Rongeurs actuels de France métropolitaine
Rodentia actuellement présents en France métropolitaine (exclut les espèces disparues ou éteintes)
108 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) | 48 | 15% | 43 | 104,88% | 43 | 122,86% | 35 | 100% |
| Aulagnier et al. (2017) | 32 | 10% | 27 | 65,85% | 27 | 77,14% | 23 | 65,71% |
| Saint et al. (1978) | 12 | 3,75% | 9 | 21,95% | 9 | 25,71% | 7 | 20% |
| Linnaeus (1758) | 10 | 3,12% | 3 | 7,32% | 3 | 8,57% | 1 | 2,86% |
| Lorvelec et al. (2007) | 10 | 3,12% | 10 | 24,39% | 10 | 28,57% | 6 | 17,14% |
| Burneleau (1983) | 7 | 2,19% | 7 | 17,07% | 7 | 20% | 5 | 14,29% |
| Krystufek (2017) | 7 | 2,19% | 5 | 12,2% | 4 | 11,43% | 4 | 11,43% |
| Ladent et al. (2021) | 6 | 1,88% | 6 | 14,63% | 6 | 17,14% | 4 | 11,43% |
| Miller (1908) | 6 | 1,88% | 1 | 2,44% | 1 | 2,86% | 0 | 0% |
| Soubeyran et al. (2011) | 6 | 1,88% | 6 | 14,63% | 6 | 17,14% | 4 | 11,43% |
| Thévenot (2014) | 5 | 1,56% | 5 | 12,2% | 5 | 14,29% | 4 | 11,43% |
| Aulagnier (2012) | 4 | 1,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beaucornu (1962) | 4 | 1,25% | 4 | 9,76% | 4 | 11,43% | 4 | 11,43% |
| Linnaeus (1766) | 4 | 1,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 4 | 1,25% | 4 | 9,76% | 4 | 11,43% | 3 | 8,57% |
| Brunet-lecomte & Volobouev (1994) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 3 | 8,57% |
| Catzeflis (2018) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 2 | 5,71% |
| Gargominy et al. (1996) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 2 | 5,71% |
| Krystufek (2017) | 3 | 0,94% | 2 | 4,88% | 2 | 5,71% | 2 | 5,71% |
| Questel & Le Quellec (2012) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 2 | 5,71% |
| Questel (2020) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 2 | 5,71% |
| Storch & Lutt (1989) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 3 | 8,57% |
| Theuerkauf et al. (2010) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 2 | 5,71% |
| Vogel et al. (1991) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 3 | 8,57% |
| Yokoyama (2013) | 3 | 0,94% | 3 | 7,32% | 3 | 8,57% | 2 | 5,71% |
| Beaucournu (1974) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 2 | 5,71% |
| Blasius (1857) | 2 | 0,62% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Bochaton et al. (2021) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 2 | 5,71% |
| Brunet-Lecomte & Chaline (1993) | 2 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brunet-Lecomte (2010) | 2 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Castiglia et al. (2008) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 2 | 5,71% |
| Dozières (2012) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 1 | 2,86% |
| Frenot et al. (2005) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 1 | 2,86% |
| Gerbe & Lisle (1880) | 2 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerbe (1873) | 2 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerbe (1879) | 2 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2021) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 0 | 0% |
| Jourdan (2020) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 1 | 2,86% |
| Krystufek (2017) | 2 | 0,62% | 2 | 4,88% | 0 | 0% | 2 | 5,71% |
| Lacoste (de) (2020) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 1 | 2,86% |
| Musser & Carleton (2005) | 2 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prévost & Mougin (1970) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 1 | 2,86% |
| Reutter et al. (2002) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 2 | 5,71% |
| Revilliod (1914) | 2 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2015) | 2 | 0,62% | 2 | 4,88% | 2 | 5,71% | 1 | 2,86% |
| Albaret (2008) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Amand et al. (2012) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Ancillotto, L., Mori, E., Sozio, G., Solano, E., Bertolino, S. & Russo, D. 2017. A novel approach to field identification of cryptic Apodemus wood mice: calls differ more than morphology. Mammal Review, 47: 6â10. | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Anonyme. (2004) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Aulagnier (2019) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Bakhoum et al. (2015) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Bastelica (2010) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Bournaud & Gautheron-Duranthon (1969) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Brunet-lecomte (1995) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Chapuis et al. (2011) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Chapuis et al. (2014) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Chapuis (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 0 | 0% |
| Chapuis (2005) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 0 | 0% |
| Chapuis (2017) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Crespon (1844) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deblock et al. (1960) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Dieme et al. (2015) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Dozières et al. (2010) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Dozières et al. (2015) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| DREAL Alsace & MEDAD (2007) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Fatio (1905) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faugier & Bulliffon (2015) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Gerbe (1852) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerbe (1879) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerriet (2009) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Heim et al. (1967) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heinrich (1951) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouanin (1986) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Jouanin (1992) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Jourdane & Mas-Coma (1977) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Kamenova (2009) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Krapp & Winking (1976) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legros, Puissauve & Haffner (2015) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Linnaeus (1761) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lurz et al. (2013) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Major (1905) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marsot et al. (2011) | 1 | 0,31% | 1 | 2,44% | 0 | 0% | 1 | 2,86% |
| Melchior (1834) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nappi et al. (2019) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Obolenskaya et al. (2009) | 1 | 0,31% | 1 | 2,44% | 0 | 0% | 1 | 2,86% |
| Pallas (1771) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1778) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal & Chapuis (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Pascal & Vigne (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 0 | 0% |
| Pascal & Vigne (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Pascal & Vigne (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Pascal (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Pascal (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Ramousse & Le Berre (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 0 | 0% |
| Renaud et al. (2013) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sardin & Bauchet (1985) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schaefer (1935) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sélys-Longchamp de (1847) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sélys-Longchamps (1838) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| SORDELLO (2012) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 0 | 0% |
| Vein et al. (2013) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Vigne (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Vigne (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Vigne (2003) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Virion (2018) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Wencel (2000) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Yoccoz (1992) | 1 | 0,31% | 1 | 2,44% | 1 | 2,86% | 1 | 2,86% |
| Zilli (2021) | 1 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
