Bivalves d'eau douce
Bivalvia d'eau douce au sens large
74 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 | 30,33% | 96 | 145,45% | 82 | 138,98% | 88 | 141,94% |
| Falkner et al. (2002) | 66 | 19,82% | 26 | 39,39% | 21 | 35,59% | 23 | 37,1% |
| Gargominy et al. (2011) | 63 | 18,92% | 42 | 63,64% | 37 | 62,71% | 39 | 62,9% |
| Lopes-Lima et al. (2016) | 12 | 3,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié (2020) | 10 | 3% | 8 | 12,12% | 8 | 13,56% | 8 | 12,9% |
| Delannoye et al. (2015) | 7 | 2,1% | 6 | 9,09% | 6 | 10,17% | 6 | 9,68% |
| Lamy & Pointier (2018) | 6 | 1,8% | 6 | 9,09% | 6 | 10,17% | 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 | 4,55% | 3 | 5,08% | 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 | 4,55% | 3 | 5,08% | 3 | 4,84% |
| Dupuy (1849) | 3 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welter-schultes (2012) | 3 | 0,9% | 3 | 4,55% | 3 | 5,08% | 3 | 4,84% |
| Bouchet & Pointier (1998) | 2 | 0,6% | 2 | 3,03% | 2 | 3,39% | 2 | 3,23% |
| Breton (2014) | 2 | 0,6% | 2 | 3,03% | 2 | 3,39% | 1 | 1,61% |
| Goulletquer (2016) | 2 | 0,6% | 2 | 3,03% | 2 | 3,39% | 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% |
| Massemin et al. (2011) | 2 | 0,6% | 2 | 3,03% | 2 | 3,39% | 2 | 3,23% |
| Payraudeau (1826) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Petit (2022) | 2 | 0,6% | 2 | 3,03% | 2 | 3,39% | 2 | 3,23% |
| Prié & Puillandre (2014) | 2 | 0,6% | 1 | 1,52% | 0 | 0% | 1 | 1,61% |
| Andrusov (1897) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Anonyme. (2004) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 0 | 0% |
| Bespalaya et al. (2017) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| bij de Vaate & Beisel (2011) | 1 | 0,3% | 1 | 1,52% | 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 | 1,52% | 0 | 0% | 1 | 1,61% |
| Conrad (1831) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coomans (1967) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Cuvier (1798) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faillettaz et al. (2020) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Fruget & Beisel (2016) | 1 | 0,3% | 1 | 1,52% | 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 | 1,52% | 1 | 1,69% | 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 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Lowe et al. (2007) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 0 | 0% |
| Marescaux et al. (2012) | 1 | 0,3% | 1 | 1,52% | 0 | 0% | 1 | 1,61% |
| Mouthon & Forcellini (2017) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Mouthon & Loiseau (2000) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mouthon et al. (2017) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Mouthon et al. (2021) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Pereira et al. (2013) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Phillips (1928) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pigneur et al. (2011) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Poli (1791) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prié & Fruget (2017) | 1 | 0,3% | 1 | 1,52% | 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 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Prime (1865) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Puissauve, Barthelemy & Lamand (2015) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 0 | 0% |
| Puissauve, Cohen, Barthelemy & Reygnaud (2015) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Quiñonero-salgado & López-soriano (2017) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 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 | 1,52% | 1 | 1,69% | 1 | 1,61% |
| Wolowicz (1992) | 1 | 0,3% | 1 | 1,52% | 1 | 1,69% | 1 | 1,61% |
