Insectes de Saint-Pierre-et-Miquelon
480 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Linnaeus (1758) | 90 | 4,7% | 13 | 2,11% | 13 | 2,18% | 12 | 2,01% |
Bousquet (2012) | 66 | 3,45% | 64 | 10,39% | 58 | 9,73% | 64 | 10,74% |
Elder & Abraham (2012) | 65 | 3,39% | 65 | 10,55% | 65 | 10,91% | 65 | 10,91% |
Roux (1984) | 65 | 3,39% | 59 | 9,58% | 58 | 9,73% | 54 | 9,06% |
Tronquet (2014) | 63 | 3,29% | 63 | 10,23% | 61 | 10,23% | 58 | 9,73% |
Noblecourt (2016) | 49 | 2,56% | 8 | 1,3% | 8 | 1,34% | 8 | 1,34% |
Hindermeyer et al. (2007) | 41 | 2,14% | 39 | 6,33% | 36 | 6,04% | 38 | 6,38% |
Albouy & Richard (2017) | 34 | 1,78% | 31 | 5,03% | 31 | 5,2% | 25 | 4,19% |
Etcheberry & Abraham (2009) | 27 | 1,41% | 25 | 4,06% | 25 | 4,19% | 23 | 3,86% |
[Denis & Schiffermüller] (1775) | 26 | 1,36% | 0 | 0% | 0 | 0% | 0 | 0% |
Albouy et al. (2017) | 25 | 1,31% | 23 | 3,73% | 23 | 3,86% | 21 | 3,52% |
Leraut (2012) | 23 | 1,2% | 21 | 3,41% | 21 | 3,52% | 21 | 3,52% |
Leraut (1997) | 19 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Ramage (2020) | 18 | 0,94% | 18 | 2,92% | 18 | 3,02% | 18 | 3,02% |
Reverté et al. (2023) | 18 | 0,94% | 17 | 2,76% | 17 | 2,85% | 17 | 2,85% |
Jourdan & Mille (2006) | 16 | 0,84% | 16 | 2,6% | 16 | 2,68% | 16 | 2,68% |
Mériguet & Zagatti (2016) | 16 | 0,84% | 16 | 2,6% | 16 | 2,68% | 12 | 2,01% |
Speight (2013) | 16 | 0,84% | 15 | 2,44% | 15 | 2,52% | 15 | 2,52% |
Ramage (2017) | 15 | 0,78% | 15 | 2,44% | 15 | 2,52% | 15 | 2,52% |
Vaillant (2000) | 15 | 0,78% | 15 | 2,44% | 13 | 2,18% | 15 | 2,52% |
Meurgey (2011) | 13 | 0,68% | 12 | 1,95% | 12 | 2,01% | 12 | 2,01% |
Lafranchis (2014) | 12 | 0,63% | 11 | 1,79% | 11 | 1,85% | 10 | 1,68% |
Lafranchis (2016) | 12 | 0,63% | 11 | 1,79% | 11 | 1,85% | 10 | 1,68% |
Lebard & Speight (2019) | 12 | 0,63% | 12 | 1,95% | 12 | 2,01% | 12 | 2,01% |
Chapelin et al. (2012) | 11 | 0,57% | 10 | 1,62% | 10 | 1,68% | 9 | 1,51% |
Linnaeus (1761) | 11 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1958) | 11 | 0,57% | 11 | 1,79% | 11 | 1,85% | 11 | 1,85% |
Boisduval (1840) | 9 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 9 | 0,47% | 9 | 1,46% | 9 | 1,51% | 8 | 1,34% |
Questel (2020) | 9 | 0,47% | 8 | 1,3% | 8 | 1,34% | 8 | 1,34% |
Séguy (1944) | 9 | 0,47% | 8 | 1,3% | 8 | 1,34% | 8 | 1,34% |
Dominique (1892) | 8 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 8 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 8 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Audinet-Serville (1823) | 7 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2004) | 7 | 0,37% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Meurgey & Picard (2011) | 7 | 0,37% | 7 | 1,14% | 7 | 1,17% | 7 | 1,17% |
Dominique (1902) | 6 | 0,31% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Geoffroy (1762) | 6 | 0,31% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Hullé et al. (2018) | 6 | 0,31% | 6 | 0,97% | 6 | 1,01% | 6 | 1,01% |
Jouveau et al. (2018) | 6 | 0,31% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Mikkola & Honey (1993) | 6 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas (2014) | 6 | 0,31% | 6 | 0,97% | 5 | 0,84% | 6 | 1,01% |
Questel & Le Quellec (2012) | 6 | 0,31% | 6 | 0,97% | 6 | 1,01% | 6 | 1,01% |
Adelski (2012) | 5 | 0,26% | 5 | 0,81% | 5 | 0,84% | 5 | 0,84% |
Bonfils (1969) | 5 | 0,26% | 5 | 0,81% | 5 | 0,84% | 5 | 0,84% |
Chevin & Savina (2013) | 5 | 0,26% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Coutanceau (2006) | 5 | 0,26% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Fabricius (1775) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1781) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Godart & Duponchel (1834) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutierrez (1981) | 5 | 0,26% | 5 | 0,81% | 5 | 0,84% | 5 | 0,84% |
Honey & Scoble (2001) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Lindberg (1958) | 5 | 0,26% | 5 | 0,81% | 5 | 0,84% | 5 | 0,84% |
Peck et al. (2014) | 5 | 0,26% | 5 | 0,81% | 5 | 0,84% | 5 | 0,84% |
Peck (2011) | 5 | 0,26% | 5 | 0,81% | 5 | 0,84% | 5 | 0,84% |
Rageau (1956) | 5 | 0,26% | 5 | 0,81% | 5 | 0,84% | 5 | 0,84% |
Abraham (2017) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Boisduval (1832-[1835]) | 4 | 0,21% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Boyer & Rivault (2003) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Coiffait (1956) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Dejean (1829) | 4 | 0,21% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Denux & Zagatti (2010) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Dijkstra et al. (2015) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Doucet (2016) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Evenhuis (2018) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Geoffroy (1762) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy (2000) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Grand & Boudot (2007) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Grand et al. (2014) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Heidemann & Seidenbusch (2002) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Heppner (1982) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Martiré & Rochat (2008) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Panzer ([1796]) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1959) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Roux et al. (2006) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Scopoli (1763) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB & MNHN (2021) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Vaillant & Brunhes (1981) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Vayssières et al. (2001) | 4 | 0,21% | 4 | 0,65% | 4 | 0,67% | 4 | 0,67% |
Walker (1863) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Binaghi (1942) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Blank & Taeger (1998) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousquet (2016) | 3 | 0,16% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Campbell (1976) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Chartois et al. (2023) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Chown & Convey (2016) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Clarke (1971) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Cochereau (1974) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Dejean (1831) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Deknuydt et al. (2016) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Esper & Charpentier (1789-[1804]) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Garrison (1984) | 3 | 0,16% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Garrouste & Hervé (2009) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Geer (1774) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Grand et al. (2014) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Hammond (1972) | 3 | 0,16% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Hartig (1840) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Haworth (1803-1828) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Heller (1916) | 3 | 0,16% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Hullé & Vernon (2021) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Acanthoscelides obtectus sur des plantes de Phaseolus vulgaris en plein champ. Bulletin de la Société Zoologique de France, 110: 395-402.">Jarry et al. (1985) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Joshi et al. (2023) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Larson (1989) | 3 | 0,16% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Le Peletier (1823) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2014) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lohez (2013) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Marsham (1802) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Meigen (1822) | 3 | 0,16% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Millière (1881) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Oberthür (1910) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulian (1998) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Remillet (1988) | 3 | 0,16% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Schrank (1781) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn & Woodward (1901) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Stenseth (1980) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Stierlin (1861) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Thunberg & Borgström (1784) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Verity (1927) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Villers (1789) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Voisin et al. (2017) | 3 | 0,16% | 3 | 0,49% | 3 | 0,5% | 3 | 0,5% |
Alonso-zarazaga & Evenhuis (2017) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Atton (1990) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Azam (1893) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Barbut & Voisin (2014) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Barbut et al. (2006) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Beaucournu et al. (1998) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Bertrand (1949) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (1950) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Beuret (1934) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval & Lacordaire (1835) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter & Glare (2010) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Casevitz-Weulersse & Galkowski (2009) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Céréghino & Lavandier (1997) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Cheesman (1927) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Clerck (1759) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Coombs & Woodroffe (1973) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Couteyen & Papazian (2012) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Daly et al. (2023) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Dewynter et al. (2022) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Douyer (1981) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Černý et al. (2020) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Esper ([1796-1805]) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (1989) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Fabricius (1798) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Fauvel (1904) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar & Kaulfuss (1817) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Giard (1879) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Goeze (1783) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy et al. (2016) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Grand et al. (2019) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Guenée ([1858]) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Handfield & Handfield (2021) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Hausmann & Viidalepp (2012) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Holloway & Peters (1976) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Horstmann (2006) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Houard (2020) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Hübner ([1790-1833]) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1793) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1766) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Iperti & Bertand (2001) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Jourdan (2020) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Karsholt et al. (2006) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Katsoyannos et al. (1997) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Kieffer (1898) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiesenwetter (1851) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Kirby (1890) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Klimaszewski et al. (2006) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Laforgue (2015) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 1 | 0,17% |
Lam et al. (2024) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Laporte de Castelnau & Brullé (1840) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lauriaut et al. (2021) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Lebas et al. (2016) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Leraut (2005) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Linné (1767) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2006) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Majka & Langor (2011) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Malloch (1933) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Meganck et al. (2017) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Nel et al. (2020) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochs (1949) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1797]) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre & Lalanne-Cassou | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Questel (2016) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Rambur (1829) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Redon & Chorein (2009) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Robineau-Desvoidy (1841) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rognes & Blackith (1990) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Rönkä et al. (2016) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi (1792) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rottemburg (1775) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sahlberg (1871) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1825) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Schattanek-Wiesmair et al. (2024) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 0 | 0% |
Schauberger (1934) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuler (1964) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Shinonaga et al. (1991) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Srot (1979) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Stewart (1934) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Stewart (1934) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Theodorides (1955) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Thomas (1991) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Thomas (2015) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Thompson (1938) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Tronquet (2006) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Vane-Wright & De Jong (2003) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Viette (1950) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Villastrigo et al. (2017) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Villeneuve (1918) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Winkler et al. (2009) | 2 | 0,1% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Zahradník & Poussereau (2022) | 2 | 0,1% | 2 | 0,32% | 2 | 0,34% | 2 | 0,34% |
Abraham (2021) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Abraham (2022) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Adler (2020) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2018) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Archaux & Chatard (2018) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Aubert & Beaucournu (1976) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Balfour-Browne (1944) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Baraniak (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Baylac (1980) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Beaucournu et al. (1985) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Beaucournu et al. (1992) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Bellmann (2019) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Bencheton et al. (2011) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Berce (1867) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (1949) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot (1862) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Blanchot (1992) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Blatchley (1910) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1833) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Bouget et al. (2019) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Brown (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (1940) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Brunhes (1979) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Callot & Rioux (1965) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Candy et al. (2018) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Casey (1884) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Casey (1896) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chainey (2005) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Chambers (1875) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chandler (2013) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Chebbah et al. (2023) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Chopard (1924) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Clemens (1861) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Clemens (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1966) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Coiffait (1976) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre (2016) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Colligros & Lebecque (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Corti (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulon et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Creighton (1950) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cresson (1865) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Croset et al. (1980) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dachy (1979) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 0 | 0% |
Dadant & Etienne (1973) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Damgaard & Zettel (2014) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
De Geer (1773) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dejean (1825) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Delbol & Perez (2020) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Delhaes et al. (2001) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Denis (1921) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Devaud & Lebouvier (2019) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Doubleday (1847) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Doubleday (1850) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Drury ([1770-1773]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Drury (1773) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois (1996) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Duftschmid (1812) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-martial et al. (2024) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Duponchel (1838-[1840]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duponchel (1842-[1845]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duquef (2021) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Eaton et al. (1879) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Edward et al. (2015) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 0 | 0% |
Edwards (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Eppo (2018) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Eppo (2018) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Esper & Charpentier (1795-[1806]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne & Vilardebó (1978) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Evenhuis (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Evenhuis (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Fabricius ([1777]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1779) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fadda (2016) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Fall (1923) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fall (1924) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Fallén (1817) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1862) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Fauvel (1867) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Fauvel (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fitch (1856) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1902) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fossen et al. (2016) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Fougère et al. (2020) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Francoeur (1977) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Frölich (1828) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gadeau de Kerville (1894) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gebler (1830) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerhard ([1850-1853]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1821) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1824) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ghiliani (1852) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Giudicelli (1964) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Gmelin (1790) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Godart (1822) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
González-Miguéns et al. (2020) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Goulson & Wright (1998) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Grenier (1950) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Grote (1873) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Guegan (1970) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Guenée (1852) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gyllenhal (1827) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamard et al. (2013) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 0 | 0% |
Hammes & Putoa (1986) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Harris (1850) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Harris (1941) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartig (1837) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hebard (1933) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Hébrard (1984) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1981) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Herbst (1783) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Hinton (1941) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway (1979) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1836]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1816-[1826]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Huemer et al. (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1766) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1767) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
ICZN (1954) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2013) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Izri & Akhoundi (2024) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Jansson (1982) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Jeannel & Jarrige (1949) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jeannel (1941) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Joannis (1909) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Joannis (1915) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdain et al. (2016) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Jourdan et al. (2023) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Kassebeer (2000) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Kassebeer (2002) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Kearfott (1907) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirby (1802) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Klug (1816) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolenati (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kugler (1967) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Kurahashi & Fauran (1980) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Labat (2023) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lacomme (2013) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lacourt (1985) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lagarde (2008) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lamy (1978) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1810) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Maitre & Chadee (1983) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lechapt (2015) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lemoine & Quindroit (2023) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lent & Wygodzinsky (1945) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1975) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lethierry (1881) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lieftinck (1966) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lieftinck (1975) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Lienig & Zeller (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin de la Société d'Histoire Naturelle des Ardennes, 97: 67-69.">Ligeron (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Majka & Langor (2011) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Malloch (1932) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Marcos-garcía et al. (2013) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Marinov et al. (2016) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Marinov et al. (2019) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Marinov et al. (2021) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Martiré (2010) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Mary (2017) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Mathias & Fournal (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Mayr (1861) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Meigen (1830) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Meurgey (2004) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Meurgey (2004) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Minot (2016) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Neunzig (2003) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Neve (2015) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Newman (1833) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nibouche et al. (202X) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Nicolas (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Nielsen & Karsholt (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noblecourt (2018) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Noblecourt (2019) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Noblecourt (2020) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Nolken (1870) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nyst (1987) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Obenberger (1917) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochsenheimer (1808) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1790) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1790) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Packard (1870) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1773) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Papazian et al. (2007) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Patrick & Patrick (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Péricart (1987) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrette (1998) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 0 | 0% |
Peyerimhoff (1862) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Peyerimhoff (1879) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollet et al. (2004) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Pont (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Poussereau et al. (2013) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Princis (1974) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Prous et al. (2014) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Prunner (1798) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Quilici et al. (1988) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Quilici et al. (1998) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Quindroit (2020) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Real (1982) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Real (1988) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Retzius (1783) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ris (1915) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Rivault et al. (1991) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Robinson & Nielsen (1983) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rome (2016) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Ronkay et al. (2017) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Roth & Rivault (2002) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Ruzsky (1926) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Samways (2003) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Sattler & Tremewan (1973) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1861) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Savina (2019) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Sawoniewicz (1986) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1831) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schönherr (1806) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sculfort & Dewynter (2024) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Séguy (1934) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Séguy (1960) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Selys & Longchamps (1840) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sharp (1882) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Slamka (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1974) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Soulsby (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stefanescu et al. (2012) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Ström (1768) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sturm (1835) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Telachebba (2022) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Tengström (1948) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tillier (2011) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Tillier (2015) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Umble & Fisher (2000) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Umble & Fisher (2002) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Usinger & Beaucournu (1967) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Vago (2007) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Verity (1919) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verity (1947-1951) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Viette (1949) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Viette (1959) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Viette (1979) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Viette (1994) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Villa & Villa (1833) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Voisin (1975) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Walker (1834) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler et al. (1994) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1908) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1927) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Yang & Landry (2019) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Yokoyama (2013) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Zaddach (1859) | 1 | 0,05% | 1 | 0,16% | 1 | 0,17% | 1 | 0,17% |
Zeller (1849) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zeller (1875) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zetterstedt (1824) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zetterstedt (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zetterstedt ([1838]-1840) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |