Insectes sociaux de métropole
Kalotermitidae, Rhinotermitidae, Formicidae, Termitidae, Serritermitidae, Polistinae, Apis, Bombus, Meliponini et Vespinae de France métropolitaine
475 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 | 16,08% | 186 | 45,15% | 186 | 53,6% | 162 | 44,38% |
Lebas et al. (2016) | 250 | 15% | 228 | 55,34% | 228 | 65,71% | 203 | 55,62% |
Colindre (2016) | 47 | 2,82% | 47 | 11,41% | 47 | 13,54% | 39 | 10,68% |
Reverté et al. (2023) | 47 | 2,82% | 46 | 11,17% | 46 | 13,26% | 29 | 7,95% |
Bellmann (2019) | 37 | 2,22% | 35 | 8,5% | 35 | 10,09% | 22 | 6,03% |
Bolton (2003) | 32 | 1,92% | 11 | 2,67% | 11 | 3,17% | 11 | 3,01% |
Seifert (2020) | 29 | 1,74% | 26 | 6,31% | 26 | 7,49% | 26 | 7,12% |
Willot & Wegnez (2024) | 27 | 1,62% | 27 | 6,55% | 27 | 7,78% | 22 | 6,03% |
Blatrix et al. (2018) | 26 | 1,56% | 26 | 6,31% | 26 | 7,49% | 26 | 7,12% |
Seifert (2021) | 24 | 1,44% | 24 | 5,83% | 24 | 6,92% | 21 | 5,75% |
Ward et al. (2015) | 23 | 1,38% | 10 | 2,43% | 10 | 2,88% | 10 | 2,74% |
Baliteau et al. (2013) | 22 | 1,32% | 21 | 5,1% | 21 | 6,05% | 15 | 4,11% |
Linnaeus (1758) | 19 | 1,14% | 3 | 0,73% | 3 | 0,86% | 0 | 0% |
Wheeler (1935) | 18 | 1,08% | 12 | 2,91% | 12 | 3,46% | 12 | 3,29% |
Kruseman (1958) | 17 | 1,02% | 3 | 0,73% | 1 | 0,29% | 3 | 0,82% |
Colindre (2017) | 16 | 0,96% | 16 | 3,88% | 16 | 4,61% | 16 | 4,38% |
Galkowski et al. (2010) | 16 | 0,96% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Bondroit (1918) | 15 | 0,9% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Mayr (1861) | 14 | 0,84% | 10 | 2,43% | 10 | 2,88% | 6 | 1,64% |
Meurgey & Ramage (2020) | 14 | 0,84% | 14 | 3,4% | 14 | 4,03% | 13 | 3,56% |
Perrault (1988) | 14 | 0,84% | 13 | 3,16% | 13 | 3,75% | 13 | 3,56% |
Ramage et al. (2023) | 14 | 0,84% | 14 | 3,4% | 14 | 4,03% | 14 | 3,84% |
Ramage (2014) | 14 | 0,84% | 14 | 3,4% | 14 | 4,03% | 14 | 3,84% |
Ramage (2017) | 14 | 0,84% | 14 | 3,4% | 14 | 4,03% | 14 | 3,84% |
Rasmont et al. (2021) | 14 | 0,84% | 11 | 2,67% | 0 | 0% | 11 | 3,01% |
Bernard (1968) | 13 | 0,78% | 8 | 1,94% | 8 | 2,31% | 8 | 2,19% |
Franco et al. (2019) | 13 | 0,78% | 13 | 3,16% | 13 | 3,75% | 13 | 3,56% |
Jaffe & Lattke (1994) | 13 | 0,78% | 12 | 2,91% | 12 | 3,46% | 12 | 3,29% |
Seifert et al. (2024) | 13 | 0,78% | 10 | 2,43% | 10 | 2,88% | 9 | 2,47% |
Galkowski (2016) | 12 | 0,72% | 12 | 2,91% | 12 | 3,46% | 12 | 3,29% |
Jennings et al. (2013) | 12 | 0,72% | 12 | 2,91% | 12 | 3,46% | 11 | 3,01% |
Jourdan & Mille (2006) | 12 | 0,72% | 12 | 2,91% | 12 | 3,46% | 11 | 3,01% |
Taylor (1987) | 12 | 0,72% | 12 | 2,91% | 12 | 3,46% | 12 | 3,29% |
Bernard (1978) | 11 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
L'Entomologiste picard, 34: 2.">Colindre et al. (2021) | 11 | 0,66% | 11 | 2,67% | 11 | 3,17% | 8 | 2,19% |
Galkowski & Cagniant (2017) | 11 | 0,66% | 7 | 1,7% | 7 | 2,02% | 7 | 1,92% |
Morrison (1997) | 11 | 0,66% | 11 | 2,67% | 11 | 3,17% | 11 | 3,01% |
Schmid-Egger et al. (2017) | 11 | 0,66% | 9 | 2,18% | 9 | 2,59% | 9 | 2,47% |
Vogt (1909) | 11 | 0,66% | 3 | 0,73% | 0 | 0% | 3 | 0,82% |
Wheeler (1932) | 11 | 0,66% | 8 | 1,94% | 8 | 2,31% | 8 | 2,19% |
Wilson & Taylor (1967) | 11 | 0,66% | 9 | 2,18% | 9 | 2,59% | 9 | 2,47% |
Annales de la Societé Entomologique de France, 1: 366-382.">Lepeletier de Saint-fargeau ([1833]) | 10 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Morrison (1996) | 10 | 0,6% | 9 | 2,18% | 9 | 2,59% | 9 | 2,47% |
Questel (2020) | 10 | 0,6% | 10 | 2,43% | 10 | 2,88% | 9 | 2,47% |
Albouy et al. (2017) | 9 | 0,54% | 9 | 2,18% | 9 | 2,59% | 3 | 0,82% |
Blard et al. (2003) | 9 | 0,54% | 9 | 2,18% | 9 | 2,59% | 9 | 2,47% |
Delmas (1976) | 9 | 0,54% | 9 | 2,18% | 9 | 2,59% | 6 | 1,64% |
Meurgey (2011) | 9 | 0,54% | 8 | 1,94% | 8 | 2,31% | 8 | 2,19% |
Seifert (2012) | 9 | 0,54% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Vidal et al. (2022) | 9 | 0,54% | 9 | 2,18% | 9 | 2,59% | 2 | 0,55% |
Vidal (2023) | 9 | 0,54% | 8 | 1,94% | 8 | 2,31% | 3 | 0,82% |
Wetterer (2002) | 9 | 0,54% | 8 | 1,94% | 8 | 2,31% | 8 | 2,19% |
Wheeler (1932) | 9 | 0,54% | 6 | 1,46% | 6 | 1,73% | 6 | 1,64% |
Wilson & Hunt (1967) | 9 | 0,54% | 8 | 1,94% | 8 | 2,31% | 8 | 2,19% |
Cheesman (1928) | 8 | 0,48% | 8 | 1,94% | 8 | 2,31% | 8 | 2,19% |
Rasmont et al. (2016) | 8 | 0,48% | 3 | 0,73% | 2 | 0,58% | 3 | 0,82% |
Seifert (2002) | 8 | 0,48% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Wheeler (1933) | 8 | 0,48% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Wheeler (1936) | 8 | 0,48% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Agosti & Collingwood (1987) | 7 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (1995) | 7 | 0,42% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Dalla Torre (1893) | 7 | 0,42% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Latreille (1798) | 7 | 0,42% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Linnaeus (1761) | 7 | 0,42% | 2 | 0,49% | 1 | 0,29% | 1 | 0,27% |
Plateaux & Cagniant (2012) | 7 | 0,42% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Seifert et al. (2017) | 7 | 0,42% | 7 | 1,7% | 7 | 2,02% | 7 | 1,92% |
Baliteau et al. (2010) | 6 | 0,36% | 6 | 1,46% | 6 | 1,73% | 6 | 1,64% |
Brasero et al. (2021) | 6 | 0,36% | 5 | 1,21% | 2 | 0,58% | 3 | 0,82% |
Emery (1914) | 6 | 0,36% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Fabricius (1793) | 6 | 0,36% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Gerstäcker (1869) | 6 | 0,36% | 4 | 0,97% | 4 | 1,15% | 3 | 0,82% |
Jourdan (2020) | 6 | 0,36% | 6 | 1,46% | 5 | 1,44% | 6 | 1,64% |
Kirschner et al. (2023) | 6 | 0,36% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Latreille (1802) | 6 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1792) | 6 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
Pérez ([1880]) | 6 | 0,36% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Questel & Le Quellec (2012) | 6 | 0,36% | 6 | 1,46% | 6 | 1,73% | 5 | 1,37% |
Rome (2016) | 6 | 0,36% | 6 | 1,46% | 6 | 1,73% | 4 | 1,1% |
Wheeler (1908) | 6 | 0,36% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Zilli (2021) | 6 | 0,36% | 2 | 0,49% | 1 | 0,29% | 1 | 0,27% |
Alicata et al. (2024) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Baroni Urbani & De Andrade (2007) | 5 | 0,3% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Bolton (2012) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1915) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher & Fong (2020) | 5 | 0,3% | 5 | 1,21% | 5 | 1,44% | 4 | 1,1% |
Forel (1874) | 5 | 0,3% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Fourcroy (1785) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Lepeletier (1836) | 5 | 0,3% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Radchenko & Elmes (2010) | 5 | 0,3% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Rasmont et al. (1995) | 5 | 0,3% | 5 | 1,21% | 3 | 0,86% | 5 | 1,37% |
Rigato (2011) | 5 | 0,3% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Roger (1863) | 5 | 0,3% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Molecular Phylogenetics and Evolution, 127: 387‑404.">Steiner et al. (2018) | 5 | 0,3% | 5 | 1,21% | 5 | 1,44% | 2 | 0,55% |
Wetterer (2012) | 5 | 0,3% | 5 | 1,21% | 5 | 1,44% | 5 | 1,37% |
Wetterer (2013) | 5 | 0,3% | 5 | 1,21% | 5 | 1,44% | 5 | 1,37% |
André (1881) | 4 | 0,24% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Anonyme (2015) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard (1977) | 4 | 0,24% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Colindre (2016) | 4 | 0,24% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Dronnet et al. (2005) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1869) | 4 | 0,24% | 3 | 0,73% | 3 | 0,86% | 2 | 0,55% |
Emery (1916) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1925) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamer et al. (2021) | 4 | 0,24% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Kirby (1802) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoir et al. (2023) | 4 | 0,24% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Lowe et al. (2007) | 4 | 0,24% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Mayr (1855) | 4 | 0,24% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Perrault (1993) | 4 | 0,24% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Rasmont & Adamski (1996) | 4 | 0,24% | 4 | 0,97% | 0 | 0% | 4 | 1,1% |
Roger (1859) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulthess-Rechberg (1886) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert et al. (2014) | 4 | 0,24% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Talaga et al. (2015) | 4 | 0,24% | 4 | 0,97% | 4 | 1,15% | 4 | 1,1% |
Wagner et al. (2017) | 4 | 0,24% | 4 | 0,97% | 4 | 1,15% | 3 | 0,82% |
Williams et al. (2023) | 4 | 0,24% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Bernard (1978) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Blatrix et al. (2013) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Bolton (2007) | 3 | 0,18% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Bondroit (1917) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Bondroit (1920) | 3 | 0,18% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Casevitz-Weulersse (1990) | 3 | 0,18% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Castro-Cobo et al. (2021) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Clément et al. (2001) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 2 | 0,55% |
Clément (1977) | 3 | 0,18% | 3 | 0,73% | 2 | 0,58% | 3 | 0,82% |
Collingwood & Yarrow (1969) | 3 | 0,18% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Darchen (1976) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Donisthorpe (1932) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1924) | 3 | 0,18% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Evenhuis (1997) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1775) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Galkowski et al. (2017) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
García et al. (2020) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Guilbert & Casevitz-Weulersse (1997) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Lepeletier & Saint-fargeau (1832) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1853) | 3 | 0,18% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Mayr (1853) | 3 | 0,18% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Nylander (1849) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Pérez (1890) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Salata & Fisher (2022) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Santschi (1925) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1927) | 3 | 0,18% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Scopoli (1763) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert & Galkowski (2016) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Seifert et al. (2014) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Seifert (1996) | 3 | 0,18% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Seifert (2019) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Selis et al. (2023) | 3 | 0,18% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Van Loon et al. (1990) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Wetterer & Hita Garcia (2015) | 3 | 0,18% | 3 | 0,73% | 3 | 0,86% | 3 | 0,82% |
Williams (1998) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen et al. (2022) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Alonso-zarazaga & Evenhuis (2017) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
André (1896) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Austin et al. (2005) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagnères et al. (2003) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Baker (1996) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Bernard (1950) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Blatrix et al. (2020) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Blight et al. (2009) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Boer (2013) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (1988) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Bondroit (1916) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Boudinot et al. (2022) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Boyer de Fonscolombe (1846) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bračko (2006) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Casevitz-Weulersse (2010) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Casevitz-weulersse (2014) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Christ (1791) | 2 | 0,12% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Clément (1978) | 2 | 0,12% | 2 | 0,49% | 0 | 0% | 2 | 0,55% |
Colindre & Galkowski (2023) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Colindre (2017) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 1 | 0,27% |
Csősz et al. (2014) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Csősz et al. (2018) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Czechowski et al. (2002) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Descamps et al. (2015) | 2 | 0,12% | 2 | 0,49% | 0 | 0% | 2 | 0,55% |
Elmes (1978) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Emery & Forel (1879) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Emery (1870) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Emery (1878) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Emery (1892) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1909) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1921) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1925) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1925) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Espadaler et al. (1984) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1894) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Galkowski & Lebas (2016) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Galkowski et al. (2019) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Galkowski et al. (2022) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Garrouste & Hervé (2009) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Gereys (2022) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Güsten et al. (2006) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
ICZN (1999) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kohl (1898) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kriechbaumer (1870) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Krüger (1951) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Krüger (1954) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kutter (1950) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kutter (1977) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Breton et al. (2005) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Leach (1825) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lecocq et al. (2015) | 2 | 0,12% | 2 | 0,49% | 0 | 0% | 2 | 0,55% |
Linné (1771) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Longino & Cox (2009) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Mann (1921) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinet et al. (2018) | 2 | 0,12% | 2 | 0,49% | 0 | 0% | 2 | 0,55% |
Meurgey (2014) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 0 | 0% |
Müller (1923) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz-López et al. (2012) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Nève de Mévergnies et al. (2024) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Nylander (1856) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1800]) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1802]) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnaudeau & Madl (2009) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Pérez (1883-[1884]) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Radoszkowski (1884) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Rasmont et al. (2008) | 2 | 0,12% | 2 | 0,49% | 0 | 0% | 2 | 0,55% |
Rasmont (1986) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Rome et al. (2009) | 2 | 0,12% | 2 | 0,49% | 1 | 0,29% | 1 | 0,27% |
Rome et al. (2011) | 2 | 0,12% | 2 | 0,49% | 1 | 0,29% | 1 | 0,27% |
Rome et al. (2013) | 2 | 0,12% | 2 | 0,49% | 1 | 0,29% | 1 | 0,27% |
Rortais et al. (2010) | 2 | 0,12% | 2 | 0,49% | 1 | 0,29% | 1 | 0,27% |
Salata et al. (2018) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanetra et al. (1999) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmitz (1950) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (1982) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Seifert (1992) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Seifert (2003) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Shattuck (1992) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Spinola (1808) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Steiner et al. (2010) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Vansteene (2022) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 1 | 0,27% |
Velona et al. (2011) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 2 | 0,55% |
Vidal (2016) | 2 | 0,12% | 2 | 0,49% | 2 | 0,58% | 1 | 0,27% |
Villemant et al. (2010) | 2 | 0,12% | 2 | 0,49% | 1 | 0,29% | 1 | 0,27% |
Villemant et al. (2011) | 2 | 0,12% | 2 | 0,49% | 1 | 0,29% | 1 | 0,27% |
Ward et al. (2016) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Wetterer et al. (2007) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Wild (2007) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Wilson (1955) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2003) | 2 | 0,12% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Agosti (1990) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Arakelian (1994) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Astric (2012) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Astric (2012) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Atanassov & Dlussky (1992) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbier (2006) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbier (2009) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Barech et al. (2020) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Baroni Urbani (1964) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Baroni Urbani (1968) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Baugnee & Godeau (2000) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Benoist (1926) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Benoist (1928) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Benoist (1950) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Berland (1928) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Bernadou et al. (2010) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Berville et al. (2013) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Betrem (1960) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bischoff (1931) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Blatrix & Galkowski (2018) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Blatrix et al. (2017) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Blatrix et al. (2018) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Blatrix (2013) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Blight et al. (2023) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Bolton & Fisher (2011) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Bolton (1987) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Bolton (2000) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Boyd et al. (2006) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Brown (1963) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Buschinger et al. (1986) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Buschinger (1981) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Buschinger (1987) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cagniant & Espadaler (1997) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cagniant (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot (2023) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Carolan et al. (2012) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Carpenter & Glare (2010) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Casevitz-Weulersse (1990) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Célini et al. (2014) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Célini et al. (2020) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Charrier et al. (2020) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Chopard (1921) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre & Bertrand (2023) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Colindre & Derozier (2023) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Colindre & Galkowski (2019) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Colindre (2016) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Colindre (2018) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Colindre (2021) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Colindre (2023) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Conte et al. (2007) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Cordonnier et al. (2020) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Creighton (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Czechowski et al. (2012) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalla Torre (1882) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Delabie & Blard (2002) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Delabie et al. (2011) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Della Santa (1993) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Delmas (1945) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dilman (2013) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Donisthorpe (1915) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Donisthorpe (1926) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Donisthorpe (1930) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Ebmer (1975) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Ebmer (2021) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Emery (1881) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Emery (1894) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Emery (1895) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1898) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1921) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Espadaler et al. (2010) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Espadaler (1983) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Eversmann (1852) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Fabricius ([1777]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1781) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Finzi (1926) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Finzi (1928) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Foerster (1850) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1881) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Forel (1886) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1890) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1890) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Forel (1892) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1895) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1901) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1902) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Forel (1916) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Friese (1907) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Frin (2018) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Gabrion et al. (1976) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Galkowski & Wegnez (2010) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Galkowski (2009) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Galkowski (2009) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Galkowski (2010) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Galkowski (2011) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Gereys et al. (2021) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Gereys (2006) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1817) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gouraud et al. (2021) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Graf (1961) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Griebenow (2020) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Groom et al. (2016) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Gutierrez (1981) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Hacala & Gouraud (2019) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Heinze & Mikó (2015) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Illiger (1806) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Iserbyt et al. (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jerdon (1851) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2014) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Karavaiev (1927) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Karavaiev (1929) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Krausse (1911) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kriechbaumer (1877) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kruger (1956) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Kutter (1963) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Kutter (1967) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Kutter (1969) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapeva-Gjonova & Radchenko (2021) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Lapeva-Gjonova (2010) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lebas & Galkowski (2016) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Lebas & Galkowski (2019) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Lebas & Galkowski (2021) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Lebas et al. (2014) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Lecocq et al. (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemoine & Vidal (2014) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Lepeletier de Saint Fargeau & Audinet-Serville (1825) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Leponce et al. (2019) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Lecocq, T., Lhomme, P., Michez, D., Dellicour, S., Valterová, I., Rasmont, P. 2011. Molecular and chemical characters to evaluate species status of two cuckoo bumblebees: Bombus barbutellus and Bombus maxillosus (Hymenoptera, Apidae, Bombini). Systematic Entomology, 36(3): 453‑469. ">Lerocq et al. (2011) |
1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Litt (2003) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Losana (1834) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Magis (2003) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mahé (2007) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Marrou (2023) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Mathieu et al. (2007) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1853) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1870) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Mayr (1886) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Dumbardon-Martial (2015) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Meurgey & Questel (2015) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Morawitz ([1868]) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Morawitz (1881) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Müller (1776) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Neumeyer et al. (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Nylander (1846) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Olivier (1791-[1792]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Orledge (1998) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortiz-Sepulveda et al. (2019) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Panis & Kreiter (2008) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Panzer (1801) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Parat (2001) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Pauly & Munzinger (2003) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Pauly et al. (2001) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Pavon et al. (2023) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Pierre et al. (2017) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Pittioni (1938) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Plateaux (1978) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Radchenko (1997) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Radchenko (2007) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Radochkoffsky (1859) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Rasmont (1984) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Remillet (1988) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Richards (1928) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1862) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Roger (1862) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1863) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi (1792) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruzsky (1902) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruzsky (1925) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruzsky (1926) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sborník Entomologického Oddeleni Národního Musea v Praze, 27: 233‑278.">Sadil (1952) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sadlier et al. (2012) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Salata et al. (2018) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1919) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1919) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1920) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1922) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1923) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1923) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1928) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1929) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Santschi (1932) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1934) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Schenck ([1861]) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Schenk (1852) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schifani et al. (2021) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Schifani (2017) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Schmiedeknecht (1882-[1884]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sebille & Morra (2022) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Seifert & Schultz (2009) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (1988) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (1991) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Seifert (1994) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (1997) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2006) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2007) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2022) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Sherborn & Woodward (1906) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Smith (1844) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1849) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Smith (1857) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1860) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Soudek (1925) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Stitz (1939) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor & Wilson (1961) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Tinaut (1987) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Tkalců (1963) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2018) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Touroult et al. (2020) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Vachal (1907) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Vantaux et al. (2010) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Villemant (2008) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |
Vogt (1911) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Walker (1859) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wegnez & Lommelen (2020) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Wegnez & Mourey (2016) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Wegnez et al. (2011) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Wegnez et al. (2015) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Westwood (1839) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Westwood (1839) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1923) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Wheeler (1929) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wild (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Yarrow (1955) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 1 | 0,27% |
Zakardjian et al. (2020) | 1 | 0,06% | 1 | 0,24% | 1 | 0,29% | 0 | 0% |
Zakardjian et al. (2023) | 1 | 0,06% | 1 | 0,24% | 0 | 0% | 1 | 0,27% |