 5,26% | 4 | 5,41% | 4 | 5,41% |
Altena et al. (1975) | 3 | 1,17% | 3 | 3,95% | 3 | 4,05% | 3 | 4,05% |
Baker (1927) | 3 | 1,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf (2007) | 3 | 1,17% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Hausdorf (2023) | 3 | 1,17% | 3 | 3,95% | 3 | 4,05% | 3 | 4,05% |
Muratov & Gargominy (2011) | 3 | 1,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1835-1838) | 3 | 1,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 3 | 1,17% | 2 | 2,63% | 2 | 2,7% | 2 | 2,7% |
Questel (2020) | 3 | 1,17% | 2 | 2,63% | 2 | 2,7% | 2 | 2,7% |
Reeve (1849) | 3 | 1,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Vernhout (1914) | 3 | 1,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1935) | 2 | 0,78% | 2 | 2,63% | 2 | 2,7% | 2 | 2,7% |
Altena (1974) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1923) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure et al. (2020) | 2 | 0,78% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Breure (1976) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Clench (1964) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Deshayes (1831) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Deshayes (1863) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Dézallier et al. (1780) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac & Deshayes (1820-51) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1822) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy & Fontaine (2015) | 2 | 0,78% | 2 | 2,63% | 2 | 2,7% | 2 | 2,7% |
Gould (1843) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1852) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Guppy (1866) | 2 | 0,78% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Higgins (1872) | 2 | 0,78% | 2 | 2,63% | 2 | 2,7% | 2 | 2,7% |
Hyman & Ponder (2010) | 2 | 0,78% | 2 | 2,63% | 2 | 2,7% | 2 | 2,7% |
Jousseaume (1889) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Küster & Pfeiffer (1845-1855) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamy & Pointier (2018) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Lightfoot (1786) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1883) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit de la Saussaye (1840) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1899) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1844) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Sowerby (1842) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Adams (1845) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Ancey (1892) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Arruda et al. (2016) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1961) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Benson (1850) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure & Ablett (2015) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Bruguière (1789-1792) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Christensen & Kahn (2017) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Cooke (1928) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Dall (1885) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
D'Ávila et al. (2020) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Dillwyn (1817) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (2022) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Gargominy et al. (2025) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Gargominy (2001) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrett (1879) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1866) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf & Bermúdez (2003) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf (2006) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Jay et al. (2009) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Jourde et al. (2017) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaire & Gerriet (2014) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1838) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelet (1860) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Naggs (1989) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Orbigny (1835) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1840) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1846) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1855) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1998) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1873-1874) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Roosen & Breure (2024) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Salvador et al. (2020) | 1 | 0,39% | 1 | 1,32% | 1 | 1,35% | 1 | 1,35% |
Tillier (1981) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidigal et al. (2018) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |