Diptères de Polynésie française
Diptera de Polynésie française
244 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) | 344 | 44,97% | 337 | 90,84% | 332 | 90,71% | 337 | 91,83% |
| Paulian (1998) | 101 | 13,2% | 98 | 26,42% | 96 | 26,23% | 98 | 26,7% |
| Malloch (1933) | 53 | 6,93% | 30 | 8,09% | 30 | 8,2% | 30 | 8,17% |
| Evenhuis (2012) | 48 | 6,27% | 48 | 12,94% | 48 | 13,11% | 48 | 13,08% |
| Evenhuis (2018) | 45 | 5,88% | 43 | 11,59% | 42 | 11,48% | 43 | 11,72% |
| Evenhuis (2013) | 44 | 5,75% | 44 | 11,86% | 44 | 12,02% | 44 | 11,99% |
| Malloch (1932) | 39 | 5,1% | 31 | 8,36% | 31 | 8,47% | 31 | 8,45% |
| Craig (1997) | 31 | 4,05% | 31 | 8,36% | 31 | 8,47% | 31 | 8,45% |
| Craig (1987) | 29 | 3,79% | 29 | 7,82% | 29 | 7,92% | 29 | 7,9% |
| Rageau (1958) | 29 | 3,79% | 27 | 7,28% | 27 | 7,38% | 25 | 6,81% |
| Malloch (1932) | 27 | 3,53% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Evenhuis (2012) | 26 | 3,4% | 26 | 7,01% | 24 | 6,56% | 26 | 7,08% |
| Evenhuis (2012) | 24 | 3,14% | 23 | 6,2% | 23 | 6,28% | 23 | 6,27% |
| Macfie (1933) | 23 | 3,01% | 19 | 5,12% | 19 | 5,19% | 19 | 5,18% |
| Ramage et al. (2018) | 23 | 3,01% | 18 | 4,85% | 18 | 4,92% | 18 | 4,9% |
| Evenhuis (2013) | 22 | 2,88% | 22 | 5,93% | 22 | 6,01% | 22 | 5,99% |
| Jourdan & Mille (2006) | 18 | 2,35% | 14 | 3,77% | 14 | 3,83% | 14 | 3,81% |
| Evenhuis (2012) | 17 | 2,22% | 15 | 4,04% | 15 | 4,1% | 15 | 4,09% |
| Evenhuis (2012) | 17 | 2,22% | 17 | 4,58% | 17 | 4,64% | 17 | 4,63% |
| Malloch (1932) | 17 | 2,22% | 8 | 2,16% | 8 | 2,19% | 8 | 2,18% |
| Meurgey & Ramage (2020) | 17 | 2,22% | 15 | 4,04% | 15 | 4,1% | 15 | 4,09% |
| Macfie (1933) | 16 | 2,09% | 12 | 3,23% | 12 | 3,28% | 12 | 3,27% |
| Edwards (1933) | 15 | 1,96% | 12 | 3,23% | 12 | 3,28% | 12 | 3,27% |
| Evenhuis (2012) | 15 | 1,96% | 14 | 3,77% | 14 | 3,83% | 14 | 3,81% |
| Evenhuis (2007) | 14 | 1,83% | 14 | 3,77% | 13 | 3,55% | 14 | 3,81% |
| Evenhuis (2011) | 13 | 1,7% | 12 | 3,23% | 12 | 3,28% | 12 | 3,27% |
| Duyck et al. (2022) | 12 | 1,57% | 12 | 3,23% | 12 | 3,28% | 12 | 3,27% |
| Edwards (1933) | 12 | 1,57% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Evenhuis (2013) | 12 | 1,57% | 12 | 3,23% | 12 | 3,28% | 12 | 3,27% |
| Malloch (1934) | 12 | 1,57% | 11 | 2,96% | 11 | 3,01% | 11 | 3% |
| Alexander (1932) | 11 | 1,44% | 11 | 2,96% | 11 | 3,01% | 11 | 3% |
| Alexander (1933) | 11 | 1,44% | 11 | 2,96% | 11 | 3,01% | 11 | 3% |
| Edwards (1932) | 11 | 1,44% | 9 | 2,43% | 9 | 2,46% | 9 | 2,45% |
| Jourdan (2020) | 11 | 1,44% | 11 | 2,96% | 10 | 2,73% | 10 | 2,72% |
| Craig et al. (1995) | 10 | 1,31% | 10 | 2,7% | 10 | 2,73% | 10 | 2,72% |
| Curran (1929) | 10 | 1,31% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Bickel (1994) | 9 | 1,18% | 8 | 2,16% | 8 | 2,19% | 8 | 2,18% |
| Craig & Evenhuis (2017) | 9 | 1,18% | 9 | 2,43% | 9 | 2,46% | 9 | 2,45% |
| Evenhuis (2004) | 9 | 1,18% | 9 | 2,43% | 9 | 2,46% | 9 | 2,45% |
| Evenhuis (2007) | 9 | 1,18% | 9 | 2,43% | 9 | 2,46% | 9 | 2,45% |
| Evenhuis (2012) | 9 | 1,18% | 9 | 2,43% | 8 | 2,19% | 9 | 2,45% |
| Lamb (1933) | 9 | 1,18% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Alexander (1932) | 8 | 1,05% | 8 | 2,16% | 8 | 2,19% | 8 | 2,18% |
| Brunhes & Boussès (2009) | 8 | 1,05% | 8 | 2,16% | 8 | 2,19% | 7 | 1,91% |
| Annals & Magazine of Natural History Series 9, 20: 236-244.">Edwards (1927) | 8 | 1,05% | 8 | 2,16% | 8 | 2,19% | 8 | 2,18% |
| Evenhuis (2011) | 8 | 1,05% | 8 | 2,16% | 8 | 2,19% | 8 | 2,18% |
| Evenhuis (2012) | 8 | 1,05% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Marie & Bossin (2013) | 8 | 1,05% | 8 | 2,16% | 7 | 1,91% | 8 | 2,18% |
| Meganck et al. (2017) | 8 | 1,05% | 8 | 2,16% | 8 | 2,19% | 8 | 2,18% |
| Rageau (1959) | 8 | 1,05% | 8 | 2,16% | 8 | 2,19% | 8 | 2,18% |
| Ramage et al. (2017) | 8 | 1,05% | 8 | 2,16% | 8 | 2,19% | 8 | 2,18% |
| Evenhuis (2007) | 7 | 0,92% | 7 | 1,89% | 7 | 1,91% | 7 | 1,91% |
| Evenhuis (2011) | 7 | 0,92% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Meurgey (2011) | 7 | 0,92% | 5 | 1,35% | 5 | 1,37% | 5 | 1,36% |
| Mohrig et al. (2019) | 7 | 0,92% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Questel (2020) | 7 | 0,92% | 5 | 1,35% | 5 | 1,37% | 5 | 1,36% |
| Rageau (1956) | 7 | 0,92% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Souza et al. (2020) | 7 | 0,92% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Alexander (1947) | 6 | 0,78% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Craig (2004) | 6 | 0,78% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Evenhuis (2011) | 6 | 0,78% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Gutierrez (1981) | 6 | 0,78% | 6 | 1,62% | 6 | 1,64% | 5 | 1,36% |
| Malloch (1932) | 6 | 0,78% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Shinonaga et al. (1991) | 6 | 0,78% | 6 | 1,62% | 6 | 1,64% | 6 | 1,63% |
| Bickel (2003) | 5 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couri et al. (2010) | 5 | 0,65% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Duval et al. (1978) | 5 | 0,65% | 5 | 1,35% | 5 | 1,37% | 5 | 1,36% |
| Kurahashi & Fauran (1980) | 5 | 0,65% | 5 | 1,35% | 5 | 1,37% | 5 | 1,36% |
| Linnaeus (1758) | 5 | 0,65% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Mathis & Zatwarnicki (2003) | 5 | 0,65% | 5 | 1,35% | 5 | 1,37% | 5 | 1,36% |
| Sasakawa (1963) | 5 | 0,65% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Theobald (1913) | 5 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bangy et al. (2009) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 4 | 0,52% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Bickel (2002) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| David & Tsacas (1975) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| David et al. (2014) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Evenhuis (1999) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Evenhuis (2012) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Hull (1937) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Malloch (1932) | 4 | 0,52% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Malloch (1932) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Martinez & Etienne (2002) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Mille (2008) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Papp (2002) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Russell et al. (2021) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Sechan & Tetuanui (2001) | 4 | 0,52% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Bequaert (1941) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Borkent & Dominiak (2020) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bousses et al. (2013) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Etienne & Martinez (2013) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Evenhuis (2007) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Evenhuis (2007) | 3 | 0,39% | 3 | 0,81% | 2 | 0,55% | 3 | 0,82% |
| Evenhuis (2011) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Evenhuis (2012) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Evenhuis (2013) | 3 | 0,39% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Hamon (1953) | 3 | 0,39% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Lamb (1914) | 3 | 0,39% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Lamb (1932) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Le Maitre & Chadee (1983) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Lyneborg & Barkemeyer (2005) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Malloch (1933) | 3 | 0,39% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Malloch (1938) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Mirouse (1958) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Munari et al. (2020) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Pont (1972) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spencer et al. (1992) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Tsacas & Chassagnard (1988) | 3 | 0,39% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Wulp (1882) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alexander (1935) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Aubertin & Cheesman (1929) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bagny et al. (2009) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Beaucournu et al. (1985) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Bickel (2000) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Bigot (1885) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dumbardon-Martial & Delblond (2019) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Etienne & Martinez (2003) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Evenhuis (2007) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Evenhuis (2011) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Evenhuis (2011) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Evenhuis (2016) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Fabricius (1775) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hery et al. (2020) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Klein et al. (1983) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Lagarde (2008) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Lehrer & Barbet (2008) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malloch (1933) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malloch (1933) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Marks (1951) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Mary (2017) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Mathis (1986) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Mcevey & Schiffer (2015) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Mengual (2018) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Minard et al. (2015) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Nibouche et al. (202X) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Norrbom & Hancock (2004) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Pierre et al. (2017) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Pollet et al. (2004) | 2 | 0,26% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Pont (1979) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Questel & Le Quellec (2012) | 2 | 0,26% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Robineau-desvoidy (1827) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sabrosky (1957) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Sasakawa (1963) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Schroder (1988) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Sechan & Loncke (2000) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Senevet (1937) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Talaga et al. (2015) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Thompson (1981) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Vayssières et al. (2001) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Vilkamaa et al. (2012) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vueti (2001) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Wiedemann (1830) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2013) | 2 | 0,26% | 2 | 0,54% | 2 | 0,55% | 2 | 0,54% |
| Albouy et al. (2017) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Aldrich (1931) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| ANSES (2019) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Belkin et al. (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot (1890) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borkent & Wirth (1997) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Brunhes (1977) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Brunhes (1979) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Cetre-sosah et al. (2023) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Chanteau et al. (1993) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Chevin (1986) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Chown & Convey (2016) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Clastrier & Delécolle (1991) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Clastrier & Delécolle (1996) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Courtiller (1854) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couteyen (2021) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Dauphin (2003) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| De Meyer et al. (2012) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deeming (2022) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Delaunay et al. (2000) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Delaunay et al. (2009) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Duhamel (2018) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Dyar & Knab (1908) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edwards (1926) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edwards (1933) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Evenhuis (1996) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Evenhuis (2011) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Evenhuis (2012) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evenhuis (2012) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Fabricius (1794) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1794) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1798) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1805) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferrington & Saether (2006) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Forcellini et al. (2012) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Garrouste & Hervé (2009) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Girod (2004) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Hancock (2008) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Hardy & Delfinado (1980) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Hardy (1980) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Hee et al. (2015) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hendrichs et al. (2015) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hering (1951) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hynes (1993) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Irish et al. (2014) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Kassebeer (2000) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Kieffer (1916) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koehler & Menzel (2013) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Leach (1817) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lebard & Hauser (2023) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Liénard et al. (2011) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Lonsdale (2017) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Lowe et al. (2007) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Maquart et al. (2020) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Marcos-garcía et al. (2013) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Marinov et al. (2016) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Martin-vega et al. (2017) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathis & Zatwarnicki (2002) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mathis (1993) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mathis (1993) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mazumdar et al. (2024) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Medlock et al. (2012) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Meigen (1818) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moquet & Delatte (2022) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Moquet et al. (2021) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Munari (1988) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Munari (2004) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Remm (1981) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reverté et al. (2023) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Robinson (1975) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rozkosny (1983) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Runyon (2020) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Say (1823) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Schaffner & Karch (2000) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Scholte & Schaffner (2007) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Séguy (1960) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Skuse (1895) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spencer (1963) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steyskal (1952) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Tokunaga (1941) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult et al. (2016) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult et al. (2018) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Touroult et al. (2020) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Touroult et al. (2021) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult et al. (2021) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Williston (1896) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wolff et al. (2016) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yassin et al. (2012) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Younes et al. (2021) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Zatwarnicki (1991) | 1 | 0,13% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
