Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/92986
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Title: Using mercury isotopes to understand the bioaccumulation of Hg in the subtropical Pearl River Estuary, South China
Authors: Yin, R 
Feng, X
Zhang, J 
Pan, K
Wang, W
Li, X 
Issue Date: Mar-2016
Source: Chemosphere, Mar. 2016, v. 147, p. 173-179
Abstract: Coastal and estuarine regions are important areas of mercury pollution. Therefore, it is important to properly characterize the sources and bioaccumulation processes of mercury in these regions. Here, we present mercury stable isotopic compositions in 18 species of wild marine fish collected from the Pearl River Estuary (PRE), south China. Our results showed variations in mass-independent fractionation (δ199Hg: +0.05 ± 0.10‰ to +0.59 ± 0.30‰) with a δ199Hg/δ201Hg of ~1.26, suggesting that aqueous MeHg underwent photo-degradation prior to incorporation into the food chain. For the results, we discovered small but significant differences of δ199Hg values among herbivorous, demersal, and carnivorous fish, indicating that different feeding guilds of fish may have incorporated MeHg with various degrees of photo-demethylation. The consistent mercury isotope compositions between fish feeding habitat and mercury sources in the estuary provide potentially important findings on the transformation and bioaccumulation of this toxic metal in subtropical coastal environments.
Keywords: Bio-accumulation
Fish
Mercury
Mercury isotopes
Pearl River Estuary
Publisher: Pergamon Press
Journal: Chemosphere 
ISSN: 0045-6535
EISSN: 1879-1298
DOI: 10.1016/j.chemosphere.2015.12.100
Rights: © 2015 Elsevier Ltd. All rights reserved.
© 2015. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/
The following publication Yin, R., Feng, X., Zhang, J., Pan, K., Wang, W., & Li, X. (2016). Using mercury isotopes to understand the bioaccumulation of Hg in the subtropical Pearl River Estuary, South China. Chemosphere, 147, 173-179 is available at https://dx.doi.org/10.1016/j.chemosphere.2015.12.100
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