Formicidae de France métropolitaine
Formicidae de France métropolitaine
347 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Casevitz-Weulersse & Galkowski (2009) | 268 | 19.34% | 186 | 62.42% | 186 | 68.38% | 162 | 59.56% |
Lebas et al. (2016) | 250 | 18.04% | 228 | 76.51% | 228 | 83.82% | 203 | 74.63% |
Colindre (2016) | 47 | 3.39% | 47 | 15.77% | 47 | 17.28% | 39 | 14.34% |
Bolton (2003) | 32 | 2.31% | 11 | 3.69% | 11 | 4.04% | 11 | 4.04% |
Seifert (2020) | 29 | 2.09% | 26 | 8.72% | 26 | 9.56% | 26 | 9.56% |
Willot & Wegnez (2024) | 27 | 1.95% | 27 | 9.06% | 27 | 9.93% | 22 | 8.09% |
Blatrix et al. (2018) | 26 | 1.88% | 26 | 8.72% | 26 | 9.56% | 26 | 9.56% |
Seifert (2021) | 24 | 1.73% | 24 | 8.05% | 24 | 8.82% | 21 | 7.72% |
Ward et al. (2015) | 23 | 1.66% | 10 | 3.36% | 10 | 3.68% | 10 | 3.68% |
Bellmann (2019) | 18 | 1.3% | 17 | 5.7% | 17 | 6.25% | 12 | 4.41% |
Wheeler (1935) | 18 | 1.3% | 12 | 4.03% | 12 | 4.41% | 12 | 4.41% |
Colindre (2017) | 16 | 1.15% | 16 | 5.37% | 16 | 5.88% | 16 | 5.88% |
Galkowski et al. (2010) | 16 | 1.15% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Bondroit (1918) | 15 | 1.08% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Mayr (1861) | 14 | 1.01% | 10 | 3.36% | 10 | 3.68% | 6 | 2.21% |
Perrault (1988) | 14 | 1.01% | 13 | 4.36% | 13 | 4.78% | 13 | 4.78% |
Ramage et al. (2023) | 14 | 1.01% | 14 | 4.7% | 14 | 5.15% | 14 | 5.15% |
Ramage (2014) | 14 | 1.01% | 14 | 4.7% | 14 | 5.15% | 14 | 5.15% |
Ramage (2017) | 14 | 1.01% | 14 | 4.7% | 14 | 5.15% | 14 | 5.15% |
Bernard (1968) | 13 | 0.94% | 8 | 2.68% | 8 | 2.94% | 8 | 2.94% |
Franco et al. (2019) | 13 | 0.94% | 13 | 4.36% | 13 | 4.78% | 13 | 4.78% |
Jaffe & Lattke (1994) | 13 | 0.94% | 12 | 4.03% | 12 | 4.41% | 12 | 4.41% |
Meurgey & Ramage (2020) | 13 | 0.94% | 13 | 4.36% | 13 | 4.78% | 13 | 4.78% |
Seifert et al. (2024) | 13 | 0.94% | 10 | 3.36% | 10 | 3.68% | 9 | 3.31% |
Galkowski (2016) | 12 | 0.87% | 12 | 4.03% | 12 | 4.41% | 12 | 4.41% |
Taylor (1987) | 12 | 0.87% | 12 | 4.03% | 12 | 4.41% | 12 | 4.41% |
Bernard (1978) | 11 | 0.79% | 0 | 0% | 0 | 0% | 0 | 0% |
L'Entomologiste picard, 34: 2.">Colindre et al. (2021) | 11 | 0.79% | 11 | 3.69% | 11 | 4.04% | 8 | 2.94% |
Galkowski & Cagniant (2017) | 11 | 0.79% | 7 | 2.35% | 7 | 2.57% | 7 | 2.57% |
Jennings et al. (2013) | 11 | 0.79% | 11 | 3.69% | 11 | 4.04% | 11 | 4.04% |
Jourdan & Mille (2006) | 11 | 0.79% | 11 | 3.69% | 11 | 4.04% | 11 | 4.04% |
Morrison (1997) | 11 | 0.79% | 11 | 3.69% | 11 | 4.04% | 11 | 4.04% |
Wheeler (1932) | 11 | 0.79% | 8 | 2.68% | 8 | 2.94% | 8 | 2.94% |
Wilson & Taylor (1967) | 11 | 0.79% | 9 | 3.02% | 9 | 3.31% | 9 | 3.31% |
Morrison (1996) | 10 | 0.72% | 9 | 3.02% | 9 | 3.31% | 9 | 3.31% |
Blard et al. (2003) | 9 | 0.65% | 9 | 3.02% | 9 | 3.31% | 9 | 3.31% |
Meurgey (2011) | 9 | 0.65% | 8 | 2.68% | 8 | 2.94% | 8 | 2.94% |
Seifert (2012) | 9 | 0.65% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Wetterer (2002) | 9 | 0.65% | 8 | 2.68% | 8 | 2.94% | 8 | 2.94% |
Wheeler (1932) | 9 | 0.65% | 6 | 2.01% | 6 | 2.21% | 6 | 2.21% |
Wilson & Hunt (1967) | 9 | 0.65% | 8 | 2.68% | 8 | 2.94% | 8 | 2.94% |
Cheesman (1928) | 8 | 0.58% | 8 | 2.68% | 8 | 2.94% | 8 | 2.94% |
Questel (2020) | 8 | 0.58% | 8 | 2.68% | 8 | 2.94% | 8 | 2.94% |
Seifert (2002) | 8 | 0.58% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Wheeler (1933) | 8 | 0.58% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Wheeler (1936) | 8 | 0.58% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Agosti & Collingwood (1987) | 7 | 0.51% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (1995) | 7 | 0.51% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Dalla Torre (1893) | 7 | 0.51% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Latreille (1798) | 7 | 0.51% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Linnaeus (1758) | 7 | 0.51% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Plateaux & Cagniant (2012) | 7 | 0.51% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Seifert et al. (2017) | 7 | 0.51% | 7 | 2.35% | 7 | 2.57% | 7 | 2.57% |
Baliteau et al. (2010) | 6 | 0.43% | 6 | 2.01% | 6 | 2.21% | 6 | 2.21% |
Emery (1914) | 6 | 0.43% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Kirschner et al. (2023) | 6 | 0.43% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Latreille (1802) | 6 | 0.43% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1792) | 6 | 0.43% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1908) | 6 | 0.43% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Alicata et al. (2024) | 5 | 0.36% | 0 | 0% | 0 | 0% | 0 | 0% |
Baroni Urbani & De Andrade (2007) | 5 | 0.36% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Bolton (2012) | 5 | 0.36% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1915) | 5 | 0.36% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher & Fong (2020) | 5 | 0.36% | 5 | 1.68% | 5 | 1.84% | 4 | 1.47% |
Forel (1874) | 5 | 0.36% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Jourdan (2020) | 5 | 0.36% | 5 | 1.68% | 5 | 1.84% | 5 | 1.84% |
Radchenko & Elmes (2010) | 5 | 0.36% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Radoszkowsky (1884) | 5 | 0.36% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Rigato (2011) | 5 | 0.36% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Roger (1863) | 5 | 0.36% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Molecular Phylogenetics and Evolution, 127: 387‑404.">Steiner et al. (2018) | 5 | 0.36% | 5 | 1.68% | 5 | 1.84% | 2 | 0.74% |
Wetterer (2012) | 5 | 0.36% | 5 | 1.68% | 5 | 1.84% | 5 | 1.84% |
Wetterer (2013) | 5 | 0.36% | 5 | 1.68% | 5 | 1.84% | 5 | 1.84% |
André (1881) | 4 | 0.29% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Bernard (1977) | 4 | 0.29% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Colindre (2016) | 4 | 0.29% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Emery (1869) | 4 | 0.29% | 3 | 1.01% | 3 | 1.1% | 2 | 0.74% |
Emery (1916) | 4 | 0.29% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1925) | 4 | 0.29% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 4 | 0.29% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Hamer et al. (2021) | 4 | 0.29% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Lenoir et al. (2023) | 4 | 0.29% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Mayr (1855) | 4 | 0.29% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Perrault (1993) | 4 | 0.29% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Questel & Le Quellec (2012) | 4 | 0.29% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Roger (1859) | 4 | 0.29% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert et al. (2014) | 4 | 0.29% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Talaga et al. (2015) | 4 | 0.29% | 4 | 1.34% | 4 | 1.47% | 4 | 1.47% |
Wagner et al. (2017) | 4 | 0.29% | 4 | 1.34% | 4 | 1.47% | 3 | 1.1% |
Bernard (1978) | 3 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
Blatrix et al. (2013) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Bolton (2007) | 3 | 0.22% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Bondroit (1917) | 3 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
Bondroit (1920) | 3 | 0.22% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Casevitz-Weulersse (1990) | 3 | 0.22% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Castro-Cobo et al. (2021) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Collingwood & Yarrow (1969) | 3 | 0.22% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Darchen (1976) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Donisthorpe (1932) | 3 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1924) | 3 | 0.22% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Galkowski et al. (2017) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
García et al. (2020) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Guilbert & Casevitz-Weulersse (1997) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Lowe et al. (2007) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Mayr (1853) | 3 | 0.22% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Mayr (1853) | 3 | 0.22% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Nylander (1849) | 3 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
Salata & Fisher (2022) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Santschi (1925) | 3 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1927) | 3 | 0.22% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Seifert & Galkowski (2016) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Seifert et al. (2014) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Seifert (1996) | 3 | 0.22% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Seifert (2019) | 3 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Loon et al. (1990) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Wetterer & Hita Garcia (2015) | 3 | 0.22% | 3 | 1.01% | 3 | 1.1% | 3 | 1.1% |
Allen et al. (2022) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
André (1896) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard (1950) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Blatrix et al. (2020) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Blight et al. (2009) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Boer (2013) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (1988) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Bondroit (1916) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Boudinot et al. (2022) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Boyer de Fonscolombe (1846) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bračko (2006) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Casevitz-Weulersse (2010) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Casevitz-weulersse (2014) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Colindre & Bertrand (2023) | 2 | 0.14% | 2 | 0.67% | 1 | 0.37% | 2 | 0.74% |
Colindre & Galkowski (2023) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Colindre (2017) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 1 | 0.37% |
Csősz et al. (2014) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Csősz et al. (2018) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Czechowski et al. (2002) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Elmes (1978) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Emery & Forel (1879) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Emery (1870) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Emery (1878) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Emery (1892) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1909) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1921) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1925) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1925) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Espadaler et al. (1984) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1894) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Galkowski & Lebas (2016) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Galkowski et al. (2019) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Galkowski et al. (2022) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Garrouste & Hervé (2009) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Güsten et al. (2006) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
ICZN (1999) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Kutter (1950) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Kutter (1977) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Breton et al. (2005) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Leach (1825) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 2 | 0.14% | 2 | 0.67% | 1 | 0.37% | 1 | 0.37% |
Longino & Cox (2009) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Mann (1921) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1923) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz-López et al. (2012) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Nève de Mévergnies et al. (2024) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Nylander (1856) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnaudeau & Madl (2009) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Salata et al. (2018) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanetra et al. (1999) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmitz (1950) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (1982) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Seifert (1992) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Seifert (2003) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Shattuck (1992) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Spinola (1808) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Steiner et al. (2010) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 2 | 0.74% |
Vansteene (2022) | 2 | 0.14% | 2 | 0.67% | 2 | 0.74% | 1 | 0.37% |
Ward et al. (2016) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Wetterer et al. (2007) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Wild (2007) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Wilson (1955) | 2 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2003) | 2 | 0.14% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Zilli (2021) | 2 | 0.14% | 2 | 0.67% | 1 | 0.37% | 1 | 0.37% |
Agosti (1990) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Arakelian (1994) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Astric (2012) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Astric (2012) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Atanassov & Dlussky (1992) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Barech et al. (2020) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Baroni Urbani (1964) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Baroni Urbani (1968) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Baugnee & Godeau (2000) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Bernadou et al. (2010) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Berville et al. (2013) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Betrem (1960) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Blatrix & Galkowski (2018) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Blatrix et al. (2017) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Blatrix et al. (2018) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Blatrix (2013) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Blight et al. (2023) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Bolton & Fisher (2011) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Bolton (1987) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Bolton (2000) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Brown (1963) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Buschinger et al. (1986) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Buschinger (1981) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Buschinger (1987) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cagniant & Espadaler (1997) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cagniant (2016) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot (2023) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Casevitz-Weulersse (1990) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Célini et al. (2014) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Célini et al. (2020) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Charrier et al. (2020) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Chopard (1921) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre & Derozier (2023) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Colindre & Galkowski (2019) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Colindre (2016) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Colindre (2018) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Colindre (2021) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Colindre (2023) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Cordonnier et al. (2020) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Creighton (1950) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Czechowski et al. (2012) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delabie & Blard (2002) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Delabie et al. (2011) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Della Santa (1993) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Donisthorpe (1915) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Donisthorpe (1926) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Donisthorpe (1930) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1881) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Emery (1894) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Emery (1895) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1898) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1905) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1921) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Espadaler et al. (2010) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Espadaler (1983) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Fabricius (1775) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Finzi (1926) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Finzi (1928) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Foerster (1850) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1881) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Forel (1886) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1890) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Forel (1890) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1892) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1895) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1901) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1902) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Forel (1916) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gabrion et al. (1976) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Galkowski & Wegnez (2010) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Galkowski (2009) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Galkowski (2009) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Galkowski (2010) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Galkowski (2011) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Gouraud et al. (2021) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Griebenow (2020) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Gutierrez (1981) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Hacala & Gouraud (2019) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Heinze & Mikó (2015) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Jerdon (1851) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2014) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Karavaiev (1927) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Karavaiev (1929) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Krausse (1911) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kutter (1963) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Kutter (1967) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Kutter (1969) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapeva-Gjonova & Radchenko (2021) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Lapeva-Gjonova (2010) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lebas & Galkowski (2016) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Lebas & Galkowski (2019) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Lebas & Galkowski (2021) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Lebas et al. (2014) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Leponce et al. (2019) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Linné (1771) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Losana (1834) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Marrou (2023) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Mathieu et al. (2007) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1853) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1870) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Mayr (1886) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nylander (1846) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Orledge (1998) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortiz-Sepulveda et al. (2019) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Panis & Kreiter (2008) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Parat (2001) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Pavon et al. (2023) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Plateaux (1978) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Radchenko (1997) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Radchenko (2007) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1862) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1862) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Roger (1863) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruzsky (1902) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruzsky (1925) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruzsky (1926) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sborník Entomologického Oddeleni Národního Musea v Praze, 27: 233‑278.">Sadil (1952) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sadlier et al. (2012) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Salata et al. (2018) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1919) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1919) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1920) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1922) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1923) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1923) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1928) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1929) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Santschi (1932) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1934) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Schenk (1852) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Schifani et al. (2021) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Schifani (2017) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Scopoli (1763) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sebille & Morra (2022) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Seifert & Schultz (2009) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (1988) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (1991) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Seifert (1994) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (1997) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2004) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2006) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2007) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2022) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Sherborn & Woodward (1906) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Smith (1857) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1860) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Soudek (1925) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Stitz (1939) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor & Wilson (1961) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Tinaut (1987) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2018) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Touroult et al. (2020) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Vantaux et al. (2010) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Walker (1859) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Wegnez & Lommelen (2020) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 0 | 0% |
Wegnez & Mourey (2016) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Wegnez et al. (2011) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Wegnez et al. (2015) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Westwood (1839) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Westwood (1839) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Wheeler (1923) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |
Wheeler (1929) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Wild (2004) | 1 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Yarrow (1955) | 1 | 0.07% | 1 | 0.34% | 1 | 0.37% | 1 | 0.37% |