Soricomorphes, Erinacéomorphes, Diprotodontes et Xénarthres de France
Eulipotyphla (anciennement Soricomorpha et Erinaceomorpha), Diprotodontia et Xenarthra
80 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Aulagnier (2009) | 29 | 12.18% | 26 | 61.9% | 26 | 92.86% | 12 | 40% |
. SFEPM, Bourges. 56 pp. ">Rigaux & Dupasquier (2012) | 14 | 5.88% | 13 | 30.95% | 13 | 46.43% | 6 | 20% |
Aulagnier et al. (2017) | 11 | 4.62% | 10 | 23.81% | 10 | 35.71% | 5 | 16.67% |
Catzeflis (2012) | 9 | 3.78% | 9 | 21.43% | 9 | 32.14% | 4 | 13.33% |
Hoff & Daszkiewicz (2001) | 9 | 3.78% | 9 | 21.43% | 9 | 32.14% | 4 | 13.33% |
Dewynter (2020) | 8 | 3.36% | 8 | 19.05% | 8 | 28.57% | 4 | 13.33% |
Uicn et al. (2017) | 8 | 3.36% | 8 | 19.05% | 8 | 28.57% | 4 | 13.33% |
Catzeflis & Thoisy (2012) | 7 | 2.94% | 7 | 16.67% | 7 | 25% | 2 | 6.67% |
Linnaeus (1758) | 7 | 2.94% | 6 | 14.29% | 6 | 21.43% | 3 | 10% |
Gilot et al. (1992) | 6 | 2.52% | 5 | 11.9% | 5 | 17.86% | 3 | 10% |
Saint et al. (1978) | 6 | 2.52% | 6 | 14.29% | 6 | 21.43% | 2 | 6.67% |
Chaezl & Chazel (2011) | 5 | 2.1% | 5 | 11.9% | 5 | 17.86% | 4 | 13.33% |
Ariagno et al. (2016) | 4 | 1.68% | 4 | 9.52% | 4 | 14.29% | 2 | 6.67% |
Barthe et al. (2024) | 4 | 1.68% | 4 | 9.52% | 3 | 10.71% | 3 | 10% |
Euzet & Jourdane (1968) | 3 | 1.26% | 3 | 7.14% | 3 | 10.71% | 0 | 0% |
Faugier (2011) | 3 | 1.26% | 3 | 7.14% | 3 | 10.71% | 2 | 6.67% |
Igea et al. (2015) | 3 | 1.26% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Nicolas et al. (2017) | 3 | 1.26% | 3 | 7.14% | 3 | 10.71% | 3 | 10% |
Raynaud et Heim de Balsac (1940) | 3 | 1.26% | 0 | 0% | 0 | 0% | 0 | 0% |
Vesmanis et al. (1982) | 3 | 1.26% | 0 | 0% | 0 | 0% | 0 | 0% |
Wagler (1832) | 3 | 1.26% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu & Gilot (1971) | 2 | 0.84% | 2 | 4.76% | 2 | 7.14% | 2 | 6.67% |
Brünner et al. (2002) | 2 | 0.84% | 2 | 4.76% | 2 | 7.14% | 2 | 6.67% |
Burneleau (1983) | 2 | 0.84% | 2 | 4.76% | 2 | 7.14% | 1 | 3.33% |
Butet & Leroux (1993) | 2 | 0.84% | 2 | 4.76% | 2 | 7.14% | 2 | 6.67% |
Castiglia et al. (2007) | 2 | 0.84% | 2 | 4.76% | 2 | 7.14% | 0 | 0% |
Charissou (2001) | 2 | 0.84% | 2 | 4.76% | 2 | 7.14% | 0 | 0% |
Grulich (1971) | 2 | 0.84% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausser (1978) | 2 | 0.84% | 2 | 4.76% | 2 | 7.14% | 1 | 3.33% |
Kahmann & Kahmann (1954) | 2 | 0.84% | 2 | 4.76% | 0 | 0% | 2 | 6.67% |
Miller (1907) | 2 | 0.84% | 0 | 0% | 0 | 0% | 0 | 0% |
Millet (1828) | 2 | 0.84% | 2 | 4.76% | 2 | 7.14% | 2 | 6.67% |
Pallas (1831) | 2 | 0.84% | 0 | 0% | 0 | 0% | 0 | 0% |
Wagler (1832) | 2 | 0.84% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Araigno (2007) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Basset & Hausser (2003) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Bechstein (1800) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1840) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Bouche (2000) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Brumpt (1923) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Burton (1995) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Chabasse et al. (1987) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Chastel et al. (1994) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Crochet (1990) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Desbrosses (1996) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Dollfus & Callot (1944) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Heim de Balsac (1940) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Hermann (1783) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdane (1977) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Kerr (1792) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1763) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Morel (1959) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1776) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Némoz & Bertrand (2008) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Nicolas et al. (2021) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Niort (1949) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Omar et al. (2011) | 1 | 0.42% | 1 | 2.38% | 0 | 0% | 1 | 3.33% |
Pascal & Vigne (2003) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Pascal (2003) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Pennant (1771) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Phillips et al. (2013) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst & Tézier (2000) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Puissauve & Haffner (2015) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Rode (1938) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Le Corre (2009) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Salamolard (2002) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Schinz (1837) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Sélys-longchamps (1839) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |
Sheftel (2018) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Taberlet (1983) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Theron (1976) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Thévenot (2014) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Tillon & Lorvelec (2004) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 1 | 3.33% |
Tournier & Miquet (1990) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Uicn et al. (2015) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Vigne & Pascal (2003) | 1 | 0.42% | 1 | 2.38% | 1 | 3.57% | 0 | 0% |
Zimmermann (1780) | 1 | 0.42% | 0 | 0% | 0 | 0% | 0 | 0% |