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Contrasting kinetics of arsenic release from As-bearing ferrihydrite coprecipitates by distinct sulfate-reducing bacteria.

作者信息

Luo Ran, Cheng Yu, Song Tenglong, Wu Zhengyu, Wang Yanhong, Li Ping

机构信息

State Key Laboratory of Geomicrobiology and Environmental Changes, China University of Geosciences, Wuhan 430074, PR China.

School of Environmental Studies, China University of Geosciences, Wuhan 430074, PR China.

出版信息

Ecotoxicol Environ Saf. 2025 Mar 15;293:118035. doi: 10.1016/j.ecoenv.2025.118035. Epub 2025 Mar 12.

Abstract

Microbial sulfate reduction plays key roles in arsenic (As) biotransformation and release in groundwater aquifers; however, influences by distinct sulfate-reducing strains on the transformation of As-bearing iron (oxyhydr)oxide under different sulfate availability and associated As mobilization are not clear. In this study, anaerobic batch experiments were conducted to clarify the transformation processes of As-bearing ferrihydrite mediated by two distinct sulfate-reducing strains. Results showed that both the purchased model strain Desulfovibrio vulgaris (D-1) and the Citrobacter sp. C-1 isolated from high As groundwater in this study were capable of sulfate, iron and arsenate reduction. However, they presented different patterns of sulfate/iron reduction and As release under As-bearing ferrihydrite conditions attributed to their preferential functions. Sulfate input accelerated the bioreduction of sulfate and ferrihydrite simultaneously by D-1, thereby facilitated arsenic release and formation of vivianite, mackinawite and goethite. The As release was accelerated by 20.7 % and 165.5 % under 1 mM and 10 mM sulfate amendment, respectively. In contrast, sulfate reduction occurred in the early stage (0-7 days) and iron reduction began afterwards in strain C-1 treatment, thus the increased sulfate hindered initial ferrihydrite reduction and suppress As release by 27.9 % and 37.9 % in 1 and 10 mM sulfate systems, respectively. The final secondary minerals were predominantly presented as amorphous goethite by C-1 due to low ferrihydrite reduction. The results highlight the necessary consideration of preferred functions of SRB when exploring the sulfate-mediated As release processes.

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