Insectes de Saint-Barthélemy
728 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Questel (2020) | 411 | 29,34% | 379 | 73,74% | 356 | 75,11% | 373 | 78,36% |
Meurgey & Ramage (2020) | 325 | 23,2% | 314 | 61,09% | 288 | 60,76% | 307 | 64,5% |
Meurgey (2011) | 275 | 19,63% | 192 | 37,35% | 173 | 36,5% | 186 | 39,08% |
Questel & Le Quellec (2012) | 192 | 13,7% | 162 | 31,52% | 149 | 31,43% | 158 | 33,19% |
Peck (2011) | 186 | 13,28% | 161 | 31,32% | 156 | 32,91% | 161 | 33,82% |
Peck (2011) | 117 | 8,35% | 103 | 20,04% | 100 | 21,1% | 103 | 21,64% |
Questel (2016) | 111 | 7,92% | 101 | 19,65% | 92 | 19,41% | 99 | 20,8% |
Peck et al. (2014) | 83 | 5,92% | 71 | 13,81% | 71 | 14,98% | 69 | 14,5% |
UICN Comité français, OFB & MNHN (2021) | 57 | 4,07% | 54 | 10,51% | 54 | 11,39% | 29 | 6,09% |
Yokoyama (2013) | 56 | 4% | 48 | 9,34% | 45 | 9,49% | 46 | 9,66% |
Colijn et al. (2020) | 55 | 3,93% | 51 | 9,92% | 51 | 10,76% | 47 | 9,87% |
Ramage (2017) | 55 | 3,93% | 53 | 10,31% | 52 | 10,97% | 51 | 10,71% |
Deknuydt et al. (2016) | 51 | 3,64% | 49 | 9,53% | 49 | 10,34% | 48 | 10,08% |
Matile-Ferrero & Etienne (2006) | 51 | 3,64% | 48 | 9,34% | 44 | 9,28% | 48 | 10,08% |
Peck (2016) | 49 | 3,5% | 47 | 9,14% | 47 | 9,92% | 47 | 9,87% |
Jourdan & Mille (2006) | 41 | 2,93% | 37 | 7,2% | 36 | 7,59% | 35 | 7,35% |
Chalumeau & Touroult (2005) | 40 | 2,86% | 33 | 6,42% | 29 | 6,12% | 33 | 6,93% |
Meurgey & Picard (2011) | 40 | 2,86% | 36 | 7% | 36 | 7,59% | 36 | 7,56% |
Soldati & Touroult (2014) | 38 | 2,71% | 36 | 7% | 36 | 7,59% | 36 | 7,56% |
Remillet (1988) | 37 | 2,64% | 33 | 6,42% | 33 | 6,96% | 27 | 5,67% |
Dewynter et al. (2022) | 33 | 2,36% | 32 | 6,23% | 32 | 6,75% | 12 | 2,52% |
Linnaeus (1758) | 28 | 2% | 3 | 0,58% | 3 | 0,63% | 2 | 0,42% |
Bonfils (1969) | 23 | 1,64% | 15 | 2,92% | 15 | 3,16% | 15 | 3,15% |
Streito et al. (2007) | 23 | 1,64% | 23 | 4,47% | 23 | 4,85% | 23 | 4,83% |
Chovet et al. (2023) | 22 | 1,57% | 19 | 3,7% | 6 | 1,27% | 15 | 3,15% |
Guenée (1852) | 21 | 1,5% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ramage et al. (2023) | 21 | 1,5% | 21 | 4,09% | 20 | 4,22% | 20 | 4,2% |
Jaffe & Lattke (1994) | 19 | 1,36% | 19 | 3,7% | 18 | 3,8% | 18 | 3,78% |
Pierre & Lalanne-Cassou | 19 | 1,36% | 16 | 3,11% | 14 | 2,95% | 7 | 1,47% |
Shpeley et al. (2017) | 19 | 1,36% | 17 | 3,31% | 17 | 3,59% | 17 | 3,57% |
Martiré & Rochat (2008) | 18 | 1,28% | 10 | 1,95% | 10 | 2,11% | 9 | 1,89% |
Sculfort & Dewynter (2024) | 18 | 1,28% | 18 | 3,5% | 5 | 1,05% | 18 | 3,78% |
Franco et al. (2019) | 17 | 1,21% | 17 | 3,31% | 17 | 3,59% | 15 | 3,15% |
Meurgey (2014) | 17 | 1,21% | 17 | 3,31% | 17 | 3,59% | 15 | 3,15% |
Brindle (1971) | 16 | 1,14% | 12 | 2,33% | 12 | 2,53% | 12 | 2,52% |
Chassain & Touroult (2012) | 16 | 1,14% | 11 | 2,14% | 11 | 2,32% | 11 | 2,31% |
Meurgey & Dumbardon-Martial (2019) | 16 | 1,14% | 16 | 3,11% | 16 | 3,38% | 16 | 3,36% |
Poussereau et al. (2018) | 16 | 1,14% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Wheeler (1935) | 16 | 1,14% | 10 | 1,95% | 10 | 2,11% | 10 | 2,1% |
Galkowski (2016) | 15 | 1,07% | 15 | 2,92% | 14 | 2,95% | 14 | 2,94% |
Etienne (2005) | 14 | 1% | 14 | 2,72% | 14 | 2,95% | 14 | 2,94% |
Jourdan (2020) | 14 | 1% | 14 | 2,72% | 14 | 2,95% | 12 | 2,52% |
Lucas (2012) | 14 | 1% | 14 | 2,72% | 14 | 2,95% | 14 | 2,94% |
Dumbardon-Martial & Delblond (2019) | 13 | 0,93% | 10 | 1,95% | 8 | 1,69% | 5 | 1,05% |
Fabricius (1775) | 13 | 0,93% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutierrez (1981) | 13 | 0,93% | 11 | 2,14% | 11 | 2,32% | 10 | 2,1% |
Lupoli (2023) | 13 | 0,93% | 13 | 2,53% | 13 | 2,74% | 13 | 2,73% |
Nicolas (2012) | 13 | 0,93% | 13 | 2,53% | 13 | 2,74% | 13 | 2,73% |
Fleutiaux & Sallé ([1890]) | 12 | 0,86% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Jennings et al. (2013) | 12 | 0,86% | 12 | 2,33% | 12 | 2,53% | 11 | 2,31% |
Anonyme (2018) | 11 | 0,79% | 10 | 1,95% | 10 | 2,11% | 9 | 1,89% |
Guillermet (2004) | 11 | 0,79% | 7 | 1,36% | 7 | 1,48% | 4 | 0,84% |
Rageau (1958) | 11 | 0,79% | 10 | 1,95% | 8 | 1,69% | 10 | 2,1% |
Touroult et al. (2018) | 11 | 0,79% | 11 | 2,14% | 11 | 2,32% | 10 | 2,1% |
Vayssières et al. (2001) | 11 | 0,79% | 10 | 1,95% | 10 | 2,11% | 10 | 2,1% |
Wilson & Taylor (1967) | 11 | 0,79% | 8 | 1,56% | 8 | 1,69% | 8 | 1,68% |
Garrouste & Hervé (2009) | 10 | 0,71% | 10 | 1,95% | 10 | 2,11% | 10 | 2,1% |
Meurgey & Questel (2015) | 10 | 0,71% | 10 | 1,95% | 10 | 2,11% | 9 | 1,89% |
Questel (2023) | 10 | 0,71% | 10 | 1,95% | 10 | 2,11% | 10 | 2,1% |
Ramage (2014) | 10 | 0,71% | 10 | 1,95% | 10 | 2,11% | 10 | 2,1% |
Cheesman (1928) | 9 | 0,64% | 9 | 1,75% | 9 | 1,9% | 9 | 1,89% |
Matile-Ferrero et al. (2000) | 9 | 0,64% | 9 | 1,75% | 9 | 1,9% | 9 | 1,89% |
Paulian (1998) | 9 | 0,64% | 8 | 1,56% | 7 | 1,48% | 8 | 1,68% |
Perrault (1988) | 9 | 0,64% | 9 | 1,75% | 9 | 1,9% | 9 | 1,89% |
Taylor (1987) | 9 | 0,64% | 9 | 1,75% | 9 | 1,9% | 9 | 1,89% |
Wheeler (1932) | 9 | 0,64% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Bonfils (1969) | 8 | 0,57% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Cochereau (1966) | 8 | 0,57% | 8 | 1,56% | 8 | 1,69% | 8 | 1,68% |
Heller (1916) | 8 | 0,57% | 5 | 0,97% | 5 | 1,05% | 4 | 0,84% |
Meurgey & Dumbardon-Martial (2015) | 8 | 0,57% | 8 | 1,56% | 7 | 1,48% | 7 | 1,47% |
Mille et al. (2016) | 8 | 0,57% | 8 | 1,56% | 8 | 1,69% | 7 | 1,47% |
Morrison (1997) | 8 | 0,57% | 8 | 1,56% | 8 | 1,69% | 8 | 1,68% |
Touroult (2005) | 8 | 0,57% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 7 | 0,5% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Bottimer (1968) | 7 | 0,5% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Cheesman (1927) | 7 | 0,5% | 7 | 1,36% | 7 | 1,48% | 7 | 1,47% |
Cochereau (1974) | 7 | 0,5% | 7 | 1,36% | 7 | 1,48% | 7 | 1,47% |
Germain et al. (2014) | 7 | 0,5% | 7 | 1,36% | 7 | 1,48% | 7 | 1,47% |
Gomy (2000) | 7 | 0,5% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Guillermet (2009) | 7 | 0,5% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Lebas et al. (2016) | 7 | 0,5% | 7 | 1,36% | 7 | 1,48% | 7 | 1,47% |
Lethierry (1881) | 7 | 0,5% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Morrison (1996) | 7 | 0,5% | 7 | 1,36% | 7 | 1,48% | 7 | 1,47% |
Touroult et al. (2019) | 7 | 0,5% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Tronquet (2014) | 7 | 0,5% | 7 | 1,36% | 7 | 1,48% | 7 | 1,47% |
Villiers (1980) | 7 | 0,5% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Wheeler (1936) | 7 | 0,5% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Blard et al. (2003) | 6 | 0,43% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Boyer & Rivault (2003) | 6 | 0,43% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Brévignon (2020) | 6 | 0,43% | 4 | 0,78% | 3 | 0,63% | 3 | 0,63% |
Ceccolini (2023) | 6 | 0,43% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Cramer ([1777]) | 6 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1914) | 6 | 0,43% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Etienne & Martinez (2003) | 6 | 0,43% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Hart & Ivie (2016) | 6 | 0,43% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Jourdan (2021) | 6 | 0,43% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Munroe (1956) | 6 | 0,43% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Rheinheimer (2014) | 6 | 0,43% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Rioux et al. (1986) | 6 | 0,43% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Scheffrahn et al. (2005) | 6 | 0,43% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Touroult (2012) | 6 | 0,43% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Wetterer (2002) | 6 | 0,43% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Wheeler (1932) | 6 | 0,43% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Wheeler (1933) | 6 | 0,43% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Wilson & Hunt (1967) | 6 | 0,43% | 6 | 1,17% | 6 | 1,27% | 6 | 1,26% |
Zagatti et al. (2006) | 6 | 0,43% | 6 | 1,17% | 0 | 0% | 6 | 1,26% |
Barbut et al. (2006) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Blatrix et al. (2018) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Casevitz-Weulersse & Galkowski (2009) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Dheurle (2012) | 5 | 0,36% | 5 | 0,97% | 2 | 0,42% | 5 | 1,05% |
Dupuis & Perrin (2020) | 5 | 0,36% | 4 | 0,78% | 4 | 0,84% | 3 | 0,63% |
Fabricius (1792) | 5 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 5 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
Gemmell et al. (2014) | 5 | 0,36% | 5 | 0,97% | 4 | 0,84% | 1 | 0,21% |
Guillermet (2009) | 5 | 0,36% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Hielkema & Hielkema (2019) | 5 | 0,36% | 4 | 0,78% | 3 | 0,63% | 4 | 0,84% |
IUCN (2013) | 5 | 0,36% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Lacomme (2013) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 3 | 0,63% |
Leavengood et al. (2024) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Marquet & Roguet (2003) | 5 | 0,36% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Nieser (1969) | 5 | 0,36% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Perrault (1993) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Rheinheimer (2012) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Touroult et al. (2015) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 4 | 0,84% |
Viette (1949) | 5 | 0,36% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Villiers (1979) | 5 | 0,36% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Wetterer (2012) | 5 | 0,36% | 5 | 0,97% | 5 | 1,05% | 5 | 1,05% |
Barbut & Lalanne-Cassou (2009) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Bigot & Etienne (2009) | 4 | 0,29% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Bolton (2012) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonadona (1981) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Bousquet et al. (2018) | 4 | 0,29% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Brévignon (2004) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter (2023) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Célini et al. (2013) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Chalumeau & Touroult (2004) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalumeau (1983) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Clarke (1971) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Cohic (1959) | 4 | 0,29% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Constantin (2012) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Cramer ([1780]-1782) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
de Kort-Gommers & Nieser (1969) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Dumbardon-martial et al. (2023) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Erwin (1991) | 4 | 0,29% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Evenhuis (2018) | 4 | 0,29% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Fabricius (1798) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1903) | 4 | 0,29% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Foldi & Germain (2018) | 4 | 0,29% | 3 | 0,58% | 3 | 0,63% | 2 | 0,42% |
Germain (2007) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 3 | 0,63% |
Guenée (1862) | 4 | 0,29% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Guillermet (2011) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Hartmann et al. (2021) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Haxaire & Rasplus (1986) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 3 | 0,63% |
Hebard (1933) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Jourdan et al. (2023) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Legros et al. (2017) | 4 | 0,29% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Lemaire (2017) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Linnaeus (1767) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Michel et al. (2008) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Mille et al. (2020) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Möschler (1890) | 4 | 0,29% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Nibouche et al. (202X) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 3 | 0,63% |
Pierre et al. (2017) | 4 | 0,29% | 3 | 0,58% | 3 | 0,63% | 2 | 0,42% |
Rageau (1959) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Remaudière & Etienne (1988) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Spinola (1841) | 4 | 0,29% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Talaga et al. (2015) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Touroult et al. (2020) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 4 | 0,84% |
Touroult et al. (2021) | 4 | 0,29% | 4 | 0,78% | 3 | 0,63% | 4 | 0,84% |
Touroult et al. (2021) | 4 | 0,29% | 4 | 0,78% | 3 | 0,63% | 4 | 0,84% |
Touroult et al. (2023) | 4 | 0,29% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Wetterer (2020) | 4 | 0,29% | 4 | 0,78% | 4 | 0,84% | 0 | 0% |
Wheeler (1908) | 4 | 0,29% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Albouy et al. (2017) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 2 | 0,42% |
Arrow (1927) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Bellmann (2019) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 2 | 0,42% |
Bernard (1968) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Boisduval (1833) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer & Rivault (2006) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Chassain & Sautière (2007) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Cordeiro & Moreira (2015) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
David & Lucas (2017) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Dejean (1825) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
[Denis & Schiffermüller] (1775) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Denux & Zagatti (2010) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
dos Santos et al. (2021) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Dumbardon-martial et al. (2024) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Etienne et al. (2018) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Fabricius (1787) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1903) | 3 | 0,21% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Girón & Franz (2012) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Gonzales et al. (2014) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Grand et al. (2014) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Guenée (1852) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Guenée (1852) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Hayden et al. (2017) | 3 | 0,21% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ivie & Geiser (2014) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Keller & Branham (2021) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Keller (2022) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Konstantinov et al. (2022) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Kuhlmann (2006) | 3 | 0,21% | 3 | 0,58% | 2 | 0,42% | 3 | 0,63% |
Lagarde (2008) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Le Maitre & Chadee (1983) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Leponce et al. (2019) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Leraut (2014) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Li et al. (2019) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Mantilleri (2014) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Meurgey & Daigle (2007) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Meurgey et al. (2015) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Meyrick (1934) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Minot (2016) | 3 | 0,21% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Mirouse (1958) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore et al. (2018) | 3 | 0,21% | 3 | 0,58% | 2 | 0,42% | 3 | 0,63% |
Nattier et al. (2015) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Olivier (1792) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnaudeau (2017) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Ponchel (2011) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 2 | 0,42% |
Princis (1974) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Ramage et al. (2015) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Ratcliffe & Cave (2015) | 3 | 0,21% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Roth & Rivault (2002) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Russell & Etienne (1985) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Salata & Fisher (2022) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Scheffrahn & Křeček (2001) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Schoenherr (1836) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Segarra-carmona et al. (2020) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Talaga et al. (2015) | 3 | 0,21% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Tavakilian & Chevillotte (2013) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 1 | 0,21% |
Thompson (1981) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Touroult et al. (2016) | 3 | 0,21% | 3 | 0,58% | 3 | 0,63% | 3 | 0,63% |
Ardoin (1977) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Azam (1893) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Balazuc & Chalumeau (1978) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ball & Shpeley (2009) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Balthasar (1966) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bangy et al. (2009) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Becker (2002) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Bigot & Drouet (2014) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Bigot (2011) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Bippus (2019) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Blackwelder (1943) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Boisduval & Guénée ([1874]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1833) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Botero et al. (2020) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouget et al. (2019) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Bousquet (2012) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousses et al. (2013) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Brévignon & Brévignon (2012) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 0 | 0% |
Brévignon (2000) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Broadhead (1989) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Brullé (1846) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bur (1907) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Cabrera-asencio et al. (2008) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Cadena-castañeda (2014) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Cassola (2011) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 1 | 0,21% |
Célini et al. (2020) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Chalumeau & Benito-Espinal (1984) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalumeau & Touroult (2004) | 2 | 0,14% | 2 | 0,39% | 0 | 0% | 2 | 0,42% |
Chazeau et al. (1974) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Chazeau (1978) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Chevrolat (1879) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Chopard (1924) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Couteyen & Papazian (2012) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Cramer ([1775-1776]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer ([1779]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1773) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Desutter-Grandcolas & Bland (2003) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Dobson (1954) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Dognin (1908) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-Martial & Pierre (2020) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Dumbardon-martial (2015) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Dyar & Knab (1906) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Ensaf et al. (2004) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Esper & Charpentier (1778-[1804]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne & Vilardebó (1978) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Evenhuis (2007) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ezzat (1958) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Fabricius (1781) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1801) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1867) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Faynel (2010) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 1 | 0,21% |
Fisher & Fong (2020) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Gemmell & Marcus (2015) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 0 | 0% |
Germain (2013) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Gielis (2011) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gielis (2013) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilmour (1963) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy et al. (2016) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Grand et al. (2019) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Gros (2020) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Guenée (1854) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Guilbert & Casevitz-Weulersse (1997) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Gusenleitner (2011) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Hammes & Putoa (1986) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Hamon (1953) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Haxaire & Rasplus (1987) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Hebard (1933) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Heidemann & Seidenbusch (2002) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Hery et al. (2020) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner ([1825-1831]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2018) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Jerdon (1851) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2014) | 2 | 0,14% | 2 | 0,39% | 1 | 0,21% | 2 | 0,42% |
Kaydan & Gullan (2012) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Kingsolver (1970) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Klyver (1932) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Labat (2023) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Lafranchis (2014) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 1 | 0,21% |
Lafranchis (2016) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 1 | 0,21% |
Latreille & Godart (1819-[1824]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Breton et al. (2005) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Lemaire (2014) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Lupoli & Dusoulier (2015) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Marie & Bossin (2013) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Martiré (2010) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Mary (2017) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Matile-Ferrero & Etienne (1996) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Matile-Ferrero & Etienne (1998) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Matile-Ferrero & Williams (2015) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Mengual et al. (2009) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1886) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mifsud et al. (2010) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Mikkola & Honey (1993) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mollot et al. (2016) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Montrouzier (1860) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Nève de Mévergnies et al. (2024) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Nicolas et al. (2015) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Olivier (1791-[1792]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Otte (1979) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Packauskas (2010) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Parnaudeau (2012) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Perez-Gelabert & Floriano (2016) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Pierre & Dumbardon-Martial (2016) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Pinto et al. (2020) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Zoosystema, 42(7) : 105-114.">Pocco & Cigliano (2020) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Pogue (2013) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Poole (1989) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Prudhomme (2022) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Rageau (1956) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ramage et al. (2018) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Rambur (1829) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Rivault et al. (1991) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Robineau-desvoidy (1827) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell (1965) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Sardet et al. (2015) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Schönherr (1806) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Schouteden (1907) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Senevet (1937) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Sinev (1993) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Stål (1875) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Taquet et al. (2019) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Touroult et al. (2022) | 2 | 0,14% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Uicn et al. (2020) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Vachal (1907) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 1 | 0,21% |
Van Duzee (1937) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Vane-Wright & De Jong (2003) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 0 | 0% |
Viette (1950) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 0 | 0% |
Villiers (1980) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Vivallo (2019) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Voisin (2020) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Votýpka et al. (2020) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Walker (1865-[1866]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Walsingham (1897) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1923) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 1 | 0,21% |
Yano (1963) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Zimmermann et al. (2005) | 2 | 0,14% | 2 | 0,39% | 2 | 0,42% | 2 | 0,42% |
Abbayes (1931) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguesse & Gaillot (1969) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Aguilar-Velasco et al. (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Albuquerque et al. (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Allen et al. (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Alonso (2019) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Amyot & Audinet-Serville (1843) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Arenberger (2010) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ascete (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Aurivillius (1909) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Bagny et al. (2009) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Balhoff et al. (2013) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Barbut & Lalanne-Cassou (2005) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut & Voisin (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Bates (1878) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Beckers et al. (1989) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Belkin et al. (1965) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellifa et al. (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Bertrand (1949) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Betz (1980) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Bielawski (1973) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Blanchot (1992) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Blight et al. (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Boisduval & Leconte (1829-1833) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (2007) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bondar (1923) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Borowiec & Moragues (2005) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Bourgogne (1983) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Bout et al. (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Boyd et al. (2006) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Boyer & Rivault (2004) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Boyer & Rivault (2006) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Braby et al. (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brévignon (2001) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Brévignon (2001) | 1 | 0,07% | 1 | 0,19% | 0 | 0% | 1 | 0,21% |
Brevignon (2002) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brindle (1971) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brindle (1975) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Brindle (1976) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Brindle (1985) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Brunhes & Boussès (2009) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Brunhes (1977) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunhes (1979) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Burr (1904) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot & Rioux (1965) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Casey (1924) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Catil et al. (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Celini et al. (2012) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Célini et al. (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Célini et al. (2018) | 1 | 0,07% | 1 | 0,19% | 0 | 0% | 1 | 0,21% |
Celini (2013) | 1 | 0,07% | 1 | 0,19% | 0 | 0% | 1 | 0,21% |
Chalumeau (1982) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Chambers (1875) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapelin-Viscardi & Lariviere (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Chassain (2005) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Chevin (1986) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Chown & Convey (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Clarke (1986) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Clément (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Cobben (1960) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Cochard et al. (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Cochereau (1966) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Cock (2017) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1950) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Cohic (1959) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre & Derozier (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Colindre (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Colindre (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Comstock (1943) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Conjard et al. (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Constantin et al. (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Constantin (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Conte et al. (2007) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Couteyen & Papazian (2007) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Dahlbom (1843-1845) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalens & Touroult (2007) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Dalla Torre (1893) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Damoiseau (1966) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Darlington (1992) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Daumal (2013) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Dauphin (2003) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
David et al. (2010) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Davis (1986) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Denier (1922) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Desutter-Grandcolas et al. (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Devaud & Lebouvier (2019) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Dijkstra et al. (2015) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Distant (1914) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Doesburg (1968) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Dominique (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dommanget & Papazian (2000) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Doucet (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Dubois (1996) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Dubrony (1879) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufay (1975) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Duhamel (2018) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-Martial et al. (2018) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Dumbleton (1961) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Dupuis (1999) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Duquef (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Duquef (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Duquef (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Duranton (2004) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Edwards (1933) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Emery (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1900) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Eppo (2018) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Eppo (2018) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Etienne & Gagné (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Etienne & Martinez (2013) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Etienne & Matile-Ferrero (2008) | 1 | 0,07% | 1 | 0,19% | 0 | 0% | 1 | 0,21% |
Etienne et al. (1989) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Etienne et al. (1998) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Etienne (1978) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Evenhuis (2011) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Evenhuis (2011) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Evenhuis (2012) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Evenhuis (2012) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Fabricius ([1777]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1803) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1805) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fall (1910) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1906) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Felder & Rogenhofer (1864-1867) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Fernández et al. (2015) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Fisher & Bolton (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Fisher (1932) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcellini et al. (2012) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Forel (1881) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Forel (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1899) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Fouquet (2000) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
França et al. (2024) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Frenot et al. (2005) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Friese (1907) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1927) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1928) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste (2015) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Geoffroy (1762) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Geyer (1837) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Giannoulis et al. (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Girod & Matzke (2020) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Giron et al. (2018) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Godart (1822-[1824]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gonzalez & Vetrovec (2021) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Goudey-Perriere et al. (1988) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Goudey-Perriere (1991) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Goux (1937) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Grand & Boudot (2007) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Grand et al. (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Grange et al. (2010) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier & Grenier (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Groom et al. (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Guenée ([1858]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Guérin-méneville (1857) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilding (1827) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Gusenleitner & Madl (2011) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Hamon (1956) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Háva (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Hebard (1921) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hebard (1935) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Hedlund et al. (2020) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Hemming (1933) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Henriot (1933) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1981) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1982) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1995) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Herbst ([1791]-1792) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hewitson (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hindermeyer et al. (2007) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Holloway & Peters (1976) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Holloway (1979) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Honey & Scoble (2001) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner et al. (3) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner [1819-1826] | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hustache (1920) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
ICZN (1954) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ivie & Hart (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirby (1890) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kozár (2004) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Kreiter et al. (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Kurahashi & Fauran (1980) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Lachaud et al. (2012) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Lamas (2004) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Lambret & Deschamps (2013) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Landry et al. (2013) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lathy (1904) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1802) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Divelec (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Le Goff et al. (2013) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Lebard & Claude (2024) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Lebard & Hauser (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Leng & Mutchler (1916) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoir et al. (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Leonard (1968) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Lepesme (1943) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1997) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesne (1901) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lieftinck (1966) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Lieftinck (1975) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Linnaeus (1761) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1763) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1764) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1771) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
López-García & Deloya (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Lorenzo-Carballa et al. (2020) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli (2019) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Machet & Duquef (2004) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Madl & Ganeshan (2008) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Magis (2003) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Malausa (1977) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Malloch (1932) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Maquart et al. (2020) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Marinov et al. (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Marinov et al. (2019) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Marinov et al. (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Marks (1951) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Martins (1971) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Matthews et al. (2018) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1886) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1887) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meganck et al. (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ménétriès (1832) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mengual et al. (2008) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Meurgey (2004) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey (2014) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1855) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1858) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Morin (2000) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Motschulsky (1858) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Motta et al. (2018) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Moulin et al. (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Munroe (1959) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Muru et al. (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Naviaux (2007) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nel & Varenne (2019) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas et al. (2024) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Nicolas (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Nieser (1970) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Núñez et al. (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Olivier (1899) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Orhant (2002) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Otte et al. (1987) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Paola et al. (2010) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Papazian et al. (2007) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Parnaudeau & Madl (2009) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Parnaudeau (2009) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Patrick & Patrick (2012) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Paulian (1991) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Pauly et al. (2001) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pavon et al. (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Perez-gelabert & Thomas (2005) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Perrette & Spill (2008) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ponchel (2015) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 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 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Praz & Bénon (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Le Coléoptériste, 7(3): 3-39. [Une mise à jour 2011 a été obtenue auprès de l'auteur.]">Queney (2004) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Questel (2014) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Questel (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Quilici et al. (1988) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ramage et al. (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ramage (2015) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ramage (2024) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ratcliffe (1976) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Rehn (1949) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Reiche ([1843]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Reinert et al. (2004) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Reverté et al. (2023) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Rheinheimer (2015) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ris (1915) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Robinson & Nielsen (1983) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rochas et al. (2022) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rogard (2010) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rogenhofer (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rome (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Rozkosny (1983) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Sadlier et al. (2012) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Samways (2003) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Santos-Silva et al. (2010) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Santschi (1928) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1861) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1862) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sauvion et al. (1999) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Say (1823) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Schaffer & Solis (1995) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulthess (1915) | 1 | 0,07% | 1 | 0,19% | 0 | 0% | 1 | 0,21% |
Scoble et al. (1999) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Scudder (1872) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Scudder (1876) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sculfort & Dewynter (2024) | 1 | 0,07% | 1 | 0,19% | 0 | 0% | 1 | 0,21% |
Segarra-carmona et al. (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Seifert (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Selys Longchamps (1839) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seurat (1934) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Shinonaga et al. (1991) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Siroux (2010) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Siroux (2015) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Siroux (2018) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Sites et al. (2024) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Skinner (1891) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1857) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1860) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Soltani et al. (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Srivastava (2002) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Stefanescu et al. (2012) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Sudre et al. (2010) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Taylor & Wilson (1961) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Tennent (2005) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Theobald (1913) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Theodorides et al. (1983) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Thomas (2015) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Touroult et al. (2017) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Touroult et al. (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Touroult et al. (2024) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Townes (1950) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Tronquet (2016) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Turlin (2002) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Ueda (2020) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Vaillant (2000) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Vantaux et al. (2010) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Vardy (2000) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Viette (1994) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Villiers (1979) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Villiers (1980) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Vincent (2008) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Vitali & Touroult (2005) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Voisin (1975) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Vorst (2008) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1860) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Warren (1907) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (1937) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Weise (1885) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Weller et al. (2004) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Wenman (2012) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiedemann ([1820]-1821) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams (1932) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Willot & Wegnez (2024) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Wilson et al. (2010) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Yamane et al. (1996) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Yersin (1860) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zagatti & Guy (2005) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Zakardjian et al. (2020) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 0 | 0% |
Zakardjian et al. (2023) | 1 | 0,07% | 1 | 0,19% | 0 | 0% | 1 | 0,21% |
Zeller (1973) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang et al. (2021) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Zhang et al. (2022) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |
Zimmerman (1968) | 1 | 0,07% | 1 | 0,19% | 1 | 0,21% | 1 | 0,21% |