Chemical forms of Pb, Zn and Cu in the sediment profiles of the Pearl River Estuary

被引:363
作者
Li, XD [1 ]
Shen, ZG
Wai, OWH
Li, YS
机构
[1] Hong Kong Polytech Univ, Dept Civil & Struct Engn, Kowloon, Hong Kong, Peoples R China
[2] Nanjing Agr Univ, Dept Agron, Nanjing 210095, Peoples R China
关键词
heavy metals; sediment core; chemical speciation; Pb isotopes; the Pearl River Estuary; China;
D O I
10.1016/S0025-326X(00)00145-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 [工学]; 0830 [环境科学与工程];
摘要
The chemical forms of heavy metals (Pb, Zn and Cu) in sediment cores of the Pearl River Estuary were studied using a sequential chemical extraction method. The isotope ratios of (206)pb/Pb-207 in various chemical fractions were also measured to assess the potential Pb sources. Zinc and Cu were mainly associated with the residual fraction, The Fe-Mn oxide and organic/sulphide fractions were the next important phases for Zn and Cu, respectively. For Pb, different chemical partitioning patterns were found among different sediment cores. Most Ph was associated with the residual fraction in the sediments. In some sediment profiles, the major phase of Pb in the top layers was the Fe-Mn oxide fraction. The proportion of Pb in the Fe-Mn oxide fraction decreased significantly with increasing depth. Among the different depths, the (206)pb/(207)pb isotope ratios in the residual fraction remained fairly stable, with a mean value of 1.202, which may represent the natural background value, The (206)pb/Pb-207 ratios in the exchangeable fraction were the lowest among the five fractions, particularly in top sediments, showing the anthropogenic inputs of heavy metals from recent rapid industrial development in the surrounding region. For the other three non-residual fractions, there was a similar trend of increasing (206)pb/(207)pb ratios down the profile. Results from this study are useful in assessing both the chemical changes for heavy metals in marine sediments and the potential of heavy metal release into the water environment of an estuary area. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:215 / 223
页数:9
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