Symphytes de France métropolitaine
Hymenoptera Symphyta de France métropolitaine
320 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Noblecourt (2016) | 2899 | 78,29% | 722 | 92,68% | 702 | 92,61% | 705 | 92,52% |
Audinet-Serville (1823) | 235 | 6,35% | 13 | 1,67% | 13 | 1,72% | 13 | 1,71% |
Chevin & Savina (2013) | 220 | 5,94% | 181 | 23,23% | 181 | 23,88% | 175 | 22,97% |
Le Peletier (1823) | 115 | 3,11% | 6 | 0,77% | 6 | 0,79% | 6 | 0,79% |
Blank & Taeger (1998) | 110 | 2,97% | 7 | 0,9% | 7 | 0,92% | 7 | 0,92% |
Sherborn & Woodward (1901) | 109 | 2,94% | 6 | 0,77% | 6 | 0,79% | 6 | 0,79% |
Hartig (1837) | 77 | 2,08% | 4 | 0,51% | 4 | 0,53% | 4 | 0,52% |
Savina et al. (2014) | 63 | 1,7% | 45 | 5,78% | 45 | 5,94% | 43 | 5,64% |
Thomson (1871) | 58 | 1,57% | 10 | 1,28% | 10 | 1,32% | 8 | 1,05% |
Prous et al. (2014) | 51 | 1,38% | 21 | 2,7% | 21 | 2,77% | 21 | 2,76% |
Klug (1818) | 49 | 1,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Klug (1816) | 47 | 1,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Prous et al. (2017) | 45 | 1,22% | 23 | 2,95% | 23 | 3,03% | 22 | 2,89% |
Linnaeus (1758) | 43 | 1,16% | 5 | 0,64% | 5 | 0,66% | 5 | 0,66% |
Fourcroy (1785) | 42 | 1,13% | 1 | 0,13% | 1 | 0,13% | 0 | 0% |
Klug (1817) | 38 | 1,03% | 8 | 1,03% | 8 | 1,06% | 8 | 1,05% |
Hartig (1840) | 32 | 0,86% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Noblecourt (2018) | 27 | 0,73% | 6 | 0,77% | 6 | 0,79% | 6 | 0,79% |
Noblecourt (2021) | 27 | 0,73% | 10 | 1,28% | 10 | 1,32% | 10 | 1,31% |
Lacourt (1985) | 24 | 0,65% | 4 | 0,51% | 4 | 0,53% | 4 | 0,52% |
Liston et al. (2017) | 23 | 0,62% | 11 | 1,41% | 11 | 1,45% | 11 | 1,44% |
Prous et al. (2021) | 19 | 0,51% | 8 | 1,03% | 8 | 1,06% | 8 | 1,05% |
Retzius (1783) | 19 | 0,51% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Savina (2019) | 17 | 0,46% | 17 | 2,18% | 17 | 2,24% | 17 | 2,23% |
Klug (1817) | 16 | 0,43% | 4 | 0,51% | 4 | 0,53% | 4 | 0,52% |
Lacourt (2001) | 16 | 0,43% | 8 | 1,03% | 8 | 1,06% | 8 | 1,05% |
Noblecourt (2020) | 16 | 0,43% | 14 | 1,8% | 14 | 1,85% | 14 | 1,84% |
Taeger et al. (2010) | 16 | 0,43% | 5 | 0,64% | 5 | 0,66% | 5 | 0,66% |
Alonso-zarazaga & Evenhuis (2017) | 12 | 0,32% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Fabricius (1781) | 12 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 12 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirby (1882) | 12 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 12 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Béguinot (2012) | 11 | 0,3% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (1988) | 10 | 0,27% | 8 | 1,03% | 8 | 1,06% | 8 | 1,05% |
Schrank (1781) | 10 | 0,27% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brischke & Zaddach (1883) | 9 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1881) | 9 | 0,24% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin & Savina (2016) | 9 | 0,24% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Klug (1814) | 9 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Zaddach (1859) | 9 | 0,24% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Fabricius (1775) | 8 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fallén (1808) | 8 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 8 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1895) | 8 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Villaret & Foulques (1832) | 8 | 0,22% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Eversmann (1847) | 7 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Fallén (1808) | 7 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 7 | 0,19% | 1 | 0,13% | 1 | 0,13% | 0 | 0% |
Magis (2003) | 7 | 0,19% | 5 | 0,64% | 3 | 0,4% | 5 | 0,66% |
Béguinot (2017) | 6 | 0,16% | 6 | 0,77% | 6 | 0,79% | 6 | 0,79% |
Chevin (1993) | 6 | 0,16% | 6 | 0,77% | 6 | 0,79% | 6 | 0,79% |
Christ (1791) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Klug (1808) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1974) | 6 | 0,16% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (1991) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1995) | 6 | 0,16% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Lacourt (2020) | 6 | 0,16% | 6 | 0,77% | 6 | 0,79% | 6 | 0,79% |
Linnaeus (1761) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Liston & Prous (2014) | 6 | 0,16% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Liston (2007) | 6 | 0,16% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Noblecourt (2006) | 6 | 0,16% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Panzer ([1803]) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Villers (1789) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Brischke & Zaddach (1883) | 5 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevin (1997) | 5 | 0,14% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Fabricius (1804) | 5 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1892) | 5 | 0,14% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noblecourt (2019) | 5 | 0,14% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Noblecourt (2019) | 5 | 0,14% | 5 | 0,64% | 5 | 0,66% | 5 | 0,66% |
Scopoli (1763) | 5 | 0,14% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Verheyde & Meert (2020) | 5 | 0,14% | 5 | 0,64% | 5 | 0,66% | 5 | 0,66% |
Zilli (2021) | 5 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellmann (2019) | 4 | 0,11% | 4 | 0,51% | 4 | 0,53% | 4 | 0,52% |
Berland (1943) | 4 | 0,11% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1984) | 4 | 0,11% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Dahlbom (1835) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 4 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Konow (1885) | 4 | 0,11% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Konow (1886) | 4 | 0,11% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lacourt (1994) | 4 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (1998) | 4 | 0,11% | 4 | 0,51% | 4 | 0,53% | 4 | 0,52% |
Lacourt (2006) | 4 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Liston et al. (2019) | 4 | 0,11% | 4 | 0,51% | 4 | 0,53% | 4 | 0,52% |
Liston et al. (2019) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Liston (2023) | 4 | 0,11% | 4 | 0,51% | 4 | 0,53% | 4 | 0,52% |
Panzer ([1797]) | 4 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Panzer ([1801]) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi (1790) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Spinola ([1807]) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Stein (1876) | 4 | 0,11% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stephens (1835) | 4 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Tischbein (1846) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Béguinot (2021) | 3 | 0,08% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Benson (1954) | 3 | 0,08% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Berland (1947) | 3 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Blank et al. (2013) | 3 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Brischke & Zaddack (1883) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cagniard & Lemoine (2021) | 3 | 0,08% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Chevin (1982) | 3 | 0,08% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Chevin (1984) | 3 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chevin (1986) | 3 | 0,08% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Chevin (1988) | 3 | 0,08% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Costa (1859) | 3 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
. Typis Brünnischianis. 18 pp.">Dahlbom (1835) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2008) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 3 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Harris (1776-[1780]) | 3 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Jurine (1807) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Klug (1815) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1887) | 3 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Konow (1904) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1985) | 3 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (1989) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1993) | 3 | 0,08% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Lacourt (1996) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Liston et al. (2023) | 3 | 0,08% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Liston (2005) | 3 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Müller (1776) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Noblecourt (2007) | 3 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Savina & Liston (2009) | 3 | 0,08% | 3 | 0,39% | 3 | 0,4% | 3 | 0,39% |
Schrank (1766) | 3 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Spinola (1843) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Taeger & Blank (1998) | 3 | 0,08% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
André (1879-1882) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Benson (1943) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Benson (1953) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Blank (2002) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Blank (2009) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brébisson (1818) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bremi-wolf (1849) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brullé (1832) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1883) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1885) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevin (1972) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1973) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1974) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chevin (1977) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1982) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevin (1983) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chevin (1988) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauphin & Aniotsbéhère (1993) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
European Nucleotide Archive (2019) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Fallén (1808) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Förster (1854) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulet et al. (2015) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Klug (1812) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Klug (1834) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Konow (1887) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Konow (1894) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1895) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1896) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1903) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1907) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kopelke (2007) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1973) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (1980) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (1985) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (1985) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1985) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1987) | 2 | 0,05% | 2 | 0,26% | 0 | 0% | 2 | 0,26% |
Lacourt (1990) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (1996) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1996) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1998) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1998) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (2003) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (2003) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lacourt (2004) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Latreille (1812) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Leach (1817) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Liston et al. (2018) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Liston et al. (2019) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Liston (1992) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Liston (2005) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noblecourt & Vallarades (2004) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noblecourt (2023) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Olivier (1811) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1797]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1799]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1799]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1799]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1799]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1800]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1801]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1802]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1802]) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Passerin d'Entréves (1983) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pigeot (1918) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Prous et al. (2019) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ruthe (1859) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schiff et al. (2012) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Shinohara (2003) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Taeger & Schmidt (1992) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Taeger (2002) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Thomson (1870) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vallot (1836) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zaddach (1863) | 2 | 0,05% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Zaddach (1876) | 2 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Zetterstedt (1838) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Altenhofer & Zombori (1987) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Anonyme (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Baker (1994) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Beneš (1961) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Benson (1933) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Benson (1938) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Benson (1952) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Benson (1959) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Benson (1960) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Benson (1965) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brice & Hallart (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brischke (1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Buratti et al. (1987) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cameron (1875) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1880) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cameron (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1882) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin & Barbier (1980) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin & Hamon (2010) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin & Withers (2007) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin et al. (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin et al. (2009) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1971) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1986) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1987) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1988) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevin (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevin (2005) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Costa (1860) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Curtis (1824-1840) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalman (1819) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dalman (1823) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Darling (1845) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauphin (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Enslin (1916) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Enslin (1919) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Fabricius (1779) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fallén (1807) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fockeu (1888-1889) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Forster (1771) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Giraud (1857) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Giraud (1861) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gravenhorst (1807) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Haris (2000) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartig (1834) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Heim (1893) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hering (1923) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hering (1932) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Huflejt (2006) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Hurabielle (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Klug (1819) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Klug (1820) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Klug (1824) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Klug (1834) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1901) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1886) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1886) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Konow (1892) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1897) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1903) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Konow (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1904) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Konow (1905) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Konow (1906) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kriechbaumer (1869) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kriechbaumer (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1978) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lacourt (1988) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lacourt (1998) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lacourt (2006) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (2017) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lemoine & Noblecourt (2020) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lhubac (1988) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lindqvist (1952) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lindqvist (1968) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Liston et al. (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Liston et al. (2015) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Liston et al. (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Liston (1993) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Liston (1995) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Marion (1979) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Matsumura (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mocsáry (1879) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Mocsáry (1883) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mocsáry (1910) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1766) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1985) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Newman (1837) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noblecourt & Le Divelec (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Norton (1872) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pesarini & Pesarini (1984) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pesarini (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pesarini (2021) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Provancher (1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Quinlan (1974) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rohwer (1910) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Rome (2016) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Savina & Chevin (2012) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Savina (2019) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Schrank (1802) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Scopoli (1786) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Shaw et al. (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Shinohara (2000) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sichel ([1857]) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Taeger & Blank (1996) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Taeger & Viitasaari (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Taeger et al. (1998) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Telachebba (2022) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Thomson (1870) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tischbein (1853) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Viitasaari & Vikberg (1985) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Westwood (1839) | 1 | 0,03% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Zaddach (1864) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Zaddach (1866) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |