Amphipodes de métropole
385 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Chevreux (1887) | 118 | 6,9% | 50 | 6,46% | 50 | 6,55% | 49 | 6,39% |
Godet et al. (2010) | 80 | 4,68% | 64 | 8,27% | 64 | 8,39% | 62 | 8,08% |
Bourcier (1988) | 77 | 4,5% | 55 | 7,11% | 55 | 7,21% | 53 | 6,91% |
Nelson-Smith et al. (2014) | 46 | 2,69% | 38 | 4,91% | 38 | 4,98% | 37 | 4,82% |
Ledoyer (1977) | 37 | 2,16% | 37 | 4,78% | 37 | 4,85% | 37 | 4,82% |
Lowry (2007) | 27 | 1,58% | 27 | 3,49% | 27 | 3,54% | 27 | 3,52% |
Bellan-Santini & Kaim-Malka (1977) | 25 | 1,46% | 25 | 3,23% | 25 | 3,28% | 25 | 3,26% |
Ann Univ Lyon, xxvi: 527-689.">Bonnier (1896) | 25 | 1,46% | 13 | 1,68% | 13 | 1,7% | 13 | 1,69% |
Poisson & Legueux (1926) | 21 | 1,23% | 11 | 1,42% | 11 | 1,44% | 11 | 1,43% |
Salmon (1962) | 16 | 0,94% | 8 | 1,03% | 8 | 1,05% | 8 | 1,04% |
Chevreux (1888) | 15 | 0,88% | 6 | 0,78% | 6 | 0,79% | 6 | 0,78% |
Dauvin et al. (1991) | 12 | 0,7% | 12 | 1,55% | 12 | 1,57% | 12 | 1,56% |
Ledoyer (1983) | 12 | 0,7% | 10 | 1,29% | 8 | 1,05% | 10 | 1,3% |
Messouli et al. (2018) | 12 | 0,7% | 9 | 1,16% | 9 | 1,18% | 9 | 1,17% |
Coineau (1968) | 11 | 0,64% | 5 | 0,65% | 2 | 0,26% | 5 | 0,65% |
Chevreux (1901) | 10 | 0,58% | 8 | 1,03% | 8 | 1,05% | 8 | 1,04% |
Labat et al. (2011) | 10 | 0,58% | 8 | 1,03% | 8 | 1,05% | 7 | 0,91% |
Ledoyer (1972) | 10 | 0,58% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Chevreux (1908) | 9 | 0,53% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dauvin & Bellan-Santini (1996) | 9 | 0,53% | 9 | 1,16% | 9 | 1,18% | 9 | 1,17% |
Breton (2014) | 8 | 0,47% | 7 | 0,9% | 7 | 0,92% | 7 | 0,91% |
Goulletquer (2016) | 8 | 0,47% | 8 | 1,03% | 8 | 1,05% | 8 | 1,04% |
Kaim-Malka (2000) | 8 | 0,47% | 8 | 1,03% | 8 | 1,05% | 8 | 1,04% |
Peart (2004) | 8 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinkster (1972) | 8 | 0,47% | 8 | 1,03% | 4 | 0,52% | 8 | 1,04% |
Reid (1951) | 8 | 0,47% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bulletin de la Société Zoologique de France, 28: 81-97.">Chevreux (1903) | 7 | 0,41% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Cuénot & Mercier (1914) | 7 | 0,41% | 4 | 0,52% | 4 | 0,52% | 3 | 0,39% |
Dewarumez et al. (2011) | 7 | 0,41% | 6 | 0,78% | 6 | 0,79% | 6 | 0,78% |
Poupin et al. (1999) | 7 | 0,41% | 7 | 0,9% | 7 | 0,92% | 7 | 0,91% |
Bellan-santini & Vader (1988) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1887) | 6 | 0,35% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Costa (1853) | 6 | 0,35% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Dauvin & Bellan-Santini (1982) | 6 | 0,35% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Dauvin & Gentil (1983) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Diviacco & Vader (1988) | 6 | 0,35% | 6 | 0,78% | 6 | 0,79% | 6 | 0,78% |
Ifremer (2009) | 6 | 0,35% | 5 | 0,65% | 5 | 0,66% | 5 | 0,65% |
Karaman (1929) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowry & Myers (2019) | 6 | 0,35% | 6 | 0,78% | 6 | 0,79% | 6 | 0,78% |
Myers et al. (1987) | 6 | 0,35% | 6 | 0,78% | 6 | 0,79% | 6 | 0,78% |
Stock (1971) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Bachelet et al. (2003) | 5 | 0,29% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Catta (1875) | 5 | 0,29% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chevreux (1893) | 5 | 0,29% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevreux (1920) | 5 | 0,29% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
DCE-Benthos Network, French Mediterranen Lagoon Monitoring Network (2022) | 5 | 0,29% | 5 | 0,65% | 5 | 0,66% | 5 | 0,65% |
Gourret (1891) | 5 | 0,29% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Hughes & Lowry (2010) | 5 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (2022) | 5 | 0,29% | 5 | 0,65% | 1 | 0,13% | 4 | 0,52% |
Laval (1968) | 5 | 0,29% | 5 | 0,65% | 5 | 0,66% | 5 | 0,65% |
Ledoyer (1975) | 5 | 0,29% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Paris (1918) | 5 | 0,29% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Razouls & Thiriot (1968) | 5 | 0,29% | 5 | 0,65% | 5 | 0,66% | 5 | 0,65% |
Ruffo et al. (2014) | 5 | 0,29% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Amanieu & Salvat (1963) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbé (1964) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Bate (1862) | 4 | 0,23% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bellan-Santini & Ledoyer (1974) | 4 | 0,23% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Bellan-Santini (1985) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Chevreux & Guernej (1892) | 4 | 0,23% | 1 | 0,13% | 1 | 0,13% | 0 | 0% |
Mémoires de la Société zoologique de France, 23(3-4): 145-285.">Chevreux (1911) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin & Bellan-santini (2002) | 4 | 0,23% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Goedmakers (1974) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 2 | 0,26% |
Graf & Straskraba (1968) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Hovencamp et al. (1983) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaim-malka (1976) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Karaman & Ruffo (1971) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Karaman (1931) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1971) | 4 | 0,23% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Karaman (1988) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Krapp-schickel (1975) | 4 | 0,23% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Laval (1980) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Ledoyer (1972) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 2 | 0,26% |
Montagu (1808) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinkster & Platvoet (1986) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Ruffo (1954) | 4 | 0,23% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Schellenberg (1950) | 4 | 0,23% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Stebbing (1888) | 4 | 0,23% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stock & Gledhill (1977) | 4 | 0,23% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Stock (1966) | 4 | 0,23% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Vonk (1988) | 4 | 0,23% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Aguesse (1960) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Alther et al. (2016) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ariyama (2004) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Arresti (1989) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Audouin (1826) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Balazuc (1957) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Barnard (1961) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 1 | 0,13% |
Bellan-Santini & Dauvin (1981) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Bellan-santini & Ruffo (1991) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Bou (1965) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Chevreux (1902) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chevreux (1912) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Coineau (1963) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Cousins et al. (2013) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Delamare et al. (1954) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Dole-Olivier et al. (2015) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gouillieux et al. (2015) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Gouillieux et al. (2016) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Gouillieux (2018) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Hoogenboom & Hennen (1985) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Hubault & Ruffo (1956) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2022) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Just (2017) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Kaim-malka (1983) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Karaman (1955) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Karaman (1969) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1980) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Kilgallen & Lowry (2014) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Krapp-Schnickel (1978) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Laubitz (1995) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Leach ([1814]) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 1 | 0,13% |
L'Hardy & Truchot (1964) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Mathieu & Taveau (1984) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Milne-Edwards (1830) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Myers et al. (2012) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Pinkster & Scholl (1984) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Pinkster & Stock (1971) | 3 | 0,18% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pinkster (1983) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Pouchet (1888) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Wichers (1964) | 3 | 0,18% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Arnal et al. (2015) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Arnaud (1974) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Barbe (1963) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1916) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Barnard (1957) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1962) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1973) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bartoli & Prévot (1986) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Beermann et al. (2018) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bellan-Santini & Diviacco (1990) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bellan-Santini & Ruffo (2003) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bellan-Santini (1972) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bigot (2006) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bou (1971) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Canadian Journal of Fisheries and Aquatic Sciences, 46(10): 1714-1725.">Bousfield (1989) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bréhier & Jaume (2009) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Catta (1877) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux & Bouvier (1892) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1890) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chevreux (1892) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1894) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1895) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chevreux (1900) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1908) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chevreux (1919) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cochard et al. (2010) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Conlan (1990) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Conlan (2021) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cuénot & Mercier (1921) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Dahl (1938) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dan & Capuse (1959) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin et al. (2014) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Dauvin et al. (2020) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Davoult (2010) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Devin et al. (2001) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Dubois et al. (2015) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Etcheberry & Abraham (2009) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
European Nucleotide Archive (2019) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Fabricius (1779) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Furnestin (1960) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Garcia-Paris et al. (2022) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Goedmakers & Pinkster (1977) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gouillieux & Sorbe (2015) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gouillieux et al. (2020) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gouillieux et al. (2020) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gouillieux et al. (2022) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gouillieux (2017) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gouillieux (2019) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Guerra-garcia et al. (2023) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Hertzog (1936) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ifremer (2023) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ifremer (2024) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Jaume et al. (1998) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kaim-Malka (2004) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kaim-malka (2012) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Karaman (1971) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Karaman (1973) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Karaman (1986) | 2 | 0,12% | 2 | 0,26% | 0 | 0% | 2 | 0,26% |
Karaman (1986) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Karaman (2022) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Krapp-Schickel & Sorbe (2006) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Krap-schickel (1974) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ledoyer (1970) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ledoyer (1986) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Margalef (1951) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Marquiegui & Perez (2006) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
100: 11-47.">Mateus & Maciel (1967) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Mathieu et al. (1994) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Mayer (1890) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Merlo et al. (2017) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Messouli et al. (2006) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Michel (2007) | 2 | 0,12% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Mills (1967) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Oliveira (1951) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Othaitz & Sorbe (2020) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pinkster (1969) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pinkster (1973) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Poupin (1994) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ramage (2017) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rathke (1843) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reid (1938) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Rigolet et al. (2014) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Robertson (1892) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rouville (1894) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ruffo (1959) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruffo (1959) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1895) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schaferna (1923) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Scheepmaker (1987) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Schellenberg (1934) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schellenberg (1937) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schiecke (1977) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Segerstrale (1947) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Senna (1908) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Shoemaker (1934) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Soika (1949) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Souben et al. (2014) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Spilmont et al. (2018) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Stephensen (1931) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Stephensen (1935) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Toulmond (1966) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Vandel (1920) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 1 | 0,13% |
Walker (1904) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Wathing & Maurer (1973) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
White (2011) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Whiteley et al. (2011) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Wildish (2014) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Wrzesniowski (1874) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Australian Museum (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Balazuc & Angelier (1952) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bulletin of the American Museum of Natural History, 127(1): 1-46.">Barnard (1964) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1969) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 0 | 0% |
Bate & Westwood (1863-68) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bate (1851) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Batisse & Dragesco (1967) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bellan-Santini (1972) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bessa et al. (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bigot et al. (2006) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeck (1871) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bollache (2004) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bovallius (1887) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brullé (1832) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brun & Brun (1964) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabezas et al. (2012) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Callame (1956) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cecchini (1928) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chauvel et al. (2023) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevreux & Fage (1925) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin de la Société Zoologique de France. 13: 31-35.">Chevreux (1888) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1890) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevreux (1909) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevreux (1922) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin de la Société Zoologique de France, 50: pp. 278-311.">Chevreux (1925) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ciavatti et al. (1993) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ciofini et al. (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ciofini et al. (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Clemente (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cochereau (1974) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Costa (1867) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Crawford (1937) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dana (1852) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Davoult et al. (1999) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Deblock et al. (1960) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Devin et al. (2005) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Droual et al. (2024) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dussart (1948) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Enequist (1950) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Evenhuis (2003) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Faasse (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Fabricius (1775) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fage (1934) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Forskål (1775) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fruget & Beisel (2016) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gambineri et al. (2008) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Glemarec (1963) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Glemarec (1965) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gouilleux (2022) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gouillieux & Droual (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gouillieux & Massé (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gouillieux et al. (2016) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gouillieux (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Grabowski et al. (2007) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Grube (1864) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Posidonia oceanica Delile. Recueil des Travaux de la Station Marine d'Endoume, 35(51): 43-105.">Harmelin (1964) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Helfer (1914) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the United States National Museum. 35(1654): 489-543; 46 figs.">Holmes (1908) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoover & Bousfield (2001) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Hynes (1959) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ifremer (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ifremer (2021) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Jazdzewski (1975) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourde et al. (2013) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Just (2009) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Karaman (1931) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1986) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kilgallen et al. (2006) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kohn & Waterstraat (1990) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Krapp et al. (1996) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bollettino del Museo Civico di Storia Naturale di Verona Botanica Zoologia, 26: 81-103.">Krapp-Schickel & Kulla (2002) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Krapp-Schickel (2013) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Krøyer (1842) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1817) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1825-[1828]) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Laubitz & Sorbe (1996) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Leitinger et al. (2021) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Liljeborg (1855) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Liljeborg (1856) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lincoln (1979) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lowry & Coleman (2011) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Marchini et al. (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Maren (1972) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Martynov 1924) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mateus et al. (1959) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayer (1882) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Mezzetti et al. (2010) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
MGnify (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Michel et al. (2019) | 1 | 0,06% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Miecherdzinski (1959) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Moniez (1887) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Montagu (1804) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1813) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Montfort (2001) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Proceedings of the Hawaiian Entomological Society, 9(1): 69-70.">Mumford (1935) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Myers & Ashelby (2022) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Myers & Mcgrath (1983) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Myers (1976) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noël (2016) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Norman & Scott (1906) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Norman (1865) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Nourisson & Scapini (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Oliveira (1954) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver & Trilles (2000) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pacaud (1944) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Paulmier (1996) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pearman et al. (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Peart & Hughes (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Perrier (1929) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Petit (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Piscart et al. (2008) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Piscart et al. (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Platvoet (1984) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Poisson (1924) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Questel (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Questel (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Reid (1939) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Roux (1964) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruffo & Schiecke (1975) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruffo (1946) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruffo (1987) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Salathe & Riera (2012) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sars (1858) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1879) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sars (1883) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Savigny (1816) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schellenberg (1925) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schellenberg (1935) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sellier et al. (2016) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sexton (1912) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sexton (1939) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sorbe & Elizalde (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stebbing (1874) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Stebbing (1906) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Steele (1968) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stephensen (1932) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephensen (1944) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Thomas et al. (1995) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Thomas (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Turquier (1965) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ugolini et al. (2015) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ugolini (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Uicn et al. (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Uicn et al. (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Van & Maren (1974) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vandel (1920) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Veloso et al. (2008) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Walker (1889) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1901) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Annals & Magazine of Natural History Series 7, 17: 452-458.">Walker (1906) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang et al. (2002) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Wildish (2018) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |