Gastéropodes continentaux de Saint-Martin
135 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Hovestadt & Neckheim (2020) | 73 | 23,78% | 59 | 89,39% | 53 | 92,98% | 54 | 91,53% |
Delannoye et al. (2015) | 67 | 21,82% | 41 | 62,12% | 39 | 68,42% | 39 | 66,1% |
Coomans (1967) | 44 | 14,33% | 16 | 24,24% | 13 | 22,81% | 13 | 22,03% |
Bouchet & Pointier (1998) | 39 | 12,7% | 22 | 33,33% | 22 | 38,6% | 20 | 33,9% |
Lamy & Pointier (2018) | 22 | 7,17% | 20 | 30,3% | 20 | 35,09% | 20 | 33,9% |
Massemin et al. (2009) | 19 | 6,19% | 13 | 19,7% | 13 | 22,81% | 13 | 22,03% |
Bouchet et al. (1991) | 18 | 5,86% | 7 | 10,61% | 7 | 12,28% | 7 | 11,86% |
Griffiths & Florens (2006) | 15 | 4,89% | 7 | 10,61% | 7 | 12,28% | 7 | 11,86% |
Questel (2017) | 13 | 4,23% | 5 | 7,58% | 5 | 8,77% | 5 | 8,47% |
Questel (2020) | 13 | 4,23% | 7 | 10,61% | 7 | 12,28% | 7 | 11,86% |
Gargominy (2016-2021) | 12 | 3,91% | 11 | 16,67% | 11 | 19,3% | 11 | 18,64% |
Pilsbry (1906-1907) | 12 | 3,91% | 0 | 0% | 0 | 0% | 0 | 0% |
Cowie (2000) | 10 | 3,26% | 6 | 9,09% | 6 | 10,53% | 5 | 8,47% |
Jourdan et al. (2014) | 8 | 2,61% | 5 | 7,58% | 5 | 8,77% | 5 | 8,47% |
Brook (2010) | 7 | 2,28% | 4 | 6,06% | 4 | 7,02% | 3 | 5,08% |
Solem (1961) | 7 | 2,28% | 5 | 7,58% | 5 | 8,77% | 4 | 6,78% |
Solem (1964) | 7 | 2,28% | 5 | 7,58% | 5 | 8,77% | 4 | 6,78% |
Yokoyama (2013) | 7 | 2,28% | 4 | 6,06% | 4 | 7,02% | 4 | 6,78% |
Drouët (1859) | 6 | 1,95% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1883) | 6 | 1,95% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB & MNHN (2021) | 6 | 1,95% | 4 | 6,06% | 4 | 7,02% | 4 | 6,78% |
Mousson (1872) | 5 | 1,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Abdou et al. (2004) | 4 | 1,3% | 3 | 4,55% | 3 | 5,26% | 3 | 5,08% |
Gould (1852) | 4 | 1,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Haynes (2001) | 4 | 1,3% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Hutton (1834) | 4 | 1,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Mary (2017) | 4 | 1,3% | 4 | 6,06% | 4 | 7,02% | 4 | 6,78% |
Pointier & Marquet (1990) | 4 | 1,3% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Questel & Le Quellec (2012) | 4 | 1,3% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Baker (1927) | 3 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure (2016) | 3 | 0,98% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Cooke (1934) | 3 | 0,98% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Deshayes (1863) | 3 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1827) | 3 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
Grimpe & Hoffmann (1925) | 3 | 0,98% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Hausdorf (2023) | 3 | 0,98% | 3 | 4,55% | 3 | 5,26% | 3 | 5,08% |
Jay et al. (2009) | 3 | 0,98% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Pointier (2001) | 3 | 0,98% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Potiez & Michaud (1835-1838) | 3 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1995) | 3 | 0,98% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Reeve (1849) | 3 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1935) | 2 | 0,65% | 2 | 3,03% | 2 | 3,51% | 1 | 1,69% |
Baker (1923) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure et al. (2020) | 2 | 0,65% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Bruguière (1789-1792) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Clapp (1918) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Clench (1964) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1867) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Falkner et al. (2002) | 2 | 0,65% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Forcellini et al. (2012) | 2 | 0,65% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Fossati & Marquet (1998) | 2 | 0,65% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Gargominy et al. (2011) | 2 | 0,65% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Gerber (2018) | 2 | 0,65% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Gould (1843) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Guppy (1878) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Jousseaume (1889) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Küster & Pfeiffer (1845-1855) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1890) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1909-1910) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1916-1918) | 2 | 0,65% | 2 | 3,03% | 2 | 3,51% | 0 | 0% |
Pointier et al. (1977) | 2 | 0,65% | 2 | 3,03% | 2 | 3,51% | 2 | 3,39% |
Rang (1831) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1873-1874) | 2 | 0,65% | 1 | 1,52% | 1 | 1,75% | 0 | 0% |
Sowerby (1843) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1840) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor (2003) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Welter-schultes (2012) | 2 | 0,65% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Ancey (1892) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Arruda et al. (2016) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1961) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Benoit (1881) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1856) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1822) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (1994) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Charles (2016) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Christensen & Kahn (2017) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Clavier et al. (2010) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Cockerell (1901) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Cooke (1928) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Crosse (1874) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Férussac (1821) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer (1868) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Bedoucha (1964) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontanilla et al. (2014) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Gamiette et al. (2023) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy & Fontaine (2014) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Garrett (1879) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1866) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomes & Thome (2004) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Gould (1859) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilding (1824) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilding (1828) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Haas (1938) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf (2007) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Johnson (1964) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Kadolsky (2012) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Lenoble (2021) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1838) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Lydeard et al. (2016) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Naggs (1989) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Orbigny (1835) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulay & Brown (2019) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Pfeiffer (1840) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1846) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1849) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1850) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1852) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1858) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1899) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Blanc (1985) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Delay (1995) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Pointier & Théron (2006) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Pointier (1976) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1844) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Questel (2023) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Rang (1834) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvador et al. (2023) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Say (1817) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Simroth (1918) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Solem (1959) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1970) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1976) | 1 | 0,33% | 1 | 1,52% | 1 | 1,75% | 1 | 1,69% |
Tillier (1980) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Tillier (1981) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1922) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Vernhout (1914) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidigal et al. (2018) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Watters (2014) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |