Bivalves marins de la Réunion
137 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Jay et al. (2009) | 307 | 17,31% | 183 | 55,96% | 183 | 55,96% | 183 | 55,96% |
Héros et al. (2007) | 114 | 6,43% | 81 | 24,77% | 81 | 24,77% | 81 | 24,77% |
Deshayes (1863) | 105 | 5,92% | 16 | 4,89% | 16 | 4,89% | 16 | 4,89% |
Tröndlé & Boutet (2009) | 84 | 4,74% | 57 | 17,43% | 57 | 17,43% | 57 | 17,43% |
Deuss et al. (2013) | 65 | 3,66% | 38 | 11,62% | 38 | 11,62% | 38 | 11,62% |
Linnaeus (1758) | 34 | 1,92% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Lamy & Pointier (2018) | 28 | 1,58% | 27 | 8,26% | 27 | 8,26% | 27 | 8,26% |
Richard (2006) | 26 | 1,47% | 22 | 6,73% | 22 | 6,73% | 22 | 6,73% |
Iredale (1939) | 24 | 1,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard et al. (1982) | 18 | 1,01% | 13 | 3,98% | 13 | 3,98% | 13 | 3,98% |
Chabanet et al. (2007) | 17 | 0,96% | 14 | 4,28% | 14 | 4,28% | 14 | 4,28% |
Dall et al. (1938) | 15 | 0,85% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Gmelin (1791) | 12 | 0,68% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 12 | 0,68% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Mulochau et al. (2020) | 12 | 0,68% | 11 | 3,36% | 11 | 3,36% | 11 | 3,36% |
Turton (1932) | 11 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 9 | 0,51% | 7 | 2,14% | 7 | 2,14% | 7 | 2,14% |
Pelorce & Hoarau (comm. pers., 2012) | 8 | 0,45% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Lamprell & Healy (2001) | 7 | 0,39% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Lamprell & Stanisic (1996) | 7 | 0,39% | 5 | 1,53% | 5 | 1,53% | 5 | 1,53% |
Pearman et al. (2020) | 7 | 0,39% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Bouchet et al. (2008) | 6 | 0,34% | 6 | 1,83% | 6 | 1,83% | 6 | 1,83% |
Cambert et al. (2011) | 6 | 0,34% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Kaiser (2009) | 6 | 0,34% | 5 | 1,53% | 5 | 1,53% | 5 | 1,53% |
Martin (2011) | 6 | 0,34% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Viader (1951) | 6 | 0,34% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Kronen et al. (2008) | 5 | 0,28% | 4 | 1,22% | 4 | 1,22% | 4 | 1,22% |
Nelson-Smith et al. (2014) | 5 | 0,28% | 3 | 0,92% | 3 | 0,92% | 3 | 0,92% |
Thiele & Jaeckel (1931) | 5 | 0,28% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Vidal (1994) | 5 | 0,28% | 3 | 0,92% | 3 | 0,92% | 3 | 0,92% |
Dijkstra & Maestrati (2010) | 4 | 0,23% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Drivas & Jay (1990) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 4 | 0,23% | 3 | 0,92% | 3 | 0,92% | 3 | 0,92% |
Gout (1991) | 4 | 0,23% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Melvill (1909) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Odhner (1919) | 4 | 0,23% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Preston (1908) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 4 | 0,23% | 3 | 0,92% | 3 | 0,92% | 3 | 0,92% |
Barnard (1964) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Born (1778) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Boshoff (1965) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourcier (1988) | 3 | 0,17% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Dijkstra (2001) | 3 | 0,17% | 3 | 0,92% | 3 | 0,92% | 3 | 0,92% |
Ifremer (2020) | 3 | 0,17% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Iredale (1929) | 3 | 0,17% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Kotaka (1977) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1818) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Prashad (1932) | 3 | 0,17% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Vergonzanne (1977) | 3 | 0,17% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Breton (2014) | 2 | 0,11% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Dijkstra (1988) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 2 | 0,11% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Habe & Kosuge (1966) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Héros (comm. pers., 2011) | 2 | 0,11% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Huber (2015) | 2 | 0,11% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Iredale (1927) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Iredale (1931) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kleemann & Maestrati (2012) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamprell & Kilburn (1999) | 2 | 0,11% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Laseron (1953) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Massemin et al. (2009) | 2 | 0,11% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Melvill (1898) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicet & Denis (2011) | 2 | 0,11% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Oliver & Holmes (2004) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Orton (1928) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Powell (1967) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Preston (1904) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Robert et al. (1991) | 2 | 0,11% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Sakurai & Habe (1966) | 2 | 0,11% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Smith (1910) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Taki & Habe (1945) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Thang & Tsi (1960) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal (1999) | 2 | 0,11% | 2 | 0,61% | 2 | 0,61% | 2 | 0,61% |
Voskuil & Onverwagt (1991) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wantiez (2001) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrefouet et al. (2014) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Arzul et al. (2011) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Australian Museum (2020) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Barnard (1962) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Beu (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot (2006) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchet (2002) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Cox (1927) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall (1924) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dautzenberg & Fischer (1897) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dautzenberg (1923) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Dewarumez et al. (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dijkstra & Beu (2018) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dijkstra & Maestrati (2013) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dijkstra (1998) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fulton (1915) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrard (1963) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Habe (1958) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Habe (1961) | 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% |
Hedley & Petterd (1906) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley (1909) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley (1921) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Huber & Schultz (2005) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Huber (2010) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Ifremer (2023) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Iredale (1924) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Iredale (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jameson (1901) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kilburn (1973) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1953) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuriakose et al. (1976) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Kuroda (1945) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Melvill (1906) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Menzel (1974) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Morris & Morris (1993) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Noda (1966) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Noseworthy et al. (2007) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver et al. (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Poutiers (1993) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Poutiers (2006) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Preston (1906) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Preston (1910) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Preston (1913) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pulteney (1799) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Quod et al. (1995) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Salisbury (1934) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schepman (1907) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1903) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1903) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Takeda (1953) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ter Poorten (2000) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal (1997) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang (1983) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (1920) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Zetek & Mclean (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Zibrowius & Arnaud (1995) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Zinke et al. (2005) | 1 | 0,06% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |