Metal-sulfide dynamics in a constructed wetland in the Southeastern United States

被引:9
|
作者
Harris, Savannah [1 ]
Xu, Xiaoyu [1 ]
Mills, Gary [1 ]
机构
[1] Univ Georgia, Savannah River Ecol Lab, PO Drawer E, Aiken, SC 29802 USA
关键词
Acid-volatile sulfide; Constructed wetland; Diffusive gradients in thin films; Metal; Resuspension; Simultaneously extracted metals; ACID-VOLATILE SULFIDE; THIN-FILMS; CONTAMINATED SEDIMENTS; ORGANIC-MATTER; TRACE-METALS; BIOAVAILABILITY; SURFACE; COPPER; PH; SPECIATION;
D O I
10.1007/s11273-020-09749-6
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Tritium Processing Facility at the Savannah River Site releases effluent containing copper (Cu), zinc (Zn), and lead (Pb) to the H-02 constructed wetland for remediation before the final release. Sediment cores were collected in the wetland cells in both summer and winter. Concentrations of total metals in all sediment layers and acid-volatile sulfide (AVS) and simultaneously extracted metals (SEM) in surface sediments were determined. Total metal concentrations suggested most metals removed from surface water were retained by the organic-rich flocculent in the top sediment layers instead of being transported to the deeper sulfide mineral layers. The seasonal difference of AVS and SEM indicated a season-related sulfur cycle and metal removal process in the wetland cells. SEM-Zn was the major contributor to total SEM. Metals accumulating in surface sediments were mainly sequestered in AVS and SEM extractable phases including metal-sulfides and organic matter complexes. The general SEM/AVS ratio was > 1, demonstrating the metals associated with sediments were potentially mobile and/or bioavailable, which becomes a concern for the long-term sustainability of the constructed wetland. The disturbance event in the sediment triggered the release of total metals, which were mostly in particulate form and were not bioavailable. Due to the high levels of reduced ion (Fe) in the sediment, the released particulate metals were likely to form metal-scavenging particulate Fe(3+)oxyhydroxides under oxic conditions.
引用
收藏
页码:847 / 861
页数:15
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