Faune cavernicole de France
Faune cavernicole au sens large (inclut les troglobies/troglophiles/trogloxènes et les stygobies/stygophiles/stygoxènes) de France, tous territoires confondus. ATTENTION : liens espèces-habitats (intérieurs des grottes) non encore pris en compte !
406 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Deharveng (2024) | 153 | 10,51% | 151 | 21,21% | 142 | 24,7% | 151 | 23,2% |
Thibaud (2017) | 141 | 9,68% | 136 | 19,1% | 132 | 22,96% | 133 | 20,43% |
Defaye & Deharveng (2024) | 122 | 8,38% | 110 | 15,45% | 92 | 16% | 103 | 15,82% |
Gargominy et al. (2011) | 104 | 7,14% | 97 | 13,62% | 80 | 13,91% | 90 | 13,82% |
Glöer (2022) | 78 | 5,36% | 75 | 10,53% | 61 | 10,61% | 75 | 11,52% |
Tronquet (2014) | 65 | 4,46% | 61 | 8,57% | 34 | 5,91% | 57 | 8,76% |
Faille et al. (2023) | 58 | 3,98% | 58 | 8,15% | 58 | 10,09% | 42 | 6,45% |
Falkner et al. (2002) | 58 | 3,98% | 52 | 7,3% | 45 | 7,83% | 45 | 6,91% |
Santamaria & Faille (2007) | 48 | 3,3% | 20 | 2,81% | 14 | 2,43% | 16 | 2,46% |
Gisin & Gama (1970) | 25 | 1,72% | 25 | 3,51% | 22 | 3,83% | 25 | 3,84% |
Gisin & Gama (1969) | 24 | 1,65% | 24 | 3,37% | 24 | 4,17% | 21 | 3,23% |
Boeters & Falkner (2003) | 20 | 1,37% | 19 | 2,67% | 19 | 3,3% | 19 | 2,92% |
Rouch (1970) | 15 | 1,03% | 15 | 2,11% | 15 | 2,61% | 15 | 2,3% |
Faille et al. (2010) | 13 | 0,89% | 11 | 1,54% | 11 | 1,91% | 7 | 1,08% |
Bonadona & Giordan (1988) | 12 | 0,82% | 12 | 1,69% | 9 | 1,57% | 12 | 1,84% |
Genest (1983) | 12 | 0,82% | 6 | 0,84% | 6 | 1,04% | 6 | 0,92% |
Gisin (1960) | 12 | 0,82% | 4 | 0,56% | 3 | 0,52% | 4 | 0,61% |
Kime & Enghoff (2017) | 12 | 0,82% | 12 | 1,69% | 12 | 2,09% | 11 | 1,69% |
Ponge et al. (2003) | 11 | 0,76% | 9 | 1,26% | 9 | 1,57% | 9 | 1,38% |
Rouch (1980) | 11 | 0,76% | 11 | 1,54% | 11 | 1,91% | 11 | 1,69% |
Balvay (2009) | 10 | 0,69% | 10 | 1,4% | 9 | 1,57% | 6 | 0,92% |
Chappuis & Rouch (1959) | 10 | 0,69% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Denis (1924) | 10 | 0,69% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Ferreira et al. (2007) | 10 | 0,69% | 7 | 0,98% | 6 | 1,04% | 7 | 1,08% |
Nicolas (1891) | 10 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Beruete et al. (2002) | 9 | 0,62% | 9 | 1,26% | 9 | 1,57% | 9 | 1,38% |
Deharveng (1978) | 9 | 0,62% | 5 | 0,7% | 5 | 0,87% | 5 | 0,77% |
Deharveng (1988) | 9 | 0,62% | 9 | 1,26% | 9 | 1,57% | 9 | 1,38% |
Dole-Olivier et al. (2015) | 9 | 0,62% | 8 | 1,12% | 7 | 1,22% | 8 | 1,23% |
Gisin & Gama (1970) | 9 | 0,62% | 9 | 1,26% | 9 | 1,57% | 9 | 1,38% |
Gisin (1963) | 9 | 0,62% | 5 | 0,7% | 5 | 0,87% | 5 | 0,77% |
Cassagnau (1955) | 8 | 0,55% | 8 | 1,12% | 8 | 1,39% | 8 | 1,23% |
Denis (1947) | 8 | 0,55% | 5 | 0,7% | 5 | 0,87% | 5 | 0,77% |
Girardi (2009) | 8 | 0,55% | 6 | 0,84% | 0 | 0% | 6 | 0,92% |
Lemaire (2016) | 8 | 0,55% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Magniez (1978) | 7 | 0,48% | 7 | 0,98% | 4 | 0,7% | 6 | 0,92% |
Apostolov (1998) | 6 | 0,41% | 6 | 0,84% | 6 | 1,04% | 6 | 0,92% |
Beauchamp (1956) | 6 | 0,41% | 6 | 0,84% | 6 | 1,04% | 6 | 0,92% |
Bernasconi (1985) | 6 | 0,41% | 3 | 0,42% | 3 | 0,52% | 2 | 0,31% |
Boeters (1981) | 6 | 0,41% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Boeters (2000) | 6 | 0,41% | 6 | 0,84% | 4 | 0,7% | 6 | 0,92% |
Callot-Girardi (2015) | 6 | 0,41% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Champeau (1967) | 6 | 0,41% | 5 | 0,7% | 5 | 0,87% | 2 | 0,31% |
Coiffait (1969) | 6 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Denis (1922) | 6 | 0,41% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Girardi (2009) | 6 | 0,41% | 6 | 0,84% | 6 | 1,04% | 6 | 0,92% |
Gouze & Deharveng (1987) | 6 | 0,41% | 6 | 0,84% | 6 | 1,04% | 6 | 0,92% |
Hondt (1967) | 6 | 0,41% | 6 | 0,84% | 6 | 1,04% | 6 | 0,92% |
Jeannel (1938) | 6 | 0,41% | 3 | 0,42% | 3 | 0,52% | 0 | 0% |
Kerhervé (1914) | 6 | 0,41% | 1 | 0,14% | 1 | 0,17% | 0 | 0% |
Kiefer (1937) | 6 | 0,41% | 6 | 0,84% | 6 | 1,04% | 6 | 0,92% |
Lindner (1859) | 6 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Magniez (1968) | 6 | 0,41% | 6 | 0,84% | 0 | 0% | 6 | 0,92% |
Paladilhe (1869) | 6 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié et al. (2024) | 6 | 0,41% | 6 | 0,84% | 6 | 1,04% | 6 | 0,92% |
Weygoldt (2006) | 6 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1931) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters & Bertrand (2001) | 5 | 0,34% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Brölemann (1921) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Condé (1980) | 5 | 0,34% | 5 | 0,7% | 5 | 0,87% | 5 | 0,77% |
Deharveng (1989) | 5 | 0,34% | 5 | 0,7% | 5 | 0,87% | 5 | 0,77% |
Fourès (1954) | 5 | 0,34% | 5 | 0,7% | 4 | 0,7% | 4 | 0,61% |
Locard (1883) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Locard (1893) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Najt (1981) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochs (1938) | 5 | 0,34% | 1 | 0,14% | 1 | 0,17% | 0 | 0% |
Pelosse (1927) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Pélosse (1930) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Route et al. (2004) | 5 | 0,34% | 5 | 0,7% | 5 | 0,87% | 5 | 0,77% |
Achurra et al. (2012) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Apostolov (2002) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Apostolov (2005) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Beauchamp (1919) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Beruete et al. (2021) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Boeters & Falkner (2003) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters & Falkner (2009) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Cottarelli et al. (2000) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Deharveng & Gouze (1984) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Deharveng (1981) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Denis (1921) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Denis (1923) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 0 | 0% |
Faille & Bourdeau (2022) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Fischer (1885) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Fresneda et al. (2010) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Fresneda, Perreau & Vanderbergh (2010) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Giani & Lafont (1982) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Girardi et al. (2002) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Girardi (2009) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Girardi (2009) | 4 | 0,27% | 4 | 0,56% | 0 | 0% | 4 | 0,61% |
Girardi (2009) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 4 | 0,61% |
Gisin (1964) | 4 | 0,27% | 4 | 0,56% | 1 | 0,17% | 4 | 0,61% |
Jeannel (1913) | 4 | 0,27% | 4 | 0,56% | 4 | 0,7% | 3 | 0,46% |
Jeannel (1916) | 4 | 0,27% | 3 | 0,42% | 2 | 0,35% | 2 | 0,31% |
Jeannel (1919) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiefer (1954) | 4 | 0,27% | 4 | 0,56% | 0 | 0% | 4 | 0,61% |
Latella (2015) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Löbl & Smetana (2004) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Nicolet (1847) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Normand (1907) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelosse (1925) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelosse (1927) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Perreau & Queinnec (1987) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Racovitza (1922) | 4 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage (2017) | 4 | 0,27% | 3 | 0,42% | 3 | 0,52% | 2 | 0,31% |
Rouch (1990) | 4 | 0,27% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Vandel (1920) | 4 | 0,27% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Apostolov (2004) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Argod-vallon (1913) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Avon (1994) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Beauchamp (1926) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Beauchamp (1929) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Beauchamp (1937) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1950) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Beauchamp (1955) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Boeters (1969) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonet (1931) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Bourguignat (1864) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Brölemann (1900) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Cabidoche (1961) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot-Girardi (2017) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Callot-girardi (2017) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Cassagnau et al. (1953) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Champeau & Thiéry (1990) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 1 | 0,15% |
Chappuis & Rouch (1960) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Chappuis (1956) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Chappuis (1956) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Chevreux (1901) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Coiffait (1976) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Coutagne (1883) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Defaye & Dussart (2011) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Deharveng & Gouze (1986) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Deharveng (1987) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Deharveng (1988) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Delamare (-) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Delamare-Deboutteville (1948) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Delay (1972) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Denis (1932) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Dieck (1869) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupre (1991) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Faille et al. (2010) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourès (1961) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Fresneda et al. (2009) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Gaudin (1938) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Gaudin (1947) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Genest (1977) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Giachino (1988) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Giani et al. (1990) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Gisin & Gama (1969) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Gourbault (1965) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Gourbault (1969) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoch et al. (2003) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Jeannel (1938) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 1 | 0,15% |
Jordana & Baquero (2005) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Juget (1967) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Juget (1987) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Kerney & Cameron (1999) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 1 | 0,15% |
Lemaire (2021) | 3 | 0,21% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Lescher-Montoue (1974) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Lescher-Moutoue (1968) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Lescher-moutoue (1968) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Lescher-moutoue (1968) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Lescher-moutoue (1969) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Lescher-Moutoue (1974) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Lescher-moutoue (1978) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Miranda et al. (2021) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Moniez (1887) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Moniez (1890) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Paladilhe (1867) | 3 | 0,21% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Pesce & Galassi (1988) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Ribaut (1947) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Richard (1890) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodriguez & Giani (1987) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Rouch & Lescher-Moutoué (1977) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Rouch (1988) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Rouch (1988) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Rouch (1992) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouch (1996) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (1922) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (1927) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Stomp & Gouze (1984) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Stomp et al. (1982) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Stomp (1974) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Thibaud & Massoud (1983) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Thibaud (1967) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Thibaud (1975) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Vargovitsh (2009) | 3 | 0,21% | 3 | 0,42% | 3 | 0,52% | 3 | 0,46% |
Abrahamsen (1969) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Absolon (1900) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Apostolov (2002) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Mémoires de Biospéologie, 28(55): 1-8.">Apostolov (2002) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Apostolov (2003) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Arbea (1991) | 2 | 0,14% | 2 | 0,28% | 0 | 0% | 2 | 0,31% |
Avon (2007) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Beauchamp & Gourbault (1964) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Beauchamp (1932) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Bernasconi (1968) | 2 | 0,14% | 2 | 0,28% | 0 | 0% | 2 | 0,31% |
Bernasconi (1989) | 2 | 0,14% | 2 | 0,28% | 0 | 0% | 2 | 0,31% |
Bertrand (2001) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Bertrand (2004) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Besuchet (1981) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Boeters & Gittenberger (1980) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Boeters (1983) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters (1999) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Bourguignat (1865) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Bourlet (1839) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Brolemann (1894) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabidoche (1965) | 2 | 0,14% | 2 | 0,28% | 0 | 0% | 2 | 0,31% |
Cabidoche (1968) | 2 | 0,14% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Callot-Girardi & Boeters (2017) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Callot-girardi et al. (2017) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Callot-Girardi (2012) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Callot-Girardi (2013) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Callot-Girardi (2015) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Callot-Girardi (2015) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Callot-Girardi (2015) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Callot-Girardi (2017) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Cassagnau et Delamare (1955) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Cassagnau (1959) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Caziot (1908) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Cesne et al. (2022) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Chappuis & Rouch (1959) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Chappuis (1928) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Condé (1981) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Condé (1989) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Cottarelli & Bruno (1993) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Deharveng & Beruete (1993) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Deharveng & Thibaud (1980) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Deharveng & Thibaud (1989) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Deharveng (1979) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Delarouzée (1857) | 2 | 0,14% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Delfosse (2024) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Denis (1935) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Dollfus (1897) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 0 | 0% |
Dugès (1830) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Dussart (1963) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 1 | 0,15% |
Dussart (1970) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Fagniez (1923) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Faille & Bourdeau (2008) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Faille et al. (2013) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire ([1857]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1980) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Ferreira (2005) | 2 | 0,14% | 2 | 0,28% | 1 | 0,17% | 2 | 0,31% |
Fiers & Pandourski (2008) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Fossati & Marquet (1998) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 1 | 0,15% |
Fresneda & Bourdeau (2012) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Fresneda & Salgado-Costas (2006) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Fresneda et al. (2010) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Galassi et al. (1999) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Galassi et al. (1999) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Galassi et al. (2019) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Gargominy (2011-2023) | 2 | 0,14% | 2 | 0,28% | 1 | 0,17% | 2 | 0,31% |
Gaudin (1925) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 0 | 0% |
Gaudin (1939) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Genest & Juberthie (1983) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy & Mauriès (2017) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Germain (1911) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi & Bertrand (2009) | 2 | 0,14% | 2 | 0,28% | 0 | 0% | 2 | 0,31% |
Girardi & Bertrand (2009) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Girardi (2001) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi (2002) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi (2004) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi (2004) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Girardi (2004) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Girardi (2009) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Girardi (2009) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Girardi (2009) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Girardi (2009) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Gisin (1965) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Gourbault et al. (1976) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Gourbault (1969) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourbault (1971) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Gourbault (1984) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Gouze (1983) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Haase (2000) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Hallez (1910) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Heurtault (1986) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Hrabe (1937) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Iorio (2009) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Isaia et al. (2023) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Jakubisiak (1922) | 2 | 0,14% | 1 | 0,14% | 1 | 0,17% | 0 | 0% |
Joubin (1894) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Juget & Des Chatelliers (2001) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Juget (1959) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Jurine (1820) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Kosel (1980) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Lecaplain (2021) | 2 | 0,14% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Lescher-Moutoué (1971) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lopez (1996) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Martinsson et al. (2013) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Michaud (1831) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mihelčič (1960) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Monard (1925) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Moniez (1889-1890) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Moniez (1894) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Moniez (1894) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Pagès (1978) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Palevody (1973) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Papp (1978) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Prie & Bichain (2009) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Rémy (1949) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Richard (1887) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Richling et al. (2016) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodriguez & Giani (1989) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Roewer (1935) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouch (1964) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Roy (1931) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 0 | 0% |
Russell et al. (2021) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 0 | 0% |
Sainte-Claire Deville (1922) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 0 | 0% |
Sayn (1889) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Secq (2013) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Sendra et al. (2017) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Stomp (1971) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Vachon & Heurtault-rossi (1964) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Vandel (1920) | 2 | 0,14% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Vannier & Thibaud (1984) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Vejdovský (1876) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 2 | 0,31% |
Vuillefroy-Cassini (1893) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Welter-schultes (2012) | 2 | 0,14% | 2 | 0,28% | 2 | 0,35% | 1 | 0,15% |
Yosii (1953) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Abeille & Perrin (1905) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Absolon (1901) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Arbea et al. (2021) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Beauchamp (1926) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernasconi (1988) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Bernasconi (1994) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernasconi (1999) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeters (1967) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Boeters (2022) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Brady (1880) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bretscher (1902) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Callot-Girardi (2015) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Carpenter (1934) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Casale (1988) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cassagnau (1958) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Chevey (1927) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Clessin (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Coutagne (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuénot & Mercier (1914) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delachaux (1921) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Delfosse (2003) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Delfosse (2004) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delfosse (2017) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Denis (1931) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
d'Hondt & Ben Ahmed (2009) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1801) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupuy (1847-1852) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2018) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Fagniez (1913) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 0 | 0% |
Faille et al. (2007) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Galassi & De Laurentiis (2004) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Geoffroy & Iorio (2009) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Giani (1976) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Girardi (2009) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Girardi (2009) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gisin (1954) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Gittenberger (1973) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Grosser (2015) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Hrabe (1963) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Hrabe (1963) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Iorio et al. (2023) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Johnson & Wellington (1983) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Jouin (1973) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Juberthie (1972) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Juberthie (1983) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Kneubühler et al. (2021) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Labbé (1926) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 0 | 0% |
Lemaire (2011) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Lilljeborg (1901) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2003) | 1 | 0,07% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Locard (1883) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Locard (1901) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Locard (1903) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Martynova (1964) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Massera (1952) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey (2011) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Monard (1928) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mrázek (1894) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolet (1842) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman & Scott (1906) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Omaly (1970) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Paladilhe (1874) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Piguet (1906) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointner (1914) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollonera (1887) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Potapov (2001) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Prieto (2008) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Pugh et al. (2002) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1888) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1890) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1897) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Saint-simon (1848) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmeil (1893) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Steinman (1910) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Templeton (1836) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibaud & Najt (1993) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Thiébaud (1927) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Usher & Hider (1975) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Vandel (1922) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Vedel et al. (2013) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Vejdovský (1883) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Westerlund (1884‑1890) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Willem (1902) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |
Zapparoli & Iorio (2012) | 1 | 0,07% | 1 | 0,14% | 1 | 0,17% | 1 | 0,15% |