Search USGS⌕ Search

USGS · 70243151

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

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 −1 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.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Brett A. Poulin, Michael T. Tate, Jacob M. Ogorek, Sara E. Breitmeyer, Austin K. Baldwin, Alysa Muir Yoder, Reed C. Harris, Jesse Naymik, Nick Gastelecutto, Charles Hoovestol, Christopher F. Larsen, Ralph Myers, George R. Aiken, David P. Krabbenhoft. 2023. Biogeochemical and hydrologic synergy control mercury fate in an arid land river-reservoir system. https://doi.org/10.1039/d3em00032j

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

Per- and polyfluoroalkyl substances (PFAS) and other contaminants of concern in tribal waters of Montana

We assessed potential exposures to a broad suite of contaminants (inorganic, organic and microbial) in culturally important surface waters from three watersheds in a northern plains Native American community (Apsáalooke [Crow Tribe of Montana]) in south-central Montana, United States, with water insecurity concerns. Inorganic (37), organic (435) and microbial (3) constituents were assessed in 12 surface water sites from the Pryor Creek ( n = 2), Bighorn River ( n = 2) and Little Bighorn River ( n = 8) valleys. Twenty-six organics, 33 inorganics and Escherichia coli were detected. Despite relatively low concentrations in surface waters within the Crow Reservation, mixture toxicity indicated prevalent chronic ecological effects and human-health secondary contact (recreation) effects at multiple sites. Further, to address Tribal concerns over the prevalence and corresponding risks of per- and polyfluoroalkyl substances (PFAS), we sampled water, sediment, biofilms and fish at a limited number of locations in the Little Bighorn River. Results indicated that PFAS were prevalent in fish tissues, including whole blood and filets, and to a lesser extent in biofilms, despite few detections in water and sediment samples. This is the first attempt to document environmental PFAS contamination within the reservation and the potential human-health concerns for the general population from consumption of recreational/subsistence fish. Overall, this effort provided preliminary information on the contaminant mixtures present and their potential health implications, which can support the protection of community health and culturally meaningful resources across the Crow Reservation.

Montana↗

Transient methylmercury formation during wetland soil rewetting is governed by organic matter availability rather than coagulant history

Rewetting of previously drained wetland soils can induce rapid redox shifts that influence mercury (Hg) cycling and methylmercury (MeHg) production. We investigated how prior exposure to common metal-salt and biopolymer coagulants influences Hg transformations during wetland soil rewetting and whether organic matter (OM) availability modulates these effects. Wetland soils (∼300 µg kg −1 total Hg) were incubated in triplicate soil-water microcosms for 16 days following rewetting. Treatments included soils previously exposed to ferric sulfate, polyaluminum chloride, or a chitosan-based coagulant, alongside untreated controls. Upon rewetting without additional OM, redox potential declined to ∼250 mV, consistent with manganese-reducing conditions, and MeHg concentrations remained relatively low in water (0.05–0.18 ng L −1 ) and soils (1–2 µg kg −1 ) across all treatments. In contrast, addition of algal-derived OM (Spirulina powder) rapidly decreased redox potential to 0–100 mV and produced a short-lived pulse of MeHg formation in all treatments, with aqueous MeHg peaking at ∼30–40 ng L −1 and soil MeHg at ∼6–8 µg kg −1 on days 2–4 before declining. Coagulant treatments increased transient inorganic Hg concentrations in overlying water (45–75 ng L −1 ) relative to controls (∼30 ng L −1 ) but did not enhance higher MeHg production. Results demonstrate that OM-driven redox dynamics, rather than prior coagulant exposure, control transient MeHg production during wetland soil rewetting, highlighting how episodic carbon inputs can regulate mercury transformation in managed and natural wetlands.

California↗

Assessing microplastics, per- and polyfluoroalkyl substances (PFAS), and other contaminants of global concern in wadable agricultural streams

Microplastics, per- and polyfluoroalkyl substances (PFAS), antibiotic resistance genes (ARGs), pharmaceuticals and personal care products (PPCPs), and pesticides may lead to unintended environmental contamination through many pathways in multiple matrices. This statewide, multi-matrix study of contaminants of global concern (CGCs) in agricultural streams across Iowa (United States) is the first to examine multiple CGCs in water, bed sediment, and fish to understand their occurrence in small streams located in regions of intense agriculture activity. Iowa plays a pivotal role in agriculture, with more than 85% of Iowa’s landscape devoted to agriculture making it an ideal location for determining the prevalence of CGCs to provide critical baseline exposure data. Fifteen sites were sampled across a range of predominant land uses (e.g., poultry, swine); all sites had detections of microplastics in all matrices. Concentrations of PFAS varied but were detected in water and sediment; all fish had detections of perfluorooctanesulfonate (PFOS), a type of PFAS. More than 50% of water and bed sediment samples had detections of ARGs. The most frequently detected PPCP was metformin. No sites had a cumulative exposure activity ratio greater than 1.0 for chemical exposures; 13 sites were above the 0.001 precautionary threshold. Toxicity quotients calculated using Aquatic Life Benchmarks were below the 0.1 moderate risk threshold for chemical exposures for all but one site. For fish, all sites exceeded the moderate and high-risk thresholds proposed for microplastic particles for food dilution (both chronic and acute exposures) and all sites exceeded the microplastic moderate threshold proposed for chronic tissue translocation, and two sites exceeded the threshold for acute tissue translocation.

Iowa↗