Crystallography and chemistry of the calcium carbonate polymorph switch in M. edulis shells

被引:69
作者
Dalbeck, Paul
England, Jennifer
Cusack, Maggie
Lee, Martin R.
Fallick, Anthony E.
机构
[1] Univ Glasgow, Dept Geog & Earth Sci, Glasgow G12 8QQ, Lanark, Scotland
[2] Scottish Univ Environm Res Ctr, E Kilbride C75 0QF, Lanark, Scotland
关键词
polymorph interface; Electron Backscatter Diffraction (EBSD); mineral bridges; carbonate chemistry;
D O I
10.1127/0935-1221/2006/0018-0601
中图分类号
P57 [矿物学];
学科分类号
070901 ;
摘要
The control exerted by some invertebrates on the calcium carbonate polymorph produced is intriguing but not understood. Mytilus edulis shells, with the abrupt polymorph switch within their valves from an outer calcite to inner aragonite layer, are excellent examples of this phenomenon. Detailed crystallography of intact valves using Electron Backscatter Diffraction (EBSD) is considered in the context of quantitative chemical analyses by electron microprobe. Apart from the outer 40 pm, individual crystals that comprise the calcite layer of M. edulis differ from each other in terms of misorientation by less than 10 degrees. Similar uniformity occurs in the inner aragonite layer with notable 'mineral bridging' between tablets of aragonite nacre. The first-formed aragonite laminae are submicron thickness and the subsequent laminae of uniform 1 mu m thickness. Variations in chemical composition through the two valves correspond in part with the distribution of the two polymorphs. Magnesium is present in notably higher concentrations within calcite than aragonite. However, the Mg2+ concentration in calcite is not uniform and increases with growth before decreasing at the polymorph switch. Sodium concentrations decrease steadily through the calcite layer. The aragonite layer is compositionally more uniform. Sulphur is not a good proxy for organic content in this system because it does not reflect the higher organic content of the aragonite. Sector zoning is not responsible for the element distribution seen here while differences in crystal size and association with organic components remain as possible explanations.
引用
收藏
页码:601 / 609
页数:9
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