Chironomidae de France métropolitaine
207 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Moubayed-Breil et al. (2017) | 170 | 7,45% | 162 | 19,38% | 160 | 19,28% | 161 | 19,4% |
Moubayed-Breil & Ashe (2016) | 108 | 4,73% | 108 | 12,92% | 107 | 12,89% | 108 | 13,01% |
Edwards (1929) | 72 | 3,16% | 9 | 1,08% | 9 | 1,08% | 9 | 1,08% |
Goetghebuer (1921) | 40 | 1,75% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Meigen (1818) | 26 | 1,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Moubayed-Breil (2007) | 26 | 1,14% | 22 | 2,63% | 22 | 2,65% | 22 | 2,65% |
Moubayed-breil & Ashe (2018) | 25 | 1,1% | 25 | 2,99% | 25 | 3,01% | 25 | 3,01% |
Kieffer (1925) | 22 | 0,96% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Brundin (1947) | 19 | 0,83% | 5 | 0,6% | 5 | 0,6% | 5 | 0,6% |
Kieffer (1911) | 15 | 0,66% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Kieffer (1911) | 14 | 0,61% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kieffer (1918) | 13 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Meigen (1830) | 13 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Goetghebuer (1934) | 11 | 0,48% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil (2020) | 11 | 0,48% | 11 | 1,32% | 11 | 1,33% | 11 | 1,33% |
Stur & Ekrem (2006) | 11 | 0,48% | 9 | 1,08% | 9 | 1,08% | 9 | 1,08% |
Chandler (2013) | 10 | 0,44% | 7 | 0,84% | 7 | 0,84% | 7 | 0,84% |
Goetghebuer (1928) | 10 | 0,44% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Kieffer (1913) | 10 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Moubayed et al. (2019) | 10 | 0,44% | 10 | 1,2% | 10 | 1,2% | 10 | 1,2% |
Meigen (1804) | 9 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Reiss (1969) | 9 | 0,39% | 9 | 1,08% | 9 | 1,08% | 9 | 1,08% |
Brundin (1949) | 8 | 0,35% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Brundin (1956) | 8 | 0,35% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Kieffer (1921) | 8 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Kruseman (1933) | 8 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Michiels & Spies (2002) | 8 | 0,35% | 7 | 0,84% | 7 | 0,84% | 7 | 0,84% |
Goetghebuer (1913) | 7 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Goetghebuer (1938) | 7 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1915) | 7 | 0,31% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Malloch (1915) | 7 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Withers (2014) | 7 | 0,31% | 7 | 0,84% | 7 | 0,84% | 7 | 0,84% |
Johannsen (1905) | 6 | 0,26% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kieffer (1922) | 6 | 0,26% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed & Langton (2019) | 6 | 0,26% | 6 | 0,72% | 6 | 0,72% | 6 | 0,72% |
Moubayed (2022) | 6 | 0,26% | 6 | 0,72% | 6 | 0,72% | 6 | 0,72% |
Moubayed-breil & Ashe (2018) | 6 | 0,26% | 6 | 0,72% | 6 | 0,72% | 6 | 0,72% |
Moubayed-Breil & Orsini (2016) | 6 | 0,26% | 6 | 0,72% | 6 | 0,72% | 6 | 0,72% |
Moubayed-Breil et al. (2012) | 6 | 0,26% | 5 | 0,6% | 5 | 0,6% | 5 | 0,6% |
Moubayed-Breil (2017) | 6 | 0,26% | 6 | 0,72% | 6 | 0,72% | 6 | 0,72% |
Saether (1990) | 6 | 0,26% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Serra-Tosio (1984) | 6 | 0,26% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Tissot et al. (2021) | 6 | 0,26% | 6 | 0,72% | 6 | 0,72% | 6 | 0,72% |
Zetterstedt (1838) | 6 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer & Thienemann (1909) | 5 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1922) | 5 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Meigen (1838) | 5 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Moubayed-Breil (2016) | 5 | 0,22% | 5 | 0,6% | 5 | 0,6% | 5 | 0,6% |
Zetterstedt (1850) | 5 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Caspers & Reiss (1989) | 4 | 0,18% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chevrel (1904) | 4 | 0,18% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Ferrington & Saether (2011) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Goetghebuer (1921) | 4 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Langton & Moubayed (2001) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Langton (2012) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Moubayed & Tissot (2023) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Moubayed et al. (2022) | 4 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Moubayed-Breil & Ashe (2019) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Moubayed-Breil & Dominici (2019) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Moubayed-breil (2007) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Moubayed-Breil (2018) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Moubayed-Breil (2020) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Moubayed-Breil (2020) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Pagast (1931) | 4 | 0,18% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pagast (1947) | 4 | 0,18% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Serra-tosio (1964) | 4 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Serra-tosio (1989) | 4 | 0,18% | 4 | 0,48% | 4 | 0,48% | 4 | 0,48% |
Binge (1970) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Casas & Langton (2001) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Fabricius (1805) | 3 | 0,13% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Freeman (1955) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Goetghebuer (1935) | 3 | 0,13% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Goetghebuer (1936) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Goetghebuer (1944) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaiser et al. (2021) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Kieffer (1912) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1913) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Lehmann (1969) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Linnaeus (1758) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Moubayed (1990) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Moubayed (1991) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Moubayed-Breil & Bitušík (2019) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Moubayed-breil & Dia (2017) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Moubayed-Breil (2013) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Moubayed-Breil (2016) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Rossaro & Delettre (1992) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Serra-tosio (1964) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Serra-Tosio (1972) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Verneanx (1970) | 3 | 0,13% | 3 | 0,36% | 3 | 0,36% | 3 | 0,36% |
Abreu (1918) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Albu (1960) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ashe & O'connor (2012) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Ashe & O'connor (2015) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Chevrel (1903) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cobo et al. (1995) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Cranston & Saether (1982) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Cranston & Saether (1986) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Eaton (1875) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Edwards (1928) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Epler (1987) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Fabricius (1787) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fittkau (1954) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Freeman (1957) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Goetghebuer (1922) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Goetghebuer (1928) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Goetghebuer (1934) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Goetghebuer (1942) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2018) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Kieffer (1906) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kieffer (1920) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1922) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1924) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lenz (1959) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Lenz (1960) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lindner (1960) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Makarchenko & Hansen (2022) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Makarchenko et al. (2022) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed & Breil & Tissot (2019) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed & Guisset (2022) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed & Langton (1999) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil & Ashe (2013) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil & Ashe (2015) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil & Ashe (2015) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil & Ashe (2018) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil & Coppa (2018) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil & Garrigue (2014) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-breil & Garrigue (2021) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil & Gaultier (2018) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-breil & Langton (1996) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Moubayed-breil & Langton (2020) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil et al. (2012) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil et al. (2012) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil (2013) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil (2013) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil (2015) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil (2017) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Moubayed-Breil (2020) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Murray & Fittkau (1985) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Namayandeh et al. (2020) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Oyewo & Saether (2008) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Reiss (1988) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Rossaro et al. (2012) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Sasa (1983) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Saunders (1930) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Serra-Tosio (1970) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Shilova (1957) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Spies & Saether (2004) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Stora (1939) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verneaux (1969) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Wang & Saether (2011) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Ashe & Cranston (1991) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewarumez et al. (2011) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Edwards (1922) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Edwards (1924) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Edwards (1924) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Edwards (1926) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ekrem (2006) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Evenhuis (1989) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fabricius (1775) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1781) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Godet et al. (2010) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Haliday (1855) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Hullé & Vernon (2021) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Johannsen (1932) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer & Thienemann (1908) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1898) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kieffer (1914) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1915) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1916) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1919) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1922) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1924) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1925) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Labat & Serrette (2015) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Langton & Garcia (2000) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Langton (2005) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lin et al. (2018) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Linnaeus (1761) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Macquart (1834) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1919) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Moubayed-Breil & Ashe (2011) | 1 | 0,04% | 1 | 0,12% | 0 | 0% | 1 | 0,12% |
Moubayed-Breil & Ashe (2015) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Moubayed-Breil & Ashe (2016) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Moubayed-breil & Ashe (2016) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Moubayed-Breil & Lounaci (2013) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Palmen (1959) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Potthast (1914) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Reiss (1991) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Rossaro & Lencioni (2015) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Rossaro & Lencioni (2015) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Saether & Spies (2013) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Saether & Wang (1995) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Silva (2023) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Spies & Dettinger-Klemm (2015) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Strenzke & Thienemanh (1942) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Strobl (1900) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Stur & Saether (2004) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Thomas (1981) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Tokunaga (1939) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1920) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Withers (2007) | 1 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Wulker (1959) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |