Névroptères
Neuroptera
254 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Aspock et al. (1980) | 53 | 7,16% | 8 | 2,61% | 8 | 2,68% | 8 | 2,65% |
Tillier (2015) | 45 | 6,08% | 40 | 13,03% | 40 | 13,38% | 40 | 13,25% |
Ohm & Hölzel (1998) | 34 | 4,59% | 28 | 9,12% | 28 | 9,36% | 27 | 8,94% |
Canard et al. (2014) | 30 | 4,05% | 20 | 6,51% | 20 | 6,69% | 19 | 6,29% |
Ohm & Hölzel (1997) | 24 | 3,24% | 21 | 6,84% | 21 | 7,02% | 21 | 6,95% |
Breitkreuz et al. (2021) | 17 | 2,3% | 17 | 5,54% | 17 | 5,69% | 16 | 5,3% |
Dobosz (2010) | 17 | 2,3% | 17 | 5,54% | 17 | 5,69% | 17 | 5,63% |
Ardila-Camacho et al. (2024) | 14 | 1,89% | 10 | 3,26% | 10 | 3,34% | 10 | 3,31% |
Ramage (2017) | 14 | 1,89% | 14 | 4,56% | 14 | 4,68% | 14 | 4,64% |
Thierry & Canard (2021) | 13 | 1,76% | 12 | 3,91% | 12 | 4,01% | 12 | 3,97% |
Esben-Petersen (1937) | 12 | 1,62% | 12 | 3,91% | 12 | 4,01% | 12 | 3,97% |
Hoffman et al. (2002) | 12 | 1,62% | 12 | 3,91% | 12 | 4,01% | 12 | 3,97% |
Meurgey & Ramage (2020) | 11 | 1,49% | 11 | 3,58% | 11 | 3,68% | 11 | 3,64% |
Thierry et al. (2022) | 11 | 1,49% | 11 | 3,58% | 11 | 3,68% | 11 | 3,64% |
Monserrat (2011) | 9 | 1,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Ardila-Camacho et al. (2023) | 7 | 0,95% | 7 | 2,28% | 7 | 2,34% | 7 | 2,32% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 7 | 0,95% | 6 | 1,95% | 6 | 2,01% | 6 | 1,99% |
Jones & Badano (2021) | 7 | 0,95% | 7 | 2,28% | 7 | 2,34% | 7 | 2,32% |
Meurgey (2011) | 7 | 0,95% | 6 | 1,95% | 6 | 2,01% | 6 | 1,99% |
Tillier (2016) | 7 | 0,95% | 7 | 2,28% | 7 | 2,34% | 7 | 2,32% |
Hölzel & Ohm (2000) | 6 | 0,81% | 2 | 0,65% | 0 | 0% | 2 | 0,66% |
Nakahara (1960) | 6 | 0,81% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Rambur (1842) | 6 | 0,81% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Thierry & Canard (2019) | 6 | 0,81% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Vayssières et al. (2001) | 6 | 0,81% | 5 | 1,63% | 5 | 1,67% | 5 | 1,66% |
Cheesman (1927) | 5 | 0,68% | 5 | 1,63% | 5 | 1,67% | 5 | 1,66% |
Nicolas (2022) | 5 | 0,68% | 5 | 1,63% | 4 | 1,34% | 5 | 1,66% |
Séméria & Quilici (1986) | 5 | 0,68% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Stephens (1835-1836) | 5 | 0,68% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier (2011) | 5 | 0,68% | 5 | 1,63% | 5 | 1,67% | 5 | 1,66% |
Albouy et al. (2017) | 4 | 0,54% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Canard et al. (2007) | 4 | 0,54% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Canard (1981) | 4 | 0,54% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Esben-petersen (1935) | 4 | 0,54% | 4 | 1,3% | 4 | 1,34% | 4 | 1,32% |
Giacomino (2016) | 4 | 0,54% | 4 | 1,3% | 4 | 1,34% | 4 | 1,32% |
Lacroix (1919) | 4 | 0,54% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Navás (1927) | 4 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Ohm (1965) | 4 | 0,54% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Pictet (1865) | 4 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Rausch & Weissmair (2007) | 4 | 0,54% | 4 | 1,3% | 4 | 1,34% | 4 | 1,32% |
Schneider (1851) | 4 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 4 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Banks (1920) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard & Labrique (1989) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard (1985) | 3 | 0,41% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Colombo & Pichard (2015) | 3 | 0,41% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Giacomino (2015) | 3 | 0,41% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Hoffman et al. (2017) | 3 | 0,41% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Hölzel (1965) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Kimmins (1932) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Kimmins (1960) | 3 | 0,41% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Lacroix (1915) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1988) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 3 | 0,41% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Navás (1901) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Tjeder (1940) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Vansteene (2018) | 3 | 0,41% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Vidal (2023) | 3 | 0,41% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Villers (1789) | 3 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 3 | 0,41% | 3 | 0,98% | 3 | 1% | 3 | 0,99% |
Abraham (2013) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Adams (1982) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Ardila Camacho & Jones (2012) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Aspock & Aspock (1964) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Aspöck & Aspöck (1995) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Aspöck et al. 2001 | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Aspock (1963) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Badano et al. (2018) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Baliteau (2016) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Borkhausen (1791) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Brauer (1851) | 2 | 0,27% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Canard & Monserrat (2019) | 2 | 0,27% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Canard & Thierry (2020) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Colombo et al. (2012) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
D'agostino (2023) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Dobosz (2008) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Duelli et al. (2024) | 2 | 0,27% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Fabricius (1793) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenescheau et al. (2020) | 2 | 0,27% | 2 | 0,65% | 0 | 0% | 2 | 0,66% |
Hagen (1864) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Henry et al. (2002) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Henry et al. (2003) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Hölzel & Ohm (1991) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Holzel & Ohm (1995) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Holzel (1974) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2020) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Kimmins (1958) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Kis & Ujhelyi (1965) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Lacroix (1913) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1913) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1915) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1915) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1988) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1989) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1991) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1992) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1764) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Machado & Rafael (2010) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Machado (2018) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Mclachlan (1893) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 0 | 0% |
Monserrat (1976) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Monserrat (1977) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Monserrat (1977) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Navás (1903) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1904) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1905) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1907) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1910) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1911) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1913) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Navás (1914) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1916) | 2 | 0,27% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Navás (1935) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Panis & Kreiter (2008) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Pantaleoni et al. (2010) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Peslier (2002) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Rausch & Aspock (1978) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Réal (1968) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi (1790) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Rousset (1964) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Séméria et al. (29-30) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Séméria (1976) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Stange & Miller (2018) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Steinmann (1963) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Sziraki (2020) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Thierry & Canard (2020) | 2 | 0,27% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier et al. (2014) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Tillier (2012) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Tillier (2013) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Vago (2009) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Zelený (1962) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Zelený (1963) | 2 | 0,27% | 2 | 0,65% | 2 | 0,67% | 2 | 0,66% |
Zilli (2021) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ábrahám & Dobosz (2011) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Andrèu (1911) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Armand & Pélissié (2023) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Aspock & Aspock (1965) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Banks (1895) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Burmeister (1839) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard & Jacquemin (2013) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard & Thierry (2015) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Canard & Thierry (2017) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard & Thierry (2019) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Canard et al. (2015) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Canard et al. (2021) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Canard et al. (2021) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Cochereau (1974) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Cocquemont & Chambon (1990) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Colombo et al. (2013) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Cotte (2018) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Dobosz et al. (2019) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Dobsz & Levente (2014) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Enderlein (1906) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne et al. (2018) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Fabricius (1787) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fitch (1855) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Fourcroy (1785) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerstaecker (1888) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Giacomino (2007) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Giacomino (2009) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Giacomino (2010) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Giacomino (2011) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Gruppe et al. (2024) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Gruppe (2007) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Hagen (1860) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hagen (1866) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Hölzel (1965) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hölzel (1972) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hölzel (1972) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hölzel (1974) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Jacquemin & Canard (2006) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Killington (1935) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Kimmins (1936) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Kimmins (1963) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1933) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1933) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lagarde & Tillier (2019) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Latreille (1807) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1988) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Leraut (1991) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Leraut (1991) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Letardi et al. (2008) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Linnaeus (1767) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Luquet (1983) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Machado & Oswald (2020) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Maclachlan (1887) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Mazel (2003) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Mazel (2004) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclachlan (1866) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Mclachlan (1898) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mille et al. (2020) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Monserrat et al. (2014) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Monserrat (1975) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Monserrat (1994) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1906) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1908) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1909) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Navás (1909) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1910) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1912) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1912) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1912) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1913) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1913) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1915) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Navás (1916) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Navás (1918) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1919) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1924) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1926) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1926) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1930) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1931) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1932) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bollettino della Societa Entomologica Italiana, 65: 105-113.">Navas (1933) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ohm (1967) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Oswald (1988) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Pallas (1771) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Poda von Neuhaus (1761) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Poujade (1878) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Rambur (1837-1840) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1838) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Selys Longchamps (1888) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Semeria (1991) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Siedle & Pfender (1988) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Stein (1863) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Tauber (2007) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier & Colombo (2016) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier & Mangot (2019) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier et al. (2018) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier et al. (2020) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier (2008) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Tillier (2009) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier (2010) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tillier (2011) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tjeder (1941) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Tjeder (1960) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Tjeder (1967) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2020) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Touroult et al. (2021) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Vincent (1984) | 1 | 0,14% | 1 | 0,33% | 1 | 0,33% | 1 | 0,33% |
Walker (1860) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Wesmael (1841) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Westwood (1867) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Zetterstedt ([1838]-1840) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |