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潮间带沉积物中溶解气态汞的形成与汞的挥发。

Dissolved gaseous mercury formation and mercury volatilization in intertidal sediments.

机构信息

Centro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal; IPMA-Instituto Português do Mar e Atmosfera, Rua Alfredo Magalhães Ramalho, 6, 1495-006 Lisboa, Portugal.

Environment and Climate Change Canada, Aquatic Contaminants Research Division, Water Science and Technology Directorate, Montréal, QC, Canada.

出版信息

Sci Total Environ. 2017 Dec 15;603-604:279-289. doi: 10.1016/j.scitotenv.2017.06.093. Epub 2017 Jun 23.

Abstract

Intertidal sediments of Tagus estuary regularly experiences complex redistribution due to tidal forcing, which affects the cycling of mercury (Hg) between sediments and the water column. This study quantifies total mercury (Hg) and methylmercury (MMHg) concentrations and fluxes in a flooded mudflat as well as the effects on water-level fluctuations on the air-surface exchange of mercury. A fast increase in dissolved Hg and MMHg concentrations was observed in overlying water in the first 10min of inundation and corresponded to a decrease in pore waters, suggesting a rapid export of Hg and MMHg from sediments to the water column. Estimations of daily advective transport exceeded the predicted diffusive fluxes by 5 orders of magnitude. A fast increase in dissolved gaseous mercury (DGM) concentration was also observed in the first 20-30min of inundation (maximum of 40pg L). Suspended particulate matter (SPM) concentrations were inversely correlated with DGM concentrations. Dissolved Hg variation suggested that biotic DGM production in pore waters is a significant factor in addition to the photochemical reduction of Hg. Mercury volatilization (ranged from 1.1 to 3.3ngmh; average of 2.1ngmh) and DGM production exhibited the same pattern with no significant time-lag suggesting a fast release of the produced DGM. These results indicate that Hg sediment/water exchanges in the physical dominated estuaries can be underestimated when the tidal effect is not considered.

摘要

由于潮汐的作用,塔古斯河口的潮间带沉积物经常经历复杂的再分布,这影响了汞(Hg)在沉积物和水柱之间的循环。本研究定量了淹没泥滩中总汞(Hg)和甲基汞(MMHg)的浓度和通量,以及水位波动对汞在空气-表面交换的影响。在淹没的最初 10 分钟内,上覆水中溶解的 Hg 和 MMHg 浓度迅速增加,而孔隙水中的浓度相应降低,表明 Hg 和 MMHg 从沉积物迅速向水柱中输出。每日平流输运的估算值超过了预测的扩散通量 5 个数量级。在淹没的最初 20-30 分钟内,也观察到溶解气态汞(DGM)浓度迅速增加(最高达 40pgL)。悬浮颗粒物(SPM)浓度与 DGM 浓度呈反比。溶解 Hg 的变化表明,生物孔隙水中的 DGM 产生是除 Hg 的光化学还原之外的一个重要因素。汞的挥发(范围为 1.1 至 3.3ngmh;平均值为 2.1ngmh)和 DGM 的产生呈现出相同的模式,没有明显的时间滞后,表明产生的 DGM 迅速释放。这些结果表明,在不考虑潮汐效应的情况下,物理主导的河口的 Hg 沉积物/水交换可能被低估。

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