Espèces terrestres de Wallis-et-Futuna
1246 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fournet (2002) | 630 | 14,5% | 507 | 58,28% | 503 | 60,1% | 491 | 58,59% |
Munzinger et al. (2016) | 515 | 11,85% | 140 | 16,09% | 138 | 16,49% | 138 | 16,47% |
Morat & Veillon (1985) | 421 | 9,69% | 339 | 38,97% | 333 | 39,78% | 333 | 39,74% |
Funk et al. (2007) | 396 | 9,11% | 121 | 13,91% | 120 | 14,34% | 115 | 13,72% |
Morat et al. (2012) | 292 | 6,72% | 147 | 16,9% | 145 | 17,32% | 143 | 17,06% |
Ramage (2017) | 163 | 3,75% | 150 | 17,24% | 147 | 17,56% | 150 | 17,9% |
Fourdrigniez & Meyer (2008) | 146 | 3,36% | 114 | 13,1% | 112 | 13,38% | 109 | 13,01% |
Hequet & Le Corre (2010) | 136 | 3,13% | 113 | 12,99% | 112 | 13,38% | 109 | 13,01% |
Hequet et al. (2009) | 136 | 3,13% | 113 | 12,99% | 112 | 13,38% | 109 | 13,01% |
MacKee (1994) | 134 | 3,08% | 108 | 12,41% | 107 | 12,78% | 104 | 12,41% |
Paton et al. (2019) | 116 | 2,67% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Tison et al. (2014) | 103 | 2,37% | 48 | 5,52% | 47 | 5,62% | 41 | 4,89% |
Jourdan & Mille (2006) | 93 | 2,14% | 81 | 9,31% | 80 | 9,56% | 80 | 9,55% |
Gutierrez (1981) | 79 | 1,82% | 67 | 7,7% | 66 | 7,89% | 65 | 7,76% |
Anonyme (2014) | 71 | 1,63% | 60 | 6,9% | 60 | 7,17% | 60 | 7,16% |
Acevedo-Rodríguez & Strong (2012) | 68 | 1,57% | 44 | 5,06% | 44 | 5,26% | 42 | 5,01% |
Molino et al. (2022) | 64 | 1,47% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Delnatte & Meyer (2012) | 58 | 1,33% | 45 | 5,17% | 45 | 5,38% | 44 | 5,25% |
Boullet et al. (2018) | 57 | 1,31% | 51 | 5,86% | 50 | 5,97% | 49 | 5,85% |
Meurgey & Ramage (2020) | 56 | 1,29% | 55 | 6,32% | 54 | 6,45% | 54 | 6,44% |
Meurgey (2011) | 51 | 1,17% | 49 | 5,63% | 48 | 5,73% | 49 | 5,85% |
Dierkens (2021) | 50 | 1,15% | 49 | 5,63% | 49 | 5,85% | 49 | 5,85% |
Matile-Ferrero & Etienne (2006) | 48 | 1,1% | 47 | 5,4% | 47 | 5,62% | 47 | 5,61% |
Léotard & Chaline (2013) | 44 | 1,01% | 38 | 4,37% | 38 | 4,54% | 37 | 4,42% |
Poupin (2010) | 43 | 0,99% | 33 | 3,79% | 33 | 3,94% | 33 | 3,94% |
Questel (2020) | 43 | 0,99% | 38 | 4,37% | 38 | 4,54% | 37 | 4,42% |
Copeland (1932) | 40 | 0,92% | 14 | 1,61% | 14 | 1,67% | 14 | 1,67% |
Thibault et al. (2014) | 40 | 0,92% | 35 | 4,02% | 31 | 3,7% | 32 | 3,82% |
Gargominy et al. (1996) | 39 | 0,9% | 34 | 3,91% | 34 | 4,06% | 34 | 4,06% |
Wheeler (1935) | 39 | 0,9% | 22 | 2,53% | 22 | 2,63% | 22 | 2,63% |
Grand et al. (2014) | 37 | 0,85% | 37 | 4,25% | 37 | 4,42% | 32 | 3,82% |
Cohic (1959) | 34 | 0,78% | 22 | 2,53% | 21 | 2,51% | 22 | 2,63% |
Questel & Le Quellec (2012) | 33 | 0,76% | 29 | 3,33% | 28 | 3,35% | 28 | 3,34% |
Gill (1995) | 32 | 0,74% | 27 | 3,1% | 27 | 3,23% | 23 | 2,74% |
Wilson & Hunt (1967) | 32 | 0,74% | 29 | 3,33% | 29 | 3,46% | 29 | 3,46% |
Jourdan et al. (2014) | 31 | 0,71% | 22 | 2,53% | 21 | 2,51% | 22 | 2,63% |
Wetterer (2002) | 31 | 0,71% | 26 | 2,99% | 26 | 3,11% | 26 | 3,1% |
Ramage (2014) | 30 | 0,69% | 29 | 3,33% | 29 | 3,46% | 29 | 3,46% |
Wilson & Taylor (1967) | 30 | 0,69% | 21 | 2,41% | 21 | 2,51% | 21 | 2,51% |
Jourdan (2020) | 29 | 0,67% | 28 | 3,22% | 27 | 3,23% | 26 | 3,1% |
Perrault (1988) | 29 | 0,67% | 27 | 3,1% | 27 | 3,23% | 27 | 3,22% |
Jennings et al. (2013) | 28 | 0,64% | 27 | 3,1% | 27 | 3,23% | 26 | 3,1% |
Mille et al. (2016) | 28 | 0,64% | 28 | 3,22% | 28 | 3,35% | 28 | 3,34% |
Linnaeus (1758) | 26 | 0,6% | 8 | 0,92% | 8 | 0,96% | 7 | 0,84% |
Rogers & Appan (1973) | 26 | 0,6% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Taylor (1987) | 25 | 0,58% | 25 | 2,87% | 25 | 2,99% | 25 | 2,98% |
Uicn et al. (2015) | 25 | 0,58% | 25 | 2,87% | 25 | 2,99% | 25 | 2,98% |
Berland (1942) | 24 | 0,55% | 11 | 1,26% | 11 | 1,31% | 11 | 1,31% |
Morrison (1996) | 24 | 0,55% | 19 | 2,18% | 19 | 2,27% | 19 | 2,27% |
Aublet (1775) | 23 | 0,53% | 10 | 1,15% | 9 | 1,08% | 9 | 1,07% |
Baaijens & Veldkamp (1991) | 23 | 0,53% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Murdock & Smith (2003) | 22 | 0,51% | 14 | 1,61% | 13 | 1,55% | 14 | 1,67% |
Yokoyama (2013) | 22 | 0,51% | 18 | 2,07% | 18 | 2,15% | 18 | 2,15% |
Grand et al. (2019) | 21 | 0,48% | 21 | 2,41% | 21 | 2,51% | 21 | 2,51% |
Clastrier & Delécolle (1996) | 20 | 0,46% | 20 | 2,3% | 20 | 2,39% | 20 | 2,39% |
Morrison (1997) | 20 | 0,46% | 16 | 1,84% | 16 | 1,91% | 16 | 1,91% |
Orchard (2013) | 20 | 0,46% | 2 | 0,23% | 1 | 0,12% | 1 | 0,12% |
Poussereau et al. (2018) | 20 | 0,46% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Remillet (1988) | 20 | 0,46% | 18 | 2,07% | 18 | 2,15% | 17 | 2,03% |
Suddee et al. (2004) | 20 | 0,46% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Wheeler (1932) | 20 | 0,46% | 12 | 1,38% | 12 | 1,43% | 12 | 1,43% |
Cohic (1950) | 19 | 0,44% | 17 | 1,95% | 17 | 2,03% | 17 | 2,03% |
Florence (1997) | 19 | 0,44% | 14 | 1,61% | 14 | 1,67% | 13 | 1,55% |
Heller (1916) | 19 | 0,44% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Lemée (1953) | 19 | 0,44% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Lowe et al. (2007) | 19 | 0,44% | 14 | 1,61% | 13 | 1,55% | 13 | 1,55% |
Molino et al. (2009) | 19 | 0,44% | 17 | 1,95% | 17 | 2,03% | 16 | 1,91% |
Rageau (1958) | 19 | 0,44% | 15 | 1,72% | 13 | 1,55% | 13 | 1,55% |
Wheeler (1936) | 19 | 0,44% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Cochereau (1966) | 18 | 0,41% | 17 | 1,95% | 17 | 2,03% | 17 | 2,03% |
Emery (1914) | 18 | 0,41% | 9 | 1,03% | 9 | 1,08% | 9 | 1,07% |
Evenhuis (2018) | 18 | 0,41% | 15 | 1,72% | 14 | 1,67% | 15 | 1,79% |
Germain et al. (2014) | 18 | 0,41% | 18 | 2,07% | 18 | 2,15% | 18 | 2,15% |
Griffiths & Florens (2006) | 18 | 0,41% | 14 | 1,61% | 14 | 1,67% | 14 | 1,67% |
Allem (1994) | 17 | 0,39% | 2 | 0,23% | 1 | 0,12% | 1 | 0,12% |
Berland (1934) | 17 | 0,39% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Cheesman (1928) | 17 | 0,39% | 17 | 1,95% | 17 | 2,03% | 17 | 2,03% |
Delannoye et al. (2015) | 17 | 0,39% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Dierkens & Ramage (2016) | 17 | 0,39% | 13 | 1,49% | 13 | 1,55% | 13 | 1,55% |
Florence (2004) | 17 | 0,39% | 15 | 1,72% | 15 | 1,79% | 15 | 1,79% |
Paulian (1998) | 17 | 0,39% | 15 | 1,72% | 13 | 1,55% | 15 | 1,79% |
Chew (1969) | 16 | 0,37% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Foldi & Germain (2018) | 16 | 0,37% | 16 | 1,84% | 16 | 1,91% | 16 | 1,91% |
Hammes & Putoa (1986) | 16 | 0,37% | 16 | 1,84% | 16 | 1,91% | 16 | 1,91% |
Jaffe & Lattke (1994) | 16 | 0,37% | 16 | 1,84% | 16 | 1,91% | 16 | 1,91% |
Migeon (2015) | 16 | 0,37% | 16 | 1,84% | 16 | 1,91% | 16 | 1,91% |
UICN Comité français, OFB & MNHN (2021) | 16 | 0,37% | 16 | 1,84% | 16 | 1,91% | 16 | 1,91% |
Berland (1933) | 15 | 0,35% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Berland (1934) | 15 | 0,35% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Clarke (1971) | 15 | 0,35% | 12 | 1,38% | 12 | 1,43% | 10 | 1,19% |
Cowie (2000) | 15 | 0,35% | 12 | 1,38% | 12 | 1,43% | 12 | 1,43% |
Dierkens & Charlat (2011) | 15 | 0,35% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Germain (2007) | 15 | 0,35% | 15 | 1,72% | 15 | 1,79% | 15 | 1,79% |
Margońska (2019) | 15 | 0,35% | 14 | 1,61% | 14 | 1,67% | 14 | 1,67% |
Marinov et al. (2021) | 15 | 0,35% | 15 | 1,72% | 14 | 1,67% | 14 | 1,67% |
Meyer et al. (2006) | 15 | 0,35% | 8 | 0,92% | 7 | 0,84% | 7 | 0,84% |
Fauvel (1867) | 14 | 0,32% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Lorvelec et al. (2007) | 14 | 0,32% | 14 | 1,61% | 14 | 1,67% | 14 | 1,67% |
Wheeler (1932) | 14 | 0,32% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Allen et al. (2022) | 13 | 0,3% | 12 | 1,38% | 12 | 1,43% | 12 | 1,43% |
Gill (1995) | 13 | 0,3% | 11 | 1,26% | 11 | 1,31% | 11 | 1,31% |
Desmodium incanum and Fall of D. canum (Fabaceae). Taxon, 27(4): 365-370.">Nicolson (1978) | 13 | 0,3% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Theuerkauf et al. (2010) | 13 | 0,3% | 13 | 1,49% | 13 | 1,55% | 13 | 1,55% |
Viette (1949) | 13 | 0,3% | 8 | 0,92% | 7 | 0,84% | 8 | 0,95% |
Viette (1950) | 13 | 0,3% | 4 | 0,46% | 3 | 0,36% | 4 | 0,48% |
Wurdack et al. (1993) | 13 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Blard et al. (2003) | 12 | 0,28% | 12 | 1,38% | 12 | 1,43% | 12 | 1,43% |
Cochereau (1974) | 12 | 0,28% | 12 | 1,38% | 12 | 1,43% | 12 | 1,43% |
Hovenkamp & Miyamoto (2005) | 12 | 0,28% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lemée (1952) | 12 | 0,28% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Martiré & Rochat (2008) | 12 | 0,28% | 8 | 0,92% | 8 | 0,96% | 7 | 0,84% |
Pilsbry (1906-1907) | 12 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage et al. (2023) | 12 | 0,28% | 12 | 1,38% | 12 | 1,43% | 12 | 1,43% |
Rocamora (2004) | 12 | 0,28% | 11 | 1,26% | 11 | 1,31% | 11 | 1,31% |
Toutain (1989) | 12 | 0,28% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Berland (1924) | 11 | 0,25% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Braun et al. (2014) | 11 | 0,25% | 11 | 1,26% | 11 | 1,31% | 11 | 1,31% |
Etienne & Vilardebó (1978) | 11 | 0,25% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Galkowski (2016) | 11 | 0,25% | 11 | 1,26% | 11 | 1,31% | 11 | 1,31% |
Gmelin (1789) | 11 | 0,25% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Hovestadt & Neckheim (2020) | 11 | 0,25% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Ledoux & Hallé (1995) | 11 | 0,25% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Uicn et al. (2017) | 11 | 0,25% | 11 | 1,26% | 11 | 1,31% | 11 | 1,31% |
Vayssières et al. (2001) | 11 | 0,25% | 9 | 1,03% | 9 | 1,08% | 9 | 1,07% |
Wheeler (1933) | 11 | 0,25% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Anonyme (2018) | 10 | 0,23% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Barau et al. (2005) | 10 | 0,23% | 9 | 1,03% | 9 | 1,08% | 9 | 1,07% |
Cazanove (2022) | 10 | 0,23% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Cooke (1934) | 10 | 0,23% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Etienne (2005) | 10 | 0,23% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Ferlay et al. (2023) | 10 | 0,23% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Franco et al. (2019) | 10 | 0,23% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Garrett (1884) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lebas et al. (2016) | 10 | 0,23% | 10 | 1,15% | 10 | 1,19% | 10 | 1,19% |
Lemée (1955) | 10 | 0,23% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Linnaeus (1753) | 10 | 0,23% | 7 | 0,8% | 6 | 0,72% | 6 | 0,72% |
Meyer (2017) | 10 | 0,23% | 10 | 1,15% | 9 | 1,08% | 9 | 1,07% |
Montrouzier (1861) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Øllgaard et al. (2020) | 10 | 0,23% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Souza et al. (2019) | 10 | 0,23% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Véron et al. (2021) | 10 | 0,23% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Berland (1935) | 9 | 0,21% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Brook (2010) | 9 | 0,21% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Christenhusz (2009) | 9 | 0,21% | 9 | 1,03% | 9 | 1,08% | 9 | 1,07% |
Cochereau (1966) | 9 | 0,21% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Miller (1768) | 9 | 0,21% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Papazian et al. (2007) | 9 | 0,21% | 9 | 1,03% | 7 | 0,84% | 9 | 1,07% |
Patrick & Policard (2015) | 9 | 0,21% | 6 | 0,69% | 3 | 0,36% | 6 | 0,72% |
Platnick (1993) | 9 | 0,21% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Remsen et al. (2013) | 9 | 0,21% | 9 | 1,03% | 9 | 1,08% | 9 | 1,07% |
Stace (2010) | 9 | 0,21% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Weimerskirch et al. (2009) | 9 | 0,21% | 9 | 1,03% | 9 | 1,08% | 9 | 1,07% |
Barré (2021) | 8 | 0,18% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Cheesman (1927) | 8 | 0,18% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Cooke & Kondo (1961) | 8 | 0,18% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Croat & Delannay (2017) | 8 | 0,18% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gomy (2000) | 8 | 0,18% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Levesque & Delcroix (2018) | 8 | 0,18% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Marinov et al. (2019) | 8 | 0,18% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Marples (1957) | 8 | 0,18% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Mitchell & Daly (2015) | 8 | 0,18% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Nattier et al. (2015) | 8 | 0,18% | 8 | 0,92% | 8 | 0,96% | 8 | 0,95% |
Øllgaard & Windisch (2016) | 8 | 0,18% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Philcox (1965) | 8 | 0,18% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Poupin et al. (2018) | 8 | 0,18% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Preece (1995) | 8 | 0,18% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Sauer (1964) | 8 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Solem (1961) | 8 | 0,18% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Aulagnier et al. (2017) | 7 | 0,16% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Bauer & Sadlier (2000) | 7 | 0,16% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Bernard (2015) | 7 | 0,16% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Borkent & Wirth (1997) | 7 | 0,16% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Flechtmann et al. (2000) | 7 | 0,16% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Gargominy (2016-2021) | 7 | 0,16% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 7 | 0,16% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Ineich (2016) | 7 | 0,16% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Jeffrey (1980) | 7 | 0,16% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Jost et al. (2019) | 7 | 0,16% | 5 | 0,57% | 4 | 0,48% | 5 | 0,6% |
Judd et al. (2018) | 7 | 0,16% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Larridon et al. (2014) | 7 | 0,16% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lavergne (2011) | 7 | 0,16% | 5 | 0,57% | 4 | 0,48% | 4 | 0,48% |
Massemin et al. (2009) | 7 | 0,16% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Moore (1933) | 7 | 0,16% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Mousson (1871) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Peck (2011) | 7 | 0,16% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Perrault (1993) | 7 | 0,16% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Poupin (2015) | 7 | 0,16% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Preece (1998) | 7 | 0,16% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Solem (1964) | 7 | 0,16% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Soubeyran et al. (2011) | 7 | 0,16% | 7 | 0,8% | 7 | 0,84% | 7 | 0,84% |
Wasshausen (2006) | 7 | 0,16% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Zerega et al. (2005) | 7 | 0,16% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Abdou et al. (2004) | 6 | 0,14% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Blatrix et al. (2018) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Bouchet & Pointier (1998) | 6 | 0,14% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bouchet et al. (1991) | 6 | 0,14% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Casevitz-Weulersse & Galkowski (2009) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Ceccolini (2023) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Couhia & Fleurot (2016) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Distant (1914) | 6 | 0,14% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Fauvel (1903) | 6 | 0,14% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Fauvel (1904) | 6 | 0,14% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Garrett (1879) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hermans & Cribb (2021) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway (1979) | 6 | 0,14% | 4 | 0,46% | 3 | 0,36% | 4 | 0,48% |
Linnaeus (1753) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 5 | 0,6% |
Matile-Ferrero & Williams (2015) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Montrouzier (1860) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Peck et al. (2014) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Peterson et al. (2014) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Pilsbry & Cooke (1915-1916) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2023) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 6 | 0,72% |
Reid et al. (2021) | 6 | 0,14% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Roux (1913) | 6 | 0,14% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Schatz & Lowry (2018) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1908) | 6 | 0,14% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Wood et al. (2020) | 6 | 0,14% | 6 | 0,69% | 6 | 0,72% | 5 | 0,6% |
Zdunek (2022) | 6 | 0,14% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Aberlenc et al. (2004) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Barabé & Gibernau (2015) | 5 | 0,12% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Berland (1929) | 5 | 0,12% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bigot (1992) | 5 | 0,12% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Blanc et al. (1993) | 5 | 0,12% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Bonfils (1969) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Couté & Garrouste (2009) | 5 | 0,12% | 4 | 0,46% | 3 | 0,36% | 4 | 0,48% |
Dewynter et al. (2023) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Dupérré (2023) | 5 | 0,12% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Fawcett & Smith (2021) | 5 | 0,12% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fernandes (1984) | 5 | 0,12% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fischer et al. (2013) | 5 | 0,12% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fosberg (1937) | 5 | 0,12% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Frenot et al. (2005) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Garrett (1887) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste & Hervé (2009) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Gillespie (2003) | 5 | 0,12% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Guinot et al. (2018) | 5 | 0,12% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Hausdorf (2023) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Holloway & Peters (1976) | 5 | 0,12% | 3 | 0,34% | 3 | 0,36% | 2 | 0,24% |
Kuschel (2008) | 5 | 0,12% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Matile-Ferrero (1979) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Mertens & Wermuth (1960) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer & Ah-Peng (2024) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Needham (1932) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Peck (2016) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Poupin et al. (2013) | 5 | 0,12% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Prévost & Mougin (1970) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Radoszkowsky (1884) | 5 | 0,12% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Ramage et al. (2015) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Rico et al. (2006) | 5 | 0,12% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Vueti (2001) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Wetterer (2012) | 5 | 0,12% | 5 | 0,57% | 5 | 0,6% | 5 | 0,6% |
Angel (1935) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Aulagnier (2009) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Baker (1941) | 4 | 0,09% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Bauters et al. (2019) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Beenen (2008) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Belfan & Conde (2016) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bochaton et al. (2021) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Bolton (2012) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer & Rivault (2003) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Braun et al. (1999) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Carpenter (2023) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Clements (2012) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Couteyen & Papazian (2012) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Cremers & Hoff (1994) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dadant & Etienne (1973) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Damoiseau (1966) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2022) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Duyck et al. (2022) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Evenhuis (2007) | 4 | 0,09% | 2 | 0,23% | 1 | 0,12% | 2 | 0,24% |
Fauvel (1891) | 4 | 0,09% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Fauvel (1903) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher & Fong (2020) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Flechtmann et al. (1999) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Forest (1954) | 4 | 0,09% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Fryxell (2001) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gasper et al. (2016) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gentry et al. (2004) | 4 | 0,09% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Gomy (2016) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 2 | 0,24% |
Gould (1852) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1862) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Guilbert & Casevitz-Weulersse (1997) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Guillermet (2009) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2009) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Hammel & Grayum (2011) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hassemer (2017) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Henderson & Breuil (2012) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hoser (2016) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutton (1834) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2007) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Jay et al. (2009) | 4 | 0,09% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Judziewicz (1990) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Kuhlmann (2006) | 4 | 0,09% | 4 | 0,46% | 3 | 0,36% | 4 | 0,48% |
Legros et al. (2017) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Leroy et al. (2021) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Lieftinck (1975) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Marie & Bossin (2013) | 4 | 0,09% | 2 | 0,23% | 1 | 0,12% | 2 | 0,24% |
Marinov et al. (2016) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Marinov (2021) | 4 | 0,09% | 4 | 0,46% | 0 | 0% | 4 | 0,48% |
Mayr (1870) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Meurgey & Picard (2011) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Mille et al. (2020) | 4 | 0,09% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Montrouzier (1861) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Nava et al. (2018) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Ocampo & Columbus (2012) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnaudeau (2012) | 4 | 0,09% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Pilsbry (1920-1921) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (2013) | 4 | 0,09% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Reinert et al. (2004) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Revilliod (1914) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ris (1915) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Roalson et al. (2010) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Routtier et al. (2023) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Rudge (1805) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Sadlier et al. (2012) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Schabetsberger et al. (2009) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Schouteden (1907) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Solem (1983) | 4 | 0,09% | 4 | 0,46% | 3 | 0,36% | 3 | 0,36% |
Talaga et al. (2015) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Ter Steege et al. (2016) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 3 | 0,36% |
Thomson et al. (2022) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Van Zwaluwenburg (1932) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Welker et al. (2020) | 4 | 0,09% | 4 | 0,46% | 4 | 0,48% | 4 | 0,48% |
Wenzel (1955) | 4 | 0,09% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Albouy et al. (2017) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 2 | 0,24% |
Arrow (1927) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Baker (1938) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Balouet & Olson (1989) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bangy et al. (2009) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bauer & Sadlier (1994) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Bauters et al. (2016) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Berg (1992) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bernard (1968) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Berry et al. (1996) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Berry et al. (1997) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bippus (2019) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Boggan et al. (1992) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1833) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulard (1996) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Brauer (1865) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunhes & Boussès (2009) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 2 | 0,24% |
Burneleau (1983) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Butaud (2021) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Candolle (1828) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Catzeflis (2018) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Coomans (1967) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cremers & Boudrie (2007) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dewynter et al. (2023) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Donisthorpe (1932) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Durant et al. (2013) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Etcheberry & Abraham (2009) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Etienne et al. (2015) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Fabricius (1793) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1849) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fauvel (1862) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Férussac (1821) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Field et al. (2016) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fort & Barrière (2021) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Gardner et al. (2021) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 2 | 0,24% |
Geneva et al. (2013) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
González‐Elizondo & Peterson (1997) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
González-sánchez et al. (2021) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Greipsson & Priest (1983) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2004) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Gusenleitner (2011) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Gutierrez (1968) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Hausdorf (2007) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Havery et al. (2018) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Hebard (1933) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Hervé & Garrouste (2009) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Hustache (1920) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Justine et al. (2021) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Ke et al. (2022) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Kormilev (1971) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lagarde (2008) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Lambert (1988) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Le Maitre & Chadee (1983) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Lenfant & Marro (1997) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Lieftinck (1966) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Lima et al. (2012) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Liu (2021) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Lucas (2012) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Maas (1985) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Massary et al. (2020) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Massary et al. (2021) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Masters et al. (2023) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Mitchell (1997) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Moench (1794) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1940) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mousson (1869) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nentwig et al. (2019) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Nève de Mévergnies et al. (2024) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Ng & Shih (2015) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas (2012) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
O’Donnell et al. (2022) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ohler et al. (2021) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Patrick & Patrick (2012) | 3 | 0,07% | 2 | 0,23% | 1 | 0,12% | 2 | 0,24% |
Pease (1861) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pease (1865) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1916-1918) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Probst et al. (2022) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Probst (2001) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Questel et al. (2023) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Questel et al. (2023) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Questel (2017) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Raspi et al. (2007) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Rheinheimer (2012) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Rheinheimer (2014) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Rhodin et al. (2017) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Ronot (2007) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Roux (1926) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Sachet (1962) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Safford & Hawkins (2013) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Salata & Fisher (2022) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Simões & Staples (2017) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Simon (1897) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Soldati et al. (2012) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Taylor et al. (2017) | 3 | 0,07% | 3 | 0,34% | 1 | 0,12% | 2 | 0,24% |
Thouvenot & Bardat (2010) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Thouvenot et al. (2011) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Tirvengadum & Bour (1985) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Van Zwaluwenburg (1959) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Vanderwerf et al. (2006) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Vane-Wright & De Jong (2003) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 2 | 0,24% |
Vedel et al. (2013) | 3 | 0,07% | 3 | 0,34% | 3 | 0,36% | 3 | 0,36% |
Videira et al. (2017) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Wallach (2020) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Walter et al. (2015) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ward et al. (2015) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Yang et al. (2012) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Zimmerman (1936) | 3 | 0,07% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Acevedo-Rodríguez (2012) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Adamson (1935) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Alvarez et al. (2023) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Aubouin et al. (2016) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Aurore et al. (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Baroni Urbani & De Andrade (2007) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Barthelat (2019) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bauer (1987) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beenen (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Behm et al. (2019) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Béreau (2017) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Berland (1927) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bielawski (1973) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Blanvillain et al. (2002) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Boggan et al. (1997) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Borth & Kons (2022) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Boulenger (1883) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bouman et al. (2022) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bournier & Mound (2000) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bournier (2000) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bousses et al. (2013) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bradley (1953) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Breuil (2002) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuning (1970) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Brun et al. (1983) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Busala et al. (2024) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Byng et al. (2016) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Carille (2012) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Chapuis et al. (2004) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Charpy et al. (2012) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Chazeau (1978) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cheke (1987) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Chemisquy et al. (2010) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Clarke (1986) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Clench (1964) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cockerell (1893) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cockerell (1895) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cole et al. (2005) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Colijn et al. (2020) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Collenette (1934) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Collinson et al. (2017) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Cramer ([1780]-1782) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Crouzier (2017) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Deblock et al. (1960) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Deshayes (1863) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2019) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Dewynter (2021) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Distant (1920) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Dognin (1908) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duay et al. (2014) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Dumbardon-Martial & Delblond (2019) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 1 | 0,12% |
Duméril & Bibron (1836) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duval et al. (2019) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Esyunin & Zamani (2020) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fabricius (1775) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1850) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Feldmann (2012) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fennah (1958) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fennah (1969) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Ferriere (1929) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fici (2014) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Flechtmann & Etienne (2001) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Flechtmann et al. (1999) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fleutiaux (1891) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gagnon et al. (2016) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Galliard (1927) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerlach (2016) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gilot et al. (1992) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Giraldo-Cañas (2012) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Girard (1858) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1788) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy et al. (2009) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulding et al. (2023) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gros (2020) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Guillermet (2006) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Guillermet (2011) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gusenleitner & Madl (2011) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gutierrez & Etienne (1986) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Hamon (1953) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartmann et al. (2021) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Hendrian & Kondo (2007) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hery et al. (2020) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoddle et al. (2008) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Hodgetts & Lockhart (2020) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Humeau et al. (2020) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Ineich et al. (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jelinek & Lason (2018) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Jerdon (1851) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
John (1942) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Johnson (1994) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Justine et al. (2014) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Justine et al. (2015) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Keith et al. (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirch (1973) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Klein et al. (2016) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Kojadinovic et al. (2007) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Kowalkowska & Margonska (2012) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Kuntze (1891) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacoste (de) (2020) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Lacroix (2015) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Lallemand (1942) | 2 | 0,05% | 2 | 0,23% | 0 | 0% | 2 | 0,24% |
Lamarck (1783) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Le Breton et al. (2005) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Leopold (1965) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Leponce et al. (2019) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Lesson (1830) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Liardet (1876) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli & Abadie (2015) | 2 | 0,05% | 2 | 0,23% | 1 | 0,12% | 1 | 0,12% |
Maddi (2014) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Maillaud et al. (2015) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Manzitto‐Tripp & Daniel (2023) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Marshall (1921) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Martiré (2010) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Mary (2017) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Mas-Coma et al. (1989) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Massary et al. (2017) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Massary et al. (2018) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Mesnil (1968) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Meurgey & Dumbardon-Martial (2015) | 2 | 0,05% | 2 | 0,23% | 1 | 0,12% | 1 | 0,12% |
Meurgey (2014) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 0 | 0% |
Meyrick (1934) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Miller & Wilson (1997) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Montrouzier (1858) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1859) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mousson (1870) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Neubert & Gosteli (2003) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nibouche et al. (202X) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Nicolas et al. (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas et al. (2015) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
N'Yeurt & Payri (2004) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Oatleya et al. (2015) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Odhner (1921) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Oliveira Pellegrini & Forzza (2017) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ollitrault et al. (2020) | 2 | 0,05% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
Panis (1969) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Parris (2007) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Pascal et al. 2006 | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Paton et al. (2018) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Payri & N'yeurt (1997) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Peale (1848) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pease (1868) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Pease (1869) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Pease (1871) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pejhanmehr (2022) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Perroud & Montrouzier (1864) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pignal et al. (2023) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Pritchard & Baker (1955) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Probst (1997) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Probst (1998) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rageau (1956) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rageau (1959) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Ramage & Gourvès (2017) | 2 | 0,05% | 2 | 0,23% | 1 | 0,12% | 1 | 0,12% |
Rang (1831) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Reichenbach (1878) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Remaudière & Etienne (1988) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Rheinheimer (2015) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Ringler et al. (2015) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Rivière (1979) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Robineau-desvoidy (1827) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ros et al. (2013) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Saint et al. (1978) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Salisbury (1796) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez & Probst (2016) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Sanchez et al. (2019) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Sanchez (2020) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Sanders (2012) | 2 | 0,05% | 1 | 0,11% | 0 | 0% | 0 | 0% |
Schulthess (1915) | 2 | 0,05% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
Séguy (1944) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Seifert (2022) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Senevet (1937) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherff (1937) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Sicart & Ruffie (1960) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Sluys (2016) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Smith (1857) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Solem (1959) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1872) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1874) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Talaga et al. (2015) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Taylor & Wilson (1961) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Teres (2006) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Theobald (1913) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thorell (1887) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thunberg (1787) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tomaszewska (2010) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Touroult et al. (2018) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Tronquet (2014) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Upton et al. (1994) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Van Dijk et al. (2012) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Van Zwaluwenburg (1932) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Veldkamp (1991) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Veldkamp (2014) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Verreaux & Des Murs (1860) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Viette (1950) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Walckenaer ([1841]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang (2003) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Wiersema et al. (2018) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Wilcox & Spotswood (2011) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Zilli et al. (2017) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Zimmerman (1943) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Zimmerman (1964) | 2 | 0,05% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Zubia et al. (2015) | 2 | 0,05% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Adams (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Albouy & Richard (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Alencar et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Allorge-Boiteau (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Alston (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrassy (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Appelhans et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Armand & Ferlay (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Arnold & Ovenden (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Astorga-acuña & Mora (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Astrongatt (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Aulagnier (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ausilio & Zotier (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Austin & Huáman (1996) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Austin & Zug (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Azam (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Badré (2008b) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bagny et al. (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailenger et al. (1965) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Baker (1940) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker-gabb (1979) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Balachowsky (1958) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bance (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Barbour (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bardat et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Barré et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Barre et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Barre (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Barrioz & Morinière (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bassett et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bauer & DeVaney (1987) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bauer et al. (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bavay (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beatty et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Beaucournu (1968) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauvieux et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Beggs et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Behm et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Belkin et al. (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bell (1982) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bellifa et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bellmann (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Bénito-espinal (1990) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Benson (1850) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernardi (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Berry et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bioinsight/diren & Guyane (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Biondi et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bippus (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Birdlife International (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Blair (1934) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Blair (1934) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Blanc (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanchot (1992) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Blancou et al. (1987) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Blight et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Blom et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Blom (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bocourt (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boddaert & Daubenton (1783) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Boettger (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boheman (1858-1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolton (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bonfils et al. (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Borroto-páez (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bosser & Heine (2000b) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Botrel et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bougeard & Siblet (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bouget et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bouman et al. (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bour et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bousquet (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bovini (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1822) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyd et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Boyer de Fonscolombe (1834) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Breuil et al. (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brindle (1975) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Brindle (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Brisbane et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Brown & Gibbons (1986) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bruguière (1789-1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brun & Chazeau (1986) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Brunhes (1977) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunhes (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Burr (1914) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bursey & Goldberg (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Bursey et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Caceres & Salamolard (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cafferty et al. (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot & Rioux (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Callou (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Camiñas et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Carini & Pinto (1926) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Carl (1915) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter & Madl (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Carpenter (1934) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Carpenter (1935) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Casale et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Caut et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Célini et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chambault et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Champagne et al. (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chance et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chapelin-Viscardi & Lariviere (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chavez et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cheke & Hume (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cheke (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevalier (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chevallier et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chew (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chopard (1924) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chown & Convey (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Christenhusz (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Christensen & Kahn (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Chûjô (1961) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ciccione et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Clause et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cohic (1959) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Colindre (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Collazos-astudillo et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Collet & Pérennec (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Collier et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Commission de l’Avifaune Française (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Conte et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Coode 1982 | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cooke (1928) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cooreman (1959) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Couté et al. (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Couteyen (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cox (1970) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cramer ([1777]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Crantz (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1990) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Crillon & Cuzange (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Crouzier (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cummings et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Cuvier (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dal Zotto et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dalla Torre (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Daly et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
D´angiolella et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Danin et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Daudin (1802) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Daudin (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1773) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deharveng (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dehgan (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Delabie & Blard (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Delcroix et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Delcroix et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Delgado-trejo et al. (2024) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delprete (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deniau & Provost (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
[Denis & Schiffermüller] (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Denoyes et al. (1986) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Denux & Zagatti (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Des et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Deuss & Jourdan (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Devaud & Lebouvier (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dewynter & Claessens (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dewynter et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dewynter et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dewynter et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dickinson & Remsen (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dieme et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dierkens (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Doleschall (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dollfus (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Donskoff (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubief & Gallais (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dubois & Frétey (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Dubois et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Dubois (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ducatez & Devore (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duffaut et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duguy et al. (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duguy et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duguy (1987) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duguy (1988) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duguy (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duguy (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Duhamel (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bibron (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Duméril (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ebihara et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Edwards et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Edwards (1933) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ellis et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Emerit & Ledoux (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Emery (1869) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Emery (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1897) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Englund & Polhemus (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Entraygues (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Étaix-bonnin et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Etienne et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Euro+Med (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Evenhuis (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Evenhuis (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Evenhuis (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fabre & Orsini (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fabres (1977) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fabricius (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1903) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fauvel (1905) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ferris (1935) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Feuillet (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Feuillet (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Filipowicz et al. (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Finnerty et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fischer-piette & Bedoucha (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fisher (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Flechtmann & Etienne (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Flechtmann & Etienne (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Flechtmann & Etienne (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Flitti & Rocha (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Flora of China (2015-) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Florschütz-de Waard et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fontanilla et al. (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Forel (1881) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Forel (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1907) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Forel (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fretey & Triplet (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Fretey et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Friese (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gamiette et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gardner et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gargominy (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gassies (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerlach (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Germar (1824) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gherghel et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gillespie (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Girard (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondo (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Girondot (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Godet et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Goldberg et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gomy (1981) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Gould et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Görts-van Rijn (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Grangaud (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Grant-mackie et al. (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffing et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Grolle (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Groom et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Guenée (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillaumin (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamon (1956) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Harman (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hassemer et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hebard (1933) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hebard (1935) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hedges et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heinicke et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Heiss (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Henao-osorio et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hett (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hill et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hinckley (1963) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Hindermeyer et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Holub (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugonnot et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
ICZN (1954) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Bauer (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Blanc (1988) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ineich et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ineich et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ineich (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ineich (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
IUCN (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Jacquinot & Guichenot (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jäger (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Janda & Abbott (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Jaramillo et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Jendrzejewska (1995) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Jiguet (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Jolinon (1987) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Jouan (1863) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Jouveau et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Justine & Winsor (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Kaltenbach (1968) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Karadjian et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Karin et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Karny (1925) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Kaszab (1982) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Kayser & Wilhelm (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Keith & Marquet (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Khaliq et al. (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Kirejtshuk (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Klonowska et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Klonowska et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Koch (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kormilev (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kozar & Benedicty (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Kreiter et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Kükenthal (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuschel (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lackner & Leschen (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lafranchis (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lafranchis (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lamarck (1798) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lamontellerie (1965) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lancastre et al. (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lapwong et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Latreille (1802) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1806) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1807) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Jouventin (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Le Goff et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Le Scao et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Leavengood et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lemée (1956) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoir et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lescure et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lescure et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lescure et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lesson (1826-1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Mathurin (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lewis (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Liardet & d'Auzon (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Liardet (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lichtenstein (1823) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Liebart et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Liebgold et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lima et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Pascal (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lorvelec & Pascal (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lorvelec et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lorvelec et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lorvelec et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lorvelec et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Louisin & Probst (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Lower (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Luo (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ma et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Macfie (1933) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Macfie (1933) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Malausa & Ehanno (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1932) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Mapaya (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Marchal et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Marchandeau & Letty (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Marchandeau et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Maréchal & Iinuma (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Marks (1951) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Marples (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Maskell (1893) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Massary et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Mayr (1862) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Mayr (1866) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Mayr (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazur & Węgrzynowicz (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Mckay & Milenkaya (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Meganck et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ménard et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Merrem (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Questel (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Meyen (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Meyrick (1912-1916) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1916-1923) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Meyrick (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mille et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Minot (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Möllendorf (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrousier (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Catalogue of Brazilian plants collected by Prince Maximilian of Wied". Plant Ecology and Evolution, 149(3): 308-315.">Moraes et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelon (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Mori et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Morinière & Dell'amico (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Mousson (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Muratet (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Murphy et al. (1978) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Naggs (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Naggs (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Nakata (1961) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Nassi et al. (1975) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Nkontcho et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Noël (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ochyra et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Orbigny (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Orhant (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
O’Shea (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Oueslati et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Parmentier et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Parnaudeau & Madl (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Parnaudeau (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Parnaudeau (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pastore et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Paudyal et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Payri et al. (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Peck (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Peron (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Perrault (1979) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Persoon (1807) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit et al. (1990) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pfeiffer (1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre & Lalanne-Cassou | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pierre et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Pilsbry & Hirase (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1927-1935) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Platnick (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pocock (1898) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pointier & Blanc (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Poisson (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ponel & Roge (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ponge et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Potin (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Transactions of the Entomological Society of London, 76: 453-468.">Poulton & Riley (1929) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Jelínek, J. & Audisio, P. 2011. A new species of Amystrops Reitter, 1875, and an updated checklist of the Nitidulidae from Réunion Island (Coleoptera). Bulletin de la Société entomologique de France, 116(4): 421-428. ">Poussereau et al. (2011) |
1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Princis (1974) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Probst et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Probst et al. (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Probst (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Pulle (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Quilici et al. (1988) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ragavan et al. (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Ramage (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Randi et al. (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rankin Rodríguez & Greuter (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rathbun (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Read & Farman (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Read & Jean (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Read et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Read et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Reed (1968) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rehn (1948) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rehn (1949) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Renaud et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Reverté et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Reynolds & Henderson (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Richard (1792) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rigouzzo et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rinaldi et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rivault et al. (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rocha et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Roger (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Roos (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Roques (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ros et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Roth & Rivault (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Rowe (1978) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Russell & Etienne (1985) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Saaristo (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Samaniego et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Samuel et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Samways (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Sanders (2006) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 0 | 0% |
Sant (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Santschi (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Saunders (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sautet (1936) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Sauvignet et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Savouré-Soubelet et al. (in prep.) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Say (1823) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Sayed (1946) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Schenck (1905) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Schneider (1783) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1799) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schönherr (1806) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schwaner & Brown (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schweigger (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Seifert et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Seifert (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Servan (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Seurat (1934) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Shaver et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Shea et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Shih et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Shine et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Shinonaga et al. (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Shrestha et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Shuttleworth (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1897) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Siroux (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Smith (1858) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Smith (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Snak et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Snyder et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Song et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Soubeyran (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Souza et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Steadman & Bollt (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Steindachner (1870) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stevenson (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Strong (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Széles et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taberlet (1983) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Tamaki et al. (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
IOBC-WPRS Bulletin, 18(5): 36-38.">Tamonte (1995) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tareau (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Terao (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thévenot (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Thibaud (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Thibault (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Thompson (1938) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Tison et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tostain et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Touroult et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Turner & Veldkamp (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Turner (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Uicn et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Váňa et al. (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Vachal (1907) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Vaillant (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Valerio (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
van den Burg et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Van Zwaluwenburg (1940) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Vantaux et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Vayssières et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Veldkamp (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Verdcourt (1970) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Verwijs et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Vieillot (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Viel (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Viette (1950) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
Viette (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Villers (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Voisin et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Waayers et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Wagner et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Walker (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Wang & Qiu (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Webb & Waddle (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Weisler et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Wells et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1898) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Weterings & Vetter (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Wheeler (1923) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Whistler (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wigginton (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Willdenow (1800) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams (1932) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Winstanley (1983) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Wood et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Yamane et al. (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Yokoyama (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Younes et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Zakardjian et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 0 | 0% |
Zakardjian et al. (2023) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,12% |
Zardini & Raven (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Zhang et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
Zimmerman (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zug et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |
(2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,12% | 1 | 0,12% |