Rhopalocères et Zygènes de Guyane
Hesperiidae, Lycaenidae, Nymphalidae, Papilionidae, Riodinidae, Pieridae et Zygaenidae de Guyane
265 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Faynel (2010) | 227 | 7,26% | 224 | 9,52% | 223 | 12,29% | 224 | 12,16% |
| Brévignon & Benmesbah (2012) | 89 | 2,85% | 46 | 1,95% | 42 | 2,32% | 39 | 2,12% |
| Brévignon & Gallard (1997) | 65 | 2,08% | 53 | 2,25% | 36 | 1,98% | 52 | 2,82% |
| Li et al. (2019) | 54 | 1,73% | 51 | 2,17% | 48 | 2,65% | 39 | 2,12% |
| Gallard & Wood (2017) | 53 | 1,69% | 36 | 1,53% | 18 | 0,99% | 36 | 1,95% |
| Zhang et al. (2022) | 51 | 1,63% | 43 | 1,83% | 42 | 2,32% | 29 | 1,57% |
| Linnaeus (1758) | 49 | 1,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Espeland et al. (2023) | 48 | 1,54% | 39 | 1,66% | 39 | 2,15% | 38 | 2,06% |
| Hall (2018) | 43 | 1,38% | 16 | 0,68% | 14 | 0,77% | 15 | 0,81% |
| Remillet (1988) | 43 | 1,38% | 27 | 1,15% | 26 | 1,43% | 18 | 0,98% |
| Hewitson (1867-1871) | 39 | 1,25% | 16 | 0,68% | 14 | 0,77% | 9 | 0,49% |
| UICN Comité français, OFB & MNHN (2021) | 36 | 1,15% | 35 | 1,49% | 35 | 1,93% | 12 | 0,65% |
| Olivier (1792) | 35 | 1,12% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Hewitson (1871) | 33 | 1,06% | 19 | 0,81% | 19 | 1,05% | 16 | 0,87% |
| Dewynter et al. (2022) | 32 | 1,02% | 32 | 1,36% | 32 | 1,76% | 12 | 0,65% |
| Lacomme (2013) | 30 | 0,96% | 26 | 1,1% | 13 | 0,72% | 21 | 1,14% |
| Cramer ([1779]) | 24 | 0,77% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brévignon (2005) | 23 | 0,74% | 19 | 0,81% | 9 | 0,5% | 16 | 0,87% |
| Cramer ([1777]) | 23 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cramer ([1780]-1782) | 23 | 0,74% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Pierre & Lalanne-Cassou | 23 | 0,74% | 19 | 0,81% | 19 | 1,05% | 11 | 0,6% |
| Brévignon & Gallard (1998) | 20 | 0,64% | 17 | 0,72% | 5 | 0,28% | 15 | 0,81% |
| Meurgey (2011) | 20 | 0,64% | 15 | 0,64% | 12 | 0,66% | 11 | 0,6% |
| Faynel et al. (2003) | 19 | 0,61% | 9 | 0,38% | 9 | 0,5% | 9 | 0,49% |
| Brévignon (2021) | 18 | 0,58% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Felder & Rogenhofer (1864-1867) | 18 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brévignon (2011) | 17 | 0,54% | 15 | 0,64% | 9 | 0,5% | 15 | 0,81% |
| Tarmann & Drouet (2015) | 17 | 0,54% | 17 | 0,72% | 17 | 0,94% | 17 | 0,92% |
| Meurgey & Ramage (2020) | 15 | 0,48% | 12 | 0,51% | 8 | 0,44% | 11 | 0,6% |
| Brévignon (2019) | 14 | 0,45% | 12 | 0,51% | 9 | 0,5% | 11 | 0,6% |
| Lamas (2004) | 14 | 0,45% | 4 | 0,17% | 2 | 0,11% | 3 | 0,16% |
| Cramer ([1775-1776]) | 12 | 0,38% | 2 | 0,08% | 2 | 0,11% | 0 | 0% |
| Sculfort & Dewynter (2024) | 12 | 0,38% | 12 | 0,51% | 8 | 0,44% | 11 | 0,6% |
| Chainey (2005) | 11 | 0,35% | 8 | 0,34% | 8 | 0,44% | 5 | 0,27% |
| Guillermet (2004) | 11 | 0,35% | 7 | 0,3% | 7 | 0,39% | 4 | 0,22% |
| Brévignon & Lamas (1993) | 10 | 0,32% | 6 | 0,25% | 0 | 0% | 6 | 0,33% |
| Brévignon (2013) | 10 | 0,32% | 8 | 0,34% | 4 | 0,22% | 8 | 0,43% |
| Dumbardon-Martial & Delblond (2019) | 10 | 0,32% | 8 | 0,34% | 8 | 0,44% | 3 | 0,16% |
| Fabricius ([1777]) | 10 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille & Boullet (1917) | 10 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 10 | 0,32% | 8 | 0,34% | 7 | 0,39% | 5 | 0,27% |
| Yokoyama (2013) | 10 | 0,32% | 9 | 0,38% | 9 | 0,5% | 6 | 0,33% |
| Brévignon (2021) | 9 | 0,29% | 6 | 0,25% | 3 | 0,17% | 6 | 0,33% |
| Faynel & Robbins (2014) | 9 | 0,29% | 9 | 0,38% | 9 | 0,5% | 9 | 0,49% |
| Heppner (1982) | 9 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brévignon (2000) | 8 | 0,26% | 8 | 0,34% | 8 | 0,44% | 8 | 0,43% |
| Chovet et al. (2023) | 8 | 0,26% | 6 | 0,25% | 2 | 0,11% | 4 | 0,22% |
| Gallard & Salk (2019) | 8 | 0,26% | 7 | 0,3% | 4 | 0,22% | 7 | 0,38% |
| Questel & Le Quellec (2012) | 8 | 0,26% | 5 | 0,21% | 4 | 0,22% | 5 | 0,27% |
| Brévignon (2011) | 7 | 0,22% | 7 | 0,3% | 5 | 0,28% | 7 | 0,38% |
| Brévignon (2016) | 7 | 0,22% | 5 | 0,21% | 4 | 0,22% | 5 | 0,27% |
| Dias (2013) | 7 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1775) | 7 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fratello et al. (2015) | 7 | 0,22% | 4 | 0,17% | 4 | 0,22% | 4 | 0,22% |
| Gallard & Fernandez (2012) | 7 | 0,22% | 7 | 0,3% | 4 | 0,22% | 7 | 0,38% |
| Siewert et al. (2020) | 7 | 0,22% | 3 | 0,13% | 3 | 0,17% | 3 | 0,16% |
| Zacca et al. (2020) | 7 | 0,22% | 7 | 0,3% | 3 | 0,17% | 5 | 0,27% |
| Brévignon (1998) | 6 | 0,19% | 6 | 0,25% | 0 | 0% | 6 | 0,33% |
| Brévignon (2005) | 6 | 0,19% | 6 | 0,25% | 2 | 0,11% | 6 | 0,33% |
| Brévignon (2006) | 6 | 0,19% | 6 | 0,25% | 0 | 0% | 6 | 0,33% |
| Brévignon (2010) | 6 | 0,19% | 6 | 0,25% | 6 | 0,33% | 6 | 0,33% |
| Brévignon (2015) | 6 | 0,19% | 4 | 0,17% | 4 | 0,22% | 4 | 0,22% |
| Brévignon (2019) | 6 | 0,19% | 5 | 0,21% | 1 | 0,06% | 5 | 0,27% |
| Gallard & Fernandez (2015) | 6 | 0,19% | 6 | 0,25% | 6 | 0,33% | 6 | 0,33% |
| Gallard (1996) | 6 | 0,19% | 4 | 0,17% | 4 | 0,22% | 2 | 0,11% |
| Latreille & Godart (1819-[1824]) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seitz (1907-[1924]) | 6 | 0,19% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Zacca et al. (2017) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhang et al. (2023) | 6 | 0,19% | 4 | 0,17% | 4 | 0,22% | 4 | 0,22% |
| Brévignon (2015) | 5 | 0,16% | 4 | 0,17% | 2 | 0,11% | 4 | 0,22% |
| Gallard (2014) | 5 | 0,16% | 4 | 0,17% | 3 | 0,17% | 4 | 0,22% |
| Martiré & Rochat (2008) | 5 | 0,16% | 5 | 0,21% | 5 | 0,28% | 4 | 0,22% |
| Toussaint et al. (2019) | 5 | 0,16% | 5 | 0,21% | 4 | 0,22% | 3 | 0,16% |
| Zhang et al. (2023) | 5 | 0,16% | 3 | 0,13% | 3 | 0,17% | 3 | 0,16% |
| Attal & Benmesbah (2014) | 4 | 0,13% | 3 | 0,13% | 0 | 0% | 3 | 0,16% |
| Benmesbah (2015) | 4 | 0,13% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Brévignon et al. (2019) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brévignon (1996) | 4 | 0,13% | 4 | 0,17% | 0 | 0% | 4 | 0,22% |
| Brévignon (2006) | 4 | 0,13% | 4 | 0,17% | 0 | 0% | 4 | 0,22% |
| Brévignon (2013) | 4 | 0,13% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Costa et al. (2021) | 4 | 0,13% | 4 | 0,17% | 3 | 0,17% | 3 | 0,16% |
| Dolibaina et al. (2015) | 4 | 0,13% | 3 | 0,13% | 3 | 0,17% | 2 | 0,11% |
| Fabricius (1781) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1787) | 4 | 0,13% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Faynel (2019) | 4 | 0,13% | 4 | 0,17% | 4 | 0,22% | 4 | 0,22% |
| Gallard & Fernandez (2017) | 4 | 0,13% | 4 | 0,17% | 4 | 0,22% | 4 | 0,22% |
| Gallard (2002) | 4 | 0,13% | 4 | 0,17% | 2 | 0,11% | 2 | 0,11% |
| Gallard (2006) | 4 | 0,13% | 4 | 0,17% | 4 | 0,22% | 4 | 0,22% |
| Hemming (1958) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Herrich-schäffer (1850-1858) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner (1816-[1826]) | 4 | 0,13% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Linné (1771) | 4 | 0,13% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Lucas (1852) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1878) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Plötz (1882) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stoll ([1787-1790]) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhang et al. (2021) | 4 | 0,13% | 4 | 0,17% | 4 | 0,22% | 3 | 0,16% |
| Attal et al. (2016) | 3 | 0,1% | 2 | 0,08% | 1 | 0,06% | 1 | 0,05% |
| Bates (1868) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Busby et al. (2017) | 3 | 0,1% | 3 | 0,13% | 3 | 0,17% | 3 | 0,16% |
| Deknuydt et al. (2024) | 3 | 0,1% | 3 | 0,13% | 2 | 0,11% | 1 | 0,05% |
| Gallard (2015) | 3 | 0,1% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Linnaeus (1763) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martins et al. (2016) | 3 | 0,1% | 3 | 0,13% | 3 | 0,17% | 3 | 0,16% |
| Neukirchen (1994) | 3 | 0,1% | 3 | 0,13% | 1 | 0,06% | 2 | 0,11% |
| Piovesan et al. (2022) | 3 | 0,1% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Stichel (1910) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult (2015) | 3 | 0,1% | 3 | 0,13% | 2 | 0,11% | 2 | 0,11% |
| Viette (1950) | 3 | 0,1% | 2 | 0,08% | 2 | 0,11% | 0 | 0% |
| Zhang et al. (2019) | 3 | 0,1% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Zhang et al. (2023) | 3 | 0,1% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Amar (2014) | 2 | 0,06% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Bates (1861) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benmesbah et al. (2018) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benmesbah et al. (2020) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Blandin et al. (2020) | 2 | 0,06% | 2 | 0,08% | 1 | 0,06% | 1 | 0,05% |
| Boisduval (1833) | 2 | 0,06% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Boisduval (1836) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brevignon & Gallard (1999) | 2 | 0,06% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Brévignon & Gallard (1999) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brévignon et al. (2021) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brévignon (1993) | 2 | 0,06% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Brévignon (1996) | 2 | 0,06% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Brévignon (1996) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Brévignon (2000) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Brévignon (2002) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Brévignon (2008) | 2 | 0,06% | 1 | 0,04% | 0 | 0% | 1 | 0,05% |
| Brévignon (2009) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Brevignon (2010) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Brévignon (2015) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Brévignon (2020) | 2 | 0,06% | 1 | 0,04% | 0 | 0% | 1 | 0,05% |
| Brévignon (2023) | 2 | 0,06% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Burns et al. (2008) | 2 | 0,06% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Butler (1866) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butler (1867) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cast (2020) | 2 | 0,06% | 2 | 0,08% | 1 | 0,06% | 1 | 0,05% |
| D'abrera (1994) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| David & Lucas (2017) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 1 | 0,05% |
| Dias et al. (2012) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Dolibaina et al. (2016) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evans (1953) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1793) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faynel & Johnson (2000) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Faynel et al. (2011) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Faynel (2006) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Faynel (2009) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Felder & Felder (1862) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1790) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hall & Harvey (2001) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hall & Willmott (2023) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Hall (1935) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Foliorum group" of Theope (Lepidoptera: Riodinidae). Lambillionea, 98(4): 562-573.">Hall (1998) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Hall (2005) | 2 | 0,06% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Hall (2005) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Hewitson (1862-1866) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hewitson (1876) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hullé et al. (2018) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Johnson (1989) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Johnson (1992) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Johnson (1993) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Krüger (1926) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacomme (2011) | 2 | 0,06% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Lafranchis (2014) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 1 | 0,05% |
| Lafranchis (2016) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 1 | 0,05% |
| Lamas (1995) | 2 | 0,06% | 1 | 0,04% | 0 | 0% | 1 | 0,05% |
| Le Cerf (1925) | 2 | 0,06% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Linné (1767) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meerburgh (1775-[1780]) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Neukirchen (1996) | 2 | 0,06% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Pallister (1956) | 2 | 0,06% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Patrick & Patrick (2012) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 1 | 0,05% |
| Penz et al. (2017) | 2 | 0,06% | 2 | 0,08% | 0 | 0% | 2 | 0,11% |
| Poirier (2015) | 2 | 0,06% | 2 | 0,08% | 1 | 0,06% | 2 | 0,11% |
| Questel (2016) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 1 | 0,05% |
| Ramage (2017) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 1 | 0,05% |
| Rambur (1829) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult et al. (2014) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vane-Wright & De Jong (2003) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 0 | 0% |
| Weymer (1911) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Willmott et al. (2001) | 2 | 0,06% | 2 | 0,08% | 2 | 0,11% | 2 | 0,11% |
| Barbut & Voisin (2014) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Bell (1941) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Braby et al. (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brévignon & Gallard (1993) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Brevignon & Gallard (1998) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Brevignon & Gallard (1998) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Brévignon (2001) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Chazal & Cast (2019) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Cock (2017) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Corecha-Jauffret (2010) | 1 | 0,03% | 1 | 0,04% | 0 | 0% | 1 | 0,05% |
| Costa et al. (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cowan (1974) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cramer (1775) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cramer ([1775-82]) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| De Medeiros et al. (2020) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| [Denis & Schiffermüller] (1775) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dias et al. (2020) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Dillon (1947) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Diringer & Bonin (2021) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Diringer (2012) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Diringer (2022) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Dos Passos (1960) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Doubleday & Westwoods (1846-1850) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draudt (1923) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois (1996) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Erschoff (1875) | 1 | 0,03% | 1 | 0,04% | 0 | 0% | 1 | 0,05% |
| Evans (1955) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1787) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faynel & Fahraeus (2023) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Felder & Felder (1862) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Felder & Rogenhofer (1864-1875) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Fuchs (1962) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gallard & Fernandez (2015) | 1 | 0,03% | 1 | 0,04% | 0 | 0% | 1 | 0,05% |
| Gallard (2013) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Gemmell & Marcus (2015) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Gemmell et al. (2014) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Godman & Salvin (1896) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godman & Salvin (1900) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Godman (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Griffin (1932) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gutierrez (1981) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Hemming (1933) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hemming (1967) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hering (1941) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hewitson (1874) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hindermeyer et al. (2007) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Holloway & Peters (1976) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Honey & Scoble (2001) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner (1806-[1808]) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner [1819-1826] | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hübner ([1825-1831]) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| ICZN (1954) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| IUCN (2013) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Jenkins (1987) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jong (1983) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1913) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Jourdan (2020) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Leraut (1997) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1759) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1764) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille & Boullet (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1888) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Mabille (1889) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mabille (1889) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Möschler (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nicolas (2023) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Núñez et al. (2021) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Orellana (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parnaudeau (2012) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Penz (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rebillard (1958) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Seraphim et al. (2018) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Staudinger ([1885]-1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stefanescu et al. (2012) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Stichel (1902) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tennent (2005) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Turlin (2002) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Vayssières et al. (2001) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Viette (1994) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 0 | 0% |
| Voisin (1975) | 1 | 0,03% | 1 | 0,04% | 1 | 0,06% | 1 | 0,05% |
| Westwood (1851) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Willmott & Hall (2001) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhang et al. (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
