Diptères de Nouvelle-Calédonie
Diptera de Nouvelle-Calédonie
315 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Evenhuis (2018) | 753 | 51,33% | 739 | 83,98% | 733 | 84,45% | 738 | 84,93% |
| Bickel (2002) | 110 | 7,5% | 110 | 12,5% | 110 | 12,67% | 110 | 12,66% |
| Hynes (1993) | 110 | 7,5% | 92 | 10,45% | 91 | 10,48% | 91 | 10,47% |
| Matile (1993) | 60 | 4,09% | 60 | 6,82% | 60 | 6,91% | 60 | 6,9% |
| Matile (1988) | 58 | 3,95% | 58 | 6,59% | 58 | 6,68% | 58 | 6,67% |
| Burger (1995) | 57 | 3,89% | 51 | 5,8% | 51 | 5,88% | 51 | 5,87% |
| Curran (1929) | 55 | 3,75% | 22 | 2,5% | 21 | 2,42% | 22 | 2,53% |
| Chassagnard & Tsacas (1997) | 51 | 3,48% | 51 | 5,8% | 51 | 5,88% | 51 | 5,87% |
| Ramage (2017) | 49 | 3,34% | 45 | 5,11% | 43 | 4,95% | 44 | 5,06% |
| Rageau (1958) | 41 | 2,79% | 30 | 3,41% | 28 | 3,23% | 28 | 3,22% |
| Trojan (1991) | 39 | 2,66% | 15 | 1,7% | 15 | 1,73% | 15 | 1,73% |
| Jourdan (2020) | 34 | 2,32% | 33 | 3,75% | 30 | 3,46% | 31 | 3,57% |
| Webb (2011) | 34 | 2,32% | 34 | 3,86% | 34 | 3,92% | 34 | 3,91% |
| Jourdan & Mille (2006) | 33 | 2,25% | 28 | 3,18% | 26 | 3% | 27 | 3,11% |
| Bickel (2008) | 32 | 2,18% | 32 | 3,64% | 32 | 3,69% | 32 | 3,68% |
| Alexander (1978) | 30 | 2,04% | 12 | 1,36% | 12 | 1,38% | 12 | 1,38% |
| Clastrier & Delécolle (1991) | 29 | 1,98% | 29 | 3,3% | 29 | 3,34% | 29 | 3,34% |
| Couri et al. (2010) | 29 | 1,98% | 28 | 3,18% | 28 | 3,23% | 28 | 3,22% |
| Irwin et al. (2020) | 28 | 1,91% | 28 | 3,18% | 27 | 3,11% | 28 | 3,22% |
| Mackerras & Rageau (1958) | 28 | 1,91% | 20 | 2,27% | 20 | 2,3% | 20 | 2,3% |
| Mille (2008) | 27 | 1,84% | 24 | 2,73% | 24 | 2,76% | 24 | 2,76% |
| Vilkamaa et al. (2012) | 26 | 1,77% | 20 | 2,27% | 20 | 2,3% | 20 | 2,3% |
| Vilkamaa et al. (2012) | 26 | 1,77% | 26 | 2,95% | 26 | 3% | 26 | 2,99% |
| Shinonaga et al. (1991) | 25 | 1,7% | 25 | 2,84% | 25 | 2,88% | 24 | 2,76% |
| Clastrier (1987) | 24 | 1,64% | 24 | 2,73% | 24 | 2,76% | 24 | 2,76% |
| Paulian (1998) | 21 | 1,43% | 18 | 2,05% | 17 | 1,96% | 17 | 1,96% |
| Clastrier & Delécolle (1993) | 20 | 1,36% | 20 | 2,27% | 20 | 2,3% | 20 | 2,3% |
| Kurahashi & Fauran (1980) | 19 | 1,3% | 16 | 1,82% | 16 | 1,84% | 16 | 1,84% |
| Mary (2017) | 19 | 1,3% | 19 | 2,16% | 19 | 2,19% | 19 | 2,19% |
| Norrbom & Hancock (2004) | 19 | 1,3% | 17 | 1,93% | 17 | 1,96% | 17 | 1,96% |
| Rageau (1956) | 19 | 1,3% | 14 | 1,59% | 12 | 1,38% | 14 | 1,61% |
| Tsacas & Chassagnard (1991) | 19 | 1,3% | 19 | 2,16% | 19 | 2,19% | 19 | 2,19% |
| Matile (1991) | 16 | 1,09% | 16 | 1,82% | 16 | 1,84% | 16 | 1,84% |
| Meurgey & Ramage (2020) | 16 | 1,09% | 15 | 1,7% | 15 | 1,73% | 14 | 1,61% |
| Vilkamaa et al. (2012) | 16 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koehler & Menzel (2013) | 14 | 0,95% | 12 | 1,36% | 12 | 1,38% | 12 | 1,38% |
| Alexander (1948) | 13 | 0,89% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Gaimari (2004) | 13 | 0,89% | 13 | 1,48% | 13 | 1,5% | 13 | 1,5% |
| Clastrier (1985) | 12 | 0,82% | 12 | 1,36% | 12 | 1,38% | 12 | 1,38% |
| Clastrier (1985) | 12 | 0,82% | 12 | 1,36% | 12 | 1,38% | 12 | 1,38% |
| Hancock (2008) | 12 | 0,82% | 11 | 1,25% | 11 | 1,27% | 11 | 1,27% |
| McAlpine (2007) | 12 | 0,82% | 12 | 1,36% | 12 | 1,38% | 12 | 1,38% |
| Tsacas & Chassagnard (1988) | 12 | 0,82% | 12 | 1,36% | 12 | 1,38% | 11 | 1,27% |
| Stuckenberg (1970) | 11 | 0,75% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Curler & Jacobson (2012) | 10 | 0,68% | 10 | 1,14% | 10 | 1,15% | 10 | 1,15% |
| Meganck et al. (2017) | 10 | 0,68% | 10 | 1,14% | 10 | 1,15% | 9 | 1,04% |
| Meuffels & Grootaert (1991) | 10 | 0,68% | 10 | 1,14% | 10 | 1,15% | 10 | 1,15% |
| Meuffels & Grootaert (2002) | 10 | 0,68% | 10 | 1,14% | 10 | 1,15% | 10 | 1,15% |
| Vilkamaa et al. (2011) | 10 | 0,68% | 10 | 1,14% | 10 | 1,15% | 10 | 1,15% |
| Evenhuis (1991) | 9 | 0,61% | 9 | 1,02% | 9 | 1,04% | 9 | 1,04% |
| Evenhuis (2012) | 9 | 0,61% | 8 | 0,91% | 8 | 0,92% | 7 | 0,81% |
| Fitzgerald (2004) | 9 | 0,61% | 9 | 1,02% | 9 | 1,04% | 9 | 1,04% |
| Mohrig et al. (2019) | 9 | 0,61% | 7 | 0,8% | 7 | 0,81% | 7 | 0,81% |
| Vilkamaa et al. (2014) | 9 | 0,61% | 9 | 1,02% | 9 | 1,04% | 9 | 1,04% |
| Bigot (1885) | 8 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clastrier (1993) | 8 | 0,55% | 8 | 0,91% | 8 | 0,92% | 8 | 0,92% |
| Falcoz (1923) | 8 | 0,55% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Sasakawa (1963) | 8 | 0,55% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Vilkamaa et al. (2012) | 8 | 0,55% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Clastrier (1985) | 7 | 0,48% | 7 | 0,8% | 7 | 0,81% | 7 | 0,81% |
| Gutierrez (1981) | 7 | 0,48% | 6 | 0,68% | 6 | 0,69% | 4 | 0,46% |
| Mesnil (1968) | 7 | 0,48% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Meurgey (2011) | 7 | 0,48% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Moubayed-breil et al. (2021) | 7 | 0,48% | 7 | 0,8% | 7 | 0,81% | 7 | 0,81% |
| Royer et al. (2019) | 7 | 0,48% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Clastrier (1985) | 6 | 0,41% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Falcoz (1921) | 6 | 0,41% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Malloch (1932) | 6 | 0,41% | 2 | 0,23% | 2 | 0,23% | 1 | 0,12% |
| Matile (1988) | 6 | 0,41% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Moubayed & Mary (2023) | 6 | 0,41% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Moubayed & Mary (2023) | 6 | 0,41% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Moubayed & Mary (2023) | 6 | 0,41% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Moubayed & Mary (2023) | 6 | 0,41% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Questel (2020) | 6 | 0,41% | 4 | 0,45% | 4 | 0,46% | 3 | 0,35% |
| Rageau (1959) | 6 | 0,41% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Souza et al. (2020) | 6 | 0,41% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Zwick & Mary-Sasal (2010) | 6 | 0,41% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Albouy et al. (2017) | 5 | 0,34% | 4 | 0,45% | 4 | 0,46% | 2 | 0,23% |
| Dobrotworsky (1972) | 5 | 0,34% | 5 | 0,57% | 5 | 0,58% | 5 | 0,58% |
| Evenhuis (2007) | 5 | 0,34% | 5 | 0,57% | 5 | 0,58% | 5 | 0,58% |
| Gilka & Dobosz (2015) | 5 | 0,34% | 5 | 0,57% | 5 | 0,58% | 5 | 0,58% |
| Linnaeus (1758) | 5 | 0,34% | 3 | 0,34% | 3 | 0,35% | 1 | 0,12% |
| Malloch (1933) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| McAlpine (2001) | 5 | 0,34% | 5 | 0,57% | 5 | 0,58% | 5 | 0,58% |
| Ramage et al. (2017) | 5 | 0,34% | 5 | 0,57% | 5 | 0,58% | 5 | 0,58% |
| Theobald (1913) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ament & Brown (2017) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Baylac & Matile (1988) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 4 | 0,27% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Bickel (1994) | 4 | 0,27% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Bickel (2013) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Bickel (2014) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Bigot (1890) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cerretti et al. (2014) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Clastrier (1989) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Daniels (1987) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| David & Tsacas (1975) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Disney (2003) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Duckhouse (1991) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Duyck et al. (2022) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Evenhuis (2005) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Evenhuis (2011) | 4 | 0,27% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Le Pont et al. (2017) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Léger & Pesson (1993) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Lonsdale (2016) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Mackerras (1962) | 4 | 0,27% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Pont (1972) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramage et al. (2018) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Séguy (1960) | 4 | 0,27% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Shima & Tachi (2008) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Tokunaga (1961) | 4 | 0,27% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
| Vilkamaa et al. (2015) | 4 | 0,27% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Bangy et al. (2009) | 3 | 0,2% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Barraclough (1991) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Brunhes & Boussès (2009) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 2 | 0,23% |
| Clastrier (1988) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Cranston (2019) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| David et al. (2014) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Disney & Chazeau (1990) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Evenhuis (2007) | 3 | 0,2% | 2 | 0,23% | 1 | 0,12% | 2 | 0,23% |
| Evenhuis (2011) | 3 | 0,2% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Galliard (1927) | 3 | 0,2% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
| Hamon (1953) | 3 | 0,2% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Le Maitre & Chadee (1983) | 3 | 0,2% | 2 | 0,23% | 2 | 0,23% | 1 | 0,12% |
| Malloch (1914) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marie & Bossin (2013) | 3 | 0,2% | 2 | 0,23% | 1 | 0,12% | 2 | 0,23% |
| Marshall & Montagnes (1990) | 3 | 0,2% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Martinez & Etienne (2002) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Mirouse (1958) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nibouche et al. (202X) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Reinert et al. (2004) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Spencer et al. (1992) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Vayssières et al. (2001) | 3 | 0,2% | 3 | 0,34% | 3 | 0,35% | 3 | 0,35% |
| Baylac & Matile (1990) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Beaucournu et al. (1985) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Bellis et al. (2013) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Bequaert (1941) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Bickel (2005) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Bickel (2008) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Bickel (2014) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Bousses et al. (2013) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Broadley et al. (2016) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Brunhes (1977) | 2 | 0,14% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Brunhes (1979) | 2 | 0,14% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Chassagnard & Groseille (1992) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Chen et al. (2015) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Chown & Convey (2016) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
| Daly et al. (2023) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Daugeron (2002) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Drew & Hancock (2000) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Elsayed & Mille (2022) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| , 3: 249-270.">Enderlein (1903) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etienne & Gagné (2017) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Etienne & Martinez (2013) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Evenhuis (2011) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Evenhuis (2012) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Evenhuis (2012) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Evenhuis (2013) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Evenhuis (2013) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Gillung & Winterton (2011) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Hamon (1956) | 2 | 0,14% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Han & Norrbom (2008) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Hery et al. (2020) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hippa (1980) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hull (1937) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Hullé et al. (2018) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Hynes (1987) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Ježek & Pont (2016) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Johnston et al. (2019) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Kieffer (1898) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lagarde (2008) | 2 | 0,14% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Laird (1954) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Lehrer & Barbet (2008) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malloch (1932) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matile (1986) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Mcevey & Schiffer (2015) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Mengual (2012) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Mengual (2016) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Mengual (2018) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Moubayed & Mary (2023) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moubayed & Mary (2023) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Moubayed-Breil & Mary (2020) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Munari (2002) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Munari (2004) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Okada (1985) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Pape (1996) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Papp (1978) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Pont (1979) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Questel & Le Quellec (2012) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
| Robineau-desvoidy (1827) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rognes & Blackith (1990) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Sasakawa (1963) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Sasakawa (2004) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Senevet (1937) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sicart & Ruffie (1960) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Sinclair (1997) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Sinclair (2008) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Stuke (2014) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Talaga et al. (2015) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Touroult et al. (2018) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Vilkamaa & Suuronen (2019) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Whitworth (2014) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Yokoyama (2013) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Younes et al. (2021) | 2 | 0,14% | 2 | 0,23% | 2 | 0,23% | 1 | 0,12% |
| Zwick & Mary-sasal (2010) | 2 | 0,14% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Alexander (1932) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Alexander (1947) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Alexander (1972) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2018) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Bagny et al. (2009) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barraclough (1992) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Belkin et al. (1965) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blanchot (1992) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
| Borkent & Wirth (1997) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Borkent (2024) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Boyd et al. (2006) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Callot & Rioux (1965) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Callot et al. (1967) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
| Cantrell & Crosskey (1989) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Chevin (1986) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Clastrier & Delécolle (1996) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Colless (1982) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Couri & Rodrigues-junior (2012) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Couri & Sousa (2019) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Cranston & Tang (2018) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Dauphin (2003) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Debenham (1969) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Deeming (2022) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Delhaes et al. (2001) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Drew (1971) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel (2018) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dumbardon-Martial & Delblond (2019) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Eaton et al. (1879) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Edwards (1926) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Edwards (1933) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Etienne & Martinez (2003) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Evenhuis (1989) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Evenhuis (2007) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Evenhuis (2007) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Evenhuis (2011) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Evenhuis (2012) | 1 | 0,07% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
| Evenhuis (2012) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Evenhuis (2012) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Evenhuis (2013) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Fabricius (1775) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1794) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1805) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcellini et al. (2012) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Frenot et al. (2005) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Froggatt (1897) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Galliard (1928) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrouste & Hervé (2009) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Germain et al. (2014) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Han & Ro (2019) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Hancock & Drew (2003) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Hardy & Delfinado (1980) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Hering (1951) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hughes et al. (2004) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Hullé & Vernon (2021) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Hynes (1988) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Irish et al. (2014) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Izri & Akhoundi (2024) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Kameneva & Korneyev (2016) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Kassebeer (2000) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Kugler (1967) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
| Lamb (1914) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Le Goff et al. (2013) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Lebard & Claude (2024) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Lebard & Hauser (2023) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Liénard et al. (2011) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Maa (1966) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macfie (1933) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Macfie (1933) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Macquart (1842) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malloch (1932) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maquart et al. (2020) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Marcos-garcía et al. (2013) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Marks (1951) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Meigen (1824) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meigen (1830) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mik (1885) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Mille & Hancock (2009) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Mille et al., 2012 | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Mouttet & Taddei (2024) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Munari et al. (2020) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Perkins (1939) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierre et al. (2017) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Pol et al. (2018) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Pont (1977) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Quindroit & Lemoine (2022) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
| Quindroit (2020) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
| Rageau & Verrent (1959) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reverté et al. (2023) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Rondani (1861) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rozkosny (1983) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Say (1823) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Schiner (1864) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1763) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shima & Tachi (2019) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Skuhravá et al. (2005) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Skuse (1888) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Speiser (1908) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Spencer (1977) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Szadziewski (1983) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thompson (1981) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Thompson (2003) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Touroult et al. (2020) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Touroult et al. (2021) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Tryon (1895) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verves (2004) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Walker (1849) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiedemann (1819) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wright & Skevington (2013) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Yassin et al. (2012) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
| Zatwarnicki (1991) | 1 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
