Crustacés d'eau douce de métropole
Branchiopoda, Oligostraca et Multicrustacea d'eau douce (sens large) de métropole
517 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Martens & Savatenalinton (2011) | 179 | 9,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Balvay (2009) | 152 | 7,83% | 129 | 16,52% | 122 | 17,33% | 117 | 15,92% |
Defaye & Deharveng (2024) | 122 | 6,28% | 110 | 14,08% | 92 | 13,07% | 103 | 14,01% |
Champeau & Thiéry (1990) | 85 | 4,38% | 68 | 8,71% | 66 | 9,38% | 60 | 8,16% |
Moniez (1887) | 75 | 3,86% | 35 | 4,48% | 35 | 4,97% | 35 | 4,76% |
Monnier (2014) | 61 | 3,14% | 53 | 6,79% | 53 | 7,53% | 53 | 7,21% |
Richard (1887) | 42 | 2,16% | 13 | 1,66% | 13 | 1,85% | 12 | 1,63% |
Champeau (1967) | 32 | 1,65% | 27 | 3,46% | 26 | 3,69% | 15 | 2,04% |
Coineau (1968) | 29 | 1,49% | 8 | 1,02% | 5 | 0,71% | 8 | 1,09% |
Monard (1928) | 29 | 1,49% | 17 | 2,18% | 17 | 2,41% | 17 | 2,31% |
Paris (1919) | 29 | 1,49% | 23 | 2,94% | 23 | 3,27% | 23 | 3,13% |
Chevey (1927) | 28 | 1,44% | 19 | 2,43% | 19 | 2,7% | 18 | 2,45% |
Pélosse (1930) | 27 | 1,39% | 13 | 1,66% | 13 | 1,85% | 12 | 1,63% |
Roy (1922) | 26 | 1,34% | 6 | 0,77% | 6 | 0,85% | 5 | 0,68% |
Richard (1890) | 25 | 1,29% | 10 | 1,28% | 10 | 1,42% | 10 | 1,36% |
Roy (1927) | 25 | 1,29% | 4 | 0,51% | 4 | 0,57% | 3 | 0,41% |
Pelosse (1925) | 23 | 1,18% | 11 | 1,41% | 11 | 1,56% | 10 | 1,36% |
Pelosse (1927) | 19 | 0,98% | 9 | 1,15% | 9 | 1,28% | 8 | 1,09% |
Roy (1931) | 19 | 0,98% | 17 | 2,18% | 17 | 2,41% | 12 | 1,63% |
Pelosse (1927) | 18 | 0,93% | 9 | 1,15% | 9 | 1,28% | 8 | 1,09% |
Richard (1897) | 18 | 0,93% | 8 | 1,02% | 8 | 1,14% | 8 | 1,09% |
Richard (1888) | 15 | 0,77% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Rouch (1970) | 15 | 0,77% | 15 | 1,92% | 15 | 2,13% | 15 | 2,04% |
Jurine (1820) | 14 | 0,72% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1776) | 14 | 0,72% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Nourisson & Thiéry (1988) | 14 | 0,72% | 13 | 1,66% | 13 | 1,85% | 12 | 1,63% |
Dole-Olivier et al. (2015) | 13 | 0,67% | 11 | 1,41% | 10 | 1,42% | 11 | 1,5% |
Kerhervé (1914) | 13 | 0,67% | 3 | 0,38% | 2 | 0,28% | 2 | 0,27% |
Paris (1918) | 13 | 0,67% | 10 | 1,28% | 10 | 1,42% | 10 | 1,36% |
Richard (1890) | 13 | 0,67% | 5 | 0,64% | 5 | 0,71% | 5 | 0,68% |
Magniez (1978) | 12 | 0,62% | 12 | 1,54% | 9 | 1,28% | 11 | 1,5% |
Rouch (1980) | 11 | 0,57% | 11 | 1,41% | 11 | 1,56% | 11 | 1,5% |
Sars (1862) | 11 | 0,57% | 7 | 0,9% | 7 | 0,99% | 7 | 0,95% |
Aguesse & Dussart (1957) | 10 | 0,51% | 4 | 0,51% | 4 | 0,57% | 2 | 0,27% |
Chappuis & Rouch (1959) | 10 | 0,51% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Chevreux (1901) | 10 | 0,51% | 8 | 1,02% | 8 | 1,14% | 8 | 1,09% |
Labat et al. (2011) | 10 | 0,51% | 8 | 1,02% | 8 | 1,14% | 7 | 0,95% |
Linnaeus (1758) | 10 | 0,51% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Paris (1916) | 10 | 0,51% | 7 | 0,9% | 7 | 0,99% | 7 | 0,95% |
Dussart (1963) | 9 | 0,46% | 9 | 1,15% | 9 | 1,28% | 6 | 0,82% |
Ferreira et al. (2007) | 9 | 0,46% | 4 | 0,51% | 0 | 0% | 4 | 0,54% |
Guerne & Richard (1891) | 9 | 0,46% | 7 | 0,9% | 7 | 0,99% | 7 | 0,95% |
Labbé (1927) | 9 | 0,46% | 6 | 0,77% | 6 | 0,85% | 6 | 0,82% |
Messouli et al. (2018) | 9 | 0,46% | 6 | 0,77% | 6 | 0,85% | 6 | 0,82% |
Jakubisiak (1922) | 8 | 0,41% | 4 | 0,51% | 4 | 0,57% | 3 | 0,41% |
Meynard (2011) | 8 | 0,41% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Alfonso et al. (2021) | 7 | 0,36% | 7 | 0,9% | 7 | 0,99% | 6 | 0,82% |
Cuénot & Mercier (1914) | 7 | 0,36% | 4 | 0,51% | 4 | 0,57% | 3 | 0,41% |
Marazanoff (1965) | 7 | 0,36% | 5 | 0,64% | 5 | 0,71% | 5 | 0,68% |
Pinkster (1972) | 7 | 0,36% | 7 | 0,9% | 4 | 0,57% | 7 | 0,95% |
Pugh et al. (2002) | 7 | 0,36% | 6 | 0,77% | 6 | 0,85% | 5 | 0,68% |
Rabet et al. (2005) | 7 | 0,36% | 6 | 0,77% | 6 | 0,85% | 6 | 0,82% |
Apostolov (1998) | 6 | 0,31% | 6 | 0,77% | 6 | 0,85% | 6 | 0,82% |
Ferreira (2005) | 6 | 0,31% | 4 | 0,51% | 1 | 0,14% | 4 | 0,54% |
Gurney (1909) | 6 | 0,31% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Karaman (1929) | 6 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiefer (1937) | 6 | 0,31% | 6 | 0,77% | 6 | 0,85% | 6 | 0,82% |
Labbé (1926) | 6 | 0,31% | 5 | 0,64% | 5 | 0,71% | 4 | 0,54% |
Low & Tan (2011) | 6 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Magniez (1968) | 6 | 0,31% | 6 | 0,77% | 0 | 0% | 6 | 0,82% |
Serban et al. (1971) | 6 | 0,31% | 6 | 0,77% | 6 | 0,85% | 6 | 0,82% |
Thiébaud & Pelosse (1929) | 6 | 0,31% | 4 | 0,51% | 4 | 0,57% | 3 | 0,41% |
Thiébaud (1927) | 6 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Wagner & Bou (2021) | 6 | 0,31% | 6 | 0,77% | 6 | 0,85% | 6 | 0,82% |
Aguesse (1960) | 5 | 0,26% | 5 | 0,64% | 5 | 0,71% | 5 | 0,68% |
Dewarumez et al. (2011) | 5 | 0,26% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Dumont (1983) | 5 | 0,26% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Karaman (2022) | 5 | 0,26% | 5 | 0,64% | 1 | 0,14% | 4 | 0,54% |
Klie (1938) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruffo et al. (2014) | 5 | 0,26% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Stifter (1988) | 5 | 0,26% | 5 | 0,64% | 5 | 0,71% | 5 | 0,68% |
Alekseev et al. (2021) | 4 | 0,21% | 2 | 0,26% | 2 | 0,28% | 1 | 0,14% |
Apostolov (2002) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Apostolov (2005) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Baldry (2007) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbé (1964) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 4 | 0,21% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Chappuis (1948) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Coineau et al. (2013) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Cottarelli et al. (2000) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Crosetti & Margaritora (1985) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Dollfus (1897) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 2 | 0,27% |
Einsle (1996) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Gaudy & Thomassin (2006) | 4 | 0,21% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Goedmakers (1974) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 2 | 0,27% |
Graf & Straskraba (1968) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Henry & Magniez (1968) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Henry & Magniez (1982) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Hovencamp et al. (1983) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1931) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1988) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Kiefer (1954) | 4 | 0,21% | 4 | 0,51% | 0 | 0% | 4 | 0,54% |
Labbé (1924) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Mirabdullayev & Defaye (2004) | 4 | 0,21% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Paris (1916) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Parpet & Gelder (2020) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Pinkster & Platvoet (1986) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Racovitza (1922) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouch (1990) | 4 | 0,21% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Roy (1932) | 4 | 0,21% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Ruffo (1954) | 4 | 0,21% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Russell et al. (2021) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 0 | 0% |
Schellenberg (1950) | 4 | 0,21% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
, 28: 3-17.">Serban (1989) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
, 31: 21-45.">Serban (1992) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Stepanova (2005) | 4 | 0,21% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Stock & Gledhill (1977) | 4 | 0,21% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Sywula (1968) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Damme et al. (2009) | 4 | 0,21% | 4 | 0,51% | 4 | 0,57% | 4 | 0,54% |
Vandel (1920) | 4 | 0,21% | 3 | 0,38% | 3 | 0,43% | 2 | 0,27% |
Vonk (1988) | 4 | 0,21% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Alther et al. (2016) | 3 | 0,15% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Amoros (1980) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Apostolov (2004) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Balazuc (1957) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Bodin (1978) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Bou (1965) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Champeau (1970) | 3 | 0,15% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
Chappuis & Rouch (1960) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Chappuis (1956) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Chappuis (1956) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Chevreux & Guernej (1892) | 3 | 0,15% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Coineau (1963) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Colin (1998) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Danielopol et al. (2012) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Danielopol (1978) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Defaye & Dussart (2011) | 3 | 0,15% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Delamare et al. (1954) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Dole & Coineau (1987) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Durr & Thiery (2020) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
European Nucleotide Archive (2019) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Filhol (1936) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Hansson (1998) | 3 | 0,15% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
Henry & Magniez (1969) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Henry & Magniez (1972) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Henry & Magniez (1972) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Henry & Magniez (1996) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Henry (1963) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Henry (1969) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Henry (1980) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Hubault & Ruffo (1956) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Jaume & Brehier (2005) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Karaman (1980) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Kiefer (1930) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescher-Montoue (1974) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Lescher-Moutoue (1968) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Lescher-moutoue (1968) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Lescher-moutoue (1968) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Lescher-moutoue (1969) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Lescher-Moutoue (1974) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Lescher-moutoue (1978) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Magniez & Henry (1969) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Magniez (1965) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathieu & Taveau (1984) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Meisch et al. (2007) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Monard (1926) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Namiotko et al. (2005) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Nelson-Smith et al. (2014) | 3 | 0,15% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Nordmann (1832) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Nourisson (1975) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Pagano (2009) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Pesce & Galassi (1988) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Petit & Schachter (1943) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinkster & Scholl (1984) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Pinkster & Stock (1971) | 3 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Pinkster (1983) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Prévost (1803) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Ramage (2017) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 2 | 0,27% |
Rehberg (1880) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Rose (1925) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Rossetti & Martens (1996) | 3 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Rouch & Lescher-Moutoué (1977) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Rouch (1988) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Rouch (1988) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Rouch (1992) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouch (1996) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (1924) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Séchet & Noël (2015) | 3 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Sinev & Dumont (2016) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Sinev (2015) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Uicn et al. (2014) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Vandel (1922) | 3 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Wichers (1964) | 3 | 0,15% | 3 | 0,38% | 3 | 0,43% | 3 | 0,41% |
Alm (1914) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Almeida et al. (2015) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Mémoires de Biospéologie, 28(55): 1-8.">Apostolov (2002) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Apostolov (2002) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Apostolov (2003) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Arcangeli (1942) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Artheau (2007) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Baird (1836) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Baird (1843) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Baltanas et al. (1993) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Bameul (2013) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Barbe (1963) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Belk & Brtek (1995) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Botello et al. (2013) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Bou (1971) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Canadian Journal of Fisheries and Aquatic Sciences, 46(10): 1714-1725.">Bousfield (1989) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Bovée et al. (1973) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 1 | 0,14% |
Brady (1880) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bréhier & Jaume (2009) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Brehm (1907) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Burckhardt (1920) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 0 | 0% |
Chappuis & Delamare-deboutteville (1952) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Chappuis & Rouch (1959) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Chappuis (1928) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Chappuis (1953) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Chatton (1912) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Chevreux (1887) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chevreux (1894) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Claus (1866) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Coineau (1963) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Colin & Hoibian (2003) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Cottarelli & Bruno (1993) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Cuénot & Mercier (1921) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Daday & Deés (1910) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Dan & Capuse (1959) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Danielopol (1977) | 2 | 0,1% | 2 | 0,26% | 0 | 0% | 2 | 0,27% |
Danielopol (1981) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Delamare-Deboutteville & Chappuis (1954) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Devin et al. (2001) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Dussart (1957) | 2 | 0,1% | 2 | 0,26% | 0 | 0% | 2 | 0,27% |
Dussart (1970) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Dussart (1984) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Dybowski & Grochowski (1894) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Fage (1937) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Fiers & Pandourski (2008) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Fischer (1848) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Fossati & Marquet (1998) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 1 | 0,14% |
Fox (1963) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Frankenberger (1938) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenzel & Alonso (1988) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Frey (1965) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Frey (1980) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Galassi et al. (1999) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Galassi et al. (1999) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Galassi et al. (2019) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Garcia-Paris et al. (2022) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Gérard et al. (2017) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Gidó et al. (2007) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Goedmakers & Pinkster (1977) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Goulletquer (2016) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Grandjean et al. (2021) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Guerne & Richard (1888) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Henry & Magniez (1978) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Henry & Magniez (1981) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Hertzog (1935) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Hertzog (1936) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Horeau et al. (2005) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Iepure et al. (2008) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Jacquet (2023) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Karaman (1971) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1986) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Karaman (2022) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Keilhack (1910) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Klie (1925) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Klie (1941) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Koelbel (1884) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Koźmiński (1933) | 2 | 0,1% | 2 | 0,26% | 0 | 0% | 2 | 0,27% |
Landé (1890) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1956) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescher-Moutoué (1971) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lilljeborg (1901) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Löffler (1963) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowndes (1926) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Magniez & Henry (2002) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Margalef (1945) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Margalef (1951) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Margaritora (1971) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Marrone et al. (2010) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Martens et al. (2019) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Bollettino di Zoologia Napoli, 3: 213-223.">Masi (1932) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathieu et al. (1994) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Messouli et al. (2006) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Milne-Edwards (1853) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Monard (1925) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Mrázek (1894) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1785) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz et al. (2009) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Neveu (2009) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ng et al. (2008) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël & Guinot (2007) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Omaly (1970) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Paulmier (2009) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Petkovski (1959) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinkster (1969) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Pinkster (1973) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Ponyi (1956) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Racovitza (1919) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rémy (1948) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 0 | 0% |
Rémy (1949) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Renon & Lefèvre (1985) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Røen (1987) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rogulj & Danielopol (1993) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Rouch (1964) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Ruffo (1959) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1895) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Schaferna (1923) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Scheepmaker (1987) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Schellenberg (1934) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Schellenberg (1937) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
, 23: 7-18.">Serban & Leclerc (1984) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Sereda et al. (2016) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Simon (1886-1887) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Sinev (2020) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Souben et al. (2014) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Soyer (1975) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Sywula (1972) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sywula (1974) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiéry & Champeau (1988) | 2 | 0,1% | 2 | 0,26% | 2 | 0,28% | 2 | 0,27% |
Van et al. (2011) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1920) | 2 | 0,1% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Alekseev et al. (2021) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Alm (1915) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anastasiadou et al. (2006) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Anker & Noël (1999) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Baird (1843) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Balazuc & Angelier (1952) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Balsamo-Crivelli (1859) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Balvay (1972) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bate (1862) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Beauchamp (1918) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1928) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Beladjal et al. (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Beldescu (1961) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Benzie (2005) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Bollache (2004) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Borza (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bosc (1801-1802) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchard (2021) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Boxshall & Bernot (2023) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Bozic (1955) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Brady & Robertson (1870) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Brehm (1923) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brehm (1923) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brehm (1925) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brehm (1953) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bronstein (1928) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brtek & Thiery (1995) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Brun & Brun (1964) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Caillot et al. (1999) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Casanova (1967) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chabrol (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chappuis (1954) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chappuis (1959) | 1 | 0,05% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
Chauvel et al. (2023) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chevreux & Fage (1925) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1908) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chevreux (1909) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chevreux (1922) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chien (1970) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chucholl & Daudey (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Claus (1857) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochard et al. (2010) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Cochereau (1974) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Colas (2019) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Collas et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Collas et al. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Daday de Deés (1908) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Daday (1884) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dana (1849) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Dana (1852) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1778) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Desmaret (1823) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Devin et al. (2005) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Dollfus et al. (1935) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dussart (1948) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Dussart (1982) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Dybowski (1860) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Esposito et al. (2023) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Filipová et al. (2013) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Filippi (2013) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Fischer de Waldheim (1834) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Frescheville de (1958) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Fruget & Beisel (2016) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Furtos (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Galassi & De Laurentiis (2004) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Gallien (1936) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Gauthier (1938) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gelder et al. (2012) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Gery (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Giesbrecht (1892-1893) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Girard (1852) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Grabowski et al. (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Graf (1964) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinot et al. (2018) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hahn (1990) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hanzelovà & Gerdeaux (2003) | 1 | 0,05% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
Harada (1930) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartmann (1964) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Henderson (1986) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hesse & Mangot (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff (1942) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Holynska & Dahms (2004) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hubault (1935) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Huguet (1973) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hynes (1959) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jamonneau et al. (2025) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Jazdzewski (1975) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1931) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1952) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1986) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Keilhack (1909) | 1 | 0,05% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
Kellogg (1906) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Klie (1938) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1844) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kohn & Waterstraat (1990) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Korovchinsky (2000) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Kouba et al. (2014) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Kruger et al. (2019) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Krynicki (1830) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kurz (1875) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Laffitte et al. (2023) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Lescher-Moutoué (1979) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Liévin (1848) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lilljeborg (1888) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Upsala, Druck der Akademischen buchdruckerei E. Berling. 701 pp.">Lilljeborg (1900) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lindner (1920) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Löffler (1960) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Löffler (1961) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Loot et al. (2001) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Lowe et al. (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Lowndes (1932) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lyko (2017) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Machino (1996) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Machino (1999) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Maddocks (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Magniez (2001) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Margalef (1946) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Margalef (1948) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Marková et al. (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Martynov 1924) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Masi (1905) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Masi (1932) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Masson (1979) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Matsuzaki et al. (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Maury (1973) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Méhes (1939) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Meisch et al. (1990) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Meisch (1979) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
MGnify (2017) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Miecherdzinski (1959) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-Edwards (1840) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Minkiewicz (1924) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Montfort (2001) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Müller (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Namiotko & Danielopol (2004) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Noël, Breton (2016) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Noël (2016) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Noël (2017) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Noël (2017) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Norman & Scott (1906) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Notenboom et al. (2006) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Okubo (1973) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier et al. (2006) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Pacaud (1944) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Parpet & Gelder (2018) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Petit & Schachter (1948) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit (1950) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petkovski (1963) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petkovski (1966) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petkowski & Keyser (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pezy et al. (2015) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Pinto & Kotzian (1961) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Piscart et al. (2008) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Platvoet (1984) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (1999) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Puissauve, Collas, & Grandjean (2015) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Puissauve, Legros, Noël & Collas (2015) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
PUISSAUVE Renaud, COLLAS Marc & GRANDJEAN Frédéric (2013) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Questel (2020) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Racovitza (1919) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Racovitza (1924) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Raibaut (1962) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Règlement d'exécution (UE) 2016/1141 | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Remy (1948) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Renon & Pineau (2013) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Rey (1966) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Richard (1896) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Roca & Baltanas (1993) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Rogers et al. (2020) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Rogers (2003) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Rome & Deckker (1977) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rome (1947) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rose (1933) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Roux (1964) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scalone & Rabet (2013) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Schabetsberger et al. (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Schachter & Champeau (1969) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schellenberg (1935) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Schmeil (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmeil (1894) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank et al. (1803) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scourfield (1947) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Sexton (1939) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Sinev et al. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sinev et al. (2023) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Sket & Zakšek (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Spandl (1925) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephensen (1935) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Sywula (1981) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Taiti & Ferrara (1996) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiebaud (1908) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiery & Pont (1987) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Thiéry & Robert (1992) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Timms (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Turner (1895) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vannier et al. (2003) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Vasileva et al. (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Vogt (1845) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wierzbicka (1959) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wittmann & Ariani (2000) | 1 | 0,05% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Zilli (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |