Phenol–Quinone Redox Couples of Natural Organic Matter Promote Mercury Methylation in Paddy Soil

IF 11.3 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL 环境科学与技术 Pub Date : 2025-01-07 DOI:10.1021/acs.est.4c07397
Yao Huang, Yingmei Huang, John R. Reinfelder, Huan Zhong, Liping Fang, Chuanping Liu, Fangbai Li
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Abstract

Methylmercury in paddy soils poses threats to food security and thus human health. Redox-active phenolic and quinone moieties of natural organic matter (NOM) mediate electron transfer between microbes and mercury during mercury reduction. However, their role in mercury methylation remains elusive. Here, artificial organic matter (AOM), i.e., biochar, wherein the phenol–quinone ratio and associated redox properties varied, was used as a redox-tunable model NOM to investigate the impact of the phenol–quinone redox couples on mercury methylation in Hg-contaminated paddy soils. Our findings confirm that AOM with higher phenol–quinone ratios (i.e., electron donor capacities) stimulated microbial methylation (4.9-fold increase) and dark abiotic methylation (2.2-fold increase). The phenol–quinone ratio had contrasting effects on the abundance of the Hg methylation gene hgcA and metabolic genes corresponding to Hg-methylating and demethylating clades (i.e., dsrA, dsrB, mcrA, and pmoA), especially under anaerobic (simulated flooding) conditions. The key Hg methylators were from Geobacteraceae, including Oryzomonas, Fundidesulfovibrio, and Geomobilimonas. The microbial methylation driven by the phenol–quinone ratio was further validated by NOM such as humic and fulvic acids. Notably, abiotic methylation was observed in aerobic sterilized soil, yet additional evidence is necessary to confirm the potential abiotic pathway, hampered by the difficulty of identifying effective methyl donors in soil. Our results reveal the potential of phenol–quinone redox properties in NOM to drive mercury methylation, offering novel insights into mercury methylation in paddy soils.

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天然有机质苯酚-醌氧化还原偶对促进水稻土汞甲基化
水稻土中的甲基汞对粮食安全以及人类健康构成威胁。天然有机物质(NOM)的氧化还原活性酚和醌部分在汞还原过程中介导微生物和汞之间的电子转移。然而,它们在汞甲基化中的作用仍然难以捉摸。本研究以人工有机物质(AOM),即生物炭为研究对象,研究了苯酚-醌氧化还原对汞甲基化的影响,其中苯酚-醌的比例和相关的氧化还原特性发生了变化。我们的研究结果证实,具有较高酚醌比(即电子供体容量)的AOM刺激微生物甲基化(增加4.9倍)和暗非生物甲基化(增加2.2倍)。酚醌比对汞甲基化基因hgcA和汞甲基化和去甲基化分支对应的代谢基因(即dsrA, dsrB, mcrA和pmoA)的丰度有不同的影响,特别是在厌氧(模拟洪水)条件下。主要的汞甲基化分子来自地菌科,包括Oryzomonas、funddidesulfovibrio和Geomobilimonas。用腐殖酸和黄腐酸等溶剂进一步验证了苯酚-醌比对微生物甲基化的驱动作用。值得注意的是,在好氧灭菌的土壤中观察到非生物甲基化,但由于难以确定土壤中有效的甲基供体,需要更多的证据来证实潜在的非生物途径。我们的研究结果揭示了NOM中苯酚-醌氧化还原特性驱动汞甲基化的潜力,为水稻土壤中汞甲基化提供了新的见解。
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来源期刊
环境科学与技术
环境科学与技术 环境科学-工程:环境
CiteScore
17.50
自引率
9.60%
发文量
12359
审稿时长
2.8 months
期刊介绍: Environmental Science & Technology (ES&T) is a co-sponsored academic and technical magazine by the Hubei Provincial Environmental Protection Bureau and the Hubei Provincial Academy of Environmental Sciences. Environmental Science & Technology (ES&T) holds the status of Chinese core journals, scientific papers source journals of China, Chinese Science Citation Database source journals, and Chinese Academic Journal Comprehensive Evaluation Database source journals. This publication focuses on the academic field of environmental protection, featuring articles related to environmental protection and technical advancements.
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