Animaux terrestres et d'eau douce introduits en Nouvelle-Calédonie
Animaux terrestres et d'eau douce introduits en Nouvelle-Calédonie
1805 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Jourdan & Mille (2006) | 432 | 10,74% | 384 | 35,92% | 380 | 36,93% | 371 | 35,91% |
Ramage (2017) | 416 | 10,35% | 395 | 36,95% | 387 | 37,61% | 386 | 37,37% |
Jourdan (2020) | 341 | 8,48% | 329 | 30,78% | 315 | 30,61% | 317 | 30,69% |
Meurgey & Ramage (2020) | 224 | 5,57% | 223 | 20,86% | 218 | 21,19% | 217 | 21,01% |
Meurgey (2011) | 194 | 4,82% | 159 | 14,87% | 155 | 15,06% | 154 | 14,91% |
Matile-Ferrero & Etienne (2006) | 103 | 2,56% | 102 | 9,54% | 96 | 9,33% | 97 | 9,39% |
Heller (1916) | 97 | 2,41% | 58 | 5,43% | 57 | 5,54% | 57 | 5,52% |
Mille et al. (2016) | 83 | 2,06% | 80 | 7,48% | 80 | 7,77% | 75 | 7,26% |
Jennings et al. (2013) | 82 | 2,04% | 80 | 7,48% | 78 | 7,58% | 79 | 7,65% |
Rageau (1958) | 80 | 1,99% | 74 | 6,92% | 70 | 6,8% | 66 | 6,39% |
Linnaeus (1758) | 78 | 1,94% | 24 | 2,25% | 24 | 2,33% | 18 | 1,74% |
Questel (2020) | 78 | 1,94% | 72 | 6,74% | 71 | 6,9% | 67 | 6,49% |
Gomy (2000) | 70 | 1,74% | 50 | 4,68% | 50 | 4,86% | 50 | 4,84% |
Séguy (1944) | 66 | 1,64% | 32 | 2,99% | 32 | 3,11% | 30 | 2,9% |
Peck et al. (2014) | 64 | 1,59% | 59 | 5,52% | 59 | 5,73% | 58 | 5,61% |
Vayssières et al. (2001) | 63 | 1,57% | 57 | 5,33% | 57 | 5,54% | 55 | 5,32% |
Tronquet (2014) | 61 | 1,52% | 58 | 5,43% | 56 | 5,44% | 58 | 5,61% |
Clarke (1971) | 55 | 1,37% | 42 | 3,93% | 42 | 4,08% | 39 | 3,78% |
Paulian (1998) | 54 | 1,34% | 51 | 4,77% | 48 | 4,66% | 50 | 4,84% |
Gutierrez (1981) | 51 | 1,27% | 44 | 4,12% | 44 | 4,28% | 41 | 3,97% |
Martiré & Rochat (2008) | 51 | 1,27% | 36 | 3,37% | 34 | 3,3% | 34 | 3,29% |
Questel & Le Quellec (2012) | 50 | 1,24% | 44 | 4,12% | 43 | 4,18% | 40 | 3,87% |
Germain et al. (2014) | 45 | 1,12% | 44 | 4,12% | 44 | 4,28% | 42 | 4,07% |
Hammes & Putoa (1986) | 44 | 1,09% | 44 | 4,12% | 44 | 4,28% | 44 | 4,26% |
Peck (2011) | 43 | 1,07% | 41 | 3,84% | 40 | 3,89% | 40 | 3,87% |
Viette (1949) | 42 | 1,04% | 28 | 2,62% | 28 | 2,72% | 27 | 2,61% |
Foldi & Germain (2018) | 41 | 1,02% | 40 | 3,74% | 39 | 3,79% | 35 | 3,39% |
Rageau (1959) | 41 | 1,02% | 38 | 3,55% | 36 | 3,5% | 38 | 3,68% |
Quénéhervé & Van Den Berg (2005) | 40 | 0,99% | 40 | 3,74% | 40 | 3,89% | 40 | 3,87% |
Ramage et al. (2023) | 39 | 0,97% | 39 | 3,65% | 38 | 3,69% | 39 | 3,78% |
Evenhuis (2018) | 38 | 0,95% | 36 | 3,37% | 35 | 3,4% | 35 | 3,39% |
Germain (2007) | 38 | 0,95% | 38 | 3,55% | 38 | 3,69% | 33 | 3,19% |
Cochereau (1966) | 37 | 0,92% | 36 | 3,37% | 36 | 3,5% | 35 | 3,39% |
Remillet (1988) | 37 | 0,92% | 28 | 2,62% | 27 | 2,62% | 24 | 2,32% |
Etienne (2005) | 35 | 0,87% | 35 | 3,27% | 35 | 3,4% | 35 | 3,39% |
Gabriac et al. (2024) | 35 | 0,87% | 35 | 3,27% | 35 | 3,4% | 35 | 3,39% |
Denux & Zagatti (2010) | 34 | 0,85% | 29 | 2,71% | 29 | 2,82% | 29 | 2,81% |
Hopkins (1915) | 34 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
Poussereau et al. (2018) | 34 | 0,85% | 10 | 0,94% | 10 | 0,97% | 10 | 0,97% |
Holloway (1979) | 33 | 0,82% | 22 | 2,06% | 21 | 2,04% | 22 | 2,13% |
Mille et al. (2020) | 33 | 0,82% | 32 | 2,99% | 32 | 3,11% | 32 | 3,1% |
Wheeler (1935) | 32 | 0,8% | 18 | 1,68% | 18 | 1,75% | 18 | 1,74% |
Anonyme (2018) | 31 | 0,77% | 30 | 2,81% | 29 | 2,82% | 30 | 2,9% |
Fauvel (1867) | 31 | 0,77% | 11 | 1,03% | 11 | 1,07% | 11 | 1,06% |
Yokoyama (2013) | 31 | 0,77% | 26 | 2,43% | 26 | 2,53% | 24 | 2,32% |
Guillermet (2009) | 30 | 0,75% | 26 | 2,43% | 26 | 2,53% | 26 | 2,52% |
Migeon (2015) | 30 | 0,75% | 30 | 2,81% | 30 | 2,92% | 30 | 2,9% |
Fauvel (1904) | 29 | 0,72% | 18 | 1,68% | 18 | 1,75% | 18 | 1,74% |
Bournier & Mound (2000) | 28 | 0,7% | 28 | 2,62% | 28 | 2,72% | 28 | 2,71% |
Cohic (1959) | 28 | 0,7% | 20 | 1,87% | 20 | 1,94% | 18 | 1,74% |
Gargominy et al. (1996) | 28 | 0,7% | 25 | 2,34% | 25 | 2,43% | 23 | 2,23% |
Bouget et al. (2019) | 27 | 0,67% | 27 | 2,53% | 27 | 2,62% | 27 | 2,61% |
Perrault (1988) | 27 | 0,67% | 25 | 2,34% | 25 | 2,43% | 25 | 2,42% |
Ramage (2014) | 27 | 0,67% | 26 | 2,43% | 26 | 2,53% | 26 | 2,52% |
Fauvel (1903) | 26 | 0,65% | 16 | 1,5% | 16 | 1,55% | 16 | 1,55% |
Griffiths & Florens (2006) | 26 | 0,65% | 16 | 1,5% | 16 | 1,55% | 16 | 1,55% |
Berland (1933) | 25 | 0,62% | 11 | 1,03% | 11 | 1,07% | 11 | 1,06% |
Platnick (1993) | 24 | 0,6% | 15 | 1,4% | 15 | 1,46% | 15 | 1,45% |
Rageau (1956) | 24 | 0,6% | 23 | 2,15% | 18 | 1,75% | 21 | 2,03% |
Wilson & Taylor (1967) | 24 | 0,6% | 18 | 1,68% | 18 | 1,75% | 18 | 1,74% |
Cochereau (1974) | 23 | 0,57% | 23 | 2,15% | 22 | 2,14% | 21 | 2,03% |
Etienne & Vilardebó (1978) | 23 | 0,57% | 22 | 2,06% | 22 | 2,14% | 19 | 1,84% |
Jaffe & Lattke (1994) | 23 | 0,57% | 20 | 1,87% | 20 | 1,94% | 20 | 1,94% |
Leraut (2014) | 23 | 0,57% | 23 | 2,15% | 23 | 2,24% | 23 | 2,23% |
Morrison (1997) | 23 | 0,57% | 20 | 1,87% | 20 | 1,94% | 20 | 1,94% |
Solem (1964) | 23 | 0,57% | 17 | 1,59% | 17 | 1,65% | 17 | 1,65% |
Taylor (1987) | 23 | 0,57% | 23 | 2,15% | 22 | 2,14% | 23 | 2,23% |
Etienne et al. (2015) | 22 | 0,55% | 22 | 2,06% | 22 | 2,14% | 22 | 2,13% |
Gomy et al. (2016) | 22 | 0,55% | 19 | 1,78% | 19 | 1,85% | 19 | 1,84% |
Morrison (1996) | 22 | 0,55% | 18 | 1,68% | 18 | 1,75% | 18 | 1,74% |
Muru et al. (2017) | 22 | 0,55% | 22 | 2,06% | 22 | 2,14% | 22 | 2,13% |
Peck (2011) | 21 | 0,52% | 21 | 1,96% | 20 | 1,94% | 21 | 2,03% |
Remaudière & Etienne (1988) | 21 | 0,52% | 21 | 1,96% | 21 | 2,04% | 21 | 2,03% |
Guillermet (2011) | 20 | 0,5% | 20 | 1,87% | 20 | 1,94% | 20 | 1,94% |
Lesne (1932) | 20 | 0,5% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Albouy & Richard (2017) | 19 | 0,47% | 17 | 1,59% | 17 | 1,65% | 17 | 1,65% |
Fauvel (1903) | 19 | 0,47% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Franco et al. (2019) | 19 | 0,47% | 18 | 1,68% | 18 | 1,75% | 18 | 1,74% |
Galkowski (2016) | 19 | 0,47% | 19 | 1,78% | 19 | 1,85% | 19 | 1,84% |
Lowe et al. (2007) | 19 | 0,47% | 17 | 1,59% | 16 | 1,55% | 15 | 1,45% |
Wheeler (1932) | 19 | 0,47% | 11 | 1,03% | 11 | 1,07% | 11 | 1,06% |
Berland (1924) | 18 | 0,45% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Berland (1934) | 18 | 0,45% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Cowie (2000) | 18 | 0,45% | 14 | 1,31% | 14 | 1,36% | 14 | 1,36% |
Delannoye et al. (2015) | 18 | 0,45% | 14 | 1,31% | 14 | 1,36% | 14 | 1,36% |
Hoddle et al. (2008) | 18 | 0,45% | 18 | 1,68% | 18 | 1,75% | 18 | 1,74% |
Nibouche et al. (202X) | 18 | 0,45% | 17 | 1,59% | 17 | 1,65% | 16 | 1,55% |
Wheeler (1936) | 18 | 0,45% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Berland (1934) | 17 | 0,42% | 10 | 0,94% | 10 | 0,97% | 10 | 0,97% |
Cheesman (1928) | 17 | 0,42% | 17 | 1,59% | 17 | 1,65% | 17 | 1,65% |
Solem (1961) | 17 | 0,42% | 13 | 1,22% | 13 | 1,26% | 13 | 1,26% |
Barré (2021) | 16 | 0,4% | 16 | 1,5% | 16 | 1,55% | 12 | 1,16% |
Bigot (1992) | 16 | 0,4% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Dupont et al. (2023) | 16 | 0,4% | 16 | 1,5% | 16 | 1,55% | 16 | 1,55% |
Montrouzier (1860) | 16 | 0,4% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Wetterer (2002) | 16 | 0,4% | 14 | 1,31% | 14 | 1,36% | 14 | 1,36% |
Wilson & Hunt (1967) | 16 | 0,4% | 15 | 1,4% | 15 | 1,46% | 15 | 1,45% |
Blard et al. (2003) | 15 | 0,37% | 15 | 1,4% | 15 | 1,46% | 15 | 1,45% |
Bournier (2000) | 15 | 0,37% | 15 | 1,4% | 15 | 1,46% | 15 | 1,45% |
Flechtmann et al. (1999) | 15 | 0,37% | 15 | 1,4% | 15 | 1,46% | 15 | 1,45% |
Kreiter et al. (2020) | 15 | 0,37% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Mary (2017) | 15 | 0,37% | 14 | 1,31% | 13 | 1,26% | 13 | 1,26% |
Streito et al. (2007) | 15 | 0,37% | 15 | 1,4% | 15 | 1,46% | 15 | 1,45% |
Theuerkauf et al. (2010) | 15 | 0,37% | 15 | 1,4% | 15 | 1,46% | 13 | 1,26% |
Wheeler (1932) | 15 | 0,37% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Dierkens & Charlat (2011) | 14 | 0,35% | 10 | 0,94% | 10 | 0,97% | 10 | 0,97% |
Lebas et al. (2016) | 14 | 0,35% | 14 | 1,31% | 14 | 1,36% | 14 | 1,36% |
Lorvelec et al. (2007) | 14 | 0,35% | 14 | 1,31% | 14 | 1,36% | 6 | 0,58% |
Perroud & Montrouzier (1864) | 14 | 0,35% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Soubeyran et al. (2011) | 14 | 0,35% | 14 | 1,31% | 14 | 1,36% | 12 | 1,16% |
Aulagnier et al. (2017) | 13 | 0,32% | 11 | 1,03% | 11 | 1,07% | 9 | 0,87% |
Bonfils (1969) | 13 | 0,32% | 11 | 1,03% | 11 | 1,07% | 11 | 1,06% |
Cazanove (2022) | 13 | 0,32% | 11 | 1,03% | 11 | 1,07% | 11 | 1,06% |
Cohic (1950) | 13 | 0,32% | 12 | 1,12% | 12 | 1,17% | 12 | 1,16% |
Fairmaire (1849) | 13 | 0,32% | 12 | 1,12% | 12 | 1,17% | 12 | 1,16% |
Fauvel (1889) | 13 | 0,32% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Fauvel (1903) | 13 | 0,32% | 7 | 0,65% | 7 | 0,68% | 5 | 0,48% |
Hebard (1933) | 13 | 0,32% | 11 | 1,03% | 11 | 1,07% | 11 | 1,06% |
Hovestadt & Neckheim (2020) | 13 | 0,32% | 12 | 1,12% | 12 | 1,17% | 12 | 1,16% |
Jourdan et al. (2014) | 13 | 0,32% | 10 | 0,94% | 9 | 0,87% | 10 | 0,97% |
Nattier et al. (2015) | 13 | 0,32% | 10 | 0,94% | 10 | 0,97% | 10 | 0,97% |
Parnaudeau (2017) | 13 | 0,32% | 11 | 1,03% | 11 | 1,07% | 11 | 1,06% |
Paulian (1991) | 13 | 0,32% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Peck (2016) | 13 | 0,32% | 10 | 0,94% | 10 | 0,97% | 10 | 0,97% |
Ruzzier et al. (2023) | 13 | 0,32% | 13 | 1,22% | 13 | 1,26% | 13 | 1,26% |
Zakardjian et al. (2023) | 13 | 0,32% | 13 | 1,22% | 11 | 1,07% | 13 | 1,26% |
Bright (2019) | 12 | 0,3% | 11 | 1,03% | 11 | 1,07% | 11 | 1,06% |
Fauvel (1906) | 12 | 0,3% | 10 | 0,94% | 10 | 0,97% | 9 | 0,87% |
Frenot et al. (2005) | 12 | 0,3% | 11 | 1,03% | 11 | 1,07% | 9 | 0,87% |
Hullé et al. (2018) | 12 | 0,3% | 12 | 1,12% | 12 | 1,17% | 12 | 1,16% |
Ledoux & Hallé (1995) | 12 | 0,3% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Niedbała (1998) | 12 | 0,3% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Tavakilian & Chevillotte (2013) | 12 | 0,3% | 10 | 0,94% | 10 | 0,97% | 8 | 0,77% |
Wheeler (1933) | 12 | 0,3% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Albouy et al. (2017) | 11 | 0,27% | 10 | 0,94% | 10 | 0,97% | 7 | 0,68% |
Fauvel (1862) | 11 | 0,27% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Niedbała & Penttinen (2007) | 11 | 0,27% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Pilsbry (1906-1907) | 11 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Berland (1935) | 10 | 0,25% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Blatrix et al. (2018) | 10 | 0,25% | 10 | 0,94% | 10 | 0,97% | 10 | 0,97% |
Brook (2010) | 10 | 0,25% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Casevitz-Weulersse & Galkowski (2009) | 10 | 0,25% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Colijn et al. (2020) | 10 | 0,25% | 9 | 0,84% | 9 | 0,87% | 8 | 0,77% |
Curran (1929) | 10 | 0,25% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Fabricius (1775) | 10 | 0,25% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Legros et al. (2017) | 10 | 0,25% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Matile-Ferrero (1979) | 10 | 0,25% | 10 | 0,94% | 10 | 0,97% | 9 | 0,87% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 10 | 0,25% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Michaelsen (1913) | 10 | 0,25% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Nicolas et al. (2015) | 10 | 0,25% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Perrault (1993) | 10 | 0,25% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Soubeyran (2008) | 10 | 0,25% | 8 | 0,75% | 8 | 0,78% | 7 | 0,68% |
Sudre et al. (2010) | 10 | 0,25% | 7 | 0,65% | 7 | 0,68% | 6 | 0,58% |
Chani-Posse et al. (2018) | 9 | 0,22% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Dierkens & Ramage (2016) | 9 | 0,22% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Emery (1914) | 9 | 0,22% | 6 | 0,56% | 5 | 0,49% | 6 | 0,58% |
Fauvel (1891) | 9 | 0,22% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Garrett (1884) | 9 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gentry et al. (2004) | 9 | 0,22% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Henderson & Breuil (2012) | 9 | 0,22% | 6 | 0,56% | 2 | 0,19% | 6 | 0,58% |
Kaszab (1982) | 9 | 0,22% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Montrouzier (1861) | 9 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Quilici et al. (1988) | 9 | 0,22% | 9 | 0,84% | 9 | 0,87% | 8 | 0,77% |
Siroux (2015) | 9 | 0,22% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Soldati & Touroult (2014) | 9 | 0,22% | 9 | 0,84% | 9 | 0,87% | 9 | 0,87% |
Wheeler (1908) | 9 | 0,22% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Beeson (1935) | 8 | 0,2% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Berland (1929) | 8 | 0,2% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Blackwelder (1943) | 8 | 0,2% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Boisduval (1833) | 8 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Corporaal (1937) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Csuzdi & Pavlíček (2009) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Dadant & Etienne (1973) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Distant (1914) | 8 | 0,2% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Dupont et al. (2023) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Fennah (1969) | 8 | 0,2% | 7 | 0,65% | 5 | 0,49% | 5 | 0,48% |
Ferrer (2015) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Fisher & Fong (2020) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Flechtmann et al. (2000) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Guenée (1862) | 8 | 0,2% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Háva (2014) | 8 | 0,2% | 7 | 0,65% | 6 | 0,58% | 7 | 0,68% |
Kuschel (2008) | 8 | 0,2% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Leijs et al. (2017) | 8 | 0,2% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Meganck et al. (2017) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 7 | 0,68% |
Pintureau et al. (2011) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
UICN Comité français, OFB & MNHN (2021) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 7 | 0,68% |
Uicn et al. (2015) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 7 | 0,68% |
Vedel et al. (2013) | 8 | 0,2% | 8 | 0,75% | 8 | 0,78% | 8 | 0,77% |
Arrow (1927) | 7 | 0,17% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Beaver & Liu (2016) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Beeson (1935) | 7 | 0,17% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Berland (1942) | 7 | 0,17% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Bouchet & Pointier (1998) | 7 | 0,17% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Brown (2009) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Carpenter (2023) | 7 | 0,17% | 7 | 0,65% | 5 | 0,49% | 6 | 0,58% |
CEN Nouvelle-Calédonie (2021) | 7 | 0,17% | 5 | 0,47% | 4 | 0,39% | 5 | 0,48% |
Chalumeau (1983) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Chazeau et al. (1974) | 7 | 0,17% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cheesman (1927) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Clarke (1986) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Cooke (1934) | 7 | 0,17% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
[Denis & Schiffermüller] (1775) | 7 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1850) | 7 | 0,17% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Garrouste & Hervé (2009) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Guillermet (2004) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 4 | 0,39% |
Gutierrez & Etienne (1986) | 7 | 0,17% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Marchán et al. (2022) | 7 | 0,17% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 6 | 0,58% |
Matile-Ferrero & Williams (2015) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Meyrick (1934) | 7 | 0,17% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Mille (2008) | 7 | 0,17% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Ortiz-Sepulveda et al. (2019) | 7 | 0,17% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Parnaudeau (2012) | 7 | 0,17% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Prévost & Mougin (1970) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 5 | 0,48% |
Ramage et al. (2015) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Ramage et al. (2017) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Souza et al. (2019) | 7 | 0,17% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Szederjesi et al. (2019) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Talaga et al. (2015) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Touroult et al. (2018) | 7 | 0,17% | 7 | 0,65% | 7 | 0,68% | 7 | 0,68% |
Welter-schultes (2012) | 7 | 0,17% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Abdou et al. (2004) | 6 | 0,15% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Aulagnier (2009) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 4 | 0,39% |
Bigot & Etienne (2009) | 6 | 0,15% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Brun et al. (1983) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Butaud (2021) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 5 | 0,48% |
Ceccolini (2023) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Collenette (1934) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 5 | 0,48% |
Coulis (2017) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Dierkens (2021) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Černosvitov (1934) | 6 | 0,15% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Fabricius (1798) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Falkner et al. (2002) | 6 | 0,15% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Fort & Barrière (2021) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 4 | 0,39% |
Fricke et al. (2011) | 6 | 0,15% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Gargominy et al. (2011) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Gould (1852) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Grimpe & Hoffmann (1925) | 6 | 0,15% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Groom et al. (2016) | 6 | 0,15% | 5 | 0,47% | 5 | 0,49% | 4 | 0,39% |
Guillermet (2006) | 6 | 0,15% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Guillermet (2009) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Gustafsson & Zou (2020) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Hebard (1933) | 6 | 0,15% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Holloway & Peters (1976) | 6 | 0,15% | 5 | 0,47% | 5 | 0,49% | 4 | 0,39% |
Hullé & Vernon (2021) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Hustache (1920) | 6 | 0,15% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Iorio & Coulis (2020) | 6 | 0,15% | 6 | 0,56% | 2 | 0,19% | 6 | 0,58% |
Jacot (1934) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2021) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Keith et al. (2006) | 6 | 0,15% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Klyver (1932) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Kreiter & Moraes (1997) | 6 | 0,15% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lagarde (2008) | 6 | 0,15% | 4 | 0,37% | 3 | 0,29% | 4 | 0,39% |
Leraut (1997) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Luc & Coomans (1992) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Montrouzier (1858) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1790) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Orhant (2002) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Pascal et al. 2006 | 6 | 0,15% | 6 | 0,56% | 5 | 0,49% | 6 | 0,58% |
Pavlíček & Csuzdi (2012) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Potin (2013) | 6 | 0,15% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Raspi et al. (2007) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 3 | 0,29% |
Savouré-Soubelet et al. (in prep.) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 5 | 0,48% |
Schouteden (1907) | 6 | 0,15% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 6 | 0,15% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Voisin et al. (2017) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Wetterer (2012) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Wetterer (2014) | 6 | 0,15% | 6 | 0,56% | 6 | 0,58% | 6 | 0,58% |
Wygodzinsky (1966) | 6 | 0,15% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Aberlenc et al. (2004) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Allen et al. (2022) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Barau et al. (2005) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Beaver (1991) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Bernard (1968) | 5 | 0,12% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Bielawski (1973) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Bochaton et al. (2021) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Boyer & Rivault (2003) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Chopard (1924) | 5 | 0,12% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Chown & Convey (2016) | 5 | 0,12% | 4 | 0,37% | 4 | 0,39% | 3 | 0,29% |
Damgaard & Zettel (2014) | 5 | 0,12% | 5 | 0,47% | 4 | 0,39% | 4 | 0,39% |
Disney & Chazeau (1990) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Distant (1920) | 5 | 0,12% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Escalona & Ślipiński (2010) | 5 | 0,12% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Evenhuis (2012) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 4 | 0,39% |
Fauvel (1883) | 5 | 0,12% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Fouquet (2000) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Fricke et al. (2009) | 5 | 0,12% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Gusenleitner & Madl (2011) | 5 | 0,12% | 5 | 0,47% | 2 | 0,19% | 5 | 0,48% |
Gutierrez (1968) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Hammer (1972) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Hayashi (1961) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
James & Gamiette (2016) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Jay et al. (2009) | 5 | 0,12% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Kuhlmann (2006) | 5 | 0,12% | 4 | 0,37% | 3 | 0,29% | 4 | 0,39% |
Kurahashi & Fauran (1980) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Laporte de Castelnau & Brullé (1840) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Leroy et al. (2021) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Levesque & Delcroix (2018) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Lucas (2012) | 5 | 0,12% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Malloch (1932) | 5 | 0,12% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Malloch (1933) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Marquet & Roguet (2003) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Massemin et al. (2009) | 5 | 0,12% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Matile-Ferrero et al. (2000) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Mériguet & Zagatti (2016) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Montrouzier (1861) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
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) |
5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Revilliod (1914) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Routtier et al. (2023) | 5 | 0,12% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Schrank (1781) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1874) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Théry & Bordat (2012) | 5 | 0,12% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Vachal (1907) | 5 | 0,12% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Wetterer (2012) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Wetterer (2013) | 5 | 0,12% | 5 | 0,47% | 5 | 0,49% | 5 | 0,48% |
Wood (1989) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ascher et al. (2016) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Aulagnier (2021) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 3 | 0,29% |
Barnouin et al. (2020) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Beaucournu et al. (1998) | 4 | 0,1% | 4 | 0,37% | 3 | 0,29% | 3 | 0,29% |
Beaucournu (1968) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Beeson (1940) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 4 | 0,1% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bellmann (2019) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 3 | 0,29% |
Bolton (2012) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonfils et al. (1994) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Bouchet et al. (1991) | 4 | 0,1% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Busala et al. (2024) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Caceres & Salamolard (2021) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 3 | 0,29% |
Cramer ([1777]) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
David & Tsacas (1975) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Dole & Cognato (2010) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Dupérré (2023) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Ermilov & Mary (2019) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Ermilov & Mary (2020) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Ermilov et al. (2013) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Fabricius (1794) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1893) | 4 | 0,1% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Flechtmann & Etienne (2000) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Forcellini et al. (2012) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Fourcroy (1785) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy (2016-2021) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Garrett (1887) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy (2016) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 2 | 0,19% |
Guilbert & Casevitz-Weulersse (1997) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Guilbert (2002) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Gusenleitner (2011) | 4 | 0,1% | 4 | 0,37% | 3 | 0,29% | 4 | 0,39% |
Halstead & Green (1979) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Hausdorf (2023) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Hebard (1935) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Holovachov (2019) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Hullé et al. (2003) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Hullé et al. (2010) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Jacot (1934) | 4 | 0,1% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Keith et al. (2002) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Keith et al. (2011) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Kim et al. (2004) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Kreiter et al. (2002) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Kreiter et al. (2018) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Kreiter et al. (2022) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Le Divelec (2024) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Lopez-Vaamonde et al. (2010) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Madl (2014) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Mauriès (1980) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 4 | 0,1% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Nava et al. (2018) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Niedbała & Liu (2023) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Niedbała (2000) | 4 | 0,1% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Norrbom & Hancock (2004) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Pascal et al. (2006) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Periasamy et al. (2015) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Pilsbry (1920-1921) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Polhemus & Herring (1970) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 3 | 0,29% |
Preece (1995) | 4 | 0,1% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Pritchard & Baker (1955) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Putshkov et al. (1999) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Questel (2016) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Quilici et al. (2000) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Radoszkowsky (1884) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Ramage (2024) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Rasplus et al. (2010) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Rheinheimer (2014) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Rigaud et al. (1997) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Russell & Etienne (1985) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Samuelson (1973) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Séguy (1960) | 4 | 0,1% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Shockley et al. (2009) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Silvestri (1935) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 3 | 0,29% |
Theobald (1913) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Thompson (1938) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 3 | 0,29% |
Timberlake (1941) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Touroult et al. (2020) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Tsacas & Chassagnard (1988) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 4 | 0,39% |
Vandenspiegel & Mathys (2021) | 4 | 0,1% | 4 | 0,37% | 4 | 0,39% | 3 | 0,29% |
Wenzel (1955) | 4 | 0,1% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Adamson (1932) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Adamson (1935) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Atyeo & Gaud (1992) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Aubert & Beaucournu (1976) | 3 | 0,07% | 3 | 0,28% | 2 | 0,19% | 3 | 0,29% |
Baker (1938) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Beatty et al. (2008) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Belon (1884) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Berry et al. (1997) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Berry et al. (1998) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bigot & Drouet (2014) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bippus (2019) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Brindle (1976) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Brun & Chazeau (1986) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Brunhes (1979) | 3 | 0,07% | 2 | 0,19% | 1 | 0,1% | 2 | 0,19% |
Burneleau (1983) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 1 | 0,1% |
Cameron (1933) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Catzeflis (2018) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Chamberlin (1920) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Coomans (1967) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Couri et al. (2010) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
David et al. (2014) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
De Geer (1778) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Des et al. (2021) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Deshayes (1863) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2019) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Dewynter et al. (2022) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Dewynter et al. (2023) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Dewynter et al. (2023) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Donisthorpe (1932) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupont & Coulis (2023) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Easteal (1981) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Esper ([1796-1805]) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2007) | 3 | 0,07% | 2 | 0,19% | 1 | 0,1% | 2 | 0,19% |
Evenhuis (2011) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Fabricius (1781) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1877) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Fauvel (1882) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1958) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Férussac (1821) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Flechtmann & Etienne (2006) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Forel (1899) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gamiette et al. (2023) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Geer (1774) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Gerber (2018) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Germain et al. (2014) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Gielis (2011) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Godefroid et al. (2017) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
González-sánchez et al. (2021) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Grandison et al. (2009) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Haas et al. (2015) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 0 | 0% |
Hamon (1953) | 3 | 0,07% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Hausdorf (2007) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Háva & McCormack (2022) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Hava (2006) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Holzschuh (1995) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Howard (1881) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hsu et al. (2020) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Jackson (1933) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
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 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Jerdon (1851) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson et al. (2021) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Justine et al. (2021) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Keith et al. (2014) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Keith (2002) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Kerney & Cameron (1999) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Kirejtshuk & Lawrence (1999) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Kormilev (1971) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lafranchis (2014) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Lafranchis (2016) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Lamy & Pointier (2018) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Le Maitre & Chadee (1983) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Lenfant & Marro (1997) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 0 | 0% |
Leraut (2012) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Lesne (1901) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Liu & Zhang (2014) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Liu (2021) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Lupoli (2023) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Mannerheim (1844) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Marie & Bossin (2013) | 3 | 0,07% | 2 | 0,19% | 1 | 0,1% | 2 | 0,19% |
Marie & Vetter (2015) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Marples (1957) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Marsham (1802) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinez & Etienne (2002) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Martinez-Torres et al. (1997) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Massary et al. (2021) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Mauriès (1983) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Mauriès (1987) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
McGregor (1949) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mesibov (2014) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Meyrick (1934) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Millière (1863) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mirouse (1958) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Monterosato (1892) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Motschulsky (1858) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Navajas et al. (2010) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Nentwig et al. (2019) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Nève de Mévergnies et al. (2024) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Nicolas (2012) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Olivier (1790) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Onteniente & Babío (2002) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pace (1991) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Pauly & Munzinger (2003) | 3 | 0,07% | 2 | 0,19% | 1 | 0,1% | 2 | 0,19% |
Perris (1866) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Poussereau (2015) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Price & Beer (1963) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Princis (1974) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Probst (2001) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Questel et al. (2023) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Questel et al. (2023) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Questel (2017) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Questel (2023) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Ramage et al. (2018) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Razowski (2013) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Rehn (1949) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Rheinheimer (2012) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Risbec (1956) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rispe et al. (1999) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Ronot (2007) | 3 | 0,07% | 2 | 0,19% | 1 | 0,1% | 2 | 0,19% |
Roth & Rivault (2002) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Salata & Fisher (2022) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Sanchez (2020) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Sasakawa (1963) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Schileyko et al. (2024) | 3 | 0,07% | 3 | 0,28% | 2 | 0,19% | 3 | 0,29% |
Schulthess (1915) | 3 | 0,07% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Séret (1997) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Seurat (1934) | 3 | 0,07% | 3 | 0,28% | 2 | 0,19% | 3 | 0,29% |
Shinonaga et al. (1991) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Silvestri (1934) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Simon et al. (1991) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Simon (1897) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Smith et al. (2020) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Solsky (1871) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Spencer et al. (1992) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Starmühlner (1970) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Stewart (1934) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Taczanowski (1871) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult (2005) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Turner (1919) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Urvois et al. (2023) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Van Duzee (1937) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Viette (1950) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Viette (1950) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 1 | 0,1% |
Viette (1979) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Wallach (2020) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ward et al. (2015) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Wetterer & Hita Garcia (2015) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Würmli (1974) | 3 | 0,07% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Yeates (1992) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Zahradník & Poussereau (2022) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Zakardjian et al. (2020) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 2 | 0,19% |
Zilli et al. (2017) | 3 | 0,07% | 3 | 0,28% | 3 | 0,29% | 3 | 0,29% |
Zimmerman (1936) | 3 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Adachi & Fullaway (1953) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ali (1993) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Alley et al. (2023) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Altson (1923) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Altson (1924) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Antheaume (2011) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Aoki (1959) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Archibald & Maddison, 1988 | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Aubouin et al. (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Azab et al. (1972) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bagnall (1919) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1941) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Baker (1986) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 0 | 0% |
Balthasar (1966) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bameul (1986) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bangy et al. (2009) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Banks (1900) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut et al. (2006) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Baroni Urbani & De Andrade (2007) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Barré & Moutou (1982) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bauer & Sadlier (2000) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer (1987) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Belfan & Conde (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bell et al. (1989) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bellemare & Brunelle (1950) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Berland (1927) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bertrand (1949) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bertrand (1950) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bhatti (1978) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bieńkowski & Orlova-Bienkowskaja (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bigot (2011) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Binney (1841) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Biondi et al. (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bippus (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Blackburn (1888) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Blair (1934) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Blair (1934) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Blanchard (1939) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1829) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (2007) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bonadona (1981) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bondroit (1916) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Borkhsenius (1958) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Borth & Kons (2022) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Bourgeois (1884) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousses et al. (2013) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Boyer de Fonscolombe (1832) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil et al. (2010) | 2 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Breuil (2002) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brindle (1971) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Brindle (1975) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Brito et al. (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Brölemann (1931) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brosse et al. (2021) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Brunhes & Boussès (2009) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Brunhes (1977) | 2 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Burr (1914) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Callot et al. (1967) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Carl (1915) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Caron et al. (2008) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cassis & Gross (2002) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cerkowniak et al. (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Chamberlin (1918) | 2 | 0,05% | 2 | 0,19% | 0 | 0% | 2 | 0,19% |
Chapuis et al. (2004) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 0 | 0% |
Chatthanabun et al. (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Chebbah et al. (2023) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cheon et al. (2023) | 2 | 0,05% | 2 | 0,19% | 0 | 0% | 2 | 0,19% |
Chevalier & Dewynter (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Chûjô (1961) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Chûjô (1964) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Coache (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cobb (1893) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1966) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cockerell (1893) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohn & Sher (1972) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Coiffait (1976) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cole et al. (2005) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Constantin (2012) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Cooke & Kondo (1961) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Courtial (2023) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cramer ([1779]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer ([1780]-1782) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1867) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1868) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dajoz (1970) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Damoiseau (1966) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Daniel et al. (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Decaëns et al. (2024) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Deknuydt et al. (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Delport (2018) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Delsalle & Sechet (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Demange (1981) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Desutter-Grandcolas et al. (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Dobson (1954) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dobson (1956) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dognin (1908) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duay et al. (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Dumbardon-Martial & Delblond (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Dumbleton (1956) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupouy (1966) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duyck et al. (2022) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Eggers (1933) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
, 3: 249-270.">Enderlein (1903) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Enders (1993) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Černosvitov (1936) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne & Dumbardon-Martial (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Etienne & Gagné (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Etienne & Martinez (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Etienne & Matile-Ferrero (2008) | 2 | 0,05% | 2 | 0,19% | 0 | 0% | 2 | 0,19% |
Evenhuis (2007) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Evenhuis (2011) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Evenhuis (2011) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Evenhuis (2012) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ezzat (1958) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Fabres (1974) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Fabricius (1781) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1805) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fall (1910) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fan & George (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Faucheux (1990) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Faucheux (2005) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Fauvel (1878) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Fauvel (1903) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1963) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferragu (1979) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ferris (1935) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Férussac (1822) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fikáček (2010) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Flechtmann & Etienne (2001) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Flechtmann & Etienne (2005) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Flechtmann et al. (1999) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Fleutiaux (1932) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Fontenot et al. (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Freyer (1842-1845) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1927) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Gargominy (2011-2023) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Genier & Moretto (2017) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Geoffroy (1762) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Gielis (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1995) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gilot et al. (1992) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Girard (2007) | 2 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Gmelin (1789) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Godet et al. (2021) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Gomes & Thome (2004) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Gomy et al. (2009) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Gonzales & Yvinec (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Gonzales et al. (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Gould (1843) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Goux (1948) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Graber et al. (1997) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Green (1930) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Gros (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Gude (1900) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1852) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1854) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gyllenhal (1827) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hagstrum & Subramanyam (2009) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hale et al. (2008) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hamon (1956) | 2 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Hancock (2008) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Harimalala et al. (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hartmann et al. (2021) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Haupt (1927) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Haynes (2001) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Heppner (1982) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hervé & Garrouste (2009) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hery et al. (2020) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hielkema & Hielkema (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hindermeyer et al. (2007) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Hodkinson (1983) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Horváth (1914) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hossain et al. (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hübner (1796-[1828]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1836]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hull (1937) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hutton (1834) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hyman & Ponder (2010) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Hynes (1993) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Ineich et al. (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ito & Hirose (1978) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Jackson (1941) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Johnson (1994) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolivet (1979) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jones et al. (2006) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Jones et al. (2007) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Jordan (1933) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jordan (1933) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Justine et al. (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Justine et al. (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Justine et al. (2021) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaszab (1985) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Kawamoto & Okado (1987) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Keith et al. (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Kieffer (1898) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Knight (1987) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kreiter et al. (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Krombein (1950) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kutschera (1987) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lackner & Leschen (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 0 | 0% |
Lacoste (de) (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Lambert (1988) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lardeux & Cheffort (1996) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lavauden (1929) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Breton et al. (2005) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ledoux (2007) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1949) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Legrand (1953) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Leponce et al. (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lescure et al. (2012) | 2 | 0,05% | 2 | 0,19% | 1 | 0,1% | 1 | 0,1% |
Lesne (1897) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Levesque & Clergeau (2002) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lim et al. (2002) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Linnaeus (1761) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lions (1966) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lis (1997) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lis (1999) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Löbl & Smetana (2007) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Logvinovskaya (1983) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lordello (1951) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lourenço (1987) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Luc (1958) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Lucas (1847) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli & Dusoulier (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Madl & van Achterberg (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mann (1921) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchal et al. (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Marquet et al. (2003) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Martoni & Brown (2018) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mas-Coma et al. (1989) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Maskell (1893) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Massary et al. (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Massary et al. (2018) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Massary et al. (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mckamey (2010) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Medkour et al. (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mengual (2018) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Meurgey & Dumbardon-Martial (2015) | 2 | 0,05% | 2 | 0,19% | 1 | 0,1% | 1 | 0,1% |
Meurgey (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Meurgey (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 0 | 0% |
Meyrick (1886) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1926) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1878) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mifsud et al. (2010) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Migeon et al. (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mille et al. (2012) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mock & Matthyssee (1977) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mollot et al. (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Moulton & Steinweden (1933) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mound & Halsey (1978) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mound & Masumoto (2005) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mound et al. (2010) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Mound (1974) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mroczkowski (1968) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 0 | 0% |
Muratet (2015) | 2 | 0,05% | 2 | 0,19% | 1 | 0,1% | 1 | 0,1% |
Nagaraja & Nagarkatti (1969) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Nageleisen et al. (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Najt & Weiner (1997) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nicolas & Scoles (1997) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Nicolas et al. (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas et al. (2024) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Niedbała (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ohm & Hölzel (1997) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ohm & Hölzel (1998) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Osborn (1934) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Otte et al. (1987) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Panis (1969) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1796]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnaudeau & Madl (2009) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Parnaudeau (2009) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Patrick & Patrick (2012) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Pelosse (1927) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Percy (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Pfeiffer (1846) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre et al. (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Pilsbry & Cooke (1915-1916) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1909-1910) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1916-1918) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Pistil & Kontykowski (1974) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Platnick & Baehr, 2006 | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Platnick & Dupérré (2009) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Platnick et al. (2012) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Pointier & Marquet (1990) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Pointier (2001) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pont (1979) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Poussereau (2007) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Probst et al. (2022) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Quentin & Villiers (1979) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Questel (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Quilici et al. (1997) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Rakowski et al. (1981) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ramage (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Rammah & Hirschmann (1988) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Raven (2015) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Razowski (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Reinert et al. (2004) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Reise et al. (2011) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Remsen et al. (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Reverté et al. (2023) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Rheinheimer (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Richard (1957) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1914) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Rivault et al. (1991) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Robin & Megnin (1877) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Robineau-desvoidy (1827) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Robinson (1975) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rocamora (2004) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Roger (2018) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Roman & Puech (1965) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Royer et al. (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ruecker (2005) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell (1958) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Russell (1965) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Ruys & Coord (2012) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Sadlier et al. (2012) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Saint et al. (1978) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Salin et al. (2003) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Sanchez & Probst (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Sanchez et al. (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Sardet et al. (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Schedl (1940) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schedl (1980) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schileyko et al. (2018) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Seifert (2003) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sellnick (1959) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Senevet (1937) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sharp (1898) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Shelley (2004) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Siroux (2012) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Siroux (2018) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Sluys (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Smith (1857) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Speare (1990) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stewart (1934) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Streito et al. (2010) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Sudre & Teocchi (1996) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Sudre & Teocchi (2000) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Swaine (1934) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1840) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1872) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1874) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Talaga et al. (2015) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Taquet et al. (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Thibault et al. (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Thierry & Canard (2021) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Thorell (1887) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tirvengadum & Bour (1985) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tomaszewska (2010) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Touroult et al. (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Tronquet (2015) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Uicn et al. (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Uicn et al. (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Vago (1997) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Van Meer & Cocquempot (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Van Zwaluwenburg (1932) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Van Zwaluwenburg (1940) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Vandel (1981) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Vane-Wright & De Jong (2003) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 0 | 0% |
Varenne & Billi (2008) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vayssières et al. (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Vedovini (1969) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1926) | 2 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Viel (2021) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Votýpka et al. (2020) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Walckenaer ([1841]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1865) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1923) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Whitworth (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Will (2011) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Will (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Williams & Watson (1988) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood & Bright (1992) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Yang et al. (2023) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Yano (1963) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Younes et al. (2021) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 1 | 0,1% |
Zanetti et al. (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Zimmerman (1968) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Zimmermann et al. (2005) | 2 | 0,05% | 2 | 0,19% | 2 | 0,19% | 2 | 0,19% |
Abdel-kader & Barak (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Abhaya et al. (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Abood & Murphy (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Abraham (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Adams (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguirre et al. (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Alencar et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Allen (1890) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Alonso-zarazaga & Evenhuis (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Alonso-Zarazaga (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Alston (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Altamirano-Benavides & Woolrich-Piña (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Altamirano-benavides & Woolrich-piña (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Alvarez-berríos et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ancey (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
André (1938) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Arenberger (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ariagno & Erome (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Arnold & Ovenden (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Ascete (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ashmead (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ashmead (1905) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Astorga-acuña & Mora (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Astrongatt (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Audouin (1826) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Auger et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Azam (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagnall (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagny et al. (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailenger et al. (1965) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Balachowsky (1958) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Balhoff et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Banks (1905) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut & Voisin (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Barré et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barrière & Fort (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Baubet & Saint-andrieux (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bauer & Sadlier (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bauer et al. (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Beaucournu et al. (1964) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Beaucournu et al. (1985) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Beaucournu et al. (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Becerra et al. (2024) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Beenen (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Beggs et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Béguinot (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Behm et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Behm et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Belkin et al. (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Belles (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Belles (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellifa et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Beltramino et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bencheton et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Benson (1850) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Berenger & Pluot-Sigwalt (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Berlese & Paoli (1916) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Berlese (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (1949) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Betrem (1961) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bippus (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bippus (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blair (1934) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blair (1940) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blakemore et al., 2006 | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blanchot (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Blancou et al. (1987) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blight et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blommers (1974) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bocquillon (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Boheman (1858-1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1827) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton & Fisher (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bolton (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bondar (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Borowiec et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bouché (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchez-Zacria et al. (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bouget & Noblecourt (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bour et al. (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Bousquet (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousquet (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bout et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bowdich (1822) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyd et al. (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Boyer & Rivault (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Boyer & Rivault (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Boyer & Rivault (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Boyer de Fonscolombe (1834) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Brahm (1791) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brandt (1833) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brinon et al. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Briones (1996) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brisbane et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Brongniart (1800) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bruguière (1789-1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brumpt (1929) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Brustel & Roge (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bur (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Buttner (1953) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cabaret et al. (1986) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot & Rioux (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Callou (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Cameron (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1933) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cameron (1936) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Candy et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Capalleras & Carretero (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Capps (1953) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Carl (1926) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Carpenter & Madl (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Carpenter (1996) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Casey (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cassis & Vanags (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Catala (1948) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cazanove (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Caziot (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Célini et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cerkowniak et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Chabrol (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Chalumeau & Touroult (2005) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Champagne et al. (1997) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Champion (1922) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapelin-Viscardi & Lariviere (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Chapuis & Eichhoff (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chastel et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Chatard (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chazeau (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chebbah et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cheke (1987) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cheke (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chen (1938) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevin (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cheylan et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Chopard (1915) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Chopard (1930) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Coatmeur (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cobb (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cobb (1913) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cobb (1917) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cobbold (1878) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochard et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cockerell (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cockerell (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1959) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coiffait (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Colin (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Colindre (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Colindre (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Collet & Pérennec (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Conte et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Cooke (1928) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cooreman (1959) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Corpuz-Raros (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cosson (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cowie et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Crotch (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Crotch (1873) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cummings et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Curtis (1823-1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Czechowski et al. (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dalla Torre (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Daly et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dard et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dard et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Darling & Génier (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Darlington (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Daudin (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauphin (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
De Geer (1773) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
de Massary et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Deblock et al. (1960) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Deeming (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Defo et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Degallier & Gomy (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Degallier (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Deharveng & Najt (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Déjean & Danflous (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Déjean et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Delabie & Blard (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Delabie et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Delobel & Guttierrez (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Delobel & Tran (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Denoyes et al. (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Denys et al. (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Derozier (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Desutter‐grandcolas (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Deuss et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dewynter & Claessens (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dewynter et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Dewynter et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Dewynter (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dewynter (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dhondt (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Dickey et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dieme et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dillon (1957) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dispons (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Distant (1920) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dobosz (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Doguet (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dollfus (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dominique (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Donini & Doody (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Donskoff (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dosse (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dozier (1937) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Drake (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
D'souza & Jagannath (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dubois & Frétey (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dubois et al. (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dubois (1996) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Ducos (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dufay (1975) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufay (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufour (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dugès (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-Martial et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Duméril & Bibron (1836) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Duponchel (1836-[1837]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupuis (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Duquef (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Duquef (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Duval et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Eason (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Eaton et al. (1879) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Edwards (1933) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Eggers (1930) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Eggers (1944) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehara & Amano (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Eichhoff (1868) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Elder & Abraham (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Elder (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Elder (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Emery (1869) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Emery (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1894) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Emery (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Černosvitov (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Esben-Petersen (1937) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Escherich (1905) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Esper (1776-1779) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Etienne et al. (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
European Commission (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Evans (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Evenhuis (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Evenhuis (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Evenhuis (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Evenhuis (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Evenhuis (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ewing (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Eyles (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fabre & Orsini (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fabres (1977) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fabricius (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1802) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernández et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ferrer & Poussereau (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ferris (1932) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ficetola & Scali (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Finnerty et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Firmat & Alibert (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer & Madl (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fischer (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Bedoucha (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Flechtmann & Atkinson (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Flechtmann & Etienne (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fleutiaux (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Floch & Abonnenc (1949) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fontanilla & Wade (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fontanilla et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Forel (1874) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Forel (1881) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Forel (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1890) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fossati & Marquet (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Frank (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Friese (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Froggatt (1897) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fueßlin (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fullaway (1942) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Furminieux (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gahan (1924) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gaimari (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gall & Beague (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Galliard (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallien-lamarche (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy & Fontaine (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gargominy (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Garrett (1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrett (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gasnier et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gassies (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gates (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gates (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gay (1953) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Geijskes (1939) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Geneva et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Geoffroy & Iorio (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gérard et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gerberg (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerlach (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Germain & Streito (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Germain et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Germain (1931) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1824) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Geyer & Frölich (1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill et al. (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Girault & Dodd (1915) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Girod & Matzke (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Girod (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Godfrey (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goeze (1783) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goldarazena et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Golovatch et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gomy (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gomy (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gonzalez & Vetrovec (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
González et al. (2018) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Goudey-Perriere et al. (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Goudey-Perriere (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gould et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourvès & Samuelson (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Goux (1937) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Goyaud & Lemarie (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gozlan et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Graber & Euzeby (1976) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Graham (1969) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Graham (1987) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Graham (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grandjean (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grange (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Grant-mackie et al. (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1831) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Green (1896) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gressitt (1960) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gressitt (1960) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Griffing et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Grote (1873) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grouvelle & Raffray (1908) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Guenée (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guernier et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Guilbert (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Guiller & Madec (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Guillermet (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gupta (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hacala et al. (2024) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hacker (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamdi et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Han & Ro (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Haouchine et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Harman (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Harold (1867) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hava & Poussereau (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Háva et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Háva (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Háva (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hazir et al. (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hebard (1921) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hedges et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heer (1838-1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heiss (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemp & Dettner (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Henao-osorio et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hengoat (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hentz (1847) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Heppner (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Herbst ([1791]-1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hering (1951) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hinckley (1963) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Honey & Scoble (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Horvàth (1895) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Howard (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Howard (1906) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hoyer (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hübner (1796) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Huchet & Labatut (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Huchet (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hudson et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hudson et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hufnagel (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugel & Blard (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hustache (1926) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
ICZN (1954) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ide et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Iković et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Ineich & Bauer (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Fischer (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ineich et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ineich et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ineich (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Iorio & Berg (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Iorio et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Iorio (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Irish et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ito (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
IUCN (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Iwan et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Iwata & Nishimoto (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Izri & Akhoundi (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jackson (1938) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jacquelin du Val (1861) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jacquot et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jäger (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jamonneau et al. (2025) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jansson (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Jena et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jiroux (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Johnson et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Johnson (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolivet (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Joubert (1985) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jourdain et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Justine & Winsor (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kaiser (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaltenbach (1968) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kameneva & Korneyev (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Karny (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Karny (1925) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kassebeer (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Keith & Marquet (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Keith et al. (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Keith (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Keith (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Keith (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Klein et al. (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Klug (1801) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Koch (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kofoid & White (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolibáč (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kormilev (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kornilev et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Kozár (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kreiter & Douin (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kronmüller (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Kugelann (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kugler (1967) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kumar et al. (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Labat (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Lacoste (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lacroix (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Laguerre (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Laidoudi et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Laidoudi et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lamb (1914) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lamontellerie (1965) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lancastre et al. (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lapwong et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Latreille (1802) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1804) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Latreille (1806) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1807) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Latzel (1892) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Le Bail et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Le Goff et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Leach ([1816]) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Leavengood et al. (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lebard & Claude (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lebard & Hauser (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Leger & Le Gallen (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemagnen (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaire (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lenoir et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lepertel & Quinette (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Leraut (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Leschen & Newton (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lescure & Marty (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lescure et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lesson (1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lethierry (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Mathurin (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Levi (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Liénard et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Light & Zimmerman (1936) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Light (1932) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Light (1932) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Likhitrakarn et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linford & Oliveira (1940) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lis (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Liu et al. (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lohez (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lonc & Modrzejewska (1987) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lordello & Costa (1961) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lordello (1955) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lorvelec et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lorvelec et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lourenço (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lovenburg (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lower (1898) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1858) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Luziau (1953) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Madl & Ganeshan (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Linzer Biologische Beitraege, 44(1): 591-594. ">Madl (2012) |
1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mahunka (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mahunka (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Maillard & David (2014) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Malausa & Ehanno (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mammola & Milano (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Maquart et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marchandeau & Letty (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Marchandeau et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Marchioro et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marcos-garcía et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Maréchal & Iinuma (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marks (1951) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marshall (1921) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Massary (2012) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Matile-Ferrero & Etienne (1996) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Matos-Maraví et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Matsuzaki et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mayr (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayr (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazur & Węgrzynowicz (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mcevey & Schiffer (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mckay & Milenkaya (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Melin et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Melot et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ménard et al. (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Menezes et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Menezes et al. (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mercet (1931) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Metcalf (1955) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Questel (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Meurgey (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Meyrick (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1907) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Meyrick (1916-1923) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Meyrick (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaelsen (1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaelsen (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mille et al., 2012 | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mille et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mille et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Miremad-gassmann (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Miyatake (1968) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Moniez (1898-1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Monné et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Monteith et al., 2006 | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Monti et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Montrouzier (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morgan (1889) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morin (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Motschulsky (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moulton (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mound & Collins (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mouttet & Taddei (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Murienne et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nakahara (1960) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nakata (1961) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nassi et al. (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Natural History Museum of London (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Naudon et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Neid (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nel & Varenne (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nentwig & Kobelt (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Neumann (1901) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Newport (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Newstead (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nicolas (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Niedbała & Starý (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Normark et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
O'brien (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ôhira (1971) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Oliver & Reichenbach-Klinke (1973) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Olivier (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
">Olliff (1889) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Onillon et al. (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Opitz (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Orbigny (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Orhant (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Osuji (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Osuji (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Oudemans (1923) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pace (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pace (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Palmer (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pang et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Parker & Fitzgerald (2024) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Patrick (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Paulay (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulian & Félice (1941) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Paulian (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pauly et al. (2001) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Peale (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Perkins (1907) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Perkins (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrault (1977) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Perrin et al. (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Persat & Keith (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Peters (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Petryszak et al. (1996) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pettit et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pfeiffer (1850) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippot et al. (2019) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Pierre & Lalanne-Cassou | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Pilsbry (1927-1935) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pintureau et al. (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pirot & Bourgain (1942) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pocock (1898) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pointier & Blanc (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Delay (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Poisson (1940) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Poisson (1957) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pol et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ponel et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Portanier et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Poussereau & Lecoq (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Poussereau (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Powell & Henderson (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Preece (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prena (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Priesner (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prins et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pritchard & Baker (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Probst (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prout (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pulawski (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Putshkov (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Quaintance (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Quindroit & Lemoine (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Quindroit (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Randi et al. (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Raphael (1970) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Reeve (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Régimbart (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rehn (1948) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Renaud et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Reynolds et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rhodin & Carr (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ringler et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rivière (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Robin & Dalens (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rocha et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Roger (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roman (1938) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Roman (1951) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Romero et al. (2010) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Rondani (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosenbaum et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ross (1955) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rossi & Godoy (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rossi (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rota (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Roth (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Martinez (1987) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Roux (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rozkosny (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rudolphi (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rungs (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Saha & Maiti (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sakimura (1955) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Salles et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Samaniego et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Santschi (1920) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sato (1966) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Saunders (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Saunders (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1867) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Sautet (1936) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sauvion et al. (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Savigny (1826) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1823) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Say (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sayed (1946) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Schedl (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schedl (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schoepff (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linzer Biologische Beitraege, 41(1): 767-801. ">Schöller (2009) |
1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Schönherr (1806) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schott & Callot (1994) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schott (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schreber (1777) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Schuurmans Stekhoven & Teunissen (1938) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sciacchitano (1932) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scoble et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Séchet & Noël (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Séméria & Quilici (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Servan & Arvy (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Seyfullah et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Shaaya (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Shahhosseini (1980) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sharp (1916) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sher (1966) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sherpa et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Shine et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Shine (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Shiraki (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Siddaiah & Kujur (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Siddiqi (1961) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Siddiqi (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Silvestri (1915) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Simon (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Simroth (1918) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Siroux (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Siroux (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Siroux (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Siu et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Skierska (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Skuhravá et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Smith (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Snyder et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Socolovschi et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Soldati et al. (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Solem (1959) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sonan (1932) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
SORDELLO (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Stahl et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Stainton (1856) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Stainton (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Starý et al. (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Steiner (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stenram (1956) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Stephens (1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stoev et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Storer et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Streito et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sturm (1807) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Subías (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Széles et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Talamas et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tamaki et al. (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
IOBC-WPRS Bulletin, 18(5): 36-38.">Tamonte (1995) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor & Wilson (1961) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Telnov (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Telnov (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tenorio (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Teunissen & Peters (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thévenot (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thibaud (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thibault (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thnberg (1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thompson (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thorell (1897) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tixier et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Touroult et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Touroult et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tronquet (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Trotignon (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tryon (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tryon (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Turner (1904) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Turpin & Probst (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Tuthill (1942) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Unruh & Gullan (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Urvois et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Usinger & Beaucournu (1967) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Valencia-zuleta et al. (2024) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Valentine (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
van den Burg et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Van Dyke (1932) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Van Zwaluwenburg (1932) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vandeschricke et al. (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vannini et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vantaux et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Varenne & Nel (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vayssières et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Veysset (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Viallet (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Viette (1949) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Viette (1959) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Viette (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Vigne et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vilardebo & Guerout (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Villa & Villa (1833) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Villers (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vinson (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vorst (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1839) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Walker (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1863) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Walker (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1865-[1866]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walt (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Warner (1970) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Watson et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Webb & Waddle (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Weterings & Vetter (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Wheeler (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wied (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiedemann (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams (1932) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Wilson (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wittmer (1968) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Wollaston (1854) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wollaston (1858) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wollaston (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Works & Olson (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Yamane et al. (1996) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Yassin et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Yasumiba et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Yokoyama (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ythier (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zagatti & Cotte (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zanetti et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zatwarnicki (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zdunek (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zeller (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zeller (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zeller (1848) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zeller (1852) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zeller (1879) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zeller (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhou et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zimmerman (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zimmerman (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zug & Zug (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zug et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |