Espèces animales introduites en Guyane
Animaux introduits au sens large en Guyane française, c'est-à-dire introduits établis (I), invasifs (J), introduits non établis (M) ou introduits éteints (Y)
849 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) | 69 | 6,76% | 66 | 35,68% | 65 | 36,11% | 65 | 36,11% |
| Meurgey & Ramage (2020) | 68 | 6,67% | 68 | 36,76% | 66 | 36,67% | 68 | 37,78% |
| Jourdan & Mille (2006) | 61 | 5,98% | 57 | 30,81% | 57 | 31,67% | 55 | 30,56% |
| Meurgey (2011) | 57 | 5,59% | 46 | 24,86% | 45 | 25% | 45 | 25% |
| Shelley & Lehtinen (1999) | 46 | 4,51% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Questel (2020) | 40 | 3,92% | 36 | 19,46% | 34 | 18,89% | 36 | 20% |
| Matile-Ferrero & Etienne (2006) | 31 | 3,04% | 31 | 16,76% | 31 | 17,22% | 29 | 16,11% |
| Jourdan (2020) | 26 | 2,55% | 25 | 13,51% | 24 | 13,33% | 24 | 13,33% |
| Questel & Le Quellec (2012) | 24 | 2,35% | 22 | 11,89% | 22 | 12,22% | 21 | 11,67% |
| Remillet (1988) | 24 | 2,35% | 21 | 11,35% | 21 | 11,67% | 20 | 11,11% |
| Delannoye et al. (2015) | 21 | 2,06% | 13 | 7,03% | 13 | 7,22% | 13 | 7,22% |
| Peck et al. (2014) | 19 | 1,86% | 18 | 9,73% | 18 | 10% | 18 | 10% |
| Ramage et al. (2023) | 19 | 1,86% | 19 | 10,27% | 19 | 10,56% | 19 | 10,56% |
| Etienne (2005) | 18 | 1,76% | 18 | 9,73% | 18 | 10% | 18 | 10% |
| Gabriac et al. (2024) | 18 | 1,76% | 18 | 9,73% | 18 | 10% | 18 | 10% |
| Linnaeus (1758) | 17 | 1,67% | 7 | 3,78% | 7 | 3,89% | 6 | 3,33% |
| Quénéhervé & Van Den Berg (2005) | 17 | 1,67% | 17 | 9,19% | 17 | 9,44% | 17 | 9,44% |
| Wheeler (1935) | 17 | 1,67% | 15 | 8,11% | 15 | 8,33% | 15 | 8,33% |
| Yokoyama (2013) | 17 | 1,67% | 15 | 8,11% | 15 | 8,33% | 14 | 7,78% |
| Gomy (2000) | 16 | 1,57% | 15 | 8,11% | 15 | 8,33% | 15 | 8,33% |
| Franco et al. (2019) | 15 | 1,47% | 15 | 8,11% | 15 | 8,33% | 15 | 8,33% |
| Griffiths & Florens (2006) | 15 | 1,47% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Luc & Coomans (1992) | 14 | 1,37% | 14 | 7,57% | 14 | 7,78% | 14 | 7,78% |
| Tronquet (2014) | 14 | 1,37% | 13 | 7,03% | 13 | 7,22% | 13 | 7,22% |
| Foldi & Germain (2018) | 13 | 1,27% | 13 | 7,03% | 13 | 7,22% | 12 | 6,67% |
| Germain (2007) | 13 | 1,27% | 13 | 7,03% | 13 | 7,22% | 12 | 6,67% |
| Henderson & Breuil (2012) | 13 | 1,27% | 12 | 6,49% | 8 | 4,44% | 12 | 6,67% |
| Jaffe & Lattke (1994) | 13 | 1,27% | 13 | 7,03% | 13 | 7,22% | 13 | 7,22% |
| Perrault (1988) | 13 | 1,27% | 13 | 7,03% | 13 | 7,22% | 13 | 7,22% |
| Ramage (2014) | 13 | 1,27% | 13 | 7,03% | 13 | 7,22% | 13 | 7,22% |
| Heller (1916) | 12 | 1,18% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Lesne (1932) | 12 | 1,18% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Mille et al. (2016) | 12 | 1,18% | 12 | 6,49% | 12 | 6,67% | 11 | 6,11% |
| Morrison (1997) | 12 | 1,18% | 11 | 5,95% | 11 | 6,11% | 11 | 6,11% |
| Vayssières et al. (2001) | 12 | 1,18% | 11 | 5,95% | 11 | 6,11% | 11 | 6,11% |
| Cheesman (1928) | 11 | 1,08% | 11 | 5,95% | 11 | 6,11% | 11 | 6,11% |
| Germain et al. (2014) | 11 | 1,08% | 11 | 5,95% | 11 | 6,11% | 10 | 5,56% |
| Justine (2018) | 11 | 1,08% | 11 | 5,95% | 11 | 6,11% | 11 | 6,11% |
| Lamy & Pointier (2018) | 11 | 1,08% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Lebas et al. (2016) | 11 | 1,08% | 11 | 5,95% | 11 | 6,11% | 11 | 6,11% |
| Massemin et al. (2009) | 11 | 1,08% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Anonyme (2018) | 10 | 0,98% | 9 | 4,86% | 8 | 4,44% | 9 | 5% |
| Dupont et al. (2023) | 10 | 0,98% | 10 | 5,41% | 10 | 5,56% | 10 | 5,56% |
| Etienne & Vilardebó (1978) | 10 | 0,98% | 10 | 5,41% | 10 | 5,56% | 9 | 5% |
| Jennings et al. (2013) | 10 | 0,98% | 10 | 5,41% | 10 | 5,56% | 10 | 5,56% |
| Lorvelec et al. (2007) | 10 | 0,98% | 10 | 5,41% | 10 | 5,56% | 10 | 5,56% |
| Taylor (1987) | 10 | 0,98% | 10 | 5,41% | 10 | 5,56% | 10 | 5,56% |
| Wetterer (2002) | 10 | 0,98% | 10 | 5,41% | 10 | 5,56% | 10 | 5,56% |
| Wheeler (1932) | 10 | 0,98% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Wilson & Hunt (1967) | 10 | 0,98% | 10 | 5,41% | 10 | 5,56% | 10 | 5,56% |
| Wilson & Taylor (1967) | 10 | 0,98% | 8 | 4,32% | 8 | 4,44% | 8 | 4,44% |
| Berland (1933) | 9 | 0,88% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Blatrix et al. (2018) | 9 | 0,88% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Cochereau (1966) | 9 | 0,88% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Galkowski (2016) | 9 | 0,88% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Gutierrez (1981) | 9 | 0,88% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Martiré & Rochat (2008) | 9 | 0,88% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Matile-Ferrero et al. (2000) | 9 | 0,88% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Morrison (1996) | 9 | 0,88% | 9 | 4,86% | 9 | 5% | 9 | 5% |
| Pavlíček & Csuzdi (2012) | 9 | 0,88% | 8 | 4,32% | 8 | 4,44% | 8 | 4,44% |
| Wheeler (1932) | 9 | 0,88% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Blard et al. (2003) | 8 | 0,78% | 8 | 4,32% | 8 | 4,44% | 8 | 4,44% |
| Brindle (1971) | 8 | 0,78% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Cochereau (1974) | 8 | 0,78% | 8 | 4,32% | 8 | 4,44% | 7 | 3,89% |
| Cohic (1959) | 8 | 0,78% | 8 | 4,32% | 8 | 4,44% | 7 | 3,89% |
| Gargominy et al. (1996) | 8 | 0,78% | 8 | 4,32% | 8 | 4,44% | 8 | 4,44% |
| Lowe et al. (2007) | 8 | 0,78% | 8 | 4,32% | 7 | 3,89% | 8 | 4,44% |
| Peck (2011) | 8 | 0,78% | 8 | 4,32% | 8 | 4,44% | 8 | 4,44% |
| Peck (2011) | 8 | 0,78% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Pilsbry (1906-1907) | 8 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2017) | 8 | 0,78% | 7 | 3,78% | 7 | 3,89% | 5 | 2,78% |
| Uicn et al. (2019) | 8 | 0,78% | 8 | 4,32% | 8 | 4,44% | 8 | 4,44% |
| Wheeler (1936) | 8 | 0,78% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Brosse et al. (2021) | 7 | 0,69% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Casevitz-Weulersse & Galkowski (2009) | 7 | 0,69% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Dupont et al. (2023) | 7 | 0,69% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Soubeyran et al. (2011) | 7 | 0,69% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Soubeyran (2008) | 7 | 0,69% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Talaga et al. (2015) | 7 | 0,69% | 7 | 3,78% | 7 | 3,89% | 7 | 3,89% |
| Wheeler (1933) | 7 | 0,69% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Aharon et al. (2017) | 6 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berland (1934) | 6 | 0,59% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Chamberlin (1918) | 6 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chani-Posse et al. (2018) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Černosvitov (1934) | 6 | 0,59% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Fauvel (1904) | 6 | 0,59% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Gargominy (2016-2021) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Garrouste & Hervé (2009) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Guillermet (2009) | 6 | 0,59% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Guillermet (2011) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Hammes & Putoa (1986) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Lupoli (2023) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Massary et al. (2021) | 6 | 0,59% | 6 | 3,24% | 5 | 2,78% | 4 | 2,22% |
| Michaelsen (1913) | 6 | 0,59% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Mille et al. (2020) | 6 | 0,59% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Rageau (1958) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 4 | 2,22% |
| Theuerkauf et al. (2010) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Wetterer (2014) | 6 | 0,59% | 6 | 3,24% | 6 | 3,33% | 6 | 3,33% |
| Aulagnier et al. (2017) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Berland (1935) | 5 | 0,49% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Bouchet & Pointier (1998) | 5 | 0,49% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Bouget et al. (2019) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Cazanove (2022) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Colijn et al. (2020) | 5 | 0,49% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Cowie (2000) | 5 | 0,49% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Csuzdi & Pavlíček (2009) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Denux & Zagatti (2010) | 5 | 0,49% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Emery (1914) | 5 | 0,49% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Fauvel (1867) | 5 | 0,49% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Fauvel (1903) | 5 | 0,49% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Fisher & Fong (2020) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Frenot et al. (2005) | 5 | 0,49% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Georgiev (2023) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| González-sánchez et al. (2021) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 4 | 2,22% |
| Hebard (1933) | 5 | 0,49% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Hovestadt & Neckheim (2020) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Justine (2017) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Mousson (1872) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olivier (1791-[1792]) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulian (1998) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Perrault (1993) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Szederjesi et al. (2019) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| UICN Comité français, OFB & MNHN (2021) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 4 | 2,22% |
| Viette (1949) | 5 | 0,49% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Wetterer (2012) | 5 | 0,49% | 5 | 2,7% | 5 | 2,78% | 5 | 2,78% |
| Berland (1924) | 4 | 0,39% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bernard (1968) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Bolton (2012) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clarke (1971) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Cohic (1950) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Coulis (2017) | 4 | 0,39% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Dewynter et al. (2020) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Dewynter et al. (2023) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 3 | 1,67% |
| Dewynter et al. (2023) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 3 | 1,67% |
| Dierkens & Charlat (2011) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Fabricius (1775) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke et al. (2009) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Gould (1852) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haynes (2001) | 4 | 0,39% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Hullé et al. (2018) | 4 | 0,39% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Hutton (1834) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ineich (2016) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Keith et al. (2002) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Keith et al. (2006) | 4 | 0,39% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Keith et al. (2013) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Ledoux & Hallé (1995) | 4 | 0,39% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Leraut (2014) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Mary (2017) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Mauriès (1980) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miers (1878) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Periasamy et al. (2015) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Pointier & Marquet (1990) | 4 | 0,39% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Questel (2017) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Remaudière & Etienne (1988) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Rigaud et al. (1997) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Séguy (1944) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 2 | 1,11% |
| Streito et al. (2007) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Uicn et al. (2015) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 2 | 1,11% |
| Vedel et al. (2013) | 4 | 0,39% | 4 | 2,16% | 4 | 2,22% | 4 | 2,22% |
| Wheeler (1908) | 4 | 0,39% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Albouy & Richard (2017) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Albouy et al. (2017) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Allen et al. (2022) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Aulagnier (2009) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Beaucournu et al. (1998) | 3 | 0,29% | 3 | 1,62% | 2 | 1,11% | 2 | 1,11% |
| Berland (1929) | 3 | 0,29% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Blackwelder (1943) | 3 | 0,29% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Blakemore (2008) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bochaton et al. (2021) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Bonfils (1969) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Brindle (1976) | 3 | 0,29% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Busala et al. (2024) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 2 | 1,11% |
| Castro-Cobo et al. (2021) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Catzeflis (2018) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Claessens (2016) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Deshayes (1863) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter et al. (2019) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 2 | 1,11% |
| Dewynter et al. (2022) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 2 | 1,11% |
| Dierkens & Ramage (2016) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Donisthorpe (1932) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etienne et al. (2015) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Firmat et al. (2012) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Fricke et al. (2011) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Girard (2007) | 3 | 0,29% | 3 | 1,62% | 2 | 1,11% | 3 | 1,67% |
| Gomy et al. (2016) | 3 | 0,29% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Gonzales & Yvinec (2016) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Guilbert & Casevitz-Weulersse (1997) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Hustache (1920) | 3 | 0,29% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| James & Gamiette (2016) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Jourdan et al. (2014) | 3 | 0,29% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Keith (2002) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Le Bail et al. (2012) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Lenfant & Marro (1997) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Lesne (1901) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Levesque & Delcroix (2018) | 3 | 0,29% | 3 | 1,62% | 2 | 1,11% | 3 | 1,67% |
| Light (1932) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary et al. (2017) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 2 | 1,11% |
| Massary et al. (2018) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 2 | 1,11% |
| Meurgey & Dumbardon-Martial (2015) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Meyrick (1934) | 3 | 0,29% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Monti et al. (2010) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Montrouzier (1860) | 3 | 0,29% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Zootaxa, 2013: 1-16.">Nemesio & Rasmussen (2009) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Nibouche et al. (202X) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Platnick (1993) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Pointier (2001) | 3 | 0,29% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Prévost & Mougin (1970) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Raspi et al. (2007) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Rehn (1949) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Rheinheimer (2012) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Rheinheimer (2014) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Salata & Fisher (2022) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Soldati & Touroult (2014) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Taczanowski (1871) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taczanowski (1874) | 3 | 0,29% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Touroult et al. (2018) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| UICN Comité français, OFB, MNHN & AsFrA (2023) | 3 | 0,29% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Urvois et al. (2023) | 3 | 0,29% | 3 | 1,62% | 3 | 1,67% | 3 | 1,67% |
| Abdou et al. (2004) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Adamson (1932) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Altson (1923) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Altson (1924) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Anderson (1949) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arrow (1927) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bance (2022) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Barau et al. (2005) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 1 | 0,56% |
| Baudry et al. (2022) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Bellmann (2019) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Berland (1934) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Bigot & Etienne (2009) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bippus (2019) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Blaisdell (1927) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blanc et al. (1993) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Blight et al. (2009) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Bolton (2007) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bos & Loof (1984) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Bournier & Mound (2000) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Boyer & Rivault (2003) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Breuil et al. (2010) | 2 | 0,2% | 2 | 1,08% | 1 | 0,56% | 2 | 1,11% |
| Breuil (2002) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 1 | 0,56% |
| Breuil (2009) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Brindle (1975) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Brito et al. (2017) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Brun & Chazeau (1986) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Bur (1907) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Burneleau (1983) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Chalumeau & Touroult (2005) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Chartier et al. (2007) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 0 | 0% |
| Chazeau et al. (1974) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Cheon et al. (2023) | 2 | 0,2% | 2 | 1,08% | 0 | 0% | 2 | 1,11% |
| Chown & Convey (2016) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Clench (1964) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cohn & Sher (1972) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Coomans (1967) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Courtial (2023) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Cramer ([1780]-1782) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dadant & Etienne (1973) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Daly et al. (2023) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Daniel et al. (2020) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 0 | 0% |
| David et al. (2014) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Delsalle & Sechet (2014) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Dognin (1908) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Draparnaud (1805) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ducarme (2023) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Dumbardon-Martial & Delblond (2019) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Duyck et al. (2022) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Ezzat (1958) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Fabricius (1781) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1793) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fairmaire (1849) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Falkner et al. (2002) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Faucheux (2005) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Fauvel (1891) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Férussac & Deshayes (1820-51) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1822) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Férussac (1827) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forcellini et al. (2012) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Fossati & Marquet (1998) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fourcroy (1785) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gamiette et al. (2023) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Gargominy et al. (2011) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Gerber (2018) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Gielis (2011) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gielis (2013) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilot et al. (1992) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Girod & Matzke (2020) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Gmelin (1789) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Gomy et al. (2009) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Gould (1846) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Graber et al. (1997) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Guenée (1862) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Haran et al. (2020) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Hartmann et al. (2021) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Havery et al. (2018) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Hebard (1933) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Hedges (2022) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Hoddle et al. (2008) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Hoff & Daszkiewicz (2001) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Hyman & Ponder (2010) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Iorio & Coulis (2020) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ito & Hirose (1978) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Jackson (1933) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Jackson (1941) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Jerdon (1851) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Justine et al. (2021) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Justine et al. (2021) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Kaszab (1982) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Keith et al. (1999) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Lacoste (de) (2020) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Legrand (1949) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legrand (1950) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Legrand (1953) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lescure et al. (2012) | 2 | 0,2% | 2 | 1,08% | 1 | 0,56% | 1 | 0,56% |
| Lesne (1897) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Levesque & Clergeau (2002) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Lim et al. (2002) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Loof & Sharma (1979) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Lordello (1951) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Luc (1958) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Luc (1961) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Lucas (1847) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas (2012) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lupoli & Dusoulier (2015) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Marquet et al. (2003) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Mas-Coma et al. (1989) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Matile-Ferrero & Etienne (1996) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Matile-Ferrero & Etienne (1998) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Matile-Ferrero (1979) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Mauriès (1987) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meurgey & Questel (2015) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Meurgey (2014) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Meyrick (1886) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Modera & Céspedes (1971) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Montrouzier (1861) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montrouzier (1861) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montrouzier (1861) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muñoz et al. (2013) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muratet (2015) | 2 | 0,2% | 2 | 1,08% | 1 | 0,56% | 1 | 0,56% |
| Nattier et al. (2015) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Nève de Mévergnies et al. (2024) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Nicholson et al. (2012) | 2 | 0,2% | 2 | 1,08% | 1 | 0,56% | 1 | 0,56% |
| Nicolas (2012) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Parnaudeau & Madl (2009) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Pascal et al. 2006 | 2 | 0,2% | 2 | 1,08% | 1 | 0,56% | 2 | 1,11% |
| Peck (2016) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierre et al. (2017) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Poupin (2010) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Poussereau et al. (2018) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Probst et al. (2022) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Probst (2001) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 1 | 0,56% |
| Questel et al. (2023) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 1 | 0,56% |
| Questel et al. (2023) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 1 | 0,56% |
| Questel (2014) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Questel (2023) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Quilici et al. (1988) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Rageau (1956) | 2 | 0,2% | 2 | 1,08% | 1 | 0,56% | 2 | 1,11% |
| Rang (1831) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Remsen et al. (2013) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Revilliod (1914) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rheinheimer (2015) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Rocamora (2004) | 2 | 0,2% | 2 | 1,08% | 1 | 0,56% | 2 | 1,11% |
| Rognes & Blackith (1990) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Roman & Puech (1965) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Ronot (2007) | 2 | 0,2% | 2 | 1,08% | 1 | 0,56% | 2 | 1,11% |
| Saint et al. (1978) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Sanchez (2020) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 1 | 0,56% |
| Sardet et al. (2015) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Seifert (2003) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Séret (1997) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Shattuck (1992) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Silvestri (1897) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Silvestri (1934) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Siu et al. (2017) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Solem (1961) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Stephenson (1925) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stewart (1934) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 1 | 0,56% |
| Taquet et al. (2019) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Taylor & Wilson (1961) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Taylor (2003) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thornton (1989) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Touroult et al. (2021) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Tronquet (2015) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Vandel (1981) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Vandenspiegel & Mathys (2021) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Verrill (1867) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Voisin et al. (2017) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Voisin (2020) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Welter-schultes (2012) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Wild (2007) | 2 | 0,2% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Yano (1963) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2012) | 2 | 0,2% | 2 | 1,08% | 2 | 1,11% | 2 | 1,11% |
| Abhaya & Probst (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Abhaya et al. (1998) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Abood & Murphy (2006) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Agarwal et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Alley et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Almeida & Vasconcelos (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Almeida et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Améziane (2007) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Angel (1935) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Anonyme. (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Anonyme (2014) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Arenberger (2010) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Armand & Ferlay (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Arnold & Ovenden (2014) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Ascete (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Aubert & Beaucournu (1976) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Aubouin et al. (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Audouin (1826) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Azam (1893) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bacchet et al. (2007) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bagnall (1919) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bailey et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Balmès & Mouttet (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Barbour (1914) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Barbut et al. (2006) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Barnouin et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Barré & Moutou (1982) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bauer & Sadlier (1994) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bauer et al. (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bavay (1869) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beatty et al. (2008) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Beaucournu (1968) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Becerra et al. (2024) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Behm et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Belfan & Conde (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Benoit (1881) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berland (1927) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Berland (1942) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Berry et al. (1997) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Berry et al. (1998) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bigot & Drouet (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot (1992) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bigot (2011) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blackburn (1888) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blair (1934) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Blanchot (1992) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bochaton et al. (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bondar (1923) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonfils et al. (1994) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Borroto-páez (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bouchet et al. (1991) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Boulenger (1883) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bour et al. (2008) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Bourgade (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bourguignat (1856) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bournier (2000) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Bousquet (2016) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bout et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Boyd et al. (2006) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Boyer de Fonscolombe (1834) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Brandt (1833) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brook (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Brown (1994) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brûlé (2011) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Burckhardt & Lauterer (1989) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Burckhardt et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Burr (1904) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Burr (1914) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butaud (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Caceres (2002) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Capalleras & Carretero (2000) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Casey (1892) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Catil et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Célini et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| CEN Nouvelle-Calédonie (2021) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Chamberlin (1920) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Champagne et al. (1997) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Chapelin-Viscardi & Maillet-Mezeray (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Charrier et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Chastel et al. (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Chatard (2016) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chazeau (1991) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cheesman (1927) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Cheke (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Chocobar et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Chopard (1921) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christensen & Kahn (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Clarke (1986) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Clements et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Coatmeur (1999) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Cobb (1893) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cochard et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Cohic (1959) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Colin (1992) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Colindre (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Colindre (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Collazos-astudillo et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Commecy et al. (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Conand et al. (2013) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conte et al. (2007) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Cooke (1934) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dal Zotto et al. (2024) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dalla Torre (1893) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| D´angiolella et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dard et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dard et al. (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dard et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| de Massary et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| De Meyer et al. (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Deblock et al. (1960) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Decaëns et al. (2024) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Defo et al. (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Degallier & Gomy (2024) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Degallier (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Deknuydt (2014) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Delabie et al. (2011) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Delhaes et al. (2001) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Delport (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Desmoulin et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Desutter-Grandcolas et al. (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Deuss et al. (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dewynter & Claessens (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dewynter et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Dewynter (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dickey et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dieme et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dierkens (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dole & Cognato (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Dollfus (1895) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dufour (1831) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril & Bibron (1836) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril & Bibron (1837) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupuis (1999) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Duquef (2014) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Duquef (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Duquef (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Duval et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Emery (1892) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etcheberry & Abraham (2009) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Etienne & Gagné (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Etienne et al. (1998) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Etienne (1972) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| European Commission (2014) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Evans et al. (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Evenhuis (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Evenhuis (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fabre & Orsini (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fabres (1977) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fabricius (1787) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1798) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1889) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fennah (1958) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fennah (1969) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ferrer (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ferry et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ferry et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Feuillet et al. (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ficetola & Scali (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Flechas et al. (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Flechtmann & Atkinson (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fontanilla & Wade (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Forel (1881) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Forel (1890) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1899) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1907) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fort & Barrière (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Fouquet (2000) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fraga & Carvalho (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Frank (1983) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Franzini et al. (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Frenot (1992) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Friese (1907) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gahan (1895) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gall & Beague (1986) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Gargominy et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Gargominy (2001) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1887) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrett (1879) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrouste (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Gassies (1866) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gates (1936) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gates (1937) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gay (1953) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Geneva et al. (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Gentry et al. (2004) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Gerberg (1957) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gerlach (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Germain & Streito (2004) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Germain et al. (2014) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Germain et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Germain (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Germar (1824) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geyer & Frölich (1830) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1995) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Girod (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Gmelin (1788) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gonzalez & Vetrovec (2021) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| González et al. (2018) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Gould (1859) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goux (1937) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Goyaud & Lemarie (2016) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gozlan et al. (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Grandison et al. (2009) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Grenand et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Groom et al. (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Grouvelle & Raffray (1908) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Guernier et al. (2014) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Guille & Vadon (1985) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guille et al. (1986) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guth (1971) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Haouchine et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Hausdorf & Bermúdez (2003) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hausdorf (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Hebard (1935) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Henao-osorio et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Hendler & Brugneaux (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Hengoat (2008) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Heppner (1995) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Hervé & Garrouste (2009) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Holovachov (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Hullé & Vernon (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ide et al. (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ifremer (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Iković et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Ineich & Massary (1997) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ineich et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ineich (1999) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ineich (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ito (1983) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Iwata & Nishimoto (1981) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Jackson (1938) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Jäger (2002) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jairam et al. (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Jamonneau et al. (2025) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Jay et al. (2009) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Johnson (1964) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kadolsky (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Kaiser & Hardy (1994) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Karin et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Keith & Dorson (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Keith & Marquet (2011) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Keith et al. (2000) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2011) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Klyver (1932) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Koch (1836) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kolibáč (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| König et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Kornilev et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Kremmer et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Kuschel (2008) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lafargue & Vasseur (1989) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lagarde (2008) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lalubie et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lambert (1988) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lancastre et al. (1976) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Latreille (1802) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Divelec (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Le Maitre & Chadee (1983) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ledoux (2007) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legros et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lemaire & Gerriet (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lenoir et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Leonhardt et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Leonhardt et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Leponce et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lescure & Marty (2000) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lescure et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lescure (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Letacq (1924) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lichtenstein & Martens (1856) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Liebgold et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Light & Zimmerman (1936) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Light (1932) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lopez-Vaamonde et al. (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lordello & Costa (1961) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lordello (1955) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lorvelec & Pascal (2009) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lorvelec et al. (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lorvelec et al. (2011) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lorvelec et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Lucas (1872) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lydeard et al. (2016) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mageski et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Maillard & David (2014) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Malloch (1932) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Mann (1921) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marchán et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Marinho (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Marion & Clergeau (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Marion & Marion (1982) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Marples (1957) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Massary et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Massary (2012) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Matile-Ferrero & Germain (2004) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Matile-Ferrero & Williams (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Matsuzaki et al. (2009) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Mayr (1886) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1883) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazé (1890) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meganck et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Melot et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Meyen (1834) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mifsud et al. (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Mille et al., 2012 | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Mollot et al. (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Monniot (1983) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (2007) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (2016) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moravec et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Moreau de Jonnès (1818) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morelet (1860) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mothes et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Motschulsky (1866) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1774) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murienne et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Nageleisen et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Naggs (1989) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Nassi et al. (1975) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Natural History Museum of London (2020) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nentwig et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Nicolas et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Nicolas et al. (2024) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Nicolas (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Nicoli et al. (1969) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Olivier (1789) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Otte et al. (1987) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Pang et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Panis (1969) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paperna & Landsberg (1989) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parmentier et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Parnaudeau (2009) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Parnaudeau (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Parnaudeau (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Pascal & Vigne (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Pascal & Vigne (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Pascal & Vigne (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Pascal et al. (2006) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Pearman et al. (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Pelosse (1927) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Perkins (1928) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippot et al. (2019) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Pointier & Delay (1995) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Poisson (1940) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Popovici et al. (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Potin (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Poupin et al. (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Poupin et al. (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Poussereau (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Powell & Henderson (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Prado et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Praz & Bénon (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Preece (1995) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Princis (1974) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Prins et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Probst & Deso (2001) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Probst et al. (2000) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Probst (2001) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Quah & Grismer (2024) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Questel (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Questel (2017) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rageau (1959) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ramage et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Renaud et al. (2013) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reverté et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Rheinheimer (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Rhodin & Carr (2009) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1914) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Robin & Dalens (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Roger (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Roguet (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Roman (1938) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Romero et al. (2010) | 1 | 0,1% | 1 | 0,54% | 0 | 0% | 1 | 0,56% |
| Roth & Rivault (2002) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Routtier et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Roux (1913) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Russell & Etienne (1985) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Ruzzier et al. (2023) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Sadlier et al. (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Safford & Hawkins (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Sanchez & Probst (2016) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Sanchez et al. (2019) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Santschi (1928) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sauvion et al. (1999) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Savigny (1826) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schoepff (1792) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schuurmans Stekhoven & Teunissen (1938) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Scudder (1876) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seifert (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Servan & Arvy (1997) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Shinonaga et al. (1991) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Shiraki (1906) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Silvestri (1935) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Simon (1897) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Singh (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Siroux (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Smith (1857) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1860) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Socolovschi et al. (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Soltani et al. (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Stainton (1856) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Stainton (1866) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1976) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Stephens (1830) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stewart (1934) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Streito & Étienne (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Sudre et al. (2010) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Taczanowski (1872) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tavakilian & Chevillotte (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Tavares & Amouroux (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Theodorides et al. (1983) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Thévenot (2014) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Thomas (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Tillier (1980) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tirvengadum & Bour (1985) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Touroult et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Turpin & Probst (1998) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Uicn et al. (2015) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Uicn et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Vachal (1907) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Vandel (1922) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Varenne & Billi (2008) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vásquez-cruz & Kelly-hernández (2024) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Vayssières et al. (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Vera-pérez et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Verhoeff (1926) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Veysset (2003) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Villiers (1980) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villiers (1980) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vivant (2005) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Von May et al. (2021) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Votýpka et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Walckenaer (1837) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Walckenaer (1837) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1859) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wang & Qiu (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Weimerskirch et al. (2009) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Wenzel (1955) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Werner (1980) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Weterings & Vetter (2017) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Wheeler (1923) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Wheeler (1929) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wied (1839) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wild (2004) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wollaston (1858) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wollaston (1867) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Works & Olson (2018) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 0 | 0% |
| Yassin et al. (2012) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Yuan et al. (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Zakardjian et al. (2020) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| Zdunek (2022) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
| (2013) | 1 | 0,1% | 1 | 0,54% | 1 | 0,56% | 1 | 0,56% |
