Bivalves marins de Nouvelle-Calédonie
197 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Héros et al. (2007) | 327 | 17,89% | 247 | 52% | 247 | 52,11% | 246 | 51,9% |
| Jay et al. (2009) | 131 | 7,17% | 77 | 16,21% | 77 | 16,24% | 77 | 16,24% |
| Tröndlé & Boutet (2009) | 98 | 5,36% | 64 | 13,47% | 64 | 13,5% | 64 | 13,5% |
| Bouchet et al. (2008) | 82 | 4,49% | 71 | 14,95% | 71 | 14,98% | 71 | 14,98% |
| Deuss et al. (2013) | 50 | 2,74% | 26 | 5,47% | 26 | 5,49% | 26 | 5,49% |
| Linnaeus (1758) | 42 | 2,3% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Glover & Taylor (2007) | 39 | 2,13% | 37 | 7,79% | 37 | 7,81% | 37 | 7,81% |
| Deshayes (1863) | 38 | 2,08% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Dijkstra (1995) | 29 | 1,59% | 25 | 5,26% | 25 | 5,27% | 25 | 5,27% |
| Iredale (1939) | 26 | 1,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamprell & Stanisic (1996) | 25 | 1,37% | 15 | 3,16% | 15 | 3,16% | 15 | 3,16% |
| Richard (2006) | 21 | 1,15% | 19 | 4% | 19 | 4,01% | 19 | 4,01% |
| Dijkstra (2001) | 20 | 1,09% | 20 | 4,21% | 20 | 4,22% | 20 | 4,22% |
| Lamprell & Healy (2001) | 19 | 1,04% | 11 | 2,32% | 11 | 2,32% | 11 | 2,32% |
| Richard et al. (1982) | 19 | 1,04% | 16 | 3,37% | 16 | 3,38% | 16 | 3,38% |
| Kleemann & Maestrati (2012) | 17 | 0,93% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal (1994) | 16 | 0,88% | 9 | 1,89% | 9 | 1,9% | 9 | 1,9% |
| Héros (comm. pers., 2011) | 13 | 0,71% | 10 | 2,11% | 10 | 2,11% | 10 | 2,11% |
| Gmelin (1791) | 12 | 0,66% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 12 | 0,66% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Australian Museum (2020) | 11 | 0,6% | 10 | 2,11% | 10 | 2,11% | 10 | 2,11% |
| Vidal & Kirkendale (2007) | 11 | 0,6% | 4 | 0,84% | 4 | 0,84% | 4 | 0,84% |
| Dall et al. (1938) | 10 | 0,55% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Vidal (1999) | 10 | 0,55% | 10 | 2,11% | 8 | 1,69% | 10 | 2,11% |
| Bergmans (1991) | 9 | 0,49% | 6 | 1,26% | 6 | 1,27% | 6 | 1,27% |
| Chabanet et al. (2007) | 9 | 0,49% | 8 | 1,68% | 8 | 1,69% | 8 | 1,69% |
| Poutiers & Bernard (1995) | 9 | 0,49% | 6 | 1,26% | 6 | 1,27% | 6 | 1,27% |
| Dijkstra (1991) | 8 | 0,44% | 7 | 1,47% | 7 | 1,48% | 7 | 1,48% |
| Souverbie (1863) | 8 | 0,44% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Dijkstra & Maestrati (2010) | 7 | 0,38% | 7 | 1,47% | 7 | 1,48% | 7 | 1,48% |
| Lamy & Pointier (2018) | 7 | 0,38% | 7 | 1,47% | 7 | 1,48% | 7 | 1,48% |
| Bartsch (1947) | 6 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kronen et al. (2008) | 6 | 0,33% | 5 | 1,05% | 5 | 1,05% | 5 | 1,05% |
| Lamarck (1818) | 6 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prashad (1932) | 6 | 0,33% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Willan (1993) | 6 | 0,33% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Huber et al. (2015) | 5 | 0,27% | 4 | 0,84% | 4 | 0,84% | 4 | 0,84% |
| Mulochau et al. (2020) | 5 | 0,27% | 4 | 0,84% | 4 | 0,84% | 4 | 0,84% |
| Pelorce & Hoarau (comm. pers., 2012) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poutiers (2006) | 5 | 0,27% | 5 | 1,05% | 5 | 1,05% | 5 | 1,05% |
| Uicn et al. (2019) | 5 | 0,27% | 3 | 0,63% | 3 | 0,63% | 3 | 0,63% |
| Dijkstra & Maestrati (2013) | 4 | 0,22% | 4 | 0,84% | 4 | 0,84% | 4 | 0,84% |
| Huber (2015) | 4 | 0,22% | 3 | 0,63% | 3 | 0,63% | 3 | 0,63% |
| Kaiser (2009) | 4 | 0,22% | 4 | 0,84% | 4 | 0,84% | 4 | 0,84% |
| Krylova (2001) | 4 | 0,22% | 4 | 0,84% | 4 | 0,84% | 4 | 0,84% |
| Martin (2011) | 4 | 0,22% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Melvill (1909) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 4 | 0,22% | 3 | 0,63% | 3 | 0,63% | 3 | 0,63% |
| Poutiers (1981) | 4 | 0,22% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Powell (1933) | 4 | 0,22% | 3 | 0,63% | 3 | 0,63% | 3 | 0,63% |
| Barnard (1964) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Born (1778) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambert et al. (2011) | 3 | 0,16% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Cox (1927) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra & Maestrati (2013) | 3 | 0,16% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Gout (1991) | 3 | 0,16% | 3 | 0,63% | 3 | 0,63% | 3 | 0,63% |
| Memoirs of the Australian Museum, iv: 287-324.">Hedley (1902) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1929) | 3 | 0,16% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Matsukuma (1996) | 3 | 0,16% | 3 | 0,63% | 3 | 0,63% | 3 | 0,63% |
| Poutiers (1982) | 3 | 0,16% | 3 | 0,63% | 3 | 0,63% | 3 | 0,63% |
| Sakurai & Habe (1966) | 3 | 0,16% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Salas & Gofas (1998) | 3 | 0,16% | 3 | 0,63% | 3 | 0,63% | 3 | 0,63% |
| Taylor & Glover (2013) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turton (1932) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vergonzanne (1977) | 3 | 0,16% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Wantiez (2001) | 3 | 0,16% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Azuma (1960) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bozzetti (1996) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dell (1956) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra & Marshall (2008) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Dijkstra (1986) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra (1990) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Drivas & Jay (1990) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fischer (1859) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Fischer-Piette (1977) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fulton (1915) | 2 | 0,11% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Garrard (1966) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Godet et al. (2010) | 2 | 0,11% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Grau (1960) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Habe & Kosuge (1966) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Habe (1958) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harte & Lamprell (1999) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Hidalgo (1903) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1936) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kleemann (1980) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kleemann (2008) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kotaka (1977) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kronen et al. (2009) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Lamprell & Healy (1997) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamprell & Kilburn (1999) | 2 | 0,11% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Lamy (1907) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas et al. (1991) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Melvill (1898) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montrouzier (1860) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Nelson-Smith et al. (2014) | 2 | 0,11% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Nielsen (1986) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Oyama (1951) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poutiers (1985) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Preston (1908) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shikama (1964) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1884) | 2 | 0,11% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Souverbie (1860) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Taylor et al. (2016) | 2 | 0,11% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Ter Poorten (2012) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Ter Poorten (2013) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| ter Poorten (2023) | 2 | 0,11% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Thang & Tsi (1960) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiele (1930) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Viader (1951) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal (1993) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walier (1972) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wang (1984) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zorina (1978) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Andrefouet et al. (2014) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Barnard (1962) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet (2002) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Breton (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cockerell (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dautzenberg (1900) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekker (2006) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delsaerdt (1986) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewarumez et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra & Beu (2018) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra & Maestrati (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Dijkstra & Maestrati (2012) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Dijkstra (1993) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Dijkstra (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dijkstra (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Dijkstra (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Dijkstra (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Dijkstra (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Dijkstra (2011) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Franc (1956) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrard (1963) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grabau & King (1928) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Habe & Tokioka (1953) | 1 | 0,05% | 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 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harry (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley & Petterd (1906) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley (1909) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedley (1921) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huber & Schultz (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Iredale (1927) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1931) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iredale (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kira (1959) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kleemann (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Knop (2007) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Kuriakose et al. (1976) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Kuroda (1945) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ladd (1934) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Lamarck (1819) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamy (1918) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorion (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Lorion (2005) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Lucas (1978) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lynge (1909) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mary (2017) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Massemin et al. (2009) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Matsukuma (1989) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Melvill (1896) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Melvill (1906) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menzel (1974) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morris & Morris (1993) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nicet & Denis (2011) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Nolf (1993) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Noseworthy et al. (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ohno et al. (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Okutani & Kawaguchi (1991) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliver et al. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orton (1928) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Otuka (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pilsbry (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poutiers (1993) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Preston (1910) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quod et al. (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeve (1850-1851) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salisbury (1934) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sartori (1993) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Sartori (1999) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Schepman (1907) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1885) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annals of Natural History, xvi: 1-19.">Smith (1895) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starmühlner (1970) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ter Poorten (2000) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Ter Poorten (2008) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tiavouane & Fauvelot (2017) | 1 | 0,05% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Wood-Mason & Alcock (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
