Gastéropodes continentaux de Nouvelle-Calédonie
201 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Solem (1961) | 221 | 22,48% | 145 | 42,65% | 144 | 44,72% | 140 | 42,04% |
| Neubert et al. (2009) | 159 | 16,17% | 25 | 7,35% | 10 | 3,11% | 21 | 6,31% |
| Pawlowska-Banasiak (2008) | 93 | 9,46% | 88 | 25,88% | 88 | 27,33% | 88 | 26,43% |
| Haase & Bouchet (1998) | 56 | 5,7% | 51 | 15% | 51 | 15,84% | 51 | 15,32% |
| Richling (2009) | 36 | 3,66% | 18 | 5,29% | 18 | 5,59% | 18 | 5,41% |
| Solem (1964) | 36 | 3,66% | 23 | 6,76% | 23 | 7,14% | 23 | 6,91% |
| Griffiths & Florens (2006) | 34 | 3,46% | 18 | 5,29% | 18 | 5,59% | 18 | 5,41% |
| Grimpe & Hoffmann (1925) | 24 | 2,44% | 15 | 4,41% | 15 | 4,66% | 15 | 4,5% |
| Cowie (2000) | 22 | 2,24% | 16 | 4,71% | 16 | 4,97% | 16 | 4,8% |
| Delannoye et al. (2015) | 20 | 2,03% | 14 | 4,12% | 14 | 4,35% | 14 | 4,2% |
| Crosse (1874) | 19 | 1,93% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Mary (2017) | 19 | 1,93% | 12 | 3,53% | 12 | 3,73% | 12 | 3,6% |
| Crosse (1870) | 18 | 1,83% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 17 | 1,73% | 9 | 2,65% | 9 | 2,8% | 9 | 2,7% |
| Crosse (1868) | 16 | 1,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2013) | 16 | 1,63% | 10 | 2,94% | 10 | 3,11% | 10 | 3% |
| Tillier (1981) | 16 | 1,63% | 16 | 4,71% | 16 | 4,97% | 15 | 4,5% |
| Crosse (1870) | 14 | 1,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hovestadt & Neckheim (2020) | 14 | 1,42% | 13 | 3,82% | 13 | 4,04% | 13 | 3,9% |
| Jourdan et al. (2014) | 13 | 1,32% | 10 | 2,94% | 10 | 3,11% | 10 | 3% |
| Brook (2010) | 12 | 1,22% | 6 | 1,76% | 6 | 1,86% | 5 | 1,5% |
| Crosse (1855) | 12 | 1,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1884) | 12 | 1,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Franc (1956) | 11 | 1,12% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| Pilsbry (1906-1907) | 11 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1874) | 10 | 1,02% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Haase & Zielske (2015) | 10 | 1,02% | 10 | 2,94% | 10 | 3,11% | 10 | 3% |
| Gassies (1863) | 9 | 0,92% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Mordan & Tillier (1986) | 9 | 0,92% | 9 | 2,65% | 9 | 2,8% | 9 | 2,7% |
| Tillier & Mordan (1995) | 9 | 0,92% | 5 | 1,47% | 5 | 1,55% | 5 | 1,5% |
| Bouchet & Pointier (1998) | 8 | 0,81% | 3 | 0,88% | 3 | 0,93% | 3 | 0,9% |
| Cooke (1934) | 8 | 0,81% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Crosse (1868) | 8 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1871) | 8 | 0,81% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Jourdan (2020) | 8 | 0,81% | 8 | 2,35% | 8 | 2,48% | 8 | 2,4% |
| Preston (1907) | 8 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1874) | 7 | 0,71% | 0 | 0% | 0 | 0% | 0 | 0% |
| Falkner et al. (2002) | 7 | 0,71% | 5 | 1,47% | 5 | 1,55% | 5 | 1,5% |
| Gargominy et al. (2011) | 7 | 0,71% | 7 | 2,06% | 7 | 2,17% | 7 | 2,1% |
| Garrett (1887) | 7 | 0,71% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welter-schultes (2012) | 7 | 0,71% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| Abdou et al. (2004) | 6 | 0,61% | 3 | 0,88% | 3 | 0,93% | 3 | 0,9% |
| Baker (1938) | 6 | 0,61% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| Dautzenberg (1923) | 6 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1852) | 6 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jay et al. (2009) | 6 | 0,61% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| Lamy & Pointier (2018) | 6 | 0,61% | 3 | 0,88% | 3 | 0,93% | 3 | 0,9% |
| Massemin et al. (2009) | 6 | 0,61% | 3 | 0,88% | 3 | 0,93% | 3 | 0,9% |
| Montrouzier (1859) | 6 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1850) | 6 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souverbie (1860) | 6 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1894) | 5 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1880) | 5 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haynes (2001) | 5 | 0,51% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Jourdan & Mille (2006) | 5 | 0,51% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Mousson (1872) | 5 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1916-1918) | 5 | 0,51% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| Pointier & Marquet (1990) | 5 | 0,51% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Questel (2020) | 5 | 0,51% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| UICN Comité français, OFB & MNHN (2021) | 5 | 0,51% | 5 | 1,47% | 5 | 1,55% | 5 | 1,5% |
| Zielske & Haase (2015) | 5 | 0,51% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| Adamson (1935) | 4 | 0,41% | 3 | 0,88% | 3 | 0,93% | 3 | 0,9% |
| Bouchet et al. (1991) | 4 | 0,41% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Coomans (1967) | 4 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1867) | 4 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1872) | 4 | 0,41% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Forcellini et al. (2012) | 4 | 0,41% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Gargominy (2016-2021) | 4 | 0,41% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| Gassies (1857) | 4 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2023) | 4 | 0,41% | 4 | 1,18% | 4 | 1,24% | 4 | 1,2% |
| Müller (1774) | 4 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1901-1902) | 4 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1920-1921) | 4 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1995) | 4 | 0,41% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Abdou et al. (2019) | 3 | 0,31% | 3 | 0,88% | 3 | 0,93% | 3 | 0,9% |
| Crosse (1870) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1871) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deshayes (1863) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1821) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1879) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1858) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1866) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerber (2018) | 3 | 0,31% | 3 | 0,88% | 3 | 0,93% | 3 | 0,9% |
| Hausdorf (2007) | 3 | 0,31% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Kerney & Cameron (1999) | 3 | 0,31% | 3 | 0,88% | 3 | 0,93% | 3 | 0,9% |
| Monterosato (1892) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preece (1998) | 3 | 0,31% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Questel (2017) | 3 | 0,31% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Solem (1959) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souverbie (1859) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Trewick et al. (2009) | 3 | 0,31% | 3 | 0,88% | 3 | 0,93% | 1 | 0,3% |
| Yokoyama (2013) | 3 | 0,31% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Abdou (2021) | 2 | 0,2% | 2 | 0,59% | 1 | 0,31% | 1 | 0,3% |
| Baker (1941) | 2 | 0,2% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Binney (1841) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Kondo (1961) | 2 | 0,2% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Crosse & Marie (1867) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1805) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupouy (1966) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1822) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1827) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1868) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fossati & Marquet (1998) | 2 | 0,2% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Gargominy (2011-2023) | 2 | 0,2% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Gassies (1867) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1874) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gomes & Thome (2004) | 2 | 0,2% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Gould (1843) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1846) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gude (1900) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley (1898) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutton (1834) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hyman & Ponder (2010) | 2 | 0,2% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Johnson (1994) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 0,2% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Marie (1870) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1865) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neiber & Glaubrecht (2018) | 2 | 0,2% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Neubert & Gosteli (2003) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pain (1958) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1865) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1869) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1869) | 2 | 0,2% | 2 | 0,59% | 2 | 0,62% | 2 | 0,6% |
| Pease (1871) | 2 | 0,2% | 1 | 0,29% | 1 | 0,31% | 0 | 0% |
| Pfeiffer (1846) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry & Cooke (1915-1916) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1909-1910) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier (2001) | 2 | 0,2% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Questel & Le Quellec (2012) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Récluz (1842) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1851-1854) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reise et al. (2011) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richling (2017) | 2 | 0,2% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Solem (1960) | 2 | 0,2% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Souverbie (1863) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson (1840) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor (2003) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tröndlé & Boutet (2009) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adams (1845) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ancey (1892) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1940) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beltramino et al. (2018) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Benoit (1881) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benson (1850) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boettger (1880) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1856) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowdich (1822) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brown (1994) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruguière (1789-1792) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cockerell (1901) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke (1928) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Cowie et al. (2009) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Cowie (1998) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse & Fischer (1870) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1868) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosse (1872) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Crosse (1887) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deuss et al. (2013) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Fischer-piette & Bedoucha (1964) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilla et al. (2014) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Gargominy & Fontaine (2014) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Gargominy (2007) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Garrett (1881) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gassies (1869) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gould (1859) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guiller & Madec (2010) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Johnson (1964) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Kaiser (2009) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kirch (1973) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Letacq (1924) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lounnas et al. (2017) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Lovenburg (2009) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Lydeard et al. (2016) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1883) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mousson (1869) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naudon et al. (2015) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Neubert & Gosteli (2005) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orbigny (1835) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1861) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pease (1861) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1850) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1860) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pfeiffer (1868) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1927-1935) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Blanc (1985) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pointier & Delay (1995) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Pointier et al. (2007) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Questel (2014) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Reeve (1849) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1873-1874) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salles et al. (2018) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Say (1817) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherpa et al. (2018) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Shuttleworth (1852) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simroth (1918) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1976) | 1 | 0,1% | 1 | 0,29% | 1 | 0,31% | 1 | 0,3% |
| Tryon (1886) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vandel (1922) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
