Mollusques continentaux de Guyane
Mollusca continentaux (sens large) de Guyane française
148 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) | 95 | 20,74% | 66 | 54,1% | 65 | 54,17% | 66 | 55% |
| Delannoye et al. (2015) | 71 | 15,5% | 43 | 35,25% | 43 | 35,83% | 43 | 35,83% |
| Gargominy (2016-2021) | 65 | 14,19% | 58 | 47,54% | 56 | 46,67% | 58 | 48,33% |
| Lamy & Pointier (2018) | 40 | 8,73% | 32 | 26,23% | 32 | 26,67% | 32 | 26,67% |
| Hovestadt & Neckheim (2020) | 29 | 6,33% | 24 | 19,67% | 24 | 20% | 24 | 20% |
| Bouchet & Pointier (1998) | 27 | 5,9% | 16 | 13,11% | 16 | 13,33% | 16 | 13,33% |
| Griffiths & Florens (2006) | 20 | 4,37% | 8 | 6,56% | 8 | 6,67% | 8 | 6,67% |
| Pilsbry (1906-1907) | 18 | 3,93% | 4 | 3,28% | 4 | 3,33% | 2 | 1,67% |
| Drouët (1859) | 16 | 3,49% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Coomans (1967) | 14 | 3,06% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Prié (2020) | 10 | 2,18% | 8 | 6,56% | 8 | 6,67% | 8 | 6,67% |
| Cowie (2000) | 9 | 1,97% | 6 | 4,92% | 6 | 5% | 6 | 5% |
| Gargominy & Muratov (2012) | 9 | 1,97% | 9 | 7,38% | 9 | 7,5% | 9 | 7,5% |
| Tillier (1980) | 9 | 1,97% | 2 | 1,64% | 1 | 0,83% | 2 | 1,67% |
| Bouchet et al. (1991) | 8 | 1,75% | 3 | 2,46% | 3 | 2,5% | 3 | 2,5% |
| Jourdan et al. (2014) | 8 | 1,75% | 5 | 4,1% | 5 | 4,17% | 5 | 4,17% |
| Brook (2010) | 6 | 1,31% | 5 | 4,1% | 5 | 4,17% | 5 | 4,17% |
| Pfeiffer (1872) | 6 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1995) | 6 | 1,31% | 3 | 2,46% | 3 | 2,5% | 3 | 2,5% |
| Questel (2020) | 6 | 1,31% | 3 | 2,46% | 3 | 2,5% | 3 | 2,5% |
| UICN Comité français, OFB & MNHN (2021) | 6 | 1,31% | 5 | 4,1% | 5 | 4,17% | 5 | 4,17% |
| Abdou et al. (2004) | 5 | 1,09% | 4 | 3,28% | 4 | 3,33% | 4 | 3,33% |
| Mousson (1872) | 5 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Solem (1961) | 5 | 1,09% | 4 | 3,28% | 4 | 3,33% | 4 | 3,33% |
| Cooke (1934) | 4 | 0,87% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Deshayes (1830-1832) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1852) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1878) | 4 | 0,87% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Haynes (2001) | 4 | 0,87% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Hutton (1834) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mary (2017) | 4 | 0,87% | 4 | 3,28% | 4 | 3,33% | 4 | 3,33% |
| Pilsbry (1916-1918) | 4 | 0,87% | 4 | 3,28% | 4 | 3,33% | 4 | 3,33% |
| Pilsbry (1920-1921) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1927-1935) | 4 | 0,87% | 3 | 2,46% | 3 | 2,5% | 3 | 2,5% |
| Pointier & Marquet (1990) | 4 | 0,87% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Reeve (1851-1854) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Solem (1964) | 4 | 0,87% | 4 | 3,28% | 4 | 3,33% | 4 | 3,33% |
| Altena et al. (1975) | 3 | 0,66% | 3 | 2,46% | 3 | 2,5% | 3 | 2,5% |
| Baker (1927) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1863) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner et al. (2002) | 3 | 0,66% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Gargominy et al. (2011) | 3 | 0,66% | 3 | 2,46% | 3 | 2,5% | 3 | 2,5% |
| Hausdorf (2007) | 3 | 0,66% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Hausdorf (2023) | 3 | 0,66% | 3 | 2,46% | 3 | 2,5% | 3 | 2,5% |
| Linnaeus (1758) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1883) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1774) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muratov & Gargominy (2011) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (2001) | 3 | 0,66% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Potiez & Michaud (1835-1838) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2017) | 3 | 0,66% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Reeve (1849) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vernhout (1914) | 3 | 0,66% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Yokoyama (2013) | 3 | 0,66% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Adamson (1935) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Altena (1974) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1923) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breure et al. (2020) | 2 | 0,44% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Breure (1976) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clench (1964) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1831) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dézallier et al. (1780) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1805) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac & Deshayes (1820-51) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1822) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1827) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcellini et al. (2012) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Fossati & Marquet (1998) | 2 | 0,44% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Gargominy & Fontaine (2015) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Gerber (2018) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Gould (1843) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1846) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1866) | 2 | 0,44% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Higgins (1872) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Hupé (1857) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hyman & Ponder (2010) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Jay et al. (2009) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Jousseaume (1889) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Küster & Pfeiffer (1845-1855) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1822) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lightfoot (1786) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massemin et al. (2011) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Petit de la Saussaye (1840) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1899) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potiez & Michaud (1844) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Petit (2022) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Prié (2017) | 2 | 0,44% | 2 | 1,64% | 2 | 1,67% | 2 | 1,67% |
| Questel (2014) | 2 | 0,44% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Rang (1831) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sowerby (1842) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (2003) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welter-schultes (2012) | 2 | 0,44% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Adams (1845) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ancey (1892) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arruda et al. (2016) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1961) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Benoit (1881) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1850) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1856) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breure & Ablett (2015) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Brown (1994) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruguière (1789-1792) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen & Kahn (2017) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Clavier et al. (2010) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Conrad (1831) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke (1928) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Crosse (1864) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1876) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dall (1885) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| D'Ávila et al. (2020) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Deuss et al. (2013) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Dewarumez et al. (2011) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Dillwyn (1817) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy (2001) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1879) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1866) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girardi (2003) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1859) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Guilding (1828) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guppy (1867) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf & Bermúdez (2003) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2006) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Johnson (1964) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourde et al. (2017) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Lydeard et al. (2016) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1860) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naggs (1989) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Orbigny (1835) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pereira et al. (2013) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Pfeiffer (1840) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1855) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Pointier & Théron (2006) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Pointier (1976) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1998) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prime (1865) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1873-1874) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salvador et al. (2020) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Say (1817) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1976) | 1 | 0,22% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
| Vandel (1922) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vernhout (1914) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidigal et al. (2018) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
