Insectes des îles Eparses
340 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Martiré & Rochat (2008) | 63 | 9,8% | 55 | 29,26% | 51 | 29,82% | 53 | 30,99% |
Parnaudeau (2012) | 52 | 8,09% | 48 | 25,53% | 40 | 23,39% | 48 | 28,07% |
Parnaudeau & Madl (2009) | 30 | 4,67% | 27 | 14,36% | 20 | 11,7% | 26 | 15,2% |
Ramage (2017) | 25 | 3,89% | 23 | 12,23% | 23 | 13,45% | 22 | 12,87% |
Boisduval (1833) | 24 | 3,73% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Ramage (2020) | 22 | 3,42% | 21 | 11,17% | 21 | 12,28% | 20 | 11,7% |
Guillermet (2004) | 21 | 3,27% | 21 | 11,17% | 18 | 10,53% | 21 | 12,28% |
Wheeler (1935) | 20 | 3,11% | 15 | 7,98% | 15 | 8,77% | 15 | 8,77% |
Guillermet (2009) | 18 | 2,8% | 18 | 9,57% | 16 | 9,36% | 18 | 10,53% |
Jourdan & Mille (2006) | 17 | 2,64% | 15 | 7,98% | 15 | 8,77% | 15 | 8,77% |
Guillermet (2009) | 15 | 2,33% | 14 | 7,45% | 14 | 8,19% | 14 | 8,19% |
Guillermet (2006) | 14 | 2,18% | 12 | 6,38% | 10 | 5,85% | 12 | 7,02% |
Meurgey (2011) | 13 | 2,02% | 10 | 5,32% | 10 | 5,85% | 10 | 5,85% |
Wilson & Taylor (1967) | 13 | 2,02% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Bangy et al. (2009) | 12 | 1,87% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Franco et al. (2019) | 12 | 1,87% | 11 | 5,85% | 11 | 6,43% | 11 | 6,43% |
Perrault (1988) | 12 | 1,87% | 12 | 6,38% | 12 | 7,02% | 12 | 7,02% |
Ramage et al. (2023) | 12 | 1,87% | 12 | 6,38% | 12 | 7,02% | 12 | 7,02% |
Ramage (2014) | 12 | 1,87% | 12 | 6,38% | 12 | 7,02% | 12 | 7,02% |
Wheeler (1932) | 12 | 1,87% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Jaffe & Lattke (1994) | 11 | 1,71% | 11 | 5,85% | 11 | 6,43% | 11 | 6,43% |
Morrison (1997) | 11 | 1,71% | 11 | 5,85% | 11 | 6,43% | 11 | 6,43% |
Parnaudeau et al. (2013) | 11 | 1,71% | 11 | 5,85% | 9 | 5,26% | 11 | 6,43% |
Questel (2020) | 11 | 1,71% | 10 | 5,32% | 10 | 5,85% | 9 | 5,26% |
Salata & Fisher (2022) | 11 | 1,71% | 6 | 3,19% | 6 | 3,51% | 6 | 3,51% |
Yassin et al. (2012) | 11 | 1,71% | 11 | 5,85% | 11 | 6,43% | 11 | 6,43% |
Blard et al. (2003) | 10 | 1,56% | 10 | 5,32% | 10 | 5,85% | 10 | 5,85% |
David et al. (2014) | 10 | 1,56% | 10 | 5,32% | 10 | 5,85% | 10 | 5,85% |
Galkowski (2016) | 10 | 1,56% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Jennings et al. (2013) | 10 | 1,56% | 10 | 5,32% | 10 | 5,85% | 10 | 5,85% |
Madl (2014) | 10 | 1,56% | 10 | 5,32% | 6 | 3,51% | 10 | 5,85% |
Morrison (1996) | 10 | 1,56% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Nicolas (2023) | 10 | 1,56% | 8 | 4,26% | 6 | 3,51% | 8 | 4,68% |
Ramage (2024) | 10 | 1,56% | 10 | 5,32% | 9 | 5,26% | 10 | 5,85% |
Taylor (1987) | 10 | 1,56% | 10 | 5,32% | 10 | 5,85% | 10 | 5,85% |
Wheeler (1932) | 10 | 1,56% | 7 | 3,72% | 7 | 4,09% | 7 | 4,09% |
Cheesman (1928) | 9 | 1,4% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Clarke (1971) | 9 | 1,4% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Fisher & Fong (2020) | 9 | 1,4% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Lebas et al. (2016) | 9 | 1,4% | 9 | 4,79% | 9 | 5,26% | 9 | 5,26% |
Linnaeus (1758) | 9 | 1,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1936) | 9 | 1,4% | 5 | 2,66% | 5 | 2,92% | 5 | 2,92% |
Guenée (1862) | 8 | 1,24% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Hamon (1953) | 8 | 1,24% | 4 | 2,13% | 4 | 2,34% | 4 | 2,34% |
Viette (1949) | 8 | 1,24% | 5 | 2,66% | 5 | 2,92% | 4 | 2,34% |
Wetterer (2002) | 8 | 1,24% | 8 | 4,26% | 8 | 4,68% | 8 | 4,68% |
Wilson & Hunt (1967) | 8 | 1,24% | 8 | 4,26% | 8 | 4,68% | 8 | 4,68% |
Blatrix et al. (2018) | 7 | 1,09% | 7 | 3,72% | 7 | 4,09% | 7 | 4,09% |
Bousses et al. (2013) | 7 | 1,09% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Lagarde (2008) | 7 | 1,09% | 4 | 2,13% | 4 | 2,34% | 4 | 2,34% |
Parnaudeau & Richoux (2010) | 7 | 1,09% | 7 | 3,72% | 7 | 4,09% | 7 | 4,09% |
Parnaudeau (2009) | 7 | 1,09% | 6 | 3,19% | 5 | 2,92% | 6 | 3,51% |
Questel & Le Quellec (2012) | 7 | 1,09% | 6 | 3,19% | 6 | 3,51% | 5 | 2,92% |
Wheeler (1933) | 7 | 1,09% | 5 | 2,66% | 5 | 2,92% | 5 | 2,92% |
Casevitz-Weulersse & Galkowski (2009) | 6 | 0,93% | 6 | 3,19% | 6 | 3,51% | 6 | 3,51% |
Duhamel (2018) | 6 | 0,93% | 4 | 2,13% | 4 | 2,34% | 4 | 2,34% |
Gutierrez (1981) | 6 | 0,93% | 5 | 2,66% | 5 | 2,92% | 5 | 2,92% |
Parnaudeau (2012) | 6 | 0,93% | 5 | 2,66% | 5 | 2,92% | 5 | 2,92% |
Perrault (1993) | 6 | 0,93% | 5 | 2,66% | 5 | 2,92% | 5 | 2,92% |
Rakotonirina & Fisher (2022) | 6 | 0,93% | 4 | 2,13% | 4 | 2,34% | 2 | 1,17% |
Wetterer (2012) | 6 | 0,93% | 6 | 3,19% | 6 | 3,51% | 6 | 3,51% |
Wetterer (2014) | 6 | 0,93% | 6 | 3,19% | 6 | 3,51% | 6 | 3,51% |
Wheeler (1908) | 6 | 0,93% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Aurivillius (1909) | 5 | 0,78% | 1 | 0,53% | 1 | 0,58% | 0 | 0% |
Brunhes (1977) | 5 | 0,78% | 4 | 2,13% | 4 | 2,34% | 4 | 2,34% |
Brunhes (1979) | 5 | 0,78% | 4 | 2,13% | 4 | 2,34% | 4 | 2,34% |
David & Tsacas (1975) | 5 | 0,78% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Fabricius (1775) | 5 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnaudeau (2016) | 5 | 0,78% | 4 | 2,13% | 4 | 2,34% | 4 | 2,34% |
Talaga et al. (2015) | 5 | 0,78% | 5 | 2,66% | 5 | 2,92% | 5 | 2,92% |
Wetterer (2012) | 5 | 0,78% | 5 | 2,66% | 5 | 2,92% | 5 | 2,92% |
Wetterer (2013) | 5 | 0,78% | 5 | 2,66% | 5 | 2,92% | 5 | 2,92% |
Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 4 | 0,62% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Bernard (1968) | 4 | 0,62% | 4 | 2,13% | 4 | 2,34% | 4 | 2,34% |
Boisduval (1833) | 4 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (2012) | 4 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Dognin (1908) | 4 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufay (1975) | 4 | 0,62% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Emery (1914) | 4 | 0,62% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Guenée (1852) | 4 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamon (1956) | 4 | 0,62% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Herbulot (1979) | 4 | 0,62% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Holloway (1979) | 4 | 0,62% | 3 | 1,6% | 3 | 1,75% | 2 | 1,17% |
Jourdan (2020) | 4 | 0,62% | 4 | 2,13% | 4 | 2,34% | 3 | 1,75% |
Kohl (1909) | 4 | 0,62% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Ortiz-Sepulveda et al. (2019) | 4 | 0,62% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Rageau (1958) | 4 | 0,62% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Russell et al. (2021) | 4 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Vayssières et al. (2001) | 4 | 0,62% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Benoist (1950) | 3 | 0,47% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Bippus (2017) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Bippus (2019) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Carpenter & Madl (2009) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
de Toulgoët (1979) | 3 | 0,47% | 2 | 1,06% | 1 | 0,58% | 2 | 1,17% |
[Denis & Schiffermüller] (1775) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2007) | 3 | 0,47% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Evenhuis (2018) | 3 | 0,47% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Fischer & Fisher (2013) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy (2000) | 3 | 0,47% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Hamon (1954) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Jarrige (1968) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Kimmins (1960) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Lafranchis (2014) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Lafranchis (2016) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Leraut (2012) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Millière (1864-1868) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulian (1998) | 3 | 0,47% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Reinert et al. (2004) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Román-Palacios et al. (2020) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Sudre & Parnaudeau (2016) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Touroult et al. (2018) | 3 | 0,47% | 3 | 1,6% | 3 | 1,75% | 3 | 1,75% |
Ward et al. (2015) | 3 | 0,47% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Yokoyama (2013) | 3 | 0,47% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Allen et al. (2022) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Bagny et al. (2009) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Bell et al. (1989) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Bippus (2016) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Bolton (2007) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Borowiec (2016) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Brunhes & Boussès (2009) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Cohic (1950) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Cramer ([1779]) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer ([1780]-1782) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Dadant & Etienne (1973) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Dejean (1825) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Dörfel & Ohl (2022) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Drury ([1770-1773]) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel (2020) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Emery (1894) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Esper ([1796-1805]) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1781) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1867) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste & Hervé (2009) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Geoffroy (1762) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilbert & Casevitz-Weulersse (1997) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Hery et al. (2020) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugel (2014) | 2 | 0,31% | 2 | 1,06% | 0 | 0% | 2 | 1,17% |
Hustache (1920) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Jerdon (1851) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Kóbor (2023) | 2 | 0,31% | 1 | 0,53% | 0 | 0% | 1 | 0,58% |
Kruger (2001) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Le Goff et al. (2013) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Le Maitre & Chadee (1983) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Léong et al. (2003) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Leraut (1997) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Madl & van Achterberg (2014) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Malloch (1932) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Mann (1921) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Marie & Bossin (2013) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Masner (1960) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Mathis & Zatwarnicki (2003) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Meyrick (1934) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Minard et al. (2015) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1860) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Munroe (1956) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Ohm & Hölzel (1998) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Parnaudeau (2017) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Pauly et al. (2001) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Perroud & Montrouzier (1864) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Poisson (1956) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Rakotonirina et al. (2017) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Régnart et al. (2022) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Richard (1977) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Robineau-desvoidy (1827) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (2018) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Sardet et al. (2015) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 1 | 0,58% |
Senevet (1937) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Sudre & Vitali (2021) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Talaga et al. (2015) | 2 | 0,31% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Tavakilian & Chevillotte (2013) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Theobald (1913) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Tsacas & Chassagnard (1999) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Turlin (2002) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 1 | 0,58% |
Wetterer et al. (2012) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1923) | 2 | 0,31% | 2 | 1,06% | 2 | 1,17% | 2 | 1,17% |
Albouy et al. (2017) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Anonyme (2018) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Ascete (2021) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Balmès & Mouttet (2019) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Barbut et al. (2006) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Baroni Urbani & De Andrade (2007) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Belkin et al. (1965) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellmann (2019) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Bergroth (1893) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Bippus (2020) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% | |
Blair (1934) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Blair (1934) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Burla (1954) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1884) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot & Rioux (1965) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Célini et al. (2020) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Cerkowniak et al. (2017) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Cerkowniak et al. (2020) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Cetre-sosah et al. (2023) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Clarke (1986) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Cochereau (1966) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Cohic (1959) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1959) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Colindre (2021) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Collet & Pérennec (2012) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Couteyen (2021) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dahlbom (1843-1845) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalla Torre (1893) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Damoiseau (1966) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Day (1974) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Deknuydt et al. (2016) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 0 | 0% |
Delabie et al. (2011) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Delatte et al. (2008) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Delaunay et al. (2000) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Delaunay et al. (2009) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Delobel & Guttierrez (1981) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 0 | 0% |
Demergès & Grandmaire (2014) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Denux & Zagatti (2010) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Derozier (2016) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Dewynter et al. (2022) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Distant (1920) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Ditter et al. (2023) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Duda (1940) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Edwards (1933) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Elissa & Karch (2005) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Emery (1892) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1895) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Esper (1776-1779) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2012) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Evenhuis (2012) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Fabricius (1794) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1805) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1849) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Fairmaire (1850) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Fairmaire (1896) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1862) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1903) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernandez-Triana et al. (2020) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Ferragu (1979) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Forel (1881) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Forel (1899) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Fourcroy (1785) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1927) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1928) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Galman et al. (2011) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Gasnier et al. (2015) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Geer (1774) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Georges et al. (2024) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Girod (2004) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Godart (1822-[1824]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy et al. (2016) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Grote (1873) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1852) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2012) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Hammes & Putoa (1986) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Häuser & Boppre (1997) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hava & Poussereau (2017) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Hava (2006) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Háva (2014) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Hayashi (1961) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Heller (1916) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1982) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway & Peters (1976) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Honey & Scoble (2001) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Huang et al. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1790) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1818) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugel (2007) | 1 | 0,16% | 1 | 0,53% | 0 | 0% | 1 | 0,58% |
Jack (1985) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Kremmer et al. (2017) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Kumar et al. (1988) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Lacomme (2013) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Lamb (1914) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Lang (1789) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1802) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoir et al. (2023) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Leponce et al. (2019) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Lucas (1872) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Madl (2016) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Maes (2014) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1933) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Marks (1951) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Martin (1964) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Mathis (1993) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Mayr (1886) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Medlock et al. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Menezes et al. (2005) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Menezes et al. (2006) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Moravec (2008) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Nève de Mévergnies et al. (2024) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Nibouche et al. (202X) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Olmi et al. (2019) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Pagenstecher (1907) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Palisot & Beauvois (1805-1821) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Patrick & Patrick (2012) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Paulian (1957) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Peck et al. (2014) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Petagna (1786) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre & Lalanne-Cassou | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Pierre (1992) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Rageau (1956) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Rakotonirina & Fisher (2014) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Robinson & Nielsen (1983) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1920) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1928) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Sattler & Tremewan (1973) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Saunders (1851) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1892) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1823) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Schaffner & Karch (2000) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Scholte & Schaffner (2007) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulthess et al. (1907) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2003) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Seifert (2022) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Siddaiah & Kujur (2016) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Sircoulomb (2013) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Siroux (2010) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Skuse (1895) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1857) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1860) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Sudre et al. (2010) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Taylor & Wilson (1961) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Tennent (2005) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Touroult et al. (2021) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Tsacas & Chassagnard (1988) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Tsacas et al. (1988) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Vane-Wright & De Jong (2003) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Viette (1950) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Viette (1979) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Villers (1789) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Voisin et al. (2017) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Wetterer & Sharaf (2017) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Williams & Henning (2023) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Younes et al. (2021) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Zeller (1847) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 1 | 0,58% |
Zhang et al. (2023) | 1 | 0,16% | 1 | 0,53% | 1 | 0,58% | 0 | 0% |