Hyménoptères de Guadeloupe
Hymenoptera de Guadeloupe
275 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Meurgey & Ramage (2020) | 189 | 23,42% | 186 | 83,04% | 179 | 82,87% | 184 | 84,79% |
| Ramage et al. (2023) | 100 | 12,39% | 100 | 44,64% | 97 | 44,91% | 99 | 45,62% |
| Galkowski (2016) | 84 | 10,41% | 80 | 35,71% | 78 | 36,11% | 79 | 36,41% |
| Meurgey (2011) | 77 | 9,54% | 65 | 29,02% | 60 | 27,78% | 64 | 29,49% |
| Franco et al. (2019) | 64 | 7,93% | 61 | 27,23% | 61 | 28,24% | 58 | 26,73% |
| Jaffe & Lattke (1994) | 51 | 6,32% | 44 | 19,64% | 43 | 19,91% | 43 | 19,82% |
| Meurgey (2014) | 40 | 4,96% | 39 | 17,41% | 39 | 18,06% | 37 | 17,05% |
| Questel (2020) | 30 | 3,72% | 30 | 13,39% | 28 | 12,96% | 28 | 12,9% |
| Ramage (2017) | 29 | 3,59% | 29 | 12,95% | 28 | 12,96% | 29 | 13,36% |
| Meurgey & Dumbardon-Martial (2019) | 24 | 2,97% | 24 | 10,71% | 24 | 11,11% | 24 | 11,06% |
| Wheeler (1935) | 23 | 2,85% | 13 | 5,8% | 13 | 6,02% | 13 | 5,99% |
| Ramage (2014) | 21 | 2,6% | 20 | 8,93% | 20 | 9,26% | 20 | 9,22% |
| Jennings et al. (2013) | 20 | 2,48% | 20 | 8,93% | 20 | 9,26% | 19 | 8,76% |
| Jourdan & Mille (2006) | 20 | 2,48% | 20 | 8,93% | 19 | 8,8% | 19 | 8,76% |
| Brown (1958) | 19 | 2,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrault (1988) | 19 | 2,35% | 18 | 8,04% | 18 | 8,33% | 18 | 8,29% |
| Morrison (1997) | 16 | 1,98% | 15 | 6,7% | 15 | 6,94% | 15 | 6,91% |
| Taylor (1987) | 16 | 1,98% | 16 | 7,14% | 16 | 7,41% | 16 | 7,37% |
| Wilson & Taylor (1967) | 16 | 1,98% | 12 | 5,36% | 12 | 5,56% | 12 | 5,53% |
| Meurgey & Dumbardon-Martial (2015) | 15 | 1,86% | 15 | 6,7% | 13 | 6,02% | 14 | 6,45% |
| Morrison (1996) | 15 | 1,86% | 14 | 6,25% | 14 | 6,48% | 14 | 6,45% |
| UICN Comité français, OFB & MNHN (2021) | 14 | 1,73% | 14 | 6,25% | 14 | 6,48% | 14 | 6,45% |
| Questel & Le Quellec (2012) | 13 | 1,61% | 13 | 5,8% | 12 | 5,56% | 12 | 5,53% |
| Santschi (1929) | 13 | 1,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buffington et al. (2017) | 12 | 1,49% | 9 | 4,02% | 9 | 4,17% | 9 | 4,15% |
| Lebas et al. (2016) | 12 | 1,49% | 11 | 4,91% | 11 | 5,09% | 11 | 5,07% |
| Wheeler (1932) | 12 | 1,49% | 7 | 3,12% | 7 | 3,24% | 7 | 3,23% |
| Wheeler (1936) | 12 | 1,49% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Blard et al. (2003) | 11 | 1,36% | 11 | 4,91% | 11 | 5,09% | 11 | 5,07% |
| Muru et al. (2017) | 11 | 1,36% | 10 | 4,46% | 10 | 4,63% | 10 | 4,61% |
| Touroult et al. (2018) | 11 | 1,36% | 11 | 4,91% | 11 | 5,09% | 11 | 5,07% |
| Cheesman (1928) | 10 | 1,24% | 10 | 4,46% | 10 | 4,63% | 10 | 4,61% |
| Fisher & Fong (2020) | 10 | 1,24% | 10 | 4,46% | 10 | 4,63% | 10 | 4,61% |
| Wetterer (2002) | 10 | 1,24% | 10 | 4,46% | 10 | 4,63% | 10 | 4,61% |
| Wilson & Hunt (1967) | 10 | 1,24% | 10 | 4,46% | 10 | 4,63% | 10 | 4,61% |
| Yokoyama (2013) | 10 | 1,24% | 9 | 4,02% | 9 | 4,17% | 9 | 4,15% |
| Delvare et al. (2008) | 9 | 1,12% | 9 | 4,02% | 9 | 4,17% | 9 | 4,15% |
| Emery (1911) | 9 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lattke (1995) | 9 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leponce et al. (2019) | 9 | 1,12% | 9 | 4,02% | 9 | 4,17% | 9 | 4,15% |
| Perrault (1993) | 9 | 1,12% | 8 | 3,57% | 8 | 3,7% | 8 | 3,69% |
| Touroult et al. (2019) | 9 | 1,12% | 9 | 4,02% | 9 | 4,17% | 8 | 3,69% |
| Wheeler (1932) | 9 | 1,12% | 5 | 2,23% | 5 | 2,31% | 5 | 2,3% |
| Wheeler (1933) | 9 | 1,12% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Casevitz-Weulersse & Galkowski (2009) | 8 | 0,99% | 7 | 3,12% | 7 | 3,24% | 7 | 3,23% |
| Gauld (1988) | 8 | 0,99% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Jourdan (2020) | 8 | 0,99% | 8 | 3,57% | 8 | 3,7% | 8 | 3,69% |
| Meurgey & Questel (2015) | 8 | 0,99% | 8 | 3,57% | 8 | 3,7% | 7 | 3,23% |
| Touroult et al. (2015) | 8 | 0,99% | 8 | 3,57% | 8 | 3,7% | 7 | 3,23% |
| Blatrix et al. (2018) | 7 | 0,87% | 7 | 3,12% | 7 | 3,24% | 7 | 3,23% |
| Lepeletier (1841) | 7 | 0,87% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Olmi et al. (2000) | 7 | 0,87% | 6 | 2,68% | 6 | 2,78% | 6 | 2,76% |
| Ortiz-Sepulveda et al. (2019) | 7 | 0,87% | 6 | 2,68% | 6 | 2,78% | 6 | 2,76% |
| Talaga et al. (2015) | 7 | 0,87% | 7 | 3,12% | 7 | 3,24% | 7 | 3,23% |
| Touroult et al. (2020) | 7 | 0,87% | 6 | 2,68% | 6 | 2,78% | 6 | 2,76% |
| Triapitsyn (2015) | 7 | 0,87% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Ceccolini (2023) | 6 | 0,74% | 6 | 2,68% | 6 | 2,78% | 6 | 2,76% |
| Forel (1908) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2021) | 6 | 0,74% | 6 | 2,68% | 6 | 2,78% | 6 | 2,76% |
| Vayssières et al. (2001) | 6 | 0,74% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Wetterer (2012) | 6 | 0,74% | 6 | 2,68% | 6 | 2,78% | 6 | 2,76% |
| Wetterer (2014) | 6 | 0,74% | 6 | 2,68% | 6 | 2,78% | 6 | 2,76% |
| Wheeler (1908) | 6 | 0,74% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Bernard (1968) | 5 | 0,62% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Emery (1914) | 5 | 0,62% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Linnaeus (1758) | 5 | 0,62% | 1 | 0,45% | 1 | 0,46% | 0 | 0% |
| Olmi (1984) | 5 | 0,62% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Pierre et al. (2017) | 5 | 0,62% | 5 | 2,23% | 5 | 2,31% | 4 | 1,84% |
| Wetterer (2012) | 5 | 0,62% | 5 | 2,23% | 5 | 2,31% | 5 | 2,3% |
| Wetterer (2013) | 5 | 0,62% | 5 | 2,23% | 5 | 2,31% | 5 | 2,3% |
| Bolton (2012) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Célini et al. (2013) | 4 | 0,5% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Delvare (1993) | 4 | 0,5% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Dumbardon-Martial & Delblond (2019) | 4 | 0,5% | 4 | 1,79% | 4 | 1,85% | 3 | 1,38% |
| Durand (2019) | 4 | 0,5% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Fernandez-Triana et al. (2020) | 4 | 0,5% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Kim et al. (2004) | 4 | 0,5% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Meurgey et al. (2015) | 4 | 0,5% | 4 | 1,79% | 4 | 1,85% | 4 | 1,84% |
| Meurgey (2014) | 4 | 0,5% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Noyes (1979) | 4 | 0,5% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Paulian (1998) | 4 | 0,5% | 4 | 1,79% | 3 | 1,39% | 4 | 1,84% |
| Remillet (1988) | 4 | 0,5% | 3 | 1,34% | 3 | 1,39% | 2 | 0,92% |
| Wetterer (2020) | 4 | 0,5% | 4 | 1,79% | 4 | 1,85% | 0 | 0% |
| Wheeler (1923) | 4 | 0,5% | 3 | 1,34% | 3 | 1,39% | 2 | 0,92% |
| Barbotin et al. (1979) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delvare (1988) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Etienne & Delvare (1991) | 3 | 0,37% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Etienne et al. (2015) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Garrouste & Hervé (2009) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Jerdon (1851) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan & Durand (2021) | 3 | 0,37% | 3 | 1,34% | 2 | 0,93% | 3 | 1,38% |
| Kimsey (1986) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Longino (2013) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Lowe et al. (2007) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Mickel (1938) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Muesebeck (1937) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Nibouche et al. (202X) | 3 | 0,37% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Rageau (1958) | 3 | 0,37% | 3 | 1,34% | 1 | 0,46% | 3 | 1,38% |
| Ramage et al. (2015) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Rasplus et al. (2010) | 3 | 0,37% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Salata & Fisher (2022) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Touroult et al. (2021) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Ward et al. (2015) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wetterer & Hita Garcia (2015) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Wetterer & Sharaf (2021) | 3 | 0,37% | 3 | 1,34% | 3 | 1,39% | 3 | 1,38% |
| Wild (2007) | 3 | 0,37% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Wilson (2003) | 3 | 0,37% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Allemand et al. (2002) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Allen et al. (2022) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Bellmann (2019) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 1 | 0,46% |
| Bequaert (1948) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Bondroit (1916) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borowiec (2016) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Camacho et al. (2022) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Célini et al. (2020) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Dumbardon-Martial & Pierre (2020) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Emery (1896) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etienne & Dumbardon-Martial (2013) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Etienne et al. (2001) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Fabricius (1793) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1804) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Fenton (1927) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1899) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1909) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gros (2020) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Guilbert & Casevitz-Weulersse (1997) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Harvard University Museum & Morris P.J. (2020) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Jourdan et al. (2014) | 2 | 0,25% | 2 | 0,89% | 1 | 0,46% | 2 | 0,92% |
| Jourdan et al. (2022) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Jourdan et al. (2023) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Kuhlmann (2006) | 2 | 0,25% | 2 | 0,89% | 1 | 0,46% | 2 | 0,92% |
| Le Breton et al. (2005) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Leclercq (2002) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Leroy et al. (2021) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Longino (2013) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Mayr (1884) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Mayr (1887) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nève de Mévergnies et al. (2024) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Nordlander (1980) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Olmi (1984) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Olmi (1989) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Olmi (1993) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Onillon et al. (1994) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Richards (1969) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rousse & Gupta (2013) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Sarnat et al. (2015) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Seifert (2003) | 2 | 0,25% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Spinola (1841) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stary et al. (1987) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Timberlake (1924) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Timberlake (1980) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Tomanović et al. (2018) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Touroult et al. (2021) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Touroult et al. (2022) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Touroult et al. (2023) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Triapitsyn et al. (2018) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Vachal (1907) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 1 | 0,46% |
| Vardy (2005) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Vayssade et al. (2012) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Viggiani (1988) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Vivallo (2019) | 2 | 0,25% | 2 | 0,89% | 2 | 0,93% | 2 | 0,92% |
| Wetterer et al. (2012) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aguilar-Velasco et al. (2016) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Albouy et al. (2017) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 0 | 0% |
| Amarante (2002) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Balhoff et al. (2013) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Beckers et al. (1989) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Blight et al. (2023) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Bolton (2000) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boyd et al. (2006) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 0 | 0% |
| Brown (1956) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brown (1960) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brown (1965) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cameron (1884) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cameron (1911) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Celini et al. (2012) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Celini (2013) | 1 | 0,12% | 1 | 0,45% | 0 | 0% | 1 | 0,46% |
| Chapelin-Viscardi & Lariviere (2014) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Cohic (1959) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Colindre (2016) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Colindre (2021) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Colindre (2023) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Conte et al. (2007) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 0 | 0% |
| Cresson (1865) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Czechowski et al. (2002) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Dalla Torre (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dejean et al. (2011) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Delabie & Blard (2002) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Dozier (1937) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Emery (1892) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Emery (1894) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Emery (1894) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Emery (1900) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Emery (1902) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etienne (1971) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Fabricius (1794) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fernández et al. (2015) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Fischer & Fisher (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fisher & Bolton (2016) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Forel (1881) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Forel (1890) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1907) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Forel (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Friese (1907) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girault & Dodd (1915) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girault (1915) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Groom et al. (2016) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 0 | 0% |
| Gutierrez (1981) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Howard (1895) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Howard (1907) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Ješovnik & Schultz (2017) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Kempf (1962) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kurczewski et al. (2020) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Lachaud et al. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ladino & Feitosa (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lapolla & Kallal (2019) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Latreille (1802) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Divelec (2021) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Lenoir et al. (2023) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Libert & Lemoine (2022) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Linnaeus (1761) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lotfalizadeh et al. (2007) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas (1872) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Madl & Ganeshan (2008) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Madl & van Achterberg (2014) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Madl (2014) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Mann (1921) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marcineiro & Lattke (2024) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Matos-Maraví et al. (2018) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Mayr (1865) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Mayr (1879) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Mayr (1886) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menozzi (1927) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moure (1960) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noyes (2010) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Olmi & Guglielmino (2016) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Paola et al. (2010) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Parnaudeau & Madl (2009) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Pauly et al. (2001) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Praz & Bénon (2023) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Remaudiere & Stary (1993) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Reverté et al. (2023) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 0 | 0% |
| Riley et al. (1894) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roger (1859) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Santschi (1920) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Santschi (1928) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidt & Shattuck (2014) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schomburgk (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schulthess (1915) | 1 | 0,12% | 1 | 0,45% | 0 | 0% | 1 | 0,46% |
| Seifert (2022) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Seurat (1934) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Smith (1857) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1860) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1874) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Solomon et al. (2019) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Soltani et al. (2017) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Taylor & Wilson (1961) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Taylor (1968) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Touroult et al. (2016) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Touroult et al. (2017) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Touroult et al. (2023) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Townes (1950) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 0 | 0% |
| Triapitsyn (2015) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vantaux et al. (2010) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Vardy (2000) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Vardy (2002) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Voelkl (1989) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Wetterer (2015) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wetterer (2020) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Wheeler (1929) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams (1932) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 1 | 0,46% |
| Zakardjian et al. (2020) | 1 | 0,12% | 1 | 0,45% | 1 | 0,46% | 0 | 0% |
| Zakardjian et al. (2023) | 1 | 0,12% | 1 | 0,45% | 0 | 0% | 1 | 0,46% |
