Psocodea de métropole
254 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) | 947 | 51,44% | 371 | 74,8% | 371 | 76,65% | 367 | 75,36% |
Beaucournu (1968) | 44 | 2,39% | 42 | 8,47% | 42 | 8,68% | 42 | 8,62% |
Price (1977) | 42 | 2,28% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Linnaeus (1758) | 24 | 1,3% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
Rageau (1958) | 19 | 1,03% | 18 | 3,63% | 18 | 3,72% | 16 | 3,29% |
Ramage (2017) | 19 | 1,03% | 18 | 3,63% | 18 | 3,72% | 17 | 3,49% |
Badonnel (1931) | 17 | 0,92% | 9 | 1,81% | 9 | 1,86% | 9 | 1,85% |
Jourdan & Mille (2006) | 17 | 0,92% | 12 | 2,42% | 12 | 2,48% | 11 | 2,26% |
Price & Emerson (1975) | 16 | 0,87% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Rageau (1959) | 14 | 0,76% | 13 | 2,62% | 13 | 2,69% | 13 | 2,67% |
Rheinwald (1968) | 14 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 14 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Price et al. (2003) | 10 | 0,54% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Dalgleish (1972) | 9 | 0,49% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Gustafsson & Zou (2020) | 9 | 0,49% | 9 | 1,81% | 9 | 1,86% | 9 | 1,85% |
Schrank et al. (1803) | 8 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Sychra et al. (2021) | 8 | 0,43% | 4 | 0,81% | 4 | 0,83% | 0 | 0% |
Badonnel (1938) | 7 | 0,38% | 5 | 1,01% | 5 | 1,03% | 5 | 1,03% |
Price (1971) | 7 | 0,38% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Badonnel (1982) | 6 | 0,33% | 4 | 0,81% | 4 | 0,83% | 4 | 0,82% |
Clay (1938) | 6 | 0,33% | 6 | 1,21% | 6 | 1,24% | 6 | 1,23% |
De Geer (1778) | 6 | 0,33% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Guillaumont (1978) | 6 | 0,33% | 6 | 1,21% | 6 | 1,24% | 6 | 1,23% |
Lienhard (1986) | 6 | 0,33% | 5 | 1,01% | 5 | 1,03% | 5 | 1,03% |
Lienhard (2002) | 6 | 0,33% | 4 | 0,81% | 4 | 0,83% | 4 | 0,82% |
Neumann (1912) | 6 | 0,33% | 6 | 1,21% | 6 | 1,24% | 6 | 1,23% |
Price & Hellenthal (1998) | 6 | 0,33% | 6 | 1,21% | 6 | 1,24% | 6 | 1,23% |
Rageau (1956) | 6 | 0,33% | 6 | 1,21% | 6 | 1,24% | 5 | 1,03% |
Stephens (1835-1836) | 6 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1936) | 5 | 0,27% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Choe & Kim (1988) | 5 | 0,27% | 5 | 1,01% | 5 | 1,03% | 5 | 1,03% |
Palma & Pilgrim (1987) | 5 | 0,27% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Palma et al. (2002) | 5 | 0,27% | 5 | 1,01% | 5 | 1,03% | 5 | 1,03% |
Zlotorzycka (1964) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1975) | 4 | 0,22% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Beaucournu et al. (2008) | 4 | 0,22% | 4 | 0,81% | 4 | 0,83% | 4 | 0,82% |
Bedford (1939) | 4 | 0,22% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Brooke & Nakamura (1998) | 4 | 0,22% | 4 | 0,81% | 4 | 0,83% | 4 | 0,82% |
Clay & Meinertzhagen (1939) | 4 | 0,22% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Clay (1935) | 4 | 0,22% | 2 | 0,4% | 2 | 0,41% | 1 | 0,21% |
Fabricius ([1777]) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1780) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallego et al. (1987) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Giebel (1876) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Harrison (1916) | 4 | 0,22% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Ledger (1971) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lienhard (1980) | 4 | 0,22% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Martin et al. (1985) | 4 | 0,22% | 4 | 0,81% | 0 | 0% | 4 | 0,82% |
Piaget (1890) | 4 | 0,22% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Price & Emerson (1966) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Price et al. (2003) | 4 | 0,22% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Price et al. (2008) | 4 | 0,22% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Thompson (1938) | 4 | 0,22% | 4 | 0,81% | 4 | 0,83% | 3 | 0,62% |
Badonnel (1935) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1970) | 3 | 0,16% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Badonnel (1977) | 3 | 0,16% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Beaucournu & Aubert (1987) | 3 | 0,16% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Boisduval & Lacordaire (1835) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cerny (1968) | 3 | 0,16% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Coquebert de Montbret (1799) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Darolova et al. (2001) | 3 | 0,16% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Eichler (1982) | 3 | 0,16% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Fabricius (1805) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gustafsson & Bush (2017) | 3 | 0,16% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Lanzarot et al. (2005) | 3 | 0,16% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Linnaeus (1761) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Palma (2000) | 3 | 0,16% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Pearman (1946) | 3 | 0,16% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Perez-Jimenez et al. (1988) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Price & Beer (1963) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Price et al. (1997) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Price (1964) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1766) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Soler-cruz et al. (1981) | 3 | 0,16% | 3 | 0,6% | 3 | 0,62% | 3 | 0,62% |
Timmermann (1969) | 3 | 0,16% | 3 | 0,6% | 1 | 0,21% | 2 | 0,41% |
Zlotorzycka (1974) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
, 47: 129-137.">Adam (2004) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Agarwal et al. (2011) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Arnold (2005) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnold (2006) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Badonnel (1943) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1963) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Bedford (1931) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanco et al. (2001) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Blancou et al. (1987) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Brooke (2010) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Buckup (1959) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Chapman (1930) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Chown & Convey (2016) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Clay & Meinertzhagen (1941) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Clayton & Price (1984) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
", 45: 173-178.">Costica (2003) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 0 | 0% |
Dauphin (2006) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Dik et al. (2015) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dik et al. (2018) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Edwards (1960) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichler (1940) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Eichler (1941) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Eichler (1986) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1904) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Fabricius (1775) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fahrenholz (1916) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Faucheux (1990) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Ferris (1916) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerwel (1953) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gómez‐Díaz et al. (2008) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Goux (1948) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Grossi et al. (2014) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Zootaxa, 3377: 1-85.">Gustafsson & Olsson (2012) | 2 | 0,11% | 1 | 0,2% | 0 | 0% | 1 | 0,21% |
Gustafsson & Olsson (2017) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Gustafsson et al. (2019) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Hamard (1959) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Harrison (1937) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Hillgarth (1996) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Johnston & Harrison (1912) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2020) | 2 | 0,11% | 2 | 0,4% | 0 | 0% | 2 | 0,41% |
Kadulski & Fryderyk (1996) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Keler (1937) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Klockenhoff (1980) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Kolbe (1882) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kozina et al. (2021) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Lacroix (1919) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lienhard (1979) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Lonc & Modrzejewska (1987) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Machacek (1977) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mateo (2006) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Meinander (1966) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Meinander (1978) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Mock & Matthyssee (1977) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Nelson & Price (1965) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Palma & Galloway (2021) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pap et al. (2013) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Perez et al. (2023) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Pfleger (1924) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Piaget (1888) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Piross et al. (2020) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Ramli et al. (2000) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Singh et al. (2022) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Smithers (1978) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Soler-Xruz et al. (1985) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Thompson (1935) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Timmermann (1955) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Timmermann (1966) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Uchida (1926) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Williams (1981) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Zlotorzycka & Danecki (1962) | 2 | 0,11% | 2 | 0,4% | 2 | 0,41% | 2 | 0,41% |
Zlotorzycka (1973) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguirre et al. (1984) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Anonymous (2011) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Badonnel (1989) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu (1990) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Bocquillon (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Btissleras (1966) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Callot (1946) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Candy et al. (2018) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 0 | 0% |
Clay & Hopkins (1958) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Clay (1951) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Dalgleish (1971) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauphin (2001) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Dauphin (2002) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Degeilh et al. (1995) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Delamare (-) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dik (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1909) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Enderlein (1912) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1925) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
European Nucleotide Archive (2019) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Fahrenholz (1912) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Fairn et al. (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ferris (1932) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ferris (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler et al. (1984) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Gómez‐Díaz et al. (2007) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Goureau (1866) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Green & Turner (2003) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Grossi & Galloway (2022) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Grubbs et al. (2007) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Gustafsson et al. (2023) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Gustafsson (2023) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Gutierrez (1981) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Hullé & Vernon (2021) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Jancke (1932) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Jena et al. (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Jimenez et al. (1980) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Keller (2011) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Kettle (1983) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Khokhlov (1982) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Kristofik et al. (1996) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Lienhard (1989) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Lyal (1987) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Martin et al. (1981) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Mey (2020) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Millan et al. (2004) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ortego et al. (2007) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Pearman (1951) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petryszak et al. (1996) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Piednoir (2021) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Piross et al. (2020) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ramchurn (1980) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ribaga (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribette (1983) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Rodriguez et al. (1979) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Rodriguez et al. (1982) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Roesler (1954) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Schrank (1781) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Smetana (1961) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Soler-Cruz et al. (1987) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Stenram (1956) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Sychra et al. (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Thornton (1981) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Timmermann (1963) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ward (1953) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Waterston (1922) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Wilson (1934) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,2% | 1 | 0,21% | 1 | 0,21% |
(1976) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |