Pycnogonides
Pycnogonida
73 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Sabroux et al. (2022) | 98 | 21,26% | 98 | 32,56% | 98 | 32,78% | 96 | 32,11% |
| Bamber (2007) | 69 | 14,97% | 65 | 21,59% | 65 | 21,74% | 65 | 21,74% |
| Munilla et al. (2009) | 50 | 10,85% | 50 | 16,61% | 50 | 16,72% | 49 | 16,39% |
| Sabroux et al. (2019) | 45 | 9,76% | 45 | 14,95% | 45 | 15,05% | 44 | 14,72% |
| Arnaud (1972) | 34 | 7,38% | 32 | 10,63% | 30 | 10,03% | 31 | 10,37% |
| Arnaud (1974) | 29 | 6,29% | 28 | 9,3% | 27 | 9,03% | 28 | 9,36% |
| Corbari et al. (2020) | 24 | 5,21% | 24 | 7,97% | 24 | 8,03% | 24 | 8,03% |
| Stock (1978) | 18 | 3,9% | 18 | 5,98% | 18 | 6,02% | 18 | 6,02% |
| Ifremer (2009) | 16 | 3,47% | 14 | 4,65% | 14 | 4,68% | 14 | 4,68% |
| Bourdillon (1955) | 12 | 2,6% | 9 | 2,99% | 9 | 3,01% | 9 | 3,01% |
| Nelson-Smith et al. (2014) | 10 | 2,17% | 6 | 1,99% | 6 | 2,01% | 6 | 2,01% |
| Stock (1986) | 9 | 1,95% | 9 | 2,99% | 7 | 2,34% | 8 | 2,68% |
| Arnaud (1974) | 8 | 1,74% | 8 | 2,66% | 8 | 2,68% | 8 | 2,68% |
| Bamber (2011) | 6 | 1,3% | 6 | 1,99% | 6 | 2,01% | 6 | 2,01% |
| Clark (1977) | 6 | 1,3% | 6 | 1,99% | 6 | 2,01% | 6 | 2,01% |
| Cuénot (1921) | 6 | 1,3% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Sabroux et al. (2017) | 6 | 1,3% | 6 | 1,99% | 6 | 2,01% | 6 | 2,01% |
| Bamber (2004) | 5 | 1,08% | 5 | 1,66% | 5 | 1,67% | 5 | 1,67% |
| Godet et al. (2010) | 5 | 1,08% | 4 | 1,33% | 4 | 1,34% | 4 | 1,34% |
| Muller (1990) | 5 | 1,08% | 5 | 1,66% | 5 | 1,67% | 5 | 1,67% |
| Bamber (2000) | 4 | 0,87% | 4 | 1,33% | 4 | 1,34% | 4 | 1,34% |
| Bourcier (1988) | 4 | 0,87% | 4 | 1,33% | 4 | 1,34% | 4 | 1,34% |
| Miers (1875) | 4 | 0,87% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Stock (1990) | 4 | 0,87% | 4 | 1,33% | 4 | 1,34% | 4 | 1,34% |
| Bamber (2013) | 3 | 0,65% | 3 | 1% | 3 | 1% | 3 | 1% |
| Bamber (1997) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Bouvier (1916) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Corbari et al. (2015) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Dohrn (1881) | 2 | 0,43% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Gout (1991) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Hodge (1864) | 2 | 0,43% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Miers (1875) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Muller (1989) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Muller (1990) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Pushkin (1984) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Stock (1963) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Stock (1993) | 2 | 0,43% | 2 | 0,66% | 2 | 0,67% | 2 | 0,67% |
| Améziane et al. (2011) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 0 | 0% |
| Arnaud (2015) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Arnaud (2015) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Arnaud (2015) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Arnaud (2015) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Arnaud (2015) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Arnaud (2015) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Arnaud (2015) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Arnaud (2016) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Arnaud (2016) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Boisseau (1952) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevaldonné et al. (2015) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Child (1977) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Child (1979) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Child (1991) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Cole (1906) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel & Welsford (2011) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 0 | 0% |
| Duquef (2022) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Gadeau de Kerville (1900) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Giltay (1934) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haswell (1885) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| British Museum (Natural History), London. 228-261.">Hodgson (1902) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Hoek (1881) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 0 | 0% |
| Ifremer (2019) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| King (1974) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Krøyer (1844) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leach (1814) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loman (1908) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montagu (1808) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pushkin (1973) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Richer de Forges et al. (2005) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Rignault & Chevallier (2017) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Roux et al. (2020) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
| Strøm (1762) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van et al. (2008) | 1 | 0,22% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
