Exceptionally low mercury concentrations and fluxes from the 2021 and 2022 eruptions of Fagradalsfjall volcano, Iceland

Mercury (Hg) is naturally released by volcanoes and geothermal systems, but the global flux from these natural sources is highly uncertain due to a lack of direct measurements and uncertainties with upscaling Hg/SO2 mass ratios to estimate Hg fluxes. The 2021 and 2022 eruptions of Fagradalsfjall volcano, southwest Iceland, provided an opportunity to measure Hg concentrations and fluxes from a hotspot/rift system using modern analytical techniques. We measured gaseous Hg and SO2 concentrations in the volcanic plume by near-source drone-based sampling and simultaneous downwind ground-based sampling. Mean Hg/SO2 was an order of magnitude higher at the downwind locations relative to near-source data. This was attributed to the elevated local background Hg at ground level (4.0 ng m-3) likely due to emissions from outgassing lava fields. The background-corrected plume Hg/SO2 mass ratio (5.6 × 10-8) therefore appeared conservative from the near-source to several hundred meters distant, which has important implications for the upscaling of volcanic Hg fluxes based on SO2 measurements. Using this ratio and the total SO2 flux from both eruptions, we estimate the total mass of gaseous Hg released from the 2021 and 2022 Fagradalsfjall eruptions was 46 ± 33 kg, equivalent to a flux of 0.23 ± 0.17 kg d-1. This is the lowest Hg flux estimate in the literature for active open-conduit volcanoes, which range from 0.6 to 12 kg d-1 for other hotspot/rift volcanoes, and 0.5-110 kg d-1 for arc volcanoes. Our results suggest that Icelandic volcanic systems are fed from a particularly Hg-poor mantle. Furthermore, we demonstrate that the aerial near-source plume Hg measurement is feasible with a drone-based active sampling configuration that captures all gaseous and particulate Hg species, and recommend this as the preferred method for quantifying volcanic Hg emissions going forward

Toward an assessment of the global inventory of present-day mercury releases to freshwater environments

Aquatic ecosystems are an essential component of the biogeochemical cycle of mercury (Hg), as inorganic Hg can be converted to toxic methylmercury (MeHg) in these environments and reemissions of elemental Hg rival anthropogenic Hg releases on a global scale. Quantification of effluent Hg releases to aquatic systems globally has focused on discharges to the global oceans, rather than contributions to freshwater systems that affect local exposures and risks associated with MeHg. Here we produce a first-estimate of sector-specific, spatially resolved global aquatic Hg discharges to freshwater systems. We compare our release estimates to atmospheric sources that have been quantified elsewhere. By analyzing available quantitative and qualitative information, we estimate that present-day global Hg releases to freshwater environments (rivers and lakes) associated with anthropogenic activities have a lower bound of ~1000 Mg· a−1. Artisanal and small-scale gold mining (ASGM) represents the single largest source, followed by disposal of mercury-containing products and domestic waste water, metal production, and releases from industrial installations such as chlor-alkali plants and oil refineries. In addition to these direct anthropogenic inputs, diffuse inputs from land management activities and remobilization of Hg previously accumulated in terrestrial ecosystems are likely comparable in magnitude. Aquatic discharges of Hg are greatly understudied and further constraining associated data gaps is crucial for reducing the uncertainties in the global biogeochemical Hg budget

Seabird Transfer of Nutrients and Trace Elements from the North Water Polynya to Land during the Mid-Holocene Warm Period, Carey Islands, Northwest Greenland + Supplementary Appendix Figure S1 (See Article Tools)

Seabird guano from large nesting colonies is known to increase trace metal levels in adjacent terrestrial environments today, when global oceans are contaminated with Hg, Cd, and other metals. But the effect of seabird guano in the pre-industrial period has rarely been studied. We used stable C and N isotopic and trace element analyses of a peat core that represents ca. 2000 years of organic matter accumulation to examine the effect on trace elements and nutrients of a seabird colony that existed in northern Baffin Bay during the Holocene Thermal Maximum (ca. 8000–5000 yr BP). Although C and N concentrations were typical of those in other peats, isotopic data identified marine organic matter as the main source of N and a minor source of C in the peat and showed that the unknown seabird was a fish-eating species that was summer-resident for the 2000 yr period. Concentrations of Cd, Br, Sr, and Zn in peat were up to an order of magnitude higher than in ombrotrophic (air-fed) bogs elsewhere, whereas Hg and Cu concentrations were similar to those in other peats, suggesting relatively low levels of Hg and Cu in the guano. This surprising result for Hg contrasts with studies on modern seabirds, in which guano markedly increased environmental Hg concentrations. It could be a consequence of Hg concentrations in Arctic marine food webs in the pre-industrial period that were an order of magnitude lower than those of today.On sait aujourd’hui que le guano d’oiseaux marins provenant des grandes colonies nicheuses fait augmenter les teneurs en métaux-traces dans les milieux terrestres adjacents et que tous les océans sont contaminés au Hg, au Cd et autres métaux. Toutefois, l’effet du guano d’oiseaux marins dans la période préindustrielle a rarement fait l’objet d’études. Nous avons utilisé des isotopes stables de carbone d’azote et des analyses d’oligoéléments d’une carotte de tourbe, qui représente environ 2000 ans d’accumulation de matières organiques, pour examiner l’effet de la présence d’une colonie d’oiseaux marins qui a existé dans le nord de la baie de Baffin pendant le maximum thermique de l’Holocène (environ 8000 à 5000 ans BP) sur les oligoéléments et les nutriments. Même si les concentrations de C et de N étaient semblables à celles se trouvant dans d’autres tourbes, les données isotopiques ont démontré que la principale source de N, et une source mineure de C, provenaient de matières organiques marines, indiquant ainsi que les oiseaux marins inconnus étaient des espèces piscivores qui y ont résidé l’été pendant 2000 ans. Les concentrations de Cd, Br, Sr et Zn dans la tourbe étaient d’un ordre de grandeur supérieur à celles des tourbières ombrotrophes (alimentées par l’air) d’ailleurs, tandis que les concentrations de Hg et de Cu étaient semblables à celles d’autres tourbes, ce qui laisse sous-entendre des niveaux relativement bas de Hg et Cu dans le guano. Ce résultat concernant le Hg est surprenant, car il est contraire aux études modernes sur les oiseaux marins démontrant que le guano a considérablement augmenté les concentrations de Hg dans l’environnement. Cette augmentation pourrait être attribuable aux concentrations de Hg dans les réseaux alimentaires marins de l’Arctique lors de la période préindustrielle, d’un ordre de grandeur inférieur aux concentrations d’aujourd’hui

How closely do mercury trends in fish and other aquatic wildlife track those in the atmosphere? – Implications for evaluating the effectiveness of the Minamata Convention

International audienceThe Minamata Convention to reduce anthropogenic mercury (Hg) emissions entered into force in 2017, and attention is now on how to best monitor its effectiveness at reducing Hg exposure to humans. To address this, a key question is how closely Hg concentrations in the human food chain, especially in fish and other aquatic wildlife, will track the changes in atmospheric Hg that are expected to occur following anthropogenic emission reductions. We investigated this question by evaluating several regional groups of case studies where Hg concentrations in aquatic biota have been monitored continuously or intermittently for several decades. Our analysis shows that in most cases Hg time-trends in biota did not agree with concurrent Hg trends in atmospheric deposition or concentrations, and the divergence between the two trends has become more apparent over the past two decades. An over-arching general explanation for these results is that the impact of changing atmospheric inputs on biotic Hg is masked by two factors: 1) The aquatic environment also contains a large inventory of legacy emitted Hg that remains available for bio-uptake leading to a substantial lag in their response time to a change in external inputs; and 2) Biotic Hg trends reflect the dominant effects of changes in multi-causal, local and regional processes (e.g., aquatic or terrestrial biogeochemical processes, feeding ecology, climate) that control the speciation, bioavailability, and bio-uptake of both present-day and legacy emitted Hg. Globally climate change has become the most prevalent contributor to the divergence. A wide range of biotic Hg outcomes can thus be expected as anthropogenic atmospheric Hg emissions decline, depending on how these processes operate on specific regions and specific organisms. Therefore, evaluating the effectiveness of the Minamata Convention will require biomonitoring of multiple species that represent different trophic and ecological niches in multiple regions of the world

High mercury accumulation in deep-ocean hadal sediments

Ocean sediments are the largest sink for mercury (Hg) sequestration and hence an important part of the global Hg cycle(1). Yet accepted global average Hg flux data for deep-ocean sediments (> 200 m depth) are not based on measurements on sediments but are inferred from sinking particulates(2). Mercury fluxes have never been reported from the deepest zone, the hadal (> 6 km depth). Here we report the first measurements of Hg fluxes from two hadal trenches (Atacama and Kermadec) and adjacent abyssal areas (2-6 km). Mercury concentrations of up to 400 ng g(-1) were the highest recorded in marine sediments remote from anthropogenic or hydrothermal sources. The two trench systems differed significantly in Hg concentrations and fluxes, but hadal and abyssal areas within each system did not. The relatively low recent mean flux at Kermadec was 6-15 times higher than the inferred deep-ocean average(1,3), while the median flux across all cores was 22-56 times higher. Thus, some hadal and abyssal sediments are Hg accumulation hot-spots. The hadal zone comprises only similar to 1% of the deep-ocean area, yet a preliminary estimate based on sediment Hg and particulate organic carbon (POC) fluxes suggests total hadal Hg accumulation may be 12-30% of the estimate for the entire deep-ocean. The few abyssal data show equally high Hg fluxes near trench systems. These results highlight a need for further research into deep-ocean Hg fluxes to better constrain global Hg models

Volcanic mercury and mutagenesis in land plants during the end-Triassic mass extinction

During the past 600 million years of Earth history, four of five major extinction events were synchronous with volcanism in large igneous provinces. Despite improved temporal frameworks for these events, the mechanisms causing extinctions remain unclear. Volcanic emissions of greenhouse gases, SO2, and halocarbons are generally considered as major factors in the biotic crises, resulting in global warming, acid deposition, and ozone layer depletion. Here, we show that pulsed elevated concentrations of mercury in marine and terrestrial sediments across the Triassic-Jurassic boundary in southern Scandinavia and northern Germany correlate with intense volcanic activity in the Central Atlantic Magmatic Province. The increased levels of mercury-the most genotoxic element on Earth-also correlate with high occurrences of abnormal fern spores, indicating severe environmental stress and genetic disturbance in the parent plants. We conclude that this offers compelling evidence that emissions of toxic volcanogenic substances contributed to the end-Triassic biotic crisis