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生物地球化学和水文协同作用控制干旱区河流-水库系统中汞的命运。

Biogeochemical and hydrologic synergy control mercury fate in an arid land river-reservoir system.

机构信息

Department of Environmental Toxicology, University of California, Davis, USA.

U.S. Geological Survey, Upper Midwest Water Science Center, USA.

出版信息

Environ Sci Process Impacts. 2023 May 25;25(5):912-928. doi: 10.1039/d3em00032j.

Abstract

Reservoirs in arid landscapes provide critical water storage and hydroelectric power but influence the transport and biogeochemical cycling of mercury (Hg). Improved management of reservoirs to mitigate the supply and uptake of bioavailable methylmercury (MeHg) in aquatic food webs will benefit from a mechanistic understanding of inorganic divalent Hg (Hg(II)) and MeHg fate within and downstream of reservoirs. Here, we quantified Hg(II), MeHg, and other pertinent biogeochemical constituents in water (filtered and associated with particles) at high temporal resolution from 2016-2020. This was done (1) at inflow and outflow locations of three successive hydroelectric reservoirs (Snake River, Idaho, Oregon) and (2) vertically and longitudinally within the first reservoir (Brownlee Reservoir). Under spring high flow, upstream inputs of particulate Hg (Hg(II) and MeHg) and filter-passing Hg(II) to Brownlee Reservoir were governed by total suspended solids and dissolved organic matter, respectively. Under redox stratified conditions in summer, net MeHg formation in the meta- and hypolimnion of Brownlee reservoir yielded elevated filter-passing and particulate MeHg concentrations, the latter exceeding 500 ng g on particles. Simultaneously, the organic matter content of particulates increased longitudinally in the reservoir (from 9-29%) and temporally with stratified duration. In late summer and fall, destratification mobilized MeHg from the upgradient metalimnion and the downgradient hypolimnion of Brownlee Reservoir, respectively, resulting in downstream export of elevated filter-passing MeHg and organic-rich particles enriched in MeHg (up to 43% MeHg). We document coupled biogeochemical and hydrologic processes that yield in-reservoir MeHg accumulation and MeHg export in water and particles, which impacts MeHg uptake in aquatic food webs within and downstream of reservoirs.

摘要

干旱景观中的水库提供了关键的储水和水力发电能力,但也影响了汞(Hg)的传输和生物地球化学循环。为了减轻水库中生物可利用的甲基汞(MeHg)的供应和吸收,改善水库管理将受益于对水库内及其下游的无机二价汞(Hg(II))和 MeHg 命运的机制理解。在这里,我们从 2016 年到 2020 年以高时间分辨率定量测定了水中(过滤和与颗粒相关)的 Hg(II)、MeHg 和其他相关生物地球化学成分。这是通过在三个连续的水力发电水库(爱达荷州的蛇河和俄勒冈州的布朗利水库)的入口和出口处(1)以及在第一个水库(布朗利水库)内进行垂直和纵向测量(2)来完成的。在春季高流量期间,布朗利水库上游输入的颗粒态 Hg(Hg(II)和 MeHg)和过滤通过的 Hg(II)分别受总悬浮固体和溶解有机物的控制。在夏季氧化还原分层条件下,布朗利水库中meta 和 hypolimnion 的净 MeHg 形成导致过滤通过和颗粒态 MeHg 浓度升高,后者在颗粒上超过 500ng g。同时,颗粒态有机物的含量在水库中沿纵向(从 9%到 29%)和随分层时间增加。在夏末和秋季,分层解除使 MeHg 从布朗利水库的上游金属层和下游的底层分别移动,导致下游出口处过滤通过的 MeHg 和富含有机物的颗粒(富含 MeHg 高达 43%)的出口增加。我们记录了耦合的生物地球化学和水文过程,这些过程导致水库内 MeHg 积累和水中和颗粒中的 MeHg 输出,这影响了水库内及其下游的水生食物网中 MeHg 的吸收。

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