Simulated Sea Level Rise in Coastal Peat Soils Stimulates Mercury Methylation

IF 2.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Bryce A. Cook, Benjamin D. Peterson, Jacob M. Ogorek, Sarah E. Janssen, Brett A. Poulin
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Abstract

Coastal wetlands are vulnerable to sea level rise with unknown consequences for mercury (Hg) cycling, particularly the potential for exacerbating neurotoxic methylmercury (MeHg) production and bioaccumulation in food webs. Here, the effect of sea level rise on MeHg formation in the Florida Everglades was evaluated by incubating peat cores from a freshwater wetland for 0–20 days in the laboratory at five salinity conditions (0.16–6.0 parts-per-thousand; 0.20–454 mg L–1 sulfate (SO42–)) to simulate the onset of sea level rise within coastal margins. Isotopically enriched inorganic mercury (201Hg(II)) was used to track MeHg formation and peat-porewater partitioning. In all five salinity treatments, porewaters became anoxic within 1 day and became progressively enriched in dissolved organic matter (DOM) of greater aromatic composition over the 20 days compared to ambient conditions. In the four highest salinity treatments, SO42– concentrations decreased and sulfide concentrations increased over time due to microbial dissimilatory SO42– reduction that was concurrent with 201Hg(II) methylation. Importantly, elevated salinity resulted in a greater proportion of produced Me201Hg observed in porewaters as opposed to bound to peat, interpreted to be due to the complexation of MeHg with aromatic DOM released from peat. The findings highlight the potential for enhanced production and mobilization of MeHg in coastal wetlands of the Florida Everglades due to the onset of saltwater intrusion.

Abstract Image

沿海泥炭土中的模拟海平面上升会刺激汞甲基化
沿海湿地很容易受到海平面上升的影响,而海平面上升对汞(Hg)循环的影响尚不清楚,特别是有可能加剧神经毒性甲基汞(MeHg)的产生和在食物网中的生物累积。在这里,通过在实验室中将淡水湿地的泥炭芯在五种盐度条件(0.16-6.0ppm;0.20-454mg L-1 硫酸盐(SO42-))下培养 0-20 天,来评估海平面上升对佛罗里达大沼泽地甲基汞形成的影响,以模拟海岸边缘海平面上升的开始。用同位素富集无机汞(201Hg(II))来跟踪甲基汞的形成和泥炭-孔隙水分配。在所有五种盐度处理中,孔隙水在 1 天内开始缺氧,并在 20 天内逐渐富集芳香族成分更多的溶解有机物(DOM)。在四个盐度最高的处理中,随着时间的推移,SO42-浓度降低,硫化物浓度升高,这是由于微生物在进行 201Hg(II)甲基化的同时,对 SO42-进行了异氨还原。重要的是,盐度升高导致孔隙水中产生的 Me201Hg 比结合在泥炭中的 Me201Hg 所占比例更大,这可能是由于 MeHg 与泥炭中释放的芳香族 DOM 发生了络合作用。研究结果表明,由于盐水入侵的开始,佛罗里达大沼泽地沿海湿地中甲基汞的产生和迁移有可能增加。
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来源期刊
ACS Earth and Space Chemistry
ACS Earth and Space Chemistry Earth and Planetary Sciences-Geochemistry and Petrology
CiteScore
5.30
自引率
11.80%
发文量
249
期刊介绍: The scope of ACS Earth and Space Chemistry includes the application of analytical, experimental and theoretical chemistry to investigate research questions relevant to the Earth and Space. The journal encompasses the highly interdisciplinary nature of research in this area, while emphasizing chemistry and chemical research tools as the unifying theme. The journal publishes broadly in the domains of high- and low-temperature geochemistry, atmospheric chemistry, marine chemistry, planetary chemistry, astrochemistry, and analytical geochemistry. ACS Earth and Space Chemistry publishes Articles, Letters, Reviews, and Features to provide flexible formats to readily communicate all aspects of research in these fields.
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