Trichoptères de France métropolitaine
Trichoptera de France métropolitaine
142 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Coppa & Tachet (2016) | 557 | 38,6% | 477 | 84,72% | 446 | 84,63% | 456 | 84,13% |
OPIE (2012) | 50 | 3,47% | 39 | 6,93% | 35 | 6,64% | 39 | 7,2% |
Thomson (2023) | 45 | 3,12% | 45 | 7,99% | 45 | 8,54% | 45 | 8,3% |
Oláh et al. (2022) | 23 | 1,59% | 21 | 3,73% | 21 | 3,98% | 21 | 3,87% |
Mosely (1932) | 22 | 1,52% | 16 | 2,84% | 16 | 3,04% | 16 | 2,95% |
Oláh et al. (2017) | 21 | 1,46% | 21 | 3,73% | 21 | 3,98% | 21 | 3,87% |
Brauer (1857) | 18 | 1,25% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Oláh et al. (2014) | 18 | 1,25% | 18 | 3,2% | 18 | 3,42% | 18 | 3,32% |
Coppa & Tachet (2023) | 16 | 1,11% | 15 | 2,66% | 14 | 2,66% | 15 | 2,77% |
Mosely (1934) | 14 | 0,97% | 11 | 1,95% | 11 | 2,09% | 11 | 2,03% |
Botosaneanu & Giudicelli (2004) | 13 | 0,9% | 12 | 2,13% | 8 | 1,52% | 12 | 2,21% |
Olah et al. (2015) | 13 | 0,9% | 13 | 2,31% | 13 | 2,47% | 13 | 2,4% |
Marle et al. (2017) | 12 | 0,83% | 12 | 2,13% | 12 | 2,28% | 11 | 2,03% |
Oláh et al. (2015) | 11 | 0,76% | 5 | 0,89% | 5 | 0,95% | 5 | 0,92% |
Coppa & Tachet (2017) | 10 | 0,69% | 7 | 1,24% | 7 | 1,33% | 7 | 1,29% |
Linnaeus (1758) | 10 | 0,69% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Archives de Zoologie Experimentale et Generale, 97: 32-50.">Botosaneanu (1959) | 9 | 0,62% | 9 | 1,6% | 9 | 1,71% | 3 | 0,55% |
Coppa & Barnasson (2016) | 9 | 0,62% | 8 | 1,42% | 8 | 1,52% | 8 | 1,48% |
Hagen (1864) | 9 | 0,62% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Mosely (1930) | 9 | 0,62% | 6 | 1,07% | 6 | 1,14% | 6 | 1,11% |
Sipahiler (1992) | 9 | 0,62% | 6 | 1,07% | 6 | 1,14% | 6 | 1,11% |
Mosely (1935) | 8 | 0,55% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Oláh et al. (2020) | 8 | 0,55% | 8 | 1,42% | 8 | 1,52% | 8 | 1,48% |
Coppa & Guellec (2017) | 7 | 0,49% | 7 | 1,24% | 7 | 1,33% | 7 | 1,29% |
Olah et al. (2013) | 7 | 0,49% | 7 | 1,24% | 7 | 1,33% | 7 | 1,29% |
Sipahiler (1993) | 7 | 0,49% | 5 | 0,89% | 5 | 0,95% | 5 | 0,92% |
Coppa (2017) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Décamps (1972) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 6 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Sipahiler (1993) | 6 | 0,42% | 6 | 1,07% | 0 | 0% | 6 | 1,11% |
Sipahiler (1999) | 6 | 0,42% | 6 | 1,07% | 6 | 1,14% | 6 | 1,11% |
Curtis (1834) | 5 | 0,35% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Curtis (1834) | 5 | 0,35% | 4 | 0,71% | 4 | 0,76% | 4 | 0,74% |
Malicky (2002) | 5 | 0,35% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Navás (1919) | 5 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Valladolid et al. (2021) | 5 | 0,35% | 4 | 0,71% | 4 | 0,76% | 4 | 0,74% |
Andersen et al. (2019) | 4 | 0,28% | 4 | 0,71% | 4 | 0,76% | 4 | 0,74% |
Barnasson (2020) | 4 | 0,28% | 4 | 0,71% | 4 | 0,76% | 0 | 0% |
Botosaneanu (1994) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousquet (2016) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppa et al. (2004) | 4 | 0,28% | 4 | 0,71% | 4 | 0,76% | 4 | 0,74% |
Malicky (2004) | 4 | 0,28% | 4 | 0,71% | 4 | 0,76% | 4 | 0,74% |
Malicky (2018) | 4 | 0,28% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Oláh et al. (2018) | 4 | 0,28% | 4 | 0,71% | 4 | 0,76% | 4 | 0,74% |
Schrank (1781) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Tachet et al. (2001) | 4 | 0,28% | 4 | 0,71% | 4 | 0,76% | 4 | 0,74% |
Vaillant (1974) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Valladolid et al. (2018) | 4 | 0,28% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Botosaneanu & Giudicelli (1983) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Botosaneanu (2000) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppa & Gonzalez (2007) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Coppa (2004) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Décamps (1966) | 3 | 0,21% | 3 | 0,53% | 2 | 0,38% | 3 | 0,55% |
Decamps & Magne (1966) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Decamps (1965) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Decamps (1971) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Despax (1933) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Fourcroy (1785) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Kelner-Pillault (1961) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Moretti et al. (1994) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmid (1971) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Sipahiler (2000) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Statzner & Bretschko (1998) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Waringer et al. (2011) | 3 | 0,21% | 3 | 0,53% | 3 | 0,57% | 3 | 0,55% |
Botosaneanu & Dumont (2003) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Botosaneanu & Giudicelli (1981) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Botosaneanu & Giudicelli (2001) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Botosaneanu & Giudicelli (2004) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Bournaud & Gautheron-Duranthon (1969) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer de Fonscolombe (1846) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppa & Guellec (2021) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Coppa & Malicky (2005) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Coppa et al. (2022) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Coppa (2011) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Coppa (2017) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Dobson (1999) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Doledec (1987) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Fabricius (1793) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Giudicelli & Botosaneanu (1999) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Graf et al. (2015) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Guellec et al. (2013) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Guellec et al. (2023) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Lavandier (1992) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Le Guellec et al. (2020) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Lenormand et al. (2019) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 1 | 0,18% |
Leraut (2024) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Malicky (1972) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Malicky (1980) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Mangot & Rousseau (2022) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Mclachlan (1879) | 2 | 0,14% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Moretti (1981) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Oláh & Kovacs (2014) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Rázuri-gonzales et al. (2024) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Sipahiler (1995) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Sipahiler (2001) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Tobias (1972) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Valladolid et al. (2023) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Waringer & Coppa (2021) | 2 | 0,14% | 2 | 0,36% | 2 | 0,38% | 2 | 0,37% |
Albouy et al. (2017) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Bertuetti et al. (2004) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Botosaneanu (1980) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppa & Tachet (2010) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Coppa et al. (2016) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Coppa et al. (2017) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Coppa et al. (2021) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Coppa (2004) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Coppa (2005) | 1 | 0,07% | 1 | 0,18% | 0 | 0% | 1 | 0,18% |
Coppa (2010) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Coppa (2016) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Fabricius (1787) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
González & Terra (1979) | 1 | 0,07% | 1 | 0,18% | 0 | 0% | 1 | 0,18% |
Guellec (2011) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Jacquemin & Coppa (2013) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Jacquemin & Coppa (2015) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Jacquemin et al. (2019) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Kirby & Spence (1826) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Labat et al. (2019) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Le Guellec et al. (2016) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Linnaeus (1761) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Malicky (1998) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Marle et al. (2019) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Mclachlan (1866) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Mclachlan (1874-1880) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Mclachlan (1895) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Moretti & Taticchi (1992) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Moretti (1991) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Morse (1975) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Navas (1915) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1917) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1932) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Neu (2015) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Oláh & Kovacs (2012) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Oláh et al. (2021) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Pictet (1865) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Rambur (1842) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ris (1903) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Schmid (1947) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Scopoli (1763) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephens (1835-1836) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Tachet (2014) | 1 | 0,07% | 1 | 0,18% | 1 | 0,19% | 1 | 0,18% |
Zilli (2021) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |