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富营养化湖水中的藻类有机质抑制甲基汞的光降解:一项动态研究。

Algal organic matter inhibits methylmercury photodegradation in eutrophic lake water: A dynamic study.

机构信息

School of Environment, Nanjing Normal University, Nanjing 210023, China; State Key Laboratory of Pollution Control and Resources Reuse, School of Environment, Nanjing University, Nanjing 210023, China.

State Key Laboratory of Pollution Control and Resources Reuse, School of Environment, Nanjing University, Nanjing 210023, China; Suzhou Wuzhong Environmental Monitoring Station, Suzhou 215104, China.

出版信息

Sci Total Environ. 2023 Nov 15;899:165661. doi: 10.1016/j.scitotenv.2023.165661. Epub 2023 Jul 18.

Abstract

Algal organic matter (AOM) is a major component of dissolved organic matter (DOM) in eutrophic lakes and could impact the photodegradation of neurotoxic methylmercury (MeHg) in water. Predicting these effects, however, is challenging, largely due to the dynamic changes of AOM during algal decomposition. Here, we investigated the effects of AOM on MeHg photodegradation throughout the algal decomposition process and elucidated these effects by characterizing dynamic changes of AOM and exploring the respective roles of various reactive oxygen species (ROS). Our results reveal that AOM derived from algal decomposition significantly inhibits MeHg photodegradation, and the extent of this inhibition varies depending on the specific lakes (8-21 %, p < 0.05) and their eutrophication states (16-28 %, p < 0.05). The inhibitory effect gradually weakened as the decomposition progressed, which may be attributed to the dynamic changes in the quantity and quality of AOM. Moreover, hydroxyl radical (·OH) was found to be the main contributor in driving MeHg photodegradation (15-23 %) during the early stages of decomposition (day 0-3), while in the later stage (day 12-24), the role of singlet oxygen (O, 15-20 %) and (DOM*, 21-30 %) gradually strengthened and these three ROS jointly drove MeHg photodegradation. Based on our findings and recent studies, we propose that AOM derived from algal decomposition plays a vital role in increasing the risk of MeHg in eutrophic lakes. It promotes MeHg formation while simultaneously inhibiting its photodegradation. Integrating AOM-MeHg interactions into Hg biogeochemical cycling models would reduce uncertainties when predicting MeHg risks.

摘要

藻类有机质 (AOM) 是富营养化湖泊中溶解有机质 (DOM) 的主要组成部分,可能会影响水中神经毒性甲基汞 (MeHg) 的光降解。然而,由于藻类分解过程中 AOM 的动态变化,预测这些影响具有挑战性。在这里,我们研究了 AOM 对整个藻类分解过程中 MeHg 光降解的影响,并通过表征 AOM 的动态变化和探索各种活性氧物种 (ROS) 的各自作用来阐明这些影响。我们的结果表明,藻类分解产生的 AOM 会显著抑制 MeHg 的光降解,这种抑制程度因特定湖泊(8-21%,p<0.05)及其富营养化状态(16-28%,p<0.05)而异。随着分解的进行,抑制作用逐渐减弱,这可能归因于 AOM 的数量和质量的动态变化。此外,羟基自由基(·OH)被发现是驱动 MeHg 光降解的主要贡献者(15-23%),在分解的早期阶段(第 0-3 天),而在后期阶段(第 12-24 天),单线态氧(O,15-20%)和(DOM*,21-30%)的作用逐渐增强,这三种 ROS 共同驱动 MeHg 光降解。基于我们的发现和最近的研究,我们提出藻类分解产生的 AOM 在增加富营养化湖泊中 MeHg 的风险方面起着至关重要的作用。它促进 MeHg 的形成,同时抑制其光降解。将 AOM-MeHg 相互作用纳入 Hg 生物地球化学循环模型中,可以减少预测 MeHg 风险时的不确定性。

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