Foraminifères de Polynésie française
118 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Vénec-Peyré (1985) | 186 | 21,93% | 147 | 44,68% | 147 | 44,68% | 147 | 44,68% |
Debenay & Cabioch (2007) | 177 | 20,87% | 125 | 37,99% | 125 | 37,99% | 125 | 37,99% |
Guilcher et al. (1965) | 109 | 12,85% | 66 | 20,06% | 66 | 20,06% | 66 | 20,06% |
Debenay (2013) | 65 | 7,67% | 48 | 14,59% | 48 | 14,59% | 48 | 14,59% |
Langer & Lipps (2006) | 42 | 4,95% | 28 | 8,51% | 28 | 8,51% | 28 | 8,51% |
Natural History Museum of London (2020) | 16 | 1,89% | 7 | 2,13% | 7 | 2,13% | 7 | 2,13% |
Bicchi et al. (2002) | 15 | 1,77% | 12 | 3,65% | 12 | 3,65% | 12 | 3,65% |
Arnaud (1974) | 13 | 1,53% | 9 | 2,74% | 9 | 2,74% | 9 | 2,74% |
Fajemila et al. (2015) | 11 | 1,3% | 10 | 3,04% | 10 | 3,04% | 10 | 3,04% |
Cabioch et al. (2008) | 10 | 1,18% | 8 | 2,43% | 8 | 2,43% | 8 | 2,43% |
Rowlands (2007) | 10 | 1,18% | 8 | 2,43% | 8 | 2,43% | 8 | 2,43% |
Brady (1884) | 9 | 1,06% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Cushman (1933) | 9 | 1,06% | 9 | 2,74% | 9 | 2,74% | 9 | 2,74% |
Vénec-Peyré (1985) | 9 | 1,06% | 5 | 1,52% | 5 | 1,52% | 5 | 1,52% |
Zinke et al. (2005) | 9 | 1,06% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Blanc-Vernet (1965) | 8 | 0,94% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Cushman (1934) | 8 | 0,94% | 8 | 2,43% | 8 | 2,43% | 8 | 2,43% |
Loeblich & Tappan (1994) | 8 | 0,94% | 7 | 2,13% | 7 | 2,13% | 7 | 2,13% |
Belasky (1996) | 6 | 0,71% | 6 | 1,82% | 6 | 1,82% | 6 | 1,82% |
Cushman (1922) | 6 | 0,71% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Parker & Gischler (2021) | 6 | 0,71% | 5 | 1,52% | 5 | 1,52% | 5 | 1,52% |
Q. J. Micr. Sci. (n.s.), xix: pp. 20 & 261.">Brady (1879) | 5 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1925) | 5 | 0,59% | 3 | 0,91% | 3 | 0,91% | 3 | 0,91% |
Mgnify (2018) | 5 | 0,59% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Vasseur (1985) | 5 | 0,59% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Vénec-Peyré (1991) | 5 | 0,59% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Mcculloch (1977) | 4 | 0,47% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Pecheux (1996) | 4 | 0,47% | 3 | 0,91% | 3 | 0,91% | 3 | 0,91% |
Said (1949) | 4 | 0,47% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Vénec-Peyré & Salvat (1981) | 4 | 0,47% | 3 | 0,91% | 3 | 0,91% | 3 | 0,91% |
Vénec-Peyré (1988) | 4 | 0,47% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Quarterly Journal of Microscopical Science, XXl: 31-71.">Brady (1881) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1915) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin de la Societe Zoologique de France, 38: 260-271.">Fauré-Fremiet (1913) | 3 | 0,35% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Sellier & Civrieux (1977) | 3 | 0,35% | 3 | 0,91% | 3 | 0,91% | 3 | 0,91% |
Vella (1957) | 3 | 0,35% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Calvez & Calvey (1958) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Collins (1958) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Todd (1944) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Cushman (1911) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Cushman (1925) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Bulletin United States National Museum, 161: 1-84.">Cushman (1932) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1946) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Gout (1991) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Hayward et al. (2021) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Heron-allen & Earland (1915) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Larsen (1976) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Loeblich & Tappan (1988) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Margerel (1982) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Parr (1945) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Parr (1950) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Perelis & Reiss (1975) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Ponder (1972) | 2 | 0,24% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Rhumbler (1906) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 2 | 0,24% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Sellier & Civrieux (1976) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Albani (1974) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Asano (1951) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Asano (1951) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1927) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Belford (1966) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Bermudez (1952) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Bourcier (1988) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Brady (1884) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Carter (1877) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Chapman & Part (1937) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapman (1900) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevaldonné et al. (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Collins (1974) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Cooke & Cushman (1922) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Bronni-mann (1948) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Cushman & Mcculloch (1942) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Cushman (1917) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1921) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1921) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Cushman (1923) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1926) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1929) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1929) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1944) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Earland (1933) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Abhandlungen der Bayerischen Akademie, xviii(No. 2): pp. 195-458.">Egger (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehrenberg (1839) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Förderer et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Gmelin (1791) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Hayward & Brazier (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hayward (1990) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Hess et al. (2005) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1940) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Langer (1992) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Linnaeus (1758) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lloyd (1967) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mamo (2016) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Montfort de Denys (1808) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Pallas (1766) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Parr (1932) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Phleger (1951) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Prenant (1927) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reuss (1850) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reuss (1863) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Richer de Forges et al. (2005) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Saidova (1975) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Seiglie & Bennudez (1965) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Sidebottom (1905) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Sidebottom (1908) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Sidebottom (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Journal of the Royal Microscopical Society London, 1918: (1-25 122-152 249-264).">Sidebottom (1918) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Smitter (1955) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Teruem (1878) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Todd (1956) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Uchio (1952) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Williamson (1868) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Zheng et al. (1978) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Zheng (1979) | 1 | 0,12% | 1 | 0,3% | 1 | 0,3% | 1 | 0,3% |
Zheng (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |