Mammifères de métropole
Mammalia de France métropolitaine
547 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) | 178 | 8,97% | 167 | 51,38% | 167 | 63,74% | 110 | 40,29% |
Aulagnier et al. (2017) | 157 | 7,91% | 140 | 43,08% | 140 | 53,44% | 105 | 38,46% |
Rinaldi (2016) | 156 | 7,86% | 152 | 46,77% | 152 | 58,02% | 100 | 36,63% |
Carzon et al. (2016) | 117 | 5,89% | 114 | 35,08% | 114 | 43,51% | 75 | 27,47% |
Estrade et al. (2016) | 117 | 5,89% | 114 | 35,08% | 114 | 43,51% | 75 | 27,47% |
Linnaeus (1758) | 70 | 3,53% | 31 | 9,54% | 31 | 11,83% | 19 | 6,96% |
Charrassin (2016) | 39 | 1,96% | 38 | 11,69% | 38 | 14,5% | 25 | 9,16% |
Charrassin (2016) | 39 | 1,96% | 38 | 11,69% | 38 | 14,5% | 25 | 9,16% |
Jarrett & Shirihai (2014) | 39 | 1,96% | 38 | 11,69% | 38 | 14,5% | 25 | 9,16% |
Moutou (2016) | 39 | 1,96% | 38 | 11,69% | 38 | 14,5% | 25 | 9,16% |
Spitz et al. (2016) | 39 | 1,96% | 38 | 11,69% | 38 | 14,5% | 25 | 9,16% |
Thoisy & Bordin (2016) | 39 | 1,96% | 38 | 11,69% | 38 | 14,5% | 25 | 9,16% |
Urtizberea (2016) | 39 | 1,96% | 38 | 11,69% | 38 | 14,5% | 25 | 9,16% |
Uicn et al. (2015) | 37 | 1,86% | 37 | 11,38% | 37 | 14,12% | 23 | 8,42% |
Arthur & Lemaire (2015) | 34 | 1,71% | 34 | 10,46% | 34 | 12,98% | 29 | 10,62% |
Dietz & Kiefer (2015) | 34 | 1,71% | 34 | 10,46% | 34 | 12,98% | 29 | 10,62% |
Godineau & Pain (2007) | 33 | 1,66% | 33 | 10,15% | 33 | 12,6% | 28 | 10,26% |
Grubb (2005) | 28 | 1,41% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Bordin et al. (2021) | 24 | 1,21% | 24 | 7,38% | 24 | 9,16% | 17 | 6,23% |
Garrigue (2007) | 22 | 1,11% | 22 | 6,77% | 22 | 8,4% | 16 | 5,86% |
Gilot et al. (1992) | 22 | 1,11% | 16 | 4,92% | 16 | 6,11% | 10 | 3,66% |
Gannier (2001) | 20 | 1,01% | 20 | 6,15% | 20 | 7,63% | 14 | 5,13% |
G.E.M.M. (2012) | 20 | 1,01% | 20 | 6,15% | 20 | 7,63% | 14 | 5,13% |
Catzeflis (2012) | 19 | 0,96% | 19 | 5,85% | 19 | 7,25% | 13 | 4,76% |
Dewynter et al. (2021) | 19 | 0,96% | 19 | 5,85% | 19 | 7,25% | 16 | 5,86% |
Tapiero et al. (2017) | 19 | 0,96% | 19 | 5,85% | 19 | 7,25% | 15 | 5,49% |
Aubouin et al. (2016) | 18 | 0,91% | 18 | 5,54% | 18 | 6,87% | 12 | 4,4% |
Aulagnier (2021) | 18 | 0,91% | 18 | 5,54% | 18 | 6,87% | 9 | 3,3% |
Saint et al. (1978) | 18 | 0,91% | 15 | 4,62% | 15 | 5,73% | 8 | 2,93% |
Lorvelec et al. (2007) | 17 | 0,86% | 17 | 5,23% | 17 | 6,49% | 9 | 3,3% |
Barré (2021) | 16 | 0,81% | 16 | 4,92% | 16 | 6,11% | 12 | 4,4% |
Questel (2020) | 16 | 0,81% | 14 | 4,31% | 14 | 5,34% | 10 | 3,66% |
Gannier (2002) | 15 | 0,76% | 15 | 4,62% | 15 | 5,73% | 13 | 4,76% |
Gannier (2009) | 15 | 0,76% | 15 | 4,62% | 15 | 5,73% | 12 | 4,4% |
Uicn et al. (2017) | 15 | 0,76% | 15 | 4,62% | 15 | 5,73% | 10 | 3,66% |
Desbrosses & Etcheberry (1987) | 14 | 0,71% | 11 | 3,38% | 11 | 4,2% | 4 | 1,47% |
Gannier (2000) | 14 | 0,71% | 14 | 4,31% | 14 | 5,34% | 11 | 4,03% |
Soubeyran et al. (2011) | 14 | 0,71% | 14 | 4,31% | 14 | 5,34% | 12 | 4,4% |
Thévenot (2014) | 14 | 0,71% | 14 | 4,31% | 14 | 5,34% | 13 | 4,76% |
Kiszka et al.(2007) | 13 | 0,65% | 13 | 4% | 13 | 4,96% | 11 | 4,03% |
Burneleau (1983) | 12 | 0,6% | 12 | 3,69% | 12 | 4,58% | 7 | 2,56% |
Gentry et al. (2004) | 12 | 0,6% | 10 | 3,08% | 10 | 3,82% | 9 | 3,3% |
Questel & Le Quellec (2012) | 12 | 0,6% | 11 | 3,38% | 11 | 4,2% | 8 | 2,93% |
Kiszka et al. (2010) | 11 | 0,55% | 11 | 3,38% | 11 | 4,2% | 10 | 3,66% |
Laran et al. (2011) | 11 | 0,55% | 11 | 3,38% | 11 | 4,2% | 10 | 3,66% |
Lowe et al. (2007) | 11 | 0,55% | 11 | 3,38% | 11 | 4,2% | 5 | 1,83% |
Prévost & Mougin (1970) | 11 | 0,55% | 11 | 3,38% | 10 | 3,82% | 8 | 2,93% |
Yokoyama (2013) | 11 | 0,55% | 10 | 3,08% | 10 | 3,82% | 9 | 3,3% |
Dulau-Drouot et al. (2008) | 10 | 0,5% | 10 | 3,08% | 10 | 3,82% | 8 | 2,93% |
Samaran & Guinet (2009) | 10 | 0,5% | 10 | 3,08% | 10 | 3,82% | 7 | 2,56% |
Theuerkauf et al. (2010) | 10 | 0,5% | 10 | 3,08% | 10 | 3,82% | 7 | 2,56% |
Gargominy et al. (1996) | 9 | 0,45% | 9 | 2,77% | 9 | 3,44% | 6 | 2,2% |
Jourdan (2020) | 9 | 0,45% | 9 | 2,77% | 8 | 3,05% | 6 | 2,2% |
Linnaeus (1766) | 9 | 0,45% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Perrin et al. (2002) | 9 | 0,45% | 9 | 2,77% | 9 | 3,44% | 5 | 1,83% |
Shirihai (2003) | 8 | 0,4% | 8 | 2,46% | 8 | 3,05% | 4 | 1,47% |
Butaud (2021) | 7 | 0,35% | 7 | 2,15% | 7 | 2,67% | 6 | 2,2% |
Frenot et al. (2005) | 7 | 0,35% | 7 | 2,15% | 7 | 2,67% | 4 | 1,47% |
Krystufek (2017) | 7 | 0,35% | 5 | 1,54% | 4 | 1,53% | 4 | 1,47% |
Bochaton et al. (2021) | 6 | 0,3% | 6 | 1,85% | 6 | 2,29% | 6 | 2,2% |
Boer et al. (1999) | 6 | 0,3% | 6 | 1,85% | 6 | 2,29% | 4 | 1,47% |
Godet et al. (2021) | 6 | 0,3% | 6 | 1,85% | 6 | 2,29% | 2 | 0,73% |
Ladent et al. (2021) | 6 | 0,3% | 6 | 1,85% | 6 | 2,29% | 4 | 1,47% |
Miller (1908) | 6 | 0,3% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Pallas (1778) | 6 | 0,3% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Robineau & Duhamel (2006) | 6 | 0,3% | 6 | 1,85% | 6 | 2,29% | 3 | 1,1% |
Savouré-Soubelet et al. (in prep.) | 6 | 0,3% | 6 | 1,85% | 6 | 2,29% | 2 | 0,73% |
Fort & Barrière (2021) | 5 | 0,25% | 5 | 1,54% | 5 | 1,91% | 4 | 1,47% |
Pallas (1831) | 5 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. 2006 | 5 | 0,25% | 5 | 1,54% | 5 | 1,91% | 3 | 1,1% |
Robineau (2005) | 5 | 0,25% | 5 | 1,54% | 5 | 1,91% | 1 | 0,37% |
Ariagno et al. (2016) | 4 | 0,2% | 4 | 1,23% | 4 | 1,53% | 2 | 0,73% |
Aulagnier (2012) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucornu (1962) | 4 | 0,2% | 4 | 1,23% | 4 | 1,53% | 4 | 1,47% |
Boer (2000) | 4 | 0,2% | 4 | 1,23% | 4 | 1,53% | 1 | 0,37% |
Caceres & Salamolard (2021) | 4 | 0,2% | 4 | 1,23% | 4 | 1,53% | 3 | 1,1% |
Des et al. (2021) | 4 | 0,2% | 4 | 1,23% | 4 | 1,53% | 3 | 1,1% |
Groves & Grubb (2011) | 4 | 0,2% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
IUCN (2012) | 4 | 0,2% | 4 | 1,23% | 4 | 1,53% | 3 | 1,1% |
Kitchener et al. (2017) | 4 | 0,2% | 4 | 1,23% | 0 | 0% | 4 | 1,47% |
Pérez et al. (2014) | 4 | 0,2% | 4 | 1,23% | 2 | 0,76% | 2 | 0,73% |
Pérez et al. (2017) | 4 | 0,2% | 4 | 1,23% | 2 | 0,76% | 2 | 0,73% |
Routtier et al. (2023) | 4 | 0,2% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Uicn et al. (2020) | 4 | 0,2% | 4 | 1,23% | 4 | 1,53% | 2 | 0,73% |
Zelhuber (2009) | 4 | 0,2% | 4 | 1,23% | 3 | 1,15% | 3 | 1,1% |
Alves et al. (2003) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 1 | 0,37% |
Bailenger et al. (1965) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 0 | 0% |
Borsa (1997) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 1 | 0,37% |
Brunet-lecomte & Volobouev (1994) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Catzeflis (2018) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 2 | 0,73% |
Chabasse et al. (1987) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 2 | 0,73% |
Deméré (2014) | 3 | 0,15% | 3 | 0,92% | 0 | 0% | 3 | 1,1% |
Euzet & Jourdane (1968) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 0 | 0% |
Faugier (2011) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 2 | 0,73% |
Guedon & Pascal (1993) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Igea et al. (2015) | 3 | 0,15% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Jacquet (2009) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Juste et al. (2018) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Kawamura (1994) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 0 | 0% |
Krystufek (2017) | 3 | 0,15% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Lacoste (de) (2020) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 1 | 0,37% |
Léger (2008) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Nicolas et al. (2017) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Puechmaille et al. (2023) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Raynaud et Heim de Balsac (1940) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi-santos et al. (2007) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 1 | 0,37% |
Stewart (2014) | 3 | 0,15% | 3 | 0,92% | 0 | 0% | 3 | 1,1% |
Storch & Lutt (1989) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Torres et al. (2008) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Vesmanis et al. (1982) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Vogel et al. (1991) | 3 | 0,15% | 3 | 0,92% | 3 | 1,15% | 3 | 1,1% |
Wagler (1832) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
AAMP (2012) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Ainley et al. (2007) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Aouraghe (1990) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Beaucournu (1968) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu (1974) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Benedetti et al. (2021) | 2 | 0,1% | 2 | 0,62% | 1 | 0,38% | 1 | 0,37% |
Blanchet et al. (1998) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Blasius (1857) | 2 | 0,1% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Boer & Simmonds (2000) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Bordes et al. (2007) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Bouchez-Zacria et al. (2024) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Brown (2008) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Brunet-Lecomte & Chaline (1993) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunet-Lecomte (2010) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünner et al. (2002) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Butet & Leroux (1993) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Castiglia et al. (2007) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Castiglia et al. (2008) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Chaline (1980) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapuis et al. (2004) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Charissou (2001) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Diaz & Cuzange (2009) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Dozières (2012) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Fabre & Orsini (2016) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Fourt et al. (2017) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Gerbe & Lisle (1880) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerbe (1873) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerbe (1879) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill & Thiele (1997) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Girard-claudon & Ribatto (2016) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Grulich (1971) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hausser (1978) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Kahmann & Kahmann (1954) | 2 | 0,1% | 2 | 0,62% | 0 | 0% | 2 | 0,73% |
Kasamatsu & Joyce (1995) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Kasamatsu et al. (2000) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Keyserling & Blasius (1839) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Kock et al. (2006) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Krystufek (2017) | 2 | 0,1% | 2 | 0,62% | 0 | 0% | 2 | 0,73% |
Laran et al. (2012) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Lavauden (1929) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Leaper et al. (2008) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Linnaeus (1761) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lustrat (1987) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Mas-Coma et al. (1989) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Matsuoka et al. (2005) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Ménard et al. (2000) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Miller (1907) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Millet (1828) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Musser & Carleton (2005) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Nyakatura & Bininda-Emonds (2012) | 2 | 0,1% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pallas (1771) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1773) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Parise et al. (2012) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Pascal et al. (2006) | 2 | 0,1% | 2 | 0,62% | 1 | 0,38% | 2 | 0,73% |
Pascal (1988) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Potin (2013) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Puechmaille et al. (2012) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Reutter et al. (2002) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Revilliod (1914) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau (1989) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Robineau (2004) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Ruys & Coord (2012) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Saint-andrieux et al. (2006) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Saint-andrieux et al. (2009) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Schreber (1774) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Schreber (1777) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Sélys-Longchamps (1839) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Spitz et al. (2015) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 0 | 0% |
Stewart (2014) | 2 | 0,1% | 2 | 0,62% | 0 | 0% | 2 | 0,73% |
Széles et al. (2018) | 2 | 0,1% | 1 | 0,31% | 0 | 0% | 1 | 0,37% |
Thiele et al. (1999) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Thiele et al. (2004) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 1 | 0,37% |
Uicn et al. (2017) | 2 | 0,1% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
UICN (2009) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Valdez (2011) | 2 | 0,1% | 2 | 0,62% | 0 | 0% | 2 | 0,73% |
Van Canneytet al. (2008) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Viel (2021) | 2 | 0,1% | 2 | 0,62% | 2 | 0,76% | 2 | 0,73% |
Wagler (1832) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Zimmermann (1780) | 2 | 0,1% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Abril et al. (1986) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Albaret (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Amand et al. (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
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 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Andrew et al. (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 0 | 0% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Anonyme (2017) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Anonymous (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Aoutil et al. (2005) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Araigno (2007) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Ariagno & Erome (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Artois & Duchene (1982) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Artois et al. (1982) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Aulagnier (2019) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Bakhoum et al. (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Basset & Hausser (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Bastelica (2010) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Baubet & Saint-andrieux (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Beaucournu (1962) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Bechstein (1800) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard (1964) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Berzins & Ruette (2014) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Best et al. (1995) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Blumenbach (1799) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Blyth (1841) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Body (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Bojanus (1827) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1840) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Boubert et al. (2019) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Bouche (2000) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Bournaud & Gautheron-Duranthon (1969) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Boussinesq et al. (1986) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Branch (2010) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Breton (2014) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Brumpt (1923) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Brunet-lecomte (1995) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Brunet-lecomte (2005) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Budylenko (1977) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Burton (1995) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Callou (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Cassinello (1998) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Cerchio et al. (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Chaline & Laborier (1981) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Chapuis et al. (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapuis et al. (2011) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Chapuis et al. (2014) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Chapuis (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Chapuis (2005) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Chapuis (2017) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Chastel et al. (1994) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Cheke & Hume (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Colas-Belcour & Rageau (1951) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Collectif (1999) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Collectif (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Combes & Clerc (1970) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Corti et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Cottarel et al. (2013) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Cotte et al. (2001) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Counihan et al. (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Crampe & Barascud (2014) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Crespon (1844) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Crochet (1990) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Croquet & Cugnasse (2013) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Cugnasse & Rigaux (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Cunha et al. (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Dalebout et al. (2005) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Deblock et al. (1960) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Delattre et al. (1990) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Desbrosses (1996) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Desmet (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Dewas et al. (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Dewynter (2020) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Dieme et al. (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Dietz (2005) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Dollfus & Callot (1944) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Dozières et al. (2010) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Dozières et al. (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
DREAL Alsace & MEDAD (2007) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
DREAL Occitanie (2014) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Dubray & Barboiron (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Dubrulle & Catusse (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Ersts & Rosenbaum (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Erxleben (1777) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Falconer & Cautley (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fatio (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Faugier & Bulliffon (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Fleming & Jackson (2011) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Gadeau de Kerville (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Galaup & Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Galibert et al. (2018) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Garnier et al. (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Geoffroy (1812) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerbe (1852) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerbe (1879) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
GEREA & DIREN (2007) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Gerriet (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Gillespie (1997) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Gonzalez et al. (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Goodall et al. (1997) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Gray (1832-1835) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Greenwood (1955) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Grisser (1987) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Gueldenstaedt (1770) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Guerin (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Guinet (1991) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Guinet (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Guitton (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Harran et al. (2023) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Heim de Balsac (1940) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Heim et al. (1967) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Heimlich-boran (1993) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Heinrich (1951) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Helversen (2001) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Hermann (1779) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hermann (1783) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hinton (1910) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff & Daszkiewicz (2001) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Houin et al. (1982) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Huvier et al. (2023) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Jaquemet et al. (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Jefferson & & Van Waerebeek (2002) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jefferson & Barros (1997) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Jehl et al. (1980) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Johnson & Wolman (1984) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Jouanin (1986) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Jouanin (1992) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Joubert & Margerit (1986) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Jouglin et al. (2019) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Jourdane & Mas-Coma (1977) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Jourdane (1977) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Kamenova (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Kasamatsu et al. (1995) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Kasamatsu et al. (1998) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Kia et al. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiefer & Veith (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al. (2007) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Kiszka et al. (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Klein & Saint-andrieux (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Krapp & Winking (1976) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kratochvil (1981) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Kuhn et al. (2019) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Kuhn (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Kuhn (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Labach et al. (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Lacoste (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Lacoste (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Lancastre et al. (1973) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Lancastre et al. (1976) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Lataste (1883) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Laurent (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Leaper et al. (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Leatherwood et al. (1979) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Lebarbenchon et al. (2010) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Léger et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Léger (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Léger (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Legros, Puissauve & Haffner (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Lesson (1828) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Letacq (1924) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Letty & Bouche (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Letty et al. (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Levesque & Mathurin (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Lorvelec & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Losinger (2007) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Lurz et al. (2013) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Macleod et al. (2006) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Maillard & Saint-Andrieux (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Maillard (2020) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Major (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Marboutin et al. (2006) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Marchandeau & Letty (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Marchandeau et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Marié et al. (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Marquet & Seronie-vivien (2016) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Marsot et al. (2011) | 1 | 0,05% | 1 | 0,31% | 0 | 0% | 1 | 0,37% |
Matschie (1901) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
MEDD (2006) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
MEDDE & MAAF (2013) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Medde (2014) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
MEEDDAT & MAP (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Melchior (1834) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Michallet et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Miller (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Miller-Butterworth et al. (2007) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Miquet (1996) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Montagu (1808) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Morel (1959) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
MTES & MAA (2018) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Müller (1776) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Murase et al. (2002) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Nappi et al. (2019) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Nassi et al. (1975) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Némoz & Bertrand (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Nesti (1825) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Neveu-Lemaire (1923) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Nicol et al. (2000) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Nicolas et al. (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Niort (1949) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2017) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
N'Zobadila et al. (1996) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Obolenskaya et al. (2009) | 1 | 0,05% | 1 | 0,31% | 0 | 0% | 1 | 0,37% |
Oremus (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pallas (1776) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1777) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal & Chapuis (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal & Lorvelec (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal et al. (2003) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Pennant (1771) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pereira et al. (2001) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Perrin et al. (1994) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Perry et al. (1999) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Phillips et al. (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierpoint et al. (1997) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Pietri et al. (2011) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pisanu et al. (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Pisanu (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pitman & Ensor (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Pons et al. (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Portanier et al. (2023) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Praderi et al. (1992) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Probst & Tézier (2000) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Puissauve & Haffner (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Puissauve, Haffner & Khun (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Puissauve, Legros, Kerbiriou & Marmet (2015) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Ramousse & Le Berre (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Randi et al. (2001) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Renaud et al. (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribic et al. (1991) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Riccialdelli et al. (2010) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Ridoux (2016) | 1 | 0,05% | 1 | 0,31% | 0 | 0% | 1 | 0,37% |
Ringler et al. (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Roche & Guinet (2007) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Rode (1938) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosenbaum & Collins (2006) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Rosenhauer (1856) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Ruedi et al. (2002) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Ruedi et al. (2019) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Rüppell (1842) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Le Corre (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Saint-andrieux & Cargnelutti (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Saint-andrieux (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Salamolard (2002) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Samaran (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Sardin & Bauchet (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scalera & Angelici (2002) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Scandola et al. (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schaefer (1935) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schinz (1837) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Sélys-Longchamp de (1847) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sélys-Longchamps (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sélys-longchamps (1839) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sheffield & King (1994) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Sheftel (2018) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Sillero-Zubiri (2009) | 1 | 0,05% | 1 | 0,31% | 0 | 0% | 1 | 0,37% |
Sirovic et al. (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Smith et al. (2005) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Soubeyran (2008) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Stahl et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Stahl et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Taberlet (1983) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Temminck (1824-1825) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Theron (1975) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Theron (1976) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Tillon & Lorvelec (2004) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Toïgo et al. (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Tournier & Miquet (1990) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Tresset et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Trotignon (1989) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
UICN Comité français, OFB & MNHN (2021) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Varanguin (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Vein et al. (2013) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Viale & Frontier (1989) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne & Pascal | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne & Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Vigne & Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne & Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Vigne & Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne & Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Vigne & Pascal (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne et al. (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Vigne et al. (2003) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vigne (2003) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vincent (1987) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vincent (2001) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Virion (2018) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Vollmer et al. (2019) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Wagner (1832) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Weerdt (2023) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Wencel (2000) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Williams et al. (2009) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 0 | 0% |
Wursig & Wursig (1980) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |
Yoccoz (1992) | 1 | 0,05% | 1 | 0,31% | 1 | 0,38% | 1 | 0,37% |