Mollusques continentaux de la Réunion
Mollusca continentaux (sens large) de la Réunion
158 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Griffiths & Florens (2006) | 223 | 48,37% | 165 | 129,92% | 165 | 130,95% | 165 | 130,95% |
Deshayes (1863) | 27 | 5,86% | 5 | 3,94% | 5 | 3,97% | 5 | 3,97% |
Falkner et al. (2002) | 23 | 4,99% | 16 | 12,6% | 16 | 12,7% | 16 | 12,7% |
Delannoye et al. (2015) | 21 | 4,56% | 12 | 9,45% | 12 | 9,52% | 12 | 9,52% |
Gargominy et al. (2011) | 21 | 4,56% | 18 | 14,17% | 18 | 14,29% | 18 | 14,29% |
Welter-schultes (2012) | 19 | 4,12% | 15 | 11,81% | 15 | 11,9% | 15 | 11,9% |
Jay et al. (2009) | 18 | 3,9% | 11 | 8,66% | 11 | 8,73% | 11 | 8,73% |
Pointier & Marquet (1990) | 16 | 3,47% | 4 | 3,15% | 4 | 3,17% | 4 | 3,17% |
Cowie (2000) | 15 | 3,25% | 12 | 9,45% | 12 | 9,52% | 12 | 9,52% |
Kerney & Cameron (1999) | 15 | 3,25% | 12 | 9,45% | 12 | 9,52% | 12 | 9,52% |
Forcellini et al. (2012) | 13 | 2,82% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Abdou et al. (2004) | 12 | 2,6% | 8 | 6,3% | 8 | 6,35% | 8 | 6,35% |
Haynes (2001) | 11 | 2,39% | 6 | 4,72% | 6 | 4,76% | 6 | 4,76% |
Hovestadt & Neckheim (2020) | 10 | 2,17% | 10 | 7,87% | 10 | 7,94% | 10 | 7,94% |
Jourdan et al. (2014) | 10 | 2,17% | 7 | 5,51% | 7 | 5,56% | 7 | 5,56% |
Lamy & Pointier (2018) | 10 | 2,17% | 5 | 3,94% | 5 | 3,97% | 5 | 3,97% |
Gargominy (2011-2023) | 9 | 1,95% | 9 | 7,09% | 9 | 7,14% | 9 | 7,14% |
Müller (1774) | 9 | 1,95% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 8 | 1,74% | 4 | 3,15% | 4 | 3,17% | 4 | 3,17% |
Massemin et al. (2009) | 8 | 1,74% | 5 | 3,94% | 5 | 3,97% | 5 | 3,97% |
Pilsbry (1906-1907) | 8 | 1,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Solem (1961) | 8 | 1,74% | 6 | 4,72% | 6 | 4,76% | 6 | 4,76% |
Bouchet & Pointier (1998) | 7 | 1,52% | 3 | 2,36% | 3 | 2,38% | 3 | 2,38% |
Hausdorf (2023) | 7 | 1,52% | 7 | 5,51% | 7 | 5,56% | 7 | 5,56% |
Mary (2017) | 7 | 1,52% | 7 | 5,51% | 7 | 5,56% | 7 | 5,56% |
Brook (2010) | 6 | 1,3% | 6 | 4,72% | 6 | 4,76% | 6 | 4,76% |
Gargominy (2016-2021) | 6 | 1,3% | 6 | 4,72% | 6 | 4,76% | 6 | 4,76% |
Questel (2020) | 6 | 1,3% | 4 | 3,15% | 4 | 3,17% | 4 | 3,17% |
Solem (1964) | 6 | 1,3% | 5 | 3,94% | 5 | 3,97% | 5 | 3,97% |
Franc (1956) | 5 | 1,08% | 3 | 2,36% | 3 | 2,38% | 3 | 2,38% |
Garrett (1884) | 5 | 1,08% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Mousson (1872) | 5 | 1,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1864) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Fossati & Marquet (1998) | 4 | 0,87% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Gould (1852) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutchinson et al. (2022) | 4 | 0,87% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Hutton (1834) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2020) | 4 | 0,87% | 4 | 3,15% | 4 | 3,17% | 4 | 3,17% |
Monterosato (1892) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier (2001) | 4 | 0,87% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Questel (2017) | 4 | 0,87% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Starmühlner (1970) | 4 | 0,87% | 3 | 2,36% | 3 | 2,38% | 3 | 2,38% |
Tröndlé & Boutet (2009) | 4 | 0,87% | 3 | 2,36% | 3 | 2,38% | 3 | 2,38% |
Cooke (1934) | 3 | 0,65% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Draparnaud (1805) | 3 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1821) | 3 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerber (2018) | 3 | 0,65% | 3 | 2,36% | 3 | 2,38% | 3 | 2,38% |
Grimpe & Hoffmann (1925) | 3 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Jousseaume (1872) | 3 | 0,65% | 3 | 2,36% | 3 | 2,38% | 3 | 2,38% |
Lamarck (1816) | 3 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 3 | 0,65% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Lowe et al. (2007) | 3 | 0,65% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Preece (1995) | 3 | 0,65% | 3 | 2,36% | 3 | 2,38% | 3 | 2,38% |
UICN Comité français, OFB & MNHN (2021) | 3 | 0,65% | 3 | 2,36% | 3 | 2,38% | 3 | 2,38% |
Abdou (2021) | 2 | 0,43% | 2 | 1,57% | 1 | 0,79% | 1 | 0,79% |
Badie (1977) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchet et al. (1991) | 2 | 0,43% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Clench (1964) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Coomans (1967) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupouy (1966) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1822) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1827) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Vukadinovic (1970) | 2 | 0,43% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Garrett (1879) | 2 | 0,43% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Gassies (1871) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffiths & Florens (2004) | 2 | 0,43% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Hyman & Ponder (2010) | 2 | 0,43% | 2 | 1,57% | 2 | 1,59% | 2 | 1,59% |
Jousseaume (1884) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Martens (1875) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollonera (1889) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Rang (1831) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Reise et al. (2011) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor (2003) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Wetherby (1879) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 2 | 0,43% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Adamson (1935) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Alder (1830) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Audibert & Paillet (2014) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Badie et al. (1992) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Benoit (1857) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Benoit (1881) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1856) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1860) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1822) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Cooke (1928) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Correa et al. (2010) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Draparnaud (1801) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichhorst (2016) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
European Nucleotide Archive (2019) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Fagot (1879) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Bedoucha (1964) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontanilla et al. (2014) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Gargominy et al. (2022) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Gargominy (2001) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy (2007) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Garrett (1887) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1866) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1869) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain (1921) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain (1931) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomes & Thome (2004) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Gould (1859) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gregorio (1895) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiller & Madec (2010) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Héros et al. (2007) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Huet (2023) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Johnson (1964) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan & Mille (2006) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Kadolsky (2012) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Kennard & Woodward (1926) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1819) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1822) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaire & Gerriet (2014) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lounnas et al. (2017) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Lydeard et al. (2016) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Mabille (1881) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Macé (1860) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1883) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1890) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelet (1848) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Moutier & Moutier (1920) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Naggs (1989) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Naggs (1994) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Paulucci (1882) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1865) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelorce & Hoarau (comm. pers., 2012) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Pfeiffer (1846) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Blanc (1985) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Delay (1995) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Pointier et al. (1998) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier et al. (2007) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Pollonera (1885) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1835-1838) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1844) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Preston (1915) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Pugh & Scott (2002) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Questel (2014) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Reeve (1849) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (2006) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Risso (1826) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Rowson et al. (2014) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1817) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Schröter (1784) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherpa et al. (2018) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Starmühlner (1976) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Stévanovich (1994) | 1 | 0,22% | 1 | 0,79% | 1 | 0,79% | 1 | 0,79% |
Swainson ([1820-1821]) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Turton (1932) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Vallot (1801) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Van & Bruggen (1991) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1922) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |