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Synchronous barium peaks in high-resolution profiles of calcite and aragonite marine bivalve shells
Gillikin, D.P.; Lorrain, A.; Paulet, Y.M.; André, L.; Dehairs, F. (2008). Synchronous barium peaks in high-resolution profiles of calcite and aragonite marine bivalve shells. Geo-Mar. Lett. 28(5-6): 351-358. dx.doi.org/10.1007/s00367-008-0111-9
In: Geo-Marine Letters. Springer: Heidelberg; Berlin. ISSN 0276-0460; e-ISSN 1432-1157, more
Peer reviewed article  

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Keyword
    Marine/Coastal

Authors  Top 
  • Gillikin, D.P., more
  • Lorrain, A.
  • Paulet, Y.M.

Abstract
    Barium/calcium profiles of bivalve shells are characterized by flat background signals periodically interrupted by sharp peaks, with the background signals correlated with water Ba/Ca. To test if the peaks are an environmental signal related to productivity, we analyzed high-resolution Ba/Ca profiles in bivalve shells that grew adjacent to one another. Two aragonitic Saxidomus giganteus show remarkable similarity over a decade of growth, clearly indicating an environmental forcing. Four calcitic Pecten maximus shells also record synchronous Ba/Ca peaks, again indicating an exogenous control. The Ba/Ca peaks, however, start similar to 40 days after the crash of a bloom, while sedimentation takes place immediately following the bloom. Barite formation in settling phytoplankton flocs, as has been previously proposed, is clearly not the cause of these peaks. Other possible causes, such as dissolved Ba in ambient water, spawning, shell organic matter content, and kinetic growth rate effects are also discussed, but none provide satisfactory explanations. Background shell Ba partition coefficients (Ba/Ca(carbonate)/Ba/Ca(water)) for both the calcitic shells (0.18) and aragonitic shells (0.16) are similar to that previously reported for the calcitic Mytilus edulis (similar to 0.1). We suggest that Ba/Ca peaks in bivalve shells are caused by an as yet undetermined environmental forcing, while background Ba/Ca levels are a good indication of dissolved Ba/Ca in the water; both are independent of shell mineralogy.

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