Lumbricina de métropole
105 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Bouché (1972) | 102 | 20,32% | 46 | 22,33% | 43 | 22,28% | 46 | 23,12% |
Marchán et al. (2022) | 42 | 8,37% | 28 | 13,59% | 27 | 13,99% | 25 | 12,56% |
Marchán et al. (2023) | 35 | 6,97% | 34 | 16,5% | 32 | 16,58% | 33 | 16,58% |
Marchán et al. (2021) | 19 | 3,78% | 19 | 9,22% | 16 | 8,29% | 17 | 8,54% |
Marchán et al. (2023) | 17 | 3,39% | 17 | 8,25% | 17 | 8,81% | 17 | 8,54% |
Zicsi & Csuzdi (1999) | 15 | 2,99% | 10 | 4,85% | 10 | 5,18% | 10 | 5,03% |
Bouché (1970) | 14 | 2,79% | 8 | 3,88% | 8 | 4,15% | 8 | 4,02% |
Gérard et al. (2023) | 13 | 2,59% | 13 | 6,31% | 7 | 3,63% | 12 | 6,03% |
Savigny (1826) | 11 | 2,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouché (1969) | 9 | 1,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchán et al. (2023) | 9 | 1,79% | 7 | 3,4% | 7 | 3,63% | 7 | 3,52% |
Qiu & Bouché (1998) | 9 | 1,79% | 9 | 4,37% | 6 | 3,11% | 9 | 4,52% |
Qiu & Bouché (1998) | 8 | 1,59% | 4 | 1,94% | 4 | 2,07% | 4 | 2,01% |
Dupont et al. (2023) | 7 | 1,39% | 7 | 3,4% | 7 | 3,63% | 7 | 3,52% |
Szederjesi et al. (2023) | 7 | 1,39% | 4 | 1,94% | 1 | 0,52% | 3 | 1,51% |
Blakemore (2012) | 6 | 1,2% | 4 | 1,94% | 4 | 2,07% | 4 | 2,01% |
Chandebois (1958) | 6 | 1,2% | 2 | 0,97% | 2 | 1,04% | 2 | 1,01% |
Hullé et al. (2018) | 6 | 1,2% | 4 | 1,94% | 4 | 2,07% | 2 | 1,01% |
Michaelsen (1913) | 6 | 1,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Qiu & Bouché (1998) | 6 | 1,2% | 6 | 2,91% | 6 | 3,11% | 6 | 3,02% |
Rota (1994) | 6 | 1,2% | 3 | 1,46% | 3 | 1,55% | 3 | 1,51% |
Dupont et al. (2023) | 5 | 1% | 5 | 2,43% | 5 | 2,59% | 5 | 2,51% |
Marchán et al. (2018) | 5 | 1% | 4 | 1,94% | 4 | 2,07% | 4 | 2,01% |
Marchán et al. (2024) | 5 | 1% | 5 | 2,43% | 5 | 2,59% | 5 | 2,51% |
Szederjesi et al. (2019) | 5 | 1% | 5 | 2,43% | 5 | 2,59% | 4 | 2,01% |
Blakemore (2008) | 4 | 0,8% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Csuzdi & Pavlíček (2009) | 4 | 0,8% | 4 | 1,94% | 4 | 2,07% | 4 | 2,01% |
Jourdan (2020) | 4 | 0,8% | 4 | 1,94% | 4 | 2,07% | 3 | 1,51% |
Marchán et al. (2020) | 4 | 0,8% | 4 | 1,94% | 4 | 2,07% | 4 | 2,01% |
Pavlíček & Csuzdi (2012) | 4 | 0,8% | 3 | 1,46% | 3 | 1,55% | 3 | 1,51% |
Qiu & Bouché (1998) | 4 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Qiu & Bouché (1998) | 4 | 0,8% | 2 | 0,97% | 2 | 1,04% | 2 | 1,01% |
Ramage et al. (2023) | 4 | 0,8% | 4 | 1,94% | 4 | 2,07% | 4 | 2,01% |
Zicsi (1977) | 4 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartoli (1963) | 3 | 0,6% | 3 | 1,46% | 3 | 1,55% | 3 | 1,51% |
Bartoli (1963) | 3 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouché (1969) | 3 | 0,6% | 3 | 1,46% | 3 | 1,55% | 3 | 1,51% |
Bouché (1982) | 3 | 0,6% | 2 | 0,97% | 2 | 1,04% | 2 | 1,01% |
Csuzdi & Zicsi (2003) | 3 | 0,6% | 1 | 0,49% | 0 | 0% | 1 | 0,5% |
Dugès (1828) | 3 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Černosvitov (1934) | 3 | 0,6% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Frenot et al. (2005) | 3 | 0,6% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Guerne & Horst (1893) | 3 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchán et al. (2018) | 3 | 0,6% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Onteniente & Babío (2002) | 3 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Qiu & Bouché (1998) | 3 | 0,6% | 3 | 1,46% | 3 | 1,55% | 3 | 1,51% |
Szederjesi et al. (2021) | 3 | 0,6% | 3 | 1,46% | 3 | 1,55% | 3 | 1,51% |
Tétry (1939) | 3 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Vedovini (1969) | 3 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Vedovini (1969) | 3 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Vedovini (1971) | 3 | 0,6% | 3 | 1,46% | 3 | 1,55% | 3 | 1,51% |
Bouche (1979) | 2 | 0,4% | 2 | 0,97% | 2 | 1,04% | 2 | 1,01% |
Bretscher (1899) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupont et al. (2019) | 2 | 0,4% | 2 | 0,97% | 2 | 1,04% | 2 | 1,01% |
Černosvitov (1936) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Martínez Navarro et al. (2023) | 2 | 0,4% | 2 | 0,97% | 2 | 1,04% | 2 | 1,01% |
Sapkarev (1971) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephenson (1925) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Tetry (1936) | 2 | 0,4% | 2 | 0,97% | 2 | 1,04% | 2 | 1,01% |
Tetry (1938) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Vedovini (1969) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Zicsi & Cuendet (2005) | 2 | 0,4% | 2 | 0,97% | 2 | 1,04% | 2 | 1,01% |
Zicsi (1982) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Alvarez (1971) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Beddard (1905) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Blakemore et al., 2006 | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Bouché (1970) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Briones (1996) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Chinaglia (1913) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Cognetti de Martiis (1914) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulis (2017) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Csuzdi & Pavlíček (2002) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Csuzdi et al. (2017) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Csuzdi et al. (2017) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Eisen (1874) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Eisen (1895) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Černosvitov (1929) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Černosvitov (1942) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernández et al. (2011) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Fletcher (1887) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot (1992) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Gates (1943) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Giani (1976) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Guerne & Horst (1896) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
James & Gamiette (2016) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
James et al. (2010) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Jourdan & Mille (2006) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Levinsen (1883) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Michaelsen (1899) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaelsen (1899) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaelsen (1913) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Örley (188) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Örley (1881) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Qiu & Bouché (1998) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Qiu & Bouché (1998) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Reynolds & Clapperton (1996) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosa (1893) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Rota et al. (2018) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Rota (2013) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Saussey (1973) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |
Sciacchitano (1932) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephenson (1915) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Vedovini (1967) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Zicsi (1963) | 1 | 0,2% | 1 | 0,49% | 1 | 0,52% | 1 | 0,5% |