Névroptères de France métropolitaine
197 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 | 11,37% | 8 | 4,42% | 8 | 4,55% | 8 | 4,49% |
Tillier (2015) | 45 | 9,66% | 40 | 22,1% | 40 | 22,73% | 40 | 22,47% |
Canard et al. (2014) | 30 | 6,44% | 20 | 11,05% | 20 | 11,36% | 19 | 10,67% |
Breitkreuz et al. (2021) | 16 | 3,43% | 16 | 8,84% | 16 | 9,09% | 15 | 8,43% |
Monserrat (2011) | 9 | 1,93% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 7 | 1,5% | 6 | 3,31% | 6 | 3,41% | 6 | 3,37% |
Tillier (2016) | 7 | 1,5% | 7 | 3,87% | 7 | 3,98% | 7 | 3,93% |
Rambur (1842) | 6 | 1,29% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Thierry & Canard (2019) | 6 | 1,29% | 3 | 1,66% | 3 | 1,7% | 3 | 1,69% |
Stephens (1835-1836) | 5 | 1,07% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier (2011) | 5 | 1,07% | 5 | 2,76% | 5 | 2,84% | 5 | 2,81% |
Albouy et al. (2017) | 4 | 0,86% | 3 | 1,66% | 3 | 1,7% | 3 | 1,69% |
Canard et al. (2007) | 4 | 0,86% | 3 | 1,66% | 3 | 1,7% | 3 | 1,69% |
Canard (1981) | 4 | 0,86% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Giacomino (2016) | 4 | 0,86% | 4 | 2,21% | 4 | 2,27% | 4 | 2,25% |
Ohm (1965) | 4 | 0,86% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Pictet (1865) | 4 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Rausch & Weissmair (2007) | 4 | 0,86% | 4 | 2,21% | 4 | 2,27% | 4 | 2,25% |
Schneider (1851) | 4 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 4 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard & Labrique (1989) | 3 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard (1985) | 3 | 0,64% | 3 | 1,66% | 3 | 1,7% | 3 | 1,69% |
Colombo & Pichard (2015) | 3 | 0,64% | 3 | 1,66% | 3 | 1,7% | 3 | 1,69% |
Hölzel (1965) | 3 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1915) | 3 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1988) | 3 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 3 | 0,64% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Navás (1901) | 3 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Tjeder (1940) | 3 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Vansteene (2018) | 3 | 0,64% | 3 | 1,66% | 3 | 1,7% | 3 | 1,69% |
Vidal (2023) | 3 | 0,64% | 3 | 1,66% | 3 | 1,7% | 3 | 1,69% |
Villers (1789) | 3 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Aspock & Aspock (1964) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Aspöck & Aspöck (1995) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Aspöck et al. 2001 | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Aspock (1963) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Baliteau (2016) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Borkhausen (1791) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Brauer (1851) | 2 | 0,43% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Canard & Monserrat (2019) | 2 | 0,43% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Canard & Thierry (2020) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Colombo et al. (2012) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
D'agostino (2023) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Duelli et al. (2024) | 2 | 0,43% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Fabricius (1793) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenescheau et al. (2020) | 2 | 0,43% | 2 | 1,1% | 0 | 0% | 2 | 1,12% |
Hagen (1864) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Henry et al. (2002) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Henry et al. (2003) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Holzel (1974) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Kis & Ujhelyi (1965) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Lacroix (1913) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1913) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1915) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1915) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1988) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1989) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1991) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1992) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1764) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclachlan (1893) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 0 | 0% |
Monserrat (1976) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Monserrat (1977) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Monserrat (1977) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Navás (1903) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1904) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1905) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1907) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1911) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1914) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1916) | 2 | 0,43% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Panis & Kreiter (2008) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Pantaleoni et al. (2010) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Peslier (2002) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Rausch & Aspock (1978) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Réal (1968) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi (1790) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Rousset (1964) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Séméria et al. (29-30) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Séméria (1976) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Steinmann (1963) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Sziraki (2020) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Thierry & Canard (2020) | 2 | 0,43% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier et al. (2014) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Tillier (2012) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Tillier (2013) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Vago (2009) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Zelený (1962) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Zelený (1963) | 2 | 0,43% | 2 | 1,1% | 2 | 1,14% | 2 | 1,12% |
Zilli (2021) | 2 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrèu (1911) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Armand & Pélissié (2023) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Aspock & Aspock (1965) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Burmeister (1839) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard & Jacquemin (2013) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard & Thierry (2015) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Canard & Thierry (2017) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Canard & Thierry (2019) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Canard et al. (2015) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Canard et al. (2021) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Canard et al. (2021) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Cocquemont & Chambon (1990) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Colombo et al. (2013) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Cotte (2018) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Dobosz et al. (2019) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1906) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Giacomino (2007) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Giacomino (2009) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Giacomino (2010) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Giacomino (2011) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Gruppe et al. (2024) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Gruppe (2007) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Hagen (1860) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hagen (1866) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Hölzel (1965) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hölzel (1972) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hölzel (1972) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hölzel (1974) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Jacquemin & Canard (2006) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Killington (1935) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Kimmins (1963) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1933) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1933) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Lagarde & Tillier (2019) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Latreille (1807) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1988) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Leraut (1991) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Leraut (1991) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Letardi et al. (2008) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Linnaeus (1767) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Luquet (1983) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Maclachlan (1887) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Mazel (2003) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Mazel (2004) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclachlan (1866) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Mclachlan (1898) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Monserrat et al. (2014) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Monserrat (1975) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Monserrat (1994) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1906) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1908) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1909) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1909) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Navás (1910) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1912) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1912) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1912) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1913) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1913) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Navás (1916) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Navás (1918) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1919) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1924) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1926) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1926) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1930) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1931) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1932) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Bollettino della Societa Entomologica Italiana, 65: 105-113.">Navas (1933) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Ohm & Hölzel (1997) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Ohm (1967) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Pallas (1771) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Poda von Neuhaus (1761) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Poujade (1878) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Rambur (1837-1840) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1838) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Selys Longchamps (1888) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Séméria & Quilici (1986) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Semeria (1991) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Siedle & Pfender (1988) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Stein (1863) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Thierry & Canard (2021) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier & Colombo (2016) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier & Mangot (2019) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier et al. (2018) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier et al. (2020) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier (2008) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Tillier (2009) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier (2010) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tillier (2011) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tjeder (1941) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Tjeder (1960) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Tjeder (1967) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Vincent (1984) | 1 | 0,21% | 1 | 0,55% | 1 | 0,57% | 1 | 0,56% |
Wesmael (1841) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Zetterstedt ([1838]-1840) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |