Seasonal Variation of Acid Volatile Sulfide and Simultaneously Extracted Metals in Sediment Cores from the Pearl River Estuary

Abstract

The simultaneously extracted metals/acid volatile sulfide (SEM/AVS) method is widely used to estimate the toxicity of metals in sediment. In this study, SEM and AVS concentrations were obtained by the cold-acid purge-and-trap technique during spring (April) and winter (December) at six sites in the Pearl River estuary. Total organic carbon, grain size distribution, and total metals were also measured in winter samples. AVS concentrations in spring sediments were slightly higher than those in winter sediments, except at site 2. AVS concentrations showed more distinct locational and temporal variation compared with SEM concentrations. Generally, AVS contents increased downcore, whereas SEM concentrations decreased slightly with depth. Higher SEM concentrations were observed in the west shoal (sites 2, 6, and 7) and site 4 (1.24 ∼ 4.28 μmol•g⁻¹) compared with those at sites 1 and 3 (0.73 ∼ 2.14 μmol•g⁻¹) in the middle shoal. Most SEM metals have a significant linear positive correlation with the total metals, especially for Cd, Zn, and Pb, which were easily extracted by 1 M HCl compared with Cr and Ni. According to the toxicity threshold value of 1.7 μmol•g⁻¹ for the difference of SEM-AVS, a toxic effect is expected at sites 1, 2, and 4 in spring and at sites 4, 6, and 7 in winter, which also indicates a relatively obvious seasonal variation in heavy metal bioavailability. However, comparisons between the total heavy metal concentrations in winter sediments with the sediment quality guidelines of ERLs/ERMs and TELs/PELs showed that adverse biological effects may occasionally occur at sites 2, 4, 6, and 7. Therefore, SEM/AVS prediction in conjunction with sediment quality guidelines can give a more reliable evaluation of the bioavailability of heavy metal in sediments.

Keywords:

• Heavy metals
• AVS
• SEM
• seasonal variation
• bioavailability

Acknowledgements

This study was financially supported by the National Natural Science Foundation of China (No. 40903047) and the Chinese Academy of Sciences (No. ZKCX2-SW-212). We thank Dr. Y. Lv, D. R. Zhang, and Mr. X. H. Xie for their help in collecting samples and Mr. C. P. Lin for his assistance with heavy metals analysis. This is contribution No. IS-1728 from GIGCAS.