Amibes à thèques
128 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Deflandre (1927) | 130 | 20,28% | 86 | 18,45% | 76 | 22,16% | 59 | 14,57% |
Thécamoebiens du Sol". Hermann, Paris. 103pp.">Bonnet & Thomas (1960) | 89 | 13,88% | 75 | 16,09% | 52 | 15,16% | 52 | 12,84% |
Bonnet (1977) | 86 | 13,42% | 71 | 15,24% | 66 | 19,24% | 38 | 9,38% |
Deflandre (1928) | 47 | 7,33% | 15 | 3,22% | 3 | 0,87% | 14 | 3,46% |
Heger et al. (2009) | 41 | 6,4% | 31 | 6,65% | 25 | 7,29% | 21 | 5,19% |
González-miguéns et al. (2021) | 36 | 5,62% | 24 | 5,15% | 18 | 5,25% | 23 | 5,68% |
Vincke et al. (2004) | 33 | 5,15% | 20 | 4,29% | 17 | 4,96% | 14 | 3,46% |
Penard (1890) | 32 | 4,99% | 14 | 3% | 14 | 4,08% | 11 | 2,72% |
Penard (1908) | 30 | 4,68% | 21 | 4,51% | 20 | 5,83% | 20 | 4,94% |
Decloitre (1981) | 29 | 4,52% | 27 | 5,79% | 13 | 3,79% | 26 | 6,42% |
Decloitre (1982) | 29 | 4,52% | 29 | 6,22% | 16 | 4,66% | 27 | 6,67% |
Ogden (1983) | 29 | 4,52% | 16 | 3,43% | 16 | 4,66% | 16 | 3,95% |
Penard (1902) | 29 | 4,52% | 15 | 3,22% | 15 | 4,37% | 12 | 2,96% |
Deflandre (1929) | 26 | 4,06% | 18 | 3,86% | 9 | 2,62% | 15 | 3,7% |
Decloitre (1978) | 21 | 3,28% | 19 | 4,08% | 11 | 3,21% | 17 | 4,2% |
Bobrov & Mazei (2017) | 20 | 3,12% | 10 | 2,15% | 8 | 2,33% | 8 | 1,98% |
Bonnet (1958) | 20 | 3,12% | 15 | 3,22% | 12 | 3,5% | 14 | 3,46% |
Bonnet (1965) | 19 | 2,96% | 17 | 3,65% | 16 | 4,66% | 8 | 1,98% |
Lahr & Lopes (2009) | 18 | 2,81% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Bonnet & Thomas (1955) | 15 | 2,34% | 13 | 2,79% | 9 | 2,62% | 6 | 1,48% |
Decloitre (1960) | 15 | 2,34% | 13 | 2,79% | 11 | 3,21% | 5 | 1,23% |
Decloitre (1979) | 15 | 2,34% | 15 | 3,22% | 9 | 2,62% | 13 | 3,21% |
Dumas (1930) | 15 | 2,34% | 15 | 3,22% | 15 | 4,37% | 15 | 3,7% |
Bonnet (1959) | 14 | 2,18% | 13 | 2,79% | 7 | 2,04% | 12 | 2,96% |
Decloitre (1968) | 14 | 2,18% | 13 | 2,79% | 10 | 2,92% | 8 | 1,98% |
Playfair (1918) | 14 | 2,18% | 8 | 1,72% | 4 | 1,17% | 7 | 1,73% |
Vincke et al. (2004) | 14 | 2,18% | 8 | 1,72% | 7 | 2,04% | 3 | 0,74% |
Bonnet & Thomas (1960) | 13 | 2,03% | 12 | 2,58% | 5 | 1,46% | 10 | 2,47% |
Gauthier-lièvre & Thomas (1958) | 13 | 2,03% | 13 | 2,79% | 7 | 2,04% | 13 | 3,21% |
Cash & Hopkinson (1909) | 12 | 1,87% | 9 | 1,93% | 7 | 2,04% | 9 | 2,22% |
Decloitre (1970) | 12 | 1,87% | 12 | 2,58% | 5 | 1,46% | 11 | 2,72% |
Deflandre (1936) | 12 | 1,87% | 8 | 1,72% | 3 | 0,87% | 8 | 1,98% |
Soler-zamora et al. (2023) | 12 | 1,87% | 4 | 0,86% | 2 | 0,58% | 4 | 0,99% |
Decloitre (1978) | 11 | 1,72% | 11 | 2,36% | 7 | 2,04% | 11 | 2,72% |
Decloitre (1979) | 11 | 1,72% | 11 | 2,36% | 8 | 2,33% | 11 | 2,72% |
Decloitre (1979) | 10 | 1,56% | 10 | 2,15% | 9 | 2,62% | 10 | 2,47% |
Penard (1900) | 10 | 1,56% | 7 | 1,5% | 6 | 1,75% | 6 | 1,48% |
Bonnet (1959) | 9 | 1,4% | 6 | 1,29% | 6 | 1,75% | 5 | 1,23% |
Decloitre (1972) | 9 | 1,4% | 7 | 1,5% | 1 | 0,29% | 7 | 1,73% |
Decloitre (1977) | 9 | 1,4% | 9 | 1,93% | 9 | 2,62% | 9 | 2,22% |
Decloitre (1979) | 9 | 1,4% | 8 | 1,72% | 6 | 1,75% | 8 | 1,98% |
Coûteaux & Golemansky (1984) | 8 | 1,25% | 7 | 1,5% | 7 | 2,04% | 7 | 1,73% |
Decloitre (1970) | 8 | 1,25% | 7 | 1,5% | 5 | 1,46% | 7 | 1,73% |
Jung (1942) | 7 | 1,09% | 7 | 1,5% | 7 | 2,04% | 7 | 1,73% |
Mazei & Warren (2015) | 7 | 1,09% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Thomas (1959) | 7 | 1,09% | 6 | 1,29% | 6 | 1,75% | 6 | 1,48% |
Bonnet (1961) | 6 | 0,94% | 4 | 0,86% | 2 | 0,58% | 4 | 0,99% |
Couteaux (1972) | 6 | 0,94% | 6 | 1,29% | 6 | 1,75% | 6 | 1,48% |
Leidy (1879) | 6 | 0,94% | 3 | 0,64% | 3 | 0,87% | 2 | 0,49% |
Badewitz (2004) | 5 | 0,78% | 3 | 0,64% | 3 | 0,87% | 3 | 0,74% |
Bonnet & Gomez-Sanchez (1994) | 5 | 0,78% | 5 | 1,07% | 5 | 1,46% | 5 | 1,23% |
Bonnet (1986) | 5 | 0,78% | 4 | 0,86% | 2 | 0,58% | 4 | 0,99% |
Décloitre (1962) | 5 | 0,78% | 2 | 0,43% | 1 | 0,29% | 2 | 0,49% |
Decloitre (1971) | 5 | 0,78% | 5 | 1,07% | 3 | 0,87% | 5 | 1,23% |
Decloitre (1975) | 5 | 0,78% | 4 | 0,86% | 2 | 0,58% | 4 | 0,99% |
Dujardin (1841) | 5 | 0,78% | 2 | 0,43% | 2 | 0,58% | 1 | 0,25% |
Kosakyan et al. (2016) | 5 | 0,78% | 5 | 1,07% | 5 | 1,46% | 5 | 1,23% |
Decloitre (1974) | 4 | 0,62% | 4 | 0,86% | 4 | 1,17% | 4 | 0,99% |
Decloitre (1982) | 4 | 0,62% | 4 | 0,86% | 2 | 0,58% | 4 | 0,99% |
Dumas (1929) | 4 | 0,62% | 4 | 0,86% | 4 | 1,17% | 4 | 0,99% |
Dumas (1937) | 4 | 0,62% | 4 | 0,86% | 4 | 1,17% | 4 | 0,99% |
Gauthier-lievre & Thomas (1960) | 4 | 0,62% | 3 | 0,64% | 1 | 0,29% | 2 | 0,49% |
González-miguéns et al. (2022) | 4 | 0,62% | 4 | 0,86% | 4 | 1,17% | 4 | 0,99% |
Kosakyan et al. (2012) | 4 | 0,62% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Medioli & Scott (1983) | 4 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Vincke et al. (2004) | 4 | 0,62% | 4 | 0,86% | 2 | 0,58% | 2 | 0,49% |
Wailes & Penard (1911) | 4 | 0,62% | 3 | 0,64% | 1 | 0,29% | 2 | 0,49% |
Bonnet & Gomez-Sanchez (1984) | 3 | 0,47% | 3 | 0,64% | 3 | 0,87% | 3 | 0,74% |
Bonnet (1960) | 3 | 0,47% | 3 | 0,64% | 3 | 0,87% | 3 | 0,74% |
Bonnet (1979) | 3 | 0,47% | 3 | 0,64% | 3 | 0,87% | 3 | 0,74% |
Decloitre (1976) | 3 | 0,47% | 3 | 0,64% | 1 | 0,29% | 3 | 0,74% |
Decloitre (1986) | 3 | 0,47% | 3 | 0,64% | 3 | 0,87% | 3 | 0,74% |
Deflandre (1931) | 3 | 0,47% | 3 | 0,64% | 1 | 0,29% | 3 | 0,74% |
Ehrenberg (1838) | 3 | 0,47% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Olivier (1944) | 3 | 0,47% | 3 | 0,64% | 3 | 0,87% | 3 | 0,74% |
Penard (1909) | 3 | 0,47% | 3 | 0,64% | 3 | 0,87% | 3 | 0,74% |
Bankov et al. (2021) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Bonnet (1974) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Bonnet (1984) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Cash et al. (1915) | 2 | 0,31% | 2 | 0,43% | 0 | 0% | 2 | 0,49% |
Decloitre (1961) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Decloitre (1970) | 2 | 0,31% | 2 | 0,43% | 1 | 0,29% | 2 | 0,49% |
Decloitre (1974) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Decloitre (1974) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 0 | 0% |
Decloitre (1977) | 2 | 0,31% | 2 | 0,43% | 0 | 0% | 2 | 0,49% |
Deflandre (1928) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Gauthier-lièvre (1953) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Golemansky (1991) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 1 | 0,25% |
Greeff (1866) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Loeblich & Tappan (1961) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Marcisz et al. (2014) | 2 | 0,31% | 2 | 0,43% | 1 | 0,29% | 2 | 0,49% |
Odgen (1981) | 2 | 0,31% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Ogden & Živković (1983) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 2 | 0,49% |
Penard (1910) | 2 | 0,31% | 1 | 0,21% | 1 | 0,29% | 0 | 0% |
Penard (1911) | 2 | 0,31% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Taranek (1881) | 2 | 0,31% | 2 | 0,43% | 2 | 0,58% | 0 | 0% |
Thomas (1953) | 2 | 0,31% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Tsyganov & Mazei (2006) | 2 | 0,31% | 2 | 0,43% | 1 | 0,29% | 1 | 0,25% |
Van Oye (1949) | 2 | 0,31% | 2 | 0,43% | 1 | 0,29% | 2 | 0,49% |
Bonnet & Comoy (1977) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Bonnet (1980) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Cash & Hopkinson (1905) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cash (1904) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cockerell (1911) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Couté & Perrette (2009) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Decloitre (1958) | 1 | 0,16% | 1 | 0,21% | 0 | 0% | 1 | 0,25% |
Decloitre (1966) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Decloitre (1969) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Decloitre (1974) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Decloitre (1975) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Decloitre (1976) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 0 | 0% |
Duckert et al. (2018) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Gomaa et al. (2017) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Guerne & Richard (1891) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Jassey et al. (2010) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Kosakyan et al. (2013) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lansac-tôha et al. (2001) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Leidy (1878) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
MGnify (2017) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Nasser et al. (2021) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Penard (1904) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Penard (1917) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Porfirio-sousa et al. (2023) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Thomas (1958) | 1 | 0,16% | 1 | 0,21% | 0 | 0% | 1 | 0,25% |
Travé (1982) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Van Oye (1939) | 1 | 0,16% | 1 | 0,21% | 1 | 0,29% | 1 | 0,25% |
Vincke et al. (2006) | 1 | 0,16% | 1 | 0,21% | 0 | 0% | 1 | 0,25% |
Wailes (1913) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |