Espèces animales introduites dans l'océan Indien
Animaux introduits au sens large dans l'océan Indien, c'est-à-dire introduits établis (I), invasifs (J), introduits non établis (M) ou introduits éteints (Y). Par "océan Indien" on entend: la Réunion, Mayotte et les îles Éparses.
1819 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Ramage (2017) | 184 | 5,74% | 176 | 22,95% | 176 | 24,04% | 174 | 23,39% |
Meurgey & Ramage (2020) | 158 | 4,93% | 156 | 20,34% | 156 | 21,31% | 155 | 20,83% |
Meurgey (2011) | 133 | 4,15% | 107 | 13,95% | 107 | 14,62% | 106 | 14,25% |
Jourdan & Mille (2006) | 131 | 4,08% | 122 | 15,91% | 122 | 16,67% | 120 | 16,13% |
Poussereau et al. (2018) | 118 | 3,68% | 56 | 7,3% | 28 | 3,83% | 50 | 6,72% |
Gomy et al. (2016) | 88 | 2,74% | 79 | 10,3% | 78 | 10,66% | 77 | 10,35% |
Griffiths & Florens (2006) | 79 | 2,46% | 41 | 5,35% | 41 | 5,6% | 41 | 5,51% |
Gomy (2000) | 71 | 2,21% | 50 | 6,52% | 50 | 6,83% | 49 | 6,59% |
Questel (2020) | 67 | 2,09% | 61 | 7,95% | 60 | 8,2% | 57 | 7,66% |
Matile-Ferrero & Etienne (2006) | 58 | 1,81% | 58 | 7,56% | 58 | 7,92% | 58 | 7,8% |
Tronquet (2014) | 58 | 1,81% | 54 | 7,04% | 53 | 7,24% | 51 | 6,85% |
Linnaeus (1758) | 57 | 1,78% | 18 | 2,35% | 18 | 2,46% | 17 | 2,28% |
Jourdan (2020) | 56 | 1,75% | 54 | 7,04% | 52 | 7,1% | 53 | 7,12% |
Vayssières et al. (2001) | 48 | 1,5% | 44 | 5,74% | 44 | 6,01% | 44 | 5,91% |
Barré & Moutou (1982) | 44 | 1,37% | 40 | 5,22% | 40 | 5,46% | 40 | 5,38% |
Peck et al. (2014) | 43 | 1,34% | 40 | 5,22% | 40 | 5,46% | 40 | 5,38% |
Cazanove (2022) | 42 | 1,31% | 40 | 5,22% | 40 | 5,46% | 40 | 5,38% |
Questel & Le Quellec (2012) | 41 | 1,28% | 36 | 4,69% | 36 | 4,92% | 32 | 4,3% |
Etienne (2005) | 34 | 1,06% | 34 | 4,43% | 34 | 4,64% | 34 | 4,57% |
Mille et al. (2016) | 32 | 1% | 32 | 4,17% | 32 | 4,37% | 32 | 4,3% |
Ramage et al. (2023) | 31 | 0,97% | 31 | 4,04% | 30 | 4,1% | 31 | 4,17% |
Martiré & Rochat (2008) | 30 | 0,94% | 23 | 3% | 19 | 2,6% | 21 | 2,82% |
Muru et al. (2017) | 30 | 0,94% | 28 | 3,65% | 28 | 3,83% | 28 | 3,76% |
Heller (1916) | 29 | 0,9% | 19 | 2,48% | 19 | 2,6% | 19 | 2,55% |
Jennings et al. (2013) | 29 | 0,9% | 29 | 3,78% | 29 | 3,96% | 28 | 3,76% |
Nicolas et al. (2015) | 29 | 0,9% | 25 | 3,26% | 18 | 2,46% | 21 | 2,82% |
Yokoyama (2013) | 28 | 0,87% | 22 | 2,87% | 22 | 3,01% | 19 | 2,55% |
Germain et al. (2014) | 27 | 0,84% | 26 | 3,39% | 26 | 3,55% | 26 | 3,49% |
Guillermet (2009) | 26 | 0,81% | 22 | 2,87% | 18 | 2,46% | 22 | 2,96% |
Wheeler (1935) | 25 | 0,78% | 15 | 1,96% | 15 | 2,05% | 15 | 2,02% |
Peck (2011) | 24 | 0,75% | 23 | 3% | 23 | 3,14% | 23 | 3,09% |
Shelley & Lehtinen (1999) | 24 | 0,75% | 0 | 0% | 0 | 0% | 0 | 0% |
Delannoye et al. (2015) | 23 | 0,72% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Etienne & Vilardebó (1978) | 23 | 0,72% | 23 | 3% | 23 | 3,14% | 23 | 3,09% |
Perrault (1988) | 23 | 0,72% | 21 | 2,74% | 21 | 2,87% | 21 | 2,82% |
Ramage (2014) | 23 | 0,72% | 22 | 2,87% | 22 | 3,01% | 22 | 2,96% |
Remillet (1988) | 23 | 0,72% | 21 | 2,74% | 21 | 2,87% | 20 | 2,69% |
Falkner et al. (2002) | 22 | 0,69% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Nibouche et al. (202X) | 22 | 0,69% | 20 | 2,61% | 20 | 2,73% | 20 | 2,69% |
Paulian (1998) | 22 | 0,69% | 22 | 2,87% | 22 | 3,01% | 22 | 2,96% |
Sanchez (2020) | 22 | 0,69% | 22 | 2,87% | 22 | 3,01% | 18 | 2,42% |
Denux & Zagatti (2010) | 21 | 0,65% | 17 | 2,22% | 17 | 2,32% | 17 | 2,28% |
Gargominy et al. (1996) | 21 | 0,65% | 19 | 2,48% | 19 | 2,6% | 18 | 2,42% |
Lowe et al. (2007) | 21 | 0,65% | 19 | 2,48% | 18 | 2,46% | 19 | 2,55% |
Mille et al. (2020) | 21 | 0,65% | 20 | 2,61% | 20 | 2,73% | 20 | 2,69% |
Remaudière & Etienne (1988) | 21 | 0,65% | 21 | 2,74% | 21 | 2,87% | 21 | 2,82% |
Barau et al. (2005) | 20 | 0,62% | 17 | 2,22% | 16 | 2,19% | 13 | 1,75% |
Foldi & Germain (2018) | 20 | 0,62% | 20 | 2,61% | 20 | 2,73% | 20 | 2,69% |
Gargominy et al. (2011) | 20 | 0,62% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Jaffe & Lattke (1994) | 20 | 0,62% | 18 | 2,35% | 18 | 2,46% | 18 | 2,42% |
Probst et al. (2022) | 20 | 0,62% | 19 | 2,48% | 17 | 2,32% | 17 | 2,28% |
Probst (2001) | 20 | 0,62% | 12 | 1,56% | 12 | 1,64% | 10 | 1,34% |
Soubeyran (2008) | 20 | 0,62% | 18 | 2,35% | 18 | 2,46% | 18 | 2,42% |
Uicn et al. (2015) | 20 | 0,62% | 20 | 2,61% | 20 | 2,73% | 18 | 2,42% |
Germain (2007) | 19 | 0,59% | 19 | 2,48% | 19 | 2,6% | 19 | 2,55% |
Grubb (2005) | 19 | 0,59% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Morrison (1997) | 19 | 0,59% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Bournier (2000) | 18 | 0,56% | 18 | 2,35% | 18 | 2,46% | 18 | 2,42% |
Chazeau et al. (1974) | 18 | 0,56% | 6 | 0,78% | 6 | 0,82% | 4 | 0,54% |
Franco et al. (2019) | 18 | 0,56% | 17 | 2,22% | 17 | 2,32% | 17 | 2,28% |
Fricke et al. (2009) | 18 | 0,56% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Galkowski (2016) | 18 | 0,56% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Welter-schultes (2012) | 18 | 0,56% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Blard et al. (2003) | 17 | 0,53% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Cowie (2000) | 17 | 0,53% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Etienne et al. (2015) | 17 | 0,53% | 17 | 2,22% | 17 | 2,32% | 17 | 2,28% |
Lebas et al. (2016) | 17 | 0,53% | 15 | 1,96% | 15 | 2,05% | 15 | 2,02% |
Morrison (1996) | 17 | 0,53% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Ronot (2007) | 17 | 0,53% | 13 | 1,69% | 11 | 1,5% | 13 | 1,75% |
Berland (1933) | 16 | 0,5% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Gibbons (1979) | 16 | 0,5% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hammes & Putoa (1986) | 16 | 0,5% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Hullé et al. (2018) | 16 | 0,5% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Leraut (2014) | 16 | 0,5% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Taylor (1987) | 16 | 0,5% | 16 | 2,09% | 16 | 2,19% | 16 | 2,15% |
Wilson & Taylor (1967) | 16 | 0,5% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Cochereau (1966) | 15 | 0,47% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Ferrer (2015) | 15 | 0,47% | 15 | 1,96% | 15 | 2,05% | 15 | 2,02% |
Fisher & Fong (2020) | 15 | 0,47% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Kerney & Cameron (1999) | 15 | 0,47% | 11 | 1,43% | 11 | 1,5% | 11 | 1,48% |
Sanchez & Probst (2016) | 15 | 0,47% | 14 | 1,83% | 14 | 1,91% | 12 | 1,61% |
Anonyme (2018) | 14 | 0,44% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Bouget et al. (2019) | 14 | 0,44% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Bright (2019) | 14 | 0,44% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Cheesman (1928) | 14 | 0,44% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Cohic (1959) | 14 | 0,44% | 11 | 1,43% | 11 | 1,5% | 11 | 1,48% |
Lorvelec et al. (2007) | 14 | 0,44% | 14 | 1,83% | 14 | 1,91% | 14 | 1,88% |
Wetterer (2002) | 14 | 0,44% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Wheeler (1932) | 14 | 0,44% | 9 | 1,17% | 9 | 1,23% | 9 | 1,21% |
Wilson & Hunt (1967) | 14 | 0,44% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Abdou et al. (2004) | 13 | 0,41% | 9 | 1,17% | 8 | 1,09% | 9 | 1,21% |
Bippus (2019) | 13 | 0,41% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Bournier & Mound (2000) | 13 | 0,41% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Clarke (1971) | 13 | 0,41% | 10 | 1,3% | 10 | 1,37% | 10 | 1,34% |
Gutierrez (1981) | 13 | 0,41% | 11 | 1,43% | 11 | 1,5% | 11 | 1,48% |
Henderson & Breuil (2012) | 13 | 0,41% | 10 | 1,3% | 6 | 0,82% | 6 | 0,81% |
Peck (2011) | 13 | 0,41% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Soubeyran et al. (2011) | 13 | 0,41% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Streito et al. (2007) | 13 | 0,41% | 13 | 1,69% | 13 | 1,78% | 13 | 1,75% |
Tirvengadum & Bour (1985) | 13 | 0,41% | 10 | 1,3% | 10 | 1,37% | 10 | 1,34% |
Wheeler (1936) | 13 | 0,41% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Albouy & Richard (2017) | 12 | 0,37% | 11 | 1,43% | 11 | 1,5% | 10 | 1,34% |
Barré (2021) | 12 | 0,37% | 12 | 1,56% | 12 | 1,64% | 12 | 1,61% |
Boyer & Rivault (2003) | 12 | 0,37% | 12 | 1,56% | 12 | 1,64% | 12 | 1,61% |
Fauvel (1904) | 12 | 0,37% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Hoddle et al. (2008) | 12 | 0,37% | 12 | 1,56% | 12 | 1,64% | 12 | 1,61% |
Jourdan et al. (2014) | 12 | 0,37% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Keith et al. (2006) | 12 | 0,37% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Levesque & Delcroix (2018) | 12 | 0,37% | 12 | 1,56% | 12 | 1,64% | 9 | 1,21% |
Nentwig et al. (2019) | 12 | 0,37% | 12 | 1,56% | 12 | 1,64% | 12 | 1,61% |
Potin (2013) | 12 | 0,37% | 10 | 1,3% | 9 | 1,23% | 9 | 1,21% |
Theuerkauf et al. (2010) | 12 | 0,37% | 12 | 1,56% | 12 | 1,64% | 12 | 1,61% |
Blatrix et al. (2018) | 11 | 0,34% | 11 | 1,43% | 11 | 1,5% | 11 | 1,48% |
Boyer & Rivault (2006) | 11 | 0,34% | 11 | 1,43% | 11 | 1,5% | 11 | 1,48% |
Fauvel (1903) | 11 | 0,34% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Hovestadt & Neckheim (2020) | 11 | 0,34% | 10 | 1,3% | 10 | 1,37% | 10 | 1,34% |
Parnaudeau (2017) | 11 | 0,34% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Roth & Rivault (2002) | 11 | 0,34% | 11 | 1,43% | 11 | 1,5% | 11 | 1,48% |
Turpin & Probst (1998) | 11 | 0,34% | 8 | 1,04% | 8 | 1,09% | 6 | 0,81% |
Wheeler (1932) | 11 | 0,34% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Aulagnier et al. (2017) | 10 | 0,31% | 10 | 1,3% | 10 | 1,37% | 9 | 1,21% |
Chani-Posse et al. (2018) | 10 | 0,31% | 10 | 1,3% | 10 | 1,37% | 10 | 1,34% |
Fauvel (1867) | 10 | 0,31% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Fauvel (1903) | 10 | 0,31% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Frenot et al. (2005) | 10 | 0,31% | 10 | 1,3% | 10 | 1,37% | 10 | 1,34% |
Hamel et al. (2009) | 10 | 0,31% | 9 | 1,17% | 9 | 1,23% | 9 | 1,21% |
Lambert (1988) | 10 | 0,31% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Ledoux & Hallé (1995) | 10 | 0,31% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Madl & van Achterberg (2014) | 10 | 0,31% | 9 | 1,17% | 9 | 1,23% | 9 | 1,21% |
Pilsbry (1906-1907) | 10 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1958) | 10 | 0,31% | 10 | 1,3% | 10 | 1,37% | 8 | 1,08% |
Wheeler (1933) | 10 | 0,31% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Aulagnier (2009) | 9 | 0,28% | 9 | 1,17% | 9 | 1,23% | 7 | 0,94% |
Berland (1934) | 9 | 0,28% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Berland (1942) | 9 | 0,28% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Casevitz-Weulersse & Galkowski (2009) | 9 | 0,28% | 9 | 1,17% | 9 | 1,23% | 9 | 1,21% |
Dierkens & Ramage (2016) | 9 | 0,28% | 9 | 1,17% | 9 | 1,23% | 9 | 1,21% |
Lacroix (2015) | 9 | 0,28% | 8 | 1,04% | 7 | 0,96% | 8 | 1,08% |
Lamy & Pointier (2018) | 9 | 0,28% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Massemin et al. (2009) | 9 | 0,28% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Matile-Ferrero et al. (2000) | 9 | 0,28% | 9 | 1,17% | 9 | 1,23% | 9 | 1,21% |
Müller (1774) | 9 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Marquet (1990) | 9 | 0,28% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Poussereau (2015) | 9 | 0,28% | 9 | 1,17% | 9 | 1,23% | 9 | 1,21% |
Uicn et al. (2019) | 9 | 0,28% | 9 | 1,17% | 9 | 1,23% | 9 | 1,21% |
Berland (1934) | 8 | 0,25% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Blackwelder (1943) | 8 | 0,25% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Bouchet & Pointier (1998) | 8 | 0,25% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Brindle (1971) | 8 | 0,25% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Chartier & Reche (1992) | 8 | 0,25% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Cochereau (1974) | 8 | 0,25% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Corporaal (1937) | 8 | 0,25% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Dierkens & Charlat (2011) | 8 | 0,25% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Eggers (1940) | 8 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1849) | 8 | 0,25% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Gabriac et al. (2024) | 8 | 0,25% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Guenée (1862) | 8 | 0,25% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hullé & Vernon (2021) | 8 | 0,25% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Iorio & Coulis (2020) | 8 | 0,25% | 7 | 0,91% | 3 | 0,41% | 7 | 0,94% |
Jay et al. (2009) | 8 | 0,25% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Legros et al. (2017) | 8 | 0,25% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Lescure et al. (2012) | 8 | 0,25% | 3 | 0,39% | 2 | 0,27% | 2 | 0,27% |
Maran & Frétey (2023) | 8 | 0,25% | 8 | 1,04% | 8 | 1,09% | 8 | 1,08% |
Montrouzier (1860) | 8 | 0,25% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Peck (2016) | 8 | 0,25% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Perrault (1993) | 8 | 0,25% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Solem (1961) | 8 | 0,25% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Vandenspiegel & Mathys (2021) | 8 | 0,25% | 8 | 1,04% | 8 | 1,09% | 7 | 0,94% |
Wheeler (1908) | 8 | 0,25% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Berland (1935) | 7 | 0,22% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
De Meyer et al. (2012) | 7 | 0,22% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Emery (1914) | 7 | 0,22% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Fabricius (1775) | 7 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcellini et al. (2012) | 7 | 0,22% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Fricke et al. (2011) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Gargominy (2011-2023) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Gargominy (2016-2021) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Gasnier et al. (2015) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 6 | 0,81% |
Gentry et al. (2004) | 7 | 0,22% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Glaw & Rösler (2015) | 7 | 0,22% | 7 | 0,91% | 6 | 0,82% | 3 | 0,4% |
Haynes (2001) | 7 | 0,22% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Kaszab (1982) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Lesne (1932) | 7 | 0,22% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Massary et al. (2020) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 6 | 0,81% |
Matile-Ferrero (1979) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Nattier et al. (2015) | 7 | 0,22% | 6 | 0,78% | 6 | 0,82% | 5 | 0,67% |
Niedbała (2017) | 7 | 0,22% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Platnick (1993) | 7 | 0,22% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Poussereau & Lecoq (2008) | 7 | 0,22% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Sanchez et al. (2019) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Soldati & Touroult (2014) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Solem (1964) | 7 | 0,22% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Vedel et al. (2013) | 7 | 0,22% | 7 | 0,91% | 7 | 0,96% | 7 | 0,94% |
Viette (1949) | 7 | 0,22% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Aharon et al. (2017) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellifa et al. (2017) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 4 | 0,54% |
Bippus (2020) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Bouchet et al. (1991) | 6 | 0,19% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Boyer & Rivault (2004) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Boyer & Rivault (2006) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Caceres & Salamolard (2021) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 5 | 0,67% |
Colijn et al. (2020) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
David & Tsacas (1975) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Dierkens (2021) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Duyck et al. (2022) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Fauvel (1889) | 6 | 0,19% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fort & Barrière (2021) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 5 | 0,67% |
Garrouste & Hervé (2009) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Guillermet (2004) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Guillermet (2011) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Hausdorf (2023) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Hervé & Garrouste (2009) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Hopkins (1915) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2021) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Justine (2017) | 6 | 0,19% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Justine (2018) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Keith et al. (2002) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Keith et al. (2011) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Leraut (2012) | 6 | 0,19% | 3 | 0,39% | 3 | 0,41% | 0 | 0% |
Mary (2017) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Mauriès (1980) | 6 | 0,19% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Meurgey & Picard (2011) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Migeon (2015) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Millière (1864-1868) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas (2012) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
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) |
6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Preece (1995) | 6 | 0,19% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Prévost & Mougin (1970) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Probst & Deso (2001) | 6 | 0,19% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Ramage et al. (2017) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Ramage (2024) | 6 | 0,19% | 6 | 0,78% | 5 | 0,68% | 6 | 0,81% |
Raspi et al. (2007) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Rocamora (2004) | 6 | 0,19% | 6 | 0,78% | 5 | 0,68% | 6 | 0,81% |
Routtier et al. (2023) | 6 | 0,19% | 4 | 0,52% | 4 | 0,55% | 3 | 0,4% |
Ruzzier et al. (2023) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Talaga et al. (2015) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Touroult et al. (2018) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
UICN Comité français, OFB & MNHN (2021) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Voisin et al. (2017) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Wetterer (2012) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Wetterer (2014) | 6 | 0,19% | 6 | 0,78% | 6 | 0,82% | 6 | 0,81% |
Wygodzinsky (1966) | 6 | 0,19% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Aberlenc et al. (2004) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Albouy et al. (2017) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 4 | 0,54% |
Beeson (1935) | 5 | 0,16% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Belfan & Conde (2016) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 4 | 0,54% |
Berland (1924) | 5 | 0,16% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bochaton et al. (2021) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Bonfils (1969) | 5 | 0,16% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Breuil (2002) | 5 | 0,16% | 3 | 0,39% | 3 | 0,41% | 1 | 0,13% |
Brook (2010) | 5 | 0,16% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Butaud (2021) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Cohic (1950) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Dadant & Etienne (1973) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 4 | 0,54% |
Dewynter et al. (2022) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 3 | 0,4% |
Dewynter et al. (2023) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 3 | 0,4% |
Dominique (1892) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupérré (2023) | 5 | 0,16% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Escalona & Ślipiński (2010) | 5 | 0,16% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Fischer & Madl (2008) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
González-sánchez et al. (2021) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 4 | 0,54% |
Gutierrez & Etienne (1986) | 5 | 0,16% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Harvey (2011) | 5 | 0,16% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Hebard (1933) | 5 | 0,16% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Hullé et al. (2010) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Ineich (2016) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Keith et al. (2013) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Keith (2002) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Mahunka (1988) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary et al. (2021) | 5 | 0,16% | 4 | 0,52% | 4 | 0,55% | 2 | 0,27% |
Mousson (1872) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Niedbała & Penttinen (2007) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Olivier (1791-[1792]) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. (2006) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Poussereau (2012) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Probst (1997) | 5 | 0,16% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Questel et al. (2023) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 3 | 0,4% |
Questel et al. (2023) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 3 | 0,4% |
Séret (1997) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Silvestri (1935) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 4 | 0,54% |
Souza et al. (2019) | 5 | 0,16% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Taczanowski (1874) | 5 | 0,16% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Wetterer (2012) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Wetterer (2013) | 5 | 0,16% | 5 | 0,65% | 5 | 0,68% | 5 | 0,67% |
Adamson (1932) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Allen et al. (2022) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Aulagnier (2021) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Barnouin et al. (2020) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Bellmann (2019) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 3 | 0,4% |
Bernard (1968) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Bigot (1992) | 4 | 0,12% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Bolton (2012) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1864) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil et al. (2010) | 4 | 0,12% | 3 | 0,39% | 2 | 0,27% | 2 | 0,27% |
Burneleau (1983) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Cabaret et al. (1986) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Célini et al. (2013) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Chamberlin (1920) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 3 | 0,4% |
Cheke (2010) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Clarke (1986) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Cooke (1934) | 4 | 0,12% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Csősz et al. (2023) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Deshayes (1863) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dole & Cognato (2010) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Dominique (1902) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubos et al. (2023) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 2 | 0,27% |
Dupont et al. (2023) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Esposito et al. (2023) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Etienne & Flechtmann (2006) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Etienne et al. (2001) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Etienne (1972) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Fabricius (1798) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1891) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Fernandez-de-Mera et al. (2003) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Fouquet (2000) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Fourcroy (1785) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Geniez & Cheylan (2012) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain et al. (2014) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Germain (2013) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Gilot et al. (1992) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Girard (1997) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Gould (1852) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hava (2006) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Howard (1881) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2003) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Hustache (1920) | 4 | 0,12% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hutchinson et al. (2022) | 4 | 0,12% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hutton (1834) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jacquot et al. (2016) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Jordan (1894) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Latzel (1892) | 4 | 0,12% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Le Divelec (2024) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Light (1932) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Matile-Ferrero & Williams (2015) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Mauriès (1987) | 4 | 0,12% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mériguet & Zagatti (2016) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 3 | 0,4% |
Meurgey (2014) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 2 | 0,27% |
Mifsud et al. (2010) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Monterosato (1892) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Monti et al. (2010) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Montrouzier (1861) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Nève de Mévergnies et al. (2024) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Niedbała & Liu (2023) | 4 | 0,12% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Niedbała (1998) | 4 | 0,12% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Ortiz-Sepulveda et al. (2019) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Parnaudeau & Madl (2009) | 4 | 0,12% | 3 | 0,39% | 2 | 0,27% | 3 | 0,4% |
Periasamy et al. (2015) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Pilsbry (1920-1921) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier (2001) | 4 | 0,12% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Poussereau (2007) | 4 | 0,12% | 4 | 0,52% | 3 | 0,41% | 3 | 0,4% |
Poussereau (2017) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Probst et al. (2001) | 4 | 0,12% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Putshkov et al. (1999) | 4 | 0,12% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Questel (2017) | 4 | 0,12% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Quilici et al. (1988) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Rang (1831) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Rasplus et al. (2010) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Rheinheimer (2014) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Rigaud et al. (1997) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Russell et al. (2021) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Sasal et al. (2008) | 4 | 0,12% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Starý et al. (1994) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Touroult et al. (2020) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Uicn et al. (2017) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 2 | 0,27% |
Walckenaer (1802) | 4 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Zahradník & Poussereau (2022) | 4 | 0,12% | 4 | 0,52% | 4 | 0,55% | 4 | 0,54% |
Annecke & Mynhardt (1974) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Arrow (1927) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Aubé (1838) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Bauer et al. (2010) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Baxter-gilbert et al. (2021) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Beaumelle et al. (2021) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Beaver (1991) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Breuil (2013) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Brindle (1976) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Brosse et al. (2021) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Brustel & Roge (1998) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Busala et al. (2024) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Caceres (2002) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cameron (1936) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Carbayo et al. (2016) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Castro-Cobo et al. (2021) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Catzeflis (2018) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Cazanove et al. (2022) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Chalumeau (1983) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Chamberlin (1918) | 3 | 0,09% | 2 | 0,26% | 0 | 0% | 2 | 0,27% |
Chartois et al. (2023) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Chopard (1924) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chown & Convey (2016) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Claudin et al. (2022) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Coulis (2017) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Couteyen & Papazian (2012) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Daudin (1802) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
de Massary et al. (2015) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Dewynter et al. (2019) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 1 | 0,13% |
Dewynter et al. (2023) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 1 | 0,13% |
Doguet (2015) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Donisthorpe (1932) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2018) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Fabricius (1792) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1862) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1877) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Fazio et al. (2008) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Férussac (1821) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Filippi (2013) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Firmat et al. (2012) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Gamiette et al. (2023) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Gerber (2018) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Girard (2007) | 3 | 0,09% | 2 | 0,26% | 1 | 0,14% | 1 | 0,13% |
Gmelin (1789) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Grech-Angelini et al. (2019) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Grillo et al. (2007) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Grimpe & Hoffmann (1925) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilbert & Casevitz-Weulersse (1997) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Hausdorf (2007) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Háva & McCormack (2022) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Háva (2014) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Hebard (1933) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Holloway (1979) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ineich et al. (2019) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
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 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Jerdon (1851) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson et al. (2021) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Kormilev (1971) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kreiter et al. (2022) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Kuschel (2008) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Lagarde (2008) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Lenfant & Marro (1997) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Lucas (2012) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Lupoli (2023) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Madl (2014) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Martinez-Torres et al. (1997) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Massary et al. (2017) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 1 | 0,13% |
Massary et al. (2018) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 1 | 0,13% |
Massary et al. (2019) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Mertens & Wermuth (1960) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1934) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Millière (1863) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Muratet (2015) | 3 | 0,09% | 2 | 0,26% | 1 | 0,14% | 1 | 0,13% |
Parola & Barré (2004) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Pascal et al. 2006 | 3 | 0,09% | 3 | 0,39% | 2 | 0,27% | 3 | 0,4% |
Pastorini et al. (2000) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Paulian (1991) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Pauly et al. (2001) | 3 | 0,09% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Philippot et al. (2019) | 3 | 0,09% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Pierre et al. (2017) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Probst (1997) | 3 | 0,09% | 3 | 0,39% | 1 | 0,14% | 3 | 0,4% |
Probst (1997) | 3 | 0,09% | 3 | 0,39% | 2 | 0,27% | 2 | 0,27% |
Probst (1998) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Quénéhervé & Van Den Berg (2005) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Questel (2016) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Questel (2023) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Rageau (1956) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Rageau (1959) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Rehn (1949) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Reitter (1877) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Remsen et al. (2013) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Rheinheimer (2012) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Rispe et al. (1999) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Rousse & Gupta (2013) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Etienne (1985) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Salata & Fisher (2022) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Schileyko et al. (2024) | 3 | 0,09% | 3 | 0,39% | 2 | 0,27% | 3 | 0,4% |
Seurat (1934) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Silvestri (1934) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Simon et al. (1991) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Siroux (2015) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Soldati et al. (2019) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Szederjesi et al. (2019) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Tsacas & Chassagnard (1988) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Urvois et al. (2023) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Vachal (1907) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 2 | 0,27% |
Vandel (1981) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Vidal & Vansteene (2021) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Wallach (2020) | 3 | 0,09% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Ward et al. (2015) | 3 | 0,09% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Wetterer & Hita Garcia (2015) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Wickel & Jamon (2010) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Zimmerman (1968) | 3 | 0,09% | 3 | 0,39% | 3 | 0,41% | 3 | 0,4% |
Adelski (2012) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 0 | 0% |
Alley et al. (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Arnold & Ovenden (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Aubouin et al. (2016) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Augros et al. (2017) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Augros et al. (2018) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Azab et al. (1972) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Azam (1893) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Badie (1977) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Baehr et al. (2013) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Bain (1981) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Baroni Urbani & De Andrade (2007) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Barre et al. (1988) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Batsch (1786) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Baudry et al. (2022) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Bauer & Sadlier (2000) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bauer (1987) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Beatty et al. (2008) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Beeson (1935) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bell et al. (1989) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Bellemare & Brunelle (1950) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Benejam et al. (2008) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Berland (1929) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Berry et al. (1997) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Bhatti (1978) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bielawski (1973) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Bippus (2019) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Blanc et al. (1993) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Blanchard (1886) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Blight et al. (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Bolton (2007) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Borges & Couri (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Borowiec et al. (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Borowiec (2016) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bour et al. (2008) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Bourdeau & Chermette (1985) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Bourgat (1970) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer de Fonscolombe (1832) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Breuil (2021) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Brindle (1975) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Brito et al. (2017) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Brown (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Brun et al. (1983) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Brunes et al. (2021) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Bryant (1942) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bur (1907) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Butler (1897 (1898)) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Cabaret et al. (2002) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Carpenter & Madl (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Carpintero & Dellapé (2006) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Cerkowniak et al. (2020) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Champagne et al. (1997) | 2 | 0,06% | 2 | 0,26% | 1 | 0,14% | 2 | 0,27% |
Chapuis et al. (2004) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Chazeau (1978) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cheke (1987) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Cheon et al. (2023) | 2 | 0,06% | 2 | 0,26% | 0 | 0% | 2 | 0,27% |
Chevallier et al. (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Clench (1964) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Coatmeur (1999) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 0 | 0% |
Cochereau (1966) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Cockerell (1893) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cocquempot & Debreuil (2006) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Coiffait (1976) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Coiffait (1980) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cole et al. (2005) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Colindre (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Constantin (2012) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Coomans (1967) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer ([1780]-1782) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Csuzdi & Pavlíček (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Damoiseau (1966) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
David et al. (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Debach (1960) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Deblock et al. (1988) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Del et al. (2024) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Delport (2018) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Demange (1981) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Des et al. (2021) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Deso et al. (2013) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Deuss et al. (2013) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Distant (1910) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dobson (1956) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dognin (1908) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Duay et al. (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Dumbardon-Martial & Delblond (2019) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Dupont et al. (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Dupouy (1966) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Edgecombe (2004) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Enders (1993) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Endrodi (1977) | 2 | 0,06% | 2 | 0,26% | 0 | 0% | 2 | 0,27% |
Etcheberry & Abraham (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Etienne (1971) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Etienne (1978) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Ezzat (1958) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Fabricius (1787) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1868) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1893) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1878) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Fernandez-Triana et al. (2020) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Ferrer & Poussereau (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Férussac (1822) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1827) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Vukadinovic (1970) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Flechtmann et al. (1999) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Foata et al. (2005) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Fontenot et al. (2015) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Fossati & Marquet (1998) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fourcroy (1785) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gedoelst (1923) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Geer (1774) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Genier & Moretto (2017) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Girod & Matzke (2020) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Glaw (2015) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Godet et al. (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Goeze (1782) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gonzales et al. (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Gould (1846) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Graber et al. (1997) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Grandjean (1933) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Gray (1842) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Grouvelle (1892) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Guenée (1845) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilbert (2002) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Guillermet (2006) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2011) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Guillermet (2012) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Guiran (1963) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gusev (1965) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hacala et al. (2024) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hagstrum & Subramanyam (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hale et al. (2008) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hartmann et al. (2021) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Havery et al. (2018) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hawlitschek et al. (2011) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Head et al. (2024) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hebard (1935) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Heidemann & Seidenbusch (2002) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hendrichs et al. (2015) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Herbulot (1979) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hinton (1941) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodkinson (1983) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Hoff & Daszkiewicz (2001) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Horváth (1914) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hossain et al. (2016) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Howard (1907) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Huber et al. (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
IUCN (2013) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Jackson (1933) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Jacquelin & Val (1853) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
James & Gamiette (2016) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Jolivet (1979) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jones et al. (2006) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Jones et al. (2007) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Jordan (1896) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Joyeux & Baer (1953) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Justine et al. (2022) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Kassebeer (2000) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Kaszab (1985) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Keith et al. (1999) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Keith et al. (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Kemal (2008) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kikuchi (1929) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Klyver (1932) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Kurahashi & Fauran (1980) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Lacoste (de) (2020) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Laurenti (1768) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lawrence (1969) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lawrence (1991) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Lehrter et al. (2016) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Leignel et al. (2002) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Lemagnen (2015) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2005) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lethierry (1881) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Levesque & Clergeau (2002) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 0 | 0% |
Lichtenfels et al. (1994) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Light & Zimmerman (1936) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Light (1932) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lim et al. (2002) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Logvinovskaya (1983) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Lopez-Vaamonde et al. (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Louette & Cousin (1999) | 2 | 0,06% | 2 | 0,26% | 1 | 0,14% | 1 | 0,13% |
Lü & Zhou (2012) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Luc & Coomans (1992) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Lucas (1847) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli & Dusoulier (2015) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Madl & Ganeshan (2008) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Mann (1921) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Marcos-garcía et al. (2013) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Marquet et al. (2003) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Marsham (1802) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2011) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Martiré (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Mas-Coma et al. (1989) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Matile-Ferrero & Etienne (1996) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Matile-Ferrero & Etienne (1998) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Mees (2006) | 2 | 0,06% | 2 | 0,26% | 0 | 0% | 2 | 0,27% |
Meurgey & Dumbardon-Martial (2019) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Meurgey & Questel (2015) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Meurgey (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Meyrick (1908) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaelsen (1913) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Miers (1878) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Migeon et al. (2019) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Minard et al. (2015) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mollot et al. (2016) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Montagnon et al. (1993) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Montrouzier (1861) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Nageleisen et al. (2015) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Nelson-Smith et al. (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Nerozzi et al. (2024) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Nicolas et al. (2024) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Nicolas (2020) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Nicolas (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Niedbała & Starý (2015) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Niedbała (1994) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Noël (2024) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Pallas [1814] | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Panis (1969) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1796]) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnaudeau (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Parnaudeau (2012) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Pavlíček & Csuzdi (2012) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Perrin et al. (2007) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Perris (1852) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Persat & Keith (1997) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Pistil & Kontykowski (1974) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Pollonera (1889) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Poussereau & Ferrer (2012) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Poussereau & Lecoq (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Poussereau & Rose (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Poussereau et al. (2013) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Poussereau (2008) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Probst (1997) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Questel (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Quilici et al. (1998) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Rakowski et al. (1981) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Ramage et al. (2015) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Ramage et al. (2018) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Raven (2015) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Reise et al. (2011) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Reverté et al. (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Revilliod (1914) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rheinheimer (2015) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Richard (1957) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Robert et al. (1991) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Roberts (2014) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rocha et al. (2022) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Rochas et al. (2022) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Roger (2018) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Röll et al. (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Rose (2009) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Rudolphi (1819) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell (1965) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Ruys & Coord (2012) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Safford & Hawkins (2013) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Saint et al. (1978) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Sakimura (1975) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Salin et al. (2003) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Sanchez (2013) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Sarnat et al. (2015) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sattler & Tremewan (1973) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Savouré-Soubelet et al. (in prep.) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Schileyko et al. (2018) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Schoenherr (1843) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Schreber (1777) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert (2003) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sellnick (1959) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Shattuck (1992) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Shelley (2004) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Siu et al. (2017) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Sluys (2016) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Smith (1857) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Starý et al. (1973) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Stoev et al. (2010) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Sudre & Teocchi (2000) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Tachikawa (1968) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1872) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1874) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Taiti & Ferrara (1983) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Taquet et al. (2019) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Taylor & Wilson (1961) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Taylor (2003) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Terefe et al. (2005) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Théry & Bordat (2012) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Thibault et al. (2014) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Touroult (2005) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Tronquet (2015) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Turpin et al. (2001) | 2 | 0,06% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
UICN France et al. (2013) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Umhang et al. (2013) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
van den Burg et al. (2021) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Vences et al. (2004) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Viel (2021) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Villanueva et al. (2021) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 0 | 0% |
Virgilio et al. (2010) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Voisin (2020) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Votýpka et al. (2020) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Walckenaer ([1841]) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Walsingham (1920) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang et al. (2021) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Weterings & Vetter (2017) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Wetherby (1879) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wetterer et al. (2012) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1923) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Wheeler (1933) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wild (2007) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Williams & Watson (1988) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (1975) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Winsor (1991) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Wondafrash et al. (2020) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Würmli (1974) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 1 | 0,13% |
Yaginuma (1972) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Yang et al. (2023) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Yin & Sproston (1948) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2012) | 2 | 0,06% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Zanetti et al. (2016) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Zimmermann et al. (2005) | 2 | 0,06% | 2 | 0,26% | 2 | 0,27% | 2 | 0,27% |
Abalos et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abalos et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abdel-kader & Barak (1979) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abhaya & Probst (1996) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Abhaya & Probst (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abhaya & Probst (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abhaya & Probst (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abhaya & Probst (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abhaya & Probst (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abhaya & Probst (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abhaya et al. (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Abhaya et al. (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Abhaya et al. (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Abhaya et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Adams (1845) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1935) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Alam et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Alcott et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Alencar et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Allemand et al. (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Alonso-zarazaga & Evenhuis (2017) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (NOI) (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Anonyme (NOI) (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Anonyme (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Anonyme (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Anonyme (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
ANSES (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Arzul et al. (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ascete (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Asselbergs (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Astrongatt (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Astudillo et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Audibert & Paillet (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Audige (1927) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Audouin (1826) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Auger et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Aurivillius (1909) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Azevedo et al. (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bacchet et al. (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Badie et al. (1992) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bagnall (1919) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagnall (1927) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagny et al. (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailenger et al. (1965) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bailey et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Baker & Pritchard (1960) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Balachowsky (1958) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Balhoff et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Balogh (1958) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bangy et al. (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Baptista et al. (2017) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Barbancey & Probst (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Barbancey (2001) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Barbour (1912) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Barbut et al. (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Barbut (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Barré et al. (2001) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Barrière & Fort (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Barthélémy (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bassitta et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bauer & Sadlier (1994) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Baxter-gilbert et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Baylis & Daubney (1922) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Baylis (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Beatty et al. (1991) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Beaucournu (1968) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaver & Liu (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Becerra et al. (2024) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Béguinot (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Behm et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Behm et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Belles (1980) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Belles (1985) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Benajiba et al. (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Benoit (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Benson (1850) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Berenger & Pluot-Sigwalt (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Berger (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Berland (1927) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Berlese & Paoli (1916) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertin (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Entomologiste (Paris), 61(1): 33-34.">Binon (2005) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Biondi et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bippus (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bippus (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bippus (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Blair (1934) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Blair (1934) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Blair (1934) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Blair (1940) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Blanchard (1891) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanchard (1940) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bleeker (1860) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bocage (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Boer et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Boettger (1880) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boettger (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1833) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton & Fisher (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bolton (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bondar (1923) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonfils et al. (1994) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Borcyk et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Bordes et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bouchy & Quentin (1988) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Boulay & Probst (1998) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulenger (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulenger (1909) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulenger (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boullet (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bourgat (1967) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgat (1968) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgat (1968) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgat (1969) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgat (1972) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1856) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousquet (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousquet (2018) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousses et al. (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bout et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Bowdich (1822) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyd et al. (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Boyer de Fonscolombe (1834) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Brandt (1833) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brèthes (1913) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Breuil et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Breuil (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Brisbane et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Brölemann (1889) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (1994) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruguière (1789-1792) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brûlé (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Brun & Chazeau (1986) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Brunke et al. (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Burr (1904) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Burr (1914) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabaret (1982) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Caceres & Mehn (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Caceres et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cahuzac & Dauphin (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Caillot et al. (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Callou (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cambridge (1879) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1933) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cameron (1933) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Capalleras & Carretero (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Carl (1926) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Carneiro et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Casey (1893) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Catil et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cazals & Dupont (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cazanove et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Cazanove (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Célini et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
CEN Nouvelle-Calédonie (2021) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Cerkowniak et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cesco et al. (2001) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cetre-sosah et al. (2023) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Chabanet & Durville (2005) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chabaud et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chabrol (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chapelin-viscardi (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chapuis & Eichhoff (1875) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Charrier et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chastel et al. (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Chebbah et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chebbah et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cheesman (1927) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cheke & Hume (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cheke (1975) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cheke (1982) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Chevin (1986) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cheylan et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cheylan (1988) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chopard (1921) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Chopard (1930) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Christensen & Kahn (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Chûjô (1964) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cicculli et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cini et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Clain et al. (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Clergeau & Pascal (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Clergeau (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cochard et al. (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cochard et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cocquempot (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cohic (1959) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Colin (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Colindre (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Colindre (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Colligros & Lebecque (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Collingwood & Agosti (1996) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Commecy et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Constant (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Conte et al. (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Cooke (1928) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Coquerel (1866) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cornuaille et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cornuaille (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Correa et al. (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Coulon & Sautet (1931) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Courtial (2023) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Couteyen & Papazian (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Couteyen (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Couteyen (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Couteyen (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Crotch (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Crotch (1873) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cummings et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Curran (1929) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Cuvier (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Czechowski et al. (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dadda et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dalla Torre (1893) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dard et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dard et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Darlington (1992) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Daudin (1803) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Daumal (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dauphin & Matile-Ferrero (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dauphin (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
De Geer (1773) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
DeBach (1959) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Deblock et al. (1960) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Decoin et al. (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Defo et al. (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Deguine et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Deknuydt et al. (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Del Guercio (1900) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Del Hoyo & Collar (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Del Hoyo & Collar (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Delabie & Blard (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Delabie et al. (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Delatte et al. (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Delaunay et al. (2000) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Delaunay et al. (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Delfosse (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Delsalle & Sechet (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dendy (1891) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Denoyes et al. (1986) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Denys et al. (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Deraniyagala (1953) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dervin et al. (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dervin (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Deso & Probst (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Déso & Probst (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Deso et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Deso et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dewarumez et al. (2011) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter & Claessens (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dewynter et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Dewynter et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dickey et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dieme et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dierkens (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dijkstra et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dikmans (1932) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Disney & Chazeau (1990) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Dispons (1965) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dollfus (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dosse (1958) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Doucet (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Draparnaud (1801) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois et al. (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dubos et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Dubos (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Duguy (1967) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel et al. (2005) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Duméril & Bibron (1836) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Duméril & Bribron (1841) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Duponchel (1836-[1837]) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupont & Petter (1988) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dupuis (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Dupuis-desormeaux et al. (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Duquef (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Duquef (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Duquef (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Duval et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Eggers (1933) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichhoff (1868) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Emerit & Ledoux (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Emery (1869) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Emery (1892) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1894) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Eppo (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Eppo (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Černosvitov (1934) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Escoriza et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Escoriza (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Esser (2017) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne & Gagné (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Etienne et al. (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Etienne et al. (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Etienne et al. (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
European Commission (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Evans et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Evenhuis (2007) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Evenhuis (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Evenhuis (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Eyles (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fabre & Orsini (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fabres (1974) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fabres (1977) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fabricius (1781) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1801) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1802) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1803) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fagot (1879) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1906) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fennah (1958) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fennah (1969) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ferragu (1979) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ferris (1935) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ficetola & Scali (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Fieldsend et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Finnerty et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Firmat & Alibert (2011) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer & Fisher (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer-piette & Bedoucha (1964) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher & Bolton (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Flechtmann & Atkinson (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Flechtmann & Etienne (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Flechtmann & Etienne (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Flechtmann & Etienne (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fleutiaux & Sallé ([1890]) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontanilla & Wade (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fontanilla et al. (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Forel (1881) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Forel (1890) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1893) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1899) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fournal (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fraga & Carvalho (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Frank (1983) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Frétey (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fricke et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Friese (1907) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritz et al. (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Fruget & Beisel (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Furminieux (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gahan (1924) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gall & Beague (1986) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ganesh & Vogel (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gargominy et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gargominy (2001) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Garrett (1879) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrett (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gassies (1866) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Geneva et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Geoffroy & Iorio (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Geoffroy Saint-Hilaire (1796) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Germain & Streito (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Germain (1931) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1821) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1824) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Geyer & Frölich (1830) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibbons (1981) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gier (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gilgado et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gill (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gillespie (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gillespie (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Girard (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Girard (1859) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Girault (1915) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Girod & Sauce (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Girod (2004) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Girod (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gmelin (1788) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gomes & Thome (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gomy (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gonzales & Yvinec (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gonzalez & Vetrovec (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
González et al. (2018) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Gouillard (1973) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourvès & Samuelson (1979) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Goux (1937) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gowande et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gozlan et al. (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Graham (1969) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Graham (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Graitson et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Graitson (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Grand & Boudot (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Grand et al. (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Grand (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Grand (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gray (1831) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gray (1834) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1845) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1870) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gregorio (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gresse et al. (2002) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffing et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Grillitsch (1997) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Groom et al. (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Grouvelle & Raffray (1908) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Grouvelle & Raffray (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1852) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Guglielmone et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Guilbert (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Guiller & Madec (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Guiller & Vacher (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Guillermet et al. (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Guillermet (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Guillermet (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Gutierrez (1968) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Haliday (1833) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Haliday (1834) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hamdi et al. (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hamilton (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hammer (1972) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hamon (1953) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamon (1956) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Haran et al. (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Haran et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Harlan (1835) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassani et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hausmann (1802) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hava & Poussereau (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Háva et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Háva (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Háva (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hayashi (1961) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hedges et al. (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedlund et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hee et al. (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Heiss (2011) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hempel (1922) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Henao-osorio et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Heppner (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Herbst ([1791]-1792) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Heym et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hielkema & Hielkema (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hindermeyer et al. (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hoffmann & Smith (2005) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hoffstetter (1946) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Holden et al. (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hollinger et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hood (1928) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoogmoed & Lescure (1975) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Howard (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Howard (1906) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hübner (1796-[1836]) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Huchet (1992) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Huet & Cadet (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Huet (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hugel (2007) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Hugel (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Hugel (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hull (1937) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Hustache (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Iković et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Ineich & Bauer (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Massary (1997) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ineich et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Iorio et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Irish et al. (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
IUCN (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Jackson (1941) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Jacquelin du Val (1861) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Jacquelin et al. (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Jacquiet et al. (1997) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Jäger (2002) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jamonneau et al. (2025) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Janák (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Jay & Probst (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Johnson et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Johnson (1964) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolivet (1998) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1892) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouffroy et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Jouveau et al. (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Joyeux & Alleaux (1924) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Julvez et al. (1990) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Justine et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Justine et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Justine et al. (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Justine et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kadolsky (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kamensky (1932) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Karner (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Karny (1925) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Keith & Dorson (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Keith & Dorson (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Keith & Dorson (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Keith & Dorson (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Keith & Marquet (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Keith (1967) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Keith (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Keith (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kelly & Ranwashe (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kemp (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Kennard & Woodward (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirby (1890) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Klaver (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Klein & Saint-andrieux (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Koch (1836) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolibáč (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
König et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kormilev (1965) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kornilev et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Kozár (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kreiter et al. (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kreiter et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kronmüller (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Kulbicki (comm. pers., 2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kumar et al. (1988) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Kury et al. (2024) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Kuwahara et al. (1974) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lacoste (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lacoste (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lacoste (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Laetsch et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Laforgue (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lafranchis (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lafranchis (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lagadec et al. (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lalubie et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lamarck (1816) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1819) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambret & Deschamps (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lamontellerie (1965) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lancastre et al. (1976) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Landemaine (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lanuza et al. (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Laporte & Sanchez (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lapwong et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Laranjo-Gonzalez et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Larivière et al. (1973) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Latham (1790) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1802) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubin et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Le Bail et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Le Goff et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Leach ([1816]) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Lebard & Claude (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lebard & Hauser (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lebard & Speight (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lecigne et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lecoq & Tronquet (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lecoq (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lefebvre & Crivelli (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Léger & Mouzels (1917) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1949) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1950) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1953) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Leignel et al. (1997) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lemaire & Gerriet (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoir et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Leponce et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Leraut (1997) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lescure et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Letacq (1924) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Letellier & Dauphin (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Levesque & Mathurin (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Liénard et al. (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Linnaeus (1761) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1763) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Löbl & Smetana (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lopez (1990) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lordello (1955) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lorvelec & Pascal (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lorvelec et al. (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lorvelec et al. (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lounnas et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lü & Zhou (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lucas (1872) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lukanov & Pavlova (2022) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Luo (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Luziau (1953) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Lydeard et al. (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lyubarsky (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lyubarsky (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mabille (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Macé (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Machet & Duquef (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Linzer Biologische Beitraege, 44(1): 591-594. ">Madl (2012) |
1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Maillard & David (2014) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Malausa & Ehanno (1988) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1932) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Malloch (1933) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mally et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mammola & Milano (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Maquart et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Marchal et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Marchandeau & Letty (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Marchandeau et al. (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Maréchal & Iinuma (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Marie & Vetter (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Marples (1957) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Marquet & Roguet (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Martin-vega et al. (2017) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Martnez-Gomez (1968) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary (2012) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Matile-Ferrero & Germain (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Matsumura (1931) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsuzaki et al. (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Maucarré (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mauriès (1983) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mayr (1862) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mayr (1879) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mayr (1886) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1890) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mcevey & Schiffer (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mckay & Milenkaya (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Medlock et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Meek et al. (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Meganck et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Melin et al. (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Melot et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ménard et al. (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Menezes et al. (2005) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Menezes et al. (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mertens (1963) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Methuen & Hewitt (1913) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Meurgey & Dumbardon-Martial (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Meurgey (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Meyen (1834) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1904) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Meyrick (1912-1916) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Meyrick (1934) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mille et al., 2012 | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mille et al. (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Miñano et al. (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
M'intosh (1855) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mitchell & Zug (1988) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Miyatake (1968) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mocquard (1895) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Momont (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Moquet & Delatte (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Moquet et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Morelet (1848) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Morgan (1889) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Morin (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Mothes et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Motschulsky (1866) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moulton (1907) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moutier & Moutier (1920) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moutou (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Mozzi et al. (2005) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
M’rad et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Murienne et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Murray (1864) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Murray (1867) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Naggs (1989) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Naggs (1994) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Nardi et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Nassi et al. (1975) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Natural History Museum of London (2020) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Navajas et al. (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Neid (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Nentwig & Kobelt (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Nicolas (1978) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Noda (1966) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël et al. (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Odin (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Olivier (1789) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Omar et al. (2011) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Onillon et al. (1994) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Opitz (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Orhant (2003) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Orton (1928) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Osuji (1975) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Osuji (1975) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ota & Ineich (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Ouvrard et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ouvrard et al. (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pace (1991) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pace (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pace (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pagenstecher (1907) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pal (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pallas (1766) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pande & Chauhan (1969) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pang et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Parnaudeau & Couteyen (2001) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pascal & Vigne (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pascal & Vigne (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pascal & Vigne (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pascal & Vigne (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pascal & Vigne (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Paulian (1979) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulucci (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pauly & Munzinger (2003) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Pelosse (1927) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pereira et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Perkins (1928) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrault (1977) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Perry et al. (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pétavy et al. (1990) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Peters (1854) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Peters (1874) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1840) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1846) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pic (1926) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pilsbry (1927-1935) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pintureau et al. (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Platnick et al. (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pointier & Blanc (1985) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Delay (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pointier et al. (1998) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier et al. (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pollonera (1885) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Porcel et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Potiez & Michaud (1835-1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Potiez & Michaud (1844) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Poussereau & Voisin (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Poussereau (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Poussereau (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Poussereau (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Power (1927) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Preece (1998) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Prena (2008) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Princis (1974) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Prins et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Probst & Calimoutouonien (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Probst & Sanchez (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Probst & Tézier (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Probst et al. (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Probst et al. (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst et al. (2000) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst et al. (2002) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst et al. (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Probst (1993) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Probst (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Probst (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Probst (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Probst (2001) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Pugh & Scott (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Puigcerver et al. (2001) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Puissauve & Poulet (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Purger et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Putshkov (1987) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Quah & Grismer (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Quaintance (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Quentin & Villiers (1979) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Questel (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Quilici et al. (1997) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Quilici et al. (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Quintard et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ragonot (1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Raingeard (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ramage & Martiré (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ramage & Roy (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ramage (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Randi et al. (2001) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ransom (1907) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Raphael (1970) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Rasamimanana et al. (1990) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ratnadass et al. (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Razowski (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Razowski (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Reeve (1849) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Reinert et al. (2004) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Renaud et al. (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rhodin & Carr (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rhodin et al. (2017) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1914) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ringler et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Risso (1826) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Robinson et al. (1994) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Rode (1938) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Romero et al. (2010) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Roques & Skrzypczyńska (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Rosenbaum et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Rosenhauer (1856) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi & Godoy (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Rossi (1790) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi (1792) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi (1794) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Martinez (1987) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Roux (1913) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rowson et al. (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rozkosny (1983) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Rücker (1981) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudolphi (1803) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudolphi (1805) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudolphi (1809) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Ruiz-Huidobro et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Russell & Le Corre (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Sadlier et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sahli & Pages (1978) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Salamolard (2002) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Salvador et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Salvi et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sanchez & Gandar (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sanchez & Gandar (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sanchez & Probst (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sanchez & Probst (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sanchez et al. (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sanchez et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Santschi (1920) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Santschi (1928) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sardet et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Saulai et al. (2001) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sauvage (1878) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sauvaget et al. (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sauvion et al. (1999) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Say (1817) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1831) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schaffner & Karch (2000) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schlegel (1865) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schoepff (1792) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Linzer Biologische Beitraege, 41(1): 767-801. ">Schöller (2009) |
1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Scholte & Schaffner (2007) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1781) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schröter (1784) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schweigger (1812) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Scudder (1876) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Séchet et al. (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Séguy (1960) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Seifert (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Selys Longchamps (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sengupta & Deb (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Servan & Arvy (1997) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Shaaya (1981) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Shahhosseini (1980) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Shaw (1794) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Shaw (1802) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn ([]) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sherpa et al. (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Shiraki (1906) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Siddaiah & Kujur (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Silvestri (1913) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Silvestri (1916) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1864) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1873) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1892) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1893) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1897) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1983) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Singh (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sircoulomb (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Siroux (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Siroux (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Skierska (1976) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Skrjabin & Mizkewitsch (1930) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Skrjabin (1942) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Skuse (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Smetana (1980) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith, F. (1861) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Smith (1858) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1976) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Snyder et al. (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sochurek (1956) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Socolovschi et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Soldati et al. (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sonan (1932) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
SORDELLO (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Spalikowski (1897) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sparacio et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Speight (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sreelatha et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Stadelman (1894) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Stainton (1856) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Staręga (1989) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Starmühlner (1970) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1976) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Stévanovich (1994) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Stierlin (1861) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Stiles (1892) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Streito et al. (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Streito et al. (2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sturm (1807) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sudre & Teocchi (1996) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sudre et al. (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Sundevall (1857) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Széles et al. (2018) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1871) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tarjan & Weischer (1965) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Tattersall (1977) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tattersall (1989) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tavakilian & Chevillotte (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Tavoillot (1997) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Temminck & Schlegel (1849) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Temminck (1813) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Theodorides et al. (1983) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Thévenot (2014) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Thirion (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Thomas (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Thompson (1981) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Timberlake (1941) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Tixier et al. (2013) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Tonnabel et al. (2011) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Torgerson et al. (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Tornier (1901) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Torres et al. (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Touroult et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Tower (1913) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brazil Medico, 28: 183.">Travassos (1914) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Treitschke (1832) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tröndlé & Boutet (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Tronquet (2006) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tronquet (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tronquet (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Tubangui (1934) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Turner (1919) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Turpin & Probst (1997) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Turpin (1996) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Turpin (1996) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Uicn et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Urvois et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Valerio (1981) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Valladares et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vallot (1801) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Van & Bruggen (1991) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
van den Burg et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Van Dijk et al. (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1922) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vannini et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vargas et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vásquez-cruz & Kelly-hernández (2024) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vayssières et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vercambre et al. (2007) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Verhoeff (1926) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Veysset (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Viallet (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vidal (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vieillot (1817) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vieira (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Viette (1971) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Viette (1979) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vigne & Pascal (2003) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Vilardebo & Guerout (1976) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Villa & Villa (1833) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Villeneuve (1911) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vinson (1863) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vinson (1871) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vogel et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Vorst (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Walbaum (1792) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer (1837) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Walckenaer (1837) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1864) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wasilewski et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Watson et al. (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wehsener & Noss (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Whalley (1973) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Wheeler (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
While & Uller (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Wied (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiegmann (1834) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wild (2004) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilkinson (1927) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Williams et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Withers & Allemand (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Wollaston (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (1977) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Works & Olson (2018) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Yadav et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Yang et al. (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Younes et al. (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Zagatti & Cotte (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Zajitschek et al. (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Zakardjian et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Zakardjian et al. (2023) | 1 | 0,03% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Zanetti et al. (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Zdunek (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Zeller (1847) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Zeller (1848) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Zeller (1973) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Zimkus et al. (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Zinke et al. (2005) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
Zug et al. (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |
(2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
(2023) | 1 | 0,03% | 1 | 0,13% | 1 | 0,14% | 1 | 0,13% |