Chilopodes
Chilopoda
206 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 | 16,36% | 129 | 47,25% | 121 | 49,39% | 119 | 46,85% |
| Iorio et al. (2022) | 72 | 8,18% | 69 | 25,27% | 68 | 27,76% | 61 | 24,02% |
| Iorio (2008) | 72 | 8,18% | 64 | 23,44% | 63 | 25,71% | 56 | 22,05% |
| Ribaut (1923) | 67 | 7,61% | 53 | 19,41% | 53 | 21,63% | 51 | 20,08% |
| Iorio et al. (2023) | 64 | 7,27% | 63 | 23,08% | 59 | 24,08% | 61 | 24,02% |
| Würmli (1974) | 46 | 5,23% | 41 | 15,02% | 41 | 16,73% | 39 | 15,35% |
| Zapparoli & Iorio (2012) | 33 | 3,75% | 30 | 10,99% | 30 | 12,24% | 28 | 11,02% |
| Verhoeff (1943) | 29 | 3,3% | 6 | 2,2% | 6 | 2,45% | 6 | 2,36% |
| Iorio & Berg (2007) | 27 | 3,07% | 22 | 8,06% | 21 | 8,57% | 21 | 8,27% |
| Iorio & Geoffroy (2019) | 25 | 2,84% | 24 | 8,79% | 23 | 9,39% | 21 | 8,27% |
| Iorio (2007) | 23 | 2,61% | 22 | 8,06% | 22 | 8,98% | 17 | 6,69% |
| Iorio & Coulis (2020) | 22 | 2,5% | 22 | 8,06% | 16 | 6,53% | 22 | 8,66% |
| Bonato & Minelli (2014) | 20 | 2,27% | 6 | 2,2% | 6 | 2,45% | 6 | 2,36% |
| Schileyko et al. (2018) | 19 | 2,16% | 19 | 6,96% | 16 | 6,53% | 18 | 7,09% |
| Ramage et al. (2023) | 16 | 1,82% | 16 | 5,86% | 13 | 5,31% | 16 | 6,3% |
| Iorio & Leccia (2021) | 15 | 1,7% | 15 | 5,49% | 14 | 5,71% | 14 | 5,51% |
| Demange (1981) | 14 | 1,59% | 12 | 4,4% | 9 | 3,67% | 11 | 4,33% |
| Demange & Pereira (1985) | 12 | 1,36% | 3 | 1,1% | 3 | 1,22% | 3 | 1,18% |
| Geoffroy (2020) | 12 | 1,36% | 12 | 4,4% | 11 | 4,49% | 10 | 3,94% |
| Iorio & Coulis (2024) | 12 | 1,36% | 12 | 4,4% | 12 | 4,9% | 12 | 4,72% |
| Iorio & Racine (2022) | 12 | 1,36% | 12 | 4,4% | 11 | 4,49% | 12 | 4,72% |
| Iorio (2014) | 12 | 1,36% | 5 | 1,83% | 5 | 2,04% | 4 | 1,57% |
| Iorio (2021) | 11 | 1,25% | 11 | 4,03% | 11 | 4,49% | 10 | 3,94% |
| Ramage (2017) | 11 | 1,25% | 11 | 4,03% | 10 | 4,08% | 10 | 3,94% |
| Eason (1974) | 10 | 1,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meurgey (2011) | 10 | 1,14% | 7 | 2,56% | 7 | 2,86% | 6 | 2,36% |
| Chamberlin (1918) | 9 | 1,02% | 6 | 2,2% | 4 | 1,63% | 6 | 2,36% |
| Iorio & Coulis (2019) | 9 | 1,02% | 9 | 3,3% | 9 | 3,67% | 9 | 3,54% |
| Léger & Duboscq (1903) | 9 | 1,02% | 4 | 1,47% | 4 | 1,63% | 4 | 1,57% |
| Chamberlin (1920) | 8 | 0,91% | 8 | 2,93% | 7 | 2,86% | 7 | 2,76% |
| Meinert (1870) | 8 | 0,91% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Silvestri (1935) | 8 | 0,91% | 8 | 2,93% | 8 | 3,27% | 7 | 2,76% |
| Iorio et al. (2020) | 7 | 0,8% | 7 | 2,56% | 7 | 2,86% | 7 | 2,76% |
| Meinert (1872) | 7 | 0,8% | 5 | 1,83% | 5 | 2,04% | 4 | 1,57% |
| Verhoeff (1928) | 7 | 0,8% | 6 | 2,2% | 6 | 2,45% | 6 | 2,36% |
| Koch ([1835]-[1844]) | 6 | 0,68% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Koch (1847) | 6 | 0,68% | 5 | 1,83% | 5 | 2,04% | 3 | 1,18% |
| Koch (1862) | 6 | 0,68% | 6 | 2,2% | 6 | 2,45% | 5 | 1,97% |
| Adamson (1932) | 5 | 0,57% | 5 | 1,83% | 5 | 2,04% | 4 | 1,57% |
| Brölemann (1904) | 5 | 0,57% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Mauriès & Nguyen Duy-Jacquemin (2001) | 5 | 0,57% | 4 | 1,47% | 4 | 1,63% | 3 | 1,18% |
| Schileyko (2018) | 5 | 0,57% | 2 | 0,73% | 1 | 0,41% | 2 | 0,79% |
| Brölemann & Ribaut (1911) | 4 | 0,45% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Brölemann (1909) | 4 | 0,45% | 4 | 1,47% | 4 | 1,63% | 4 | 1,57% |
| Brölemann (1909) | 4 | 0,45% | 4 | 1,47% | 4 | 1,63% | 4 | 1,57% |
| Brölemann (1926) | 4 | 0,45% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Demange (1963) | 4 | 0,45% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Fanzago (1877) | 4 | 0,45% | 4 | 1,47% | 4 | 1,63% | 4 | 1,57% |
| Jeannel (1926) | 4 | 0,45% | 4 | 1,47% | 4 | 1,63% | 2 | 0,79% |
| Latzel (1880) | 4 | 0,45% | 3 | 1,1% | 3 | 1,22% | 3 | 1,18% |
| Linnaeus (1758) | 4 | 0,45% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Matic (1958) | 4 | 0,45% | 4 | 1,47% | 4 | 1,63% | 4 | 1,57% |
| Newport (1844) | 4 | 0,45% | 3 | 1,1% | 3 | 1,22% | 2 | 0,79% |
| Questel & Le Quellec (2012) | 4 | 0,45% | 4 | 1,47% | 4 | 1,63% | 3 | 1,18% |
| Rageau (1958) | 4 | 0,45% | 4 | 1,47% | 4 | 1,63% | 2 | 0,79% |
| Risso (1827) | 4 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schileyko & Cupul-Magaña (2021) | 4 | 0,45% | 3 | 1,1% | 3 | 1,22% | 3 | 1,18% |
| Silvestri (1934) | 4 | 0,45% | 4 | 1,47% | 4 | 1,63% | 3 | 1,18% |
| Bonato et al. (2023) | 3 | 0,34% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Brölemann (1924) | 3 | 0,34% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Edgecombe (2003) | 3 | 0,34% | 3 | 1,1% | 3 | 1,22% | 3 | 1,18% |
| 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 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Iorio et al. (2015) | 3 | 0,34% | 3 | 1,1% | 3 | 1,22% | 3 | 1,18% |
| Matic (1961) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matic (1976) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pereira (2010) | 3 | 0,34% | 3 | 1,1% | 3 | 1,22% | 3 | 1,18% |
| Questel (2020) | 3 | 0,34% | 3 | 1,1% | 3 | 1,22% | 2 | 0,79% |
| Quindroit & Iorio (2023) | 3 | 0,34% | 3 | 1,1% | 3 | 1,22% | 3 | 1,18% |
| Quindroit (2021) | 3 | 0,34% | 3 | 1,1% | 3 | 1,22% | 3 | 1,18% |
| Bonato et al. (2011) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Brölemann (1897) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Brölemann (1897) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brölemann (1898) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brölemann (1901) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Brölemann (1902) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brölemann (1907) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brölemann (1908) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brölemann (1920) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Brölemann (1927) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Brolemann (1930) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chalande & Ribaut (1909) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chalande (1907) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Chalande (1909) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Chalande (1910) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Demange (1955) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Desmots & Racine (2023) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Eason (1972) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edgecombe (2004) | 2 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Fanzago (1875) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Foddai & Minelli (1999) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Gilgado et al. (2022) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Grube (1872) | 2 | 0,23% | 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 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Iorio (2009) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Cryptops umbricus VERHOEFF, 1931 (Chilopoda, Scolopendromorpha, Cryptopidae). Bulletin de la Société linnéenne de Bordeaux, 144 (N.S.) 37(4): 471-481.">Iorio (2010) | 2 | 0,23% | 2 | 0,73% | 0 | 0% | 2 | 0,79% |
| Iorio (2010) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Iorio (2015) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Jones (1998) | 2 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Jourdan & Mille (2006) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 1 | 0,39% |
| Latreille (1829) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Latzel (1886) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Latzel (1886) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 0 | 0% |
| Latzel (1888) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leach (1814) | 2 | 0,23% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| Leach (1815) | 2 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Legendre (1966) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Lewis (2013) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Linné (1767) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas (1846) | 2 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Meinert (1868) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 1 | 0,39% |
| Murienne et al. (2011) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Newport (1845) | 2 | 0,23% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| Pereira et al. (1995) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Pereira et al. (2006) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Pereira (1999) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Pocock (1898) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Quindroit (2020) | 2 | 0,23% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Ribaut (1911) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shelley (2004) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 1 | 0,39% |
| Silvestri (1908) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Thomas (2015) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 2 | 0,79% |
| Verhoeff (1931) | 2 | 0,23% | 2 | 0,73% | 2 | 0,82% | 1 | 0,39% |
| Verhoeff (1935) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alberto & Pereira (2015) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Arthur et al. (2001) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Attems (1903) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Balazuc & Reveillet (1980) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Bergsøe & Meinert (1866) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| Billi et al. (2011) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Bonato & Minelli (2015) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Brölemann (1889) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brölemann (1892) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Cabanillas et al. (2023) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| 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 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Cochard (2019) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Coulis (2017) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Crabill (1960) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cupul-Magaña et al. (2021) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| De Geer (1778) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Demange & Serra (1978) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Demange (1958) | 1 | 0,11% | 1 | 0,37% | 0 | 0% | 1 | 0,39% |
| Demange (1958) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| 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 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Edgecombe (2004) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| 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 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Iorio et al. (2019) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Iorio (2003) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| 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 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Iorio (2016) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| Iorio (2016) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Iorio (2019) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Jacquemin & Iorio (2017) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Jacquemin & Iorio (2022) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Jacquemin (2019) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Jacquemin (2024) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| Jourdan (2020) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Kos (1995) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kronmüller (2012) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| Latzel (1880) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Latzel (1887) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Latzel (1892) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 0 | 0% |
| Leach (1817) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lewis (1989) | 1 | 0,11% | 1 | 0,37% | 0 | 0% | 1 | 0,39% |
| Livory (2022) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| 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% |
| Pereira & Minelli (1993) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pereira (2013) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| 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 | 0,37% | 1 | 0,41% | 0 | 0% |
| Rossi (1790) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rothenbühler (1899) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Serra (1980) | 1 | 0,11% | 1 | 0,37% | 0 | 0% | 1 | 0,39% |
| Shaw (1794) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Silvestri (1898) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Sivestri (1896) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stoev et al. (2010) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| 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 | 0,37% | 1 | 0,41% | 0 | 0% |
| Verhoeff (1898) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| 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 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Verhoeff (1925) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| Verhoeff (1934) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verhoeff (1935) | 1 | 0,11% | 1 | 0,37% | 1 | 0,41% | 1 | 0,39% |
| 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 | 0,37% | 1 | 0,41% | 0 | 0% |
