Psocodea
311 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Séguy (1944) | 962 | 45,02% | 371 | 53,85% | 371 | 55,21% | 367 | 54,21% |
Ramage (2017) | 83 | 3,88% | 81 | 11,76% | 81 | 12,05% | 79 | 11,67% |
Thornton & Smithers (1974) | 78 | 3,65% | 70 | 10,16% | 70 | 10,42% | 70 | 10,34% |
Thornton (1989) | 55 | 2,57% | 50 | 7,26% | 50 | 7,44% | 49 | 7,24% |
Beaucournu (1968) | 44 | 2,06% | 42 | 6,1% | 42 | 6,25% | 42 | 6,2% |
Price (1977) | 42 | 1,97% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Jourdan & Mille (2006) | 27 | 1,26% | 21 | 3,05% | 21 | 3,12% | 20 | 2,95% |
Rageau (1958) | 27 | 1,26% | 24 | 3,48% | 24 | 3,57% | 22 | 3,25% |
Badonnel (1977) | 26 | 1,22% | 19 | 2,76% | 19 | 2,83% | 19 | 2,81% |
Rageau (1959) | 26 | 1,22% | 24 | 3,48% | 24 | 3,57% | 24 | 3,55% |
Ferris (1932) | 25 | 1,17% | 8 | 1,16% | 8 | 1,19% | 8 | 1,18% |
Linnaeus (1758) | 25 | 1,17% | 1 | 0,15% | 1 | 0,15% | 0 | 0% |
Badonnel (1931) | 17 | 0,8% | 9 | 1,31% | 9 | 1,34% | 9 | 1,33% |
Meurgey & Ramage (2020) | 17 | 0,8% | 17 | 2,47% | 15 | 2,23% | 16 | 2,36% |
Price & Emerson (1975) | 16 | 0,75% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Meurgey (2011) | 15 | 0,7% | 13 | 1,89% | 13 | 1,93% | 11 | 1,62% |
Scopoli (1763) | 15 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Rheinwald (1968) | 14 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1989) | 13 | 0,61% | 13 | 1,89% | 9 | 1,34% | 11 | 1,62% |
Georgiev (2023) | 13 | 0,61% | 13 | 1,89% | 13 | 1,93% | 13 | 1,92% |
Turner (1976) | 12 | 0,56% | 10 | 1,45% | 10 | 1,49% | 10 | 1,48% |
Palma (2011) | 10 | 0,47% | 10 | 1,45% | 9 | 1,34% | 10 | 1,48% |
Price et al. (2003) | 10 | 0,47% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Badonnel (1981) | 9 | 0,42% | 9 | 1,31% | 6 | 0,89% | 9 | 1,33% |
Dalgleish (1972) | 9 | 0,42% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Giebel (1876) | 9 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Gustafsson & Zou (2020) | 9 | 0,42% | 9 | 1,31% | 9 | 1,34% | 9 | 1,33% |
Price & Hellenthal (1998) | 9 | 0,42% | 9 | 1,31% | 9 | 1,34% | 9 | 1,33% |
Ferris (1932) | 8 | 0,37% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Rageau (1956) | 8 | 0,37% | 8 | 1,16% | 8 | 1,19% | 7 | 1,03% |
Schrank et al. (1803) | 8 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Sychra et al. (2021) | 8 | 0,37% | 4 | 0,58% | 4 | 0,6% | 0 | 0% |
Badonnel (1938) | 7 | 0,33% | 5 | 0,73% | 5 | 0,74% | 5 | 0,74% |
Price (1971) | 7 | 0,33% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Thornton (1981) | 7 | 0,33% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Badonnel (1982) | 6 | 0,28% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Clay (1938) | 6 | 0,28% | 6 | 0,87% | 6 | 0,89% | 6 | 0,89% |
De Geer (1778) | 6 | 0,28% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Guillaumont (1978) | 6 | 0,28% | 6 | 0,87% | 6 | 0,89% | 6 | 0,89% |
Lienhard (1986) | 6 | 0,28% | 5 | 0,73% | 5 | 0,74% | 5 | 0,74% |
Lienhard (2002) | 6 | 0,28% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Neumann (1912) | 6 | 0,28% | 6 | 0,87% | 6 | 0,89% | 6 | 0,89% |
New (1973) | 6 | 0,28% | 6 | 0,87% | 6 | 0,89% | 6 | 0,89% |
Smithers & Thornton (1974) | 6 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephens (1835-1836) | 6 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1936) | 5 | 0,23% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Choe & Kim (1988) | 5 | 0,23% | 5 | 0,73% | 5 | 0,74% | 5 | 0,74% |
Ferris (1932) | 5 | 0,23% | 5 | 0,73% | 5 | 0,74% | 5 | 0,74% |
Palma & Pilgrim (1987) | 5 | 0,23% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Palma et al. (2002) | 5 | 0,23% | 5 | 0,73% | 5 | 0,74% | 5 | 0,74% |
Zlotorzycka (1964) | 5 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1975) | 4 | 0,19% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Beaucournu et al. (2008) | 4 | 0,19% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Bedford (1939) | 4 | 0,19% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Brooke & Nakamura (1998) | 4 | 0,19% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Clay & Meinertzhagen (1939) | 4 | 0,19% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Clay (1935) | 4 | 0,19% | 2 | 0,29% | 2 | 0,3% | 1 | 0,15% |
Fabricius ([1777]) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1780) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallego et al. (1987) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Garcia & Aldrete (2000) | 4 | 0,19% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Harrison (1916) | 4 | 0,19% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Jourdan (2020) | 4 | 0,19% | 4 | 0,58% | 2 | 0,3% | 4 | 0,59% |
Klockenhoff (1977) | 4 | 0,19% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Ledger (1971) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Lienhard & Smithers (2002) | 4 | 0,19% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Lienhard (1980) | 4 | 0,19% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Martin et al. (1985) | 4 | 0,19% | 4 | 0,58% | 0 | 0% | 4 | 0,59% |
Mockford (1982) | 4 | 0,19% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Piaget (1890) | 4 | 0,19% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Price & Emerson (1966) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Price et al. (2003) | 4 | 0,19% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Price et al. (2008) | 4 | 0,19% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Thompson (1938) | 4 | 0,19% | 4 | 0,58% | 4 | 0,6% | 4 | 0,59% |
Thompson (1938) | 4 | 0,19% | 4 | 0,58% | 4 | 0,6% | 3 | 0,44% |
Badonnel (1935) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1947) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Badonnel (1966) | 3 | 0,14% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Badonnel (1970) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Beaucournu & Aubert (1987) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Boisduval & Lacordaire (1835) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Cerny (1968) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Chown & Convey (2016) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Coquebert de Montbret (1799) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Darolova et al. (2001) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Eertmoed (1973) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Eichler (1982) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Fabricius (1805) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gustafsson & Bush (2017) | 3 | 0,14% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Hullé & Vernon (2021) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Lanzarot et al. (2005) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Lienhard (2012) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Linnaeus (1761) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Palma (1994) | 3 | 0,14% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Palma (2000) | 3 | 0,14% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Pearman (1946) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Perez-Jimenez et al. (1988) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Price & Beer (1963) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Price & Beer (1963) | 3 | 0,14% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Price et al. (1997) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Price (1964) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1766) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1781) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Smithers & Thornton (1990) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Soler-cruz et al. (1981) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Thompson (1939) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Thornton & Smithers (1984) | 3 | 0,14% | 3 | 0,44% | 3 | 0,45% | 3 | 0,44% |
Timmermann (1969) | 3 | 0,14% | 3 | 0,44% | 1 | 0,15% | 2 | 0,3% |
Zlotorzycka (1974) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
, 47: 129-137.">Adam (2004) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Agarwal et al. (2011) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Arnold (2005) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnold (2006) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Badonnel & Pearman (1971) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Badonnel (1943) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1963) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Badonnel (1970) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Badonnel (1976) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Badonnel (1988) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Bedford (1931) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Beugnet et al. (1996) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Blanco et al. (2001) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Blancou et al. (1987) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Brooke (2010) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Buckup (1959) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Chapman (1930) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Clay & Meinertzhagen (1941) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Clayton & Price (1984) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Cohic (1959) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
", 45: 173-178.">Costica (2003) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 0 | 0% |
Dauphin (2006) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Dik et al. (2015) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Dik et al. (2018) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Dreux & Voisin (1993) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Edwards (1960) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichler (1940) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Eichler (1941) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichler (1986) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1904) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Fabricius (1775) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fahrenholz (1916) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Faucheux (1990) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Ferris (1916) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Garcia & Aldrete (1991) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
García Aldrete (1996) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Georgiev (2023) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Gerwel (1953) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Gómez‐Díaz et al. (2008) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Goux (1948) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Grossi et al. (2014) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Zootaxa, 3377: 1-85.">Gustafsson & Olsson (2012) | 2 | 0,09% | 1 | 0,15% | 0 | 0% | 1 | 0,15% |
Gustafsson & Olsson (2017) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Gustafsson et al. (2019) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Hamard (1959) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Harrison (1937) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Hellenthal & Price (2003) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Hillgarth (1996) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Johnston & Harrison (1912) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Kadulski & Fryderyk (1996) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Keler (1937) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Klockenhoff (1980) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Kolbe (1882) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Kozina et al. (2021) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Lacroix (1919) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lienhard (1979) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Lonc & Modrzejewska (1987) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Machacek (1977) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Mateo (2006) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Meinander (1966) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Meinander (1978) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Mey (2010) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Mock & Matthyssee (1977) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Mockford (1965) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Nelson & Price (1965) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Palma & Galloway (2021) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Pap et al. (2013) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Perez et al. (2023) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Pfleger (1924) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Piaget (1888) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Piross et al. (2020) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Ramli et al. (2000) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Singh et al. (2022) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Smithers (1978) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Soler-Xruz et al. (1985) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Thompson (1935) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Thompson (1939) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Thompson (1939) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Timmermann (1955) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Zeitschrift fuer Parasitenkunde, 20: 317-334.">Timmermann (1960) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Timmermann (1966) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Uchida (1926) | 2 | 0,09% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Williams (1981) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Zlotorzycka & Danecki (1962) | 2 | 0,09% | 2 | 0,29% | 2 | 0,3% | 2 | 0,3% |
Zlotorzycka (1973) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguirre et al. (1984) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Anonymous (2011) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Badonnel (1931) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1935) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1974) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Badonnel (1989) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu (1990) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bocquillon (2016) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Btissleras (1966) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Callot (1946) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Candy et al. (2018) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 0 | 0% |
Clay & Hopkins (1958) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Clay (1951) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Dalgleish (1971) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauphin (2001) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Dauphin (2002) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Degeilh et al. (1995) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Delamare (-) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dik (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Eaton et al. (1879) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Enderlein (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1906) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Enderlein (1907) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1909) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Enderlein (1912) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1925) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
European Nucleotide Archive (2019) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Fabricius (1787) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fahrenholz (1910) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Fahrenholz (1912) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Fairn et al. (2014) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ferris (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler et al. (1984) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Frenot et al. (2005) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Geoffroy (1762) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Giebel (1866) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomez & Gallego (1988) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Gómez‐Díaz et al. (2007) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Goureau (1866) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Green & Turner (2003) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Grossi & Galloway (2022) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Grubbs et al. (2007) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Gustafsson et al. (2023) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Gustafsson (2023) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Gutierrez (1981) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Jancke (1932) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Jena et al. (2017) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Jimenez et al. (1980) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Keller (2011) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Kettle (1983) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Khokhlov (1982) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Kolbe (1885) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kristofik et al. (1996) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Lacroix (1915) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1794) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger (2019) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Lienhard (1989) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Lienhard (1990) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lienhard (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1768) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lonc & Modrzejewska (1986) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Lyal (1987) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Martin et al. (1981) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Mclachlan (1877) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclachlan (1883) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclachlan (1899) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Mey (2005) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Mey (2020) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Millan et al. (2004) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Mockford et al. (1974) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mockford (1979) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1764) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Najer et al. (2020) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Navás (1909) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nitzsch (1866) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noordijk & Belgers (2019) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ortego et al. (2007) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Pearman (1951) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petryszak et al. (1996) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Piednoir (2021) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Piross et al. (2020) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Price & Emerson (1967) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Price (1970) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Quintin (2021) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ramchurn (1980) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ribaga (1899) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ribaga (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribette (1983) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Rodriguez et al. (1979) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Rodriguez et al. (1982) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Roesler (1954) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Rostock (1876) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudow (1869) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ryan & Price (1969) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1989) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Smetana (1961) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Soler-Cruz et al. (1987) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Stenram (1956) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Sychra et al. (2014) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Thompson (1939) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Thornton & Wong (1968) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Thornton (1981) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Timmermann (1963) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Valim & Palma (2007) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Vernon & Voisin (1991) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ward (1953) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Waterston (1922) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Wilson (1934) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Zilli (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zlotorzycka & Kassner (1986) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zlotorzycka & Modrzejewska (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
(1955) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
(1976) | 1 | 0,05% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |