Gastéropodes continentaux de Guadeloupe
177 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Delannoye et al. (2015) | 118 | 27% | 78 | 72,9% | 78 | 73,58% | 78 | 73,58% |
Bouchet & Pointier (1998) | 66 | 15,1% | 42 | 39,25% | 42 | 39,62% | 41 | 38,68% |
Hovestadt & Neckheim (2020) | 64 | 14,65% | 50 | 46,73% | 50 | 47,17% | 50 | 47,17% |
Lamy & Pointier (2018) | 48 | 10,98% | 38 | 35,51% | 38 | 35,85% | 38 | 35,85% |
Coomans (1967) | 31 | 7,09% | 10 | 9,35% | 10 | 9,43% | 10 | 9,43% |
Griffiths & Florens (2006) | 29 | 6,64% | 14 | 13,08% | 14 | 13,21% | 14 | 13,21% |
Massemin et al. (2009) | 29 | 6,64% | 18 | 16,82% | 18 | 16,98% | 18 | 16,98% |
Cowie (2000) | 16 | 3,66% | 10 | 9,35% | 10 | 9,43% | 10 | 9,43% |
Gargominy (2016-2021) | 16 | 3,66% | 14 | 13,08% | 14 | 13,21% | 14 | 13,21% |
UICN Comité français, OFB & MNHN (2021) | 15 | 3,43% | 13 | 12,15% | 13 | 12,26% | 13 | 12,26% |
Bouchet et al. (1991) | 14 | 3,2% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Jourdan et al. (2014) | 12 | 2,75% | 8 | 7,48% | 8 | 7,55% | 8 | 7,55% |
Pilsbry (1906-1907) | 12 | 2,75% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 12 | 2,75% | 6 | 5,61% | 6 | 5,66% | 6 | 5,66% |
Questel (2017) | 11 | 2,52% | 5 | 4,67% | 5 | 4,72% | 5 | 4,72% |
Solem (1961) | 10 | 2,29% | 8 | 7,48% | 8 | 7,55% | 8 | 7,55% |
Solem (1964) | 10 | 2,29% | 8 | 7,48% | 8 | 7,55% | 8 | 7,55% |
Pointier & Marquet (1990) | 9 | 2,06% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Brook (2010) | 8 | 1,83% | 4 | 3,74% | 4 | 3,77% | 4 | 3,77% |
Haynes (2001) | 7 | 1,6% | 4 | 3,74% | 4 | 3,77% | 4 | 3,77% |
Welter-schultes (2012) | 7 | 1,6% | 5 | 4,67% | 5 | 4,72% | 5 | 4,72% |
Yokoyama (2013) | 7 | 1,6% | 4 | 3,74% | 4 | 3,77% | 4 | 3,77% |
Drouët (1859) | 6 | 1,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (2011) | 6 | 1,37% | 6 | 5,61% | 6 | 5,66% | 6 | 5,66% |
Hausdorf (2023) | 6 | 1,37% | 6 | 5,61% | 6 | 5,66% | 6 | 5,66% |
Mary (2017) | 6 | 1,37% | 6 | 5,61% | 6 | 5,66% | 6 | 5,66% |
Abdou et al. (2004) | 5 | 1,14% | 3 | 2,8% | 3 | 2,83% | 3 | 2,83% |
Cooke (1934) | 5 | 1,14% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Falkner et al. (2002) | 5 | 1,14% | 4 | 3,74% | 4 | 3,77% | 4 | 3,77% |
Forcellini et al. (2012) | 5 | 1,14% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Grimpe & Hoffmann (1925) | 5 | 1,14% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Mousson (1872) | 5 | 1,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier (2001) | 5 | 1,14% | 3 | 2,8% | 3 | 2,83% | 3 | 2,83% |
Preece (1995) | 5 | 1,14% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Reeve (1873-1874) | 5 | 1,14% | 4 | 3,74% | 4 | 3,77% | 4 | 3,77% |
Gould (1852) | 4 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutton (1834) | 4 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1883) | 4 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 4 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1920-1921) | 4 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 4 | 0,92% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Baker (1927) | 3 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure (2016) | 3 | 0,69% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Charles (2016) | 3 | 0,69% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Deshayes (1863) | 3 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1827) | 3 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1824) | 3 | 0,69% | 3 | 2,8% | 3 | 2,83% | 3 | 2,83% |
Hausdorf (2007) | 3 | 0,69% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Jay et al. (2009) | 3 | 0,69% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Jourdan (2020) | 3 | 0,69% | 3 | 2,8% | 3 | 2,83% | 3 | 2,83% |
Potiez & Michaud (1835-1838) | 3 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1849) | 3 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Sowerby (1842-1887) | 3 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1935) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Baker (1923) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1926) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartsch (1942) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Binney (1841) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure et al. (2020) | 2 | 0,46% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Bruguière (1789-1792) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Charles (2014) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Clench (1964) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1867) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1874) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Deshayes (1834) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac & Deshayes (1820-51) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1822) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Fossati & Marquet (1998) | 2 | 0,46% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Gerber (2018) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Gould (1843) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Guppy (1878) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Jousseaume (1889) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Küster & Pfeiffer (1845-1855) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1890) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Moricand (1837) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1841) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1846) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1889-1890) | 2 | 0,46% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Pilsbry (1899) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1909-1910) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1916-1918) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Rang (1831) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Reise et al. (2011) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Robinson et al. (2009) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Salvador et al. (2023) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Say (1817) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Sowerby (1842) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Starmühlner (1976) | 2 | 0,46% | 2 | 1,87% | 2 | 1,89% | 2 | 1,89% |
Swainson (1840) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor (2003) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Tillier (1980) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Wetherby (1879) | 2 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Adams (1845) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Ancey (1892) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Arruda et al. (2016) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Audibert & Paillet (2014) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Baker (1941) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Baker (1961) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Benoit (1881) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Benson (1850) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1856) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1822) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (1994) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Christensen & Kahn (2017) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Clavier et al. (2010) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Cockerell (1901) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cooke (1928) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Crosse (1864) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Dunker (1848) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1821) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer (1868) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Bedoucha (1964) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontanilla et al. (2014) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Gargominy & Fontaine (2014) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Garrett (1879) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrett (1884) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1866) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomes & Thome (2004) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Gould (1859) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilding (1825) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf & Bermúdez (2003) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Huet (2023) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Johnson (1964) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourde et al. (2017) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Kadolsky (2012) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Kerney & Cameron (1999) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Lamarck (1816) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1819) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1822) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoble et al. (2018) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Lenoble et al. (2018) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Lenoble (2021) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lounnas et al. (2017) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Lowe et al. (2007) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lydeard et al. (2016) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelet (1851) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelet (1860) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Naggs (1989) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Naggs (1994) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Naudon et al. (2015) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Orbigny (1835) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1839) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1840) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1847) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1849) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1850) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1852) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1852) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Pfeiffer (1857) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1858) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1927-1935) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Blanc (1985) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Delay (1995) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Pointier & Théron (2006) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Pointier et al. (1998) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier et al. (2007) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Pointier (2008) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1844) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1998) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Rang (1834) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Récluz (1841) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Rocha & D'ávila (2019) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Saito et al. (2023) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Simroth (1918) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Singh et al. (2022) | 1 | 0,23% | 1 | 0,93% | 1 | 0,94% | 1 | 0,94% |
Solem (1959) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1970) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1922) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Vernhout (1914) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidigal et al. (2018) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Watters (2014) | 1 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |