Lépidoptères de Martinique
Lepidoptera de Martinique
224 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Meurgey & Ramage (2020) | 254 | 39,87% | 250 | 66,14% | 218 | 65,66% | 245 | 73,8% |
Deknuydt et al. (2016) | 198 | 31,08% | 191 | 50,53% | 187 | 56,33% | 185 | 55,72% |
Meurgey (2011) | 131 | 20,57% | 103 | 27,25% | 80 | 24,1% | 95 | 28,61% |
Questel (2020) | 92 | 14,44% | 83 | 21,96% | 69 | 20,78% | 78 | 23,49% |
Questel (2016) | 50 | 7,85% | 46 | 12,17% | 37 | 11,14% | 44 | 13,25% |
Questel & Le Quellec (2012) | 47 | 7,38% | 42 | 11,11% | 35 | 10,54% | 39 | 11,75% |
Guenée (1852) | 45 | 7,06% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
UICN Comité français, OFB & MNHN (2021) | 45 | 7,06% | 41 | 10,85% | 41 | 12,35% | 16 | 4,82% |
Sculfort & Dewynter (2024) | 39 | 6,12% | 39 | 10,32% | 14 | 4,22% | 39 | 11,75% |
Pierre & Lalanne-Cassou | 36 | 5,65% | 27 | 7,14% | 21 | 6,33% | 16 | 4,82% |
Dewynter et al. (2022) | 33 | 5,18% | 32 | 8,47% | 32 | 9,64% | 9 | 2,71% |
Remillet (1988) | 28 | 4,4% | 22 | 5,82% | 22 | 6,63% | 16 | 4,82% |
Martiré & Rochat (2008) | 21 | 3,3% | 14 | 3,7% | 14 | 4,22% | 13 | 3,92% |
Munroe (1956) | 21 | 3,3% | 14 | 3,7% | 14 | 4,22% | 14 | 4,22% |
Yokoyama (2013) | 21 | 3,3% | 17 | 4,5% | 15 | 4,52% | 14 | 4,22% |
Bigot & Etienne (2009) | 18 | 2,83% | 16 | 4,23% | 16 | 4,82% | 16 | 4,82% |
Chovet et al. (2023) | 15 | 2,35% | 14 | 3,7% | 5 | 1,51% | 12 | 3,61% |
Cramer ([1777]) | 14 | 2,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-Martial & Delblond (2019) | 14 | 2,2% | 10 | 2,65% | 8 | 2,41% | 3 | 0,9% |
Linnaeus (1758) | 14 | 2,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Möschler (1890) | 13 | 2,04% | 4 | 1,06% | 4 | 1,2% | 3 | 0,9% |
Guillermet (2004) | 11 | 1,73% | 7 | 1,85% | 7 | 2,11% | 4 | 1,2% |
Guillermet (2011) | 11 | 1,73% | 10 | 2,65% | 10 | 3,01% | 10 | 3,01% |
Deknuydt et al. (2018) | 10 | 1,57% | 9 | 2,38% | 9 | 2,71% | 8 | 2,41% |
Barbut & Lalanne-Cassou (2009) | 9 | 1,41% | 9 | 2,38% | 9 | 2,71% | 9 | 2,71% |
Guillermet (2009) | 9 | 1,41% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Haxaire & Rasplus (1986) | 9 | 1,41% | 8 | 2,12% | 8 | 2,41% | 7 | 2,11% |
Cook & Scoble (1995) | 8 | 1,26% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Guenée (1852) | 8 | 1,26% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Herbulot (1986) | 8 | 1,26% | 8 | 2,12% | 8 | 2,41% | 8 | 2,41% |
Lacomme (2013) | 8 | 1,26% | 7 | 1,85% | 6 | 1,81% | 3 | 0,9% |
Lévêque (2015) | 8 | 1,26% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Poole (1989) | 8 | 1,26% | 8 | 2,12% | 8 | 2,41% | 8 | 2,41% |
Touroult et al. (2021) | 8 | 1,26% | 7 | 1,85% | 6 | 1,81% | 7 | 2,11% |
Zagatti et al. (2006) | 8 | 1,26% | 8 | 2,12% | 1 | 0,3% | 8 | 2,41% |
Boisduval & Guénée ([1874]) | 7 | 1,1% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Cramer ([1779]) | 7 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1852) | 7 | 1,1% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Touroult et al. (2023) | 7 | 1,1% | 7 | 1,85% | 6 | 1,81% | 7 | 2,11% |
Anonyme (2018) | 6 | 0,94% | 5 | 1,32% | 5 | 1,51% | 5 | 1,51% |
David & Lucas (2017) | 6 | 0,94% | 6 | 1,59% | 6 | 1,81% | 6 | 1,81% |
Guenée (1854) | 6 | 0,94% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Haxaire & Rasplus (1987) | 6 | 0,94% | 5 | 1,32% | 5 | 1,51% | 5 | 1,51% |
Jourdan (2020) | 6 | 0,94% | 5 | 1,32% | 5 | 1,51% | 4 | 1,2% |
Li et al. (2019) | 6 | 0,94% | 6 | 1,59% | 5 | 1,51% | 5 | 1,51% |
Ramage (2017) | 6 | 0,94% | 5 | 1,32% | 5 | 1,51% | 4 | 1,2% |
Scoble et al. (1999) | 6 | 0,94% | 5 | 1,32% | 5 | 1,51% | 4 | 1,2% |
Barbut et al. (2006) | 5 | 0,78% | 5 | 1,32% | 5 | 1,51% | 5 | 1,51% |
Heppner (1995) | 5 | 0,78% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Olivier (1792) | 5 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot & Drouet (2014) | 4 | 0,63% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Cramer ([1780]-1782) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste & Hervé (2009) | 4 | 0,63% | 4 | 1,06% | 4 | 1,2% | 4 | 1,2% |
Gemmell et al. (2014) | 4 | 0,63% | 4 | 1,06% | 4 | 1,2% | 2 | 0,6% |
Kitching et al. (2018) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Núñez et al. (2021) | 4 | 0,63% | 3 | 0,79% | 2 | 0,6% | 2 | 0,6% |
Pierre & Pierre-Baltus (2003) | 4 | 0,63% | 4 | 1,06% | 4 | 1,2% | 4 | 1,2% |
Poole (1989) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2020) | 4 | 0,63% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Viette (1949) | 4 | 0,63% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Walker (1865-[1866]) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut & Lalanne-Cassou (2019) | 3 | 0,47% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Barbut (2022) | 3 | 0,47% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Becker (2023) | 3 | 0,47% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Bigot (2011) | 3 | 0,47% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Boisduval (1833) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Brévignon (2020) | 3 | 0,47% | 3 | 0,79% | 0 | 0% | 3 | 0,9% |
Chalumeau & Benito-Espinal (1984) | 3 | 0,47% | 3 | 0,79% | 0 | 0% | 3 | 0,9% |
Deknuydt et al. (2024) | 3 | 0,47% | 3 | 0,79% | 2 | 0,6% | 1 | 0,3% |
[Denis & Schiffermüller] (1775) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Dillon (1947) | 3 | 0,47% | 1 | 0,26% | 0 | 0% | 1 | 0,3% |
Gielis (2011) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1958) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway (1979) | 3 | 0,47% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Laguerre et al. (2014) | 3 | 0,47% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Laguerre (2018) | 3 | 0,47% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Latreille & Godart (1819-[1824]) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2016) | 3 | 0,47% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Touroult et al. (2019) | 3 | 0,47% | 3 | 0,79% | 3 | 0,9% | 3 | 0,9% |
Barnes et al. (1913) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Becker (2002) | 2 | 0,31% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Boisduval (1833) | 2 | 0,31% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Boisduval (1836) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Brévignon & Brévignon (2012) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 1 | 0,3% |
Brévignon et al. (2021) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Brévignon (2004) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Brito et al. (2017) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Butler (1878) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer (1775) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer ([1775-1776]) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Dias (2013) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Dognin (1914) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Eitschberger (2006) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1775) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 2 | 0,31% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Gemmell & Marcus (2015) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 1 | 0,3% |
Gielis (2013) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée (1862) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Guérin-Méneville & Perrotet (1842) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Hampson (1898) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner & Thiele (2017) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Herbulot (1985) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Herbulot (1995) | 2 | 0,31% | 2 | 0,53% | 0 | 0% | 2 | 0,6% |
Hübner et al. (3) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner ([1825-1831]) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2018) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Jourdan & Mille (2006) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Lafranchis (2014) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 1 | 0,3% |
Lafranchis (2016) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 1 | 0,3% |
Lamas (1995) | 2 | 0,31% | 1 | 0,26% | 0 | 0% | 1 | 0,3% |
Lévêque (2014) | 2 | 0,31% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Meyrick (1886) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Naydenov et al. (2020) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Naydenov et al. (2021) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Pitkin (2002) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Poey (1832) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2023) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Rambur (1829) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Scoble (1994) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Shaw & Nodder (1795-1796) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiaucourt (2018) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Touroult et al. (2014) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2021) | 2 | 0,31% | 2 | 0,53% | 1 | 0,3% | 2 | 0,6% |
Touroult et al. (2022) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 2 | 0,6% |
Vane-Wright & De Jong (2003) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 0 | 0% |
Viette (1950) | 2 | 0,31% | 2 | 0,53% | 2 | 0,6% | 0 | 0% |
Yano (1963) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Arenberger (2010) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Aurivillius (1909) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Bar (1875) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut & Voisin (2014) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Betz (1980) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Bigot (1992) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Bippus (2020) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Boisduval (1859) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgogne (1983) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Braby et al. (2015) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1875) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Butler (1893) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Chainey (2005) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cock (2017) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalman (1823) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
David et al. (2010) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Dubois (1996) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Dumbardon-Martial et al. (2018) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Dumbardon-Martial et al. (2018) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Dyar (1914) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Eppo (2018) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Eppo (2018) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Fabricius ([1777]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Faynel (2010) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Felder & Rogenhofer (1864-1867) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Fougère et al. (2020) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Geyer (1837) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Godart (1822-[1824]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Godman & Salvin (1896) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier & Grenier (2014) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Guillermet (2009) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutierrez (1981) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Hemming (1933) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Henriot (1933) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1982) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (2016) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hewitson (1867) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hindermeyer et al. (2007) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Holloway & Peters (1976) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Honey & Scoble (2001) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner [1819-1826] | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1823) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
ICZN (1954) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2023) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Lafontaine & Schmidt (2010) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Lamas (2004) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Leraut (1997) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1763) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1764) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1771) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1934) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Munroe (1942) | 1 | 0,16% | 1 | 0,26% | 0 | 0% | 1 | 0,3% |
Nel & Varenne (2019) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Nibouche et al. (202X) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Nicolas (2023) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Orhant (2002) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Pallister (1956) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Parnaudeau (2012) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Patrick & Patrick (2012) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Pierre et al. (2008) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Poey (1851-1854) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pogue (2013) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Poole (1987) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Prins et al. (2019) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Queiroz-Santos et al. (2024) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Questel (2014) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Ramage (2024) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Robinson & Nielsen (1983) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Rogenhofer (1882) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Schaffer & Solis (1995) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Scudder (1872) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn (1895) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Stainton (1856) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Stefanescu et al. (2012) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Tennent (2005) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Touroult et al. (2015) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Touroult et al. (2018) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Touroult et al. (2024) | 1 | 0,16% | 1 | 0,26% | 0 | 0% | 1 | 0,3% |
Toussaint et al. (2019) | 1 | 0,16% | 1 | 0,26% | 0 | 0% | 1 | 0,3% |
Turlin (2002) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Uicn et al. (2020) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Vayssières et al. (2001) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Viette (1994) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 0 | 0% |
Vincent (2008) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Voisin (1975) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |
Walker (1860) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1864) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Warren (1897) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Warren (1907) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (1937) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang et al. (2019) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang et al. (2021) | 1 | 0,16% | 1 | 0,26% | 1 | 0,3% | 1 | 0,3% |