Gastéropodes terrestres de Wallis-et-Futuna
90 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Jourdan et al. (2014) | 25 | 19,08% | 16 | 53,33% | 16 | 55,17% | 16 | 55,17% |
| Griffiths & Florens (2006) | 18 | 13,74% | 14 | 46,67% | 14 | 48,28% | 14 | 48,28% |
| Delannoye et al. (2015) | 17 | 12,98% | 10 | 33,33% | 10 | 34,48% | 10 | 34,48% |
| Cowie (2000) | 15 | 11,45% | 12 | 40% | 12 | 41,38% | 12 | 41,38% |
| Pilsbry (1906-1907) | 12 | 9,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hovestadt & Neckheim (2020) | 11 | 8,4% | 10 | 33,33% | 10 | 34,48% | 10 | 34,48% |
| Cooke (1934) | 10 | 7,63% | 3 | 10% | 3 | 10,34% | 3 | 10,34% |
| Garrett (1884) | 10 | 7,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brook (2010) | 9 | 6,87% | 7 | 23,33% | 7 | 24,14% | 7 | 24,14% |
| Cooke & Kondo (1961) | 8 | 6,11% | 4 | 13,33% | 4 | 13,79% | 4 | 13,79% |
| Preece (1995) | 8 | 6,11% | 4 | 13,33% | 4 | 13,79% | 4 | 13,79% |
| Solem (1961) | 8 | 6,11% | 6 | 20% | 6 | 20,69% | 6 | 20,69% |
| Gargominy (2016-2021) | 7 | 5,34% | 7 | 23,33% | 7 | 24,14% | 7 | 24,14% |
| Massemin et al. (2009) | 7 | 5,34% | 4 | 13,33% | 4 | 13,79% | 4 | 13,79% |
| Mousson (1871) | 7 | 5,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1998) | 7 | 5,34% | 4 | 13,33% | 4 | 13,79% | 4 | 13,79% |
| Solem (1964) | 7 | 5,34% | 7 | 23,33% | 7 | 24,14% | 7 | 24,14% |
| Abdou et al. (2004) | 6 | 4,58% | 4 | 13,33% | 4 | 13,79% | 4 | 13,79% |
| Bouchet & Pointier (1998) | 6 | 4,58% | 2 | 6,67% | 2 | 6,9% | 2 | 6,9% |
| Bouchet et al. (1991) | 6 | 4,58% | 2 | 6,67% | 2 | 6,9% | 2 | 6,9% |
| Garrett (1879) | 6 | 4,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry & Cooke (1915-1916) | 6 | 4,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1887) | 5 | 3,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2023) | 5 | 3,82% | 5 | 16,67% | 5 | 17,24% | 5 | 17,24% |
| Baker (1941) | 4 | 3,05% | 3 | 10% | 3 | 10,34% | 3 | 10,34% |
| Gould (1852) | 4 | 3,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutton (1834) | 4 | 3,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jay et al. (2009) | 4 | 3,05% | 3 | 10% | 3 | 10,34% | 3 | 10,34% |
| Pilsbry (1920-1921) | 4 | 3,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 4 | 3,05% | 3 | 10% | 3 | 10,34% | 3 | 10,34% |
| Solem (1983) | 4 | 3,05% | 4 | 13,33% | 3 | 10,34% | 3 | 10,34% |
| UICN Comité français, OFB & MNHN (2021) | 4 | 3,05% | 4 | 13,33% | 4 | 13,79% | 4 | 13,79% |
| Baker (1938) | 3 | 2,29% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Coomans (1967) | 3 | 2,29% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Férussac (1821) | 3 | 2,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2007) | 3 | 2,29% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Mousson (1869) | 3 | 2,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1861) | 3 | 2,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1865) | 3 | 2,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1916-1918) | 3 | 2,29% | 2 | 6,67% | 2 | 6,9% | 2 | 6,9% |
| Questel (2017) | 3 | 2,29% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Adamson (1935) | 2 | 1,53% | 2 | 6,67% | 2 | 6,9% | 2 | 6,9% |
| Clench (1964) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1863) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerlach (2016) | 2 | 1,53% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Goulding et al. (2023) | 2 | 1,53% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Johnson (1994) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 1,53% | 2 | 6,67% | 2 | 6,9% | 2 | 6,9% |
| Kirch (1973) | 2 | 1,53% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Liardet (1876) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 1,53% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Montrouzier (1859) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1870) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neubert & Gosteli (2003) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Odhner (1921) | 2 | 1,53% | 2 | 6,67% | 2 | 6,9% | 2 | 6,9% |
| Pease (1868) | 2 | 1,53% | 2 | 6,67% | 2 | 6,9% | 2 | 6,9% |
| Pease (1869) | 2 | 1,53% | 2 | 6,67% | 2 | 6,9% | 2 | 6,9% |
| Pease (1871) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rang (1831) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Solem (1959) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2013) | 2 | 1,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adams (1845) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1940) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1850) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boettger (1880) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1822) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruguière (1789-1792) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen & Kahn (2017) | 1 | 0,76% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Cooke (1928) | 1 | 0,76% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Fischer-piette & Bedoucha (1964) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilla et al. (2014) | 1 | 0,76% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Gamiette et al. (2023) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy (2007) | 1 | 0,76% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Gassies (1866) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1846) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1847) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Möllendorf (1888) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1865) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naggs (1989) | 1 | 0,76% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Naggs (1994) | 1 | 0,76% | 1 | 3,33% | 1 | 3,45% | 1 | 3,45% |
| Orbigny (1835) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1840) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1846) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1868) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry & Hirase (1904) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1927-1935) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Blanc (1985) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1849) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shuttleworth (1852) | 1 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
