Hyménoptères de Polynésie française
Hymenoptera de Polynésie française
267 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Ramage (2017) | 195 | 27,58% | 191 | 85,65% | 176 | 85,02% | 190 | 90,48% |
Jennings et al. (2013) | 58 | 8,2% | 56 | 25,11% | 56 | 27,05% | 54 | 25,71% |
Wheeler (1935) | 52 | 7,36% | 25 | 11,21% | 25 | 12,08% | 25 | 11,9% |
Ramage (2014) | 50 | 7,07% | 46 | 20,63% | 46 | 22,22% | 46 | 21,9% |
Perrault (1988) | 47 | 6,65% | 41 | 18,39% | 41 | 19,81% | 41 | 19,52% |
Wilson & Taylor (1967) | 45 | 6,36% | 28 | 12,56% | 28 | 13,53% | 28 | 13,33% |
Paulian (1998) | 42 | 5,94% | 42 | 18,83% | 36 | 17,39% | 41 | 19,52% |
Morrison (1996) | 34 | 4,81% | 27 | 12,11% | 27 | 13,04% | 27 | 12,86% |
Wheeler (1936) | 31 | 4,38% | 9 | 4,04% | 9 | 4,35% | 9 | 4,29% |
Fouts (1936) | 30 | 4,24% | 26 | 11,66% | 21 | 10,14% | 26 | 12,38% |
Jourdan & Mille (2006) | 30 | 4,24% | 27 | 12,11% | 26 | 12,56% | 26 | 12,38% |
Morrison (1997) | 30 | 4,24% | 25 | 11,21% | 25 | 12,08% | 25 | 11,9% |
Meurgey & Ramage (2020) | 29 | 4,1% | 29 | 13% | 28 | 13,53% | 28 | 13,33% |
Taylor (1987) | 29 | 4,1% | 29 | 13% | 29 | 14,01% | 29 | 13,81% |
Wheeler (1932) | 29 | 4,1% | 14 | 6,28% | 14 | 6,76% | 14 | 6,67% |
Fullaway (1934) | 28 | 3,96% | 26 | 11,66% | 19 | 9,18% | 25 | 11,9% |
Wilson & Hunt (1967) | 28 | 3,96% | 26 | 11,66% | 26 | 12,56% | 26 | 12,38% |
Wetterer (2002) | 27 | 3,82% | 23 | 10,31% | 23 | 11,11% | 23 | 10,95% |
Cheesman (1928) | 23 | 3,25% | 23 | 10,31% | 23 | 11,11% | 23 | 10,95% |
Fouts (1935) | 23 | 3,25% | 13 | 5,83% | 13 | 6,28% | 13 | 6,19% |
Jaffe & Lattke (1994) | 22 | 3,11% | 20 | 8,97% | 20 | 9,66% | 20 | 9,52% |
Wheeler (1932) | 22 | 3,11% | 11 | 4,93% | 11 | 5,31% | 11 | 5,24% |
Jourdan (2020) | 21 | 2,97% | 21 | 9,42% | 20 | 9,66% | 20 | 9,52% |
Ramage et al. (2023) | 21 | 2,97% | 21 | 9,42% | 21 | 10,14% | 21 | 10% |
Franco et al. (2019) | 18 | 2,55% | 18 | 8,07% | 18 | 8,7% | 18 | 8,57% |
Galkowski (2016) | 18 | 2,55% | 18 | 8,07% | 18 | 8,7% | 18 | 8,57% |
Emery (1914) | 17 | 2,4% | 7 | 3,14% | 7 | 3,38% | 7 | 3,33% |
Muru et al. (2017) | 16 | 2,26% | 16 | 7,17% | 16 | 7,73% | 16 | 7,62% |
Meurgey (2011) | 15 | 2,12% | 13 | 5,83% | 12 | 5,8% | 13 | 6,19% |
Blard et al. (2003) | 14 | 1,98% | 14 | 6,28% | 14 | 6,76% | 14 | 6,67% |
Wheeler (1933) | 14 | 1,98% | 5 | 2,24% | 5 | 2,42% | 5 | 2,38% |
Questel (2020) | 13 | 1,84% | 13 | 5,83% | 13 | 6,28% | 12 | 5,71% |
Zakardjian et al. (2023) | 13 | 1,84% | 13 | 5,83% | 12 | 5,8% | 13 | 6,19% |
Lebas et al. (2016) | 12 | 1,7% | 12 | 5,38% | 12 | 5,8% | 12 | 5,71% |
Perrault (1993) | 12 | 1,7% | 8 | 3,59% | 8 | 3,86% | 8 | 3,81% |
Timberlake (1941) | 12 | 1,7% | 11 | 4,93% | 11 | 5,31% | 11 | 5,24% |
Carpenter (2023) | 11 | 1,56% | 11 | 4,93% | 6 | 2,9% | 11 | 5,24% |
Kuhlmann (2006) | 11 | 1,56% | 10 | 4,48% | 8 | 3,86% | 10 | 4,76% |
Wheeler (1908) | 11 | 1,56% | 5 | 2,24% | 5 | 2,42% | 5 | 2,38% |
Groom et al. (2016) | 10 | 1,41% | 9 | 4,04% | 9 | 4,35% | 8 | 3,81% |
Blatrix et al. (2018) | 9 | 1,27% | 9 | 4,04% | 9 | 4,35% | 9 | 4,29% |
Rousse & Villemant (2012) | 9 | 1,27% | 9 | 4,04% | 9 | 4,35% | 9 | 4,29% |
Holmgren (1868) | 8 | 1,13% | 8 | 3,59% | 8 | 3,86% | 8 | 3,81% |
Leijs et al. (2017) | 8 | 1,13% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Ramage et al. (2015) | 8 | 1,13% | 8 | 3,59% | 8 | 3,86% | 8 | 3,81% |
Williams (1932) | 8 | 1,13% | 8 | 3,59% | 7 | 3,38% | 7 | 3,33% |
Casevitz-Weulersse & Galkowski (2009) | 7 | 0,99% | 7 | 3,14% | 7 | 3,38% | 7 | 3,33% |
Csősz et al. (2023) | 7 | 0,99% | 6 | 2,69% | 6 | 2,9% | 6 | 2,86% |
Fisher & Fong (2020) | 7 | 0,99% | 7 | 3,14% | 7 | 3,38% | 7 | 3,33% |
Gusenleitner (2011) | 7 | 0,99% | 7 | 3,14% | 4 | 1,93% | 6 | 2,86% |
Menke (1979) | 7 | 0,99% | 7 | 3,14% | 6 | 2,9% | 7 | 3,33% |
Questel & Le Quellec (2012) | 7 | 0,99% | 7 | 3,14% | 6 | 2,9% | 6 | 2,86% |
Rageau (1958) | 7 | 0,99% | 5 | 2,24% | 3 | 1,45% | 5 | 2,38% |
Yoshimoto (1963) | 7 | 0,99% | 7 | 3,14% | 7 | 3,38% | 7 | 3,33% |
Ceccolini (2023) | 6 | 0,85% | 6 | 2,69% | 6 | 2,9% | 6 | 2,86% |
Dorey et al. (2024) | 6 | 0,85% | 6 | 2,69% | 6 | 2,9% | 6 | 2,86% |
Jourdan (2021) | 6 | 0,85% | 6 | 2,69% | 6 | 2,9% | 6 | 2,86% |
Perkins (1952) | 6 | 0,85% | 6 | 2,69% | 4 | 1,93% | 6 | 2,86% |
Schulthess (1915) | 6 | 0,85% | 1 | 0,45% | 0 | 0% | 1 | 0,48% |
Talaga et al. (2015) | 6 | 0,85% | 6 | 2,69% | 6 | 2,9% | 6 | 2,86% |
Triapitsyn (2015) | 6 | 0,85% | 6 | 2,69% | 6 | 2,9% | 6 | 2,86% |
Vayssières et al. (2001) | 6 | 0,85% | 5 | 2,24% | 5 | 2,42% | 5 | 2,38% |
Wetterer (2012) | 6 | 0,85% | 6 | 2,69% | 6 | 2,9% | 6 | 2,86% |
Wetterer (2014) | 6 | 0,85% | 6 | 2,69% | 6 | 2,9% | 6 | 2,86% |
Bellmann (2019) | 5 | 0,71% | 5 | 2,24% | 5 | 2,42% | 4 | 1,9% |
Cushman (1938) | 5 | 0,71% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Fernandez-Triana et al. (2020) | 5 | 0,71% | 5 | 2,24% | 5 | 2,42% | 5 | 2,38% |
Fouts (1934) | 5 | 0,71% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Krombein (1950) | 5 | 0,71% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Wetterer (2012) | 5 | 0,71% | 5 | 2,24% | 5 | 2,42% | 5 | 2,38% |
Wetterer (2013) | 5 | 0,71% | 5 | 2,24% | 5 | 2,42% | 5 | 2,38% |
Ascher et al. (2016) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Bernard (1968) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Bolton (2012) | 4 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter (1996) | 4 | 0,57% | 4 | 1,79% | 3 | 1,45% | 4 | 1,9% |
Chen et al. (2017) | 4 | 0,57% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Gusenleitner & Madl (2011) | 4 | 0,57% | 4 | 1,79% | 2 | 0,97% | 4 | 1,9% |
Kim et al. (2004) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Kinsey (1938) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Le Divelec (2024) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Linnaeus (1758) | 4 | 0,57% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Lowe et al. (2007) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Mayr (1870) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Seurat (1934) | 4 | 0,57% | 4 | 1,79% | 3 | 1,45% | 4 | 1,9% |
Vachal (1907) | 4 | 0,57% | 2 | 0,9% | 2 | 0,97% | 1 | 0,48% |
Ward et al. (2015) | 4 | 0,57% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Yasumatsu (1953) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Yoshimoto (1963) | 4 | 0,57% | 4 | 1,79% | 4 | 1,93% | 4 | 1,9% |
Allen et al. (2022) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Bolton (2000) | 3 | 0,42% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Forel (1899) | 3 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Fullaway (1942) | 3 | 0,42% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Garrouste & Hervé (2009) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Grandgirard et al. (2007) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Guilbert & Casevitz-Weulersse (1997) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Jerdon (1851) | 3 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2014) | 3 | 0,42% | 3 | 1,35% | 2 | 0,97% | 3 | 1,43% |
Kieffer (1907-1911) | 3 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Mollot et al. (2016) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Nakahashi & Nishida (1980) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Nève de Mévergnies et al. (2024) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Nibouche et al. (202X) | 3 | 0,42% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Olmi & Villemant (2009) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Olmi (1982) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Pauly & Munzinger (2003) | 3 | 0,42% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Ramage (2020) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Risbec (1956) | 3 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Salata & Fisher (2022) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Smith (1858) | 3 | 0,42% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Touroult et al. (2018) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Wetterer & Hita Garcia (2015) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 3 | 1,43% |
Zakardjian et al. (2020) | 3 | 0,42% | 3 | 1,35% | 3 | 1,45% | 2 | 0,95% |
Balhoff et al. (2013) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Baroni Urbani & De Andrade (2007) | 2 | 0,28% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bocquillon (2018) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Bolton (2007) | 2 | 0,28% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Cameron (1883) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Célini et al. (2020) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Chatthanabun et al. (2020) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Etienne & Dumbardon-Martial (2013) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Fabricius (1793) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Grissell & Desjardins (2002) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Gros (2020) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Howard (1881) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Breton et al. (2005) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Leponce et al. (2019) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Madl & van Achterberg (2014) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Mann (1921) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Marie & Vetter (2015) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Meurgey & Dumbardon-Martial (2015) | 2 | 0,28% | 2 | 0,9% | 1 | 0,48% | 1 | 0,48% |
Meurgey (2014) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 0 | 0% |
Olmi et al. (2014) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Parnaudeau & Madl (2009) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Perrault (1976) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit et al. (2008) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Pintureau et al. (2011) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Remillet (1988) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 1 | 0,48% |
Santschi (1920) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1867) | 2 | 0,28% | 2 | 0,9% | 1 | 0,48% | 2 | 0,95% |
Seifert (2003) | 2 | 0,28% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Seifert (2022) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Sheffield et al. (2020) | 2 | 0,28% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Shimizu et al. (2020) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Smith (1857) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1869) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Stary et al. (1987) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Taylor & Wilson (1961) | 2 | 0,28% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Tomanović et al. (2018) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Tortorici et al. (2016) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Triapitsyn (2001) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Triapitsyn (2013) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Turner (1919) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Viggiani (1988) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Walker (1862) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Wheeler (1933) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 2 | 0,28% | 2 | 0,9% | 2 | 0,97% | 2 | 0,95% |
Albouy et al. (2017) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Beggs et al. (2011) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bitsch et al. (2013) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Blight et al. (2023) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Boyd et al. (2006) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Carpenter & Glare (2010) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Carpenter & Madl (2009) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Chapelin-Viscardi & Lariviere (2014) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Cohic (1959) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre (2016) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Colindre (2021) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Conte et al. (2007) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Cresson (1865) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1938) | 1 | 0,14% | 1 | 0,45% | 0 | 0% | 1 | 0,48% |
Czechowski et al. (2002) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Dalla Torre (1893) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1773) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Delabie & Blard (2002) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Delabie et al. (2011) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Dozier (1937) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Emery (1869) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Emery (1892) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1893) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1894) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Emery (1897) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Emery (1900) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Evans (1966) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Fabricius (1781) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer & Madl (2008) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Forel (1881) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Forel (1886) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1890) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1893) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1901) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Fourcroy (1785) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Friese (1907) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fullaway (1940) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Gahan (1924) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Girault & Dodd (1915) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gonseth et al. (2001) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Graham (1987) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Grandi (1938) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Gutierrez (1981) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Hamdi et al. (2011) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Jacobi (2005) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Johnson (1991) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Kempf (1962) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Krombein (1949) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Latreille (1802) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoir et al. (2023) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Leroy et al. (2021) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Linnaeus (1761) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Madl & Ganeshan (2008) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Madl (2014) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Mayr (1862) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Mayr (1866) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Mayr (1886) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1887) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Questel (2015) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Monteith et al., 2006 | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Onillon et al. (1994) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Pauly & Villemant (2009) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Pierre et al. (2017) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Rahola (2005) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Ramage et al. (2015) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Ramage et al. (2015) | 1 | 0,14% | 1 | 0,45% | 0 | 0% | 1 | 0,48% |
Ramage et al. (2017) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Ramage (2024) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Rasplus et al. (2010) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Remaudiere & Stary (1993) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Reverté et al. (2023) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Robert (2018) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Roger (1859) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1860) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1863) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Rome (2016) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Rosa (2024) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Rousse et al. (2014) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Sadlier et al. (2012) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Santschi (1928) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1859) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1860) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1874) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Somavilla et al. (2018) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Sonan (1932) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Starý et al. (1994) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Taylor (1968) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Tosquinet (1896) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2015) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Touroult et al. (2020) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Triapitsyn (2015) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Trjapitzin (2008) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
van Achterberg (2006) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Van et al. (2023) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Vantaux et al. (2010) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Vargas et al. (2012) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Vidal (2023) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Voelkl (1989) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Wheeler (1923) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Wheeler (1929) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiebes (1986) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Wiebes (1994) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Wilson (1957) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Woolley & Molin (2017) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Yamane et al. (1996) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Yefremova (2017) | 1 | 0,14% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |