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.
394 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% |
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% |