Gastéropodes continentaux de Saint-Barthélemy
109 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) | 42 | 23,46% | 30 | 93,75% | 30 | 96,77% | 27 | 87,1% |
Delannoye et al. (2015) | 37 | 20,67% | 19 | 59,38% | 19 | 61,29% | 17 | 54,84% |
Coomans (1967) | 23 | 12,85% | 4 | 12,5% | 4 | 12,9% | 4 | 12,9% |
Bouchet & Pointier (1998) | 22 | 12,29% | 10 | 31,25% | 10 | 32,26% | 10 | 32,26% |
Griffiths & Florens (2006) | 21 | 11,73% | 10 | 31,25% | 10 | 32,26% | 10 | 32,26% |
Questel (2020) | 15 | 8,38% | 9 | 28,12% | 8 | 25,81% | 9 | 29,03% |
Bouchet et al. (1991) | 14 | 7,82% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Questel (2017) | 14 | 7,82% | 8 | 25% | 6 | 19,35% | 8 | 25,81% |
Pilsbry (1906-1907) | 12 | 6,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamy & Pointier (2018) | 11 | 6,15% | 9 | 28,12% | 9 | 29,03% | 9 | 29,03% |
Cowie (2000) | 10 | 5,59% | 7 | 21,88% | 7 | 22,58% | 7 | 22,58% |
Massemin et al. (2009) | 10 | 5,59% | 7 | 21,88% | 7 | 22,58% | 7 | 22,58% |
Jourdan et al. (2014) | 8 | 4,47% | 5 | 15,62% | 5 | 16,13% | 5 | 16,13% |
Solem (1961) | 8 | 4,47% | 5 | 15,62% | 5 | 16,13% | 5 | 16,13% |
Solem (1964) | 8 | 4,47% | 6 | 18,75% | 6 | 19,35% | 6 | 19,35% |
Gargominy (2016-2021) | 7 | 3,91% | 7 | 21,88% | 7 | 22,58% | 7 | 22,58% |
Yokoyama (2013) | 6 | 3,35% | 3 | 9,38% | 3 | 9,68% | 3 | 9,68% |
Abdou et al. (2004) | 5 | 2,79% | 4 | 12,5% | 4 | 12,9% | 4 | 12,9% |
Brook (2010) | 5 | 2,79% | 4 | 12,5% | 4 | 12,9% | 4 | 12,9% |
Jay et al. (2009) | 5 | 2,79% | 3 | 9,38% | 3 | 9,68% | 3 | 9,68% |
Mousson (1872) | 5 | 2,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 5 | 2,79% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
UICN Comité français, OFB & MNHN (2021) | 5 | 2,79% | 4 | 12,5% | 4 | 12,9% | 4 | 12,9% |
Falkner et al. (2002) | 4 | 2,23% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Gould (1852) | 4 | 2,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Haynes (2001) | 4 | 2,23% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Hutton (1834) | 4 | 2,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Mary (2017) | 4 | 2,23% | 4 | 12,5% | 4 | 12,9% | 4 | 12,9% |
Pointier & Marquet (1990) | 4 | 2,23% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Baker (1927) | 3 | 1,68% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure (2016) | 3 | 1,68% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Cooke (1934) | 3 | 1,68% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Deshayes (1863) | 3 | 1,68% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (2011) | 3 | 1,68% | 3 | 9,38% | 3 | 9,68% | 3 | 9,68% |
Monterosato (1892) | 3 | 1,68% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier (2001) | 3 | 1,68% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Preece (1995) | 3 | 1,68% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Reeve (1849) | 3 | 1,68% | 0 | 0% | 0 | 0% | 0 | 0% |
Welter-schultes (2012) | 3 | 1,68% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Adamson (1935) | 2 | 1,12% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Baker (1923) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Breure et al. (2020) | 2 | 1,12% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Bruguière (1789-1792) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Clench (1964) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1867) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1821) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1827) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcellini et al. (2012) | 2 | 1,12% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Fossati & Marquet (1998) | 2 | 1,12% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Gerber (2018) | 2 | 1,12% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Gould (1843) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf (2023) | 2 | 1,12% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Jousseaume (1889) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Küster & Pfeiffer (1845-1855) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1883) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1899) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1909-1910) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1916-1918) | 2 | 1,12% | 2 | 6,25% | 2 | 6,45% | 2 | 6,45% |
Potiez & Michaud (1835-1838) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Rang (1831) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1840) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor (2003) | 2 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ancey (1892) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1961) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Benoit (1881) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1856) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1822) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (1994) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Charles (2016) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Christensen & Kahn (2017) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Cooke (1928) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Deuss et al. (2013) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Fischer-piette & Bedoucha (1964) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontanilla et al. (2014) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Gargominy & Fontaine (2014) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Gargominy (2011-2023) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Garrett (1879) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1866) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1859) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiller & Madec (2010) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Johnson (1964) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Kadolsky (2012) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Kerney & Cameron (1999) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Lenoble (2021) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Lydeard et al. (2016) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1890) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Naggs (1989) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Orbigny (1835) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1840) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1846) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1850) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1852) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1858) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Blanc (1985) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Delay (1995) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Potiez & Michaud (1844) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Salvador et al. (2023) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Sherpa et al. (2018) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Starmühlner (1970) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1976) | 1 | 0,56% | 1 | 3,12% | 1 | 3,23% | 1 | 3,23% |
Vandel (1922) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Vernhout (1914) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Watters (2014) | 1 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |