Coléoptères de Polynésie française
Coleoptera de Polynésie française
487 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Ramage (2017) | 781 | 45,46% | 757 | 92,2% | 749 | 92,13% | 757 | 92,77% |
Zimmerman (1957) | 233 | 13,56% | 153 | 18,64% | 153 | 18,82% | 153 | 18,75% |
Paulay (1985) | 128 | 7,45% | 120 | 14,62% | 120 | 14,76% | 120 | 14,71% |
Liebherr (2013) | 118 | 6,87% | 118 | 14,37% | 118 | 14,51% | 118 | 14,46% |
Zimmerman (1936) | 112 | 6,52% | 37 | 4,51% | 37 | 4,55% | 37 | 4,53% |
Gomy (2000) | 88 | 5,12% | 66 | 8,04% | 66 | 8,12% | 66 | 8,09% |
Heller (1916) | 86 | 5,01% | 45 | 5,48% | 45 | 5,54% | 45 | 5,51% |
Van Dyke (1937) | 81 | 4,71% | 81 | 9,87% | 81 | 9,96% | 81 | 9,93% |
Zimmerman (1936) | 78 | 4,54% | 78 | 9,5% | 75 | 9,23% | 75 | 9,19% |
Meurgey (2011) | 67 | 3,9% | 41 | 4,99% | 41 | 5,04% | 41 | 5,02% |
Meurgey & Ramage (2020) | 65 | 3,78% | 65 | 7,92% | 65 | 8% | 65 | 7,97% |
Peck et al. (2014) | 64 | 3,73% | 59 | 7,19% | 59 | 7,26% | 59 | 7,23% |
Van Dyke (1932) | 62 | 3,61% | 62 | 7,55% | 61 | 7,5% | 62 | 7,6% |
Van Dyke (1932) | 52 | 3,03% | 52 | 6,33% | 52 | 6,4% | 52 | 6,37% |
Coiffait (1976) | 50 | 2,91% | 44 | 5,36% | 44 | 5,41% | 44 | 5,39% |
Jourdan & Mille (2006) | 49 | 2,85% | 43 | 5,24% | 43 | 5,29% | 43 | 5,27% |
Van Zwaluwenburg (1932) | 48 | 2,79% | 16 | 1,95% | 16 | 1,97% | 16 | 1,96% |
Poussereau et al. (2018) | 47 | 2,74% | 10 | 1,22% | 10 | 1,23% | 10 | 1,23% |
Coiffait (1980) | 45 | 2,62% | 42 | 5,12% | 42 | 5,17% | 42 | 5,15% |
Tronquet (2014) | 43 | 2,5% | 40 | 4,87% | 40 | 4,92% | 39 | 4,78% |
Zimmerman (1936) | 43 | 2,5% | 20 | 2,44% | 18 | 2,21% | 19 | 2,33% |
Fairmaire (1849) | 40 | 2,33% | 32 | 3,9% | 31 | 3,81% | 32 | 3,92% |
Cameron (1933) | 38 | 2,21% | 20 | 2,44% | 20 | 2,46% | 20 | 2,45% |
Hammes & Putoa (1986) | 38 | 2,21% | 37 | 4,51% | 37 | 4,55% | 37 | 4,53% |
Hopkins (1915) | 37 | 2,15% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fauvel (1867) | 36 | 2,1% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Paulian (1998) | 34 | 1,98% | 33 | 4,02% | 33 | 4,06% | 33 | 4,04% |
Peck (2011) | 34 | 1,98% | 33 | 4,02% | 33 | 4,06% | 33 | 4,04% |
Denux & Zagatti (2010) | 33 | 1,92% | 29 | 3,53% | 29 | 3,57% | 29 | 3,55% |
Fauvel (1903) | 33 | 1,92% | 20 | 2,44% | 20 | 2,46% | 20 | 2,45% |
Jourdan (2020) | 33 | 1,92% | 32 | 3,9% | 32 | 3,94% | 32 | 3,92% |
Montrouzier (1860) | 28 | 1,63% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Cochereau (1966) | 26 | 1,51% | 22 | 2,68% | 22 | 2,71% | 22 | 2,7% |
Beeson (1935) | 25 | 1,46% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Boheman (1858-1859) | 25 | 1,46% | 17 | 2,07% | 17 | 2,09% | 17 | 2,08% |
Coiffait (1977) | 24 | 1,4% | 23 | 2,8% | 23 | 2,83% | 23 | 2,82% |
Fauvel (1904) | 24 | 1,4% | 15 | 1,83% | 15 | 1,85% | 15 | 1,84% |
Bouget et al. (2019) | 23 | 1,34% | 23 | 2,8% | 23 | 2,83% | 23 | 2,82% |
Arrow (1927) | 22 | 1,28% | 19 | 2,31% | 18 | 2,21% | 19 | 2,33% |
Cameron (1936) | 22 | 1,28% | 20 | 2,44% | 20 | 2,46% | 20 | 2,45% |
Fairmaire (1850) | 21 | 1,22% | 14 | 1,71% | 14 | 1,72% | 14 | 1,72% |
Kolibáč et al. (2020) | 21 | 1,22% | 21 | 2,56% | 21 | 2,58% | 21 | 2,57% |
Peck (2011) | 21 | 1,22% | 20 | 2,44% | 20 | 2,46% | 20 | 2,45% |
Fauvel (1877) | 20 | 1,16% | 11 | 1,34% | 11 | 1,35% | 11 | 1,35% |
Van Zwaluwenburg (1932) | 20 | 1,16% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Blair (1934) | 18 | 1,05% | 17 | 2,07% | 17 | 2,09% | 17 | 2,08% |
Gomy et al. (2016) | 18 | 1,05% | 15 | 1,83% | 15 | 1,85% | 15 | 1,84% |
Beeson (1935) | 17 | 0,99% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Montrouzier (1861) | 17 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrault (1977) | 17 | 0,99% | 17 | 2,07% | 17 | 2,09% | 17 | 2,08% |
Fauvel (1889) | 16 | 0,93% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Lesne (1932) | 16 | 0,93% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Bright (2019) | 15 | 0,87% | 14 | 1,71% | 14 | 1,72% | 14 | 1,72% |
Fauvel (1903) | 15 | 0,87% | 9 | 1,1% | 9 | 1,11% | 9 | 1,1% |
Parnaudeau (2017) | 15 | 0,87% | 13 | 1,58% | 13 | 1,6% | 13 | 1,59% |
Peck (2016) | 15 | 0,87% | 13 | 1,58% | 13 | 1,6% | 13 | 1,59% |
Porch et al. (2020) | 15 | 0,87% | 15 | 1,83% | 15 | 1,85% | 15 | 1,84% |
Beaver (1991) | 14 | 0,81% | 10 | 1,22% | 10 | 1,23% | 10 | 1,23% |
Blackwelder (1943) | 14 | 0,81% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Liebherr (2012) | 14 | 0,81% | 14 | 1,71% | 14 | 1,72% | 14 | 1,72% |
Liebherr (2012) | 14 | 0,81% | 14 | 1,71% | 14 | 1,72% | 14 | 1,72% |
Blair (1932) | 13 | 0,76% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Blair (1934) | 13 | 0,76% | 9 | 1,1% | 9 | 1,11% | 9 | 1,1% |
Jordan (1933) | 13 | 0,76% | 11 | 1,34% | 9 | 1,11% | 11 | 1,35% |
Nattier et al. (2015) | 13 | 0,76% | 11 | 1,34% | 11 | 1,35% | 11 | 1,35% |
Chassain (2001) | 12 | 0,7% | 12 | 1,46% | 9 | 1,11% | 10 | 1,23% |
Fauvel (1891) | 12 | 0,7% | 11 | 1,34% | 11 | 1,35% | 11 | 1,35% |
Johnson et al. (2021) | 12 | 0,7% | 11 | 1,34% | 11 | 1,35% | 11 | 1,35% |
Kuschel (2008) | 12 | 0,7% | 9 | 1,1% | 9 | 1,11% | 9 | 1,1% |
Remillet (1988) | 12 | 0,7% | 9 | 1,1% | 9 | 1,11% | 9 | 1,1% |
Cameron (1933) | 11 | 0,64% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Fauvel (1903) | 11 | 0,64% | 6 | 0,73% | 6 | 0,74% | 6 | 0,74% |
Albouy & Richard (2017) | 10 | 0,58% | 9 | 1,1% | 9 | 1,11% | 8 | 0,98% |
Gutierrez (1981) | 10 | 0,58% | 9 | 1,1% | 9 | 1,11% | 9 | 1,1% |
Kaszab (1982) | 10 | 0,58% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Nicolas et al. (2015) | 10 | 0,58% | 9 | 1,1% | 9 | 1,11% | 9 | 1,1% |
Ramage & Lagarde (2021) | 10 | 0,58% | 10 | 1,22% | 10 | 1,23% | 10 | 1,23% |
Ruzzier et al. (2023) | 10 | 0,58% | 10 | 1,22% | 10 | 1,23% | 10 | 1,23% |
Fauvel (1862) | 9 | 0,52% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zimmerman & Perrault (1989) | 9 | 0,52% | 9 | 1,1% | 9 | 1,11% | 9 | 1,1% |
Beeson (1940) | 8 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Blair (1934) | 8 | 0,47% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Bordoni (2013) | 8 | 0,47% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Brown (2009) | 8 | 0,47% | 8 | 0,97% | 7 | 0,86% | 8 | 0,98% |
Chani-Posse et al. (2018) | 8 | 0,47% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Corporaal (1937) | 8 | 0,47% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Eggers (1940) | 8 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer (2015) | 8 | 0,47% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Franz (1971) | 8 | 0,47% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Jelínek, J. & Audisio, P. 2011. A new species of Amystrops Reitter, 1875, and an updated checklist of the Nitidulidae from Réunion Island (Coleoptera). Bulletin de la Société entomologique de France, 116(4): 421-428. ">Poussereau et al. (2011) |
8 | 0,47% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Sharp (1899) | 8 | 0,47% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Tavakilian & Chevillotte (2013) | 8 | 0,47% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Balfour-Browne (1945) | 7 | 0,41% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Colijn et al. (2020) | 7 | 0,41% | 6 | 0,73% | 6 | 0,74% | 6 | 0,74% |
Damoiseau (1966) | 7 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1906) | 7 | 0,41% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Kaszab (1985) | 7 | 0,41% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Legalov (2009) | 7 | 0,41% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Linnaeus (1758) | 7 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (2012) | 7 | 0,41% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Montrouzier (1861) | 7 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 7 | 0,41% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Soldati & Touroult (2014) | 7 | 0,41% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Zimmerman (1936) | 7 | 0,41% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Bigot (1992) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Blair (1927) | 6 | 0,35% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Britton (1938) | 6 | 0,35% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Casari (2002) | 6 | 0,35% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Chazeau et al. (1974) | 6 | 0,35% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Fabricius (1775) | 6 | 0,35% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Hustache (1920) | 6 | 0,35% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Jordan (1933) | 6 | 0,35% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Perkins (1932) | 6 | 0,35% | 6 | 0,73% | 6 | 0,74% | 6 | 0,74% |
Voisin et al. (2017) | 6 | 0,35% | 6 | 0,73% | 6 | 0,74% | 6 | 0,74% |
Zimmerman (1938) | 6 | 0,35% | 6 | 0,73% | 6 | 0,74% | 6 | 0,74% |
Aberlenc et al. (2004) | 5 | 0,29% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Balke (1993) | 5 | 0,29% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Cohic (1959) | 5 | 0,29% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Escalona & Ślipiński (2010) | 5 | 0,29% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Fauvel (1874) | 5 | 0,29% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Frisch (2016) | 5 | 0,29% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Hołyński (2016) | 5 | 0,29% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lesne (1901) | 5 | 0,29% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Liebherr (2017) | 5 | 0,29% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Nicolas (2012) | 5 | 0,29% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Ramage & Duhamel (2015) | 5 | 0,29% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Shaw & Solodovnikov (2016) | 5 | 0,29% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Zimmerman (1968) | 5 | 0,29% | 5 | 0,61% | 5 | 0,62% | 5 | 0,61% |
Anonyme (2018) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Balke (1990) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Barnouin et al. (2020) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Cochereau (1974) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Fabricius (1792) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1878) | 4 | 0,23% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Fauvel (1883) | 4 | 0,23% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fauvel (1903) | 4 | 0,23% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gillogly (1982) | 4 | 0,23% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gomy et al. (2009) | 4 | 0,23% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Gomy (1981) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Hava (2006) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Háva (2014) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Kaszab (1982) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Kolibáč (2013) | 4 | 0,23% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Lambert & Lemaire (2014) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Lesne (1897) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Malcolm (1981) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Mériguet & Zagatti (2016) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 3 | 0,37% |
Paulian (1991) | 4 | 0,23% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Perrault (1988) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Perroud & Montrouzier (1864) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Porch & Smith (2017) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Ramage (2021) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Rheinheimer (2014) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Wenzel (1955) | 4 | 0,23% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zimmerman (1936) | 4 | 0,23% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zimmerman (1936) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Allen et al. (2022) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Besuchet (1975) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Bezděk & Konstantinov (2017) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 2 | 0,25% |
Clarke (2011) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Cohic (1950) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Constantin (2012) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Fabricius (1781) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1849) | 3 | 0,17% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fairmaire (1893) | 3 | 0,17% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fall (1910) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Frisch (2005) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Gourvès & Samuelson (1979) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Háva & McCormack (2022) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Hayashi (1961) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Jelinek & Lason (2018) | 3 | 0,17% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Johnson et al. (2020) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Kirejtshuk & Lawrence (1999) | 3 | 0,17% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Kurochkin (2005) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Liebherr & Maddison (2013) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Liu (2021) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Marshall (1921) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1790) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrault (1990) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Ramage & Löbl (2022) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Ramage et al. (2017) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Rheinheimer (2012) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Sharp (1879) | 3 | 0,17% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Short (2010) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Siroux (2015) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Sudre et al. (2010) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Théry & Bordat (2012) | 3 | 0,17% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Tottenham (1941) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Urvois et al. (2023) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Van Dyke (1933) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Wood & Bright (1992) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Zimmerman (1943) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Zimmerman (1963) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Altson (1923) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Altson (1924) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Azab et al. (1972) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Balke & Ramsdale (2006) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Bell et al. (1989) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Bellemare & Brunelle (1950) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Bellifa et al. (2017) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Besuchet (1993) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Bieńkowski & Orlova-Bienkowskaja (2017) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Bielawski (1973) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Bourgeois (1884) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousquet (2018) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuning (1942) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Breuning (1948) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Breuning (1964) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Brustel & Roge (1998) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Caron et al. (2008) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cerkowniak et al. (2020) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Chalumeau & Touroult (2005) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Chassain & Touroult (2010) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Chazeau (1978) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chûjô (1961) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chûjô (1964) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Coache (2013) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Constantin (2012) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Deane (1931) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Delobel & Tran (1993) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Delport (2018) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Dobson (1954) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dobson (1956) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dole & Cognato (2010) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
European Nucleotide Archive (2019) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Fabricius (1787) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1801) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1881) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Faucheux (2005) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Fauvel (1882) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1905) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Ferragu (1979) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fleutiaux (1932) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Fontenot et al. (2015) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Frieser (1981) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Geer (1774) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Gomy (2016) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Gonzales et al. (2014) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Guérin-Méneville (1847) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hagstrum & Subramanyam (2009) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Hale et al. (2008) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Hartmann et al. (2021) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Háva et al. (2013) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Hetschko (1928) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Hossain et al. (2016) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Hołyński (1992) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ito & Hirose (1978) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Jarrige (1938) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolivet (1979) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jones et al. (2006) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Jones et al. (2007) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Kerremans (1919) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Kirejtshuk (2008) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Kuschel (1982) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Kuschel (1998) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Kuschel (2008) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Lazarev (2014) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lü & Zhou (2012) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Marchal et al. (2017) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Marshall (1912) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Marsham (1802) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Motschulsky (1858) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Nibouche et al. (202X) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Olivier (1790) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pace (1991) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pace (2014) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Pace (2014) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Panzer ([1796]) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulian (1979) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Perkins (1936) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Perrault (1979) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Perrault (1982) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Pistil & Kontykowski (1974) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Ponel & Roge (2000) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Poussereau (2015) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Quentin & Villiers (1979) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Questel & Le Quellec (2012) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Questel (2023) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Quilici et al. (1988) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Rakowski et al. (1981) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Ramage (2015) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Rheinheimer (2015) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Rücker (2015) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Salin et al. (2003) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Sato (1966) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Souza-Gonçalves et al. (2020) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Sudre & Teocchi (1996) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Sudre & Teocchi (2000) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Telnov (2019) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Telnov (2024) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Tomaszewska (2010) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Tronquet (2015) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Valentine (1989) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Van Zwaluwenburg (1940) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Vayssières et al. (2001) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Vinson (1967) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Waqa-sakiti et al. (2015) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Wollaston (1867) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (1972) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Yadav et al. (2021) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Yokoyama (2013) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Zahradník & Poussereau (2022) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Zanetti et al. (2016) | 2 | 0,12% | 2 | 0,24% | 2 | 0,25% | 2 | 0,25% |
Zimmerman (1964) | 2 | 0,12% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Abdel-kader & Barak (1979) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Adelski (2012) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Albouy et al. (2017) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Alencar et al. (2022) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Alonso-zarazaga & Evenhuis (2017) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Alonso-Zarazaga & Lyal (1999) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Alonso-Zarazaga (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrewes (1925) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bameul (1986) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Beaver & Liu (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Berger (2012) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Blackburn (1888) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Blair (1940) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Borowiec et al. (2019) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bousquet (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1926) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cantot (1990) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cantot (2007) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Casey (1892) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cerkowniak et al. (2017) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chabrol (1995) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chalumeau (1983) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapuis & Eichhoff (1875) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chazeau (1991) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1966) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Crotch (1867) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Crotch (1873) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Decelle (1979) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Degallier & Gomy (2024) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Degallier (2012) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Dillon (1957) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Disney & Chazeau (1990) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Doguet (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
d'Orchymont (1937) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Eggers (1933) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichhoff (1868) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Erichson (1839-1840) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Erwin (1974) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Escalona (2012) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Etienne et al. (2018) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
European Commission (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fabricius (1802) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1884) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer & Poussereau (2010) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fery (2013) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fikáček (2010) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fiori (1915) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Flechtmann & Atkinson (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fleutiaux & Sallé ([1890]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleutiaux (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Franz (1977) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gay (1953) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Geoffroy (1762) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerberg (1957) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1824) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy (2017) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gonzales & Yvinec (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gonzalez & Vetrovec (2021) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Goyaud & Lemarie (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gressitt (1960) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gressitt (1960) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Grouvelle (1878) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Hava & Poussereau (2017) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Háva (2022) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Heer (1838-1841) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hendrich et al. (2010) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Herbst ([1791]-1792) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Herman (1970) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Herman (2001) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Ide et al. (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Ito (1983) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Iwata & Nishimoto (1981) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jarrige (1964) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Johnson (2001) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jolivet (1998) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouveau et al. (2018) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Kaszab (1986) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kiesenwetter (1851) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kingsolver & Ribeiro-Costa (2001) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kumar et al. (1988) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lackner & Leschen (2017) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lacoste (2007) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lacroix (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lagarde (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Laporte de Castelnau & Brullé (1840) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemagnen (2015) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Liebherr (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Linnaeus (1767) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2007) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lowe et al. (2007) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lü & Zhou (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Luziau (1953) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Macleay (1888) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Maes et al. (2010) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Marchioro et al. (2022) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Marquet & Roguet (2003) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Marseul (1855) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Menezes et al. (2005) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Menezes et al. (2006) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Meurgey (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Meurgey (2017) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Mille et al. (2007) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Miyatake (1968) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Motschulsky (1866) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mouttet et al. (-) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Murray (1864) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Nageleisen et al. (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Neid (1999) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Nicolas (2020) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Notman (1924) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ôhira (1971) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Olivier (1791-[1792]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Opitz (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Osuji (1975) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Osuji (1975) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pace (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pace (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pang et al. (2020) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pang et al. (2020) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Paśnik (2006) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Parnaudeau (2012) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Perkins (1907) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Perrin et al. (2007) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pic (1902) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pic (1924) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Poisson (1940) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Poussereau & Lecoq (2010) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Poussereau (2007) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Poussereau (2012) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Questel (2022) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Raffray (1896) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Rosenbaum et al. (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Rossi (1792) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schedl (1940) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schedl (1951) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Linzer Biologische Beitraege, 41(1): 767-801. ">Schöller (2009) |
1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Shaaya (1981) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Shahhosseini (1980) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Sharp (1882) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Siddaiah & Kujur (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Siroux (2010) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Siroux (2012) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Siroux (2018) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Skierska (1976) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Smith et al. (2020) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Soldati et al. (2018) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Soldati et al. (2024) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Soldati et al. (2024) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Solsky (1871) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephens (1830) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Storer et al. (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Telnov (2010) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Touroult et al. (2023) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Tronquet (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Tronquet (2018) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Urvois et al. (2021) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Van & Zwaluwenburg (1943) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Zwaluwenburg (1959) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Vannini et al. (2017) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Villa & Villa (1833) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Vives et al. (2015) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Vorst (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Weigel & Skale (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Wewalka et al. (2023) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Wewalka (2023) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Wittmer (1968) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Wood (1977) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Wood (1989) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zagatti & Cotte (2017) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zanetti et al. (2020) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zimmerman (1935) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zimmerman (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Zimmerman (1940) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zimmerman (1966) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zimmerman (1994) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zimmerman (1994) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |