Psocodea
184 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) | 219 | 26,74% | 131 | 31,87% | 131 | 32,51% | 129 | 31,77% |
Ramage (2017) | 83 | 10,13% | 81 | 19,71% | 81 | 20,1% | 79 | 19,46% |
Thornton & Smithers (1974) | 78 | 9,52% | 70 | 17,03% | 70 | 17,37% | 70 | 17,24% |
Thornton (1989) | 55 | 6,72% | 50 | 12,17% | 50 | 12,41% | 49 | 12,07% |
Price (1977) | 42 | 5,13% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Jourdan & Mille (2006) | 27 | 3,3% | 22 | 5,35% | 22 | 5,46% | 21 | 5,17% |
Rageau (1958) | 27 | 3,3% | 24 | 5,84% | 24 | 5,96% | 22 | 5,42% |
Badonnel (1977) | 26 | 3,17% | 19 | 4,62% | 19 | 4,71% | 19 | 4,68% |
Rageau (1959) | 26 | 3,17% | 24 | 5,84% | 24 | 5,96% | 24 | 5,91% |
Ferris (1932) | 25 | 3,05% | 8 | 1,95% | 8 | 1,99% | 8 | 1,97% |
Badonnel (1931) | 17 | 2,08% | 9 | 2,19% | 9 | 2,23% | 9 | 2,22% |
Meurgey & Ramage (2020) | 17 | 2,08% | 17 | 4,14% | 15 | 3,72% | 16 | 3,94% |
Price & Emerson (1975) | 16 | 1,95% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Meurgey (2011) | 15 | 1,83% | 13 | 3,16% | 13 | 3,23% | 11 | 2,71% |
Badonnel (1989) | 13 | 1,59% | 13 | 3,16% | 9 | 2,23% | 11 | 2,71% |
Georgiev (2023) | 13 | 1,59% | 13 | 3,16% | 13 | 3,23% | 13 | 3,2% |
Turner (1976) | 12 | 1,47% | 10 | 2,43% | 10 | 2,48% | 10 | 2,46% |
Palma (2011) | 10 | 1,22% | 10 | 2,43% | 9 | 2,23% | 10 | 2,46% |
Badonnel (1981) | 9 | 1,1% | 9 | 2,19% | 6 | 1,49% | 9 | 2,22% |
Giebel (1876) | 9 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gustafsson & Zou (2020) | 9 | 1,1% | 9 | 2,19% | 9 | 2,23% | 9 | 2,22% |
Ferris (1932) | 8 | 0,98% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Rageau (1956) | 8 | 0,98% | 8 | 1,95% | 8 | 1,99% | 7 | 1,72% |
Badonnel (1938) | 7 | 0,85% | 5 | 1,22% | 5 | 1,24% | 5 | 1,23% |
Linnaeus (1758) | 7 | 0,85% | 1 | 0,24% | 1 | 0,25% | 0 | 0% |
Price (1971) | 7 | 0,85% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Thornton (1981) | 7 | 0,85% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Badonnel (1982) | 6 | 0,73% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Guillaumont (1978) | 6 | 0,73% | 6 | 1,46% | 6 | 1,49% | 6 | 1,48% |
Lienhard (1986) | 6 | 0,73% | 5 | 1,22% | 5 | 1,24% | 5 | 1,23% |
Lienhard (2002) | 6 | 0,73% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Neumann (1912) | 6 | 0,73% | 6 | 1,46% | 6 | 1,49% | 6 | 1,48% |
New (1973) | 6 | 0,73% | 6 | 1,46% | 6 | 1,49% | 6 | 1,48% |
Smithers & Thornton (1974) | 6 | 0,73% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephens (1835-1836) | 6 | 0,73% | 0 | 0% | 0 | 0% | 0 | 0% |
Sychra et al. (2021) | 6 | 0,73% | 4 | 0,97% | 4 | 0,99% | 0 | 0% |
Badonnel (1936) | 5 | 0,61% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Ferris (1932) | 5 | 0,61% | 5 | 1,22% | 5 | 1,24% | 5 | 1,23% |
Palma et al. (2002) | 5 | 0,61% | 5 | 1,22% | 5 | 1,24% | 5 | 1,23% |
Beaucournu et al. (2008) | 4 | 0,49% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Bedford (1939) | 4 | 0,49% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Garcia & Aldrete (2000) | 4 | 0,49% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Jourdan (2020) | 4 | 0,49% | 4 | 0,97% | 2 | 0,5% | 4 | 0,99% |
Klockenhoff (1977) | 4 | 0,49% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Lienhard & Smithers (2002) | 4 | 0,49% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Lienhard (1980) | 4 | 0,49% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Mockford (1982) | 4 | 0,49% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Piaget (1890) | 4 | 0,49% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Price & Emerson (1966) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Price & Hellenthal (1998) | 4 | 0,49% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Price et al. (2008) | 4 | 0,49% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Thompson (1938) | 4 | 0,49% | 4 | 0,97% | 4 | 0,99% | 3 | 0,74% |
Thompson (1938) | 4 | 0,49% | 4 | 0,97% | 4 | 0,99% | 4 | 0,99% |
Zlotorzycka (1964) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1935) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1947) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Badonnel (1966) | 3 | 0,37% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Badonnel (1970) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Badonnel (1975) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu & Aubert (1987) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Boisduval & Lacordaire (1835) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Chown & Convey (2016) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Coquebert de Montbret (1799) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Eertmoed (1973) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Hullé & Vernon (2021) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Lienhard (2012) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Palma (1994) | 3 | 0,37% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Pearman (1946) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Price & Beer (1963) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Price & Beer (1963) | 3 | 0,37% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Smithers & Thornton (1990) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Thompson (1939) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Thornton & Smithers (1984) | 3 | 0,37% | 3 | 0,73% | 3 | 0,74% | 3 | 0,74% |
Badonnel & Pearman (1971) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Badonnel (1943) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1970) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Badonnel (1976) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Badonnel (1988) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Beugnet et al. (1996) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Blancou et al. (1987) | 2 | 0,24% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Buckup (1959) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Chapman (1930) | 2 | 0,24% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Clay & Meinertzhagen (1941) | 2 | 0,24% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Cohic (1959) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Dauphin (2006) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Dik et al. (2018) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Dreux & Voisin (1993) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Edwards (1960) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichler (1941) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichler (1986) | 2 | 0,24% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Fahrenholz (1916) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Ferris (1916) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Garcia & Aldrete (1991) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
García Aldrete (1996) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Georgiev (2023) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Hamard (1959) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Harrison (1916) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Hellenthal & Price (2003) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Lacroix (1919) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Lienhard (1979) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Linnaeus (1761) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Meinander (1978) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Mey (2010) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Mockford (1965) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Palma & Galloway (2021) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Piaget (1888) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Schrank et al. (1803) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1781) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Smithers (1978) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Thompson (1939) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Thompson (1939) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Zeitschrift fuer Parasitenkunde, 20: 317-334.">Timmermann (1960) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Uchida (1926) | 2 | 0,24% | 2 | 0,49% | 2 | 0,5% | 2 | 0,49% |
Anonymous (2011) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Badonnel (1931) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1935) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1974) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Badonnel (1989) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu (1990) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Bocquillon (2016) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Candy et al. (2018) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 0 | 0% |
Clay (1951) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Dauphin (2001) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Dauphin (2002) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Delamare (-) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Eaton et al. (1879) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Enderlein (1903) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1906) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Enderlein (1907) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1909) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Enderlein (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1925) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
European Nucleotide Archive (2019) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Fabricius ([1777]) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1805) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferris (1933) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Giebel (1866) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Goureau (1866) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Gutierrez (1981) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Jancke (1932) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Keller (2011) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Klockenhoff (1980) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Kolbe (1882) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolbe (1885) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacroix (1915) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1794) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger (2019) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Lienhard (1989) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Lienhard (1990) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lienhard (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1768) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclachlan (1877) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclachlan (1883) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclachlan (1899) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Mey (2005) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Millan et al. (2004) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Mockford et al. (1974) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mockford (1979) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1764) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Noordijk & Belgers (2019) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Pearman (1951) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Piednoir (2021) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Quintin (2021) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Ribaga (1899) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Ribaga (1904) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribette (1983) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Roesler (1954) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Rostock (1876) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ryan & Price (1969) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1989) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Schrank (1766) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Thompson (1939) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Thornton & Wong (1968) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Thornton (1981) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Timmermann (1963) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Valim & Palma (2007) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Vernon & Voisin (1991) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Waterston (1922) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Yokoyama (2013) | 1 | 0,12% | 1 | 0,24% | 1 | 0,25% | 1 | 0,25% |
Zilli (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |