Trichoptères
Trichoptera
214 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) | 558 | 27,82% | 477 | 45,13% | 446 | 43,81% | 456 | 44,1% |
Thomson (2023) | 203 | 10,12% | 203 | 19,21% | 200 | 19,65% | 203 | 19,63% |
Espeland et al. (2020) | 167 | 8,33% | 167 | 15,8% | 167 | 16,4% | 167 | 16,15% |
Oláh & Johanson (2011) | 74 | 3,69% | 70 | 6,62% | 70 | 6,88% | 70 | 6,77% |
Botosaneanu (2002) | 69 | 3,44% | 68 | 6,43% | 65 | 6,39% | 68 | 6,58% |
Johanson et al. (2020) | 54 | 2,69% | 54 | 5,11% | 54 | 5,3% | 54 | 5,22% |
Johanson & Wells (2019) | 52 | 2,59% | 51 | 4,82% | 51 | 5,01% | 51 | 4,93% |
Olah et al. (2006) | 52 | 2,59% | 0 | 0% | 0 | 0% | 0 | 0% |
OPIE (2012) | 50 | 2,49% | 39 | 3,69% | 35 | 3,44% | 39 | 3,77% |
Botosaneanu (1994) | 48 | 2,39% | 40 | 3,78% | 34 | 3,34% | 40 | 3,87% |
Wells & Johanson (2015) | 47 | 2,34% | 45 | 4,26% | 45 | 4,42% | 45 | 4,35% |
Meurgey (2011) | 43 | 2,14% | 40 | 3,78% | 38 | 3,73% | 40 | 3,87% |
Meurgey & Ramage (2020) | 42 | 2,09% | 41 | 3,88% | 39 | 3,83% | 41 | 3,97% |
Johanson & Ward (2009) | 40 | 1,99% | 40 | 3,78% | 40 | 3,93% | 40 | 3,87% |
Ward & Schefter (2000) | 40 | 1,99% | 38 | 3,6% | 38 | 3,73% | 38 | 3,68% |
Mary (2017) | 37 | 1,84% | 35 | 3,31% | 35 | 3,44% | 35 | 3,38% |
Kelley (1989) | 36 | 1,79% | 36 | 3,41% | 36 | 3,54% | 36 | 3,48% |
Johanson (1999) | 34 | 1,69% | 34 | 3,22% | 34 | 3,34% | 34 | 3,29% |
Oláh & Oláh (2017) | 30 | 1,5% | 30 | 2,84% | 30 | 2,95% | 30 | 2,9% |
Geraci et al. (2010) | 28 | 1,4% | 28 | 2,65% | 28 | 2,75% | 28 | 2,71% |
Johanson & Schefter (1999) | 28 | 1,4% | 28 | 2,65% | 28 | 2,75% | 28 | 2,71% |
Ross (1975) | 25 | 1,25% | 25 | 2,37% | 25 | 2,46% | 25 | 2,42% |
Malm & Johanson (2008) | 23 | 1,15% | 23 | 2,18% | 23 | 2,26% | 23 | 2,22% |
Oláh et al. (2022) | 23 | 1,15% | 21 | 1,99% | 21 | 2,06% | 21 | 2,03% |
Mosely (1932) | 22 | 1,1% | 16 | 1,51% | 16 | 1,57% | 16 | 1,55% |
Johanson & Keijsner (2008) | 21 | 1,05% | 21 | 1,99% | 21 | 2,06% | 21 | 2,03% |
Oláh et al. (2017) | 21 | 1,05% | 21 | 1,99% | 21 | 2,06% | 21 | 2,03% |
Botosaneanu (1988) | 19 | 0,95% | 15 | 1,42% | 15 | 1,47% | 15 | 1,45% |
Brauer (1857) | 18 | 0,9% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Oláh & Johanson (2012) | 18 | 0,9% | 18 | 1,7% | 18 | 1,77% | 18 | 1,74% |
Oláh et al. (2014) | 18 | 0,9% | 18 | 1,7% | 18 | 1,77% | 18 | 1,74% |
Wells & Johanson (2012) | 18 | 0,9% | 18 | 1,7% | 18 | 1,77% | 18 | 1,74% |
Coppa & Tachet (2023) | 17 | 0,85% | 16 | 1,51% | 15 | 1,47% | 16 | 1,55% |
Malicky (1983) | 17 | 0,85% | 17 | 1,61% | 17 | 1,67% | 16 | 1,55% |
Espeland & Johanson (2007) | 16 | 0,8% | 16 | 1,51% | 16 | 1,57% | 16 | 1,55% |
Ward (2003) | 16 | 0,8% | 16 | 1,51% | 16 | 1,57% | 16 | 1,55% |
Wells et al. (2013) | 16 | 0,8% | 16 | 1,51% | 16 | 1,57% | 16 | 1,55% |
Johanson & Mary (2009) | 15 | 0,75% | 15 | 1,42% | 15 | 1,47% | 15 | 1,45% |
Mosely (1934) | 14 | 0,7% | 11 | 1,04% | 11 | 1,08% | 11 | 1,06% |
Botosaneanu & Giudicelli (2004) | 13 | 0,65% | 12 | 1,14% | 8 | 0,79% | 12 | 1,16% |
Malm & Johanson (2008) | 13 | 0,65% | 13 | 1,23% | 13 | 1,28% | 13 | 1,26% |
Olah et al. (2015) | 13 | 0,65% | 13 | 1,23% | 13 | 1,28% | 13 | 1,26% |
Johanson (2003) | 12 | 0,6% | 12 | 1,14% | 12 | 1,18% | 12 | 1,16% |
Marle et al. (2017) | 12 | 0,6% | 12 | 1,14% | 12 | 1,18% | 11 | 1,06% |
Olah & Johanson (2010) | 12 | 0,6% | 6 | 0,57% | 6 | 0,59% | 6 | 0,58% |
Gibon & Sganga (2019) | 11 | 0,55% | 11 | 1,04% | 11 | 1,08% | 11 | 1,06% |
Oláh et al. (2015) | 11 | 0,55% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Botosaneanu (1989) | 10 | 0,5% | 9 | 0,85% | 9 | 0,88% | 8 | 0,77% |
Coppa & Tachet (2017) | 10 | 0,5% | 7 | 0,66% | 7 | 0,69% | 7 | 0,68% |
Johanson (2017) | 10 | 0,5% | 10 | 0,95% | 10 | 0,98% | 10 | 0,97% |
Linnaeus (1758) | 10 | 0,5% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Schefter & Ward (2002) | 10 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Archives de Zoologie Experimentale et Generale, 97: 32-50.">Botosaneanu (1959) | 9 | 0,45% | 9 | 0,85% | 9 | 0,88% | 3 | 0,29% |
Coppa & Barnasson (2016) | 9 | 0,45% | 8 | 0,76% | 8 | 0,79% | 8 | 0,77% |
Hagen (1864) | 9 | 0,45% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lagarde (2008) | 9 | 0,45% | 9 | 0,85% | 9 | 0,88% | 9 | 0,87% |
Malicky (1992) | 9 | 0,45% | 9 | 0,85% | 9 | 0,88% | 9 | 0,87% |
Mosely (1930) | 9 | 0,45% | 6 | 0,57% | 6 | 0,59% | 6 | 0,58% |
Sipahiler (1992) | 9 | 0,45% | 6 | 0,57% | 6 | 0,59% | 6 | 0,58% |
Espeland & Johanson (2008) | 8 | 0,4% | 8 | 0,76% | 8 | 0,79% | 8 | 0,77% |
Gibon (2019) | 8 | 0,4% | 8 | 0,76% | 8 | 0,79% | 8 | 0,77% |
Johanson & Ward (2001) | 8 | 0,4% | 6 | 0,57% | 6 | 0,59% | 6 | 0,58% |
Malicky (1980) | 8 | 0,4% | 8 | 0,76% | 8 | 0,79% | 8 | 0,77% |
Mosely (1935) | 8 | 0,4% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Oláh et al. (2020) | 8 | 0,4% | 8 | 0,76% | 8 | 0,79% | 8 | 0,77% |
Schmid (1989) | 8 | 0,4% | 8 | 0,76% | 8 | 0,79% | 8 | 0,77% |
Wells & Johanson (2014) | 8 | 0,4% | 7 | 0,66% | 7 | 0,69% | 7 | 0,68% |
Coppa & Guellec (2017) | 7 | 0,35% | 7 | 0,66% | 7 | 0,69% | 7 | 0,68% |
Forcellini et al. (2012) | 7 | 0,35% | 7 | 0,66% | 7 | 0,69% | 7 | 0,68% |
Olah et al. (2013) | 7 | 0,35% | 7 | 0,66% | 7 | 0,69% | 7 | 0,68% |
Sipahiler (1993) | 7 | 0,35% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Cavalcante & Johanson (2022) | 6 | 0,3% | 6 | 0,57% | 6 | 0,59% | 6 | 0,58% |
Coppa (2017) | 6 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Décamps (1972) | 6 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Malm & Johanson (2007) | 6 | 0,3% | 6 | 0,57% | 6 | 0,59% | 6 | 0,58% |
Mary & Ward (2001) | 6 | 0,3% | 6 | 0,57% | 6 | 0,59% | 6 | 0,58% |
Olivier (1791-[1792]) | 6 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Sipahiler (1993) | 6 | 0,3% | 6 | 0,57% | 0 | 0% | 6 | 0,58% |
Sipahiler (1999) | 6 | 0,3% | 6 | 0,57% | 6 | 0,59% | 6 | 0,58% |
Sykora (1967) | 6 | 0,3% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Curtis (1834) | 5 | 0,25% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Curtis (1834) | 5 | 0,25% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Joahnson (2002) | 5 | 0,25% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Johanson (2003) | 5 | 0,25% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Malicky (2002) | 5 | 0,25% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Navás (1919) | 5 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Valladolid et al. (2021) | 5 | 0,25% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Andersen et al. (2019) | 4 | 0,2% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Barnasson (2020) | 4 | 0,2% | 4 | 0,38% | 4 | 0,39% | 0 | 0% |
Botosaneanu & Thomas (2005) | 4 | 0,2% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Botosaneanu (1994) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousquet (2016) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppa et al. (2004) | 4 | 0,2% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Malicky (2004) | 4 | 0,2% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Malicky (2018) | 4 | 0,2% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Oláh et al. (2018) | 4 | 0,2% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Schrank (1781) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Tachet et al. (2001) | 4 | 0,2% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Vaillant (1974) | 4 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Valladolid et al. (2018) | 4 | 0,2% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Vilarino & Calor (2024) | 4 | 0,2% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Ward (2001) | 4 | 0,2% | 4 | 0,38% | 4 | 0,39% | 4 | 0,39% |
Botosaneanu & Giudicelli (1983) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Botosaneanu (2000) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppa & Gonzalez (2007) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Coppa (2004) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Décamps (1966) | 3 | 0,15% | 3 | 0,28% | 2 | 0,2% | 3 | 0,29% |
Decamps & Magne (1966) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Decamps (1965) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Decamps (1971) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Despax (1933) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Fourcroy (1785) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Kelner-Pillault (1961) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Moretti et al. (1994) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmid (1971) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Sipahiler (2000) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Statzner & Bretschko (1998) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Waringer et al. (2011) | 3 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Banks (1920) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Botosaneanu & Dumont (2003) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Botosaneanu & Giudicelli (1981) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Botosaneanu & Giudicelli (2001) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Botosaneanu & Giudicelli (2004) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Botosaseanu (2000) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Bournaud & Gautheron-Duranthon (1969) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer de Fonscolombe (1846) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppa & Guellec (2021) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Coppa & Malicky (2005) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Coppa et al. (2022) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Coppa (2011) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Coppa (2017) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Dobson (1999) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Doledec (1987) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Fabricius (1793) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcellini (2021) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Giudicelli & Botosaneanu (1999) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Graf et al. (2015) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Guellec et al. (2013) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Guellec et al. (2023) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Johanson & Mary (2001) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Johanson (2011) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Kimmins (1953) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Lavandier (1992) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Le Guellec et al. (2020) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Lenormand et al. (2019) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 1 | 0,1% |
Leraut (2024) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Malicky (1972) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Malicky (1980) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Malicky (1981) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Malicky (1987) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Mangot & Rousseau (2022) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Mclachlan (1879) | 2 | 0,1% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Moretti (1981) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Olah & Johanson (2008) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Oláh & Kovacs (2014) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Perroud & Montrouzier (1864) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Rázuri-gonzales et al. (2024) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Sipahiler (1995) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Sipahiler (2001) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Tobias (1972) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Valladolid et al. (2023) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Ward & Mary (2000) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Waringer & Coppa (2021) | 2 | 0,1% | 2 | 0,19% | 2 | 0,2% | 2 | 0,19% |
Albouy et al. (2017) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bertuetti et al. (2004) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Botosaneanu (1980) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppa & Tachet (2010) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Coppa et al. (2016) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Coppa et al. (2017) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Coppa et al. (2021) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Coppa (2004) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Coppa (2005) | 1 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Coppa (2010) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Coppa (2016) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Espeland & Johanson (2010) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Espeland & Johanson (2010) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
European Nucleotide Archive (2019) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fabricius (1787) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Flint (1974) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gmelin (1790) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
González & Terra (1979) | 1 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Guellec (2011) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jacquemin & Coppa (2013) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jacquemin & Coppa (2015) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jacquemin et al. (2019) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kirby & Spence (1826) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Labat et al. (2019) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Le Guellec et al. (2016) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Linnaeus (1761) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Malicky (1998) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marle et al. (2019) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mclachlan (1866) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mclachlan (1874-1880) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mclachlan (1895) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Moretti & Taticchi (1992) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Moretti (1991) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Morse (1975) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Navas (1915) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1917) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1932) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Neboiss (1986) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Neu (2015) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Oláh & Kovacs (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Oláh et al. (2021) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pictet (1865) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rambur (1842) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ris (1903) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Santos (2020) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Schmid (1947) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Scopoli (1763) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephens (1835-1836) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tachet (2014) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Wells (1995) | 1 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zilli (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |