Coléoptères de Martinique
Coleoptera de Martinique
463 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Peck (2011) | 460 | 28,86% | 399 | 57,33% | 391 | 57,25% | 395 | 57,83% |
Meurgey (2011) | 441 | 27,67% | 247 | 35,49% | 245 | 35,87% | 245 | 35,87% |
Peck et al. (2014) | 394 | 24,72% | 327 | 46,98% | 325 | 47,58% | 320 | 46,85% |
Meurgey & Ramage (2020) | 392 | 24,59% | 377 | 54,17% | 373 | 54,61% | 370 | 54,17% |
Peck (2011) | 174 | 10,92% | 157 | 22,56% | 152 | 22,25% | 157 | 22,99% |
Bright (2019) | 154 | 9,66% | 144 | 20,69% | 144 | 21,08% | 144 | 21,08% |
Peck (2016) | 133 | 8,34% | 123 | 17,67% | 123 | 18,01% | 123 | 18,01% |
Chalumeau & Touroult (2005) | 101 | 6,34% | 88 | 12,64% | 81 | 11,86% | 87 | 12,74% |
Rheinheimer (2014) | 94 | 5,9% | 89 | 12,79% | 89 | 13,03% | 89 | 13,03% |
Soldati & Touroult (2014) | 64 | 4,02% | 52 | 7,47% | 52 | 7,61% | 50 | 7,32% |
Rheinheimer (2012) | 61 | 3,83% | 56 | 8,05% | 56 | 8,2% | 56 | 8,2% |
Fleutiaux & Sallé ([1890]) | 54 | 3,39% | 18 | 2,59% | 18 | 2,64% | 18 | 2,64% |
Colijn et al. (2020) | 52 | 3,26% | 49 | 7,04% | 49 | 7,17% | 46 | 6,73% |
Questel (2020) | 52 | 3,26% | 51 | 7,33% | 51 | 7,47% | 50 | 7,32% |
Hopkins (1915) | 48 | 3,01% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Constantin (2012) | 47 | 2,95% | 47 | 6,75% | 47 | 6,88% | 47 | 6,88% |
Chassain & Touroult (2012) | 46 | 2,89% | 34 | 4,89% | 32 | 4,69% | 34 | 4,98% |
Rheinheimer (2017) | 42 | 2,63% | 40 | 5,75% | 40 | 5,86% | 40 | 5,86% |
Marquet & Roguet (2003) | 40 | 2,51% | 33 | 4,74% | 33 | 4,83% | 33 | 4,83% |
Touroult (2005) | 35 | 2,2% | 25 | 3,59% | 24 | 3,51% | 23 | 3,37% |
Eggers (1940) | 31 | 1,94% | 9 | 1,29% | 9 | 1,32% | 9 | 1,32% |
Gomy (2000) | 31 | 1,94% | 21 | 3,02% | 20 | 2,93% | 20 | 2,93% |
Ramage (2017) | 31 | 1,94% | 30 | 4,31% | 30 | 4,39% | 28 | 4,1% |
Questel & Le Quellec (2012) | 30 | 1,88% | 27 | 3,88% | 27 | 3,95% | 27 | 3,95% |
Shpeley et al. (2017) | 30 | 1,88% | 28 | 4,02% | 25 | 3,66% | 28 | 4,1% |
Hustache (1930) | 29 | 1,82% | 18 | 2,59% | 18 | 2,64% | 18 | 2,64% |
Lucas (2012) | 29 | 1,82% | 27 | 3,88% | 27 | 3,95% | 27 | 3,95% |
Remillet (1988) | 29 | 1,82% | 17 | 2,44% | 17 | 2,49% | 15 | 2,2% |
Tronquet (2014) | 29 | 1,82% | 26 | 3,74% | 26 | 3,81% | 26 | 3,81% |
Heller (1916) | 28 | 1,76% | 14 | 2,01% | 14 | 2,05% | 13 | 1,9% |
Nicolas (2012) | 26 | 1,63% | 24 | 3,45% | 24 | 3,51% | 24 | 3,51% |
Rheinheimer (2024) | 26 | 1,63% | 26 | 3,74% | 26 | 3,81% | 26 | 3,81% |
Chalumeau (1983) | 23 | 1,44% | 21 | 3,02% | 21 | 3,07% | 21 | 3,07% |
Hustache (1932) | 23 | 1,44% | 23 | 3,3% | 23 | 3,37% | 23 | 3,37% |
Jourdan & Mille (2006) | 22 | 1,38% | 19 | 2,73% | 19 | 2,78% | 19 | 2,78% |
Rheinheimer (2019) | 21 | 1,32% | 21 | 3,02% | 21 | 3,07% | 21 | 3,07% |
Touroult (2012) | 21 | 1,32% | 21 | 3,02% | 21 | 3,07% | 21 | 3,07% |
Ruzzier et al. (2023) | 20 | 1,25% | 20 | 2,87% | 20 | 2,93% | 20 | 2,93% |
Poussereau et al. (2018) | 19 | 1,19% | 6 | 0,86% | 6 | 0,88% | 6 | 0,88% |
Brûlé (2012) | 18 | 1,13% | 18 | 2,59% | 17 | 2,49% | 18 | 2,64% |
Hustache (1929) | 17 | 1,07% | 8 | 1,15% | 8 | 1,17% | 8 | 1,17% |
Blackwelder (1943) | 16 | 1% | 11 | 1,58% | 11 | 1,61% | 11 | 1,61% |
Rose (2017) | 16 | 1% | 16 | 2,3% | 16 | 2,34% | 16 | 2,34% |
Chassain & Touroult (2014) | 15 | 0,94% | 15 | 2,16% | 15 | 2,2% | 15 | 2,2% |
Denux & Zagatti (2010) | 15 | 0,94% | 12 | 1,72% | 12 | 1,76% | 12 | 1,76% |
Jourdan (2020) | 15 | 0,94% | 15 | 2,16% | 14 | 2,05% | 13 | 1,9% |
Linnaeus (1758) | 15 | 0,94% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Touroult et al. (2022) | 15 | 0,94% | 14 | 2,01% | 14 | 2,05% | 14 | 2,05% |
Villiers (1980) | 15 | 0,94% | 7 | 1,01% | 7 | 1,02% | 6 | 0,88% |
Touroult et al. (2021) | 14 | 0,88% | 14 | 2,01% | 13 | 1,9% | 14 | 2,05% |
Bouget et al. (2019) | 13 | 0,82% | 13 | 1,87% | 13 | 1,9% | 13 | 1,9% |
Meurgey (2014) | 13 | 0,82% | 10 | 1,44% | 10 | 1,46% | 10 | 1,46% |
Peck & Cook (2014) | 13 | 0,82% | 13 | 1,87% | 13 | 1,9% | 13 | 1,9% |
Schoenherr (1837) | 13 | 0,82% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Tavakilian & Chevillotte (2013) | 13 | 0,82% | 12 | 1,72% | 12 | 1,76% | 8 | 1,17% |
Lemaire et al. (2024) | 12 | 0,75% | 12 | 1,72% | 12 | 1,76% | 12 | 1,76% |
Lemaire (2017) | 12 | 0,75% | 11 | 1,58% | 10 | 1,46% | 11 | 1,61% |
Chassain (2005) | 11 | 0,69% | 10 | 1,44% | 10 | 1,46% | 10 | 1,46% |
Gomy et al. (2016) | 11 | 0,69% | 8 | 1,15% | 8 | 1,17% | 8 | 1,17% |
Laporte de Castelnau & Brullé (1840) | 11 | 0,69% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Touroult et al. (2020) | 11 | 0,69% | 10 | 1,44% | 10 | 1,46% | 10 | 1,46% |
Albouy & Richard (2017) | 10 | 0,63% | 9 | 1,29% | 9 | 1,32% | 9 | 1,32% |
Chalumeau & Touroult (2004) | 10 | 0,63% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Chassain & Sautière (2007) | 10 | 0,63% | 6 | 0,86% | 6 | 0,88% | 6 | 0,88% |
Fauvel (1904) | 10 | 0,63% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
Keller & Branham (2021) | 10 | 0,63% | 10 | 1,44% | 10 | 1,46% | 10 | 1,46% |
Bousquet et al. (2018) | 9 | 0,56% | 7 | 1,01% | 7 | 1,02% | 7 | 1,02% |
Brûlé & Deknuydt (2014) | 9 | 0,56% | 9 | 1,29% | 9 | 1,32% | 9 | 1,32% |
Chevrolat (1879) | 9 | 0,56% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chevrolat (1880) | 9 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 9 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Hielkema & Hielkema (2019) | 9 | 0,56% | 7 | 1,01% | 7 | 1,02% | 7 | 1,02% |
Lemaire (2021) | 9 | 0,56% | 9 | 1,29% | 9 | 1,32% | 9 | 1,32% |
Smith & Cognato (2021) | 9 | 0,56% | 8 | 1,15% | 8 | 1,17% | 8 | 1,17% |
Touroult et al. (2023) | 9 | 0,56% | 8 | 1,15% | 8 | 1,17% | 8 | 1,17% |
Yokoyama (2013) | 9 | 0,56% | 8 | 1,15% | 8 | 1,17% | 8 | 1,17% |
Fauvel (1867) | 8 | 0,5% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Gonzales et al. (2014) | 8 | 0,5% | 8 | 1,15% | 8 | 1,17% | 8 | 1,17% |
Lesne (1932) | 8 | 0,5% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Pecci-Maddalena & Lopes-Andrade (2017) | 8 | 0,5% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ratcliffe & Cave (2015) | 8 | 0,5% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Rheinheimer (2015) | 8 | 0,5% | 6 | 0,86% | 6 | 0,88% | 6 | 0,88% |
Touroult et al. (2022) | 8 | 0,5% | 8 | 1,15% | 8 | 1,17% | 8 | 1,17% |
Degallier (2012) | 7 | 0,44% | 7 | 1,01% | 7 | 1,02% | 7 | 1,02% |
Fauvel (1903) | 7 | 0,44% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Liebherr & Ivie (2021) | 7 | 0,44% | 7 | 1,01% | 7 | 1,02% | 7 | 1,02% |
Montrouzier (1860) | 7 | 0,44% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Rheinheimer (2021) | 7 | 0,44% | 6 | 0,86% | 6 | 0,88% | 6 | 0,88% |
Touroult & Poirier (2021) | 7 | 0,44% | 7 | 1,01% | 7 | 1,02% | 7 | 1,02% |
Touroult et al. (2024) | 7 | 0,44% | 7 | 1,01% | 7 | 1,02% | 7 | 1,02% |
Ball & Shpeley (2009) | 6 | 0,38% | 6 | 0,86% | 6 | 0,88% | 6 | 0,88% |
Beeson (1935) | 6 | 0,38% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Breuning (1980) | 6 | 0,38% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chevrolat (1880) | 6 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 6 | 0,38% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Dupuis & Perrin (2020) | 6 | 0,38% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Lemaire & Jourdan (2021) | 6 | 0,38% | 6 | 0,86% | 6 | 0,88% | 6 | 0,88% |
Parnaudeau (2017) | 6 | 0,38% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Touroult et al. (2015) | 6 | 0,38% | 6 | 0,86% | 6 | 0,88% | 6 | 0,88% |
Touroult (2017) | 6 | 0,38% | 6 | 0,86% | 6 | 0,88% | 6 | 0,88% |
Arrow (1927) | 5 | 0,31% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Barnouin et al. (2020) | 5 | 0,31% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
Beeson (1935) | 5 | 0,31% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Denier (1922) | 5 | 0,31% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Dheurle (2012) | 5 | 0,31% | 5 | 0,72% | 0 | 0% | 5 | 0,73% |
Fabricius (1801) | 5 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1849) | 5 | 0,31% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
Fauvel (1903) | 5 | 0,31% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Gahan (1895) | 5 | 0,31% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Hammes & Putoa (1986) | 5 | 0,31% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
Kuijten (1983) | 5 | 0,31% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Liebherr (1986) | 5 | 0,31% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Mellié (1849) | 5 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Nattier et al. (2015) | 5 | 0,31% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Rheinheimer (2015) | 5 | 0,31% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
Beaver (1991) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Beeson (1940) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonadona (1981) | 4 | 0,25% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Bousquet (2016) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Corporaal (1937) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Dejean (1825) | 4 | 0,25% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Descarpentries (1981) | 4 | 0,25% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Dole & Cognato (2010) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Erwin (1991) | 4 | 0,25% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Fabricius (1775) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer (2015) | 4 | 0,25% | 4 | 0,57% | 3 | 0,44% | 4 | 0,59% |
Fleutiaux (1907) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Girón & Franz (2012) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Grouvelle & Raffray (1908) | 4 | 0,25% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Halstead & Green (1979) | 4 | 0,25% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Hustache (1920) | 4 | 0,25% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Kaszab (1982) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Lohez (2015) | 4 | 0,25% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Paulian (1991) | 4 | 0,25% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Paulian (1998) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Schiller (2004) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Schoenherr (1843) | 4 | 0,25% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Shockley et al. (2009) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Touroult et al. (2017) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Touroult (2004) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Touroult (2007) | 4 | 0,25% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
Borowiec & Świętojańska (2021) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Boucher et al. (2015) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Brûlé (2012) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Casari (2002) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Chani-Posse et al. (2018) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Chapuis (1865) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Chassain & Touroult (2011) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chassain et al. (2014) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Chassain (2017) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Chevrolat (1879) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1966) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Darlington (1934) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Degallier & Gomy (2024) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Dégallier et al. (2017) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Dejean (1831) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Eggers (1933) | 3 | 0,19% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Etienne et al. (2018) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Fabricius (1792) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1862) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1903) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Ferragu (1964) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Franz (1984) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Girón & Short (2021) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Gutierrez (1981) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Ivie & Geiser (2014) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Johnson et al. (2020) | 3 | 0,19% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Konstantinov et al. (2022) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Lemaire (2023) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Mantilleri & Sforzi (2006) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Nicolas et al. (2015) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Paulian (1979) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Ponchel (2011) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Ratcliffe (2019) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Rose (2012) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Théry & Bordat (2012) | 3 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Touroult et al. (2016) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Touroult et al. (2018) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Touroult et al. (2021) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Voisin et al. (2017) | 3 | 0,19% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
Adelski (2012) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ali (1993) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Ardoin (1977) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1986) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Ball & Maddison (1987) | 2 | 0,13% | 2 | 0,29% | 1 | 0,15% | 1 | 0,15% |
Balthasar (1938) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Balthasar (1966) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Bell & Bell (1985) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Boilly (2012) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Boucher (2015) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Bousquet (2012) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Brûlé et al. (2017) | 2 | 0,13% | 2 | 0,29% | 0 | 0% | 2 | 0,29% |
Candèze (1863) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chalumeau & Touroult (2004) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chalumeau & Touroult (2005) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chalumeau (1982) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chalumeau (1984) | 2 | 0,13% | 2 | 0,29% | 0 | 0% | 2 | 0,29% |
Chandler (2023) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chapin (1940) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chassain & Touroult (2010) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chazeau et al. (1974) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chazeau (1978) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Chevrolat (1858) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1879) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Clavier et al. (2019) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Clavier et al. (2021) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Constantin (2017) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Coombs (1979) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Costa (1975) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Dupuis (2016) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Fabricius (1781) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1802) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1850) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Fairmaire (1893) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1906) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Fernandez (1982) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleutiaux (1930) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Fourcroy (1785) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Genier & Moretto (2017) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Germar (1824) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Giannoulis et al. (2014) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Grouvelle (1902) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Hagstrum & Subramanyam (2009) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Halstead (1973) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Hart & Ivie (2016) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hartmann et al. (2021) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Huang (2017) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ivie & Hart (2017) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Joly & Escalona (2010) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Jouveau et al. (2018) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Kaszab (1985) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Labat (2023) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Lawrence (1987) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lemaire (2014) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ślipiński et al. (2021) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
López-García & Deloya (2022) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Marsham (1802) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Mériguet & Zagatti (2016) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Meurgey & Poiron (2012) | 2 | 0,13% | 2 | 0,29% | 0 | 0% | 2 | 0,29% |
Montrouzier (1861) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore et al. (2018) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Mroczkowski (1968) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Nibouche et al. (202X) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1790) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Opitz (2013) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Panzer ([1796]) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Perkins (1980) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Perroud & Montrouzier (1864) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Pic (1914) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Pic (1922) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Poussereau (2007) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Rojkoff & Frolov (2017) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Rossi (1792) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Santos-silva & Bezark (2021) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Santos-silva et al. (2018) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Schoenherr (1840) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Spiessberger & Ivie (2018) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Telnov (2010) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Touroult et al. (2021) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Touroult et al. (2023) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Uicn et al. (2020) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Van Zwaluwenburg (1932) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 0 | 0% |
Van Zwaluwenburg (1940) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 0 | 0% |
Villiers (1979) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Villiers (1980) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Vinson (1967) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Vitrac (1913) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Wolcott (1943) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood & Bright (1992) | 2 | 0,13% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Woodley & Touroult (2012) | 2 | 0,13% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Aalbu et al. (2023) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Abood & Murphy (2006) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Albouy et al. (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Alonso-zarazaga & Evenhuis (2017) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2018) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ballerio et al. (2018) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Beaver & Liu (2016) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Belles (1985) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellifa et al. (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Belon (1884) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bielawski (1973) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Blair (1934) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Blair (1934) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Boheman (1858-1859) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Borowiec & Moragues (2005) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Boucher & Salazar (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousquet (2018) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Brahm (1791) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Brustel & Roge (1998) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Casey (1924) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cassola (2011) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Chalumeau (1982) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Chapelin-viscardi (2011) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Chapuis & Eichhoff (1875) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chassain & Touroult (2014) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Chazeau (1991) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chûjô (1964) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Cohic (1950) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Cohic (1959) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Colindre & Yvinec (2022) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Constantin et al. (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Constantin (2021) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Czenpinski (1778) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalens & Touroult (2007) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Damoiseau (1966) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Darlington (1939) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Degallier et al. (2010) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Degallier et al. (2018) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Degallier (1981) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Deknuydt & Dumbardon-Martial (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Deknuydt & Romé (2012) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Deknuydt & Romé (2014) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Deknuydt (2014) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Delport (2018) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Duranton (2004) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Dutrillaux et al. (2013) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Dutrillaux (2016) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Eichhoff (1868) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Eichhoff (1868) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Erwin (1974) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Esser (2017) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius ([1777]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1781) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1881) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Fauvel (1884) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1903) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferragu (1979) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Fisher (1926) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Fisher (1932) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher (1935) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleutiaux (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleutiaux (1932) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Frieser (1959) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Frieser (1978) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Geer (1774) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gimmel (2011) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Gmelin (1790) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy (2004) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Gonzales & Yvinec (2016) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Gonzalez & Vetrovec (2021) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gorham (1898) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Goyaud & Lemarie (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Grouvelle ([1877]) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Grouvelle (1898) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Grouvelle (1898) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Harold (1867) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hava (2006) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Háva (2014) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Háva (2014) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hemp & Dettner (2003) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hespenheide (1980) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hespenheide (2006) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hindermeyer et al. (2007) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Horn (1936) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Huchet & Labatut (2022) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Huchet et al. (2020) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Huchet (1992) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ivie & Hart (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ivie et al. (2016) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Jameson (1997) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jiroux (2018) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Jourdan et al. (2022) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Jourdan et al. (2023) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Kippenhan et al. (2013) | 1 | 0,06% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Kuschel (1951) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Legalov (2003) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lemaire (2020) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lemaire (2024) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Leng & Mutchler (1916) | 1 | 0,06% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Lepeletier de Saint Fargeau & Audinet-Serville (1825) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesne (1897) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lesne (1901) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ligeron (2010) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Linnaeus (1766) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2007) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lopes-Andrade (2008) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lyubarsky (2013) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Malausa (1977) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Marchal et al. (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Marchioro et al. (2022) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Marshall (1912) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Martins & Santos-silva (2012) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Martins (1971) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Nageleisen et al. (2015) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Neid (1999) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Nicolas (2014) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
O'Brien (2011) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Olivier (1790) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1790-[1791]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Opitz (2016) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pal (2000) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pang et al. (2020) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Peacock (1976) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Perrault (1977) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pic (1916) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pittino & Mariani (1986) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ponel & Roge (2000) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
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) |
1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Poussereau (2015) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Questel (2022) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Quilici et al. (1988) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ramage et al. (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Reiche ([1843]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Reiche (1843) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Reitter (1884) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rheinheimer (2023) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Roguet (2022) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Rosenhauer (1856) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Roth (1851) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sampson (1921) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Santos-silva & Shute (2009) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Santos-Silva et al. (2010) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sautière (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Schedl (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schedl (1940) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmidt (1909) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Schoenherr (1839) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schoenherr (1844) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Schönherr (1806) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1781) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sharp (1882) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Siroux (2010) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Siroux (2015) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Siroux (2018) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Smith et al. (2022) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Smith (1883) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sudre et al. (2010) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Telnov (2019) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Théry (1940) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Thnberg (1795) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult (2004) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Touroult (2012) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Tronquet (2016) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Urvois et al. (2021) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Van Zwaluwenburg (1932) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Vannini et al. (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Villa & Villa (1833) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Villiers (1979) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Villiers (1980) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Vitali & Touroult (2005) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Vlasak & Santos-silva (2018) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wollaston (1858) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (1977) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Zagatti & Cotte (2017) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Zimmerman (1968) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
(2013) | 1 | 0,06% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |