Analysis of fish otoliths by electrothermal vaporization inductively coupled plasma mass spectrometry: aspects of precipitating otolith calcium with hydrofluoric acid for trace element determination

被引:17
作者
Arslan, Z [1 ]
机构
[1] NOAA, NE Fisheries Sci Ctr, James J Howard Marine Sci Lab, Highlands, NJ 07732 USA
基金
美国海洋和大气管理局;
关键词
fish otoliths; trace elements; calcium fluoride precipitation; electrothermal vaporization; inductively coupled plasma mass spectrometry;
D O I
10.1016/j.talanta.2004.09.009
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method is developed for determination of trace elements, including Ag, As, Cd, Co, Cr, Cu, Mn, Ni, Se, TI and Zn, in fish otoliths by electrothermal vaporization inductively coupled plasma mass spectrometry (ETV-ICP-MS). Hydrofluoric acid was used to precipitate calcium resulting from acid dissolution of otolith calcium carbonate. Initial acidity of the sample solution influenced the precipitation efficiency of calcium fluoride. Up to 99.5% of Ca was precipitated in solutions that contained less than 2% (v/v) HNO3. Recoveries of the elements obtained from spiked artificial otolith solutions were between 90 and 103%. Stabilization of the elements within the ETV cell was achieved with 0.3 mu g Pd/0.2 mu g Rh chemical modifier that also afforded optimum sensitivity for multielement determination. The method was validated by the analysis of a fish otolith reference material (CRM) of emperor snapper. and then applied to the determination of the trace elements in otoliths of several fish species captured in Raritan Bay, New Jersey. Results indicated that fish physiology and biological processes could influence the levels of Cu, Mn, Se and Zn in the otoliths of fish inhabiting a similar aqueous environment. Otolith concentrations of Cr and Ni did not show any significant differences among different species. Concentrations for Ag, As, Cd, Co and TI were also not significantly different, but were very low indicating low affinity of otolith calcium carbonate to these elements. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1326 / 1334
页数:9
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