Myriapodes
Myriapoda
377 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 | 6,58% | 129 | 14,97% | 121 | 14,83% | 119 | 14,3% |
Kime & Enghoff (2017) | 117 | 5,34% | 98 | 11,37% | 98 | 12,01% | 95 | 11,42% |
Carl (1926) | 88 | 4,02% | 72 | 8,35% | 72 | 8,82% | 72 | 8,65% |
Iorio et al. (2022) | 72 | 3,29% | 69 | 8% | 68 | 8,33% | 61 | 7,33% |
Iorio (2008) | 72 | 3,29% | 64 | 7,42% | 63 | 7,72% | 56 | 6,73% |
Ribaut (1923) | 67 | 3,06% | 53 | 6,15% | 53 | 6,5% | 51 | 6,13% |
Brolemann (1935) | 64 | 2,92% | 52 | 6,03% | 49 | 6% | 49 | 5,89% |
Iorio et al. (2023) | 64 | 2,92% | 63 | 7,31% | 59 | 7,23% | 61 | 7,33% |
Shelley & Lehtinen (1999) | 46 | 2,1% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Würmli (1974) | 46 | 2,1% | 41 | 4,76% | 41 | 5,02% | 39 | 4,69% |
Ramage et al. (2023) | 41 | 1,87% | 41 | 4,76% | 34 | 4,17% | 41 | 4,93% |
Mauriès (1980) | 40 | 1,83% | 28 | 3,25% | 18 | 2,21% | 28 | 3,37% |
Meurgey (2011) | 40 | 1,83% | 28 | 3,25% | 24 | 2,94% | 26 | 3,12% |
Iorio & Coulis (2020) | 39 | 1,78% | 37 | 4,29% | 28 | 3,43% | 37 | 4,45% |
Scheller (1993) | 39 | 1,78% | 37 | 4,29% | 37 | 4,53% | 37 | 4,45% |
Zapparoli & Iorio (2012) | 33 | 1,51% | 30 | 3,48% | 30 | 3,68% | 28 | 3,37% |
Verhoeff (1943) | 29 | 1,32% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Iorio & Berg (2007) | 27 | 1,23% | 22 | 2,55% | 21 | 2,57% | 21 | 2,52% |
Geoffroy (2020) | 26 | 1,19% | 26 | 3,02% | 25 | 3,06% | 22 | 2,64% |
Ribaut (1913) | 26 | 1,19% | 20 | 2,32% | 20 | 2,45% | 20 | 2,4% |
Iorio & Geoffroy (2019) | 25 | 1,14% | 24 | 2,78% | 23 | 2,82% | 21 | 2,52% |
Mauriès (1961) | 24 | 1,1% | 18 | 2,09% | 17 | 2,08% | 17 | 2,04% |
Iorio (2007) | 23 | 1,05% | 22 | 2,55% | 22 | 2,7% | 17 | 2,04% |
Mauriès (1987) | 23 | 1,05% | 16 | 1,86% | 14 | 1,72% | 14 | 1,68% |
Chamberlin (1918) | 22 | 1,01% | 7 | 0,81% | 5 | 0,61% | 7 | 0,84% |
Mauriès (1969) | 22 | 1,01% | 9 | 1,04% | 9 | 1,1% | 9 | 1,08% |
Ramage (2017) | 22 | 1,01% | 21 | 2,44% | 20 | 2,45% | 20 | 2,4% |
Bonato & Minelli (2014) | 20 | 0,91% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Schileyko et al. (2018) | 19 | 0,87% | 19 | 2,2% | 16 | 1,96% | 18 | 2,16% |
Duborget (2017) | 16 | 0,73% | 16 | 1,86% | 16 | 1,96% | 15 | 1,8% |
Iorio & Leccia (2021) | 15 | 0,69% | 15 | 1,74% | 14 | 1,72% | 14 | 1,68% |
Léger & Duboscq (1903) | 15 | 0,69% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Remy (1940) | 15 | 0,69% | 15 | 1,74% | 15 | 1,84% | 15 | 1,8% |
Ribaut (1920) | 15 | 0,69% | 6 | 0,7% | 6 | 0,74% | 3 | 0,36% |
Vandenspiegel & Mathys (2021) | 15 | 0,69% | 15 | 1,74% | 15 | 1,84% | 14 | 1,68% |
Demange (1981) | 14 | 0,64% | 12 | 1,39% | 9 | 1,1% | 11 | 1,32% |
Risso (1827) | 14 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Silvestri (1935) | 14 | 0,64% | 14 | 1,62% | 14 | 1,72% | 13 | 1,56% |
Schubart & Husson (1937) | 13 | 0,59% | 5 | 0,58% | 5 | 0,61% | 5 | 0,6% |
Demange & Pereira (1985) | 12 | 0,55% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Iorio & Racine (2022) | 12 | 0,55% | 12 | 1,39% | 11 | 1,35% | 12 | 1,44% |
Iorio (2014) | 12 | 0,55% | 5 | 0,58% | 5 | 0,61% | 4 | 0,48% |
Mauriès & Nguyen Duy-Jacquemin (2001) | 12 | 0,55% | 9 | 1,04% | 9 | 1,1% | 8 | 0,96% |
Mauriès (1990) | 12 | 0,55% | 11 | 1,28% | 6 | 0,74% | 11 | 1,32% |
Mauriès (2010) | 12 | 0,55% | 12 | 1,39% | 12 | 1,47% | 12 | 1,44% |
Silvestri (1897) | 12 | 0,55% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Chamberlin (1920) | 11 | 0,5% | 10 | 1,16% | 9 | 1,1% | 9 | 1,08% |
Coulis (2017) | 11 | 0,5% | 9 | 1,04% | 8 | 0,98% | 9 | 1,08% |
Iorio (2021) | 11 | 0,5% | 11 | 1,28% | 11 | 1,35% | 10 | 1,2% |
Adamson (1932) | 10 | 0,46% | 8 | 0,93% | 8 | 0,98% | 7 | 0,84% |
Eason (1974) | 10 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Silvestri (1934) | 10 | 0,46% | 8 | 0,93% | 8 | 0,98% | 7 | 0,84% |
Brölemann (1900) | 9 | 0,41% | 9 | 1,04% | 9 | 1,1% | 9 | 1,08% |
Brölemann (1926) | 9 | 0,41% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Fanzago (1877) | 9 | 0,41% | 7 | 0,81% | 7 | 0,86% | 7 | 0,84% |
Iorio & Coulis (2019) | 9 | 0,41% | 9 | 1,04% | 9 | 1,1% | 9 | 1,08% |
Mauriès (1969) | 9 | 0,41% | 9 | 1,04% | 9 | 1,1% | 9 | 1,08% |
Brolemann (1894) | 8 | 0,37% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Brölemann (1931) | 8 | 0,37% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Brölemann (1921) | 8 | 0,37% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Jupeau (1954) | 8 | 0,37% | 7 | 0,81% | 7 | 0,86% | 7 | 0,84% |
Meinert (1870) | 8 | 0,37% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Porat (1888) | 8 | 0,37% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Iorio et al. (2020) | 7 | 0,32% | 7 | 0,81% | 7 | 0,86% | 7 | 0,84% |
Mauriès (1959) | 7 | 0,32% | 7 | 0,81% | 7 | 0,86% | 7 | 0,84% |
Meinert (1872) | 7 | 0,32% | 5 | 0,58% | 5 | 0,61% | 4 | 0,48% |
Pocock (1898) | 7 | 0,32% | 5 | 0,58% | 5 | 0,61% | 5 | 0,6% |
Scheller (1996) | 7 | 0,32% | 7 | 0,81% | 7 | 0,86% | 7 | 0,84% |
Verhoeff (1928) | 7 | 0,32% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Verhoeff (1930) | 7 | 0,32% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Demange (1963) | 6 | 0,27% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Geoffroy & Mauries (1992) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Koch ([1835]-[1844]) | 6 | 0,27% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Koch (1847) | 6 | 0,27% | 5 | 0,58% | 5 | 0,61% | 3 | 0,36% |
Koch (1862) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 5 | 0,6% |
Leclerc (1953) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Lemaire et al. (2018) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Linnaeus (1758) | 6 | 0,27% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Marek et al. (2003) | 6 | 0,27% | 5 | 0,58% | 5 | 0,61% | 5 | 0,6% |
Mauriès & Kime (1999) | 6 | 0,27% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Mauries (2019) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Nguyen Duy-Jacquemin (2002) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Questel & Le Quellec (2012) | 6 | 0,27% | 4 | 0,46% | 4 | 0,49% | 3 | 0,36% |
Questel (2020) | 6 | 0,27% | 5 | 0,58% | 5 | 0,61% | 4 | 0,48% |
Remy (1954) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Ribaut (1908) | 6 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1947) | 6 | 0,27% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Ribaut (1952) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Stoev et al. (2010) | 6 | 0,27% | 6 | 0,7% | 6 | 0,74% | 6 | 0,72% |
Brölemann (1904) | 5 | 0,23% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Gervais (1837) | 5 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Mauriès (1976) | 5 | 0,23% | 5 | 0,58% | 5 | 0,61% | 5 | 0,6% |
Ribaut (1955) | 5 | 0,23% | 2 | 0,23% | 2 | 0,25% | 0 | 0% |
Schileyko (2018) | 5 | 0,23% | 2 | 0,23% | 1 | 0,12% | 2 | 0,24% |
Yokoyama (2013) | 5 | 0,23% | 2 | 0,23% | 2 | 0,25% | 1 | 0,12% |
Brölemann & Ribaut (1911) | 4 | 0,18% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Brölemann (1897) | 4 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1900) | 4 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1909) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Brölemann (1909) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Ceuca (1962) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
De Almeida et al. (2021) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Golovatch & Sierwald (2001) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Jeannel (1926) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 2 | 0,24% |
Jeekel (1963) | 4 | 0,18% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Jourdan (2020) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Latzel (1880) | 4 | 0,18% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Latzel (1892) | 4 | 0,18% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Leach (1815) | 4 | 0,18% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Matic (1958) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Mauriès (1983) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Newport (1844) | 4 | 0,18% | 3 | 0,35% | 3 | 0,37% | 2 | 0,24% |
Rageau (1958) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 2 | 0,24% |
Remy (1947) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Scheller (1974) | 4 | 0,18% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Scheller (2014) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Schileyko & Cupul-Magaña (2021) | 4 | 0,18% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Silvestri (1902) | 4 | 0,18% | 4 | 0,46% | 4 | 0,49% | 4 | 0,48% |
Bonato et al. (2023) | 3 | 0,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bouzan et al. (2022) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Brölemann (1924) | 3 | 0,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Edgecombe (2003) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Geoffroy et al. (2022) | 3 | 0,14% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Gilgado et al. (2022) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Golovatch et al. (2014) | 3 | 0,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
GOUX, 1950 | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hansen (1903) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
ICZN (2020) | 3 | 0,14% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Iorio et al. (2015) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Matic (1961) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Matic (1976) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mauriès (1963) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Mauriès (1967) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mauriès (1974) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Mauriès (1983) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Mauries (1990) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Mesibov (2014) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Newport (1845) | 3 | 0,14% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Pereira (2010) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Quindroit & Iorio (2023) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Quindroit (2021) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Remy (1930) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Remy (1937) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Remy (1940) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Remy (1956) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Ribaut (1907) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1951) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Schubart (1958) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Shelley (2014) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Strasser (1978) | 3 | 0,14% | 3 | 0,35% | 3 | 0,37% | 3 | 0,36% |
Théodoridès & Ormières (1959) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Adis et al. (1998) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Attems (1914) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonato et al. (2011) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Brölemann (1896) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brolemann (1897) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1897) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Brölemann (1898) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1901) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Brölemann (1902) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1907) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1908) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1920) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Brölemann (1927) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Brolemann (1930) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande & Ribaut (1909) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande (1907) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Chalande (1909) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Chalande (1910) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Condé & Jacquemin (1962) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Condé (1953) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Demange (1955) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Desmots & Racine (2023) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Eason (1972) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Edgecombe (2004) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fanzago (1875) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Foddai & Minelli (1999) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Geoffroy & Mauriès (2017) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Gervais (1840) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Grube (1872) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffman (1977) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Hoffman (1981) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Lithobius (s. str.) Leach, 1814 (Chilopoda, Lithobiomorpha, Lithobiidae). Bulletin de la Société linnéenne de Bordeaux, 141(34(4)): 277-285.">Iorio & Geoffroy (2007) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Iorio (2009) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Iorio (2010) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Cryptops umbricus VERHOEFF, 1931 (Chilopoda, Scolopendromorpha, Cryptopidae). Bulletin de la Société linnéenne de Bordeaux, 144 (N.S.) 37(4): 471-481.">Iorio (2010) | 2 | 0,09% | 2 | 0,23% | 0 | 0% | 2 | 0,24% |
Iorio (2015) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Jeekel (1964) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Jeekel (1980) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Jeekel (2000) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Jones (1998) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jourdan & Mille (2006) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 1 | 0,12% |
Karsch (1881) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Latreille (1829) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Latzel (1884) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Latzel (1884) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Latzel (1886) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 0 | 0% |
Latzel (1886) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Latzel (1888) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Latzel (1895) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach (1814) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Legendre (1966) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Léger & Duboscq (1903) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lewis (2013) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Linné (1767) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1846) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Mauriès (1960) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Mauriès (1981) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Meinert (1868) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 1 | 0,12% |
Murienne et al. (2011) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Nguyen Duy-Jacquemin (2014) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Pereira et al. (1995) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Pereira et al. (2006) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Pereira (1999) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Quindroit (2020) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Remy (1935) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Remy (1936) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Remy (1957) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Ribaut (1909) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Ribaut (1911) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1931) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1951) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Ribaut (1954) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Rothenbühler (1899) | 2 | 0,09% | 2 | 0,23% | 1 | 0,12% | 2 | 0,24% |
Scheller (1973) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Scheller (1990) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Schubart (1958) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Schubart (1962) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Shelley (2002) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Shelley (2004) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 1 | 0,12% |
Silvestri (1903) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Silvestri (1908) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Thomas (2015) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Vandenspiegel et al. (2021) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Verhoeff (1894) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1931) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 1 | 0,12% |
Verhoeff (1935) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1936) | 2 | 0,09% | 2 | 0,23% | 2 | 0,25% | 2 | 0,24% |
Verhoeff (1943) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Aberlenc (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1984) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Alberto & Pereira (2015) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Antić & Spelda (2022) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Arthur et al. (2001) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Attems (1900) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Attems (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Attems (1953) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Balazuc & Reveillet (1980) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bergsøe & Meinert (1866) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Bigler (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Billi et al. (2011) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bonato & Minelli (2015) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Borreguero & Preisig (2023) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Brade-Birks (1920) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1889) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1892) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Brolemann (1897) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brolemann (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1932) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Brölemann (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabanillas et al. (2023) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chalande (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalande (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chamberlin (1920) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chéreau et al. (2016) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cochard (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Condé & Demange (1961) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Conde (1950) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Crabill (1960) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cupul-Magaña et al. (2021) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
De Geer (1778) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Demange & Serra (1978) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Demange (1958) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Demange (1958) | 1 | 0,05% | 1 | 0,12% | 0 | 0% | 1 | 0,12% |
Denis (1925) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Djursvoll (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Donovan (1810) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Eason & Minelli (1976) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Eason (1973) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Edgecombe & Giribet (2004) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Edgecombe (2004) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Faës (1902) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fanzago (1874) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Foddai et al. (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1990) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Geoffroy (2016) | 1 | 0,05% | 1 | 0,12% | 0 | 0% | 1 | 0,12% |
Geoffroy (2020) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Geoffroy (2021) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Golovatch et al. (2007) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Haase (1880) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Hansen (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoess & Scholl (2001) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Iorio et al. (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Iorio (2003) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Iorio (2005) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Iorio (2005) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Iorio (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Iorio (2016) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Iorio (2016) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Iorio (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jacquemin & Iorio (2017) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jacquemin & Iorio (2022) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jacquemin (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kime & Enghoff (2011) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kime & Enghoff (2021) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kos (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kronmüller (2012) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Latzel (1880) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Latzel (1884) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latzel (1887) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Latzel (1895) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach (1817) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lewis (1989) | 1 | 0,05% | 1 | 0,12% | 0 | 0% | 1 | 0,12% |
Likhitrakarn et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Livory (2022) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Loomis (1934) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Machado (1952) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Manfredi (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Matic (1959) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Matic (1980) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mauriès & Vicente (1977) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Mauriès (1988) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Mauriès (2015) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Meinert (1886) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mendes (1986) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mesibov (2009) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Muhr (1881) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nguyen & Duy-jacquemin (2000) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Noël & Geoffroy (2020) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pereira & Minelli (1993) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pereira (2013) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Peters (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Picard (1930) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pocock (1893) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Porat (1876) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Porath (1871) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rabaud (1918) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1956) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 0 | 0% |
Remy (1937) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Remy (1938) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Ribaut (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1909) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi (1790) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sahli & Pages (1978) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Scheller (2007) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Scopoli (1763) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Serra (1980) | 1 | 0,05% | 1 | 0,12% | 0 | 0% | 1 | 0,12% |
Seurat (1934) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Shaw (1794) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Shelley & Martinez-Torres (2013) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Sierwald (2009) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Silvestri (1894) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Silvestri (1898) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Silvestri (1904) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Sivestri (1896) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Spelda (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Srisonchai et al. (2018) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Ting et al. (2022) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Touroult et al. (2018) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandenspiegel & Golovatch (2007) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Verhoeff (1896) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1898) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Verhoeff (1899) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1902) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Verhoeff (1902) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1925) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Verhoeff (1932) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1934) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1935) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Verhoeff (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Villers (1789) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer & Gervais (1847) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (1867) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |