Hyménoptères de la Réunion
Hymenoptera de la Réunion
332 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Muru et al. (2017) | 283 | 26,28% | 269 | 62,85% | 269 | 63,44% | 269 | 63,29% |
Rousse & Villemant (2012) | 136 | 12,63% | 134 | 31,31% | 134 | 31,6% | 134 | 31,53% |
Rousse & Gupta (2013) | 88 | 8,17% | 83 | 19,39% | 83 | 19,58% | 83 | 19,53% |
Madl & van Achterberg (2014) | 69 | 6,41% | 65 | 15,19% | 65 | 15,33% | 65 | 15,29% |
Risbec (1957) | 44 | 4,09% | 20 | 4,67% | 20 | 4,72% | 20 | 4,71% |
Jennings et al. (2013) | 43 | 3,99% | 42 | 9,81% | 42 | 9,91% | 41 | 9,65% |
Fernandez-Triana et al. (2020) | 41 | 3,81% | 40 | 9,35% | 40 | 9,43% | 40 | 9,41% |
Ramage (2017) | 40 | 3,71% | 40 | 9,35% | 40 | 9,43% | 40 | 9,41% |
Meurgey & Ramage (2020) | 36 | 3,34% | 36 | 8,41% | 36 | 8,49% | 35 | 8,24% |
Nibouche et al. (202X) | 32 | 2,97% | 31 | 7,24% | 31 | 7,31% | 31 | 7,29% |
Vayssières et al. (2001) | 32 | 2,97% | 29 | 6,78% | 29 | 6,84% | 29 | 6,82% |
Jourdan & Mille (2006) | 29 | 2,69% | 26 | 6,07% | 26 | 6,13% | 25 | 5,88% |
Fischer (2014) | 28 | 2,6% | 28 | 6,54% | 28 | 6,6% | 28 | 6,59% |
Wiebes (1981) | 27 | 2,51% | 15 | 3,5% | 15 | 3,54% | 15 | 3,53% |
Wheeler (1935) | 25 | 2,32% | 14 | 3,27% | 14 | 3,3% | 14 | 3,29% |
Blard et al. (2003) | 24 | 2,23% | 23 | 5,37% | 23 | 5,42% | 23 | 5,41% |
Perrault (1988) | 22 | 2,04% | 21 | 4,91% | 21 | 4,95% | 21 | 4,94% |
Ramage (2014) | 22 | 2,04% | 21 | 4,91% | 21 | 4,95% | 21 | 4,94% |
Rousse & Braet (2012) | 22 | 2,04% | 22 | 5,14% | 22 | 5,19% | 22 | 5,18% |
Wilson & Taylor (1967) | 21 | 1,95% | 14 | 3,27% | 14 | 3,3% | 14 | 3,29% |
Jaffe & Lattke (1994) | 20 | 1,86% | 18 | 4,21% | 18 | 4,25% | 18 | 4,24% |
Morrison (1997) | 19 | 1,76% | 15 | 3,5% | 15 | 3,54% | 15 | 3,53% |
Ramage et al. (2023) | 19 | 1,76% | 19 | 4,44% | 19 | 4,48% | 19 | 4,47% |
Taylor (1987) | 18 | 1,67% | 18 | 4,21% | 18 | 4,25% | 18 | 4,24% |
Franco et al. (2019) | 17 | 1,58% | 16 | 3,74% | 16 | 3,77% | 16 | 3,76% |
Galkowski (2016) | 17 | 1,58% | 16 | 3,74% | 16 | 3,77% | 16 | 3,76% |
Lebas et al. (2016) | 17 | 1,58% | 16 | 3,74% | 16 | 3,77% | 16 | 3,76% |
Fisher & Fong (2020) | 16 | 1,49% | 15 | 3,5% | 15 | 3,54% | 15 | 3,53% |
Jourdan (2020) | 16 | 1,49% | 16 | 3,74% | 15 | 3,54% | 16 | 3,76% |
Morrison (1996) | 16 | 1,49% | 13 | 3,04% | 13 | 3,07% | 13 | 3,06% |
Wheeler (1932) | 15 | 1,39% | 9 | 2,1% | 9 | 2,12% | 9 | 2,12% |
Meurgey (2011) | 14 | 1,3% | 12 | 2,8% | 12 | 2,83% | 12 | 2,82% |
Wetterer (2002) | 13 | 1,21% | 12 | 2,8% | 12 | 2,83% | 12 | 2,82% |
Wheeler (1936) | 13 | 1,21% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Wilson & Hunt (1967) | 13 | 1,21% | 13 | 3,04% | 13 | 3,07% | 13 | 3,06% |
Blatrix et al. (2018) | 12 | 1,11% | 12 | 2,8% | 12 | 2,83% | 12 | 2,82% |
Cheesman (1928) | 12 | 1,11% | 12 | 2,8% | 12 | 2,83% | 12 | 2,82% |
Questel (2020) | 12 | 1,11% | 12 | 2,8% | 12 | 2,83% | 11 | 2,59% |
Braet et al. (2012) | 11 | 1,02% | 11 | 2,57% | 11 | 2,59% | 11 | 2,59% |
Fischer & Madl (2008) | 11 | 1,02% | 11 | 2,57% | 11 | 2,59% | 11 | 2,59% |
Madl (2014) | 11 | 1,02% | 11 | 2,57% | 10 | 2,36% | 11 | 2,59% |
Wheeler (1932) | 11 | 1,02% | 6 | 1,4% | 6 | 1,42% | 6 | 1,41% |
Wheeler (1933) | 11 | 1,02% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Allemand et al. (2002) | 9 | 0,84% | 9 | 2,1% | 9 | 2,12% | 9 | 2,12% |
Casevitz-Weulersse & Galkowski (2009) | 9 | 0,84% | 9 | 2,1% | 9 | 2,12% | 9 | 2,12% |
Emery (1914) | 9 | 0,84% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Delvare et al. (2008) | 8 | 0,74% | 8 | 1,87% | 8 | 1,89% | 8 | 1,88% |
Madl (2015) | 8 | 0,74% | 8 | 1,87% | 8 | 1,89% | 8 | 1,88% |
Perrault (1993) | 8 | 0,74% | 6 | 1,4% | 6 | 1,42% | 6 | 1,41% |
Rasplus et al. (2010) | 8 | 0,74% | 7 | 1,64% | 7 | 1,65% | 7 | 1,65% |
Wheeler (1908) | 8 | 0,74% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Eardley (2012) | 7 | 0,65% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Paulian (1998) | 7 | 0,65% | 7 | 1,64% | 7 | 1,65% | 7 | 1,65% |
Pauly et al. (2001) | 7 | 0,65% | 2 | 0,47% | 1 | 0,24% | 2 | 0,47% |
Azevedo et al. (2010) | 6 | 0,56% | 6 | 1,4% | 6 | 1,42% | 6 | 1,41% |
Brullé (1846) | 6 | 0,56% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Howard (1881) | 6 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2021) | 6 | 0,56% | 6 | 1,4% | 6 | 1,42% | 6 | 1,41% |
Kieffer (1902) | 6 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage (2024) | 6 | 0,56% | 6 | 1,4% | 5 | 1,18% | 6 | 1,41% |
Talaga et al. (2015) | 6 | 0,56% | 6 | 1,4% | 6 | 1,42% | 6 | 1,41% |
Vago (1997) | 6 | 0,56% | 6 | 1,4% | 6 | 1,42% | 6 | 1,41% |
Wetterer (2012) | 6 | 0,56% | 6 | 1,4% | 6 | 1,42% | 6 | 1,41% |
Nève de Mévergnies et al. (2024) | 5 | 0,46% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Parnaudeau & Madl (2009) | 5 | 0,46% | 5 | 1,17% | 4 | 0,94% | 5 | 1,18% |
Questel & Le Quellec (2012) | 5 | 0,46% | 5 | 1,17% | 5 | 1,18% | 4 | 0,94% |
Starý et al. (1994) | 5 | 0,46% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Vachal (1907) | 5 | 0,46% | 3 | 0,7% | 3 | 0,71% | 2 | 0,47% |
Ward et al. (2015) | 5 | 0,46% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Wetterer (2012) | 5 | 0,46% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Wetterer (2013) | 5 | 0,46% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Bellmann (2019) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 3 | 0,71% |
Belokobylskij & Zaldívar-Riverón (2021) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard (1968) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Bolton (2012) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Célini et al. (2013) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Coquerel (1955) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Csősz et al. (2023) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Haran et al. (2018) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Kieffer (1902-1904) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Kim et al. (2004) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Le Divelec (2024) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Meurgey (2014) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 2 | 0,47% |
Ortiz-Sepulveda et al. (2019) | 4 | 0,37% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Rageau (1958) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Touroult et al. (2018) | 4 | 0,37% | 4 | 0,93% | 4 | 0,94% | 4 | 0,94% |
Annecke & Mynhardt (1974) | 3 | 0,28% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Blanchot (1995) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Bolton (2007) | 3 | 0,28% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Bouček et al. (1981) | 3 | 0,28% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Carpenter & Madl (2009) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Castro-Cobo et al. (2021) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Delvare et al. (2019) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Donisthorpe (1932) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste & Hervé (2009) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Graham (1987) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Granger (1949) | 3 | 0,28% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Guilbert & Casevitz-Weulersse (1997) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Jerdon (1851) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 3 | 0,28% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Lowe et al. (2007) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Madl (2016) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Mollot et al. (2016) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Olmi et al. (2019) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Olmi et al. (2020) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Onillon et al. (1994) | 3 | 0,28% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Rousse (2013) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Salata & Fisher (2022) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Seifert et al. (2017) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Turner (1919) | 3 | 0,28% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Wetterer & Hita Garcia (2015) | 3 | 0,28% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Wiebes (1975) | 3 | 0,28% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Allen et al. (2022) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Bakkendorf (1960) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Blight et al. (2009) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Borowiec (2016) | 2 | 0,19% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Boucek (1976) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Boyer de Fonscolombe (1832) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre (2023) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Coquerel (1955) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Czechowski et al. (2002) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Debach (1960) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Delvare (2005) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Dessart (1989) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Emery (1894) | 2 | 0,19% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Etienne & Dumbardon-Martial (2013) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Etienne et al. (2001) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Etienne (1971) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Evenhuis & Barbotin (1977) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Friese (1907) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Goubault et al. (2004) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Howard (1907) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Hullé et al. (2010) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Kelly & Ranwashe (2018) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Kimsey (2005) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Kremmer et al. (2017) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Logvinovskaya (1983) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Madl & Ganeshan (2008) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Madl (2016) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Mann (1921) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Masner (1960) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Meurgey & Dumbardon-Martial (2019) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Meurgey & Questel (2015) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 1 | 0,24% |
Perry & Heraty (2021) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Pintureau et al. (2011) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Pujade-Villar et al. (2007) | 2 | 0,19% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Ramage et al. (2015) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Remillet (1988) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 1 | 0,24% |
Rousse et al. (2014) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Shattuck (1992) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Silvestri (1913) | 2 | 0,19% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Smith (1857) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Starý et al. (1973) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Tachikawa (1968) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor & Wilson (1961) | 2 | 0,19% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Timberlake (1941) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Tosquinet (1896) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Triapitsyn (2015) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Viggiani (1988) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Walker (1839) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Wang (2003) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Wesmael (1835) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Wetterer et al. (2012) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1923) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Wheeler (1933) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiebes & Compton (1990) | 2 | 0,19% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Wild (2007) | 2 | 0,19% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Abeille de Perrin (1879) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Albouy et al. (2017) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Annecke (1971) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Balhoff et al. (2013) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Baroni Urbani & De Andrade (2007) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Beggs et al. (2011) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Berlese & Paoli (1916) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Biondi et al. (2013) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Blanchard (1940) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Boer et al. (2020) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Bolton & Fisher (2011) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Bouček (1963) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Boyd et al. (2006) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Brèthes (1913) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Cameron (1883) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1897) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1906) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Cameron (1911) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Carpenter (1996) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Célini et al. (2014) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Célini et al. (2020) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Charrier et al. (2020) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Chopard (1921) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1959) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre & Bertrand (2023) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Colindre (2016) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Colindre (2017) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Colindre (2021) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Collingwood & Agosti (1996) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Conte et al. (2007) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Cresson (1865) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cruaud et al. (2013) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalla Torre (1893) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalman (1820) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1773) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
DeBach (1959) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Delabie & Blard (2002) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Delabie et al. (2011) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Bulletin de la Societe Entomologique de France, 79: 98-104.">Delobel (1974) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Dozier (1937) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Dumbardon-Martial et al. (2018) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Emery (1892) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1895) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne (1978) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Etienne (1978) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Fabricius (1781) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-Suay et al. (2012) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-Suay et al. (2015) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Ferrer-Suay et al. (2018) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Fisher & Bolton (2016) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Forel (1881) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Forel (1886) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1890) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1892) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Förster (1840) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fullaway (1942) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Gahan (1924) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Ganeshan & Madl (2016) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Garcia & Fisher (2014) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Gibson (2006) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Girault & Dodd (1915) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Girault (1915) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Graham (1969) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Graham (1991) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Graham (1992) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffin (1931) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Groom et al. (2016) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Gusenleitner & Madl (2011) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Gusenleitner (2011) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Hagstrum & Subramanyam (2009) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Haliday (1833) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Haliday (1834) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Hamdi et al. (2011) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Hartig (1841) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Holmgren (1868) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Howard (1895) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Howard (1895) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Howard (1906) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Hoyer (1986) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Jacquot (2016) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Johansson et al. (2021) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2014) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Kittel & Maeto (2018) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Klug (1801) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Kreiter et al. (2022) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Kuhlmann (2006) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Latreille (1802) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoir et al. (2023) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Leponce et al. (2019) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Leroy et al. (2021) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Linnaeus (1761) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Masi (1935) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Mason (1981) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Mayr (1862) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Mayr (1886) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Mercet (1931) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Meurgey & Dumbardon-Martial (2015) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Michel (1969) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
M'intosh (1855) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Morley (1912) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Notton (2004) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Noyes (1979) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Özdikmen (2011) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Parr (1960) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Pauly & Munzinger (2003) | 1 | 0,09% | 1 | 0,23% | 0 | 0% | 1 | 0,24% |
Pauly (2008) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Perkins (1910) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Pierre et al. (2017) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Podoler & Mazor (1981) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Pulawski (2020) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Quednau (1964) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Quilici (1993) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Rakotonirina & Fisher (2014) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Rakotonirina & Fisher (2022) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Ramage & Martiré (2016) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Ramage et al. (2017) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Reverté et al. (2023) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Risbec (1951) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Risbec (1952) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Robert (2018) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Roger (1859) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Rondani (1875) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Roques & Skrzypczyńska (2003) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Russell & Etienne (1985) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Ryckewaert & Fabre (2001) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Santschi (1920) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1928) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Saunders (1883) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Say (1836) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulthess (1915) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2003) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2022) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Seurat (1934) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Sharkey & Chapman (2017) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Sichel (1862) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Silvestri (1916) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith, F. (1861) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1858) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1860) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1976) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Sonan (1932) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Squarzoni (2001) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Timberlake (1924) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Tortorici et al. (2016) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Tower (1913) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Townes & Townes (1973) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Vargas et al. (2012) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Walker (1859) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Wetterer & Sharaf (2017) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Wheeler (1929) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiebes (1977) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Wild (2004) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilkinson (1927) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Wondafrash et al. (2020) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Yokoyama (2013) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Zakardjian et al. (2020) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 0 | 0% |
Zakardjian et al. (2023) | 1 | 0,09% | 1 | 0,23% | 0 | 0% | 1 | 0,24% |
Zolnerowich & Rose (1998) | 1 | 0,09% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |