Espèces venimeuses
501 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Geoffroy & Iorio (2009) | 144 | 12,12% | 129 | 35,34% | 121 | 37,93% | 120 | 36,04% |
Iorio et al. (2022) | 72 | 6,06% | 69 | 18,9% | 68 | 21,32% | 61 | 18,32% |
Iorio (2008) | 72 | 6,06% | 64 | 17,53% | 63 | 19,75% | 57 | 17,12% |
Ribaut (1923) | 67 | 5,64% | 53 | 14,52% | 53 | 16,61% | 49 | 14,71% |
Iorio et al. (2023) | 63 | 5,3% | 62 | 16,99% | 58 | 18,18% | 60 | 18,02% |
Würmli (1974) | 46 | 3,87% | 41 | 11,23% | 41 | 12,85% | 38 | 11,41% |
Zapparoli & Iorio (2012) | 32 | 2,69% | 29 | 7,95% | 29 | 9,09% | 27 | 8,11% |
Verhoeff (1943) | 29 | 2,44% | 6 | 1,64% | 6 | 1,88% | 6 | 1,8% |
Schileyko et al. (2024) | 28 | 2,36% | 28 | 7,67% | 22 | 6,9% | 28 | 8,41% |
Iorio & Berg (2007) | 27 | 2,27% | 22 | 6,03% | 21 | 6,58% | 21 | 6,31% |
Iorio & Geoffroy (2019) | 25 | 2,1% | 24 | 6,58% | 23 | 7,21% | 21 | 6,31% |
Iorio (2007) | 23 | 1,94% | 22 | 6,03% | 22 | 6,9% | 17 | 5,11% |
Iorio & Coulis (2020) | 22 | 1,85% | 22 | 6,03% | 16 | 5,02% | 21 | 6,31% |
Hoff & Daszkiewicz (2001) | 21 | 1,77% | 16 | 4,38% | 10 | 3,13% | 9 | 2,7% |
Linnaeus (1758) | 21 | 1,77% | 10 | 2,74% | 10 | 3,13% | 8 | 2,4% |
Bonato & Minelli (2014) | 20 | 1,68% | 6 | 1,64% | 6 | 1,88% | 6 | 1,8% |
Schileyko et al. (2018) | 19 | 1,6% | 18 | 4,93% | 16 | 5,02% | 17 | 5,11% |
Ramage et al. (2023) | 16 | 1,35% | 16 | 4,38% | 13 | 4,08% | 15 | 4,5% |
Ineich (2007) | 15 | 1,26% | 11 | 3,01% | 10 | 3,13% | 11 | 3,3% |
Iorio & Leccia (2021) | 15 | 1,26% | 15 | 4,11% | 14 | 4,39% | 14 | 4,2% |
Tröndlé & Boutet (2009) | 15 | 1,26% | 13 | 3,56% | 13 | 4,08% | 13 | 3,9% |
Demange (1981) | 14 | 1,18% | 12 | 3,29% | 9 | 2,82% | 9 | 2,7% |
Héros et al. (2007) | 14 | 1,18% | 14 | 3,84% | 14 | 4,39% | 14 | 4,2% |
Jay et al. (2009) | 14 | 1,18% | 13 | 3,56% | 13 | 4,08% | 13 | 3,9% |
Lescure et al. (2012) | 14 | 1,18% | 9 | 2,47% | 4 | 1,25% | 5 | 1,5% |
Bauer & Sadlier (2000) | 13 | 1,09% | 10 | 2,74% | 10 | 3,13% | 9 | 2,7% |
Brischoux et al. (2018) | 13 | 1,09% | 11 | 3,01% | 11 | 3,45% | 10 | 3% |
Demange & Pereira (1985) | 12 | 1,01% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Geoffroy (2020) | 12 | 1,01% | 12 | 3,29% | 11 | 3,45% | 10 | 3% |
Iorio & Coulis (2024) | 12 | 1,01% | 12 | 3,29% | 12 | 3,76% | 12 | 3,6% |
Iorio & Racine (2022) | 12 | 1,01% | 12 | 3,29% | 11 | 3,45% | 12 | 3,6% |
Iorio (2014) | 12 | 1,01% | 5 | 1,37% | 5 | 1,57% | 4 | 1,2% |
Meurgey (2011) | 12 | 1,01% | 9 | 2,47% | 7 | 2,19% | 8 | 2,4% |
Morelon (2015) | 12 | 1,01% | 9 | 2,47% | 9 | 2,82% | 9 | 2,7% |
Ramage (2017) | 12 | 1,01% | 12 | 3,29% | 10 | 3,13% | 11 | 3,3% |
Uicn et al. (2017) | 12 | 1,01% | 11 | 3,01% | 11 | 3,45% | 4 | 1,2% |
Iorio (2021) | 11 | 0,93% | 11 | 3,01% | 11 | 3,45% | 11 | 3,3% |
Eason (1974) | 10 | 0,84% | 0 | 0% | 0 | 0% | 0 | 0% |
Goiran et al. (2022) | 10 | 0,84% | 7 | 1,92% | 7 | 2,19% | 6 | 1,8% |
Chamberlin (1918) | 9 | 0,76% | 6 | 1,64% | 4 | 1,25% | 6 | 1,8% |
Iorio & Coulis (2019) | 9 | 0,76% | 9 | 2,47% | 9 | 2,82% | 9 | 2,7% |
Léger & Duboscq (1903) | 9 | 0,76% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Chamberlin (1920) | 8 | 0,67% | 8 | 2,19% | 7 | 2,19% | 7 | 2,1% |
Meinert (1870) | 8 | 0,67% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Silvestri (1935) | 8 | 0,67% | 8 | 2,19% | 8 | 2,51% | 7 | 2,1% |
Gherghel et al. (2016) | 7 | 0,59% | 7 | 1,92% | 7 | 2,19% | 7 | 2,1% |
Iorio et al. (2020) | 7 | 0,59% | 7 | 1,92% | 7 | 2,19% | 7 | 2,1% |
Meinert (1872) | 7 | 0,59% | 5 | 1,37% | 5 | 1,57% | 4 | 1,2% |
Mertens & Wermuth (1960) | 7 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 7 | 0,59% | 7 | 1,92% | 6 | 1,88% | 5 | 1,5% |
Verhoeff (1928) | 7 | 0,59% | 6 | 1,64% | 6 | 1,88% | 6 | 1,8% |
Cogger & Heatwole (2006) | 6 | 0,51% | 6 | 1,64% | 6 | 1,88% | 6 | 1,8% |
Deshayes (1863) | 6 | 0,51% | 5 | 1,37% | 5 | 1,57% | 5 | 1,5% |
Iorio (2024) | 6 | 0,51% | 6 | 1,64% | 6 | 1,88% | 6 | 1,8% |
Koch ([1835]-[1844]) | 6 | 0,51% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Koch (1847) | 6 | 0,51% | 5 | 1,37% | 5 | 1,57% | 3 | 0,9% |
Koch (1862) | 6 | 0,51% | 6 | 1,64% | 6 | 1,88% | 5 | 1,5% |
Kronen et al. (2008) | 6 | 0,51% | 6 | 1,64% | 6 | 1,88% | 6 | 1,8% |
Muratet (2015) | 6 | 0,51% | 6 | 1,64% | 1 | 0,31% | 5 | 1,5% |
Rageau (1958) | 6 | 0,51% | 6 | 1,64% | 4 | 1,25% | 4 | 1,2% |
Roux (1913) | 6 | 0,51% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Verneau (2007) | 6 | 0,51% | 5 | 1,37% | 5 | 1,57% | 5 | 1,5% |
Adamson (1932) | 5 | 0,42% | 5 | 1,37% | 5 | 1,57% | 4 | 1,2% |
Brölemann (1904) | 5 | 0,42% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Chabanet et al. (2007) | 5 | 0,42% | 5 | 1,37% | 5 | 1,57% | 5 | 1,5% |
Goiran & Shine (2020) | 5 | 0,42% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Jourdan & Mille (2006) | 5 | 0,42% | 5 | 1,37% | 3 | 0,94% | 3 | 0,9% |
Mauriès & Nguyen Duy-Jacquemin (2001) | 5 | 0,42% | 4 | 1,1% | 4 | 1,25% | 3 | 0,9% |
Questel (2020) | 5 | 0,42% | 5 | 1,37% | 5 | 1,57% | 3 | 0,9% |
Richard et al. (1982) | 5 | 0,42% | 5 | 1,37% | 5 | 1,57% | 5 | 1,5% |
Richard (2006) | 5 | 0,42% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Schileyko (2018) | 5 | 0,42% | 2 | 0,55% | 1 | 0,31% | 2 | 0,6% |
Shaw (1802) | 5 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Bour et al. (2008) | 4 | 0,34% | 3 | 0,82% | 3 | 0,94% | 0 | 0% |
Brechlin & Meister (2019) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Brölemann & Ribaut (1911) | 4 | 0,34% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Brölemann (1909) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Brölemann (1909) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Brölemann (1926) | 4 | 0,34% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Carrasco et al. (2012) | 4 | 0,34% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
de Massary et al. (2015) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 0 | 0% |
Demange (1963) | 4 | 0,34% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Deuss et al. (2013) | 4 | 0,34% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Fanzago (1877) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Jeannel (1926) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 2 | 0,6% |
Kallel et al. (2018) | 4 | 0,34% | 3 | 0,82% | 3 | 0,94% | 2 | 0,6% |
Latzel (1880) | 4 | 0,34% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Leach ([1816]) | 4 | 0,34% | 3 | 0,82% | 3 | 0,94% | 2 | 0,6% |
Massary et al. (2019) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 0 | 0% |
Matic (1958) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Morris (2012) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Newport (1844) | 4 | 0,34% | 3 | 0,82% | 3 | 0,94% | 2 | 0,6% |
Raphael (1970) | 4 | 0,34% | 3 | 0,82% | 3 | 0,94% | 2 | 0,6% |
Rasmussen & Ineich (2000) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Saint & Girons (1976) | 4 | 0,34% | 3 | 0,82% | 0 | 0% | 3 | 0,9% |
Schileyko & Cupul-Magaña (2021) | 4 | 0,34% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Silvestri (1934) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 3 | 0,9% |
Udyawer et al. (2023) | 4 | 0,34% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Uicn et al. (2019) | 4 | 0,34% | 4 | 1,1% | 4 | 1,25% | 4 | 1,2% |
Ursenbacher et al. (2006) | 4 | 0,34% | 3 | 0,82% | 1 | 0,31% | 2 | 0,6% |
Arnold & Ovenden (2014) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 0 | 0% |
Bénéluz (2021) | 3 | 0,25% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Bonato et al. (2023) | 3 | 0,25% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Brölemann (1924) | 3 | 0,25% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Conand & Ducarme (2018) | 3 | 0,25% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Edgecombe (2003) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Garrigues et al. (2020) | 3 | 0,25% | 2 | 0,55% | 0 | 0% | 2 | 0,6% |
Gervais (1837) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Goiran & Shine (2013) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
GOUX, 1950 | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Heatwole & Cogger (2013) | 3 | 0,25% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
ICZN (2020) | 3 | 0,25% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Iorio & Bonato (2024) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Iorio et al. (2015) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Iorio et al. (2024) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Maldonado (2017) | 3 | 0,25% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Matic (1961) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Matic (1976) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Dumbardon-Martial (2015) | 3 | 0,25% | 3 | 0,82% | 1 | 0,31% | 2 | 0,6% |
Meurgey & Ramage (2020) | 3 | 0,25% | 3 | 0,82% | 1 | 0,31% | 2 | 0,6% |
Mulochau et al. (2020) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Naulleau et al. (1998) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 0 | 0% |
Naulleau (1983) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 0 | 0% |
Noël et al. (2024) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Pereira (2010) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Petuch & Berschauer (2018) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Quindroit & Iorio (2023) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Quindroit (2021) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Shine et al. (2019) | 3 | 0,25% | 3 | 0,82% | 3 | 0,94% | 3 | 0,9% |
Uicn et al. (2015) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Zuffi (2002) | 3 | 0,25% | 2 | 0,55% | 1 | 0,31% | 1 | 0,3% |
Almeida et al. (2022) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 1 | 0,3% |
Bauer & Powell (2024) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Bavay (1869) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Bernarde et al. (2021) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Bonato et al. (2011) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Bonnet et al. (1999) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Bourmaud (2003) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Brechlin et al. (2011) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Brischoux & Bonnet (2009) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Brölemann (1897) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1897) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Brölemann (1898) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1901) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Brölemann (1902) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1907) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1908) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1920) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Brölemann (1927) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Brolemann (1930) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande & Ribaut (1909) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande (1907) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Chalande (1909) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Chalande (1910) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Cramer ([1777]) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Dal Vechioet al. (2021) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Demange (1955) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Desmots & Racine (2023) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Draudt (1929-1930) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Eason (1972) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Edgecombe (2004) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Fanzago (1875) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernandes et al. (2004) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Foddai & Minelli (1999) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Fraga & Carvalho (2021) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 1 | 0,3% |
Fricke et al. (2011) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Galloo & Lourdais (2007) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Geneva et al. (2013) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Gilgado et al. (2022) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Grube (1872) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiller et al. (2016) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Guillon et al. (2009) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Hamdan et al. (2023) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 1 | 0,3% |
Henderson & Breuil (2012) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Hoser (2023) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2007) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Lithobius (s. str.) Leach, 1814 (Chilopoda, Lithobiomorpha, Lithobiidae). Bulletin de la Société linnéenne de Bordeaux, 141(34(4)): 277-285.">Iorio & Geoffroy (2007) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Iorio (2009) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Iorio (2010) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Cryptops umbricus VERHOEFF, 1931 (Chilopoda, Scolopendromorpha, Cryptopidae). Bulletin de la Société linnéenne de Bordeaux, 144 (N.S.) 37(4): 471-481.">Iorio (2010) | 2 | 0,17% | 2 | 0,55% | 0 | 0% | 2 | 0,6% |
Iorio (2015) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Jones (1998) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Jourdan (2020) | 2 | 0,17% | 2 | 0,55% | 1 | 0,31% | 2 | 0,6% |
Latreille (1829) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Latzel (1886) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Latzel (1886) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Latzel (1888) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach ([1814]) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Legendre (1966) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Lemaire (1972) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Lemaire (2002) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Lewis (1989) | 2 | 0,17% | 2 | 0,55% | 0 | 0% | 2 | 0,6% |
Lewis (2013) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Linné (1767) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Lourdais et al. (2013) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Lucas (1846) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Meinert (1868) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 1 | 0,3% |
Meurgey (2014) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Motta (1982) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Murienne et al. (2011) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Newport (1845) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Pereira et al. (1995) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Pereira et al. (2006) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Pereira (1999) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Pereira (2013) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Pocock (1898) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Probst et al. (2022) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Quindroit (2020) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Remillet (1988) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 1 | 0,3% |
Ribaut (1911) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez (2020) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Sanders et al. (2013) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Santos (2003) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Sebat et al. (2005) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Shelley (2004) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 1 | 0,3% |
Shine et al. (2002) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Silvestri (1908) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Siu et al. (2017) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Solórzano & Sasa (2024) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Spix (1824) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Starace (2013) | 2 | 0,17% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Taczanowski (1874) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Thomas (2015) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 2 | 0,6% |
Trochet et al. (2024) | 2 | 0,17% | 2 | 0,55% | 0 | 0% | 2 | 0,6% |
Tucker & Tenorio (2009) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1931) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 1 | 0,3% |
Verhoeff (1935) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 1 | 0,3% |
Zakardjian et al. (2023) | 2 | 0,17% | 2 | 0,55% | 0 | 0% | 2 | 0,6% |
Zwahlen et al. (2022) | 2 | 0,17% | 2 | 0,55% | 2 | 0,63% | 0 | 0% |
Alberto & Pereira (2015) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Albouy et al. (2017) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Almeida et al. (2024) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Améziane (2007) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Anonyme. (2004) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Arribas (1997) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Arthur et al. (2001) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Arvy (1972) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Attems (1903) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bacchet et al. (2007) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Balazuc & Reveillet (1980) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Balvay (2009) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Barbour (1912) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Baron (1987) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Bauer & Sadlier (1994) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (2024) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Baumgart et al. (1983) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Bellmann (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Bentz (2002) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Bergsøe & Meinert (1866) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Billi et al. (2011) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Bodin & Duguy (1958) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Bonaparte (1832-1841) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonato & Minelli (2015) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Bonnaterre (1790) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnet et al. (2001) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Bonnet et al. (2002) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Boulenger (1876) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Boyd et al. (2006) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Breuil (2009) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Brölemann (1889) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1892) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Burger (1955) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabanillas et al. (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Catala (1950) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Caut et al. (2013) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Cavalcante et al. (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Cazanove (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Chalande (1905) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande (1905) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Chéreau et al. (2016) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Cheyrezy et al. (2012) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Ciccione (2000) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochard (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Conte et al. (2007) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Costal-oliveira et al. (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Coulis (2017) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Crabill (1960) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Crowe-riddell et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Cupul-Magaña et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Le règne animal distribué d'après son organisation, pour servir de base à l'histoire naturelle des animaux et d'introduction à l'anatomie comparée. Tome 2, contenant les reptiles, les poissons, les mollusques et les annélides. Déterville, Paris. i-xviii+1-532 pp. ">Cuvier (1816) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Daudin (1803) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1778) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
de Vis (1905) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Delafontaine et al. (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Delrieu-Trottin et al. (2015) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Demange & Serra (1978) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Demange (1958) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Demange (1958) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Deso (2001) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Despax (1925) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Dewynter & Rufray (2012) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Dewynter et al. (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Dewynter et al. (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Dezetter et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Diaz-ricaurte et al. (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Dierkens (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Donovan (1810) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dotsenko (2011) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreux & Saint Girons (1951) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Duguy & Saint Girons (1950) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Vipera berus seoanei" (Lataste) des Pyérénées françaises. Bulletin de la Société Zoologique de France, LXXVI(1-2): 45-46.">Duguy (1951) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Duguy (1995) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Duméril (1853) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupérré (2023) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Eason & Minelli (1976) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Eason (1973) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Edgecombe & Giribet (2004) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Edgecombe (2004) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Espasandín et al. (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Falck (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Fanzago (1874) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Farias et al. (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Foddai et al. (1995) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Franco et al. (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
François et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Fricke et al. (2009) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Friese (1907) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1887) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrard (1966) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Goiran & Shine (2014) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Goiran et al. (2013) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Goiran et al. (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Goiran et al. (2020) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Goiran et al. (2020) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Goiran et al. (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Golay et al. (2008) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Golvan (1962) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Graitson et al. (2012) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Graitson et al. (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Gray (1842) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1842) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Groen (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Groom et al. (2016) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Gros-désormeaux et al. (2017) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Guilbert (2007) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Guiller et al. (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Haase (1880) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Heatwole et al. (2005) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Hervé & Garrouste (2009) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Hingray (2014) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Hodges & Seabrook (2016) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Hodges et al. (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Hodges et al. (2024) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Ineich & Laboute (2002) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2017) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Ineich (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Iorio et al. (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Iorio (2003) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Iorio (2005) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Iorio (2005) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Iorio (2008) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Iorio (2016) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Iorio (2016) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Iorio (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Jacquemin & Iorio (2017) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Jacquemin & Iorio (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Jacquemin (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Jacquemin (2024) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Jan (1858) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Jennings et al. (2013) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Jouan (1864) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2014) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Kharin & Dotsenko (2012) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Kharin (1983) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Kharin (1984) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Knoepffler & Sochurek (1955) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Kordi & Shabanipour (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Kos (1995) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Kramer (1958) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Krefft (1869) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Kronmüller (2012) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Kuhlmann (2006) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Kulbicki et al. (2000) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
La Cepède (1789) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacépède (1804) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lankester (1880) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lanza & Boscherini (2000) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lataste (1879) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Latzel (1887) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Latzel (1892) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Laurenti (1768) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach (1817) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lillywhite & Menon (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lima et al. (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Linnaeus (1761) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lisse & Delauje (2012) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Livory (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lizé (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Loeuillet et al. (2017) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lorvelec et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lourdais et al. (2002) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Lourdais et al. (2004) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Luo (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lyet et al. (2005) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Lynch et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Lynch et al. (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Machado (1952) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Madsen et al. (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Manfredi (1936) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchand (2020) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Martínez-freiría et al. (2020) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Martoja et al. (1961) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Massary et al. (2020) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Mathon & Tomaselli (1959) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Matic (1959) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Matic (1980) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Meinert (1886) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Meisner (1820) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Questel (2015) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Moolenbeek & Röckel (1996) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Moreau de Jonnès (1816) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Mourgaud (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Naulleau & Bonnet (1995) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Nicet & Denis (2011) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Noël (2024) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Parnaudeau & Madl (2009) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Paulian (1998) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Pauly & Munzinger (2003) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Pauly et al. (2001) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Paysant et al. (2003) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Pereira & Minelli (1993) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre et al. (2017) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Pinto-coelho et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Porat (1876) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Porath (1871) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Prémel et al. (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Probst (2001) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Quiñones-betancourt et al. (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Rageau (1956) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Ramage (2024) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Renner (2002) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Résière et al. (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Reverté et al. (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Rey & Timmerman (2018) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Rojas-morales et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Ross et al. (2009) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Rossi (1790) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rothenbühler (1899) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Rufz (1859 | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Saint & Girons (1948) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Saint & Girons (1978) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Saint Girons & Martoja (1963) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Schlegel (1837) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1799) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulthess (1915) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Serra (1980) | 1 | 0,08% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
Shaw (1794) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Shine & Gorian (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Shine et al. (2012) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Shine et al. (2019) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Shine et al. (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Shine et al. (2020) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Shine et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Shine et al. (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Shine et al. (2022) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Shine et al. (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Silvestri (1898) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Simon (1892) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Sivestri (1896) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Soissons et al. (2007) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
SORDELLO (2012) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Sowerby (1941) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Spalikowski (1897) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Starace & Ineich (2024) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Stoev et al. (2010) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Tan et al. (2019) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Théodoridès & Ormières (1959) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2018) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Tregarot et al. (2015) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Udyawer et al. (2020) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Vachal (1907) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Valerio (1981) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandenspiegel & Mathys (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Vedel et al. (2013) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Vergonzanne (1977) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Verhoeff (1898) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Verhoeff (1899) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1901) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1902) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Verhoeff (1925) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Verhoeff (1934) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1935) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Verhoeff (1937) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach et al. (2014) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Weerdt et al. (2021) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Weinberg & Ridder (1998) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Wickel & Jamon (2010) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Wied-neuwied (1821) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2006) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Wood (1867) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Wüster et al. (2002) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 1 | 0,3% |
Zakardjian et al. (2020) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |
Zwahlen et al. (2023) | 1 | 0,08% | 1 | 0,27% | 1 | 0,31% | 0 | 0% |