Chilopodes
Chilopoda
213 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 | 16,13% | 129 | 46,07% | 121 | 48,02% | 120 | 45,98% |
Iorio et al. (2022) | 72 | 8,06% | 69 | 24,64% | 68 | 26,98% | 61 | 23,37% |
Iorio (2008) | 72 | 8,06% | 64 | 22,86% | 63 | 25% | 57 | 21,84% |
Ribaut (1923) | 67 | 7,5% | 53 | 18,93% | 53 | 21,03% | 49 | 18,77% |
Iorio et al. (2023) | 64 | 7,17% | 63 | 22,5% | 59 | 23,41% | 61 | 23,37% |
Würmli (1974) | 46 | 5,15% | 41 | 14,64% | 41 | 16,27% | 38 | 14,56% |
Zapparoli & Iorio (2012) | 33 | 3,7% | 30 | 10,71% | 30 | 11,9% | 28 | 10,73% |
Verhoeff (1943) | 29 | 3,25% | 6 | 2,14% | 6 | 2,38% | 6 | 2,3% |
Schileyko et al. (2024) | 28 | 3,14% | 28 | 10% | 22 | 8,73% | 28 | 10,73% |
Iorio & Berg (2007) | 27 | 3,02% | 22 | 7,86% | 21 | 8,33% | 21 | 8,05% |
Iorio & Geoffroy (2019) | 25 | 2,8% | 24 | 8,57% | 23 | 9,13% | 21 | 8,05% |
Iorio (2007) | 23 | 2,58% | 22 | 7,86% | 22 | 8,73% | 17 | 6,51% |
Iorio & Coulis (2020) | 22 | 2,46% | 22 | 7,86% | 16 | 6,35% | 21 | 8,05% |
Bonato & Minelli (2014) | 20 | 2,24% | 6 | 2,14% | 6 | 2,38% | 6 | 2,3% |
Schileyko et al. (2018) | 19 | 2,13% | 18 | 6,43% | 16 | 6,35% | 17 | 6,51% |
Ramage et al. (2023) | 16 | 1,79% | 16 | 5,71% | 13 | 5,16% | 15 | 5,75% |
Iorio & Leccia (2021) | 15 | 1,68% | 15 | 5,36% | 14 | 5,56% | 14 | 5,36% |
Demange (1981) | 14 | 1,57% | 12 | 4,29% | 9 | 3,57% | 9 | 3,45% |
Demange & Pereira (1985) | 12 | 1,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Geoffroy (2020) | 12 | 1,34% | 12 | 4,29% | 11 | 4,37% | 10 | 3,83% |
Iorio & Coulis (2024) | 12 | 1,34% | 12 | 4,29% | 12 | 4,76% | 12 | 4,6% |
Iorio & Racine (2022) | 12 | 1,34% | 12 | 4,29% | 11 | 4,37% | 12 | 4,6% |
Iorio (2014) | 12 | 1,34% | 5 | 1,79% | 5 | 1,98% | 4 | 1,53% |
Iorio (2021) | 11 | 1,23% | 11 | 3,93% | 11 | 4,37% | 11 | 4,21% |
Ramage (2017) | 11 | 1,23% | 11 | 3,93% | 10 | 3,97% | 10 | 3,83% |
Eason (1974) | 10 | 1,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey (2011) | 10 | 1,12% | 7 | 2,5% | 7 | 2,78% | 6 | 2,3% |
Chamberlin (1918) | 9 | 1,01% | 6 | 2,14% | 4 | 1,59% | 6 | 2,3% |
Iorio & Coulis (2019) | 9 | 1,01% | 9 | 3,21% | 9 | 3,57% | 9 | 3,45% |
Léger & Duboscq (1903) | 9 | 1,01% | 4 | 1,43% | 4 | 1,59% | 4 | 1,53% |
Chamberlin (1920) | 8 | 0,9% | 8 | 2,86% | 7 | 2,78% | 7 | 2,68% |
Meinert (1870) | 8 | 0,9% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Silvestri (1935) | 8 | 0,9% | 8 | 2,86% | 8 | 3,17% | 7 | 2,68% |
Iorio et al. (2020) | 7 | 0,78% | 7 | 2,5% | 7 | 2,78% | 7 | 2,68% |
Meinert (1872) | 7 | 0,78% | 5 | 1,79% | 5 | 1,98% | 4 | 1,53% |
Verhoeff (1928) | 7 | 0,78% | 6 | 2,14% | 6 | 2,38% | 6 | 2,3% |
Iorio (2024) | 6 | 0,67% | 6 | 2,14% | 6 | 2,38% | 6 | 2,3% |
Koch ([1835]-[1844]) | 6 | 0,67% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Koch (1847) | 6 | 0,67% | 5 | 1,79% | 5 | 1,98% | 3 | 1,15% |
Koch (1862) | 6 | 0,67% | 6 | 2,14% | 6 | 2,38% | 5 | 1,92% |
Adamson (1932) | 5 | 0,56% | 5 | 1,79% | 5 | 1,98% | 4 | 1,53% |
Brölemann (1904) | 5 | 0,56% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Mauriès & Nguyen Duy-Jacquemin (2001) | 5 | 0,56% | 4 | 1,43% | 4 | 1,59% | 3 | 1,15% |
Schileyko (2018) | 5 | 0,56% | 2 | 0,71% | 1 | 0,4% | 2 | 0,77% |
Brölemann & Ribaut (1911) | 4 | 0,45% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Brölemann (1909) | 4 | 0,45% | 4 | 1,43% | 4 | 1,59% | 4 | 1,53% |
Brölemann (1909) | 4 | 0,45% | 4 | 1,43% | 4 | 1,59% | 4 | 1,53% |
Brölemann (1926) | 4 | 0,45% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Demange (1963) | 4 | 0,45% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Fanzago (1877) | 4 | 0,45% | 4 | 1,43% | 4 | 1,59% | 4 | 1,53% |
Jeannel (1926) | 4 | 0,45% | 4 | 1,43% | 4 | 1,59% | 2 | 0,77% |
Latzel (1880) | 4 | 0,45% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Leach ([1816]) | 4 | 0,45% | 3 | 1,07% | 3 | 1,19% | 2 | 0,77% |
Linnaeus (1758) | 4 | 0,45% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Matic (1958) | 4 | 0,45% | 4 | 1,43% | 4 | 1,59% | 4 | 1,53% |
Newport (1844) | 4 | 0,45% | 3 | 1,07% | 3 | 1,19% | 2 | 0,77% |
Questel & Le Quellec (2012) | 4 | 0,45% | 4 | 1,43% | 4 | 1,59% | 3 | 1,15% |
Rageau (1958) | 4 | 0,45% | 4 | 1,43% | 4 | 1,59% | 2 | 0,77% |
Raphael (1970) | 4 | 0,45% | 3 | 1,07% | 3 | 1,19% | 2 | 0,77% |
Risso (1827) | 4 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Schileyko & Cupul-Magaña (2021) | 4 | 0,45% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Silvestri (1934) | 4 | 0,45% | 4 | 1,43% | 4 | 1,59% | 3 | 1,15% |
Bonato et al. (2023) | 3 | 0,34% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Brölemann (1924) | 3 | 0,34% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Edgecombe (2003) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Gervais (1837) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
GOUX, 1950 | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
ICZN (2020) | 3 | 0,34% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Iorio & Bonato (2024) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Iorio et al. (2015) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Iorio et al. (2024) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Matic (1961) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Matic (1976) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël et al. (2024) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Pereira (2010) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Questel (2020) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 2 | 0,77% |
Quindroit & Iorio (2023) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Quindroit (2021) | 3 | 0,34% | 3 | 1,07% | 3 | 1,19% | 3 | 1,15% |
Bonato et al. (2011) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Brölemann (1897) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Brölemann (1897) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1898) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1901) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Brölemann (1902) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1907) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1908) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1920) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Brölemann (1927) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Brolemann (1930) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande & Ribaut (1909) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande (1907) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Chalande (1909) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Chalande (1910) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Demange (1955) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Desmots & Racine (2023) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Eason (1972) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Edgecombe (2004) | 2 | 0,22% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Fanzago (1875) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Foddai & Minelli (1999) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Gilgado et al. (2022) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Grube (1872) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lithobius (s. str.) Leach, 1814 (Chilopoda, Lithobiomorpha, Lithobiidae). Bulletin de la Société linnéenne de Bordeaux, 141(34(4)): 277-285.">Iorio & Geoffroy (2007) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Iorio (2009) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Iorio (2010) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Cryptops umbricus VERHOEFF, 1931 (Chilopoda, Scolopendromorpha, Cryptopidae). Bulletin de la Société linnéenne de Bordeaux, 144 (N.S.) 37(4): 471-481.">Iorio (2010) | 2 | 0,22% | 2 | 0,71% | 0 | 0% | 2 | 0,77% |
Iorio (2015) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Jones (1998) | 2 | 0,22% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Jourdan & Mille (2006) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 1 | 0,38% |
Latreille (1829) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Latzel (1886) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Latzel (1886) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 0 | 0% |
Latzel (1888) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach ([1814]) | 2 | 0,22% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Legendre (1966) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Lewis (1989) | 2 | 0,22% | 2 | 0,71% | 0 | 0% | 2 | 0,77% |
Lewis (2013) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Linné (1767) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1846) | 2 | 0,22% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Meinert (1868) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 1 | 0,38% |
Murienne et al. (2011) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Newport (1845) | 2 | 0,22% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Pereira et al. (1995) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Pereira et al. (2006) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Pereira (1999) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Pereira (2013) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Pocock (1898) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Quindroit (2020) | 2 | 0,22% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Ribaut (1911) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Shelley (2004) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 1 | 0,38% |
Silvestri (1908) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Thomas (2015) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 2 | 0,77% |
Verhoeff (1931) | 2 | 0,22% | 2 | 0,71% | 2 | 0,79% | 1 | 0,38% |
Verhoeff (1935) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Alberto & Pereira (2015) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Arthur et al. (2001) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Attems (1903) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Balazuc & Reveillet (1980) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Bergsøe & Meinert (1866) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Billi et al. (2011) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Bonato & Minelli (2015) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Brölemann (1889) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1892) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Cabanillas et al. (2023) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Chalande (1905) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande (1905) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chéreau et al. (2016) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Cochard (2019) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Coulis (2017) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Crabill (1960) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cupul-Magaña et al. (2021) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
De Geer (1778) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Demange & Serra (1978) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Demange (1958) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Demange (1958) | 1 | 0,11% | 1 | 0,36% | 0 | 0% | 1 | 0,38% |
Donovan (1810) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Eason & Minelli (1976) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Eason (1973) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Edgecombe & Giribet (2004) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Edgecombe (2004) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Fanzago (1874) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Foddai et al. (1995) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Haase (1880) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Iorio et al. (2019) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Iorio (2003) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Iorio (2005) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Iorio (2005) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Iorio (2008) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Iorio (2016) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Iorio (2016) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Iorio (2019) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Jacquemin & Iorio (2017) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Jacquemin & Iorio (2022) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Jacquemin (2019) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Jacquemin (2024) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Jourdan (2020) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Kos (1995) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kronmüller (2012) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Latzel (1880) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Latzel (1887) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Latzel (1892) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Leach (1817) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Livory (2022) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Machado (1952) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Manfredi (1936) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Matic (1959) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Matic (1980) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Meinert (1886) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2024) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Pereira & Minelli (1993) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Porat (1876) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Porath (1871) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1956) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Rossi (1790) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rothenbühler (1899) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Serra (1980) | 1 | 0,11% | 1 | 0,36% | 0 | 0% | 1 | 0,38% |
Shaw (1794) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Silvestri (1898) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Sivestri (1896) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Stoev et al. (2010) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Théodoridès & Ormières (1959) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandenspiegel & Mathys (2021) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |
Verhoeff (1898) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Verhoeff (1899) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1901) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1902) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Verhoeff (1925) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Verhoeff (1934) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1935) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 1 | 0,38% |
Verhoeff (1937) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (1867) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,11% | 1 | 0,36% | 1 | 0,4% | 0 | 0% |