Gastéropodes terrestres de la Réunion
107 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) | 181 | 48,27% | 148 | 155,79% | 148 | 155,79% | 148 | 155,79% |
Deshayes (1863) | 22 | 5,87% | 4 | 4,21% | 4 | 4,21% | 4 | 4,21% |
Falkner et al. (2002) | 19 | 5,07% | 12 | 12,63% | 12 | 12,63% | 12 | 12,63% |
Gargominy et al. (2011) | 16 | 4,27% | 12 | 12,63% | 12 | 12,63% | 12 | 12,63% |
Kerney & Cameron (1999) | 15 | 4% | 11 | 11,58% | 11 | 11,58% | 11 | 11,58% |
Welter-schultes (2012) | 15 | 4% | 12 | 12,63% | 12 | 12,63% | 12 | 12,63% |
Delannoye et al. (2015) | 13 | 3,47% | 8 | 8,42% | 8 | 8,42% | 8 | 8,42% |
Cowie (2000) | 12 | 3,2% | 10 | 10,53% | 10 | 10,53% | 10 | 10,53% |
Abdou et al. (2004) | 11 | 2,93% | 8 | 8,42% | 8 | 8,42% | 8 | 8,42% |
Jay et al. (2009) | 9 | 2,4% | 5 | 5,26% | 5 | 5,26% | 5 | 5,26% |
Gargominy (2011-2023) | 8 | 2,13% | 8 | 8,42% | 8 | 8,42% | 8 | 8,42% |
Hovestadt & Neckheim (2020) | 8 | 2,13% | 8 | 8,42% | 8 | 8,42% | 8 | 8,42% |
Jourdan et al. (2014) | 8 | 2,13% | 6 | 6,32% | 6 | 6,32% | 6 | 6,32% |
Pilsbry (1906-1907) | 8 | 2,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Solem (1961) | 8 | 2,13% | 5 | 5,26% | 5 | 5,26% | 5 | 5,26% |
Hausdorf (2023) | 7 | 1,87% | 7 | 7,37% | 7 | 7,37% | 7 | 7,37% |
Müller (1774) | 7 | 1,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy (2016-2021) | 6 | 1,6% | 6 | 6,32% | 6 | 6,32% | 6 | 6,32% |
Massemin et al. (2009) | 6 | 1,6% | 4 | 4,21% | 4 | 4,21% | 4 | 4,21% |
Solem (1964) | 6 | 1,6% | 5 | 5,26% | 5 | 5,26% | 5 | 5,26% |
Bouchet & Pointier (1998) | 4 | 1,07% | 2 | 2,11% | 2 | 2,11% | 2 | 2,11% |
Bourguignat (1864) | 4 | 1,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brook (2010) | 4 | 1,07% | 4 | 4,21% | 4 | 4,21% | 4 | 4,21% |
Hutchinson et al. (2022) | 4 | 1,07% | 2 | 2,11% | 2 | 2,11% | 2 | 2,11% |
Hutton (1834) | 4 | 1,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Monterosato (1892) | 4 | 1,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 4 | 1,07% | 2 | 2,11% | 2 | 2,11% | 2 | 2,11% |
Questel (2020) | 4 | 1,07% | 3 | 3,16% | 3 | 3,16% | 3 | 3,16% |
Bouchet et al. (1991) | 3 | 0,8% | 2 | 2,11% | 2 | 2,11% | 2 | 2,11% |
Cooke (1934) | 3 | 0,8% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Deuss et al. (2013) | 3 | 0,8% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Férussac (1821) | 3 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Franc (1956) | 3 | 0,8% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Garrett (1884) | 3 | 0,8% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Grimpe & Hoffmann (1925) | 3 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2020) | 3 | 0,8% | 3 | 3,16% | 3 | 3,16% | 3 | 3,16% |
Preece (1995) | 3 | 0,8% | 3 | 3,16% | 3 | 3,16% | 3 | 3,16% |
UICN Comité français, OFB & MNHN (2021) | 3 | 0,8% | 3 | 3,16% | 3 | 3,16% | 3 | 3,16% |
Badie (1977) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabaret et al. (1986) | 2 | 0,53% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Clench (1964) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupouy (1966) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1822) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Vukadinovic (1970) | 2 | 0,53% | 2 | 2,11% | 2 | 2,11% | 2 | 2,11% |
Gould (1852) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffiths & Florens (2004) | 2 | 0,53% | 2 | 2,11% | 2 | 2,11% | 2 | 2,11% |
Hyman & Ponder (2010) | 2 | 0,53% | 2 | 2,11% | 2 | 2,11% | 2 | 2,11% |
Letacq (1924) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,53% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Lowe et al. (2007) | 2 | 0,53% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Pollonera (1889) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Rang (1831) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Reise et al. (2011) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1935) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Audibert & Paillet (2014) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Badie et al. (1992) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Bourguignat (1860) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1822) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruguière (1789-1792) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Christensen & Kahn (2017) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Cooke (1928) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Coomans (1967) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1879) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Bedoucha (1964) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontanilla et al. (2014) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Forcellini et al. (2012) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gamiette et al. (2023) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (2022) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Gargominy (2001) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy (2007) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Garrett (1879) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1866) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain (1931) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomes & Thome (2004) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Gould (1846) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gregorio (1895) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiller & Madec (2010) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Huet & Cadet (2024) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Kennard & Woodward (1926) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaire & Gerriet (2014) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Macé (1860) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelet (1848) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Moutier & Moutier (1920) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Naggs (1989) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Naggs (1994) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Paulucci (1882) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1846) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Blanc (1985) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollonera (1885) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1835-1838) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1844) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Pugh & Scott (2002) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Reeve (1849) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1826) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Rowson et al. (2014) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvador et al. (2023) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Schröter (1784) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherpa et al. (2018) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Stévanovich (1994) | 1 | 0,27% | 1 | 1,05% | 1 | 1,05% | 1 | 1,05% |
Swainson ([1820-1821]) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Tröndlé & Boutet (2009) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Vallot (1801) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Van & Bruggen (1991) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |