Foraminifères de Nouvelle-Calédonie
237 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 | 24,39% | 516 | 47,96% | 514 | 47,99% | 514 | 47,99% |
Debenay & Cabioch (2007) | 508 | 19,55% | 351 | 32,62% | 350 | 32,68% | 350 | 32,68% |
Guilcher et al. (1965) | 181 | 6,96% | 104 | 9,67% | 104 | 9,71% | 103 | 9,62% |
Vénec-Peyré (1985) | 146 | 5,62% | 113 | 10,5% | 113 | 10,55% | 111 | 10,36% |
Mcculloch (1977) | 64 | 2,46% | 36 | 3,35% | 35 | 3,27% | 35 | 3,27% |
Arnaud (1974) | 40 | 1,54% | 25 | 2,32% | 25 | 2,33% | 25 | 2,33% |
Langer & Lipps (2006) | 31 | 1,19% | 20 | 1,86% | 20 | 1,87% | 20 | 1,87% |
Loeblich & Tappan (1994) | 30 | 1,15% | 23 | 2,14% | 23 | 2,15% | 23 | 2,15% |
Brady (1884) | 27 | 1,04% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Collins (1958) | 23 | 0,88% | 11 | 1,02% | 10 | 0,93% | 11 | 1,03% |
Blanc-Vernet (1965) | 22 | 0,85% | 9 | 0,84% | 9 | 0,84% | 9 | 0,84% |
Q. J. Micr. Sci. (n.s.), xix: pp. 20 & 261.">Brady (1879) | 19 | 0,73% | 5 | 0,46% | 5 | 0,47% | 5 | 0,47% |
Zheng (1979) | 19 | 0,73% | 12 | 1,12% | 12 | 1,12% | 12 | 1,12% |
Parr (1950) | 18 | 0,69% | 11 | 1,02% | 11 | 1,03% | 11 | 1,03% |
Bicchi et al. (2002) | 13 | 0,5% | 11 | 1,02% | 11 | 1,03% | 11 | 1,03% |
Cushman (1911) | 12 | 0,46% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Cushman (1922) | 11 | 0,42% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Zheng (1988) | 11 | 0,42% | 4 | 0,37% | 4 | 0,37% | 4 | 0,37% |
Vella (1957) | 10 | 0,38% | 5 | 0,46% | 5 | 0,47% | 5 | 0,47% |
Zinke et al. (2005) | 10 | 0,38% | 6 | 0,56% | 6 | 0,56% | 6 | 0,56% |
Cushman (1921) | 9 | 0,35% | 6 | 0,56% | 6 | 0,56% | 6 | 0,56% |
Heron-allen & Earland (1915) | 9 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Said (1949) | 9 | 0,35% | 6 | 0,56% | 6 | 0,56% | 6 | 0,56% |
Cushman (1923) | 8 | 0,31% | 4 | 0,37% | 4 | 0,37% | 4 | 0,37% |
Cushman (1925) | 8 | 0,31% | 5 | 0,46% | 5 | 0,47% | 5 | 0,47% |
Bulletin United States National Museum, 161: 1-84.">Cushman (1932) | 8 | 0,31% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Perelis & Reiss (1975) | 8 | 0,31% | 8 | 0,74% | 8 | 0,75% | 8 | 0,75% |
Bulletin de la Societe Zoologique de France, 38: 260-271.">Fauré-Fremiet (1913) | 7 | 0,27% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Natural History Museum of London (2020) | 7 | 0,27% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Quarterly Journal of Microscopical Science, XXl: 31-71.">Brady (1881) | 6 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabioch et al. (2008) | 6 | 0,23% | 5 | 0,46% | 5 | 0,47% | 5 | 0,47% |
Abhandlungen der Bayerischen Akademie, xviii(No. 2): pp. 195-458.">Egger (1893) | 6 | 0,23% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Ifremer (2009) | 6 | 0,23% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Richer de Forges et al. (2005) | 6 | 0,23% | 6 | 0,56% | 6 | 0,56% | 6 | 0,56% |
Rowlands (2007) | 6 | 0,23% | 5 | 0,46% | 5 | 0,47% | 4 | 0,37% |
Saidova (1975) | 6 | 0,23% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Albani (1974) | 5 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Washington Smithsonian Inst Proc US Nat Mus, 44: 633-638.">Cushman (1913) | 5 | 0,19% | 4 | 0,37% | 4 | 0,37% | 4 | 0,37% |
Hatta & Ujiie (1992) | 5 | 0,19% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hess et al. (2005) | 5 | 0,19% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Vénec-Peyré (1985) | 5 | 0,19% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Albani & Yassini (1989) | 4 | 0,15% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Belasky (1996) | 4 | 0,15% | 4 | 0,37% | 4 | 0,37% | 4 | 0,37% |
Chapman & Part (1937) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Todd (1944) | 4 | 0,15% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Cushman (1913) | 4 | 0,15% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hasegawa & Nomura (1995) | 4 | 0,15% | 4 | 0,37% | 4 | 0,37% | 4 | 0,37% |
Hayward (1990) | 4 | 0,15% | 4 | 0,37% | 4 | 0,37% | 4 | 0,37% |
Hodgkinson (1992) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Margerel (1982) | 4 | 0,15% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Parr (1945) | 4 | 0,15% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pecheux (1996) | 4 | 0,15% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Vénec-Peyré (1991) | 4 | 0,15% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Zheng (1980) | 4 | 0,15% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Asano (1951) | 3 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapman (1902) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Collen (1998) | 3 | 0,12% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Collins (1974) | 3 | 0,12% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cushman & Bronnimann (1948) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman & Mcculloch (1939) | 3 | 0,12% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cushman (1933) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman (1946) | 3 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fajemila et al. (2015) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Galloway & Wissler (1927) | 3 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gout (1991) | 3 | 0,12% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Hayward et al. (1997) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Heron-allen & Earland (1932) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Langer (1992) | 3 | 0,12% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Levy et al. (1981) | 3 | 0,12% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
McCulloch (1981) | 3 | 0,12% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ponder (1972) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rignault & Chevallier (2017) | 3 | 0,12% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Seiglie (1964) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Journal of the Royal Microscopical Society London, 1918: (1-25 122-152 249-264).">Sidebottom (1918) | 3 | 0,12% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Teruem (1878) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ujiie (1990) | 3 | 0,12% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Vasseur (1985) | 3 | 0,12% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Vénec-Peyré & Salvat (1981) | 3 | 0,12% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Warren (1957) | 3 | 0,12% | 3 | 0,28% | 3 | 0,28% | 3 | 0,28% |
Wiesner (1923) | 3 | 0,12% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Wiesner (1931) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Williamson (1868) | 3 | 0,12% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Albani et al. (1982) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Barker (1960) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Belford (1966) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bronnimann & Whittaker (1983) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bronnimann et al. (1992) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cushman & Edwards (1937) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman & Galliher (1934) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Mcculloch (1950) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1910) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cushman (1915) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Washington DC Proceedings U S National Museum, 51: (651-662).">Cushman (1917) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1921) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1925) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cushman (1927) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cushman (1929) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin of the United States National Museum. 161(2): 1-79">Cushman (1933) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Dolan (2014) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Earland (1933) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Earland (1934) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Goulletquer (2016) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hayward & Brazier (1980) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hayward et al. (1999) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hofker (1956) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hofker (1976) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lacroix (1927) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lacroix (1930) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lankford & Phleger (1973) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Larsen (1976) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lee et al. (2004) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Loeblich & Tappan (1988) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mamo (2016) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Millett (190O) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Nomura (1984) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Oki (1989) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Parr (1932) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Phleger (1951) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Revets (1996) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rhumbler (1906) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Sidebottom (1910) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Takayanagi (1951) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Todd (1956) | 2 | 0,08% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Yassini & Jones (1995) | 2 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Zheng et al. (1978) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Albani (1981) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Andersen (1953) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Arnal (1958) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Asano & Nakamura (1937) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Asano (1936) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Asano (1951) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagg (1912) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Balkwill & Wright (1885) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1927) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Beckmann (1953) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Blow (1959) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bouchet et al. (2007) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bourcier (1988) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Brady (1876) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Brady (1884) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brady (1890) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Buchner (1940) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Carter (1876) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Carter (1877) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Carter (1877) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Carter (1880) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapman (1900) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapman (1907) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevaldonné et al. (2015) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Clark (1993) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Clark (1995) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cole (1931) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cooke & Cushman (1922) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Gray (1946) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman & Gray (1947) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Hanzawa (1937) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman & Mcculloch (1940) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman & Mcculloch (1948) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman & Ozawa (1929) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Ozawa (1930) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman & Parker (1931) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Parker (1947) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman & Valentine (1930) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman & Wickenden (1929) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman et al. (1954) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1917) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1919) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman (1925) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1926) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Contributions from the Cushman Laboratory for Foraminiferal Research, 2: pp. 70 & 71.">Cushman (1926) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1926) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1927) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman (1929) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1936) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman (1944) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1944) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman (1945) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ehrenberg (1839) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
European Nucleotide Archive (2019) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Finlay (1940) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleisher (1974) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Report U S Museum, i: pp. 249-349.">Flint (1897) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Förderer et al. (2018) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Glaçon & Lys (1968) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hansen & Revets (1992) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedberg (1937) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Journal of the Royal Microscopical Society London, 1912: 382-389.">Heron-Allen & Earland (1912) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Heron-allen & Earland (1913) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Heron-Allen & Earland (1924) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Heron-Allen & Earland (1928) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Heron-allen & Earland (1929) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffer (1972) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Howchin (1889) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ishizaki (1943) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ishizaki (1948) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaminski et al. (2008) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Karrer (1868) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Karrer (1878) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kornfeld (1931) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lalicker & Mcculloch (1940) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Leroy (1944) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lloyd (1967) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsunaga (1963) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclean (1956) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
MGnify (2017) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mgnify (2018) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikhalevich (1976) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Millett (1898) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Millett (1901) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Millett (1902) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Millett (1903) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Möbius (1880) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Montfort de Denys (1808) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Norman (1878) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pallas (1766) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Parker & Gischler (2021) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Parker (1952) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Parker (1954) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Parker (1962) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Parker (1967) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Prenant (1927) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Quilty (1974) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rasheed (1971) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Reuss (1850) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rhumbler (1913) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Shuto (1953) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Sidebottom (1905) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sidebottom (1906) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sidebottom (1908) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Trauth (1918) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Uchio (1953) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Uchio (1960) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Yabe & Hanzawa (1930) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Zheng (1988) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
(1967) | 1 | 0,04% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |