Tardigrades
Tardigrada
86 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Kaczmarek et al. (2015) | 16 | 6,58% | 16 | 9,76% | 14 | 9,09% | 16 | 10,19% |
Bartels et al. (2015) | 14 | 5,76% | 14 | 8,54% | 10 | 6,49% | 11 | 7,01% |
Renaud-Mornant (1983) | 12 | 4,94% | 12 | 7,32% | 12 | 7,79% | 12 | 7,64% |
Renaud-Mornant & Gourbault (1984) | 11 | 4,53% | 10 | 6,1% | 10 | 6,49% | 9 | 5,73% |
Renaud-Mornant (1984) | 11 | 4,53% | 11 | 6,71% | 11 | 7,14% | 11 | 7,01% |
Gąsiorek & Vončina (2023) | 9 | 3,7% | 4 | 2,44% | 4 | 2,6% | 4 | 2,55% |
d'Hondt (1970) | 8 | 3,29% | 8 | 4,88% | 8 | 5,19% | 6 | 3,82% |
Majdi et al. (2024) | 8 | 3,29% | 8 | 4,88% | 8 | 5,19% | 8 | 5,1% |
Renaud-Mornant (1968) | 8 | 3,29% | 5 | 3,05% | 5 | 3,25% | 5 | 3,18% |
Renaud-Mornant (1989) | 8 | 3,29% | 8 | 4,88% | 8 | 5,19% | 8 | 5,1% |
Semeria (1994) | 8 | 3,29% | 8 | 4,88% | 8 | 5,19% | 8 | 5,1% |
Renaud-Debyser (1959) | 7 | 2,88% | 7 | 4,27% | 7 | 4,55% | 6 | 3,82% |
Doyère (1840) | 6 | 2,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Hansen & Kristensen (2021) | 6 | 2,47% | 6 | 3,66% | 6 | 3,9% | 6 | 3,82% |
Renaud-Mornant (1981) | 6 | 2,47% | 6 | 3,66% | 4 | 2,6% | 4 | 2,55% |
Renaud-mornant (1984) | 6 | 2,47% | 6 | 3,66% | 4 | 2,6% | 6 | 3,82% |
Iharos (1966) | 5 | 2,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Delamare Deboutteville & Renaud-Mornant (1965) | 4 | 1,65% | 4 | 2,44% | 4 | 2,6% | 4 | 2,55% |
Ifremer (2009) | 4 | 1,65% | 4 | 2,44% | 4 | 2,6% | 3 | 1,91% |
Mihelčič (1960) | 4 | 1,65% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Renaud-Mornant (1987) | 4 | 1,65% | 4 | 2,44% | 4 | 2,6% | 4 | 2,55% |
Thulin (1942) | 4 | 1,65% | 4 | 2,44% | 4 | 2,6% | 4 | 2,55% |
Cantacuzène (1951) | 3 | 1,23% | 3 | 1,83% | 3 | 1,95% | 3 | 1,91% |
Cuénot (1891-1892) | 3 | 1,23% | 3 | 1,83% | 3 | 1,95% | 3 | 1,91% |
Fize (1958) | 3 | 1,23% | 3 | 1,83% | 3 | 1,95% | 3 | 1,91% |
Kristensen (1978) | 3 | 1,23% | 3 | 1,83% | 3 | 1,95% | 3 | 1,91% |
Meyer (2011) | 3 | 1,23% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Pogwizd & Stec (2020) | 3 | 1,23% | 3 | 1,83% | 3 | 1,95% | 3 | 1,91% |
Renaud-Mornant & Deroux (1976) | 3 | 1,23% | 3 | 1,83% | 3 | 1,95% | 3 | 1,91% |
Renaud-Mornant (1976) | 3 | 1,23% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Renaud-Mornant (1981) | 3 | 1,23% | 3 | 1,83% | 3 | 1,95% | 3 | 1,91% |
Thulin (1928) | 3 | 1,23% | 3 | 1,83% | 3 | 1,95% | 3 | 1,91% |
Arcidiacono (1962) | 2 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellido & Bertrand (1981) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Bertolani (1981) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Binda & Pilato (1972) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Chang & Rho (1997) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Dastych (1999) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Dastych (2002) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Dastych (2006) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Gąsiorek & Kristensen (2022) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 1 | 0,64% |
Gąsiorek et al. (2019) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Jorgensen & Mobjerg (2015) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Kristensen & Hallas (1980) | 2 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Marcus (1946) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Marcus (1952) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Maucci (1993) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Mckirdy et al. (1977) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Mobjerg et al. (2016) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Møbjerg et al. (2020) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Nelson et al. (1999) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Pollock (1975) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Ramazzotti (1972) | 2 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Renaud-Debyser (1959) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Renaud-Mornant & Jouin (1965) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Renaud-mornant (1980) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Renaud-mornant (1981) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Richters (1903) | 2 | 0,82% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Robotti (1970) | 2 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulze et al. (2014) | 2 | 0,82% | 2 | 1,22% | 1 | 0,65% | 1 | 0,64% |
Semeria (1984) | 2 | 0,82% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Stec et al. (2020) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Van et al. (1968) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Villora-Moreno (1996) | 2 | 0,82% | 2 | 1,22% | 2 | 1,3% | 2 | 1,27% |
Bertrand (1975) | 1 | 0,41% | 1 | 0,61% | 0 | 0% | 1 | 0,64% |
Gasiorek et al. (2021) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Gąsiorek et al. (2019) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Heinis (1908) | 1 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Kristensen & Higgins (1984) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Kristensen & Renaud-Mornant (1983) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 0 | 0% |
Kristensen (1980) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Pearman et al. (2020) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 0 | 0% |
Pilato (1997) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Pollock (1971) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Pollock (1983) | 1 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Renaud-mornant (1970) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Renaud-mornant (1975) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Renaud-mornant (1976) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Renaud-mornant (1981) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Richters (1904) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Richters (1912) | 1 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulz (1935) | 1 | 0,41% | 1 | 0,61% | 0 | 0% | 1 | 0,64% |
Schulz (1953) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Séméria (2003) | 1 | 0,41% | 1 | 0,61% | 1 | 0,65% | 1 | 0,64% |
Swedmark & Teissier (1967) | 1 | 0,41% | 1 | 0,61% | 0 | 0% | 1 | 0,64% |
Urbanowicz (1925) | 1 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |