Lépidoptères de Guadeloupe
Lepidoptera de Guadeloupe
272 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Meurgey & Ramage (2020) | 450 | 47,32% | 444 | 79,71% | 387 | 79,3% | 435 | 88,59% |
Meurgey (2011) | 249 | 26,18% | 192 | 34,47% | 153 | 31,35% | 183 | 37,27% |
Deknuydt et al. (2016) | 163 | 17,14% | 156 | 28,01% | 154 | 31,56% | 150 | 30,55% |
Questel (2020) | 128 | 13,46% | 110 | 19,75% | 96 | 19,67% | 103 | 20,98% |
Questel (2016) | 73 | 7,68% | 64 | 11,49% | 57 | 11,68% | 62 | 12,63% |
UICN Comité français, OFB & MNHN (2021) | 70 | 7,36% | 66 | 11,85% | 66 | 13,52% | 26 | 5,3% |
Questel & Le Quellec (2012) | 65 | 6,83% | 51 | 9,16% | 42 | 8,61% | 47 | 9,57% |
Dewynter et al. (2022) | 54 | 5,68% | 53 | 9,52% | 53 | 10,86% | 19 | 3,87% |
Guenée (1852) | 48 | 5,05% | 5 | 0,9% | 5 | 1,02% | 5 | 1,02% |
Munroe (1956) | 48 | 5,05% | 32 | 5,75% | 28 | 5,74% | 32 | 6,52% |
Martiré & Rochat (2008) | 40 | 4,21% | 31 | 5,57% | 31 | 6,35% | 30 | 6,11% |
Yokoyama (2013) | 34 | 3,58% | 27 | 4,85% | 24 | 4,92% | 24 | 4,89% |
Pierre & Lalanne-Cassou | 30 | 3,15% | 24 | 4,31% | 17 | 3,48% | 13 | 2,65% |
Sculfort & Dewynter (2024) | 28 | 2,94% | 28 | 5,03% | 8 | 1,64% | 28 | 5,7% |
Remillet (1988) | 27 | 2,84% | 23 | 4,13% | 23 | 4,71% | 17 | 3,46% |
Chovet et al. (2023) | 24 | 2,52% | 21 | 3,77% | 7 | 1,43% | 16 | 3,26% |
Bigot & Etienne (2009) | 22 | 2,31% | 20 | 3,59% | 20 | 4,1% | 20 | 4,07% |
Heppner (1995) | 20 | 2,1% | 11 | 1,97% | 11 | 2,25% | 11 | 2,24% |
Linnaeus (1758) | 19 | 2% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1854) | 17 | 1,79% | 4 | 0,72% | 4 | 0,82% | 4 | 0,81% |
Cramer ([1777]) | 16 | 1,68% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2009) | 15 | 1,58% | 14 | 2,51% | 14 | 2,87% | 14 | 2,85% |
Guillermet (2011) | 15 | 1,58% | 14 | 2,51% | 14 | 2,87% | 14 | 2,85% |
Möschler (1890) | 15 | 1,58% | 6 | 1,08% | 6 | 1,23% | 5 | 1,02% |
Scoble et al. (1999) | 14 | 1,47% | 8 | 1,44% | 7 | 1,43% | 6 | 1,22% |
Dumbardon-Martial & Delblond (2019) | 12 | 1,26% | 10 | 1,8% | 8 | 1,64% | 3 | 0,61% |
Touroult et al. (2023) | 12 | 1,26% | 11 | 1,97% | 10 | 2,05% | 11 | 2,24% |
Barbut & Lalanne-Cassou (2009) | 11 | 1,16% | 10 | 1,8% | 10 | 2,05% | 10 | 2,04% |
Guillermet (2004) | 11 | 1,16% | 7 | 1,26% | 7 | 1,43% | 4 | 0,81% |
Jourdan et al. (2023) | 11 | 1,16% | 11 | 1,97% | 11 | 2,25% | 11 | 2,24% |
Guenée (1852) | 10 | 1,05% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Haxaire & Rasplus (1986) | 10 | 1,05% | 9 | 1,62% | 9 | 1,84% | 8 | 1,63% |
Herbulot (1986) | 10 | 1,05% | 10 | 1,8% | 10 | 2,05% | 10 | 2,04% |
Anonyme (2018) | 9 | 0,95% | 8 | 1,44% | 8 | 1,64% | 8 | 1,63% |
Guenée (1852) | 9 | 0,95% | 5 | 0,9% | 5 | 1,02% | 5 | 1,02% |
Guillermet (2009) | 9 | 0,95% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Boisduval & Guénée ([1874]) | 8 | 0,84% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Cook & Scoble (1995) | 8 | 0,84% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Cramer ([1780]-1782) | 8 | 0,84% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 8 | 0,84% | 0 | 0% | 0 | 0% | 0 | 0% |
Haxaire & Rasplus (1987) | 8 | 0,84% | 7 | 1,26% | 7 | 1,43% | 7 | 1,43% |
Lalanne-Cassou & le Duchat d'Aubigny (1992) | 8 | 0,84% | 6 | 1,08% | 6 | 1,23% | 4 | 0,81% |
Lévêque (2015) | 8 | 0,84% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Li et al. (2019) | 8 | 0,84% | 6 | 1,08% | 5 | 1,02% | 5 | 1,02% |
Ramage (2017) | 8 | 0,84% | 7 | 1,26% | 7 | 1,43% | 6 | 1,22% |
Viette (1949) | 8 | 0,84% | 4 | 0,72% | 4 | 0,82% | 4 | 0,81% |
Zagatti et al. (2006) | 8 | 0,84% | 8 | 1,44% | 1 | 0,2% | 8 | 1,63% |
Barbut et al. (2006) | 7 | 0,74% | 7 | 1,26% | 7 | 1,43% | 7 | 1,43% |
Clarke (1971) | 7 | 0,74% | 7 | 1,26% | 7 | 1,43% | 7 | 1,43% |
Cramer ([1779]) | 7 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Deknuydt et al. (2018) | 7 | 0,74% | 6 | 1,08% | 6 | 1,23% | 5 | 1,02% |
Jourdan & Mille (2006) | 7 | 0,74% | 6 | 1,08% | 6 | 1,23% | 6 | 1,22% |
Lacomme (2013) | 7 | 0,74% | 7 | 1,26% | 7 | 1,43% | 3 | 0,61% |
Poole (1989) | 7 | 0,74% | 7 | 1,26% | 7 | 1,43% | 7 | 1,43% |
Brévignon (2020) | 6 | 0,63% | 5 | 0,9% | 1 | 0,2% | 4 | 0,81% |
Garrouste & Hervé (2009) | 6 | 0,63% | 6 | 1,08% | 6 | 1,23% | 6 | 1,22% |
Guenée (1862) | 6 | 0,63% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Jourdan (2020) | 6 | 0,63% | 5 | 0,9% | 5 | 1,02% | 4 | 0,81% |
Chalumeau & Benito-Espinal (1984) | 5 | 0,53% | 3 | 0,54% | 0 | 0% | 3 | 0,61% |
David & Lucas (2017) | 5 | 0,53% | 5 | 0,9% | 5 | 1,02% | 5 | 1,02% |
Gemmell et al. (2014) | 5 | 0,53% | 5 | 0,9% | 4 | 0,82% | 1 | 0,2% |
Kitching et al. (2018) | 5 | 0,53% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Olivier (1792) | 5 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Pitkin (2002) | 5 | 0,53% | 4 | 0,72% | 3 | 0,61% | 3 | 0,61% |
Thiaucourt (2003) | 5 | 0,53% | 5 | 0,9% | 5 | 1,02% | 5 | 1,02% |
Touroult et al. (2021) | 5 | 0,53% | 5 | 0,9% | 3 | 0,61% | 5 | 1,02% |
Walker (1865-[1866]) | 5 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot & Drouet (2014) | 4 | 0,42% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Brévignon (2004) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
[Denis & Schiffermüller] (1775) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Dognin (1908) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1775) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée ([1858]) | 4 | 0,42% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Herbulot (1995) | 4 | 0,42% | 4 | 0,72% | 2 | 0,41% | 4 | 0,81% |
Holloway (1979) | 4 | 0,42% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Parnaudeau (2012) | 4 | 0,42% | 4 | 0,72% | 4 | 0,82% | 4 | 0,81% |
Periasamy et al. (2015) | 4 | 0,42% | 4 | 0,72% | 4 | 0,82% | 4 | 0,81% |
Poole (1989) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Austin & Dombroskie (2020) | 3 | 0,32% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Barbut & Lalanne-Cassou (2019) | 3 | 0,32% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Barbut (2022) | 3 | 0,32% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Bigot (2011) | 3 | 0,32% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Bippus (2019) | 3 | 0,32% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Boisduval (1833) | 3 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1836) | 3 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 3 | 0,32% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Gielis (2011) | 3 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Hayden et al. (2017) | 3 | 0,32% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Hemming (1958) | 3 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Laguerre (2022) | 3 | 0,32% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Leraut (1997) | 3 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2014) | 3 | 0,32% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Meyrick (1934) | 3 | 0,32% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Munroe (1959) | 3 | 0,32% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Questel (2023) | 3 | 0,32% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Rambur (1834) | 3 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2021) | 3 | 0,32% | 3 | 0,54% | 2 | 0,41% | 3 | 0,61% |
Vayssières et al. (2001) | 3 | 0,32% | 3 | 0,54% | 3 | 0,61% | 3 | 0,61% |
Vincent & Laguerre (2017) | 3 | 0,32% | 3 | 0,54% | 0 | 0% | 3 | 0,61% |
Vincent (2008) | 3 | 0,32% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Barbut & Lalanne-cassou (2014) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Barnes et al. (1913) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Becker (2002) | 2 | 0,21% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Boisduval (1833) | 2 | 0,21% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
. Mauritius (H. Plaideau). 46 pp. ">Bojer (1956) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Brévignon & Brévignon (2012) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 0 | 0% |
Brévignon (2000) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Brévignon (2003) | 2 | 0,21% | 2 | 0,36% | 0 | 0% | 2 | 0,41% |
Brito et al. (2017) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Brown (1929) | 2 | 0,21% | 1 | 0,18% | 0 | 0% | 1 | 0,2% |
Clarke (1986) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Cramer (1775) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer ([1775-1776]) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Davis & Prins (2011) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Dognin (1911) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Dognin (1914) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Eitschberger (2006) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Esper & Charpentier (1778-[1804]) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Faynel (2010) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 1 | 0,2% |
Gemmell & Marcus (2015) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 0 | 0% |
Gielis (2013) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Guérin-Méneville & Perrotet (1842) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2006) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Gutierrez (1981) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 1 | 0,2% |
Heppner (1982) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Herbulot (1985) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Hübner ([1825-1831]) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2018) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Lafranchis (2014) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 1 | 0,2% |
Lafranchis (2016) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 1 | 0,2% |
Laguerre et al. (2014) | 2 | 0,21% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Lalanne-cassou & Pogue (2003) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Latreille & Godart (1819-[1824]) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1988) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Lévêque (2009) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Meyrick (1886) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Naydenov et al. (2020) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Naydenov et al. (2021) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Núñez et al. (2021) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 1 | 0,2% |
Parnaudeau (2009) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Pitkin (1993) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Poey (1832) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Pogue (2013) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Rambur (1829) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramel et al. (2009) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Schaffer & Solis (1995) | 2 | 0,21% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Schaus (1905) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Touroult et al. (2019) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Touroult et al. (2020) | 2 | 0,21% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Vane-Wright & De Jong (2003) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 0 | 0% |
Viette (1950) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 0 | 0% |
Yano (1963) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Zimmermann et al. (2005) | 2 | 0,21% | 2 | 0,36% | 2 | 0,41% | 2 | 0,41% |
Abbayes (1931) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Arenberger (2010) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Aurivillius (1909) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Bar (1875) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut & Lalanne-Cassou (2010) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Barbut & Voisin (2014) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Betz (1980) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Bigot (1992) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Bippus (2020) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Boisduval & Leconte (1829-1833) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1859) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1870) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgogne (1983) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Braby et al. (2015) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Brévignon (2001) | 1 | 0,11% | 1 | 0,18% | 0 | 0% | 1 | 0,2% |
Brévignon (2001) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Brevignon (2002) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1875) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1878) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1893) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chainey (2005) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cock (2017) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1950) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Cohic (1959) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Comstock (1943) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Curtis (1823-1840) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
David et al. (2010) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Dillon (1947) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois (1996) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Dumbardon-Martial et al. (2018) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Dyar (1914) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Eppo (2018) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Eppo (2018) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Eppo (2019) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Fabricius ([1777]) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Felder & Rogenhofer (1864-1867) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Fitch (1856) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fougère et al. (2020) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Fruhstorfer (1916) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain et al. (2014) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Geyer & Frölich (1830) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Geyer (1837) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Godart (1822-[1824]) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier & Grenier (2014) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Guilding (1827) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Hall (1917) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hampson (1898) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Haworth (1803-1828) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hazir et al. (2001) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Hemming (1933) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1937) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Henriot (1933) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1981) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (2016) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hewitson (1867) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hindermeyer et al. (2007) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Holloway & Peters (1976) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Honey & Scoble (2001) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner et al. (3) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner [1819-1826] | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1823) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
ICZN (1954) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lafontaine & Schmidt (2010) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Lamas (2004) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Lathy (1904) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2005) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Linnaeus (1763) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1764) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1771) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1852) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mally et al. (2019) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Matthews et al. (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ménétriès (1832) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Munroe (1942) | 1 | 0,11% | 1 | 0,18% | 0 | 0% | 1 | 0,2% |
Nel & Varenne (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Nibouche et al. (202X) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Nicolas (2023) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Orhant (2002) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Pallister (1956) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Patrick & Patrick (2012) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Poey (1851-1854) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Prins et al. (2019) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Prout (1916) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Prout (1932-1938) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Ramage (2024) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Robinson & Nielsen (1983) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rogenhofer (1882) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rutherford & Auguste (2018) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Scoble (1994) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Scudder (1872) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Sculfort & Dewynter (2024) | 1 | 0,11% | 1 | 0,18% | 0 | 0% | 1 | 0,2% |
Skinner (1891) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Stainton (1856) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Stefanescu et al. (2012) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Tennent (2005) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Thiaucourt (2016) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Touroult et al. (2015) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Touroult et al. (2016) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Touroult et al. (2022) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Touroult et al. (2024) | 1 | 0,11% | 1 | 0,18% | 0 | 0% | 1 | 0,2% |
Turlin (2002) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Viette (1994) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 0 | 0% |
Voisin (1975) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Walker (1854) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |
Walker (1860) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1864) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Warren (1906) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Warren (1907) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (1937) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Weller et al. (2004) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Zeller (1852) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang et al. (2021) | 1 | 0,11% | 1 | 0,18% | 1 | 0,2% | 1 | 0,2% |