Bivalves marins de Guyane
58 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Lamy & Pointier (2018) | 311 | 39,12% | 285 | 172,73% | 285 | 172,73% | 285 | 172,73% |
Massemin et al. (2009) | 128 | 16,1% | 88 | 53,33% | 88 | 53,33% | 88 | 53,33% |
Taylor & Glover (2016) | 25 | 3,14% | 25 | 15,15% | 25 | 15,15% | 25 | 15,15% |
Questel (2020) | 22 | 2,77% | 20 | 12,12% | 20 | 12,12% | 20 | 12,12% |
Questel & Le Quellec (2012) | 21 | 2,64% | 15 | 9,09% | 15 | 9,09% | 15 | 9,09% |
Linnaeus (1758) | 17 | 2,14% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Taylor et al. (2016) | 9 | 1,13% | 9 | 5,45% | 9 | 5,45% | 9 | 5,45% |
Gmelin (1791) | 6 | 0,75% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 6 | 0,75% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Dall et al. (1938) | 5 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Jay et al. (2009) | 5 | 0,63% | 3 | 1,82% | 3 | 1,82% | 3 | 1,82% |
Deshayes (1863) | 4 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2011) | 4 | 0,5% | 4 | 2,42% | 4 | 2,42% | 4 | 2,42% |
Olsson (1961) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Boss (1964) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Dautzenberg (1900) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Delannoye et al. (2015) | 2 | 0,25% | 2 | 1,21% | 2 | 1,21% | 2 | 1,21% |
Fourt et al. (2017) | 2 | 0,25% | 2 | 1,21% | 2 | 1,21% | 2 | 1,21% |
Jourde et al. (2017) | 2 | 0,25% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Narchi (1975) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Pilsbry & Lowe (1932) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié (2017) | 2 | 0,25% | 2 | 1,21% | 2 | 1,21% | 2 | 1,21% |
Pulteney (1799) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Rehder & Abbott (1951) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Taki & Habe (1945) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Clapp (1923) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Clapp (1924) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Coan (1988) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Conrad (1831) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall & Simpson (1901) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Dall (1901) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall (1908) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall (1915) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewarumez et al. (2011) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Falkner et al. (2002) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Gargominy et al. (2011) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Girardi (2003) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Guppy (1882) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Hendrickx (1980) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Héros et al. (2007) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoagland (1986) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Ifremer (2009) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Kaiser (2009) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Lamprell & Healy (2001) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1759) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Macsotay et al. (2001) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicet & Denis (2011) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Nicolay (1981) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié (2020) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Questel (2022) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Rehder (1943) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Richards (1955) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiele & Jaeckel (1931) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Journal of Conchology London, 18: 307-310.">Tomlin (1929) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Verrill & Bush (1898) | 1 | 0,13% | 1 | 0,61% | 1 | 0,61% | 1 | 0,61% |
Zetek & Mclean (1936) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |