Foraminifères de Mayotte
84 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Guilcher et al. (1965) | 250 | 34,11% | 147 | 54,85% | 143 | 54,17% | 146 | 55,09% |
| Debenay & Cabioch (2007) | 167 | 22,78% | 113 | 42,16% | 113 | 42,8% | 112 | 42,26% |
| Vénec-Peyré (1985) | 101 | 13,78% | 78 | 29,1% | 78 | 29,55% | 77 | 29,06% |
| Debenay (2013) | 58 | 7,91% | 42 | 15,67% | 42 | 15,91% | 41 | 15,47% |
| Brady (1884) | 11 | 1,5% | 2 | 0,75% | 2 | 0,76% | 2 | 0,75% |
| Zinke et al. (2005) | 11 | 1,5% | 6 | 2,24% | 6 | 2,27% | 6 | 2,26% |
| Arnaud (1974) | 9 | 1,23% | 8 | 2,99% | 8 | 3,03% | 8 | 3,02% |
| Bicchi et al. (2002) | 8 | 1,09% | 6 | 2,24% | 6 | 2,27% | 6 | 2,26% |
| Blanc-Vernet (1965) | 7 | 0,95% | 4 | 1,49% | 4 | 1,52% | 4 | 1,51% |
| Q. J. Micr. Sci. (n.s.), xix: pp. 20 & 261.">Brady (1879) | 6 | 0,82% | 1 | 0,37% | 1 | 0,38% | 0 | 0% |
| Langer & Lipps (2006) | 6 | 0,82% | 4 | 1,49% | 4 | 1,52% | 4 | 1,51% |
| Cabioch et al. (2008) | 5 | 0,68% | 3 | 1,12% | 3 | 1,14% | 3 | 1,13% |
| Bulletin United States National Museum, 161: 1-84.">Cushman (1932) | 5 | 0,68% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Cushman (1911) | 4 | 0,55% | 2 | 0,75% | 2 | 0,76% | 2 | 0,75% |
| Cushman (1915) | 4 | 0,55% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Cushman (1921) | 4 | 0,55% | 3 | 1,12% | 3 | 1,14% | 2 | 0,75% |
| Cushman (1922) | 4 | 0,55% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Gout (1991) | 3 | 0,41% | 3 | 1,12% | 3 | 1,14% | 3 | 1,13% |
| Linnaeus (1758) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quarterly Journal of Microscopical Science, XXl: 31-71.">Brady (1881) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Todd (1944) | 2 | 0,27% | 2 | 0,75% | 2 | 0,76% | 2 | 0,75% |
| Cushman et al. (1954) | 2 | 0,27% | 1 | 0,37% | 0 | 0% | 1 | 0,38% |
| Cushman (1925) | 2 | 0,27% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Bulletin de la Societe Zoologique de France, 38: 260-271.">Fauré-Fremiet (1913) | 2 | 0,27% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Heron-allen & Earland (1915) | 2 | 0,27% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Hodgkinson (1992) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loeblich & Tappan (1988) | 2 | 0,27% | 2 | 0,75% | 2 | 0,76% | 2 | 0,75% |
| Mamo (2016) | 2 | 0,27% | 2 | 0,75% | 2 | 0,76% | 2 | 0,75% |
| Revets (1996) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Todd (1956) | 2 | 0,27% | 2 | 0,75% | 2 | 0,76% | 2 | 0,75% |
| Vénec-Peyré & Salvat (1981) | 2 | 0,27% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Vénec-Peyré (1991) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Asano (1951) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brady (1876) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Brady (1884) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1876) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1877) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chapman (1900) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chapman (1902) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Chapman (1907) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Cushman (1922) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Mcculloch (1939) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Cushman & Mcculloch (1940) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Cushman & Mcculloch (1948) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Cushman (1913) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Cushman (1923) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Cushman (1925) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1926) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1929) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1929) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1933) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Cushman (1946) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abhandlungen der Bayerischen Akademie, xviii(No. 2): pp. 195-458.">Egger (1893) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ehrenberg (1839) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Fajemila et al. (2015) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Förderer et al. (2018) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Heron-allen & Earland (1913) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heron-Allen & Earland (1928) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heron-allen & Earland (1932) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hess et al. (2005) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2009) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Karrer (1868) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Loeblich & Tappan (1994) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| MGnify (2017) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Mgnify (2018) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millett (190O) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Möbius (1880) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Natural History Museum of London (2020) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parr (1932) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Parr (1945) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Parr (1950) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pecheux (1996) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Reuss (1850) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richer de Forges et al. (2005) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Rignault & Chevallier (2017) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Rowlands (2007) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Journal of the Royal Microscopical Society London, 1918: (1-25 122-152 249-264).">Sidebottom (1918) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Teruem (1878) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vasseur (1985) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vénec-Peyré (1985) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
| Wallich (1877) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiesner (1923) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiesner (1931) | 1 | 0,14% | 1 | 0,37% | 0 | 0% | 1 | 0,38% |
| Williamson (1848) | 1 | 0,14% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |