Foraminifères de métropole
56 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Hess et al. (2005) | 33 | 14,41% | 22 | 23,91% | 22 | 23,91% | 22 | 23,91% |
Ifremer (2009) | 20 | 8,73% | 12 | 13,04% | 12 | 13,04% | 12 | 13,04% |
Debenay (2013) | 13 | 5,68% | 12 | 13,04% | 12 | 13,04% | 12 | 13,04% |
Dolan (2014) | 10 | 4,37% | 8 | 8,7% | 8 | 8,7% | 8 | 8,7% |
Debenay & Cabioch (2007) | 9 | 3,93% | 6 | 6,52% | 6 | 6,52% | 6 | 6,52% |
Siemensma & Holzmann (2023) | 8 | 3,49% | 8 | 8,7% | 8 | 8,7% | 8 | 8,7% |
Guilcher et al. (1965) | 5 | 2,18% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
MGnify (2017) | 3 | 1,31% | 3 | 3,26% | 3 | 3,26% | 3 | 3,26% |
Rignault & Chevallier (2017) | 3 | 1,31% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Vénec-Peyré (1985) | 3 | 1,31% | 3 | 3,26% | 3 | 3,26% | 3 | 3,26% |
Arnaud (1974) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Q. J. Micr. Sci. (n.s.), xix: pp. 20 & 261.">Brady (1879) | 2 | 0,87% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Brady (1884) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Calvez & Calvey (1958) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Calvez (1936) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Cushman (1923) | 2 | 0,87% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Dellinger et al. (2014) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Ferrández-Cañadell (1997) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Fourt et al. (2017) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Geslin et al. (2004) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Holzmann et al. (2018) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Lacroix (1927) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Lacroix (1930) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Langer & Lipps (2006) | 2 | 0,87% | 2 | 2,17% | 2 | 2,17% | 2 | 2,17% |
Natural History Museum of London (2020) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1927) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Belasky (1996) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Blanc-Vernet (1965) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourcier (1988) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Buchner (1940) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Cépède (1914) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Chevaldonné et al. (2015) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Cushman & Mcculloch (1942) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Cushman (1911) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Cushman (1926) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Earland (1934) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
European Nucleotide Archive (2019) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Bulletin de la Societe Zoologique de France, 38: 260-271.">Fauré-Fremiet (1913) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Report U S Museum, i: pp. 249-349.">Flint (1897) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Folin & Périer (1872) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Gmelin (1791) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Heron-allen & Earland (1932) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Hofker (1932) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Loeblich & Tappan (1994) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Mgnify (2019) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Pallas (1766) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Parr (1950) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Prenant (1927) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Rhumbler (1913) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Siemensma et al. (2020) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Siemensma (2020) | 1 | 0,44% | 1 | 1,09% | 1 | 1,09% | 1 | 1,09% |
Vella (1957) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Williamson (1868) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |