Lépidoptères de Nouvelle-Calédonie
Lepidoptera de Nouvelle-Calédonie
284 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Holloway (1979) | 533 | 39,66% | 426 | 54,69% | 383 | 55,75% | 420 | 59,91% |
Viette (1949) | 147 | 10,94% | 79 | 10,14% | 75 | 10,92% | 74 | 10,56% |
Clarke (1971) | 95 | 7,07% | 59 | 7,57% | 59 | 8,59% | 54 | 7,7% |
Martiré & Rochat (2008) | 94 | 6,99% | 66 | 8,47% | 64 | 9,32% | 61 | 8,7% |
Razowski (2014) | 91 | 6,77% | 91 | 11,68% | 91 | 13,25% | 91 | 12,98% |
Holloway & Peters (1976) | 76 | 5,65% | 58 | 7,45% | 31 | 4,51% | 49 | 6,99% |
Ramage (2017) | 70 | 5,21% | 61 | 7,83% | 59 | 8,59% | 58 | 8,27% |
Viette (1950) | 65 | 4,84% | 34 | 4,36% | 18 | 2,62% | 26 | 3,71% |
Jourdan & Mille (2006) | 58 | 4,32% | 49 | 6,29% | 49 | 7,13% | 48 | 6,85% |
Razowski (2013) | 57 | 4,24% | 57 | 7,32% | 57 | 8,3% | 57 | 8,13% |
Jourdan (2020) | 40 | 2,98% | 38 | 4,88% | 36 | 5,24% | 37 | 5,28% |
Guillermet (2009) | 36 | 2,68% | 18 | 2,31% | 18 | 2,62% | 18 | 2,57% |
Guillermet (2009) | 34 | 2,53% | 30 | 3,85% | 30 | 4,37% | 30 | 4,28% |
Guillermet (2011) | 24 | 1,79% | 24 | 3,08% | 24 | 3,49% | 24 | 3,42% |
Leraut (2014) | 23 | 1,71% | 23 | 2,95% | 23 | 3,35% | 23 | 3,28% |
Vane-Wright & De Jong (2003) | 23 | 1,71% | 22 | 2,82% | 21 | 3,06% | 5 | 0,71% |
Kaila (2017) | 22 | 1,64% | 22 | 2,82% | 22 | 3,2% | 22 | 3,14% |
Holloway (1977) | 21 | 1,56% | 18 | 2,31% | 15 | 2,18% | 15 | 2,14% |
Linnaeus (1758) | 20 | 1,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2004) | 18 | 1,34% | 18 | 2,31% | 18 | 2,62% | 12 | 1,71% |
Guenée (1862) | 17 | 1,26% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Meurgey & Ramage (2020) | 15 | 1,12% | 15 | 1,93% | 15 | 2,18% | 15 | 2,14% |
Boisduval (1833) | 12 | 0,89% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 12 | 0,89% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Orhant (2002) | 11 | 0,82% | 9 | 1,16% | 9 | 1,31% | 9 | 1,28% |
Robinson (1975) | 11 | 0,82% | 8 | 1,03% | 8 | 1,16% | 7 | 1% |
Viette (1950) | 11 | 0,82% | 7 | 0,9% | 7 | 1,02% | 6 | 0,86% |
Bigot & Drouet (2014) | 10 | 0,74% | 9 | 1,16% | 7 | 1,02% | 9 | 1,28% |
Collenette (1934) | 10 | 0,74% | 9 | 1,16% | 9 | 1,31% | 8 | 1,14% |
Gutierrez (1981) | 10 | 0,74% | 9 | 1,16% | 9 | 1,31% | 7 | 1% |
Parnaudeau (2012) | 10 | 0,74% | 9 | 1,16% | 9 | 1,31% | 8 | 1,14% |
Perroud & Montrouzier (1864) | 10 | 0,74% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Agassiz (2014) | 9 | 0,67% | 9 | 1,16% | 9 | 1,31% | 9 | 1,28% |
Fabricius (1775) | 9 | 0,67% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway & Miller (2003) | 9 | 0,67% | 9 | 1,16% | 7 | 1,02% | 7 | 1% |
Questel (2020) | 9 | 0,67% | 8 | 1,03% | 8 | 1,16% | 8 | 1,14% |
Vayssières et al. (2001) | 9 | 0,67% | 7 | 0,9% | 7 | 1,02% | 7 | 1% |
Viette (1949) | 9 | 0,67% | 6 | 0,77% | 6 | 0,87% | 6 | 0,86% |
Viette (1950) | 9 | 0,67% | 3 | 0,39% | 0 | 0% | 3 | 0,43% |
Adamski & Brown (2002) | 8 | 0,6% | 8 | 1,03% | 8 | 1,16% | 8 | 1,14% |
Bigot & Etienne (2009) | 8 | 0,6% | 6 | 0,77% | 6 | 0,87% | 6 | 0,86% |
Clarke (1986) | 8 | 0,6% | 7 | 0,9% | 7 | 1,02% | 7 | 1% |
Guillermet (2006) | 8 | 0,6% | 6 | 0,77% | 6 | 0,87% | 6 | 0,86% |
Kaila (2019) | 8 | 0,6% | 8 | 1,03% | 8 | 1,16% | 8 | 1,14% |
Patrick & Patrick (2012) | 8 | 0,6% | 7 | 0,9% | 6 | 0,87% | 4 | 0,57% |
Tennent (2005) | 8 | 0,6% | 8 | 1,03% | 8 | 1,16% | 6 | 0,86% |
Brun & Chazeau (1986) | 7 | 0,52% | 7 | 0,9% | 7 | 1,02% | 7 | 1% |
[Denis & Schiffermüller] (1775) | 7 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1997) | 7 | 0,52% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Meurgey (2011) | 7 | 0,52% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 7 | 0,52% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Meyrick (1934) | 7 | 0,52% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Scoble et al. (1999) | 7 | 0,52% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Cohic (1950) | 6 | 0,45% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Dugdale (2005) | 6 | 0,45% | 6 | 0,77% | 6 | 0,87% | 6 | 0,86% |
Felder & Rogenhofer (1864-1875) | 6 | 0,45% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Parnaudeau (2009) | 6 | 0,45% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Patrick & Policard (2015) | 6 | 0,45% | 3 | 0,39% | 2 | 0,29% | 1 | 0,14% |
Bigot (1992) | 5 | 0,37% | 5 | 0,64% | 4 | 0,58% | 5 | 0,71% |
Bippus (2016) | 5 | 0,37% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Bippus (2018) | 5 | 0,37% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Bippus (2019) | 5 | 0,37% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Cramer ([1777]) | 5 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Esper ([1796-1805]) | 5 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 5 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1852) | 5 | 0,37% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Nicolas (2023) | 5 | 0,37% | 4 | 0,51% | 4 | 0,58% | 3 | 0,43% |
Questel & Le Quellec (2012) | 5 | 0,37% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Questel (2016) | 5 | 0,37% | 5 | 0,64% | 5 | 0,73% | 5 | 0,71% |
Bippus (2020) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Bradley (1982) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Cramer ([1779]) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Dadant & Etienne (1973) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 3 | 0,43% |
Deknuydt et al. (2016) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Geoffroy (1762) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibbs (2010) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Heppner (1982) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Lafranchis (2014) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 2 | 0,29% |
Lafranchis (2016) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 2 | 0,29% |
Leroy et al. (2021) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Lopez-Vaamonde et al. (2010) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Meyrick (1910) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Minet (1985) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Periasamy et al. (2015) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Razowski (2012) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Tuck (1981) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Walker (1865-[1866]) | 4 | 0,3% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Zilli et al. (2017) | 4 | 0,3% | 4 | 0,51% | 4 | 0,58% | 4 | 0,57% |
Albouy et al. (2017) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Anonyme (2018) | 3 | 0,22% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Boisduval (1833) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1959) | 3 | 0,22% | 2 | 0,26% | 1 | 0,15% | 2 | 0,29% |
Transactions of the Entomological Society of London, 76: 469-487.">Collenette (1929) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Drury (1773) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Duponchel (1827-[1828]) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibbs & Lees (2014) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Gielis (2011) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Haxaire & Salesne (2016) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Holloway (1974) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Leraut (2012) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Meyrick (1911) | 3 | 0,22% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Meyrick (1923-1930) | 3 | 0,22% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Meyrick (1934) | 3 | 0,22% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Millière (1863) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Poole (1989) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Ramage (2024) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Renevier-Faure (2014) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Robinson (1968) | 3 | 0,22% | 2 | 0,26% | 2 | 0,29% | 0 | 0% |
Salesne (2010) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Viette (1979) | 3 | 0,22% | 2 | 0,26% | 2 | 0,29% | 1 | 0,14% |
Walker (1865) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Yata et al. (2010) | 3 | 0,22% | 3 | 0,39% | 2 | 0,29% | 1 | 0,14% |
Zilli et al. (2005) | 3 | 0,22% | 3 | 0,39% | 3 | 0,44% | 3 | 0,43% |
Aurivillius (1909) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut et al. (2006) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Beaver (2020) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Bigot (2011) | 2 | 0,15% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Bippus (2016) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Boisduval (1829) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Borth & Kons (2022) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Braby & Müller (2014) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Brito et al. (2017) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Clarke (1976) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Condamine et al. (2023) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Cramer ([1780]-1782) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Derozier (2016) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Dewynter et al. (2022) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 1 | 0,14% |
Dognin (1908) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufay (1975) | 2 | 0,15% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Fabricius (1781) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Freyer (1842-1845) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaedike (1981) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Garrouste & Hervé (2009) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Gaskin (1975) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Gielis (2013) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1852) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1852) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1854) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Herbulot (1988) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Hindermeyer et al. (2007) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 1 | 0,14% |
Honey & Scoble (2001) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1836]) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Inoue (1997) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Kawamoto & Okado (1987) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Lachlan (2004) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Li & Sattler (2012) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Lower (1901) | 2 | 0,15% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Meyrick (1886) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1886) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1926) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Mille et al. (2012) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Orhant (2003) | 2 | 0,15% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Pierre & Lalanne-Cassou | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 1 | 0,14% |
Remillet (1988) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Sobczyk (2013) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Turner (1916) | 2 | 0,15% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 1 | 0,14% |
Varenne & Billi (2008) | 2 | 0,15% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Viette (1950) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Viette (1978) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Walker (1862) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1863) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker ([1865]) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Yano (1963) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Zhang et al. (2023) | 2 | 0,15% | 2 | 0,26% | 1 | 0,15% | 1 | 0,14% |
Zilli (2000) | 2 | 0,15% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Zimmermann et al. (2005) | 2 | 0,15% | 2 | 0,26% | 2 | 0,29% | 2 | 0,29% |
Arenberger (2010) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut & Voisin (2014) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Bigot & Aguesse (2011) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bippus (2017) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Boisduval (1827) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1832-[1835]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boudinot (1991) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1881) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Capps (1953) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Catala & Viette (1948) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Chatard (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Clerck (1759) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1959) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Collet & Pérennec (2012) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Cosson (2009) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Curtis (1823-1840) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
de Toulgoët (1979) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Deknuydt et al. (2018) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delobel & Guttierrez (1981) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Dubois (1996) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 0 | 0% |
Dufay (1982) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbleton (1952) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Duponchel (1836-[1837]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Eitschberger (2009) | 1 | 0,07% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
Esper (1776-1779) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne & Vilardebó (1978) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Fabricius (1787) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain et al. (2014) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Geyer & Frölich (1830) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Goeze (1783) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Grange (2014) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Grote (1873) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2012) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Hacker (1998) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hazir et al. (2001) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Hemming (1933) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1958) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1995) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Heppner (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hinckley (1963) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Hiroshi (1957) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hofmann (1898) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway (1999) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1790) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1766) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
ICZN (1954) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Jack (1985) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 0 | 0% |
Kostrowicki (1961) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Kristensen (1984) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Kugler (1967) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacomme (2013) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Lafontaine & Schmidt (2010) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Laguerre (1999) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Lane & Lane (2006) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lepertel & Quinette (2004) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Leraut (2009) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lower (1898) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1858) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1881) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1883) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1897) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Meyrick (1907) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Meyrick (1909) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1916-1923) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Meyrick (1919) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1921) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nel & Varenne (2019) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nibouche et al. (202X) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Nye (1975) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1789) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (2000) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Orhant (2003) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Prins et al. (2019) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Prout (1934) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage et al. (2017) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Rungs (1982) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Saunders (1843) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Saunders (1851) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Seurat (1934) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Stainton (1856) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Stainton (1866) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Swinhoe (1890) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Tamaki et al. (1973) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Tennent (2003) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 0 | 0% |
Touroult et al. (2023) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Turlin (2002) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Turner (1904) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Turner (1945) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Varenne & Nel (2001) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Viallet (2021) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Viette (1959) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Viette (1961) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Viette (1994) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 0 | 0% |
Villers (1789) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker ([1858]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1859) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Walker (1859) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1863) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Walker (1864) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1866) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Warren (1903) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams & Henning (2023) | 1 | 0,07% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
Zeller (1847) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zeller (1847) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zeller (1848) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Zeller (1852) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Zeller (1879) | 1 | 0,07% | 1 | 0,13% | 1 | 0,15% | 1 | 0,14% |
Zeller (1973) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |