Bivalves marins de Polynésie française
107 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Tröndlé & Boutet (2009) | 196 | 19,18% | 132 | 58,67% | 132 | 58,67% | 132 | 58,67% |
Jay et al. (2009) | 84 | 8,22% | 51 | 22,67% | 51 | 22,67% | 51 | 22,67% |
Héros et al. (2007) | 82 | 8,02% | 65 | 28,89% | 65 | 28,89% | 65 | 28,89% |
Deshayes (1863) | 40 | 3,91% | 3 | 1,33% | 3 | 1,33% | 3 | 1,33% |
Deuss et al. (2013) | 34 | 3,33% | 21 | 9,33% | 21 | 9,33% | 21 | 9,33% |
Linnaeus (1758) | 21 | 2,05% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Dall et al. (1938) | 20 | 1,96% | 8 | 3,56% | 8 | 3,56% | 8 | 3,56% |
Iredale (1939) | 19 | 1,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Dijkstra & Maestrati (2010) | 18 | 1,76% | 16 | 7,11% | 16 | 7,11% | 16 | 7,11% |
Richard et al. (1982) | 18 | 1,76% | 14 | 6,22% | 14 | 6,22% | 14 | 6,22% |
Richard (2006) | 18 | 1,76% | 16 | 7,11% | 16 | 7,11% | 16 | 7,11% |
Bouchet et al. (2008) | 14 | 1,37% | 13 | 5,78% | 13 | 5,78% | 13 | 5,78% |
Huber et al. (2015) | 13 | 1,27% | 13 | 5,78% | 13 | 5,78% | 13 | 5,78% |
Dijkstra & Maestrati (2013) | 11 | 1,08% | 10 | 4,44% | 10 | 4,44% | 10 | 4,44% |
Chabanet et al. (2007) | 10 | 0,98% | 9 | 4% | 9 | 4% | 9 | 4% |
Dijkstra (1995) | 9 | 0,88% | 9 | 4% | 9 | 4% | 9 | 4% |
Uicn et al. (2019) | 9 | 0,88% | 7 | 3,11% | 7 | 3,11% | 7 | 3,11% |
Dijkstra (2001) | 8 | 0,78% | 8 | 3,56% | 8 | 3,56% | 8 | 3,56% |
Huber (2010) | 8 | 0,78% | 4 | 1,78% | 4 | 1,78% | 4 | 1,78% |
Pearman et al. (2020) | 8 | 0,78% | 4 | 1,78% | 4 | 1,78% | 4 | 1,78% |
Kaiser (2009) | 7 | 0,68% | 6 | 2,67% | 6 | 2,67% | 6 | 2,67% |
Kleemann & Maestrati (2012) | 7 | 0,68% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartsch (1947) | 6 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamy & Pointier (2018) | 6 | 0,59% | 6 | 2,67% | 6 | 2,67% | 6 | 2,67% |
Mulochau et al. (2020) | 6 | 0,59% | 5 | 2,22% | 5 | 2,22% | 5 | 2,22% |
Gmelin (1791) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Kronen et al. (2008) | 5 | 0,49% | 4 | 1,78% | 4 | 1,78% | 4 | 1,78% |
Turton (1932) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal & Kirkendale (2007) | 5 | 0,49% | 2 | 0,89% | 2 | 0,89% | 2 | 0,89% |
Glover & Taylor (2007) | 4 | 0,39% | 4 | 1,78% | 4 | 1,78% | 4 | 1,78% |
Martin (2011) | 4 | 0,39% | 2 | 0,89% | 2 | 0,89% | 2 | 0,89% |
Wang (1983) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Born (1778) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Calvez & Guillou (1998) | 3 | 0,29% | 3 | 1,33% | 3 | 1,33% | 3 | 1,33% |
Dijkstra (1991) | 3 | 0,29% | 3 | 1,33% | 3 | 1,33% | 3 | 1,33% |
Héros (comm. pers., 2011) | 3 | 0,29% | 3 | 1,33% | 3 | 1,33% | 3 | 1,33% |
Iredale (1931) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamprell & Stanisic (1996) | 3 | 0,29% | 3 | 1,33% | 3 | 1,33% | 3 | 1,33% |
Melvill (1909) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelorce & Hoarau (comm. pers., 2012) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry (1921) | 3 | 0,29% | 2 | 0,89% | 2 | 0,89% | 2 | 0,89% |
Vergonzanne (1977) | 3 | 0,29% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Vidal (1999) | 3 | 0,29% | 3 | 1,33% | 3 | 1,33% | 3 | 1,33% |
Azuma (1960) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Cambert et al. (2011) | 2 | 0,2% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Dewarumez et al. (2011) | 2 | 0,2% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Dijkstra (1990) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Dijkstra (2011) | 2 | 0,2% | 2 | 0,89% | 2 | 0,89% | 2 | 0,89% |
Fourt et al. (2017) | 2 | 0,2% | 2 | 0,89% | 2 | 0,89% | 2 | 0,89% |
Godet et al. (2010) | 2 | 0,2% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Goulletquer (2016) | 2 | 0,2% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Grau (1960) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Habe (1976) | 2 | 0,2% | 2 | 0,89% | 2 | 0,89% | 2 | 0,89% |
Harte (1993) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Huber (2015) | 2 | 0,2% | 2 | 0,89% | 2 | 0,89% | 2 | 0,89% |
Laseron (1953) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Preston (1908) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Schultz & Huber (2013) | 2 | 0,2% | 2 | 0,89% | 2 | 0,89% | 2 | 0,89% |
Shikama (1964) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Walier (1972) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrefouet et al. (2014) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Australian Museum (2020) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Bouchet (2002) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Dall (1908) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall (1924) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Dang et al. (2008) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Delsaerdt (1986) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Dijkstra & Maestrati (2012) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Dijkstra (1998) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Fulton (1915) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gout (1991) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Harry (1985) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley & Petterd (1906) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley (1909) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley (1921) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Huber & Schultz (2005) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Huber (2010) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Iredale (1927) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Iredale (1929) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Kleemann (2008) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1953) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuriakose et al. (1976) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Lamprell & Healy (2001) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Melvill (1898) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Menzel (1974) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Nelson-Smith et al. (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Noda (1966) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Nolf (1993) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Noseworthy et al. (2007) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Orton (1928) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Poutiers (1981) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Prashad (1932) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Preston (1915) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Quayle (1938) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Quayle (1939) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rehder (1980) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sakurai & Habe (1966) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sartori (1993) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |
Smith (1903) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Wantiez (2001) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama 1922 | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Zinke et al. (2005) | 1 | 0,1% | 1 | 0,44% | 1 | 0,44% | 1 | 0,44% |