Tuniciers
Tunicata
219 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Monniot (2007) | 289 | 13,44% | 239 | 29,11% | 238 | 29,13% | 237 | 28,97% |
Bay-nouailhat & Bay-nouailhat (2020) | 196 | 9,12% | 196 | 23,87% | 196 | 23,99% | 196 | 23,96% |
Monniot & Monniot (1983) | 100 | 4,65% | 87 | 10,6% | 87 | 10,65% | 87 | 10,64% |
Monniot & Monniot (1987) | 96 | 4,47% | 84 | 10,23% | 84 | 10,28% | 82 | 10,02% |
Ifremer (2009) | 78 | 3,63% | 73 | 8,89% | 73 | 8,94% | 73 | 8,92% |
Monniot & Monniot (1991) | 66 | 3,07% | 60 | 7,31% | 60 | 7,34% | 60 | 7,33% |
Giard (1872) | 58 | 2,7% | 6 | 0,73% | 6 | 0,73% | 6 | 0,73% |
Milne-Edwards (1841) | 58 | 2,7% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Kott (2001) | 49 | 2,28% | 44 | 5,36% | 44 | 5,39% | 44 | 5,38% |
Monniot (2016) | 45 | 2,09% | 40 | 4,87% | 40 | 4,9% | 40 | 4,89% |
Lafargue & Vasseur (1989) | 41 | 1,91% | 29 | 3,53% | 29 | 3,55% | 27 | 3,3% |
Monniot et al. (2011) | 38 | 1,77% | 38 | 4,63% | 38 | 4,65% | 38 | 4,65% |
Monniot (1978) | 38 | 1,77% | 34 | 4,14% | 34 | 4,16% | 34 | 4,16% |
Godet et al. (2010) | 32 | 1,49% | 29 | 3,53% | 29 | 3,55% | 29 | 3,55% |
Gravier (1955) | 31 | 1,44% | 17 | 2,07% | 17 | 2,08% | 16 | 1,96% |
Monniot & Gaill (1978) | 30 | 1,4% | 24 | 2,92% | 24 | 2,94% | 24 | 2,93% |
Monniot & Monniot (1974) | 29 | 1,35% | 22 | 2,68% | 22 | 2,69% | 22 | 2,69% |
Monniot (1988) | 29 | 1,35% | 22 | 2,68% | 22 | 2,69% | 22 | 2,69% |
Monniot (1983) | 28 | 1,3% | 16 | 1,95% | 16 | 1,96% | 16 | 1,96% |
Uicn et al. (2019) | 28 | 1,3% | 27 | 3,29% | 27 | 3,3% | 20 | 2,44% |
Monniot & Monniot (1985) | 27 | 1,26% | 18 | 2,19% | 18 | 2,2% | 18 | 2,2% |
Breton (2014) | 25 | 1,16% | 25 | 3,05% | 25 | 3,06% | 25 | 3,06% |
Monniot & Monniot (1974) | 24 | 1,12% | 19 | 2,31% | 19 | 2,33% | 19 | 2,32% |
Nelson-Smith et al. (2014) | 24 | 1,12% | 20 | 2,44% | 20 | 2,45% | 20 | 2,44% |
Monniot (1983) | 20 | 0,93% | 17 | 2,07% | 17 | 2,08% | 16 | 1,96% |
Poupin et al. (1999) | 20 | 0,93% | 13 | 1,58% | 13 | 1,59% | 13 | 1,59% |
Arnaud (1974) | 19 | 0,88% | 17 | 2,07% | 17 | 2,08% | 17 | 2,08% |
Monniot (2018) | 19 | 0,88% | 18 | 2,19% | 18 | 2,2% | 18 | 2,2% |
Monniot (1983) | 18 | 0,84% | 17 | 2,07% | 17 | 2,08% | 16 | 1,96% |
Monniot (1983) | 17 | 0,79% | 13 | 1,58% | 13 | 1,59% | 13 | 1,59% |
Monniot & Dettai (2015) | 15 | 0,7% | 9 | 1,1% | 9 | 1,1% | 9 | 1,1% |
Bourcier (1988) | 14 | 0,65% | 13 | 1,58% | 13 | 1,59% | 13 | 1,59% |
Harant (1924) | 14 | 0,65% | 7 | 0,85% | 7 | 0,86% | 7 | 0,86% |
Monniot & Monniot (1984) | 13 | 0,6% | 9 | 1,1% | 9 | 1,1% | 9 | 1,1% |
Monniot & Monniot (2003) | 13 | 0,6% | 12 | 1,46% | 12 | 1,47% | 12 | 1,47% |
Monniot (1969) | 13 | 0,6% | 10 | 1,22% | 10 | 1,22% | 10 | 1,22% |
Monniot (1983) | 13 | 0,6% | 13 | 1,58% | 13 | 1,59% | 13 | 1,59% |
Monniot (1989) | 13 | 0,6% | 13 | 1,58% | 13 | 1,59% | 13 | 1,59% |
Goulletquer (2016) | 12 | 0,56% | 12 | 1,46% | 12 | 1,47% | 12 | 1,47% |
Monniot (1994) | 12 | 0,56% | 11 | 1,34% | 11 | 1,35% | 11 | 1,34% |
Monniot (2018) | 12 | 0,56% | 12 | 1,46% | 12 | 1,47% | 12 | 1,47% |
Monniot & Monniot (1977) | 11 | 0,51% | 9 | 1,1% | 9 | 1,1% | 9 | 1,1% |
Monniot & Monniot (1977) | 11 | 0,51% | 11 | 1,34% | 11 | 1,35% | 11 | 1,34% |
Caziot (1921) | 10 | 0,47% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Monniot (1992) | 10 | 0,47% | 10 | 1,22% | 10 | 1,22% | 10 | 1,22% |
Monniot (1969) | 9 | 0,42% | 9 | 1,1% | 9 | 1,1% | 9 | 1,1% |
Monniot (1984) | 9 | 0,42% | 8 | 0,97% | 6 | 0,73% | 8 | 0,98% |
Monniot & Monniot (2008) | 8 | 0,37% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Monniot (2021) | 8 | 0,37% | 8 | 0,97% | 8 | 0,98% | 8 | 0,98% |
Monniot (1983) | 7 | 0,33% | 6 | 0,73% | 6 | 0,73% | 6 | 0,73% |
Monniot (2018) | 7 | 0,33% | 7 | 0,85% | 7 | 0,86% | 6 | 0,73% |
Pagano (2009) | 7 | 0,33% | 7 | 0,85% | 5 | 0,61% | 6 | 0,73% |
Questel (2020) | 7 | 0,33% | 6 | 0,73% | 6 | 0,73% | 6 | 0,73% |
MGnify (2017) | 6 | 0,28% | 6 | 0,73% | 6 | 0,73% | 6 | 0,73% |
Monniot (1994) | 6 | 0,28% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Monniot (2007) | 6 | 0,28% | 6 | 0,73% | 6 | 0,73% | 6 | 0,73% |
Renon & Lefèvre (1985) | 6 | 0,28% | 5 | 0,61% | 4 | 0,49% | 5 | 0,61% |
Canu (1891) | 5 | 0,23% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Dewarumez et al. (2011) | 5 | 0,23% | 5 | 0,61% | 5 | 0,61% | 5 | 0,61% |
Monniot & Monniot (1973) | 5 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Monniot (2022) | 5 | 0,23% | 5 | 0,61% | 5 | 0,61% | 5 | 0,61% |
Sellier et al. (2016) | 5 | 0,23% | 5 | 0,61% | 5 | 0,61% | 5 | 0,61% |
Fourt et al. (2017) | 4 | 0,19% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Medioni (1970) | 4 | 0,19% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Millar (1977) | 4 | 0,19% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Monniot (1990) | 4 | 0,19% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Schleyer et al. (2016) | 4 | 0,19% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Sentz‐Braconnot (1966) | 4 | 0,19% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
Shenkar & Swalla (2010) | 4 | 0,19% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Breton (2005) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Brunetti (1991) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Caullery (1914) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Chatton & Brément (1909) | 3 | 0,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fenaux (1960) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Fenaux (1961) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Fenaux (1992) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Forsskål & Niebuhr (1775) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutt et al. (2007) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Harant (1930) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Kim & Boxshall (2020) | 3 | 0,14% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Lafargue & Wahl (1987) | 3 | 0,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lahille (1890) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Legendre (1922) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 3 | 0,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot & Debitus (2015) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Monniot & Monniot (1987) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Monniot & Monniot (2006) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Monniot (comm. pers., 2012) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Monniot (1970) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Monniot (1978) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Monniot (2011) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Monniot (2013) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Olivier et al. (2015) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Ordóñez et al. (2016) | 3 | 0,14% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Selys-Longchamps (1916) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Sluiter (1906) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Vernières (1934) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Vogt (1854) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Weinstein (1961) | 3 | 0,14% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
Australian Museum (2020) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Bay-Nouailhat et al. (2020) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Bocquet (1953) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bonnet & Lotufo (2015) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Bouzon et al. (2014) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Braconnot et al. (1988) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Brément (1912) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brement (1913) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Brunetti et al. (2015) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Caullery (1927) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chatton (1912) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Dauvin et al. (1991) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Davis & Davis (2009) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Dolan (2014) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Fenaux (1976) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Fol (1872) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Glemarec & Monniot (1966) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Harant (1927) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Herdman (1882) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Herdman (1888) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Koechlin (1977) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Korotneff (1891) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Kott (1984) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Lafargue (1975) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Martin (2011) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Maurice (1888) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Médioni (1968) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Millar & Goodbody (1974) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Rep, 30: 1-160.">Millar (1960) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Monniot & Monniot (1984) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot & Monniot (1984) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot & Monniot (1990) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
In: Crosnier, A. [Ed]. Résultats des Campagnes MUSORSTOM, Volume 21. Mémoires du Muséum national d'Histoire naturelle. Série A, Zoologie, 184: 703-721.">Monniot & Monniot (2000) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot (1970) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Monniot (1994) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Monniot (2002) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Monniot (2016) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Müller (1776) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pearman et al. (2020) | 2 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pérez-Portela et al. (2007) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Pineda et al. (2011) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Pruvot-Fol (1929) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Questel & Le Quellec (2012) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Rocha & Monniot (1993) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Sluiter (1904) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Turon et al. (2020) | 2 | 0,09% | 2 | 0,24% | 2 | 0,24% | 2 | 0,24% |
Alder (1863) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bishop et al. (2013) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bishop et al. (2015) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bone et al. (1991) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Borgne & Moll (1987) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Brunetti & Mastrototaro (2004) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Brunetti (2007) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Busch (1851) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Canu (1892) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chatton & Séguéla (1936) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chevaldonné et al. (2015) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cuvier (1804) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Davis & Davis (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Delle & Chiaje (1828) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupont et al. (2007) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Eldredge (1967) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fauré-fremiet (1910) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Forskål (1775) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fougue (1961) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gaudy & Thomassin (2006) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Hartmeyer (1903) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Heller (1878) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Herdman (1883) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Herdman (1884) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Herdman (1886) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hipeau-Jacquotte & Coste (1989) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kim & Boxshall (2021) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kott (1977) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lamare (2012) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lambert (2009) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Langherans (1880) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lizé (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lizé (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lohmann (1899) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
, 7: 181-260.">Michaelsen (1904) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Michaelsen (1921) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Michel et al. (1971) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot & Monniot (1970) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot & Monniot (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot & Monniot (1991) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot & Monniot (2001) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot & Tatián (2020) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot et al. (1991) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot (1961) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot (1971) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot (1972) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot (1974) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot (1981) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot (1988) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot (1997) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Monniot (2016) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Nival et al. (1972) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Nydam & Harrison (2007) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Ono & Moteki (2016) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Ooishi (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pallas (1766) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1774) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Péron (1804) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Richer de Forges et al. (2005) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Ritter (1905) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Roupsard & Caillot (2018) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Salfi (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Savigny (1816) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Stimpson (1852) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tokioka (1954) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Tokioka (1967) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Traustedt (1881) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Uljanin (1884) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ulman et al. (2017) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Van Name (1918) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Varela et al. (2007) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Zirpolo (1925) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |