Insectes des îles subantarctiques
335 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) | 136 | 23,41% | 116 | 63,04% | 116 | 69,05% | 104 | 60,12% |
Hullé & Vernon (2021) | 75 | 12,91% | 65 | 35,33% | 65 | 38,69% | 59 | 34,1% |
Voisin et al. (2017) | 53 | 9,12% | 52 | 28,26% | 41 | 24,4% | 52 | 30,06% |
Kuschel & Chown (1995) | 31 | 5,34% | 13 | 7,07% | 13 | 7,74% | 11 | 6,36% |
Morrone (1998) | 31 | 5,34% | 13 | 7,07% | 13 | 7,74% | 11 | 6,36% |
Dreux & Voisin (1993) | 29 | 4,99% | 21 | 11,41% | 21 | 12,5% | 20 | 11,56% |
Evenhuis (1989) | 25 | 4,3% | 24 | 13,04% | 21 | 12,5% | 23 | 13,29% |
Chown & Convey (2016) | 23 | 3,96% | 21 | 11,41% | 21 | 12,5% | 21 | 12,14% |
Séguy (1960) | 20 | 3,44% | 14 | 7,61% | 14 | 8,33% | 14 | 8,09% |
Frenot et al. (2005) | 18 | 3,1% | 16 | 8,7% | 16 | 9,52% | 16 | 9,25% |
Meurgey & Ramage (2020) | 17 | 2,93% | 17 | 9,24% | 17 | 10,12% | 17 | 9,83% |
Ramage (2017) | 16 | 2,75% | 15 | 8,15% | 15 | 8,93% | 15 | 8,67% |
Eaton (1875) | 14 | 2,41% | 10 | 5,43% | 10 | 5,95% | 6 | 3,47% |
Meurgey (2011) | 13 | 2,24% | 11 | 5,98% | 11 | 6,55% | 11 | 6,36% |
Waterhouse (1875) | 13 | 2,24% | 2 | 1,09% | 2 | 1,19% | 0 | 0% |
Jourdan & Mille (2006) | 12 | 2,07% | 11 | 5,98% | 11 | 6,55% | 11 | 6,36% |
Linnaeus (1758) | 12 | 2,07% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Vernon & Voisin (1991) | 12 | 2,07% | 8 | 4,35% | 8 | 4,76% | 7 | 4,05% |
Voisin et al. (2016) | 12 | 2,07% | 6 | 3,26% | 6 | 3,57% | 6 | 3,47% |
Viette (1959) | 11 | 1,89% | 5 | 2,72% | 5 | 2,98% | 5 | 2,89% |
Enderlein (1909) | 10 | 1,72% | 7 | 3,8% | 7 | 4,17% | 7 | 4,05% |
Hullé et al. (2010) | 10 | 1,72% | 10 | 5,43% | 10 | 5,95% | 10 | 5,78% |
Schiner (1868) | 10 | 1,72% | 6 | 3,26% | 6 | 3,57% | 6 | 3,47% |
Séguy (1944) | 10 | 1,72% | 6 | 3,26% | 6 | 3,57% | 6 | 3,47% |
Chown & Kuschel (1994) | 9 | 1,55% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Dreux & Voisin (1969) | 9 | 1,55% | 7 | 3,8% | 7 | 4,17% | 6 | 3,47% |
Eaton et al. (1879) | 9 | 1,55% | 5 | 2,72% | 5 | 2,98% | 3 | 1,73% |
Giebel (1876) | 9 | 1,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Vayssières et al. (2001) | 9 | 1,55% | 8 | 4,35% | 8 | 4,76% | 8 | 4,62% |
Denux & Zagatti (2010) | 8 | 1,38% | 8 | 4,35% | 8 | 4,76% | 8 | 4,62% |
Etienne (2005) | 8 | 1,38% | 8 | 4,35% | 8 | 4,76% | 8 | 4,62% |
Frenot et al. (1988) | 8 | 1,38% | 7 | 3,8% | 7 | 4,17% | 4 | 2,31% |
Tronquet (2014) | 8 | 1,38% | 8 | 4,35% | 8 | 4,76% | 8 | 4,62% |
Albouy & Richard (2017) | 7 | 1,2% | 6 | 3,26% | 6 | 3,57% | 6 | 3,47% |
Remaudière & Etienne (1988) | 7 | 1,2% | 7 | 3,8% | 7 | 4,17% | 7 | 4,05% |
Dreux & Voisin (1986) | 6 | 1,03% | 2 | 1,09% | 0 | 0% | 2 | 1,16% |
Gomy (2000) | 6 | 1,03% | 4 | 2,17% | 4 | 2,38% | 4 | 2,31% |
Kieffer (1902) | 6 | 1,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Peck et al. (2014) | 6 | 1,03% | 6 | 3,26% | 6 | 3,57% | 6 | 3,47% |
Albouy et al. (2017) | 5 | 0,86% | 5 | 2,72% | 5 | 2,98% | 5 | 2,89% |
Chastel & Beaucournu (1992) | 5 | 0,86% | 3 | 1,63% | 2 | 1,19% | 3 | 1,73% |
Fauvel (1867) | 5 | 0,86% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Hullé et al. (2003) | 5 | 0,86% | 5 | 2,72% | 5 | 2,98% | 5 | 2,89% |
Mille et al. (2020) | 5 | 0,86% | 5 | 2,72% | 5 | 2,98% | 5 | 2,89% |
Monod & Dollfus (1932) | 5 | 0,86% | 5 | 2,72% | 5 | 2,98% | 3 | 1,73% |
Voisin et al. (2014) | 5 | 0,86% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Clarke (1971) | 4 | 0,69% | 4 | 2,17% | 4 | 2,38% | 4 | 2,31% |
[Denis & Schiffermüller] (1775) | 4 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1905) | 4 | 0,69% | 4 | 2,17% | 4 | 2,38% | 4 | 2,31% |
Gomy et al. (2016) | 4 | 0,69% | 4 | 2,17% | 4 | 2,38% | 4 | 2,31% |
Guillermet (2004) | 4 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Heller (1916) | 4 | 0,69% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Kieffer (1902-1904) | 4 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1907-1911) | 4 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Martiré & Rochat (2008) | 4 | 0,69% | 4 | 2,17% | 4 | 2,38% | 4 | 2,31% |
Meurgey & Picard (2011) | 4 | 0,69% | 4 | 2,17% | 4 | 2,38% | 4 | 2,31% |
Questel & Le Quellec (2012) | 4 | 0,69% | 4 | 2,17% | 4 | 2,38% | 4 | 2,31% |
Questel (2020) | 4 | 0,69% | 4 | 2,17% | 4 | 2,38% | 4 | 2,31% |
Azam (1893) | 3 | 0,52% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Badonnel (1947) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Barbut & Voisin (2014) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Beaucournu-Saguez & Vernon (1990) | 3 | 0,52% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Chapelin-Viscardi et al. (2010) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Delettre (1985) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Delettre (1986) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
, 3: 249-270.">Enderlein (1903) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne & Vilardebó (1978) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Evenhuis (2018) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Fairmaire (1849) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Geer (1774) | 3 | 0,52% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Grand et al. (2014) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Gutierrez (1981) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Hammes & Putoa (1986) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Jourdan (2020) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Martinez-Torres et al. (1997) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Matile (1975) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1860) | 3 | 0,52% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Peck (2011) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Renault (2011) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Rispe et al. (1999) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Seguy (1965) | 3 | 0,52% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Séguy (1965) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 0 | 0% |
Simon et al. (1991) | 3 | 0,52% | 3 | 1,63% | 3 | 1,79% | 3 | 1,73% |
Voisin et al. (2015) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamska & Grzywacz (2019) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Aubert & Beaucournu (1976) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Azab et al. (1972) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Badonnel (1970) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Beaucournu & Chastel (1992) | 2 | 0,34% | 2 | 1,09% | 0 | 0% | 2 | 1,16% |
Beaucournu & Rodhain (1990) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Bell et al. (1989) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Bellemare & Brunelle (1950) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Bonfils (1969) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Borovec (1991) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer & Rivault (2003) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Cerkowniak et al. (2020) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Couteyen & Papazian (2012) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Dadant & Etienne (1973) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Daly et al. (2023) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
De Meillon (1952) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreux & Voisin (1984) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreux & Voisin (1987) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Dreux & Voisin (1988) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1909) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne et al. (2015) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Evenhuis & Barbotin (1977) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1862) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1891) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Fauvel (1903) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Fauvel (1903) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontenot et al. (2015) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Fourcroy (1785) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Frey (1948) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Grand et al. (2019) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Guillermet (2011) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Hale et al. (2008) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Hava (2006) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Háva (2014) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Hidalgo et al. (2013) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Hindermeyer et al. (2007) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Hossain et al. (2016) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Jeannel (1947) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Jones et al. (2006) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Jones et al. (2007) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Kieffer (1898) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Laparie & Renault (2014) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Leraut (1997) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1847) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Macquart (1835) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1933) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Meganck et al. (2017) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Mey (2010) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Montrouzier (1861) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulian (1998) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Pilgrim (1998) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 0 | 0% |
Pistil & Kontykowski (1974) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Pujade-Villar et al. (2007) | 2 | 0,34% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rakowski et al. (1981) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Rambur (1829) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Renault et al. (2014) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 0 | 0% |
Robineau-Desvoidy (1841) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Rognes & Blackith (1990) | 2 | 0,34% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Séguy (1954) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Serra-Tosio (1986) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Soldati & Touroult (2014) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Tavakilian & Chevillotte (2013) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Thomas (2015) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Vilkamaa & Menzel (2019) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Withers & Chandler (2019) | 2 | 0,34% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Yang et al. (2023) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Yokoyama (2013) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Zanetti et al. (2016) | 2 | 0,34% | 2 | 1,09% | 2 | 1,19% | 2 | 1,16% |
Abdel-kader & Barak (1979) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Allen et al. (2022) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Anonyme (2018) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Ascete (2021) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Bagnall (1927) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Baylac (1980) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Belon & Mulsant (1881) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Błeszyński & Collins (1962) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Bigot (1992) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Billi (2009) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Blair (1934) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Blair (1934) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Blanchot (1992) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Blas (2014) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Bleeckere (2001) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Boisduval (1833) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Bouget et al. (2019) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Bournier & Mound (2000) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Bournier (2000) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Brindle (1971) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Brindle (1975) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Brindle (1976) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Brown (1929) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Burr (1914) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Cerkowniak et al. (2017) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Cheesman (1927) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Cheesman (1928) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Chekchak et al. (2000) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Chopard (1924) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Clemens (1860) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1966) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Cochereau (1974) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Cohic (1959) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Colijn et al. (2020) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Crotch (1867) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Damoiseau (1966) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Davies (1965) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1773) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Deeming (1979) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Delhaes et al. (2001) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Devaud & Lebouvier (2019) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Dewynter et al. (2022) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Dreux et al. (1992) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Enderlein (1903) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1936) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2012) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Evenhuis (2012) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Fabricius (1775) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fain & Beaucournu (1984) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 0 | 0% |
Fain (1977) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 0 | 0% |
Fairmaire (1850) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Fallén (1823) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1877) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer (2015) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Ferrer-Suay et al. (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-Suay et al. (2015) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Ferrer-Suay et al. (2018) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Frauenfeld (1858) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Gadeau de Kerville (1894) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste & Hervé (2009) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Geoffroy (1762) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Goetghebuer (1944) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Goeze (1777) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Gonzales et al. (2014) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
González-Miguéns et al. (2020) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Green & Turner (2003) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Haliday (1834) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Hartig (1841) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hava & Poussereau (2017) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Hayashi (1961) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Hebard (1933) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Hebard (1933) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Heppner (2010) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Hinton (1941) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoddle et al. (2008) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Holloway (1979) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Honey & Scoble (2001) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1766) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hustache (1920) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hynes (1993) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2013) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Jarrige & Voisin (1968) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Jeannel (1953) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Johannsen (1912) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaszab (1982) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Kaszab (1985) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Kolenati (1846) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolibáč (2013) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Kumar et al. (1988) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Kuschel (2008) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacomme (2013) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Lafranchis (2014) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Lafranchis (2016) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Lagarde (2008) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Lamb (1914) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
.">Lambret & Lebouvier (2006) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Maitre & Chadee (1983) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Lemagnen (2015) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Lieftinck (1966) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Lieftinck (1975) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Linnaeus (1767) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1932) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Malloch (1932) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Marinov et al. (2016) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Marinov et al. (2019) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Marinov et al. (2021) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Martin-vega et al. (2017) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Martiré (2010) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Meigen (1818) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Menezes et al. (2005) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Menezes et al. (2006) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Menzel & Vilkamaa (2021) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Mercier (1924) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Mériguet & Zagatti (2016) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Meyrick (1893) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Minot (2016) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Moubayed-Breil et al. (2017) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Moulton (1907) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Munari et al. (2020) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Munari (1988) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Munari (2007) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Munari (2013) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Muru et al. (2017) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Olivier (1791-[1792]) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Osuji (1975) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Osuji (1975) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Papazian et al. (2007) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Parnaudeau (2012) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Perrin et al. (2007) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre & Lalanne-Cassou | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Poussereau et al. (2013) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Quindroit & Lemoine (2022) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Quindroit (2020) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rageau (1956) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rageau (1959) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Reeves et al. (2004) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rehn (1949) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Remillet (1988) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rheinheimer (2014) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rheinheimer (2015) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Ris (1915) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rivault et al. (1991) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rosenbaum et al. (2015) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Rossi (1792) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruecker (2005) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Samways (2003) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Sardet et al. (2015) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Schrank (1781) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Sculfort & Dewynter (2024) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Shaaya (1981) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Shahhosseini (1980) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Shinonaga et al. (1991) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Shiraki (1906) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Siddaiah & Kujur (2016) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Siroux (2010) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Skierska (1976) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Starý et al. (1994) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Stefanescu et al. (2012) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Steffan (1972) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Stein (1911) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Stierlin (1861) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Sudre et al. (2010) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Theodorides (1955) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Tonnoir (1940) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Tourlan (2018) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Touroult et al. (2015) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Trehen & Voisin (1984) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Tronquet (2016) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaillant (2000) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Viette (1949) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Viette (1979) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Vincent & Voisin (1991) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Voisin (1975) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Voisin (1986) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |
Walker (1865) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Westwood (1839) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Zanetti et al. (2020) | 1 | 0,17% | 1 | 0,54% | 1 | 0,6% | 1 | 0,58% |