Diptères de la Réunion
Diptera de la Réunion
267 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Lagarde (2008) | 40 | 5,04% | 37 | 13,45% | 36 | 13,19% | 37 | 13,55% |
| Kassebeer (2000) | 30 | 3,78% | 30 | 10,91% | 30 | 10,99% | 30 | 10,99% |
| Alexander (1957) | 28 | 3,53% | 17 | 6,18% | 17 | 6,23% | 17 | 6,23% |
| Meganck et al. (2017) | 25 | 3,15% | 24 | 8,73% | 24 | 8,79% | 23 | 8,42% |
| Ramage (2017) | 23 | 2,9% | 21 | 7,64% | 21 | 7,69% | 20 | 7,33% |
| David & Tsacas (1975) | 20 | 2,52% | 16 | 5,82% | 16 | 5,86% | 16 | 5,86% |
| Grichanov (2003) | 20 | 2,52% | 20 | 7,27% | 20 | 7,33% | 20 | 7,33% |
| Marcos-garcía et al. (2013) | 20 | 2,52% | 20 | 7,27% | 20 | 7,33% | 20 | 7,33% |
| Vayssières et al. (2001) | 17 | 2,14% | 16 | 5,82% | 16 | 5,86% | 16 | 5,86% |
| David et al. (2014) | 15 | 1,89% | 15 | 5,45% | 15 | 5,49% | 15 | 5,49% |
| Meurgey & Ramage (2020) | 15 | 1,89% | 14 | 5,09% | 14 | 5,13% | 13 | 4,76% |
| Evenhuis (2018) | 14 | 1,76% | 13 | 4,73% | 13 | 4,76% | 12 | 4,4% |
| Jourdan & Mille (2006) | 14 | 1,76% | 13 | 4,73% | 12 | 4,4% | 13 | 4,76% |
| Bousses et al. (2013) | 13 | 1,64% | 9 | 3,27% | 9 | 3,3% | 9 | 3,3% |
| De Meyer et al. (2012) | 13 | 1,64% | 11 | 4% | 11 | 4,03% | 11 | 4,03% |
| Pont (1979) | 13 | 1,64% | 13 | 4,73% | 11 | 4,03% | 13 | 4,76% |
| Hamon (1953) | 12 | 1,51% | 8 | 2,91% | 7 | 2,56% | 8 | 2,93% |
| Giudicelli (2008) | 11 | 1,39% | 11 | 4% | 11 | 4,03% | 11 | 4,03% |
| Paulian (1998) | 10 | 1,26% | 9 | 3,27% | 9 | 3,3% | 8 | 2,93% |
| Bigot (1862) | 9 | 1,13% | 9 | 3,27% | 9 | 3,3% | 9 | 3,3% |
| Clastrier (1959) | 8 | 1,01% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Duyck et al. (2022) | 8 | 1,01% | 8 | 2,91% | 8 | 2,93% | 8 | 2,93% |
| Rageau (1958) | 8 | 1,01% | 7 | 2,55% | 6 | 2,2% | 7 | 2,56% |
| Yassin et al. (2012) | 8 | 1,01% | 8 | 2,91% | 8 | 2,93% | 8 | 2,93% |
| Bangy et al. (2009) | 7 | 0,88% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Brunhes (1979) | 7 | 0,88% | 6 | 2,18% | 5 | 1,83% | 6 | 2,2% |
| Etienne (1972) | 7 | 0,88% | 6 | 2,18% | 6 | 2,2% | 6 | 2,2% |
| Jourdan (2020) | 7 | 0,88% | 7 | 2,55% | 7 | 2,56% | 7 | 2,56% |
| Lyneborg & Barkemeyer (2005) | 7 | 0,88% | 7 | 2,55% | 7 | 2,56% | 7 | 2,56% |
| Meurgey (2011) | 7 | 0,88% | 5 | 1,82% | 5 | 1,83% | 5 | 1,83% |
| Nibouche et al. (202X) | 7 | 0,88% | 7 | 2,55% | 7 | 2,56% | 7 | 2,56% |
| O'Hara & Cerretti (2016) | 7 | 0,88% | 7 | 2,55% | 7 | 2,56% | 7 | 2,56% |
| Desvars et al. (2015) | 6 | 0,76% | 6 | 2,18% | 6 | 2,2% | 6 | 2,2% |
| Dirickx (2001) | 6 | 0,76% | 6 | 2,18% | 6 | 2,2% | 6 | 2,2% |
| Linnaeus (1758) | 6 | 0,76% | 2 | 0,73% | 2 | 0,73% | 0 | 0% |
| Malloch (1932) | 6 | 0,76% | 2 | 0,73% | 2 | 0,73% | 1 | 0,37% |
| Pont (2012) | 6 | 0,76% | 6 | 2,18% | 6 | 2,2% | 6 | 2,2% |
| Questel (2020) | 6 | 0,76% | 4 | 1,45% | 4 | 1,47% | 3 | 1,1% |
| Rageau (1956) | 6 | 0,76% | 5 | 1,82% | 4 | 1,47% | 5 | 1,83% |
| Tsacas & David (1975) | 6 | 0,76% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Albouy et al. (2017) | 5 | 0,63% | 4 | 1,45% | 4 | 1,47% | 2 | 0,73% |
| Bickel (1994) | 5 | 0,63% | 5 | 1,82% | 5 | 1,83% | 5 | 1,83% |
| Brunhes (1977) | 5 | 0,63% | 4 | 1,45% | 3 | 1,1% | 4 | 1,47% |
| Evenhuis (2012) | 5 | 0,63% | 5 | 1,82% | 5 | 1,83% | 4 | 1,47% |
| Hamon (1956) | 5 | 0,63% | 3 | 1,09% | 2 | 0,73% | 3 | 1,1% |
| Malloch (1933) | 5 | 0,63% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Martinez & Etienne (2002) | 5 | 0,63% | 5 | 1,82% | 5 | 1,83% | 5 | 1,83% |
| Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 4 | 0,5% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Grichanov (2010) | 4 | 0,5% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Grichanov (2017) | 4 | 0,5% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Lamb (1914) | 4 | 0,5% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Macquart (1835) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macquart (1851) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Munari et al. (2020) | 4 | 0,5% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Ramage et al. (2017) | 4 | 0,5% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Reverté et al. (2023) | 4 | 0,5% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Russell et al. (2021) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shinonaga et al. (1991) | 4 | 0,5% | 4 | 1,45% | 4 | 1,47% | 3 | 1,1% |
| Tsacas & Chassagnard (1988) | 4 | 0,5% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Tsacas & David (1975) | 4 | 0,5% | 4 | 1,45% | 4 | 1,47% | 4 | 1,47% |
| Brunhes & Hervy (1995) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Couri et al. (2010) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Curran (1929) | 3 | 0,38% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Deguine et al. (2012) | 3 | 0,38% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Evenhuis (2007) | 3 | 0,38% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Fabricius (1805) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcellini et al. (2012) | 3 | 0,38% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Gagné & Jaschhof (2014) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Gutierrez (1981) | 3 | 0,38% | 2 | 0,73% | 2 | 0,73% | 1 | 0,37% |
| Hamon (1954) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hilger & Kassebeer (2000) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Irish et al. (2014) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Kurahashi & Fauran (1980) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Le Maitre & Chadee (1983) | 3 | 0,38% | 2 | 0,73% | 2 | 0,73% | 1 | 0,37% |
| Macquart (1842) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meigen (1830) | 3 | 0,38% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Mirouse (1958) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Munari (1988) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Ramage (2024) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Raspi et al. (2007) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Reinert et al. (2004) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Sabrosky (1975) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Scopoli (1763) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Speight (2013) | 3 | 0,38% | 3 | 1,09% | 3 | 1,1% | 3 | 1,1% |
| Alexander (1959) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alexander (1979) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Amouroux et al. (2013) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Anonyme (2018) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Bagny et al. (2009) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| D'Aguilar & Martinez (1979) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| De Meyer et al. (2016) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Disney (2005) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Etienne & Gagné (2017) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Etienne & Vilardebó (1978) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Etienne (1971) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Evenhuis (2006) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evenhuis (2011) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Evenhuis (2012) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Evenhuis (2012) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Galliard (1927) | 2 | 0,25% | 1 | 0,36% | 1 | 0,37% | 0 | 0% |
| Germain et al. (2014) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Greathead (1971) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Hendrichs et al. (2015) | 2 | 0,25% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Hery et al. (2020) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jupp & Harbach (1990) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Kameneva & Korneyev (2016) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Kieffer (1898) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Goff et al. (2013) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Macquart (1839) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malloch (1932) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Marie & Bossin (2013) | 2 | 0,25% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Martin-vega et al. (2017) | 2 | 0,25% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Mary (2017) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Matile (1979) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Mengual (2018) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Minard et al. (2015) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Munari (2013) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Pont (2006) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Questel & Le Quellec (2012) | 2 | 0,25% | 1 | 0,36% | 1 | 0,37% | 0 | 0% |
| Rageau (1959) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Ramage et al. (2018) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Robineau-desvoidy (1827) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séguy (1960) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Senevet (1937) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spencer et al. (1992) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Talaga et al. (2015) | 2 | 0,25% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Thomas et al. (2007) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Touroult et al. (2018) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Tsacas & Chassagnard (1999) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Vikhrev (2014) | 2 | 0,25% | 2 | 0,73% | 2 | 0,73% | 2 | 0,73% |
| Virgilio et al. (2010) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiedemann (1830) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2013) | 2 | 0,25% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Younes et al. (2021) | 2 | 0,25% | 1 | 0,36% | 1 | 0,37% | 0 | 0% |
| Aldrich (1931) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| ANSES (2019) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Austen (1909) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Baldet et al. (2004) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Balmès & Mouttet (2019) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Barraclough (1993) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Beaucournu et al. (1985) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Belkin et al. (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertin et al. (1993) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Bezzi (1917) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bickel (2002) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Blanchard (1926) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blanchot (1992) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 0 | 0% |
| Brunhes & Boussès (2009) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Burla (1954) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Callot & Rioux (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Callot et al. (1967) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 0 | 0% |
| Carter (1911) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cetre-sosah et al. (2023) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevin (1986) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Chown & Convey (2016) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 0 | 0% |
| Cini et al. (2012) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Couteyen (2021) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dadant & Etienne (1973) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Dauphin (2003) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Decoin et al. (2011) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Deeming (2022) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Delatte et al. (2008) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delaunay et al. (2000) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delaunay et al. (2009) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delpoux et al. (2013) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Duda (1940) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel (2018) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dumbardon-Martial & Delblond (2019) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Eaton et al. (1879) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Edwards (1933) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Černý et al. (2020) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Etienne & Martinez (1996) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Etienne & Martinez (2013) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Etienne (1978) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Evenhuis (1989) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Evenhuis (1996) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Evenhuis (1997) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evenhuis (2011) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Evenhuis (2011) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Evenhuis (2012) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Evenhuis (2013) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Fabricius (1775) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1787) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1794) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gagne (2004) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Galliard (1928) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geer (1776) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Georges et al. (2024) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Girod (2004) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hardy & Delfinado (1980) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Hassani et al. (2020) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Hee et al. (2015) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huang et al. (2012) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hull (1937) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Jacquet et al. (2016) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Johannsen (1905) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johannsen (1934) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jupp (1972) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Kassebeer (1999) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Kassebeer (2002) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Khalaf (1957) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| König et al. (2022) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Kremmer et al. (2017) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Kurina (2020) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Kvifte & Andersen (2018) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Lachaise et al. (1996) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Lamb (1912) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lebard & Claude (2024) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Lebard & Hauser (2023) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Lebard & Speight (2019) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Lebard et al. (2019) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Lehrer (2007) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Liénard et al. (2011) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Lowe et al. (2007) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| MacGowan (2023) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Malloch (1932) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Maquart et al. (2020) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Marks (1951) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Marshall (2019) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Matsumura (1931) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mcevey & Schiffer (2015) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Medlock et al. (2012) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meigen (1818) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mercier (1928) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Meyer et al. (1990) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Mille et al., 2012 | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Moquet & Delatte (2022) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Moquet et al. (2021) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Moubayed-Breil & Ashe (2016) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Mouttet & Taddei (2024) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Munari et al. (2021) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Munari (2004) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Patton (1905) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierre et al. (2017) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Plénet (1965) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Quilici et al. (1988) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Rapp (1943) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Remillet (1988) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Rondani (1861) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossi (1790) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rozkosny (1983) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Say (1823) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Schaffner & Karch (2000) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scholte & Schaffner (2007) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schönberger et al. (2022) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Sepulveda & Carvalho (2019) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Skuhravá et al. (2005) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Skuse (1895) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Speight & Ricarte (2012) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Speight et al. (2021) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Stoffolano (1969) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Theobald (1906) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Theobald (1913) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thompson (1981) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Touroult et al. (2020) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Touroult et al. (2021) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Touroult et al. (2021) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Tryon (1895) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tsacas (1980) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Vayssière (1933) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villeneuve (1911) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villeneuve (1916) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| White et al. (2000) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
| Wiedemann (1824) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williston (1888) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Withers & Allemand (2012) | 1 | 0,13% | 1 | 0,36% | 1 | 0,37% | 1 | 0,37% |
