Espèces animales introduites dans les îles subantarctiques
Animaux introduits au sens large dans les îles subantarctiques, c'est-à-dire introduits établis (I), invasifs (J), introduits non établis (M) ou introduits éteints (Y). Par "îles subantarctiques" on entend : l'archipel de Crozet, l'archipel des Kerguélen et les îles Saint-Paul et Amsterdam.
395 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Hullé et al. (2018) | 61 | 7,31% | 59 | 50% | 59 | 50,86% | 59 | 50,86% |
| Frenot et al. (2005) | 49 | 5,88% | 39 | 33,05% | 39 | 33,62% | 38 | 32,76% |
| Hullé & Vernon (2021) | 29 | 3,48% | 29 | 24,58% | 29 | 25% | 29 | 25% |
| Linnaeus (1758) | 26 | 3,12% | 9 | 7,63% | 9 | 7,76% | 9 | 7,76% |
| Chown & Convey (2016) | 19 | 2,28% | 18 | 15,25% | 18 | 15,52% | 18 | 15,52% |
| Meurgey & Ramage (2020) | 16 | 1,92% | 16 | 13,56% | 16 | 13,79% | 16 | 13,79% |
| Lorvelec et al. (2007) | 14 | 1,68% | 14 | 11,86% | 14 | 12,07% | 14 | 12,07% |
| Ramage (2017) | 14 | 1,68% | 14 | 11,86% | 14 | 12,07% | 14 | 12,07% |
| Séguy (1960) | 13 | 1,56% | 7 | 5,93% | 7 | 6,03% | 7 | 6,03% |
| Meurgey (2011) | 12 | 1,44% | 10 | 8,47% | 10 | 8,62% | 10 | 8,62% |
| Cuvier & Valenciennes (1848) | 11 | 1,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan & Mille (2006) | 11 | 1,32% | 11 | 9,32% | 11 | 9,48% | 11 | 9,48% |
| Voisin et al. (2017) | 11 | 1,32% | 11 | 9,32% | 10 | 8,62% | 11 | 9,48% |
| Aulagnier et al. (2017) | 10 | 1,2% | 9 | 7,63% | 9 | 7,76% | 8 | 6,9% |
| Hullé et al. (2010) | 10 | 1,2% | 10 | 8,47% | 10 | 8,62% | 10 | 8,62% |
| Jourdan (2020) | 10 | 1,2% | 9 | 7,63% | 9 | 7,76% | 9 | 7,76% |
| Questel (2020) | 10 | 1,2% | 9 | 7,63% | 9 | 7,76% | 9 | 7,76% |
| Soubeyran et al. (2011) | 9 | 1,08% | 9 | 7,63% | 9 | 7,76% | 9 | 7,76% |
| Thibaud (2017) | 9 | 1,08% | 8 | 6,78% | 8 | 6,9% | 8 | 6,9% |
| Walbaum (1792) | 9 | 1,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barré (2021) | 8 | 0,96% | 8 | 6,78% | 8 | 6,9% | 8 | 6,9% |
| Deharveng (1981) | 8 | 0,96% | 7 | 5,93% | 7 | 6,03% | 7 | 6,03% |
| Denux & Zagatti (2010) | 8 | 0,96% | 8 | 6,78% | 8 | 6,9% | 8 | 6,9% |
| Etienne (2005) | 8 | 0,96% | 8 | 6,78% | 8 | 6,9% | 8 | 6,9% |
| Gargominy et al. (1996) | 8 | 0,96% | 8 | 6,78% | 8 | 6,9% | 8 | 6,9% |
| Prévost & Mougin (1970) | 8 | 0,96% | 8 | 6,78% | 7 | 6,03% | 8 | 6,9% |
| Vayssières et al. (2001) | 8 | 0,96% | 8 | 6,78% | 8 | 6,9% | 8 | 6,9% |
| Yokoyama (2013) | 8 | 0,96% | 8 | 6,78% | 8 | 6,9% | 8 | 6,9% |
| Albouy & Richard (2017) | 7 | 0,84% | 6 | 5,08% | 6 | 5,17% | 6 | 5,17% |
| Duhamel et al. (2005) | 7 | 0,84% | 7 | 5,93% | 7 | 6,03% | 7 | 6,03% |
| Lacepède (1803) | 7 | 0,84% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 7 | 0,84% | 7 | 5,93% | 7 | 6,03% | 7 | 6,03% |
| Remaudière & Etienne (1988) | 7 | 0,84% | 7 | 5,93% | 7 | 6,03% | 7 | 6,03% |
| Soubeyran (2008) | 7 | 0,84% | 6 | 5,08% | 6 | 5,17% | 6 | 5,17% |
| Tronquet (2014) | 7 | 0,84% | 7 | 5,93% | 7 | 6,03% | 7 | 6,03% |
| Aulagnier (2009) | 6 | 0,72% | 5 | 4,24% | 5 | 4,31% | 4 | 3,45% |
| Evenhuis (1989) | 6 | 0,72% | 6 | 5,08% | 6 | 5,17% | 6 | 5,17% |
| Günther (1866) | 6 | 0,72% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kieffer (1902) | 6 | 0,72% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 6 | 0,72% | 6 | 5,08% | 6 | 5,17% | 6 | 5,17% |
| Pallas [1814] | 6 | 0,72% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peck et al. (2014) | 6 | 0,72% | 6 | 5,08% | 6 | 5,17% | 6 | 5,17% |
| Theuerkauf et al. (2010) | 6 | 0,72% | 6 | 5,08% | 6 | 5,17% | 6 | 5,17% |
| Albouy et al. (2017) | 5 | 0,6% | 5 | 4,24% | 5 | 4,31% | 5 | 4,31% |
| Gomy (2000) | 5 | 0,6% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Hullé et al. (2003) | 5 | 0,6% | 5 | 4,24% | 5 | 4,31% | 5 | 4,31% |
| Marchán et al. (2022) | 5 | 0,6% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Mille et al. (2020) | 5 | 0,6% | 5 | 4,24% | 5 | 4,31% | 5 | 4,31% |
| Blakemore (2008) | 4 | 0,48% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Cazanove (2022) | 4 | 0,48% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Clarke (1971) | 4 | 0,48% | 4 | 3,39% | 4 | 3,45% | 4 | 3,45% |
| [Denis & Schiffermüller] (1775) | 4 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Des et al. (2021) | 4 | 0,48% | 4 | 3,39% | 4 | 3,45% | 4 | 3,45% |
| Fauvel (1867) | 4 | 0,48% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Gentry et al. (2004) | 4 | 0,48% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Guillermet (2004) | 4 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heller (1916) | 4 | 0,48% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Jordan (1894) | 4 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kieffer (1902-1904) | 4 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kieffer (1907-1911) | 4 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martiré & Rochat (2008) | 4 | 0,48% | 4 | 3,39% | 4 | 3,45% | 4 | 3,45% |
| Uicn et al. (2015) | 4 | 0,48% | 4 | 3,39% | 4 | 3,45% | 4 | 3,45% |
| Aulagnier (2021) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 2 | 1,72% |
| Azam (1893) | 3 | 0,36% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Barbut & Voisin (2014) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Bochaton et al. (2021) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Burneleau (1983) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Butaud (2021) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Catzeflis (2018) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Chapelin-Viscardi & Maillet-Mezeray (2013) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| , 3: 249-270.">Enderlein (1903) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etienne & Vilardebó (1978) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Fairmaire (1849) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Geer (1774) | 3 | 0,36% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Gmelin (1789) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gomy et al. (2016) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Hammes & Putoa (1986) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Jeannenot (1955) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2011) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Lessona & Pollonera (1882) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montrouzier (1860) | 3 | 0,36% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Nicolet (1847) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nilsson (1832) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. (2006) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Peck (2011) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Ponge et al. (2003) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Renault (2011) | 3 | 0,36% | 3 | 2,54% | 3 | 2,59% | 3 | 2,59% |
| Savigny (1826) | 3 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal (2012) | 3 | 0,36% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Viette (1959) | 3 | 0,36% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Adamska & Grzywacz (2019) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Azab et al. (1972) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Béarez et al. (2017) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Bell et al. (1989) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Bellemare & Brunelle (1950) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Benedetti et al. (2021) | 2 | 0,24% | 2 | 1,69% | 1 | 0,86% | 1 | 0,86% |
| Berrebi et al. (2018) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Betsch & Massoud (1970) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonfils (1969) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Borovec (1991) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boyer & Rivault (2003) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Cazanove et al. (2022) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Cerkowniak et al. (2020) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Chandebois (1958) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Chapuis et al. (2004) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Cochereau (1974) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Couch (1877) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dadant & Etienne (1973) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Daly et al. (2023) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Denis (1921) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Denis (1922) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Denys et al. (2022) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Eaton et al. (1879) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Eaton (1875) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etienne et al. (2015) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Evenhuis & Barbotin (1977) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evenhuis (2018) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Falkner et al. (2002) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Fauvel (1891) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Fauvel (1903) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Fauvel (1903) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontenot et al. (2015) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Forsslund (1964) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Fort & Barrière (2021) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Fourcroy (1785) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frey (1948) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy et al. (2011) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Griffiths & Florens (2006) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Guillermet (2011) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Gutierrez (1981) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Hale et al. (2008) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Hava (2006) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Háva (2014) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Heckel & Kner (1858) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hindermeyer et al. (2007) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Hossain et al. (2016) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Jones et al. (2006) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Jones et al. (2007) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Jordan (1896) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kerney & Cameron (1999) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Kieffer (1898) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacoste (de) (2020) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Laparie & Renault (2014) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Leraut (1997) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas (1847) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macquart (1835) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meganck et al. (2017) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Montrouzier (1861) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nentwig & Kobelt (2010) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Pallas (1831) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. 2006 | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Paulian (1998) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Pickard-Cambridge (1876) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pistil & Kontykowski (1974) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Potin (2013) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Preynat (2013) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Pujade-Villar et al. (2007) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Rakowski et al. (1981) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Rambur (1829) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Revilliod (1914) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roberts (2014) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Robineau-Desvoidy (1841) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rognes & Blackith (1990) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Routtier et al. (2023) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saaristo & Tanasevitch (1996) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Saint et al. (1978) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Savouré-Soubelet et al. (in prep.) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Schiner (1868) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1876) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Soldati & Touroult (2014) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Thomas (2015) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Vidal & Vansteene (2021) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Vilkamaa & Menzel (2019) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1802) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welter-schultes (2012) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Withers & Chandler (2019) | 2 | 0,24% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Yang et al. (2023) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Zanetti et al. (2016) | 2 | 0,24% | 2 | 1,69% | 2 | 1,72% | 2 | 1,72% |
| Abdel-kader & Barak (1979) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Allen et al. (2022) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Anonyme. (2004) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Anonyme. (2004) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2018) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Aubouin et al. (2016) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Audige (1927) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bagnall (1927) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barau et al. (2005) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Beatty et al. (1991) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Belon & Mulsant (1881) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berland (1942) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Bernard (1961) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Beslagic et al. (2013) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Bigot (1992) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Billi (2009) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Blackwall (1852) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeckere (2001) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Bloch (1782-1784) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1784) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blyth (1841) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 0 | 0% |
| Body (2021) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Boisduval (1833) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Bonnaterre (1788) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouché (1982) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Bouget et al. (2019) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Bournier & Mound (2000) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Bournier (2000) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Brindle (1971) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Brindle (1975) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Brindle (1976) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Brown (1929) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Burr (1914) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caceres & Salamolard (2021) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Callou (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Cambridge (1879) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carapelli et al. (1995) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carapelli et al. (2001) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Carpenter (1934) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Carpenter (1935) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Cerkowniak et al. (2017) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Chapuis et al. (2001) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cheesman (1928) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Cherbonnier & Guille (1975) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cheylan et al. (2022) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Chopard (1924) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Clemens (1860) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cohic (1959) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Colijn et al. (2020) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Couteyen (2006) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Cowie (2000) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Damoiseau (1966) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| De Geer (1773) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deblock et al. (1960) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Deeming (1979) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Déjan (2012) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Delhaes et al. (2001) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Dewynter et al. (2022) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Dieme et al. (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Dreux & Voisin (1993) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Dreux et al. (1992) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Enderlein (1903) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Enderlein (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Enderlein (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Enderlein (1936) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Černosvitov (1934) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evenhuis (2012) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Fabricius (1775) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1780) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fallén (1823) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1862) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferrer (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Ferrer-Suay et al. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferrer-Suay et al. (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Ferrer-Suay et al. (2018) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Frenot (1992) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke et al. (2009) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Fueßlin (1775) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gadeau de Kerville (1894) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrouste & Hervé (2009) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Geoffroy (1762) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Giani (1976) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Girard (1859) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2021) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Goetghebuer (1944) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goeze (1777) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gonzales et al. (2014) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| González-Miguéns et al. (2020) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Groves & Grubb (2011) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guglielmone et al. (2023) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Guiguen et al. (1987) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Haliday (1834) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Hartig (1841) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hava & Poussereau (2017) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Hebard (1933) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Hebard (1933) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Hinton (1941) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoddle et al. (2008) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Holloway (1979) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Honey & Scoble (2001) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hufnagel (1766) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hustache (1920) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hynes (1993) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| IUCN (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Johannsen (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1892) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaszab (1982) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Kaszab (1985) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Keith & Dorson (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Keith & Machino (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Keith et al. (2002) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Keith et al. (2006) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Keith (2002) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Keith (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Kolenati (1846) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kolibáč (2013) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Kumar et al. (1988) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Lacomme (2013) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Lafranchis (2014) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Lafranchis (2016) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| .">Lambret & Lebouvier (2006) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Maitre & Chadee (1983) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Ledoux & Hallé (1995) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Letacq (1924) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levesque & Mathurin (2008) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Linnaeus (1767) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linné (1767) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Machino (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Malloch (1932) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Malloch (1932) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Mammola & Milano (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marchandeau & Letty (2021) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Marchandeau et al. (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Martin-vega et al. (2017) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meigen (1818) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menezes et al. (2005) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Menezes et al. (2006) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Menzel & Vilkamaa (2021) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Mercier (1924) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mériguet & Zagatti (2016) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Meyrick (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mikkola & Honey (1993) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1881) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moubayed-Breil et al. (2017) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Moulton (1907) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1774) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muru et al. (2017) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Nentwig et al. (2019) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Nicolet (1842) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olivier (1791-[1792]) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osuji (1975) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Osuji (1975) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Pascal & Vigne (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Pascal & Vigne (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Pascal & Vigne (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Pascal et al. (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Pascal et al. (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pavlíček & Csuzdi (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierre & Lalanne-Cassou | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Pisanu et al. (2003) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Poussereau et al. (2013) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Pugh & Scott (2002) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Puissauve, Legros & Poulet (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Quindroit & Lemoine (2022) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Quindroit (2020) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Rageau (1956) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Rageau (1959) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Randi et al. (2001) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Rehn (1949) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Remillet (1988) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Renaud et al. (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rheinheimer (2014) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Rheinheimer (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Rosenbaum et al. (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Rossi (1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roux & Martinez (1987) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Ruecker (2005) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ruys & Coord (2012) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Sardet et al. (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Schrank (1781) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sculfort & Dewynter (2024) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Séchet & Noël (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Shaaya (1981) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Shahhosseini (1980) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Shinonaga et al. (1991) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Shiraki (1906) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siddaiah & Kujur (2016) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Skierska (1976) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Starý et al. (1994) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Stefanescu et al. (2012) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Steffan (1972) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stein (1911) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Stierlin (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Szederjesi et al. (2019) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Széles et al. (2018) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Theodorides (1955) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thévenot (2014) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Tonnoir (1940) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tourlan (2018) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Touroult et al. (2015) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Trehen & Voisin (1984) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| UICN Comité français, OFB & MNHN (2021) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| UICN Comité français, OFB, MNHN & AsFrA (2023) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Viette (1949) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Viette (1979) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Vincent & Voisin (1991) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Vinson (1863) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Voisin (1975) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Walker (1865) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Westwood (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zanetti et al. (2020) | 1 | 0,12% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
