Lépidoptères de la Réunion
Lepidoptera de la Réunion
405 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Martiré & Rochat (2008) | 916 | 60,94% | 736 | 94,48% | 661 | 91,42% | 691 | 95,57% |
| Guillermet (2009) | 292 | 19,43% | 239 | 30,68% | 227 | 31,4% | 239 | 33,06% |
| Guillermet (2011) | 283 | 18,83% | 246 | 31,58% | 238 | 32,92% | 246 | 34,02% |
| Guillermet (2009) | 262 | 17,43% | 202 | 25,93% | 194 | 26,83% | 202 | 27,94% |
| Guillermet (2006) | 220 | 14,64% | 204 | 26,19% | 160 | 22,13% | 204 | 28,22% |
| Nicolas (2025) | 136 | 9,05% | 134 | 17,2% | 133 | 18,4% | 114 | 15,77% |
| Guenée (1862) | 121 | 8,05% | 28 | 3,59% | 28 | 3,87% | 28 | 3,87% |
| Bippus (2020) | 112 | 7,45% | 107 | 13,74% | 107 | 14,8% | 107 | 14,8% |
| Guillermet (2004) | 103 | 6,85% | 86 | 11,04% | 62 | 8,58% | 83 | 11,48% |
| Boisduval (1833) | 76 | 5,06% | 7 | 0,9% | 7 | 0,97% | 4 | 0,55% |
| Clarke (1971) | 67 | 4,46% | 51 | 6,55% | 47 | 6,5% | 45 | 6,22% |
| Bippus (2018) | 47 | 3,13% | 40 | 5,13% | 40 | 5,53% | 39 | 5,39% |
| Leraut (2014) | 47 | 3,13% | 42 | 5,39% | 42 | 5,81% | 42 | 5,81% |
| Ramage (2017) | 41 | 2,73% | 32 | 4,11% | 31 | 4,29% | 28 | 3,87% |
| Viette (1949) | 41 | 2,73% | 29 | 3,72% | 28 | 3,87% | 25 | 3,46% |
| Leraut (2012) | 40 | 2,66% | 37 | 4,75% | 37 | 5,12% | 34 | 4,7% |
| Bippus (2019) | 39 | 2,59% | 38 | 4,88% | 38 | 5,26% | 38 | 5,26% |
| Parnaudeau (2012) | 36 | 2,4% | 34 | 4,36% | 31 | 4,29% | 30 | 4,15% |
| Guillermet (2012) | 30 | 2% | 28 | 3,59% | 28 | 3,87% | 28 | 3,87% |
| Orhant (2003) | 29 | 1,93% | 25 | 3,21% | 23 | 3,18% | 25 | 3,46% |
| Bippus (2016) | 25 | 1,66% | 24 | 3,08% | 22 | 3,04% | 24 | 3,32% |
| Parnaudeau (2009) | 24 | 1,6% | 20 | 2,57% | 19 | 2,63% | 18 | 2,49% |
| Holloway (1979) | 23 | 1,53% | 16 | 2,05% | 16 | 2,21% | 13 | 1,8% |
| Viette (1975) | 23 | 1,53% | 22 | 2,82% | 16 | 2,21% | 21 | 2,9% |
| Linnaeus (1758) | 22 | 1,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan & Mille (2006) | 21 | 1,4% | 16 | 2,05% | 16 | 2,21% | 13 | 1,8% |
| Jourdan (2020) | 21 | 1,4% | 19 | 2,44% | 18 | 2,49% | 16 | 2,21% |
| Guillermet (1992) | 20 | 1,33% | 13 | 1,67% | 13 | 1,8% | 13 | 1,8% |
| Meurgey & Ramage (2020) | 20 | 1,33% | 20 | 2,57% | 20 | 2,77% | 18 | 2,49% |
| Herbulot (1967) | 18 | 1,2% | 17 | 2,18% | 15 | 2,07% | 16 | 2,21% |
| Nicolas (2023) | 18 | 1,2% | 16 | 2,05% | 13 | 1,8% | 14 | 1,94% |
| [Denis & Schiffermüller] (1775) | 17 | 1,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guillermet (2004) | 17 | 1,13% | 15 | 1,93% | 15 | 2,07% | 15 | 2,07% |
| Vayssières et al. (2001) | 16 | 1,06% | 12 | 1,54% | 12 | 1,66% | 11 | 1,52% |
| Viette (1988) | 16 | 1,06% | 10 | 1,28% | 8 | 1,11% | 10 | 1,38% |
| Bippus (2017) | 14 | 0,93% | 14 | 1,8% | 14 | 1,94% | 11 | 1,52% |
| Guillermet (2011) | 14 | 0,93% | 10 | 1,28% | 8 | 1,11% | 10 | 1,38% |
| Dadant & Etienne (1973) | 13 | 0,86% | 12 | 1,54% | 12 | 1,66% | 7 | 0,97% |
| Dufay (1975) | 13 | 0,86% | 11 | 1,41% | 11 | 1,52% | 9 | 1,24% |
| Guillermet (2013) | 13 | 0,86% | 11 | 1,41% | 11 | 1,52% | 11 | 1,52% |
| Bippus (2016) | 12 | 0,8% | 11 | 1,41% | 11 | 1,52% | 11 | 1,52% |
| Clarke (1986) | 12 | 0,8% | 10 | 1,28% | 10 | 1,38% | 10 | 1,38% |
| Guillermet (2010) | 12 | 0,8% | 10 | 1,28% | 10 | 1,38% | 10 | 1,38% |
| Guillermet (2011) | 12 | 0,8% | 12 | 1,54% | 12 | 1,66% | 12 | 1,66% |
| Questel (2020) | 12 | 0,8% | 12 | 1,54% | 12 | 1,66% | 11 | 1,52% |
| Guenée (1852) | 11 | 0,73% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Guenée (1854) | 11 | 0,73% | 6 | 0,77% | 6 | 0,83% | 6 | 0,83% |
| Diakonoff (1977) | 10 | 0,67% | 6 | 0,77% | 6 | 0,83% | 6 | 0,83% |
| Duponchel (1831-[1834]) | 10 | 0,67% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leraut (1997) | 10 | 0,67% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 10 | 0,67% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Ramage (2024) | 10 | 0,67% | 9 | 1,16% | 8 | 1,11% | 9 | 1,24% |
| Boisduval (1833) | 9 | 0,6% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Fabricius (1775) | 9 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lafranchis (2014) | 9 | 0,6% | 8 | 1,03% | 8 | 1,11% | 7 | 0,97% |
| Lafranchis (2016) | 9 | 0,6% | 8 | 1,03% | 8 | 1,11% | 7 | 0,97% |
| Meurgey (2011) | 9 | 0,6% | 7 | 0,9% | 7 | 0,97% | 7 | 0,97% |
| Meyrick (1908) | 9 | 0,6% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Razowski (2015) | 9 | 0,6% | 8 | 1,03% | 8 | 1,11% | 8 | 1,11% |
| Bippus (2019) | 8 | 0,53% | 8 | 1,03% | 8 | 1,11% | 8 | 1,11% |
| Guillermet (2009) | 8 | 0,53% | 8 | 1,03% | 8 | 1,11% | 8 | 1,11% |
| Herbulot (1979) | 8 | 0,53% | 6 | 0,77% | 5 | 0,69% | 5 | 0,69% |
| Questel (2016) | 8 | 0,53% | 8 | 1,03% | 8 | 1,11% | 8 | 1,11% |
| Viette (1979) | 8 | 0,53% | 5 | 0,64% | 5 | 0,69% | 2 | 0,28% |
| Aurivillius (1909) | 7 | 0,47% | 3 | 0,39% | 3 | 0,41% | 1 | 0,14% |
| Fabricius (1794) | 7 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guenée (1852) | 7 | 0,47% | 3 | 0,39% | 3 | 0,41% | 2 | 0,28% |
| Leraut (2019) | 7 | 0,47% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Meyrick (1934) | 7 | 0,47% | 5 | 0,64% | 5 | 0,69% | 5 | 0,69% |
| Viette (1962) | 7 | 0,47% | 6 | 0,77% | 6 | 0,83% | 6 | 0,83% |
| Bigot & Etienne (2009) | 6 | 0,4% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Cramer ([1779]) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cramer ([1780]-1782) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duponchel (1827-[1828]) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etienne & Vilardebó (1978) | 6 | 0,4% | 6 | 0,77% | 6 | 0,83% | 5 | 0,69% |
| Meyrick (1910) | 6 | 0,4% | 2 | 0,26% | 2 | 0,28% | 1 | 0,14% |
| Millière (1864-1868) | 6 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nibouche et al. (202X) | 6 | 0,4% | 6 | 0,77% | 6 | 0,83% | 6 | 0,83% |
| Timm & Brown (2014) | 6 | 0,4% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Viette (1995) | 6 | 0,4% | 6 | 0,77% | 6 | 0,83% | 6 | 0,83% |
| Cramer ([1777]) | 5 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deknuydt et al. (2016) | 5 | 0,33% | 5 | 0,64% | 5 | 0,69% | 3 | 0,41% |
| Drury (1773) | 5 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Esper ([1796-1805]) | 5 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gielis (2011) | 5 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guillermet (2016) | 5 | 0,33% | 5 | 0,64% | 5 | 0,69% | 5 | 0,69% |
| Gutierrez (1981) | 5 | 0,33% | 4 | 0,51% | 4 | 0,55% | 2 | 0,28% |
| Haxaire (2010) | 5 | 0,33% | 3 | 0,39% | 1 | 0,14% | 2 | 0,28% |
| Heppner (1982) | 5 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lagarde (2008) | 5 | 0,33% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Meyrick (1912-1916) | 5 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pagenstecher (1907) | 5 | 0,33% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Questel & Le Quellec (2012) | 5 | 0,33% | 5 | 0,64% | 5 | 0,69% | 4 | 0,55% |
| Viette (1971) | 5 | 0,33% | 2 | 0,26% | 2 | 0,28% | 1 | 0,14% |
| Woodward (1922) | 5 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot & Drouet (2014) | 4 | 0,27% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Diakonoff (1974) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dognin (1908) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guenée (1852) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guenée ([1858]) | 4 | 0,27% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Guillermet (2005) | 4 | 0,27% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Hacker et al. (2021) | 4 | 0,27% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Hübner (1796-[1828]) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Joannis (1906) | 4 | 0,27% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Leraut (2019) | 4 | 0,27% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Leroy et al. (2021) | 4 | 0,27% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Lopez-Vaamonde et al. (2010) | 4 | 0,27% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Meyrick (1887) | 4 | 0,27% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Meyrick (1913) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 4 | 0,27% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Periasamy et al. (2015) | 4 | 0,27% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Prins & Kawahara (2012) | 4 | 0,27% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Régnart et al. (2022) | 4 | 0,27% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| UICN Comité français, OFB & MNHN (2021) | 4 | 0,27% | 4 | 0,51% | 4 | 0,55% | 2 | 0,28% |
| Viette (1950) | 4 | 0,27% | 3 | 0,39% | 3 | 0,41% | 1 | 0,14% |
| Viette (1982) | 4 | 0,27% | 4 | 0,51% | 4 | 0,55% | 4 | 0,55% |
| Viette (1994) | 4 | 0,27% | 4 | 0,51% | 2 | 0,28% | 3 | 0,41% |
| Albouy et al. (2017) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Anonyme (2018) | 3 | 0,2% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Attie & Morel (1997) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 0 | 0% |
| Bippus (2016) | 3 | 0,2% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Bippus (2019) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Bippus (2020) | 3 | 0,2% | 3 | 0,39% | 2 | 0,28% | 3 | 0,41% |
| Borth & Kons (2022) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Cohic (1950) | 3 | 0,2% | 2 | 0,26% | 2 | 0,28% | 1 | 0,14% |
| Collenette (1934) | 3 | 0,2% | 3 | 0,39% | 2 | 0,28% | 2 | 0,28% |
| Curtis (1823-1840) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| de Toulgoët (1979) | 3 | 0,2% | 2 | 0,26% | 1 | 0,14% | 2 | 0,28% |
| Dewynter et al. (2022) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 2 | 0,28% |
| Duponchel (1836-[1837]) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Esper & Charpentier (1795-[1806]) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1781) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1798) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flores et al 2024 | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Geoffroy (1762) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gielis & Bippus (2016) | 3 | 0,2% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Griveaud (1960) | 3 | 0,2% | 3 | 0,39% | 2 | 0,28% | 3 | 0,41% |
| Holloway & Peters (1976) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 2 | 0,28% |
| Hübner (1796-[1828]) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Joannis (1915) | 3 | 0,2% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Linné (1767) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1934) | 3 | 0,2% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Millière (1863) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Munroe (1956) | 3 | 0,2% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Patrick & Patrick (2012) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 1 | 0,14% |
| Pierre & Lalanne-Cassou | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 2 | 0,28% |
| Poole (1989) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Ragonot (1888) | 3 | 0,2% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Rambur (1834) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vane-Wright & De Jong (2003) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 1 | 0,14% |
| Viette (1949) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Viette (1985) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Yokoyama (2013) | 3 | 0,2% | 3 | 0,39% | 3 | 0,41% | 3 | 0,41% |
| Zeller (1852) | 3 | 0,2% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Barbut & Voisin (2014) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 1 | 0,14% |
| Barbut et al. (2006) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Bigot (1992) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Boisduval (1833) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| . Mauritius (H. Plaideau). 46 pp. ">Bojer (1956) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brito et al. (2017) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Brown (1886) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brun & Chazeau (1986) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Butler (1881) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butler (1897 (1898)) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Cohic (1959) | 2 | 0,13% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Constant (1893-1894) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Derozier (2016) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Diakonoff (1978) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Diakonoff (1988) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Diakonoff (1989) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Drury ([1770-1773]) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Drury ([1782]) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Feisthamel (1837) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Felder & Rogenhofer (1864-1875) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Freyer ([1831]-1833) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fric et al. (2019) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Garrouste & Hervé (2009) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Gibeaux (1991) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gielis (2013) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guenée (1845) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guenée ([1858]) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guérin-Méneville & Perrotet (1842) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guillermet (2000) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guillermet (2006) | 2 | 0,13% | 2 | 0,26% | 0 | 0% | 2 | 0,28% |
| Hemming (1958) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Honey & Scoble (2001) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner (1796-[1836]) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hullé et al. (2018) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| IUCN (2013) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Joannis ([1901]) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kawamoto & Okado (1987) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Kruger (2001) | 2 | 0,13% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Lacomme (2013) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Leraut (2005) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maes (2014) | 2 | 0,13% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Mally & Nuss (2011) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Mally et al. (2019) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Meyrick (1886) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1911) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1921) | 2 | 0,13% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Meyrick (1922) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1926) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millière (1873) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orhant (2002) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 1 | 0,14% |
| Perroud & Montrouzier (1864) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quilici et al. (1988) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Rambur (1829) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rambur (1858-[1866]) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramel et al. (2009) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Razowski (2013) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Remillet (1988) | 2 | 0,13% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Sattler & Tremewan (1973) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Slamka (2019) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thunberg & Borgström (1784) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turlin (2002) | 2 | 0,13% | 2 | 0,26% | 1 | 0,14% | 2 | 0,28% |
| Varenne & Billi (2008) | 2 | 0,13% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Viette (1954) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Viette (1959) | 2 | 0,13% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
| Viette (1991) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Villers (1789) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1859) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1859) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Walker (1863) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1864) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walsingham (1891) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walsingham (1908) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walsingham (1920) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Waltemathe (2010) | 2 | 0,13% | 2 | 0,26% | 1 | 0,14% | 2 | 0,28% |
| Yano (1963) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zeller (1867) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zilli et al. (2017) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Zimmermann et al. (2005) | 2 | 0,13% | 2 | 0,26% | 2 | 0,28% | 2 | 0,28% |
| Anglade et al. (1971) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Anonyme (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arenberger (2010) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Asselbergs (1998) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Barbut (2003) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Bassi & Trematerra (2014) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bério (1954) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berio (1967) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Bertin (2004) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Bigot & Aguesse (2011) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot (2011) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Billi (2009) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Entomologiste (Paris), 61(1): 33-34.">Binon (2005) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Biondi et al. (2013) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Bippus (2014) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Boisduval & Guénée ([1874]) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Boisduval (1827) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boisduval (1847) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butler (1878) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Capps (1953) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Cazals & Dupont (2022) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Chatard (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chrétien (1904) | 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 | 0,14% | 0 | 0% |
| Condamine et al. (2023) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Constant (1883) | 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 | 0,14% | 0 | 0% |
| Demergès & Grandmaire (2014) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Doubleday & Westwoods (1850-1852) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois (1996) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
| Dufay (1982) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edward et al. (2015) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Enderlein (1903) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| , 3: 249-270.">Enderlein (1903) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eppo (2018) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Eppo (2018) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Eppo (2019) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Esper (1776-1779) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1787) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fibiger & Hacker (2005) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fletcher (1910) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourcroy (1785) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fournal (2012) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Fournier (2016) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Gasnier et al. (2015) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Geyer & Frölich (1830) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ghesquière (1940) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Girod & Sauce (2002) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Godart (1822-[1824]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gozmány et al. (18) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Grange (2014) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Gros (1992) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Grote (1873) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guillermet (2010) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Hacker (1998) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hampson (1907) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
| Haworth (1803-1828) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hazir et al. (2001) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Hemming (1933) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heppner (1995) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Heppner (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hindermeyer et al. (2007) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
| Hiroshi (1957) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hofmann (1898) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner (1790) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner ([1799-1838]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner (1806-[1808]) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner (1818) | 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 | 0,14% | 1 | 0,14% |
| Kalchberg (1876) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Karsholt & Nielsen (1985) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krueger (2007) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Lafontaine & Schmidt (2010) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Laguerre (1999) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Lambert (2008) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Landemaine (2002) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Lang (1789) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leraut (2002) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leraut (2006) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Lhomme (1937) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Linnaeus (1761) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linné (1771) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Lödl (1995) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Mabille (1880) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mackay (1972) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Maes (1987) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Mann (1957) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Meyrick (1883) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1885) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Meyrick (1886) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1893) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1904) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Meyrick (1911) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Meyrick (1912) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Meyrick (1917) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1922) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1923-1930) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1926) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyrick (1930) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
| Mothiron (2015) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Motschulsky (1859) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nel (2009) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Oberthür (1879-1880) | 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% |
| Orhant (2006) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Patrick & Policard (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Petagna (1786) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prins et al. (2019) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Ragonot & Hampson (1901) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ragonot (1887) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Raingeard (1999) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Razowski (2014) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Robinson & Nielsen (1983) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robinson et al. (1994) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Rogard (2015) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Rossi (1794) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rothschild (1913) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rungs (1982) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Saalmüller (1880) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saunders (1851) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sculfort & Dewynter (2024) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Sircoulomb (2013) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Snellen (1872) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Snellen (1891) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stainton (1856) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Stainton (1866) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stainton (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Staudinger (1870) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stefanescu et al. (2012) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Stephens (1834-1835) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sylla et al. (2019) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Tabone et al. (2012) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Tavoillot (1997) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Tennent (2005) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Thirion (2007) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Touroult et al. (2015) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
| Touroult et al. (2023) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Treitschke (1832) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Trimen (1862) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Trottin-Caudal et al. (2012) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| UICN France et al. (2013) | 1 | 0,07% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
| Viallet (2021) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Viette (1950) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Viette (1964) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Voisin (1975) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Walker (1856) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker ([1858]) | 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% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1863) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1864) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1865) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walsingham (1897) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Whalley (1973) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Wollaston (1879) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zeller (1846) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zeller (1847) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
| Zeller (1847) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zeller (1848) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Zeller (1853) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Zeller (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zeller (1879) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
| Zeller (1973) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhang et al. (2023) | 1 | 0,07% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
| Zilli (2021) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
