Hg Emissions Research Articles

Artificial Intelligence Modeling-Based Optimization of an Industrial-Scale Steam Turbine for Moving toward Net-Zero in the Energy Sector.

Augmentation of energy efficiency in the power generation systems can aid in decarbonizing the energy sector, which is also recognized by the International Energy Agency (IEA) as a solution to attain net-zero from the energy sector. With this reference, this article presents a framework incorporating artificial intelligence (AI) for improving the isentropic efficiency of a high-pressure (HP) steam turbine installed at a supercritical power plant. The data of the operating parameters taken from a supercritical 660 MW coal-fired power plant is well-distributed in the input and output spaces of the operating parameters. Based on hyperparameter tuning, two advanced AI modeling algorithms, i.e., artificial neural network (ANN) and support vector machine (SVM), are trained and, subsequently, validated. ANN, as turned out to be a better-performing model, is utilized to conduct the Monte Carlo technique-based sensitivity analysis toward the high-pressure (HP) turbine efficiency. Subsequently, the ANN model is deployed for evaluating the impact of individual or combination of operating parameters on the HP turbine efficiency under three real-power generation capacities of the power plant. The parametric study and nonlinear programming-based optimization techniques are applied to optimize the HP turbine efficiency. It is estimated that the HP turbine efficiency can be improved by 1.43, 5.09, and 3.40% as compared to that of the average values of input parameters for half-load, mid-load, and full-load power generation modes, respectively. The annual reduction in CO2 measuring 58.3, 123.5, and 70.8 kilo ton/year (kt/y) corresponds to half-load, mid-load, and full load, respectively, and noticeable mitigation of SO2, CH4, N2O, and Hg emissions is estimated for the three power generation modes of the power plant. The AI-based modeling and optimization analysis is conducted to enhance the operation excellence of the industrial-scale steam turbine that promotes higher-energy efficiency and contributes to the net-zero target from the energy sector.

Improved Anthropogenic Mercury Emission Inventories for China from 1980 to 2020: Toward More Accurate Effectiveness Evaluation for the Minamata Convention.

Anthropogenic mercury (Hg) emission inventories are crucial for the effectiveness evaluation of the Minamata Convention on Mercury. In this study, we developed an integrated Dynamic Inventory for Mercury Emission (DIME) model and improved the accuracy of emission estimates for primary sources in China. Long-term historical speciated Hg emission inventories for China were established. The total Hg emissions increased from 217.0 t in 1980 to 357.8 t in 2020 with a peak value of 506.6 t in 2010. Three stages with distinct leading drivers were identified. At Stage 1 (1980-1997), Hg emissions doubled with the rapid growth of economy; the driver was offset by the increase of dust and SO2 control measures at Stage 2 (1997-2010) except for cement production; and co-benefits from strict control measures induced the decoupling of Hg emissions from the economy at Stage 3 (2010-2020). The ultralow emission (ULE) retrofits in key industries had pronounced Hg removal efficiencies. Large emission reduction potential still exists in the cement industry. The improved emission estimation methods for key sectors, the consistency in methodology for historical Hg emission inventories, and the more accurate spatial distribution of speciated Hg emissions in this study provide a practical toolkit for the effectiveness evaluation of the Minamata Convention.

Isotopic investigation of sources and processes affecting gaseous and particulate bound mercury in the east coast, South Korea

Understanding sources and processes affecting atmospheric mercury (Hg) are key to enabling targeted Hg managements under the Minamata Convention on Mercury. We employed stable isotopes (δ202Hg, Δ199Hg, Δ201Hg, Δ200Hg, Δ204Hg) and backward air trajectories to characterize sources and processes affecting total gaseous Hg (TGM) and particulate bound Hg (PBM) in a coastal city, South Korea, subjected to atmospheric Hg sources of a local steel manufacturing industry, coastal evasion from the East Sea, and long-distance transport from East Asian countries. Based on the simulated airmasses and the isotopic comparison with TGM characterized from other urban, remote, and coastal sites, TGM evaded from the coastal surface of the East Sea (warm seasons) and from the land surface in high latitude regions (cold seasons) act as important sources relative to local anthropogenic emissions at our study location. Conversely, a significant relationship between Δ199Hg and concentrations of PBM (r2 = 0.39, p < 0.05) and a seasonally uniform Δ199Hg/Δ201Hg slope (1.15), except for summer (0.26), suggest that PBM is generally sourced from local anthropogenic emissions and subjected to Hg2+ photo-reduction on particles. The striking isotopic similarity between our PBM (δ202Hg; −0.86 to 0.49 ‰, Δ199Hg; −0.15 to 1.10 ‰) and those previously characterized along the coastal and offshore regions of the Northwest Pacific (δ202Hg; −0.78 to 1.1 ‰, Δ199Hg; −0.22 to 0.47 ‰) infer that anthropogenically emitted PBM from East Asia and those processed in the coastal atmosphere serves as a regional isotopic end-member. The implementation of air pollution control devices can reduce local PBM, while regional and/or multilateral efforts are required to manage TGM evasion and transport. We also anticipate that the regional isotopic end-member can be used to quantify the relative influence of local anthropogenic Hg emissions and complex processes affecting PBM in East Asia and other coastal regions.

Changes in Atmospheric Gaseous Elemental Mercury Concentrations and Isotopic Compositions at Mt. Changbai During 2015–2021 and Mt. Ailao During 2017–2021 in China

AbstractChina is the largest contributor to the global total anthropogenic mercury (Hg) emissions. However, the trend in anthropogenic Hg emissions in recent years in China has not been effectively evaluated due to the lack of long‐term atmospheric Hg observations. This study documents the changes in atmospheric gaseous elemental mercury (GEM) concentrations and isotopic compositions at Mt. Changbai (MCB) in northeastern China during 2015–2021 and Mt. Ailao (MAL) in southwestern China during 2017–2021, and explores the potential factors controlling these changes. GEM concentrations showed continuous declines from 2015 to 2021 (−2.1 ± 0.6% yr−1) at MCB and from 2017 to 2021 (−4.0 ± 1.4% yr−1) at MAL. Accompanied with these GEM declines are positive shifts in δ202Hg (medians: from 0.42 to 0.46‰ at MCB and from 0.17 to 0.57‰ at MAL), and negative shifts in Δ199Hg (medians: from −0.17‰ to −0.21‰ at MCB and from −0.10‰ to −0.17‰ at MAL) and Δ200Hg values (medians: from −0.07‰ to −0.08‰ at MCB and from −0.03‰ to −0.05‰ at MAL) (at significant levels for Δ199Hg at MCB and δ202Hg and Δ199Hg at MAL). These changes were mainly caused by the decreases in regional anthropogenic emissions in the study areas. Based on a ternary mixing model with Δ199Hg and Δ200Hg as input, we estimate decline rates of 5.8 ± 2.8 and 4.8 ± 3.0% yr−1 for the regional anthropogenic GEM emissions in northeastern and southwestern China, respectively.

Tree Rings Record of Long-Term Atmospheric Hg Pollution in the Monte Amiata Mining District (Central Italy): Lessons from the Past for a Better Future

Trees may represent useful long-term monitors of historical trends of atmospheric pollution due to the trace elements stored along the tree rings caused by modifications in the environment during a tree’s life. Chestnut (Castanea sativa Mill.) tree trunk sections were used to document the yearly evolution of atmospheric Hg in the world-class mining district of Monte Amiata (MAMD; Central Italy) and were exploited until 1982. An additional source of Hg emissions in the area have been the active geothermal power plants. A marked decrease (from &gt;200 µg/kg to &lt;100 µg/kg) in Hg contents in heartwood tree rings is recorded, likely because of mine closure; the average contents (tens of µg/kg) in recent years remain higher than in a reference area ~150 km away from the district (average 4.6 µg/kg). Chestnut barks, recording present-day Hg pollution, systematically show higher Hg concentrations than sapwood (up to 394 µg/kg in the mining area). This study shows that tree rings may be a good record of the atmospheric Hg changes in areas affected by mining activity and geothermal plants and can be used as a low-cost biomonitoring method for impact minimization and optimal resource and land management.

Health and Safety Protocol for the Management of Building Demolition Waste with High Mercury Contamination

The LIFE-funded European research project SUBproducts4LIFE seeks to demonstrate the use of industrial subproducts for the large-scale remediation of contaminated soils and industrial building debris connected to Hg mining. The main purpose of the present research was to ensure worker health and safety by creating a protocol for working in a highly mercury-contaminated demolition debris. A methodology consisting of sampling campaigns with a Lumex RA-915 mercury analyser, evaluating the accuracy of an empirical Hg emission model, evaluating each working task, providing recommendations for minimising the workers’ exposure and calculating the maximum work period in each area was proposed. It was also shown to forecast Hg biological markers. As a result, a work protocol was developed with three scenarios which allow planning the work and forecasting the workers’ mercury exposure as a function of the daily temperature, ensuring that the workers’ mercury exposure is below occupational mercury levels. The working protocol allows planning the works safely with minimum exposure to gaseous mercury and working fulfilling standard requirements. Plans for restoration or new use of industrial mercury-contaminated sites have increased in recent years, and the research improves the knowledge of Hg gas distribution and worker Hg exposure.

Bioaccumulation and trophic transfer of total mercury through the aquatic food webs of an African sub-tropical wetland system

Anthropogenic activities, including combustion of fossil fuels, coal, and gold mining, are significant sources of mercury (Hg) emissions into aquatic ecosystems. South Africa is a major contributor to global Hg emissions (46.4 tons Hg in 2018), with coal-fired power stations as the main source. Atmospheric transport of Hg emissions is the dominant cause of contamination, especially on the east coast of southern Africa where the Phongolo River Floodplain (PRF) is located. The PRF is the largest floodplain system in South Africa, with unique wetlands and high biodiversity, and provides essential ecosystem services to local communities who rely on fish as a protein source. We assessed the bioaccumulation of Hg in various biota, the trophic positions and food webs, as well as the biomagnification of Hg through the food webs in the PRF. Elevated Hg concentrations were found in sediments, macroinvertebrates and fish from the main rivers and associated floodplains in the PRF. Mercury biomagnification was observed through the food webs, with the apex predator tigerfish, Hydrocynus vittatus, having the highest Hg concentration. Our study shows that Hg in the PRF is bioavailable, accumulates in biota and biomagnifies in food webs.

Atmospheric Mercury Isotope Shifts in Response to Mercury Emissions from Underground Coal Fires.

Pollutant emissions from coal fires have caused serious concerns in major coal-producing countries. Great efforts have been devoted to suppressing them in China, notably at the notorious Wuda Coalfield in Inner Mongolia. Recent surveys revealed that while fires in this coalfield have been nearly extinguished near the surface, they persist underground. However, the impacts of Hg volatilized from underground coal fires remain unclear. Here, we measured concentrations and isotope compositions of atmospheric Hg in both gaseous and particulate phases at an urban site near the Wuda Coalfield. The atmospheric Hg displayed strong seasonality in terms of both Hg concentrations (5-7-fold higher in fall than in winter) and isotope compositions. Combining characteristic isotope compositions of potential Hg sources and air mass trajectories, we conclude that underground coal fires were still emitting large amounts of Hg into the atmosphere that have been transported to the adjacent urban area in the prevailing downwind direction. The other local anthropogenic Hg emissions were only evident in the urban atmosphere when the arriving air masses did not pass directly through the coalfield. Our study demonstrates that atmospheric Hg isotope measurement is a useful tool for detecting concealed underground coal fires.

International trade shapes global mercury-related health impacts.

Mercury (Hg) is a strong neurotoxin with substantial dangers to human health. Hg undergoes active global cycles, and the emission sources there of can also be geographically relocated through economic trade. Through investigation of a longer chain of the global biogeochemical Hg cycle from economic production to human health, international cooperation on Hg control strategies in Minamata Convention can be facilitated. In the present study, four global models are combined to investigate the effect of international trade on the relocation of Hg emissions, pollution, exposure, and related human health impacts across the world. The results show that 47% of global Hg emissions are related to commodities consumed outside of the countries where the emissions are produced, which has largely influenced the environmental Hg levels and human exposure thereto across the world. Consequently, international trade is found to enable the whole world to avoid 5.7 × 105 points for intelligence quotient (IQ) decline and 1,197 deaths from fatal heart attacks, saving a total of $12.5 billion (2020 USD) in economic loss. Regionally, international trade exacerbates Hg challenges in less developed countries, while resulting in an alleviation in developed countries. The change in economic loss therefore varies from the United States (-$4.0 billion) and Japan (-$2.4 billion) to China (+$2.7 billion). The present results reveal that international trade is a critical factor but might be largely overlooked in global Hg pollution mitigation.

Research on Waste Combustion in the Aspect of Mercury Emissions.

The topic of waste combustion/co-combustion is critical, given the increasingly restrictive legal regulations regarding its environmental aspects. In this paper, the authors present the test results of selected fuels of different compositions: hard coal, coal sludge, coke waste, sewage sludge, paper waste, biomass waste and polymer waste. The authors conducted a proximate and ultimate analysis of the materials and mercury content in them and their ashes. An interesting element of the paper was the chemical analysis of the XRF of the fuels. The authors conducted the preliminary combustion research using a new research bench. The authors provide a comparative analysis of pollutant emissions-especially mercury emission-during the combustion of the material; this is an innovative element of this paper. The authors state that coke waste and sewage sludge are distinguished by their high mercury content. The value of Hg emission during the combustion depends on the initial mercury content in the waste. The results of the combustion tests showed the adequacy of mercury release compared to the emissions of other compounds considered. Small amounts of mercury were found in waste ashes. The addition of a polymer to 10% of coal fuels leads to a reduction in mercury emissions in exhaust gases.

Acute ecotoxicological effects of Hg(CN)2 in Danio rerio (zebrafish).

Artisanal and small-scale gold mining (ASGM) is the largest source of anthropogenic Hg emissions on the planet. In addition, Hg-contaminated tailings are often reprocessed with sodium cyanide (NaCN) to extract the residual gold remaining in the material. This leads to the formation of mercury cyanide (Hg(CN)2) complexes, which are often discharged in untreated form into local drainages, leading to large amounts of free cyanide being released. However, data on mercury-cyanide interactions are scarce. In this study, we investigated the impact of cyanide and Hg bioavailability in zebrafish when added as Hg(CN)2. Different concentrations of Hg(CN)2 and NaCN were used, leading to an LC50 of 0.53 mg.L-1 for NaCN and 0.16 mg.L-1 for Hg(CN)2. Analyzing free cyanide concentrations in aquarium water, >40% dissociation was observed for NaCN and about 5% for Hg(CN)2. The accumulation of total Hg (THg) in the brain, gills, muscle and kidney was quantified. All fish exposed to Hg(CN)2 had higher THg levels than their controls and kidney was the tissue with higher Hg(CN)2 accumulation. Histological effects on the kidney and gills of both cyanides in D. rerio tissues were investigated, suggesting renal alterations in fish exposed to Hg(CN)2 and showing hyperplasia in the gills of animals exposed to NaCN and Hg(CN)2. The results alert to the risks of the presence of these complexes in aquatic environments.

Mercury flow network and its emission reduction in the steelworks

The steel industry is an important source of anthropogenic mercury (Hg) emissions. Hg is harmful to human health, causing symptoms such as dizziness, pneumonia, and renal failure. So, how do we reduce Hg emissions from the steelworks? What possibilities exist for Hg emission reduction? Firstly, in this study, the flow paths of Hg in the steelworks were described quantitatively using the substance flow analysis method, and the characteristics of the input and output of Hg-containing subjects were analyzed. Secondly, based on the Hg flow network, the circulation characteristics of Hg and the emission characteristics of Hg-containing pollutants were analyzed in the steelworks. Finally, according to the distribution of Hg in the steelworks, the emission reduction potential was examined at the source and end-of-pipe. The results showed that Hg, which mostly originated from coal, limestone, and iron ore concentrate in the steel production process, was mostly exported with waste gas and wastewater, primarily in the form of waste gas. The input, circulation, and output of Hg were 362.77, 3.25, and 392.55 mg/t crude steel (CS), respectively. Through source reduction and end-of-pipe treatment, the reduction rates of pollutants in the steelworks were 28.74% and 75.37%, respectively.

Distribution and bioavailability of mercury in size-fractioned atmospheric particles around an ultra-low emission power plant in Southwest China

Ultra-low emission (ULE) technology retrofits significantly impact the particulate-bound mercury (Hg) emissions from coal-fired power plants (CFPPs); however, the distribution and bioavailability of Hg in size-fractioned particulate matter (PM) around the ULE-retrofitted CFPPs are less understood. Here, total Hg and its chemical speciation in TSP (total suspended particles), PM10 (aerodynamic particle diameter ≤ 10 µm) and PM2.5 (aerodynamic particle diameter ≤ 2.5 µm) around a ULE-retrofitted CFPP in Guizhou Province were quantified. Atmospheric PM2.5 concentration was higher around this ULE-retrofitted CFPP than that in the intra-regional urban cities, and it had higher mass Hg concentration than other size-fractioned PM. Total Hg concentrations in PM had multifarious sources including CFPP, vehicle exhaust and biomass combustion, while they were significantly higher in autumn and winter than those in other seasons (P < 0.05). Regardless of particulate size, atmospheric PM-bound Hg had lower residual fractions (< 21%) while higher HCl-soluble fractions (> 40%). Mass concentrations of exchangeable, HCl-soluble, elemental, and residual Hg in PM2.5 were higher than those in other size-fractioned PM, and were markedly elevated in autumn and winter (P < 0.05). In PM2.5, HCl-soluble Hg presented a significantly positive relationship with elemental Hg (P < 0.05), while residual Hg showed the significantly positive relationships with HCl-soluble Hg and elemental Hg (P < 0.01). Overall, these results suggested that atmospheric PM-bound Hg around the ULE-retrofitted CFPP tends to accumulate in finer PM, and has higher bioavailable fractions, while has potential transformation between chemical speciation.

Trace mercury migration and human exposure in typical mercury-emission areas by compound-specific stable isotope analysis

Anthropogenic mercury (Hg) emissions have increased significantly since the Industrial Revolution, resulting in severe health impacts to humans. The consumptions of fish and rice were primary human methylmercury (MeHg) exposure pathways in Asia. However, the lifecycle from anthropogenic Hg emissions to human MeHg exposure is not fully understood. In this study, a recently developed approach, termed MeHg Compound-Specific Isotope Analysis (CSIA), was employed to track lifecycle of Hg in four typical Hg-emission areas. Distinct Δ199Hg of MeHg and inorganic Hg (IHg) were observed among rice, fish and hair. The Δ199Hg of MeHg averaged at 0.07 ± 0.15 ‰, 0.80 ± 0.55 ‰ and 0.43 ± 0.29 ‰ in rice, fish and hair, respectively, while those of IHg averaged at − 0.08 ± 0.24 ‰, 0.85 ± 0.43 ‰ and − 0.28 ± 0.68 ‰. In paddy ecosystem, Δ199Hg of MeHg in rice showed slightly positive shifts (∼0.2 ‰) from those of IHg, and comparable Δ199Hg of IHg between rice grain and raw/processed materials (coal, Hg ore, gold ore and sphalerite) were observed. Simultaneously, it was proved that IHg in fish muscle was partially derived from in vivo demethylation of MeHg. By a binary model, we estimated the relative contributions of rice consumption to human MeHg exposure to be 84 ± 14 %, 58 ± 26 %, 52 ± 20 % and 34 ± 15 % on average in Hg mining area, gold mining area, zinc smelting area and coal-fired power plant area, respectively, and positive shifts of δ202HgMeHg from fish/rice to human hair occurred during human metabolic processes. Therefore, the CSIA approach can be an effective tool for tracking Hg biogeochemical cycle and human exposure, from which new scientific knowledge can be generated to support Hg pollution control policies and to protect human health.

Isotopic Fractionation Characteristics of Speciated Mercury from Local Biomass Combustion in the Tibetan Plateau.

As the Third Pole of the world, the Tibetan Plateau (TP) is sensitive to anthropogenic influences. Biomass combustion is one of the most important anthropogenic sources of mercury (Hg) emissions in the TP. However, due to the lack of knowledge about Hg emission characteristics and activity levels in the plateau, atmospheric Hg emissions from biomass combustion in the TP are under large uncertainties. Here, based on pilot-scale experiments, we found that particle-bound mercury (PBM; mean of 83.1-87.7 ng/m3) occupied 17.93-49.31% of the total emitted Hg and the PBM δ202Hg values (average -1.65‰ to -0.77‰) were significantly higher than those of the corresponding feeding biomass. The Δ200Hg values of total gaseous mercury and PBM were more negative (-0.08‰ to -0.05‰) than other anthropogenic emissions, providing unique isotopic fingerprints for this sector. Together with the investigated local activity levels, Hg emissions from biomass combustion reached 402 ± 74 kg/a, which were dozens of times higher than previous estimates. The emissions were characterized by conspicuous spatial heterogeneity, concentrated in the northern and central TP. Specialized Hg emissions and the Hg isotope fingerprint of local biomass combustion can aid in evaluating the influence of this sector on the fragile ecosystems of the TP.

Quantum Chemical Investigation of Snow–Mercury Interactions and Their Implication of Mercury Deposition in the Arctic

Elemental gaseous Hg is emitted into the atmosphere through various anthropogenic and natural processes. Mercury's different species and respective transport ranges, atmospheric physical and chemical transformations, and interaction with the earth's surfaces all contribute to the global cycling of toxic mercury. Under sunlight, halogens, ozone, and nitro species oxidize the emitted elemental Hg to gaseous Hg (II) molecules, which deposit onto the snow and ice surfaces in the Arctic. To investigate the fate of deposited mercury, a quantum chemical investigation was conducted using first-principles density functional theory (DFT) to analyze the interaction between various mercury molecules and snow clusters of differing sizes. Results show that all oxidized mercury molecules: XHgY, BrHgOX, BrHgXO XHgOH, XHgO2H, and XHgNO2, with X, Y = Cl, Br, and I atoms have thermodynamically stable interactions with snow clusters. Further, the adsorption energy of all mercury molecules increases with increasing size of snow clusters. Additionally, the orientations of deposited mercury molecules on the cluster surface also influence the mercury-snow interactions.

Regulated adsorption sites using atomically single cluster over biochar for efficient elemental mercury uptake

Carbon-based materials have been widely used in gaseous pollutant removal because of their sufficient surface functional groups; however, its removal efficiency for elemental mercury (Hg0) is low. In this study, we fabricated biomass using a chelated coupled pyrolysis strategy and further constructed the regulated adsorption sites for gaseous Hg0 uptake. A series of Mnδ-N2O2/BC with different manganese cluster sizes demonstrated that manganese clusters anchored on biochar acted as highly active and durable adsorbents for Hg0 immobilization, which increased the adsorption efficiency of Hg0 by up to 50%. Shrimp- and crab-based biochar adsorbents exhibited excellent Hg0 removal because of their chitosan-like structure. In particular, small Mn clusters and oxygen species around the defect led to a boost in the Hg0 adsorption by carbon. The results of density functional theory calculation revealed that the presence of oxygen in the carbon skeleton can tune the electrons of small-sized Mn clusters, thereby promoting the affinity of mercury atoms. The newly developed Mnδ-N2O2/BCshrimp had an adsorption capacity of 7.98–11.52 mg g−1 over a broad temperature range (50–200 °C) and showed a high tolerance to different industrial flue gases (H2O, NO, HCl, and SO2). These results provide novel green and low-carbon disposal methods for biomass resource utilization and industrial Hg0 emission control.Graphical

Seven-year monitoring of mercury in wet precipitation and atmosphere at the Amsterdam Island GMOS station

Mercury (Hg) fate and transport research requires more effort to obtain a deep knowledge of its biogeochemical cycle, particularly in the Southern Hemisphere and Tropics that are still missing of distributed monitoring sites.Continuous monitoring of atmospheric Hg concentrations and trend worldwide is relevant for the effectiveness evaluation of the Minamata Convention on Mercury (MCM) actions. In this context, Gaseous Elemental Mercury (GEM) and total mercury (THg) in precipitations were monitored from 2013 to 2019 at the Amsterdam Island Observatory (AMS - 37°48′S, 77°34′E) to provide insights into the Hg pathway in the remote southern Indian Ocean, also considering ancillary dataset of Rn-222, CO2, CO, and CH4. GEM average concentration was 1.06 ± 0.07 ng m−3, with a slight increase during the austral winter due to both higher wind speed over the surface ocean and contributions from southern Africa. In wet depositions, THg average concentration was 2.39 ± 1.17 ng L−1, whereas the annual flux averaged 2.04 ± 0.80 μg m−2 year−1. In general, both GEM and Volume-Weighted Mean Concentration (VWMC) of THg did not show an increasing/decreasing trend over the seven-year period, suggesting a substantial lack of evolution about emission of Hg reaching AMS.Air masses Cluster Analysis and Potential Source Contribution Function showed that oceanic evasion was the main Hg contributor at AMS, while further contributions were attributable to long-range transport events from southern Africa, particularly when the occurrence of El Niño increased the frequency of wildfires.

Estimates of volcanic mercury emissions from Redoubt Volcano, Augustine Volcano, and Mount Spurr eruption ash

Ash is a potential sink of volcanically sourced atmospheric mercury (Hg), and the concentration of particle-bound Hg may provide constraints on Hg emissions during eruptions. We analyze Hg concentrations in 227 bulk ash samples from the Mount Spurr (1992), Redoubt Volcano (2009), and Augustine Volcano (2006) volcanic eruptions to investigate large-scale spatial, temporal, and volcanic-source trends. We find no significant difference in Hg concentrations in bulk ash by distance or discrete eruptive events at each volcano, suggesting that in-plume reactions converting gaseous Hg0 to adsorbed Hg2+ are happening on shorter timescales than considered in this study (minutes) and any additional in-plume controls are not discernable within intra-volcanic sample variability. However, we do find a significant difference in Hg concentration of ash among volcanic sources, which indicates that volcanoes may emit comparatively high or low quantities of Hg. We combine our Hg findings with total mass estimates of ashfall deposits to calculate minimum, first-order Hg emissions of 8.23 t Hg for Mount Spurr (1992), 1.25 t Hg for Redoubt Volcano (2009), and 0.16 t Hg for Augustine Volcano (2006). In particular, we find that Mount Spurr is a high Hg emitting volcano, and that its 1992 particulate Hg emissions likely contributed substantially to the global eruptive volcanic Hg budget for that year. Based on our findings, previous approaches that use long-term Hg/SO2 mass ratios to estimate eruptive total Hg under-account for Hg emitted in explosive events, and global volcanogenic Total Hg estimates need revisiting.

Estimation of Probabilistic Environmental Risk of Heavy Metal(loid)s in Resuspended Megacity Street Dust with Monte Carlo Simulation

To improve the ecological environment quality of industrial cities and protect the health of residents, we determined the priority control factors of heavy metal(loid)s (HMs) pollution and risk in the resuspended street dust (RSD) of Shijiazhuang, an emblematic heavy-industrial city in North China, according to the probabilistic risk assessment method. The results showed that the HMs studied in Shijiazhuang RSD exhibited different pollution levels, that is, Hg showed moderate-to-severe pollution and above; Zn showed moderate-and-above pollution; Co, Cu and Pb showed non-pollution to moderate pollution; while As, Cr, Mn and Ni showed no pollution. The overall contamination of HMs in the RSD presented moderate-to-above contamination levels in &gt;94% of samples. Mercury exhibited considerable-to-very-high ecological risk. The synthetic ecological risks of the HMs were considerable-to-above. The comprehensive pollution and synthetic ecological risk of HMs in Shijiazhuang RSD were mainly caused by Hg. The carcinogenic risk of HMs in RSD to local inhabitants and their non-carcinogenic risk to children should not be ignored. Coal-related industrial sources are a priority source to control. Hg and As are priority HMs to control. We suggest that local governments should strengthen the management of coal-related industrial sources and As and Hg emissions.