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1. Mercury mobilization and export from the Greenland Ice Sheet using an ice-to-ocean approach

   https://doi.org/10.1038/s43247-026-03818-z  

   Youssef, Amina N; Janssen, Sarah E; Lamborg, Carl; Tate, Michael T; Despins, Marissa; Doting, Eva L; Poulin, Brett A; McCabe, David; Hopf, Leah M; Ferrer, Emma K; et al (July 2026, Communications Earth & Environment)

   Abstract The Greenland Ice Sheet (GrIS) is a poorly constrained source of mercury (Hg) to Arctic ecosystems. We measured Hg concentrations and stable isotopes along an ice-to-ocean continuum to identify controls on GrIS Hg export. Early-season permafrost melt and rainfall produced high filtered total mercury (fTHg, ~17 pM) and monomethylmercury (MMHg, ~2 pM). As subglacial drainage evolved, particulate Hg doubled (from ~8 to 17 pM) and MMHg production remained elevated, indicating Hg mobilization from subglacial environments. Shifts in Hg stable isotope ratios and$$\Delta$$ $\Delta$ ¹⁹⁹Hg mass balance show supraglacial sources contribute 20–48% of exported Hg, suggesting subglacial inputs dominate the seasonal Hg flux. Fjord waters were enriched in fTHg ( ~ 10 pM) and MMHg ( ~ 2 pM) relative to rivers, consistent with particulate Hg transformations and terrestrial Hg inputs. The estimated GrIS Hg yield ( ~ 23 mmol km⁻²yr⁻¹) is similar to that of Arctic rivers and will likely increase with climate-driven mass loss. 

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2. 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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3. 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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4. 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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5. Mercury Distribution and Speciation Along the U.S. GEOTRACES GP15 Pacific Meridional Transect

   https://doi.org/10.1029/2024JC021672  

   Starr, Lindsay D; He, Yipeng; Mason, Robert P; Hammerschmidt, Chad R; Newell, Silvia E; Lamborg, Carl H (April 2025, Journal of Geophysical Research: Oceans)

   Abstract Mercury (Hg) is a bioaccumulative neurotoxin that can concentrate to potentially harmful levels in higher levels of marine food webs following conversion to methylmercury (MeHg). This is of public health concern as seafood is a main protein source for many in the Pacific region. To better understand Hg partitioning and transformations in the Pacific Ocean, Hg species and phases were measured along a meridional section from Alaska to Tahiti in 2018. This allowed the description of Hg concentrations and speciation under a variety of biogeochemical conditions such as the Alaskan shelf, the oligotrophic North Pacific gyre, and near the hydrothermally active Loihi seamount. Filtered HgT concentrations were elevated below 1,000 m near the Loihi Seamount with an average concentration of 1.45 pM, possibly indicating enrichment from hydrothermal venting. Filtered MeHg concentrations were notably higher at depth at the equator and generally lower south of the equator. Total Hg in suspended particles was greatest in the upper 1,000 m near the Alaskan Shelf and decreased in concentration southward. Suspended particle MeHg was greatest in the surface ocean in the upper 300 m near the Intertropical Convergence Zone (ITCZ). For both HgT and MeHg, particle‐associated concentrations appear to be related to organic fraction, and concentrations decreased southward. In general, all measured Hg species had greater concentrations in the northern than southern Pacific Ocean consistent with prior measurements. 

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