Insectes de Wallis-et-Futuna
459 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) | 123 | 15,39% | 117 | 53,18% | 114 | 54,81% | 117 | 55,98% |
Jourdan & Mille (2006) | 80 | 10,01% | 70 | 31,82% | 69 | 33,17% | 69 | 33,01% |
Gutierrez (1981) | 67 | 8,39% | 56 | 25,45% | 55 | 26,44% | 54 | 25,84% |
Meurgey & Ramage (2020) | 56 | 7,01% | 55 | 25% | 54 | 25,96% | 54 | 25,84% |
Matile-Ferrero & Etienne (2006) | 48 | 6,01% | 47 | 21,36% | 47 | 22,6% | 47 | 22,49% |
Meurgey (2011) | 47 | 5,88% | 45 | 20,45% | 44 | 21,15% | 45 | 21,53% |
Wheeler (1935) | 39 | 4,88% | 22 | 10% | 22 | 10,58% | 22 | 10,53% |
Grand et al. (2014) | 37 | 4,63% | 37 | 16,82% | 37 | 17,79% | 32 | 15,31% |
Cohic (1959) | 34 | 4,26% | 22 | 10% | 21 | 10,1% | 22 | 10,53% |
Wilson & Hunt (1967) | 32 | 4,01% | 29 | 13,18% | 29 | 13,94% | 29 | 13,88% |
Wetterer (2002) | 31 | 3,88% | 26 | 11,82% | 26 | 12,5% | 26 | 12,44% |
Ramage (2014) | 30 | 3,75% | 29 | 13,18% | 29 | 13,94% | 29 | 13,88% |
Wilson & Taylor (1967) | 30 | 3,75% | 21 | 9,55% | 21 | 10,1% | 21 | 10,05% |
Perrault (1988) | 29 | 3,63% | 27 | 12,27% | 27 | 12,98% | 27 | 12,92% |
Jennings et al. (2013) | 28 | 3,5% | 27 | 12,27% | 27 | 12,98% | 26 | 12,44% |
Mille et al. (2016) | 28 | 3,5% | 28 | 12,73% | 28 | 13,46% | 28 | 13,4% |
Taylor (1987) | 25 | 3,13% | 25 | 11,36% | 25 | 12,02% | 25 | 11,96% |
Morrison (1996) | 24 | 3% | 19 | 8,64% | 19 | 9,13% | 19 | 9,09% |
Questel (2020) | 23 | 2,88% | 22 | 10% | 22 | 10,58% | 21 | 10,05% |
Grand et al. (2019) | 21 | 2,63% | 21 | 9,55% | 21 | 10,1% | 21 | 10,05% |
Clastrier & Delécolle (1996) | 20 | 2,5% | 20 | 9,09% | 20 | 9,62% | 20 | 9,57% |
Heller (1916) | 20 | 2,5% | 10 | 4,55% | 10 | 4,81% | 10 | 4,78% |
Morrison (1997) | 20 | 2,5% | 16 | 7,27% | 16 | 7,69% | 16 | 7,66% |
Poussereau et al. (2018) | 20 | 2,5% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Remillet (1988) | 20 | 2,5% | 18 | 8,18% | 18 | 8,65% | 17 | 8,13% |
Wheeler (1932) | 20 | 2,5% | 12 | 5,45% | 12 | 5,77% | 12 | 5,74% |
Cohic (1950) | 19 | 2,38% | 17 | 7,73% | 17 | 8,17% | 17 | 8,13% |
Wheeler (1936) | 19 | 2,38% | 8 | 3,64% | 8 | 3,85% | 8 | 3,83% |
Emery (1914) | 18 | 2,25% | 9 | 4,09% | 9 | 4,33% | 9 | 4,31% |
Evenhuis (2018) | 18 | 2,25% | 15 | 6,82% | 14 | 6,73% | 15 | 7,18% |
Germain et al. (2014) | 18 | 2,25% | 18 | 8,18% | 18 | 8,65% | 18 | 8,61% |
Rageau (1958) | 18 | 2,25% | 14 | 6,36% | 12 | 5,77% | 12 | 5,74% |
Cheesman (1928) | 17 | 2,13% | 17 | 7,73% | 17 | 8,17% | 17 | 8,13% |
Jourdan (2020) | 17 | 2,13% | 17 | 7,73% | 16 | 7,69% | 15 | 7,18% |
Paulian (1998) | 17 | 2,13% | 15 | 6,82% | 13 | 6,25% | 15 | 7,18% |
Cochereau (1966) | 16 | 2% | 15 | 6,82% | 15 | 7,21% | 15 | 7,18% |
Foldi & Germain (2018) | 16 | 2% | 16 | 7,27% | 16 | 7,69% | 16 | 7,66% |
Jaffe & Lattke (1994) | 16 | 2% | 16 | 7,27% | 16 | 7,69% | 16 | 7,66% |
Questel & Le Quellec (2012) | 16 | 2% | 15 | 6,82% | 14 | 6,73% | 14 | 6,7% |
Clarke (1971) | 15 | 1,88% | 12 | 5,45% | 12 | 5,77% | 10 | 4,78% |
Germain (2007) | 15 | 1,88% | 15 | 6,82% | 15 | 7,21% | 15 | 7,18% |
Marinov et al. (2021) | 15 | 1,88% | 15 | 6,82% | 14 | 6,73% | 14 | 6,7% |
Fauvel (1867) | 14 | 1,75% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Wheeler (1932) | 14 | 1,75% | 8 | 3,64% | 8 | 3,85% | 8 | 3,83% |
Viette (1949) | 13 | 1,63% | 8 | 3,64% | 7 | 3,37% | 8 | 3,83% |
Viette (1950) | 13 | 1,63% | 4 | 1,82% | 3 | 1,44% | 4 | 1,91% |
Blard et al. (2003) | 12 | 1,5% | 12 | 5,45% | 12 | 5,77% | 12 | 5,74% |
Cochereau (1974) | 12 | 1,5% | 12 | 5,45% | 12 | 5,77% | 12 | 5,74% |
Linnaeus (1758) | 12 | 1,5% | 3 | 1,36% | 3 | 1,44% | 2 | 0,96% |
Martiré & Rochat (2008) | 12 | 1,5% | 8 | 3,64% | 8 | 3,85% | 7 | 3,35% |
Ramage et al. (2023) | 12 | 1,5% | 12 | 5,45% | 12 | 5,77% | 12 | 5,74% |
Galkowski (2016) | 11 | 1,38% | 11 | 5% | 11 | 5,29% | 11 | 5,26% |
Wheeler (1933) | 11 | 1,38% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Etienne (2005) | 10 | 1,25% | 10 | 4,55% | 10 | 4,81% | 10 | 4,78% |
Franco et al. (2019) | 10 | 1,25% | 10 | 4,55% | 10 | 4,81% | 10 | 4,78% |
Lebas et al. (2016) | 10 | 1,25% | 10 | 4,55% | 10 | 4,81% | 10 | 4,78% |
Montrouzier (1861) | 10 | 1,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Vayssières et al. (2001) | 10 | 1,25% | 8 | 3,64% | 8 | 3,85% | 8 | 3,83% |
Cochereau (1966) | 9 | 1,13% | 8 | 3,64% | 8 | 3,85% | 8 | 3,83% |
Etienne & Vilardebó (1978) | 9 | 1,13% | 9 | 4,09% | 9 | 4,33% | 9 | 4,31% |
Papazian et al. (2007) | 9 | 1,13% | 9 | 4,09% | 7 | 3,37% | 9 | 4,31% |
Patrick & Policard (2015) | 9 | 1,13% | 6 | 2,73% | 3 | 1,44% | 6 | 2,87% |
Cheesman (1927) | 8 | 1% | 8 | 3,64% | 8 | 3,85% | 8 | 3,83% |
Gomy (2000) | 8 | 1% | 6 | 2,73% | 6 | 2,88% | 6 | 2,87% |
Marinov et al. (2019) | 8 | 1% | 8 | 3,64% | 8 | 3,85% | 8 | 3,83% |
Nattier et al. (2015) | 8 | 1% | 8 | 3,64% | 8 | 3,85% | 8 | 3,83% |
Anonyme (2018) | 7 | 0,88% | 7 | 3,18% | 7 | 3,37% | 7 | 3,35% |
Borkent & Wirth (1997) | 7 | 0,88% | 7 | 3,18% | 7 | 3,37% | 7 | 3,35% |
Hammes & Putoa (1986) | 7 | 0,88% | 7 | 3,18% | 7 | 3,37% | 7 | 3,35% |
Peck (2011) | 7 | 0,88% | 6 | 2,73% | 6 | 2,88% | 6 | 2,87% |
Perrault (1993) | 7 | 0,88% | 6 | 2,73% | 6 | 2,88% | 6 | 2,87% |
Blatrix et al. (2018) | 6 | 0,75% | 6 | 2,73% | 6 | 2,88% | 6 | 2,87% |
Casevitz-Weulersse & Galkowski (2009) | 6 | 0,75% | 6 | 2,73% | 6 | 2,88% | 6 | 2,87% |
Ceccolini (2023) | 6 | 0,75% | 6 | 2,73% | 6 | 2,88% | 6 | 2,87% |
Distant (1914) | 6 | 0,75% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Fauvel (1903) | 6 | 0,75% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Fauvel (1904) | 6 | 0,75% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Holloway (1979) | 6 | 0,75% | 4 | 1,82% | 3 | 1,44% | 4 | 1,91% |
Matile-Ferrero & Williams (2015) | 6 | 0,75% | 6 | 2,73% | 6 | 2,88% | 6 | 2,87% |
Montrouzier (1860) | 6 | 0,75% | 0 | 0% | 0 | 0% | 0 | 0% |
Peck et al. (2014) | 6 | 0,75% | 6 | 2,73% | 6 | 2,88% | 6 | 2,87% |
Reid et al. (2021) | 6 | 0,75% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Wheeler (1908) | 6 | 0,75% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Aberlenc et al. (2004) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Bonfils (1969) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Garrouste & Hervé (2009) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Holloway & Peters (1976) | 5 | 0,63% | 3 | 1,36% | 3 | 1,44% | 2 | 0,96% |
Kuschel (2008) | 5 | 0,63% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Matile-Ferrero (1979) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Needham (1932) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Peck (2016) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Ramage et al. (2015) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Vueti (2001) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Wetterer (2012) | 5 | 0,63% | 5 | 2,27% | 5 | 2,4% | 5 | 2,39% |
Allen et al. (2022) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Beenen (2008) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 4 | 0,5% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Bolton (2012) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer & Rivault (2003) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Carpenter (2023) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Couteyen & Papazian (2012) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Damoiseau (1966) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Duyck et al. (2022) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Evenhuis (2007) | 4 | 0,5% | 2 | 0,91% | 1 | 0,48% | 2 | 0,96% |
Fauvel (1891) | 4 | 0,5% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Fauvel (1903) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher & Fong (2020) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Gomy (2016) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 2 | 0,96% |
Guenée (1862) | 4 | 0,5% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Guilbert & Casevitz-Weulersse (1997) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Guillermet (2009) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Guillermet (2009) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuhlmann (2006) | 4 | 0,5% | 4 | 1,82% | 3 | 1,44% | 4 | 1,91% |
Legros et al. (2017) | 4 | 0,5% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Leroy et al. (2021) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Lieftinck (1975) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Marie & Bossin (2013) | 4 | 0,5% | 2 | 0,91% | 1 | 0,48% | 2 | 0,96% |
Marinov et al. (2016) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Marinov (2021) | 4 | 0,5% | 4 | 1,82% | 0 | 0% | 4 | 1,91% |
Mayr (1870) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Meurgey & Picard (2011) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Mille et al. (2020) | 4 | 0,5% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Montrouzier (1861) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 4 | 0,5% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Parnaudeau (2012) | 4 | 0,5% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Reinert et al. (2004) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Ris (1915) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Schouteden (1907) | 4 | 0,5% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Talaga et al. (2015) | 4 | 0,5% | 4 | 1,82% | 4 | 1,92% | 4 | 1,91% |
Van Zwaluwenburg (1932) | 4 | 0,5% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Wenzel (1955) | 4 | 0,5% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Albouy et al. (2017) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 2 | 0,96% |
Arrow (1927) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Bangy et al. (2009) | 3 | 0,38% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Bernard (1968) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Bigot (1992) | 3 | 0,38% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bippus (2019) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Boisduval (1833) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulard (1996) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Brauer (1865) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunhes & Boussès (2009) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 2 | 0,96% |
Dadant & Etienne (1973) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Donisthorpe (1932) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne et al. (2015) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Fairmaire (1849) | 3 | 0,38% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Fauvel (1862) | 3 | 0,38% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Guillermet (2004) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Gusenleitner (2011) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Hebard (1933) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Hustache (1920) | 3 | 0,38% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Jourdan et al. (2014) | 3 | 0,38% | 3 | 1,36% | 2 | 0,96% | 3 | 1,44% |
Kormilev (1971) | 3 | 0,38% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Lagarde (2008) | 3 | 0,38% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Le Maitre & Chadee (1983) | 3 | 0,38% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Lenfant & Marro (1997) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Lieftinck (1966) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Liu (2021) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Lowe et al. (2007) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Lucas (2012) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Nève de Mévergnies et al. (2024) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Nicolas (2012) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Patrick & Patrick (2012) | 3 | 0,38% | 2 | 0,91% | 1 | 0,48% | 2 | 0,96% |
Raspi et al. (2007) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Rheinheimer (2012) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Rheinheimer (2014) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Salata & Fisher (2022) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Soldati et al. (2012) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 3 | 1,44% |
Van Zwaluwenburg (1959) | 3 | 0,38% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Vane-Wright & De Jong (2003) | 3 | 0,38% | 3 | 1,36% | 3 | 1,44% | 2 | 0,96% |
Ward et al. (2015) | 3 | 0,38% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Zimmerman (1936) | 3 | 0,38% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Baroni Urbani & De Andrade (2007) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Beenen (2013) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Bielawski (1973) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Borth & Kons (2022) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Bournier & Mound (2000) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Bournier (2000) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Bousses et al. (2013) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bradley (1953) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Breuning (1970) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Chazeau (1978) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Clarke (1986) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Cockerell (1893) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Cockerell (1895) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Colijn et al. (2020) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Collenette (1934) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Cramer ([1780]-1782) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Distant (1920) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Dognin (1908) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Duay et al. (2014) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Fabricius (1775) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1850) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Fauvel (1883) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1903) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Fennah (1958) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Fennah (1969) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Ferriere (1929) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Fleutiaux (1891) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Galliard (1927) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy et al. (2009) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Gros (2020) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Guillermet (2006) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Guillermet (2011) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Gusenleitner & Madl (2011) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Hamon (1953) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartmann et al. (2021) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Hery et al. (2020) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoddle et al. (2008) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Jelinek & Lason (2018) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Jerdon (1851) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (2015) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Lallemand (1942) | 2 | 0,25% | 2 | 0,91% | 0 | 0% | 2 | 0,96% |
Le Breton et al. (2005) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Leponce et al. (2019) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Lupoli & Abadie (2015) | 2 | 0,25% | 2 | 0,91% | 1 | 0,48% | 1 | 0,48% |
Marshall (1921) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Martiré (2010) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Mary (2017) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Mesnil (1968) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Meurgey & Dumbardon-Martial (2015) | 2 | 0,25% | 2 | 0,91% | 1 | 0,48% | 1 | 0,48% |
Meurgey (2014) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 0 | 0% |
Meyrick (1934) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Montrouzier (1858) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Nibouche et al. (202X) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Nicolas et al. (2015) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Olivier (1791-[1792]) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Panis (1969) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Perroud & Montrouzier (1864) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2023) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Rageau (1956) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Rageau (1959) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Ramage & Gourvès (2017) | 2 | 0,25% | 2 | 0,91% | 1 | 0,48% | 1 | 0,48% |
Remaudière & Etienne (1988) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Rheinheimer (2015) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Robineau-desvoidy (1827) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulthess (1915) | 2 | 0,25% | 1 | 0,45% | 0 | 0% | 1 | 0,48% |
Séguy (1944) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Seifert (2022) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Senevet (1937) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Short (2010) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Sicart & Ruffie (1960) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Smith (1857) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Talaga et al. (2015) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Taylor & Wilson (1961) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Theobald (1913) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Toledo (2010) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Tomaszewska (2010) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Touroult et al. (2018) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Tronquet (2014) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Van Zwaluwenburg (1932) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Viette (1950) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Wang (2003) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Yokoyama (2013) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Zilli et al. (2017) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Zimmerman (1943) | 2 | 0,25% | 2 | 0,91% | 2 | 0,96% | 2 | 0,96% |
Zimmerman (1964) | 2 | 0,25% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Albouy & Richard (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Azam (1893) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagny et al. (2009) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Balachowsky (1958) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Balfour-Browne (1945) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Barbut et al. (2006) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Beggs et al. (2011) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Belkin et al. (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellifa et al. (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bellmann (2019) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Biondi et al. (2013) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bippus (2019) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Blair (1934) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Blair (1934) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Blanchot (1992) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Blancou et al. (1987) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Blight et al. (2023) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Boheman (1858-1859) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (2000) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bonfils et al. (1994) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bouget et al. (2019) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Bousquet (2016) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyd et al. (2006) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Boyer de Fonscolombe (1834) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Brindle (1975) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Brindle (1976) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Brun & Chazeau (1986) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Brunhes (1977) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunhes (1979) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Burr (1914) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Callot & Rioux (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Carl (1915) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter & Madl (2009) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Carpenter (1996) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Célini et al. (2020) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Chapelin-Viscardi & Lariviere (2014) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Chopard (1924) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Chown & Convey (2016) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Chûjô (1961) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1959) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre (2016) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Colindre (2021) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Collet & Pérennec (2012) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Conte et al. (2007) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Couteyen (2009) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Cramer ([1777]) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalla Torre (1893) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1773) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Delabie & Blard (2002) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
[Denis & Schiffermüller] (1775) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Denoyes et al. (1986) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Denux & Zagatti (2010) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Devaud & Lebouvier (2019) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Dewynter et al. (2022) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Donskoff (1988) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois (1996) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Duhamel (2018) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Edwards (1933) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Emery (1869) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Emery (1892) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1893) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1897) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Englund & Polhemus (2010) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Etienne et al. (2018) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Evenhuis (2011) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Evenhuis (2012) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Evenhuis (2012) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Fabres (1977) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Fabricius (1787) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1805) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1905) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer (2015) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Ferris (1935) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Fisher (1950) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1881) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Forel (1886) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1901) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Forel (1907) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Friese (1907) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1928) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1824) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy (1981) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Groom et al. (2016) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Guenée (1852) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamon (1956) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Harman (1999) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Hebard (1933) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Hebard (1935) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Heiss (2011) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1933) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Hinckley (1963) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Hindermeyer et al. (2007) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Hübner (1796-[1828]) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
ICZN (1954) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2013) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Jouveau et al. (2018) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Kaltenbach (1968) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Karny (1925) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Kaszab (1982) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Khaliq et al. (1996) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Kirejtshuk (2008) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Kormilev (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Kozar & Benedicty (2003) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Kreiter et al. (2022) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Kuschel (1998) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Lackner & Leschen (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Lafranchis (2014) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Lafranchis (2016) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Latreille (1802) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Goff et al. (2013) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Leavengood et al. (2024) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Lenoir et al. (2023) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Linnaeus (1761) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Lower (1900) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Macfie (1933) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Macfie (1933) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Malausa & Ehanno (1988) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1932) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Marchal et al. (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Marks (1951) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Maskell (1893) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Mayr (1862) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Mayr (1866) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Mayr (1886) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazur & Węgrzynowicz (2008) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Meganck et al. (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Meurgey & Questel (2015) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Meyrick (1912-1916) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1916-1923) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Meyrick (1919) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Mille et al. (2007) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Minot (2016) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Montrouzier (1855) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Nakata (1961) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Orhant (2002) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Parnaudeau & Madl (2009) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Parnaudeau (2009) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Parnaudeau (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Peck (2011) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Perrault (1979) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Pierre & Lalanne-Cassou | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Pierre et al. (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Ponel & Roge (2000) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Transactions of the Entomological Society of London, 76: 453-468.">Poulton & Riley (1929) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Jelínek, J. & Audisio, P. 2011. A new species of Amystrops Reitter, 1875, and an updated checklist of the Nitidulidae from Réunion Island (Coleoptera). Bulletin de la Société entomologique de France, 116(4): 421-428. ">Poussereau et al. (2011) |
1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Princis (1974) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Questel (2022) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Quilici et al. (1988) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Ramage (2024) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Rehn (1948) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Rehn (1949) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Reverté et al. (2023) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Rivault et al. (1991) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Roger (1859) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1863) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Roth & Rivault (2002) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Rowe (1978) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Russell & Etienne (1985) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Sadlier et al. (2012) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Samways (2003) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Santschi (1928) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Saunders (1851) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1823) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Schönherr (1806) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert et al. (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Seifert (2003) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Shinonaga et al. (1991) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Siroux (2015) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Smith (1858) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Smith (1860) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Tamaki et al. (1973) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Thompson (1938) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Turner (1919) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Vachal (1907) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Vaillant (2000) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Van Zwaluwenburg (1940) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Vantaux et al. (2010) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Vayssières et al. (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Viette (1950) | 1 | 0,13% | 1 | 0,45% | 0 | 0% | 1 | 0,48% |
Viette (1994) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Villers (1789) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Voisin et al. (2017) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Walker (1859) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1923) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Williams (1932) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Winstanley (1983) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Yamane et al. (1996) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Younes et al. (2021) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 1 | 0,48% |
Zakardjian et al. (2020) | 1 | 0,13% | 1 | 0,45% | 1 | 0,48% | 0 | 0% |
Zakardjian et al. (2023) | 1 | 0,13% | 1 | 0,45% | 0 | 0% | 1 | 0,48% |
Zimmerman (1936) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |