Bivalves d'eau douce
Bivalvia d'eau douce au sens large
78 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Prié (2017) | 101 | 30,24% | 92 | 141,54% | 82 | 136,67% | 86 | 138,71% |
Falkner et al. (2002) | 66 | 19,76% | 25 | 38,46% | 21 | 35% | 23 | 37,1% |
Gargominy et al. (2011) | 63 | 18,86% | 41 | 63,08% | 37 | 61,67% | 39 | 62,9% |
Lopes-Lima et al. (2016) | 12 | 3,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié (2020) | 10 | 2,99% | 8 | 12,31% | 8 | 13,33% | 8 | 12,9% |
Delannoye et al. (2015) | 7 | 2,1% | 6 | 9,23% | 6 | 10% | 6 | 9,68% |
Lamy & Pointier (2018) | 6 | 1,8% | 6 | 9,23% | 6 | 10% | 6 | 9,68% |
Linnaeus (1758) | 5 | 1,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Macé (1860) | 5 | 1,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Massemin et al. (2009) | 5 | 1,5% | 3 | 4,62% | 3 | 5% | 3 | 4,84% |
Müller (1774) | 5 | 1,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié et al. (2012) | 4 | 1,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewarumez et al. (2011) | 3 | 0,9% | 3 | 4,62% | 3 | 5% | 3 | 4,84% |
Dupuy (1849) | 3 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Welter-schultes (2012) | 3 | 0,9% | 3 | 4,62% | 3 | 5% | 3 | 4,84% |
Bouchet & Pointier (1998) | 2 | 0,6% | 2 | 3,08% | 2 | 3,33% | 2 | 3,23% |
Breton (2014) | 2 | 0,6% | 2 | 3,08% | 2 | 3,33% | 1 | 1,61% |
Goulletquer (2016) | 2 | 0,6% | 2 | 3,08% | 2 | 3,33% | 2 | 3,23% |
Griffiths & Florens (2006) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Høpner et al. (1971) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1818) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Lopes-lima et al. (2024) | 2 | 0,6% | 2 | 3,08% | 2 | 3,33% | 2 | 3,23% |
Massemin et al. (2011) | 2 | 0,6% | 2 | 3,08% | 2 | 3,33% | 2 | 3,23% |
Payraudeau (1826) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié & Petit (2022) | 2 | 0,6% | 2 | 3,08% | 2 | 3,33% | 2 | 3,23% |
Prié & Puillandre (2014) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrusov (1897) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Anonyme. (2004) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Bespalaya et al. (2017) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
bij de Vaate & Beisel (2011) | 1 | 0,3% | 1 | 1,54% | 0 | 0% | 1 | 1,61% |
Bonhomme (1840) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Boubée (1833-1834) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Combrisson (2023) | 1 | 0,3% | 1 | 1,54% | 0 | 0% | 1 | 1,61% |
Conrad (1831) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Coomans (1967) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Cuvier (1798) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Faillettaz et al. (2020) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Fruget & Beisel (2016) | 1 | 0,3% | 1 | 1,54% | 0 | 0% | 1 | 1,61% |
Girardi (2003) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Groh et al. (2020) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Guppy (1867) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Haas (1969) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Hovestadt & Neckheim (2020) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Kerckhof et al. (2017) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Lea (1834) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Locard (1882) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Lopes-lima et al. (2018) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Lowe et al. (2007) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 0 | 0% |
Marescaux et al. (2012) | 1 | 0,3% | 1 | 1,54% | 0 | 0% | 1 | 1,61% |
Mouthon & Forcellini (2017) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Mouthon & Loiseau (2000) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Mouthon et al. (2017) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Mouthon et al. (2021) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Nakamura et al. (2024) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Normand (1844) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1771) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Pasco et al. (2023) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Pereira et al. (2013) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Pezy et al. (2022) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Phillips (1928) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Pigneur et al. (2011) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Poli (1791) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié & Fruget (2017) | 1 | 0,3% | 1 | 1,54% | 0 | 0% | 1 | 1,61% |
Prié et al. (2012) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié et al. (2012) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Prime (1865) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Puissauve, Barthelemy & Lamand (2015) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Puissauve, Cohen, Barthelemy & Reygnaud (2015) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Quiñonero-salgado & López-soriano (2017) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Rossmässler (1842) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1829) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Sheppard (1823) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Spengler (1793) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Stepien et al. (2013) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Vernhout (1914) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |
Wolowicz (1992) | 1 | 0,3% | 1 | 1,54% | 1 | 1,67% | 1 | 1,61% |