Gastéropodes terrestres de Nouvelle-Calédonie
Gastropoda de Nouvelle-Calédonie
170 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) | 201 | 24,63% | 129 | 52,23% | 128 | 55,41% | 125 | 51,65% |
Neubert et al. (2009) | 159 | 19,49% | 25 | 10,12% | 10 | 4,33% | 21 | 8,68% |
Pawlowska-Banasiak (2008) | 93 | 11,4% | 88 | 35,63% | 88 | 38,1% | 88 | 36,36% |
Richling (2009) | 36 | 4,41% | 18 | 7,29% | 18 | 7,79% | 18 | 7,44% |
Solem (1964) | 30 | 3,68% | 21 | 8,5% | 21 | 9,09% | 21 | 8,68% |
Grimpe & Hoffmann (1925) | 24 | 2,94% | 15 | 6,07% | 15 | 6,49% | 15 | 6,2% |
Griffiths & Florens (2006) | 23 | 2,82% | 16 | 6,48% | 16 | 6,93% | 16 | 6,61% |
Cowie (2000) | 19 | 2,33% | 15 | 6,07% | 15 | 6,49% | 15 | 6,2% |
Crosse (1870) | 18 | 2,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1874) | 17 | 2,08% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Crosse (1868) | 16 | 1,96% | 0 | 0% | 0 | 0% | 0 | 0% |
Delannoye et al. (2015) | 16 | 1,96% | 12 | 4,86% | 12 | 5,19% | 12 | 4,96% |
Hausdorf (2013) | 16 | 1,96% | 10 | 4,05% | 10 | 4,33% | 10 | 4,13% |
Tillier (1981) | 16 | 1,96% | 16 | 6,48% | 16 | 6,93% | 16 | 6,61% |
Crosse (1870) | 14 | 1,72% | 0 | 0% | 0 | 0% | 0 | 0% |
Brook (2010) | 13 | 1,59% | 7 | 2,83% | 7 | 3,03% | 6 | 2,48% |
Garrett (1884) | 13 | 1,59% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Crosse (1855) | 12 | 1,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Hovestadt & Neckheim (2020) | 12 | 1,47% | 11 | 4,45% | 11 | 4,76% | 11 | 4,55% |
Jourdan et al. (2014) | 11 | 1,35% | 9 | 3,64% | 9 | 3,9% | 9 | 3,72% |
Pilsbry (1906-1907) | 11 | 1,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Franc (1956) | 10 | 1,23% | 5 | 2,02% | 5 | 2,16% | 5 | 2,07% |
Mordan & Tillier (1986) | 9 | 1,1% | 9 | 3,64% | 9 | 3,9% | 9 | 3,72% |
Tillier & Mordan (1995) | 9 | 1,1% | 5 | 2,02% | 5 | 2,16% | 5 | 2,07% |
Cooke (1934) | 8 | 0,98% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Crosse (1868) | 8 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1871) | 8 | 0,98% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Preston (1907) | 8 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrett (1887) | 7 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1863) | 7 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Jay et al. (2009) | 7 | 0,86% | 4 | 1,62% | 4 | 1,73% | 4 | 1,65% |
Abdou et al. (2004) | 6 | 0,74% | 3 | 1,21% | 3 | 1,3% | 3 | 1,24% |
Baker (1938) | 6 | 0,74% | 4 | 1,62% | 4 | 1,73% | 4 | 1,65% |
Bouchet & Pointier (1998) | 6 | 0,74% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Crosse (1874) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Dautzenberg (1923) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1874) | 6 | 0,74% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Jourdan (2020) | 6 | 0,74% | 6 | 2,43% | 6 | 2,6% | 6 | 2,48% |
Montrouzier (1859) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Souverbie (1860) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1880) | 5 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1916-1918) | 5 | 0,61% | 4 | 1,62% | 4 | 1,73% | 4 | 1,65% |
UICN Comité français, OFB & MNHN (2021) | 5 | 0,61% | 5 | 2,02% | 5 | 2,16% | 5 | 2,07% |
Adamson (1935) | 4 | 0,49% | 3 | 1,21% | 3 | 1,3% | 3 | 1,24% |
Bouchet et al. (1991) | 4 | 0,49% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Crosse (1867) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1894) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Falkner et al. (2002) | 4 | 0,49% | 3 | 1,21% | 3 | 1,3% | 3 | 1,24% |
Gargominy (2016-2021) | 4 | 0,49% | 4 | 1,62% | 4 | 1,73% | 4 | 1,65% |
Gassies (1857) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1852) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf (2023) | 4 | 0,49% | 4 | 1,62% | 4 | 1,73% | 4 | 1,65% |
Massemin et al. (2009) | 4 | 0,49% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Pilsbry (1901-1902) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1920-1921) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1995) | 4 | 0,49% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Welter-schultes (2012) | 4 | 0,49% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Coomans (1967) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1870) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1821) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (2011) | 3 | 0,37% | 3 | 1,21% | 3 | 1,3% | 3 | 1,24% |
Garrett (1879) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1858) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1866) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausdorf (2007) | 3 | 0,37% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Jourdan & Mille (2006) | 3 | 0,37% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Kerney & Cameron (1999) | 3 | 0,37% | 3 | 1,21% | 3 | 1,3% | 3 | 1,24% |
Monterosato (1892) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1998) | 3 | 0,37% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Questel (2017) | 3 | 0,37% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Questel (2020) | 3 | 0,37% | 3 | 1,21% | 3 | 1,3% | 3 | 1,24% |
Solem (1959) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Souverbie (1859) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Trewick et al. (2009) | 3 | 0,37% | 3 | 1,21% | 3 | 1,3% | 1 | 0,41% |
Baker (1941) | 2 | 0,25% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Binney (1841) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Cooke & Kondo (1961) | 2 | 0,25% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Crosse & Marie (1867) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1871) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Deshayes (1863) | 2 | 0,25% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Dupouy (1966) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1822) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer (1868) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy (2011-2023) | 2 | 0,25% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Gassies (1867) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1874) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomes & Thome (2004) | 2 | 0,25% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Gould (1843) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gude (1900) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley (1898) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Houart (1991) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutton (1834) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Hyman & Ponder (2010) | 2 | 0,25% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Johnson (1994) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 2 | 0,25% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Marie (1870) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Martins (1995) | 2 | 0,25% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Mousson (1865) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Neubert & Gosteli (2003) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pain (1958) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1865) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1869) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1869) | 2 | 0,25% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Pease (1871) | 2 | 0,25% | 1 | 0,4% | 1 | 0,43% | 0 | 0% |
Pfeiffer (1846) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry & Cooke (1915-1916) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1909-1910) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1851-1854) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Reise et al. (2011) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Richling (2017) | 2 | 0,25% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Solem (1960) | 2 | 0,25% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Souverbie (1863) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1970) | 2 | 0,25% | 2 | 0,81% | 2 | 0,87% | 2 | 0,83% |
Swainson (1840) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Tröndlé & Boutet (2009) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 2 | 0,25% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Adams (1845) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ancey (1892) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1940) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Beltramino et al. (2018) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Benson (1850) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Boettger (1880) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchet et al. (2008) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1822) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruguière (1789-1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabaret et al. (1986) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cockerell (1901) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cooke (1928) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Cowie et al. (2009) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Cowie (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse & Fischer (1870) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1868) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Fischer-piette & Bedoucha (1964) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontanilla et al. (2014) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Gamiette et al. (2023) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy & Fontaine (2014) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Gargominy (2007) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Garrett (1881) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1869) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiller & Madec (2010) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Haase & Bouchet (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Houart et al. (2021) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Kaiser (2009) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirch (1973) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Letacq (1924) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lovenburg (2009) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Mousson (1869) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Naudon et al. (2015) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Neubert & Gosteli (2005) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Orbigny (1835) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1850) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1860) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1868) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1927-1935) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Blanc (1985) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1849) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1873-1874) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Salles et al. (2018) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Sherpa et al. (2018) | 1 | 0,12% | 1 | 0,4% | 1 | 0,43% | 1 | 0,41% |
Shuttleworth (1852) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Simroth (1918) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Tryon (1886) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |