Bivalves marins de métropole
165 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Martin (2011) | 242 | 8,74% | 202 | 43,63% | 202 | 43,91% | 202 | 43,91% |
Nelson-Smith et al. (2014) | 146 | 5,27% | 111 | 23,97% | 111 | 24,13% | 111 | 24,13% |
Ifremer (2009) | 129 | 4,66% | 91 | 19,65% | 91 | 19,78% | 89 | 19,35% |
Godet et al. (2010) | 97 | 3,5% | 75 | 16,2% | 75 | 16,3% | 75 | 16,3% |
Linnaeus (1758) | 72 | 2,6% | 15 | 3,24% | 15 | 3,26% | 15 | 3,26% |
Krylova & Janssen (2019) | 63 | 2,28% | 63 | 13,61% | 62 | 13,48% | 62 | 13,48% |
Bourcier (1988) | 55 | 1,99% | 28 | 6,05% | 28 | 6,09% | 28 | 6,09% |
Lamy & Pointier (2018) | 27 | 0,98% | 26 | 5,62% | 26 | 5,65% | 26 | 5,65% |
Breton (2014) | 24 | 0,87% | 20 | 4,32% | 20 | 4,35% | 20 | 4,35% |
Bucquoy et al. (1892) | 24 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 18 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 18 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 16 | 0,58% | 13 | 2,81% | 13 | 2,83% | 13 | 2,83% |
Rignault & Chevallier (2017) | 13 | 0,47% | 7 | 1,51% | 7 | 1,52% | 7 | 1,52% |
Fourt et al. (2017) | 11 | 0,4% | 11 | 2,38% | 11 | 2,39% | 11 | 2,39% |
Dewarumez et al. (2011) | 10 | 0,36% | 8 | 1,73% | 8 | 1,74% | 8 | 1,74% |
Goud et al. (2020) | 8 | 0,29% | 8 | 1,73% | 8 | 1,74% | 8 | 1,74% |
Prié (2017) | 8 | 0,29% | 8 | 1,73% | 6 | 1,3% | 6 | 1,3% |
Verrill & Bush (1898) | 8 | 0,29% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Dall et al. (1938) | 7 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Massemin et al. (2009) | 7 | 0,25% | 4 | 0,86% | 4 | 0,87% | 4 | 0,87% |
Jay et al. (2009) | 6 | 0,22% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Dautzenberg & Fischer (1897) | 5 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Deshayes (1863) | 5 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Langeveld et al. (2020) | 5 | 0,18% | 5 | 1,08% | 5 | 1,09% | 5 | 1,09% |
MGnify (2017) | 5 | 0,18% | 5 | 1,08% | 5 | 1,09% | 5 | 1,09% |
Bouchet et al. (2022) | 4 | 0,14% | 4 | 0,86% | 4 | 0,87% | 4 | 0,87% |
Cépède (1914) | 4 | 0,14% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Dall (1916) | 4 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Poulicek (2020) | 4 | 0,14% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Turton (1932) | 4 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 4 | 0,14% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Allen & Hannah (1989) | 3 | 0,11% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Cosel (1995) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Costa (1778) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 3 | 0,11% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Etcheberry & Abraham (2009) | 3 | 0,11% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Linnaeus (1767) | 3 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Lucas (1984) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Orton (1928) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Roch & Moll (1931) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal (2005) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vierna et al. (2012) | 3 | 0,11% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Bernard (1983) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisseau & Lubet (1955) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourcier & Zibrowius (1969) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delannoye et al. (2015) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Falkner et al. (2002) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Fischer-Piette (1977) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (2011) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Posidonia oceanica Delile. Recueil des Travaux de la Station Marine d'Endoume, 35(51): 43-105.">Harmelin (1964) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hertlein & Grant (1972) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Høpner et al. (1971) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaltenbach (1943) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaltenbach (1949) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuriakose et al. (1976) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuronuma (1931) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1818) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Mao et al. (2020) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Linnaeus (1767) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Lucas (1984) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Mars (1965) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Menzel (1974) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelorce & Poutiers (2009) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Pennant (1777) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 2 | 0,07% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Questel (2020) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Robert et al. (1991) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Smith (1910) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Von & Cosel (2009) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Wisshak et al. (2009) | 2 | 0,07% | 2 | 0,43% | 2 | 0,43% | 2 | 0,43% |
Allen (2015) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Allen (2015) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Andrusov (1897) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Arzul et al. (2011) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Arzul et al. (2013) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Bartsch (1921) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1914) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Berry (1947) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
bij de Vaate & Beisel (2011) | 1 | 0,04% | 1 | 0,22% | 0 | 0% | 1 | 0,22% |
Bogi (2015) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Canu (1891) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevaldonné et al. (2015) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Coen (1915) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Coen (1933) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Coen (1941) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Combrisson (2023) | 1 | 0,04% | 1 | 0,22% | 0 | 0% | 1 | 0,22% |
Comfort (1938) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Conrad (1831) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Costa (1830) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dautzenberg (1891) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin et al. (2022) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Davoult et al. (1999) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Davoult (1990) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
de Folin & Périer (1875) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Delongueville & Scaillet (2007) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Desgué (2020) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Faillettaz et al. (2020) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Fruget & Beisel (2016) | 1 | 0,04% | 1 | 0,22% | 0 | 0% | 1 | 0,22% |
Girardi (2003) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Girscher (1938) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gouillieux (2018) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Grizel et al. (1983) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Héros et al. (2007) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Hoenselaar & Hoenselaar (1989) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Huber (2015) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Ifremer (2019) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Ifremer (2020) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Jeffreys (1860) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Keen (1962) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kilburn (1973) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kilburn (1975) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1801) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Marescaux et al. (2012) | 1 | 0,04% | 1 | 0,22% | 0 | 0% | 1 | 0,22% |
Mars (1951) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Journal of Conchology Leeds, 14: 182-190; 200-213.">Marshall (1914) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Massé et al. (2022) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
McGill (1964) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Mohr (1786) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Monod & Dollfus (1932) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Monterosato (1899) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Nair (1956) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Nair (1958) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Neuthiec (1991) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Nicet & Denis (2011) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Nolf (2010) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Olivi (1792) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1771) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Payraudeau (1826) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Perna & D'Abramo (2009) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Poli (1791) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Porta et al. (2009) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Poutiers (1984) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Powell (1960) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Preston (1913) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié & Fruget (2017) | 1 | 0,04% | 1 | 0,22% | 0 | 0% | 1 | 0,22% |
Pulteney (1799) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Quayle (1938) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Quayle (1939) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (2006) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosewater (1984) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Salisbury (1934) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Severijns (2000) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Severijns (2004) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Skarlato (1981) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Smriglio & Buzzurro (1999) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Stepien et al. (2013) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Denkschriften der Kaiserlichen Akademie der Wissenschaften, Mathematische-Naturwissenschaftlischen Classe. 63: 1-36.">Sturany (1896) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sykes (1903) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Takeda (1953) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Taki & Habe (1945) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiele & Jaeckel (1931) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
van Aartsen & Giannuzzi-Savelli (1991) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
van Aartsen et al. (1984) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Van Guelpen (2016) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Van Rooijet al. (2010) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Warén (1978) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Watson (1897) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Winckworth (1931) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Wolowicz (1992) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Yokoyama (1920) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Zenetos et al. (2005) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |