Chemical composition of two mineralogically contrasting Arctic bivalves' shells and their relationships to environmental variables

被引:11
|
作者
Iglikowska, A. [1 ]
Beldowski, J. [2 ]
Chelchowski, M. [1 ]
Chierici, M. [3 ,4 ]
Kedra, M. [1 ]
Przytarska, J. [1 ]
Sowa, A. [1 ]
Kuklinski, P. [1 ]
机构
[1] Polish Acad Sci, Inst Oceanol, Marine Ecol Dept, Powstancow Warszawy 55, PL-81712 Sopot, Poland
[2] Polish Acad Sci, Inst Oceanol, Marine Chem & Biochem Dept, Powstancow Warszawy 55, PL-81712 Sopot, Poland
[3] Inst Marine Res, Sykehusveien 23, N-9294 Tromso, Norway
[4] Univ Ctr Svalbard, Longyearbyen, Norway
关键词
Trace metals; Shell mineralogy; Arctic; Bivalves; Seawater carbonates; COCKLE CLINOCARDIUM-CILIATUM; OCEAN ACIDIFICATION; CHLAMYS-ISLANDICA; ICELAND SCALLOP; CARBONIC-ACID; CALCITE; SEAWATER; GROWTH; DISSOCIATION; SVALBARD;
D O I
10.1016/j.marpolbul.2016.10.071
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The main goal of this study was to determine the concentrations of trace elements in the mineralogically contrasting shells of two Arctic bivalves: Chlamys islandica and Ciliatocardium ciliatum. Aragonite shells seem to be more susceptible to the binding of metal ions, which is most likely a result of their crystal lattice structure. We suggest that less biologically controlled aragonite mineralization tends to incorporate more metal impurities into the crystal lattice in waters with a lower pH, where metal ions are more available. Higher concentrations of impurities may further increase the lattice distortion causing lower crystal lattice stability and higher susceptibility to dissolution. Calcitic shells seem to be less prone to bind metal ions than aragonite shells most likely because under strict biological control, the uptake of ions from ambient seawater is more selective; thus, the final crystal lattice is less contaminated by other metals and is more resistant to dissolution. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:903 / 916
页数:14
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