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1. Low mercury concentrations in a Greenland glacial fjord attributed to oceanic sources

   https://doi.org/10.1038/s43247-024-01474-9  

   Lindeman, M R; Straneo, F; Adams, H M; Nelson, M_J S; Schartup, A T (December 2024, Communications Earth & Environment)

   Abstract As the role of the Greenland Ice Sheet in the Arctic mercury (Hg) budget draws scrutiny, it is crucial to understand mercury cycling in glacial fjords, which control exchanges with the ocean. We present full water column measurements of total mercury (THg) and methylmercury (MeHg) in Sermilik Fjord, a large fjord in southeast Greenland fed by multiple marine-terminating glaciers, whose circulation and water mass transformations have been extensively studied. We show that THg (0.23-1.1 pM) and MeHg (0.02-0.17 pM) concentrations are similar to those in nearby coastal waters, while the exported glacially-modified waters are relatively depleted in inorganic mercury (Hg(II)), suggesting that inflowing ocean waters from the continental shelf are the dominant source of mercury species to the fjord. We propose that sediments initially suspended in glacier meltwaters scavenge particle-reactive Hg(II) and are subsequently buried, making the fjord a net sink of oceanic mercury. 

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2. Linked mercury methylation and nitrification across oxic subpolar regions

   https://doi.org/10.3389/fenvc.2023.1109537  

   Despins, Marissa C.; Mason, Robert P.; Aguilar-Islas, Ana M.; Lamborg, Carl H.; Hammerschmidt, Chad R.; Newell, Silvia E. (May 2023, Frontiers in Environmental Chemistry)

   Methylmercury (MeHg) is a neurotoxin that bioaccumulates to potentially harmful concentrations in Arctic and Subarctic marine predators and those that consume them. Monitoring and modeling MeHg bioaccumulation and biogeochemical cycling in the ocean requires an understanding of the mechanisms behind net mercury (Hg) methylation. The key functional gene pair for Hg methylation,hgcAB, is widely distributed throughout ocean basins and spans multiple microbial phyla. While multiple microbially mediated anaerobic pathways for Hg methylation in the ocean are known, the majority ofhgcAhomologs have been found in oxic subsurface waters, in contrast to other ecosystems. In particular, microaerophilicNitrospina, a genera of nitrite-oxidizing bacteria containing ahgcA-like sequence, have been proposed as a potentially important Hg methylator in the upper ocean. The objective of this work was therefore to examine the potential of nitrifiers as Hg methylators and quantify total Hg and MeHg across three Arctic and Subarctic seas (the Gulf of Alaska, the Bering Sea and the Chukchi Sea) in regions whereNitrospinaare likely present. In Spring 2021, samples for Hg analysis were obtained with a trace metal clean rosette across these seas. Mercury methylation rates were quantified in concert with nitrification rates using onboard incubation experiments with additions of stable isotope-labeled Hg and NH₄⁺. A significant correlation between Hg methylation and nitrification was observed across all sites (R²= 0.34,p< 0.05), with the strongest correlation in the Chukchi Sea (R²= 0.99,p< 0.001).Nitrospina-specifichgcA-like genes were detected at all sites. This study, linking Hg methylation and nitrification in oxic seawater, furthers understanding of MeHg cycling in these high latitude waters, and the ocean in general. Furthermore, these studies inform predictions of how climate and human interactions could influence MeHg concentrations across the Arctic in the future. 

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3. Mercury source changes and food web shifts alter contamination signatures of predatory fish from Lake Michigan

   https://doi.org/10.1073/pnas.1907484116  

   Lepak, Ryan F.; Hoffman, Joel C.; Janssen, Sarah E.; Krabbenhoft, David P.; Ogorek, Jacob M.; DeWild, John F.; Tate, Michael T.; Babiarz, Christopher L.; Yin, Runsheng; Murphy, Elizabeth W.; et al (November 2019, Proceedings of the National Academy of Sciences)

   To understand the impact reduced mercury (Hg) loading and invasive species have had on methylmercury bioaccumulation in predator fish of Lake Michigan, we reconstructed bioaccumulation trends from a fish archive (1978 to 2012). By measuring fish Hg stable isotope ratios, we related temporal changes in Hg concentrations to varying Hg sources. Additionally, dietary tracers were necessary to identify food web influences. Through combined Hg, C, and N stable isotopic analyses, we were able to differentiate between a shift in Hg sources to fish and periods when energetic transitions (from dreissenid mussels) led to the assimilation of contrasting Hg pools (2000 to present). In the late 1980s, lake trout δ 202 Hg increased (0.4‰) from regulatory reductions in regional Hg emissions. After 2000, C and N isotopes ratios revealed altered food web pathways, resulting in a benthic energetic shift and changes to Hg bioaccumulation. Continued increases in δ 202 Hg indicate fish are responding to several United States mercury emission mitigation strategies that were initiated circa 1990 and continued through the 2011 promulgation of the Mercury and Air Toxics Standards rule. Unlike archives of sediments, this fish archive tracks Hg sources susceptible to bioaccumulation in Great Lakes fisheries. Analysis reveals that trends in fish Hg concentrations can be substantially affected by shifts in trophic structure and dietary preferences initiated by invasive species in the Great Lakes. This does not diminish the benefits of declining emissions over this period, as fish Hg concentrations would have been higher without these actions. 

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4. Elevated methylmercury in Arctic rain and aerosol linked to air-sea exchange of dimethylmercury

   https://doi.org/10.1126/sciadv.adr3805  

   He, Yipeng; Inman, Hannah; Kadko, David C; Stephens, Mark P; Hammond, Douglas E; Landing, William M; Mason, Robert P (March 2025, Science Advances)

   Mercury (Hg) is a global pollutant with substantial human health impacts. While most studies focus on atmospheric total Hg (THg) deposition, contributions of methylated Hg (MeHg), including monomethylmercury (MMHg) and dimethylmercury (DMHg), remain poorly understood. To examine this, we use rain and aerosol Hg speciation data and high-resolution surface DMHg measurements, collected on a transect from Alaskan coastal waters to the Bering and Chukchi Seas. We observed a significant fivefold increase in the MeHg:THg fraction in rain and a 10-fold increase for aerosols, closely linked to elevated surface DMHg and the highest DMHg evasion (~9.4 picomoles per square meter per hour) found in upwelling waters near the Aleutian Islands. These data highlight a previously underexplored aspect of MeHg air-sea exchange and its importance to Hg cycling and human health concerns. Our findings emphasize the importance of DMHg evasion by demonstrating that atmospheric MeHg can be transported long distances (~1700 kilometers) in the Arctic, posing risks to human health and ecosystems. 

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5. Diet shifts drive mercury bioaccumulation and distribution in tissues of the longnose lancetfish (Alepisaurus ferox)

   https://doi.org/10.1016/j.marpolbul.2025.117590  

   Chen, Rachel S; Paulson, Erik T; Schartup, Amina T; Choy, C Anela (April 2025, Marine Pollution Bulletin)

   Monitoring the impacts of global efforts to reduce mercury (Hg) emissions is limited by the collection of biological samples at appropriate spatiotemporal scales. This is especially true in the deep sea, a vast region with food webs that cycle bioaccumulative methylmercury (MeHg). Within a species, understanding the distribution of Hg across tissue types can reveal how Hg accumulates in the body and inform how useful a species is for biomonitoring geographic regions or vertical habitats of the ocean. We focus on a globally distributed deep-sea fish, the longnose lancetfish (Alepisaurus ferox, n = 69 individuals), and measure total mercury (THg) and MeHg concentrations in 10 tissue types (brain, caudal white muscle, dorsal white muscle, gallbladder, gill filament, gonad, heart, intestine, liver, and stomach lining). Across all tissue types, THg and MeHg concentrations were higher in large lancetfish (≥1.8 kg) than small lancetfish (<1.8 kg), but concentrations were relatively stable within size classes. THg levels were highest in liver, intestine, and heart, followed by caudal white muscle, dorsal white muscle, stomach lining, and gill filament, then by gonad and gallbladder. We describe how ontogenetic diet shifts explain Hg bioaccumulation in pelagic predators inhabiting similar waters to lancetfish. We hypothesize that diet shifts to deeper-dwelling prey and fishes drive increases in THg and MeHg concentrations in large lancetfish. We propose lancetfish as a strong candidate for monitoring spatiotemporal variability of Hg in the deep pelagic – they are commonly captured in global fisheries and may reflect Hg sources in two distinct vertical habitats of the ocean. 

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