Foraminifères
Foraminifera
276 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Debenay (2013) | 634 | 19,97% | 516 | 37,94% | 514 | 38,07% | 513 | 37,94% |
| Debenay & Cabioch (2007) | 508 | 16,01% | 351 | 25,81% | 350 | 25,93% | 350 | 25,89% |
| Guilcher et al. (1965) | 250 | 7,88% | 147 | 10,81% | 143 | 10,59% | 146 | 10,8% |
| Vénec-Peyré (1985) | 186 | 5,86% | 147 | 10,81% | 147 | 10,89% | 145 | 10,72% |
| Arnaud (1974) | 74 | 2,33% | 48 | 3,53% | 48 | 3,56% | 48 | 3,55% |
| Mcculloch (1977) | 66 | 2,08% | 38 | 2,79% | 37 | 2,74% | 37 | 2,74% |
| Blanc-Vernet (1965) | 54 | 1,7% | 34 | 2,5% | 34 | 2,52% | 34 | 2,51% |
| Langer & Lipps (2006) | 42 | 1,32% | 28 | 2,06% | 28 | 2,07% | 28 | 2,07% |
| Loeblich & Tappan (1994) | 36 | 1,13% | 29 | 2,13% | 29 | 2,15% | 29 | 2,14% |
| Hess et al. (2005) | 34 | 1,07% | 22 | 1,62% | 22 | 1,63% | 22 | 1,63% |
| Brady (1884) | 31 | 0,98% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Q. J. Micr. Sci. (n.s.), xix: pp. 20 & 261.">Brady (1879) | 27 | 0,85% | 11 | 0,81% | 11 | 0,81% | 10 | 0,74% |
| Collins (1958) | 23 | 0,72% | 11 | 0,81% | 10 | 0,74% | 11 | 0,81% |
| Natural History Museum of London (2020) | 23 | 0,72% | 9 | 0,66% | 9 | 0,67% | 9 | 0,67% |
| Parr (1950) | 23 | 0,72% | 14 | 1,03% | 14 | 1,04% | 14 | 1,04% |
| Ifremer (2009) | 20 | 0,63% | 12 | 0,88% | 12 | 0,89% | 12 | 0,89% |
| Zheng (1979) | 20 | 0,63% | 13 | 0,96% | 13 | 0,96% | 13 | 0,96% |
| Bicchi et al. (2002) | 15 | 0,47% | 12 | 0,88% | 12 | 0,89% | 12 | 0,89% |
| Cushman (1911) | 14 | 0,44% | 5 | 0,37% | 5 | 0,37% | 5 | 0,37% |
| Cushman (1921) | 12 | 0,38% | 8 | 0,59% | 8 | 0,59% | 7 | 0,52% |
| Cushman (1922) | 12 | 0,38% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Cushman (1933) | 12 | 0,38% | 10 | 0,74% | 10 | 0,74% | 10 | 0,74% |
| Fajemila et al. (2015) | 12 | 0,38% | 11 | 0,81% | 11 | 0,81% | 11 | 0,81% |
| Vella (1957) | 11 | 0,35% | 6 | 0,44% | 6 | 0,44% | 6 | 0,44% |
| Zheng (1988) | 11 | 0,35% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Zinke et al. (2005) | 11 | 0,35% | 6 | 0,44% | 6 | 0,44% | 6 | 0,44% |
| Cabioch et al. (2008) | 10 | 0,32% | 8 | 0,59% | 8 | 0,59% | 8 | 0,59% |
| Cushman (1923) | 10 | 0,32% | 5 | 0,37% | 5 | 0,37% | 5 | 0,37% |
| Dolan (2014) | 10 | 0,32% | 8 | 0,59% | 8 | 0,59% | 8 | 0,59% |
| Heron-allen & Earland (1915) | 10 | 0,32% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Rowlands (2007) | 10 | 0,32% | 8 | 0,59% | 8 | 0,59% | 7 | 0,52% |
| Said (1949) | 10 | 0,32% | 6 | 0,44% | 6 | 0,44% | 6 | 0,44% |
| Vénec-Peyré (1985) | 9 | 0,28% | 5 | 0,37% | 5 | 0,37% | 5 | 0,37% |
| Quarterly Journal of Microscopical Science, XXl: 31-71.">Brady (1881) | 8 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1925) | 8 | 0,25% | 5 | 0,37% | 5 | 0,37% | 5 | 0,37% |
| Bulletin United States National Museum, 161: 1-84.">Cushman (1932) | 8 | 0,25% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Cushman (1934) | 8 | 0,25% | 8 | 0,59% | 8 | 0,59% | 8 | 0,59% |
| Perelis & Reiss (1975) | 8 | 0,25% | 8 | 0,59% | 8 | 0,59% | 8 | 0,59% |
| Siemensma & Holzmann (2023) | 8 | 0,25% | 8 | 0,59% | 8 | 0,59% | 8 | 0,59% |
| Bulletin de la Societe Zoologique de France, 38: 260-271.">Fauré-Fremiet (1913) | 7 | 0,22% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Saidova (1975) | 7 | 0,22% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Belasky (1996) | 6 | 0,19% | 6 | 0,44% | 6 | 0,44% | 6 | 0,44% |
| Abhandlungen der Bayerischen Akademie, xviii(No. 2): pp. 195-458.">Egger (1893) | 6 | 0,19% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Parker & Gischler (2021) | 6 | 0,19% | 5 | 0,37% | 5 | 0,37% | 5 | 0,37% |
| Richer de Forges et al. (2005) | 6 | 0,19% | 6 | 0,44% | 6 | 0,44% | 6 | 0,44% |
| Albani (1974) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Washington Smithsonian Inst Proc US Nat Mus, 44: 633-638.">Cushman (1913) | 5 | 0,16% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Hatta & Ujiie (1992) | 5 | 0,16% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Linnaeus (1758) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mgnify (2018) | 5 | 0,16% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Vasseur (1985) | 5 | 0,16% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Vénec-Peyré (1991) | 5 | 0,16% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Zheng (1980) | 5 | 0,16% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Albani & Yassini (1989) | 4 | 0,13% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Chapman & Part (1937) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collins (1974) | 4 | 0,13% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Cushman & Mcculloch (1939) | 4 | 0,13% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Cushman & Todd (1944) | 4 | 0,13% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Cushman (1913) | 4 | 0,13% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman (1915) | 4 | 0,13% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Earland (1933) | 4 | 0,13% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Earland (1934) | 4 | 0,13% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Hasegawa & Nomura (1995) | 4 | 0,13% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Hayward (1990) | 4 | 0,13% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Heron-allen & Earland (1932) | 4 | 0,13% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Hodgkinson (1992) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Margerel (1982) | 4 | 0,13% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Parr (1945) | 4 | 0,13% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Pecheux (1996) | 4 | 0,13% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Rhumbler (1906) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vénec-Peyré & Salvat (1981) | 4 | 0,13% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Vénec-Peyré (1988) | 4 | 0,13% | 4 | 0,29% | 4 | 0,3% | 4 | 0,3% |
| Wiesner (1931) | 4 | 0,13% | 2 | 0,15% | 1 | 0,07% | 2 | 0,15% |
| Asano (1951) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chapman (1902) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Collen (1998) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Cushman & Bronnimann (1948) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman (1946) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| European Nucleotide Archive (2019) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Galloway & Wissler (1927) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gout (1991) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Hayward et al. (1997) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Expedition 1910 Nat History Report Zoology, 6(No. 2): pp. 25-268.">Heron-allen & Earland (1922) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Langer (1992) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Levy et al. (1981) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| McCulloch (1981) | 3 | 0,09% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| MGnify (2017) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Phleger (1951) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Ponder (1972) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Rignault & Chevallier (2017) | 3 | 0,09% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Seiglie (1964) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Sellier & Civrieux (1977) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Journal of the Royal Microscopical Society London, 1918: (1-25 122-152 249-264).">Sidebottom (1918) | 3 | 0,09% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Teruem (1878) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Todd (1956) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Ujiie (1990) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Warren (1957) | 3 | 0,09% | 3 | 0,22% | 3 | 0,22% | 3 | 0,22% |
| Wiesner (1923) | 3 | 0,09% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Williamson (1868) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Zheng et al. (1978) | 3 | 0,09% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Albani et al. (1982) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Barker (1960) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Belford (1966) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bronnimann & Whittaker (1983) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Bronnimann et al. (1992) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Buchner (1940) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Calvez & Calvey (1958) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Calvez (1936) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Chapman (1907) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Edwards (1937) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman & Galliher (1934) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Mcculloch (1940) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Cushman & Mcculloch (1942) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Cushman & Mcculloch (1948) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Cushman & Mcculloch (1950) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman et al. (1954) | 2 | 0,06% | 1 | 0,07% | 0 | 0% | 1 | 0,07% |
| Cushman (1910) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Washington DC Proceedings U S National Museum, 51: (651-662).">Cushman (1917) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1921) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1925) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Cushman (1927) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Cushman (1929) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bulletin of the United States National Museum. 161(2): 1-79">Cushman (1933) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Dellinger et al. (2014) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Ferrández-Cañadell (1997) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Report U S Museum, i: pp. 249-349.">Flint (1897) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Fourt et al. (2017) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Geslin et al. (2004) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Gmelin (1791) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hayward & Brazier (1980) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hayward et al. (1999) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hayward et al. (2021) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Heron-allen & Earland (1929) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hofker (1956) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hofker (1976) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Holzmann et al. (2018) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacroix (1927) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Lacroix (1930) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Lankford & Phleger (1973) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Larsen (1976) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Lee et al. (2004) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Loeblich & Tappan (1988) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Mamo (2016) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Millett (190O) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nomura (1984) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Oki (1989) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Parr (1932) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Revets (1996) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rhumbler (1913) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Sellier & Civrieux (1976) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sidebottom (1908) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sidebottom (1910) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Takayanagi (1951) | 2 | 0,06% | 2 | 0,15% | 2 | 0,15% | 2 | 0,15% |
| Yassini & Jones (1995) | 2 | 0,06% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Albani (1981) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Andersen (1953) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Arnal (1958) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Asano & Nakamura (1937) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Asano (1936) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Asano (1951) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bagg (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Balkwill & Wright (1885) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1927) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beckmann (1953) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bermudez (1952) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Blow (1959) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bouchet et al. (2007) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bouchet et al. (2023) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Bourcier (1988) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Brady (1876) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Brady (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brady (1890) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Carter (1876) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1877) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Carter (1880) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cépède (1914) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Chapman (1900) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chapman (1916) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Chevaldonné et al. (2015) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Clark (1993) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Clark (1995) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cole (1931) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cooke & Cushman (1922) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Bronni-mann (1948) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman & Gray (1946) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman & Gray (1947) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Hanzawa (1937) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman & Ozawa (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Ozawa (1930) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman & Parker (1931) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Parker (1947) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman & Valentine (1930) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman & Wickenden (1929) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman (1917) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1919) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman (1920) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman (1925) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Contributions from the Cushman Laboratory for Foraminiferal Research, 2: pp. 70 & 71.">Cushman (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1927) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1936) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman (1944) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cushman (1944) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Cushman (1945) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Ehrenberg (1839) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Finlay (1940) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleisher (1974) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Folin & Périer (1872) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Förderer et al. (2018) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Glaçon & Lys (1968) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hansen & Revets (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedberg (1937) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Journal of the Royal Microscopical Society London, 1912: 382-389.">Heron-Allen & Earland (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heron-allen & Earland (1913) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heron-Allen & Earland (1924) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heron-Allen & Earland (1928) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heron-allen & Earland (1932) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Hoffer (1972) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hofker (1932) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Howchin (1889) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ishizaki (1943) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ishizaki (1948) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaminski et al. (2008) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Karrer (1868) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Karrer (1878) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kornfeld (1931) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacroix (1940) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Lalicker & Mcculloch (1940) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Leroy (1944) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lloyd (1967) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matsunaga (1963) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mclean (1956) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mgnify (2019) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Mikhalevich (1976) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Millett (1898) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millett (1901) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Millett (1902) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millett (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Möbius (1880) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Montagu (1803) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montfort de Denys (1808) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Norman (1878) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Pallas (1766) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parker (1952) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parker (1954) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Parker (1962) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parker (1967) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prenant (1927) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quilty (1974) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rasheed (1971) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Reuss (1850) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reuss (1863) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Rhumbler (1905) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Seiglie & Bennudez (1965) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Shuto (1953) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Sidebottom (1905) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sidebottom (1906) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sidebottom (1909) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siemensma et al. (2020) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Siemensma (2020) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Smitter (1955) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Trauth (1918) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uchio (1952) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uchio (1953) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Uchio (1960) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Uchio (1962) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Wallich (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williamson (1848) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Yabe & Hanzawa (1930) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| Zheng (1988) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
| (1967) | 1 | 0,03% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
