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Human activities have emitted substantial mercury into the atmosphere, significantly impacting ecosystems and human health worldwide. Currently, consistent methodologies to evaluate long-term mercury emissions across countries and industries are scant, hindering efforts to prioritize emission controls. Here, we develop a high-spatiotemporal-resolution dataset to comprehensively analyze global anthropogenic mercury emission patterns. We show that global emissions increased 330% during 1960-2021, with declines in developed Global North countries since the 1990s and China since the 2010s completely offset by rapid growth in Global South countries (excluding China). Consequently, global emissions have continued to rise slightly since the 2013 Minamata Convention. In 2021, Global South countries produced two-thirds of global emissions, despite comprising only one-fifth of the global economy. We predict that, although large uncertainties exist, continued emission growth in Global South countries under a business-as-usual scenario could increase 10%-50% global mercury emissions by 2030. Our findings demonstrate that global control of anthropogenic mercury emissions has reached a critical juncture, highlighting the urgent need to target reductions in Global South countries to prevent worsening health and environmental impacts., Competing Interests: Competing interests: The authors declare no competing interests., (© 2025. The Author(s).)

Vegetation assimilation of atmospheric gaseous elemental mercury (GEM) represents the largest dry deposition pathway in global terrestrial ecosystems. This study investigated Hg accumulation mechanisms in deciduous broadleaves and evergreen needles, focusing on how ecophysiological strategies─reflected by δ 13 C, δ 18 O, leaf mass per area, and leaf dry matter content-mediated Hg accumulation. Results showed that deciduous leaves exhibited higher total Hg (THg) concentrations and accumulation rates (THg rate ), which were 85.3 ± 17.7 and 110.0 ± 0.3% higher than those in evergreen needles. The two tree types exhibited distinct ecophysiological strategies: deciduous broadleaves, with higher stomatal conductance and photosynthetic rates, rapidly adjust stomata to changes in meteorological and pollutant factors, playing a key role in controlling THg rate . In contrast, evergreen needles featured stable stomatal control, highlighting the direct positive effect of GEM on their THg rate . Precipitation and wind speed negatively influenced foliar THg rate . Correlations between PM 2.5 , NO 2 , and THg rate in evergreen needles suggested synergistic patterns between atmospheric Hg and pollutants. This study underscores distinct GEM accumulation mechanisms across tree functional types and emphasizes the importance of species-specific foliar ecophysiological strategies. An empirical model linking THg rate with ecophysiological, meteorological, and atmospheric pollution factors was provided, contributing to the refinement of foliar Hg accumulation models.

The neurotoxin methylmercury in seafood threatens food safety worldwide. China has implemented stringent wastewater policies, established numerous treatment facilities and enforced rigorous water quality standards to address pollution in its waterways. However, the impact of these policies on seafood safety and methylmercury exposure remains unknown. Here we developed a process-based model showing that, although mercury reductions from municipal wastewater policies accounted for only 9% of atmospheric mercury emissions during 1980-2022, these measures unexpectedly prevented 102,000 - 6,600 + 11,000 mercury-related deaths and counteracted nearly two thirds of potential deaths from those emissions. Furthermore, these policies ensured that 146 - 9 + 8 megatonnes of freshwater seafood met the World Health Organization and China's mercury-safety standards, preventing US $ 498 - 29 + 32 billion in economic losses. Finally, we explore how China, as the primary global seafood producer and exporter, could develop municipal wastewater policies at the regional level to reduce aquatic pollutants and unlock the health benefits of seafood consumption., Competing Interests: Competing interests: The authors declare no competing interests., (© 2025. The Author(s), under exclusive licence to Springer Nature Limited.)

Mercury, a neurotoxic substance, circulates globally, significantly stored in soils through atmospheric deposition and plant decay. Despite being deposited, mercury can be remobilized and released into the atmosphere and water, enhancing its global cycle. Recent research suggests that climate warming may amplify the remobilization of soil mercury, facilitating its incorporation into food webs that humans exploit. However, the potential geospatial feedback of soil mercury levels in response to warming remains unclear. By leveraging up-to-date soil measurements and observation-driven models, we determined the amount of mercury stored in global 0-100 cm soils to be 4.3 Tg (interquartile range: 2.5-6.3 Tg). Furthermore, our analysis indicates that warming likely aggravates global soil mercury levels, particularly in many temperate areas in East Asia, North Europe, and North America (>20 ng g -1 increase by 2100) due to warming-induced vegetation greening. Critically, observation-driven models raise the possibility that implementing ambitious mercury-emission-control schemes alone may be insufficient to counterbalance the positive feedback of soil mercury concentration, while process-based biogeochemical modeling demonstrates consistent patterns that reinforce this concern. These findings hold broad implications; for example, such feedback may catalyze mercury remobilization in land-ocean continuums and exacerbate human risks, stressing the necessity for continued reductions in greenhouse gas and mercury emissions.

Coastal wetland soils play a critical role in the global mercury (Hg) cycle, serving as both an important repository for total mercury (THg) and a hotspot for methylmercury (MeHg) production. This study investigated Hg pollution in soils dominated by Phragmites australis (PA) and Spartina alterniflora (SA) across five representative China's coastal wetlands (Yellow River (YR), Linhong River (LHR), Yangtze River (CJR), Min River (MR), and Nanliu River (NLR)). The THg concentrations ranged from 16.7 to 446.0 (96.3 ± 59.3 ng g -1 , dw), while MeHg concentrations varied from 0.01 to 0.81 (0.12 ± 0.12 ng g -1 , dw). We further evaluated Hg risk in these wetlands using potential ecological risk index (E r ) and geographical enrichment factor (I geo ). Most wetlands exhibited low to moderate ecological risk, except the PA habitat in the YR wetland, showing moderate to high risk. Soil organic matter significantly influenced THg and MeHg distribution, while MeHg% correlated well with soil salinity and pH. These findings highlight the importance of organic-rich coastal wetland soils in THg and MeHg accumulation, with the soil properties influencing net MeHg production. Furthermore, SA habitat generally exhibited higher MeHg%, suggesting its invasion elevates the ecological risk of MeHg in coastal wetlands. ENVIRONMENTAL IMPLICATION: Mercury (Hg), a global pollutant, poses great risks to wildlife and humans. Since industrialization, anthropogenic Hg release surpassed natural sources. Long-term exposure leads to biomagnification of Hg. This study assessed Hg and methylmercury pollution and risks in soils of five China's coastal wetlands dominated by Phragmites australis and Spartina alterniflora. Environmental factors (total carbon, total organic carbon, total nitrogen, salinity, pH) were analyzed to reveal key variables influencing Hg pollution and methylation. Essential for quantifying Hg pollution in coastal wetlands, the findings provide a scientific basis for effective wetland conservation policies and addressing environmental health in these regions., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Outdoor air pollution causes millions of premature deaths annually worldwide. Sulfate is a major component of particulate pollution. Winter sulfate observations in China show both high concentrations and an accumulation mode with a modal size >1 μm. However, we find that this observed size distribution cannot be simulated using classical gaseous and aqueous phase formation (CSF) or proposed aerosol-processing formation (APF) mechanisms. Specifically, the CSF simulation underestimates sulfate concentrations by 76% over megacities in China and predicts particle size distributions with a modal size of ∼0.35 μm, significantly smaller than observations. Although incorporating the APF mechanism in the atmospheric chemical model notably improves sulfate concentration simulation with reasonable parameters, the simulated sulfate particle size distribution remains similar to that using the CSF mechanism. We further conduct theoretical analyses and show that particles with diameters <0.3 μm grow rapidly (2-3 s) to 1 μm through the condensation of sulfuric acid in fresh high-temperature exhaust plumes, referred to as in-source formation (ISF). An ISF sulfate source equivalent to 15% of sulfur emissions from fossil fuel combustion largely explains both observed size distributions and mass concentrations of sulfate particles. The findings imply that ISF is a major source of wintertime micron-sized sulfate in China and underscore the importance of considering the size distribution of aerosols for accurately assessing the impacts of inorganic aerosols on radiative forcing and human health.

Mercury, a pervasive global pollutant, primarily enters the atmosphere through human activities and legacy emissions from the land and oceans. A significant portion of this mercury subsequently settles on land through vegetation uptake. Characterizing mercury storage and distribution within vegetation is essential for comprehending regional and global mercury cycles. We conducted an unprecedented large-scale aboveground vegetation mercury survey across the expansive Tibetan Plateau. We find that mosses (31.1 ± 0.5 ng/g) and cushion plants (15.2 ± 0.7 ng/g) outstood high mercury concentrations. Despite exceptionally low anthropogenic mercury emissions, mercury concentrations of all biomes exceeded at least one-third of their respective global averages. While acknowledging the role of plant physiological factors, statistical models emphasize the predominant impact of atmospheric mercury on driving variations in mercury concentrations. Our estimations indicate that aboveground vegetation on the plateau accumulates 32 -12 +21 Mg (interquartile range) mercury. Forests occupy the highest biomass and store 82% of mercury, while mosses, representing only 3% of the biomass, disproportionally contribute 13% to mercury storage and account for 43% (2.5 -1.4 +3.0 Mg/year) of annual mercury assimilation by vegetation. Additionally, our study underscores that extrapolating aboveground vegetation mercury storage from lower-altitude regions to the Tibetan Plateau can lead to substantial overestimation, inspiring further exploration in alpine ecosystems worldwide.

Rivers are important sources of Hg for adjacent seas, and seafood from nearshore waters is a major source of Hg exposure for humans. There is thus a key scientific concern regarding how much riverine Hg inputs influence Hg loads in nearshore waters as well as how far the impact range can extend from the river to the open sea. In addition, it is important to understand the influence of anthropogenic hydro-facilities and activities on Hg levels in downstream seas. Because of the concise mass exchange pattern between the seas and the previously demonstrated intensive Hg inputs under anthropogenic regulation from the Yellow River, the Bohai and Yellow Seas, which are key fishery and marine breeding areas for China, are an ideal research area for exploring the impacts of riverine Hg on nearshore and adjacent open seas. Field surveys were conducted in eight major rivers and two seas, and 433 water samples were collected. The main Hg input and output terms (rivers, ocean currents, underground discharge, sewage, coastal erosion, atmospheric deposition, surface evasion, sedimentation, and fisheries) were quantified in the Bohai and Yellow Seas. Owing to the high inputs from the Yellow and Yalu Rivers, elevated THg concentrations were found. Apart from direct MeHg discharge, riverine nutrients may also seemingly affect nearshore MeHg. Using mass balance models, we found that the Yellow River (9.8 t) was the dominant Hg source in the Bohai Sea, which accounted for more than half of all contributions, and the Bohai Sea played the role of a secondary source of Hg to the Yellow Sea, with a flux of 3.3 t. Anthropogenic hydro-activities in large rivers could significantly influence Hg outputs and loads in the nearshore and even open seas. This study provides useful information for water resource management applications to reduce potential MeHg risks., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Estuaries are an important food source for the world's growing population, yet human health is at risk from elevated exposure to methylmercury (MeHg) via the consumption of estuarine fish. Moreover, the sources and cycling of MeHg in temperate estuarine ecosystems are poorly understood. Here, we investigated the seasonal and tidal patterns of mercury (Hg) forms in Long Island Sound (LIS), in a location where North Atlantic Ocean waters mix with the Connecticut River. We found that seasonal variations in Hg and MeHg in LIS followed the extent of riverine Hg delivery, while tides further exacerbated the remobilization of earlier deposited riverine Hg. The net production of MeHg near the river plume was significant compared to that in other locations and enhanced during high tide, possibly resulting from the enhanced microbial activity and organic carbon remineralization in the river plume. Statistical models, driven by our novel data, further support the hypothesis that the river-delivered organic matter and inorganic Hg drive net MeHg production in the estuarine water column. Our study sheds light on the significance of water column biogeochemical processes in temperate tidal estuaries in regulating MeHg levels and inspires new questions in our quest to understand MeHg sources and dynamics in coastal oceans.

Seafood is a major source of Hg exposure for humans, and rivers are an important source of Hg for adjacent seas. The Yellow River is an extremely high-sediment river that is heavily influenced by anthropogenic water facilities, especially sediment regulations, which might result in significant intra- and inter- year flux variations on pollutants. Overestimations of Hg flux were found in previous studies on high-sediment rivers, and a comprehensive study of Hg transport along such a river has not yet been attempted. In this study, we quantified the fates of Hg and methylmercury (MeHg) in the Yellow River and its main branches, as well as the impacts of anthropogenic activities, including deposition of contaminants in the reservoirs, diversion in the downstream, and sediment regulation, by sampling in 2017 and 2018,and comparing the two typical years with and without sediment regulation. The total Hg (THg) and MeHg concentrations in the Yellow River and its tributaries were high, and extremely high MeHg/THg ratios were found in the three sampled reservoirs. The river discharges substantial amounts of THg and MeHg into the Bohai Sea, and particulate Hg in the humid period accounts for a large proportion. A significant increase in Hg flux into the ocean was found in 2018 compared with that in 2017, which was primarily attributed to the altered hydrology caused by sediment regulation. Substantial amounts of Hg were impounded in the reservoirs, and only a small fraction was discharged downstream of the reservoir in the non-regulation years. Moreover, Hg fluxes to the coastal ocean were impacted by downstream water diversion in non-regulation years, whereas the contributions of diversions in regulation years were small. In conclusion, models showed that in recent 15 years, sediment regulation can enhance the Hg burden and risk to coastal ecosystem of Bohai Sea., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Ammonia (NH 3 ) is an important precursor of secondary inorganic aerosols and greatly impacts nitrogen deposition and acid rain. Previous studies have mainly focused on the agricultural NH 3 emissions, while recent research has noted that industrial sources could be significant in China. However, detailed estimates of NH 3 emitted from industrial sectors in China are lacking. Here, we established an unprecedented high-spatial-resolution data set of China's industrial NH 3 emissions using up-to-date measurements of NH 3 and point source-level information covering eight major industries and 27 subdivided process categories. We found that China emitted 798 (90% confidence interval: 668-933) gigagrams of industrial NH 3 into the atmosphere in 2019, equivalent to 44 ± 20% of the industrial emissions worldwide; this flux is 3-fold larger than that in 1998 and has fluctuated since 2014. Furthermore, although fertilizer production is responsible for approximately half of the emissions in China, the emissions from cement production and coal-fired power plants increased dramatically from near zero to 164 and 41 gigagrams, respectively, in the past two decades, primarily due to the NH 3 escape caused by the large-scale application of the denitration process. Our results reveal that, unlike other major air pollutants, China's industrial NH 3 emission control is still in a critical period, and stricter NH 3 emission standards and innovation in pollution control technologies are highly desirable.

Anthropogenic activities have led to widespread contamination with mercury (Hg), a potent neurotoxin that bioaccumulates through food webs. Recent models estimated that, presently, 200 to 600 t of Hg is sequestered annually in deep-sea sediments, approximately doubling since industrialization. However, most studies did not extend to the hadal zone (6,000- to 11,000-m depth), the deepest ocean realm. Here, we report on measurements of Hg and related parameters in sediment cores from four trench regions (1,560 to 10,840 m), showing that the world's deepest ocean realm is accumulating Hg at remarkably high rates (depth-integrated minimum-maximum: 24 to 220 μg ⋅ m -2 ⋅ y -1 ) greater than the global deep-sea average by a factor of up to 400, with most Hg in these trenches being derived from the surface ocean. Furthermore, vertical profiles of Hg concentrations in trench cores show notable increasing trends from pre-1900 [average 51 ± 14 (1σ) ng ⋅ g -1 ] to post-1950 (81 ± 32 ng ⋅ g -1 ). This increase cannot be explained by changes in the delivery rate of organic carbon alone but also need increasing Hg delivery from anthropogenic sources. This evidence, along with recent findings on the high abundance of methylmercury in hadal biota [R. Sun et al , Nat. Commun. 11, 3389 (2020); J. D. Blum et al , Proc. Natl. Acad. Sci. U. S. A. 117, 29292-29298 (2020)], leads us to propose that hadal trenches are a large marine sink for Hg and may play an important role in the regulation of the global biogeochemical cycle of Hg., Competing Interests: The authors declare no competing interest.

Globally, the consumption of coastal fish is the predominant source of human exposure to methylmercury, a potent neurotoxicant that poses health risks to humans. However, the relative importance of riverine inputs and atmospheric deposition of mercury into coastal oceans remains uncertain owing to a lack of riverine mercury observations. Here, we present comprehensive seasonal observations of riverine mercury and methylmercury loads, including dissolved and particulate phases, to East Asia's coastal oceans, which supply nearly half of the world's seafood products. We found that East Asia's rivers annually exported 95 ± 29 megagrams of mercury to adjacent seas, 3-fold greater than the corresponding atmospheric deposition. Three rivers alone accounted for 71% of East Asia's riverine mercury exports, namely: Yangtze, Yellow, and Pearl rivers. We further conducted a metadata analysis to discuss the mercury burden on seawater and found that riverine export, combined with atmospheric deposition and terrestrial nutrients, quantitatively elevated the levels of total, methylated, and dissolved gaseous mercury in seawater by an order of magnitude. Our observations support that massive amounts of riverine mercury are exported to coastal oceans on a continental scale, intensifying their spread from coastal seawater to the atmosphere, marine sediments, and open oceans. We suggest that the impact of mercury transport along the land-ocean aquatic continuum should be considered in human exposure risk assessments.

Methylmercury presents potent neurotoxicity to humans. Fish consumption is the leading source of human exposure to methylmercury worldwide. However, the exposure source in Tibet remains poorly understood because of the scarcity of observational data on most Tibetan foods, although high mercury levels were recently detected in some traditional Tibetan medicines. Here, the results of field investigations show that the joint consumption of traditional Tibetan medicines (TTMs), fish, and rice constitutes a primary exposure pathway to methylmercury in Tibetans and that the probable daily intake of methylmercury is close to that for many coastal regions. People who are young and high-income may have higher methylmercury exposure levels mainly because of economic development and cultural exchanges among regions. Our analysis indicates that a large proportion of the Tibetan population are likely to face a high methylmercury exposure risk and that mercury-susceptible populations in Tibet should be attentive to consuming TTMs with fish., (© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

Exposure to methylmercury (MeHg) has various toxic effects on humans. The evaluation of human MeHg exposure has previously focused on fish consumption. However, in this study, we found that MeHg levels in domestic crabs in China were also relatively high (range: 50-1400 ng/g, dry weight). The high MeHg levels in crabs and their high consumption do not match the risk assessment of MeHg, indicating an underestimated exposure risk, especially in MeHg-sensitive groups such as pregnant women. The annual crab MeHg content output in China was estimated to be 30 ± 27 kg. A total of 6.8% of the country's land area contributes 71% of the MeHg output. However, 66% of the output is redistributed to non-crab-producing regions via interregional food trade, posing risks to the population on a national scale. The daily intake of MeHg from crabs could easily exceed the reference dose (0.1 µg/kg of body weight per day) suggested by the United States Environmental Protection Agency with consideration of coexposure from fish, rice, and other food sources. We suggest that future MeHg exposure analysis includes crab MeHg as a coexposure pathway to estimate the dietary MeHg limit accurately and emphasize the influence of interregional food trade on MeHg exposure., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Lake sediments are key materials for mercury deposition and methylation. To understand the mercury concentrations in China's lakes, 100 lake surface sediment samples were collected from 35 lakes in 2014. Total mercury (THg), methylmercury (MeHg) concentrations and the annual Hg burial rates in lake sediments were measured. THg and MeHg concentrations in the sediment ranged from 13.6 to 1488 ng‧g -1 and 0.05 to 1.70 ng‧g -1 , respectively, and urban lakes reported most high values, indicating direct anthropogenic inputs. The Inner Mongolia-Xinjiang Region (MX) and Qinghai-Tibet Plateau Region (QT) reported relatively lower mercury burial rates, while the Eastern Plain Region (EP), Northeast Mountain and Plain Region (NE), and Yunnan-Guizhou Plateau Region (YG) reported higher mercury burial rates. Regional variances of THg burial fluxes were dominated by atmospheric deposition, terrestrial input, and sediment accumulation rates in different lakes. In 2014, the estimated average THg burial rate in China's lakes was 139 μg‧m -2 ‧yr -1 , comparable to the average in mid-latitude North America in recent years; however, due to China's much smaller lake area relative to NA, the annual THg burial flux in China was much lower than that in North America. EP and NE, where most freshwater aquatic products in China are harvested, accounted for 58.2% and 22.9%, respectively, of the THg burial flux. High sedimentary MeHg concentrations and MeHg:THg ratios were reported in most of the NE but low MeHg concentrations and MeHg:THg ratios were reported in EP. MeHg concentrations and MeHg:THg ratios were positively correlated with water COD levels and negatively correlated with average temperature. The results of this study indicate that in addition to the adjacent seas, lake sediments are an important mercury sink in China's aquatic environment, which could cause health risks due to MeHg intake, especially in NE., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

The cement industry has become the largest mercury (Hg) emission source in China. Better understanding Hg emission and deposition characteristics and drivers of Hg emission changes can increase the awareness of related risks and support effective policy making. The results show that due to the substantial increase in the use of new suspension preheater and precalciner (NSP) technology in China, an approximate two-fold increase from 80.0 to 144.0 Mg year -1 was observed for the cement-related Hg emissions during 2005-2015, which has resulted in a considerable increase in atmospheric deposition over terrestrial China from 37.9 to 75.9 Mg year -1 . Compared to the great majority of emission sectors, the same increase in Hg emissions from cement production can cause more deposition due to the large share of highly water-soluble divalent Hg in the sector. Each 1% increase in the share of divalent Hg can result in an increase of 0.37 Mg year -1 in deposition over terrestrial China. Technical improvement and diversification of cement products are two major driving forces offsetting the economy-induced growth in cement-related Hg emissions during 2005-2015. Measures aimed at reducing the Hg emission intensity against the further increase in the use of NSP technology and avoiding overcapacity against the stimulation of real estate and increasing cement demands are urgently needed for the cement industry in China.

China is the world's largest cement-related mercury emitter. Atmospheric mercury inventories for China's cement industry are essential for appraising global mercury emissions and have been widely developed in previous studies associated with considerable uncertainties. In this study, we compiled high tempo-spatial resolution atmospheric mercury emission inventories for Chinese cement plants using the mass balance method and plant-level input-output data. The effects of industry policies were investigated based on the inventories for 2007 and 2015. Nationwide emissions increased from 80 to 113 t due to rapid expansion of production and kiln-type substitution yet partly offset by policies involving capacity structure reformation. Pollution decreased in winter in northern China, thanks to the targeting policies. Mercury input, output, and storage in cement kilns in China were estimated. The uncertainty remarkably decreased relative to previous inventories. This study demonstrates the feasibility of establishing high-resolution emission inventories with the application of the mass balance method for all the individual plants nationwide and thus has implications for similar studies. This work also improves our understanding of the spatial patterns and temporal evolution of mercury emissions in China, thus offering references for the implementation of environment policies and the Minamata Convention on Mercury in China.

The Three Gorges Dam (TGD) is the world's largest hydropower construction. It can significantly impact contaminant transport in the Yangtze River-East China Sea Continuum (YR-ECSC). In addition to evaluating the impact of the TGD on the deposition of contaminants in the reservoir, we also address their cycles in the river below the dam and in the coastal East China Sea. A comprehensive study of metal contaminant transport along the YR-ECSC has not been previously attempted. We quantified the fates of mercury (Hg), arsenic (As), lead (Pb), cadmium (Cd) and chromium (Cr) within the YR-ECSC, and the impacts of the TGD, by sampling water and suspended particles along the Yangtze River during spring, summer, fall, and winter and by modeling. We found that the Yangtze River transports substantial amounts of heavy metals into the coastal ocean. In 2016, riverine transport amounted to 48, 5900, 11,000, 230, and 15,000 megagrams (Mg) for Hg, As, Pb, Cd, and Cr, respectively, while other terrestrial contributions were negligible. Metal flux into the coastal ocean was primarily derived from the downstream portion of the river (84-97%), while metals transported from upstream were largely trapped in the Three Gorges Reservoir (TGR, 72%-96%). For example, 34 Mg of Hg accumulated in the TGR owing to river damming, large-scale soil erosion, and anthropogenic point source releases, while 21 Mg of Hg was depleted from the riverbed downstream owing to the altered river hydrology caused by the TGD. Overall the construction of TGD resulted in a 6.9% net decrease in the Hg burden of the East China Sea, compared to the pre-TGD period., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Methylmercury (MeHg) poses health risks to humans worldwide. The investigation of a longer chain of biogeochemical MeHg transport from production to consumption than that addressed in previous studies could provide additional scientific foundation for the reduction of risks. The main objective of this study is to identify the impacts of the interregional food trade along with the age, gender and socioeconomic status of people on human MeHg exposure in a developing megacity. Based on a field investigation, sampling and measurements, we provide experimental evidence regarding the substantial displacement of human MeHg exposure from production areas to consumption areas induced by the food trade. In 2018, 20% and 64% of the exposure in Beijing originated from the international and interprovincial food trade, respectively. Meanwhile, the ingestion of fish contributed 79% to the total exposure, followed by rice (4.4%), crab (3.8%) and shrimp (2.7%), and the exposure risk in urban districts was higher than that in rural areas by a factor of 2.2. A significantly higher contribution of imported deep-sea species to exposure among young people than among older people was observed (P < 0.01**), and a larger contribution of the international food trade to the MeHg exposure risk for women of childbearing age (average: 27%) than that among other groups (average: 10%) was found. Overall, our efforts demonstrate the dramatic impact of the food trade on MeHg exposure in a developing megacity, and we suggest that MeHg-susceptible populations in China should choose indigenous fish species (e.g., hairtail, yellow croaker and carp species) rather than imported deep-sea species as their dietary protein source., (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Using 2025 as the target year, we quantitatively assessed the reduction potentials of emissions of primary pollutants (including CO, HC, NO x , PM 2.5 and PM 10 ) under different vehicle control policies and the impacts of vehicle emission control policies in the BTH region on the regional PM 2.5 concentration in winter and the surface ozone (O 3 ) concentration in summer. Comparing the different scenarios, we found that (1) vehicle control policies will bring significant reductions in the emissions of primary pollutants. Among the individual policies, upgrading new vehicle emission standards and fuel quality in Beijing, Tianjin, and Hebei will be the most effective policy, with emission reductions of primary pollutants of 26.3%-54.7%, 38.0%-70.3% and 46.0%-81.6% in 2025, respectively; (2) for PM 2.5 in winter, the Combined Scenario (CS) will lead to a reduction of 0.5-3.9 μg m -3 (3.5%-11.6%) for the monthly average PM 2.5 concentrations in most areas. The monthly nitrate and ammonium concentrations would reduce by 5.8% and 5.3%, respectively, in the whole BTH region, indicating that vehicle emission control policies may play an important role in the reduction of PM 2.5 concentrations in winter, especially for nitrate aerosols; and (3) for O 3 concentrations in summer, vehicle emission control policies will lead to significant decreases. Under the CS scenario, the maximum reduction of monthly average O 3 concentrations in the summer is approximately 3.6 ppb (5.9%). Most areas in the BTH region have a decrease of 15 ppb (7.5%) in peak values compared to the base scenario. However, in some VOC-sensitive areas in the BTH region, such as the southern urban areas, significant reductions in NO x may lead to increases in ozone concentrations. Our results highlight that season- and location-specific vehicle emission control measures are needed to alleviate ambient PM 2.5 and O 3 pollution effectively in this region due to the complex meteorological conditions and atmospheric chemical reactions., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

The magnitude of environmental change due to anthropogenic impacts might greatly exceed that of natural disturbances. In this work, we quantitatively examine the impacts of river damming, soil erosion, and point-source release on the transport of methylmercury (MeHg) throughout the Yangtze River, the third longest river in the world. Based on seasonal observations and the subsequent material flow analysis, we found that in 2016, the Yangtze River discharged 470 ± 200 kg MeHg to the coastal and shelf areas, a value at least ten-fold larger than existing observations in other large rivers around the world. The construction of the Three Gorges Dam (TGD), the world's largest hydropower dam, induced a substantial amount of MeHg (at least 250 ± 220 kg) accumulation in the reservoir and a relatively small amount of MeHg (150 ± 37 kg) discharge to the downstream region in 2016. The reservoir itself is not expected to be more contaminated by MeHg than the downstream areas of the river after the TGD, and the TGD has an additive effect on downstream MeHg transport. The riverine MeHg flux in the river mouth was 3-fold that discharged from the TGD mainly due to TGD-induced resuspension of MeHg from the downstream riverbed, as well as MeHg imports to the downstream area from tributaries, soil erosion, municipal wastewater, and in situ production. Our analysis offers new evidence that in future decades, the increase in estuarine MeHg contamination resulting from the increasing construction of large dams might pose a challenge for global coastal fisheries., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Protecting the environment and enhancing food security are among the world's greatest challenges. Fish consumption is widely considered to be the single significant dietary source of methylmercury. Nevertheless, by synthesizing data from the past six decades and using a variety of models, we find that rice could be a significant global dietary source of human methylmercury exposure, especially in South and Southeast Asia. In 2013, globalization caused 9.9% of human methylmercury exposure via the international rice trade and significantly aggravated rice-derived exposure in Africa (62%), Central Asia (98%) and Europe (42%). In 2016, 180 metric tons of mercury were generated in rice plants, 14-fold greater than that exported from oceans via global fisheries. We suggest that future research should consider both the joint ingestion of rice with fish and the food trade in methylmercury exposure assessments, and anthropogenic biovectors such as crops should be considered in the global mercury cycle.

Production system-related air pollution emissions are dominant components in global emission reduction targets and in realizing relevant sustainable development goals (SDGs). To better understand the air pollution emissions induced by globalized production systems through a life cycle perspective, environmental extended multiregional input-output (EE-MRIO) analysis was applied to calculate the primary product-based emissions and the final product-based emissions embodied in the global production systems. Combined with two types of linkage analysis, named the hypothetical extraction method (HEM) and the emissions pure backward linkage (EPBL), emissions were analysed at three scopes at the sector level from macro sector linkage perspectives. An illustrative analysis was presented based on the global EXIOBASE MRIO database and primary PM 2.5 emissions from 1995 to 2011. The results show that from 1995 to 2011, the primary PM 2.5 emissions in the global production systems increased by 35%. In 2011, China's production system generated the highest primary product-based and final product-based primary PM 2.5 emissions, which accounted for 30.7% and 29.6% of the global total, respectively. The emission flows balance between primary product-based emissions and final product-based emissions revealed that most developing countries are sources of emissions and that developed countries are sinks of emissions in production systems. An approximately U-shaped relationship was found in the primary PM 2.5 emissions embodied in final products, while the opposite relationship was found embodied in primary products. Meanwhile, sector-specific protocols for controlling the high indirect emissions sectors can make the supply chain cleaner. Our findings further indicated that focusing more on industries can help relevant emissions control policymaking processes., (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Mercury (Hg) emission from natural soil is one of the most important contributors to global Hg cycles. Research on Hg emission from soil to air has been carried out in China. Currently, most of the research focuses on contaminated sites in China, while research in other regions is rare. To provide more accurate information on Hg emissions from soil to air in China and obtain additional laboratory data to verify the role of solar radiation and temperature in this process, we sampled and measured Hg emission fluxes from various natural soils (range, 48-240 ng/g) across mainland China under different solar radiation (0-900 W·m -2 ) and temperature (15-45 °C) conditions in a laboratory. We found that in different places in China, Hg emissions from natural soils occurred more easily when the soil Hg concentration, temperature, and solar radiation were high, but the impacts were different among the regions due to different soil types. Hg emissions from natural soils (0.071-24 ng·m 2 ·h -1 ) were typically lower than those from contaminated sites, suggesting that additional measurements in natural soils are desirable. The results of this study could provide more accurate information on Hg emission from natural soil to air and help establish a nationwide natural soil Hg emission inventory in China.

In the past two decades, neonicotinoid insecticides have been widely used in agricultural activities in China. Many previous studies have investigated the neonicotinoid pollution in aquatic ecosystems, but the status of water safety of neonicotinoid uses in China is very scarce. The present study aims to reveal the spatial and temporal distribution of neonicotinoids in rivers, and then evaluate the ecological risks to aquatic animals. Water samples were collected from all sixteen rivers along the east coast of China during the dry and wet seasons in 2016, and nine individual commercialized neonicotinoids were quantified. Higher concentrations were found during the dry season (343 ± 210 ng/L) compared to those during the wet season (174 ± 162 ng/L). The concentration of neonicotinoid insecticides in river water is mainly affected by the intensity of agricultural activities. The spatial and temporal pollution patterns we discovered suggested the use of neonicotinoids has shifted from old types (i.e., imidacloprid and acetamiprid) to new types (i.e., dinotefuran and nitenpyram) in some areas. The estimated annual quantity of neonicotinoids released into the adjacent seas totaled 1256 ± 780 tons, most of which (95%) ran into the East China Sea due to heavy agricultural use in the Yangtze River Basin. Using the species sensitive distribution (SSD) method, the thresholds for aquatic animals were determined (acute: 362 ng/L; chronic: 58 ng/L). Under current agricultural practices, 27% and 84% of the river water samples exceeded the thresholds for acute and chronic ecological risks, suggesting intervention programs are in urgent need to ensure river water safety for aquatic life in China., (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Soil erosion, which has been recently shown to significantly perturb carbon cycling, occurs naturally but can be either enhanced or reduced by human activities. However, the impacts of soil erosion on terrestrial contaminant cycles remain unclear. Here, we select eight trace elements, i.e., arsenic, cadmium, chromium, copper, nickel, lead, zinc, and mercury, to examine the erosional impacts of the elements' fate and transport across China. By synthesizing the detailed distribution of soil erosion fluxes, soil element inventories, and diverse modeling methods, we reveal that while human activities have reduced the lateral transport of these elements in the Loess Plateau (Central North China, a 56% decline in the past two decades with a range of 46% to 110%) due to soil conservation projects, they have increased these transport fluxes in China's major karst regions (Southwest China, a 84% increase with a range of 55% to 150%) because of severe rocky desertification. These fluxes have completely overwhelmed the soil conservation efforts in the Loess Plateau. Fluxes of these elements into aquatic environments from Southwest China reached 46% of the total input in China in 2010. These fluxes were higher than the inputs from point sources in the region by a factor of 50 because of impacts of excessive agricultural cultivation and geographical and climatic factors. These findings indicate the enormous perturbation of terrestrial contaminant cycles caused by soil erosion in karst regions and demonstrate the need for long-term sustainable management of soil erosion and contaminant discharge to protect fragile terrestrial ecosystems.

Mercury (Hg) exposure poses substantial risks to human health. Investigating a longer chain from economic activities to human health can reveal the sources and critical processes of Hg-related health risks. Thus, we develop a more comprehensive assessment method which is applied to mainland China-the largest global Hg emitter. We present a map of Hg-related health risks in China and estimate that 0.14 points of per-foetus intelligence quotient (IQ) decrements and 7,360 deaths from fatal heart attacks are related to the intake of methylmercury in 2010. This study, for the first time, reveals the significant impacts of interprovincial trade on Hg-related health risks across the whole country. For instance, interprovincial trade induced by final consumption prevents 0.39 × 10 -2 points for per-foetus IQ decrements and 194 deaths from fatal heart attacks. These findings highlight the importance of policy decisions in different stages of economic supply chains to reduce Hg-related health risks.

Neonicotinoid insecticides have been widely consumed worldwide, particularly in China. There is a growing interest in the environmental research community about the occurrence, fates, sources, and risks of neonicotinoids. Nine neonicotinoids in river/lake water were measured at 12 sites along the Yangtze River Basin during the dry and wet seasons in 2016, and nonpoint sources were also identified based on a modified mass balance method. A significantly higher concentration of neonicotinoids was found during the dry season probably due to the dilution effect and insecticide consumption. The high pollution levels are due to posing high ecological risks compared with the recommended thresholds. In 2016, 1190 (95% confidence interval (CI) = 822-1690) tons of neonicotinoids were transferred into the adjacent sea. Nonpoint source pollution (1700 (CI = 1200-2370) tons) was the major contributor (91.3%) to the total input of neonicotinoids into the system. Composition profiles identifying specific neonicotinoid sources indicated some changes in usage patterns from old to new types of neonicotinoids. This spatial and seasonal field study and source identification is expected to fill the data gap regarding the limited information on neonicotinoid use patterns and to inform further effective policy-making and intervention programs in China that should be urgently promoted in the near future.

Mercury (Hg) is characterized by its ability to migrate between continents and its adverse effects on human health, arousing great concern around the world. The transboundary transport of large anthropogenic Hg emissions from China has attracted particular attention, especially from neighboring countries. Here, we combine an atmospheric transport model, a mass budget analysis, and a multiregional input-output model to simulate the atmospheric Hg outflow from China and investigate the impacts of Chinese interprovincial trade on the outflow. The results show outflows of 423.0 Mg of anthropogenic Hg, consisting of 65.9% of the total Chinese anthropogenic emissions, from China in 2010. Chinese interprovincial trade promotes the transfer of atmospheric outflow from the eastern terrestrial boundary (-6.4 Mg year -1 ) to the western terrestrial boundary (+4.5 Mg year -1 ) and a net decrease in the atmospheric outflow for the whole boundary, reducing the chance of risks to foreign countries derived from transboundary Hg pollution from China. These impacts of interprovincial trade will be amplified due to the expected strengthened interprovincial trade in the future. The synergistic promotional effects of interprovincial trade versus Hg controls should be considered to reduce the transboundary Hg pollution from China.

The global pollutant mercury (Hg), especially as methylmercury (MeHg), threatens human and ecosystem health. But major contributors of MeHg exposure to people in China remain highly debated. We developed the China Mercury Exposure Assessment (CMEA) model, which incorporates human exposure pathways for MeHg and total Hg (THg), the interregional, including international and interprovincial, food trading as well as human physiology to provide a comprehensive system that can evaluate the pathway of Hg forms to human consumers in China. Based on the CMEA model that employed the most comprehensive and recent data, we have found that the Probable Daily Intake (PDI) of MeHg for the Chinese population was 0.057 (range: 0.036-0.091 as 60% confidence interval) μg·kg -1 ·day -1 , while that of THg was 0.35 (range: 0.22-0.55) μg·kg -1 ·day -1 . MeHg exposure was dominated by fish intake, especially by farm-raised freshwater fish due to higher consumption of these fish. In 2011, fish intake contributed to 56% to the total MeHg exposure, followed by rice (26%). Consumption of farm-raised fish reduced human exposure to MeHg by 33%. On the other hand, interregional food trading increased MeHg exposure of the Chinese population, as a whole, by 7.6%. The international and interprovincial food trades contributed to 5.1% and 22% of MeHg intake, respectively. For the whole China, fish intake related exposure to MeHg was highest for the Eastern and Northeastern populations, while Tibetans were chronically exposed to the highest MeHg from other sources. Our findings highlight the importance of farmed fish and food trade for MeHg exposure., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Highly elevated concentrations of total mercury (THg) and methylmercury (MeHg) were found in the municipal sewage in Tibet. Material flow analysis supports the hypothesis that these elevated concentrations are related to regular ingestion of Hg-containing Traditional Tibetan Medicine (TTM). In Tibet in 2015, a total of 3600 kg of THg was released from human body into the terrestrial environment as a result of TTM ingestion, amounting to 45% of the total THg release into the terrestrial environment in Tibet, hence substantially enhancing the environmental Hg burden. Regular ingestion of TTM leads to chronic exposure of Tibetans to inorganic Hg (IHg) and MeHg, which is 34 to 3000-fold and 0-12-fold higher than from any other known dietary sources, respectively. Application of a human physiology model demonstrated that ingestion of TTM can induce high blood IHg and MeHg levels in the human body. Moreover, 180 days would be required for the MeHg to be cleared out of the human body and return to the initial concentration i.e. prior to the ingestion of 1 TTM pill. Our analysis suggests that high Hg level contained in TTM could be harmful to human health and elevate the environmental Hg burden in Tibet.

Terrestrial mercury (Hg) transport, induced by water erosion and exacerbated by human activities, constitutes a major disturbance of the natural Hg cycle, but the processes are still not well understood. In this study, we modeled these processes using detailed information on erosion and Hg in soils and found that vast quantities of total Hg (THg) are being removed from land surfaces in China as a result of water erosion, which were estimated at 420 Mg/yr around 2010. This was significantly higher than the 240 Mg/yr mobilized around 1990. The erosion mechanism excavated substantial soil THg, which contributed to enhanced Hg(0) emissions to the atmosphere (4.9 Mg/yr around 2010) and its transport horizontally into streams (310 Mg/yr). Erosion-induced THg transport was driven by the extent of precipitation but was further enhanced or reduced by vegetation cover and land use changes in some regions. Surface air temperature may exacerbate the horizontal THg release into water. Our analyses quantified the processes of erosion-induced THg transport in terrestrial ecosystems, demonstrated its importance, and discussed how this transport is impacted by anthropogenic inputs and legacy THg in soils. We suggest that policy makers should pay more attention to legacy anthropogenic THg sources buried in soil.

Mercury (Hg) is of global concern because of its adverse effects on humans and the environment. In addition to long-range atmospheric transport, Hg emissions can be geographically relocated through economic trade. Here, we investigate the effect of China's interregional trade on atmospheric Hg deposition over China, using an atmospheric transport model and multiregional input-output analysis. In general, total atmospheric Hg deposition over China is 408.8 Mg yr -1 , and 32% of this is embodied in China's interregional trade, with the hotspots occurring over Gansu, Henan, Hebei, and Yunnan provinces. Interprovincial trade considerably redistributes atmospheric Hg deposition over China, with a range in deposition flux from -104% to +28%. Developed regions, such as the Yangtze River Delta (Shanghai, Jiangsu, and Zhejiang) and Guangdong, avoid Hg deposition over their geographical boundaries, instead causing additional Hg deposition over developing provinces. Bilateral interaction among provinces is strong over some regions, suggesting a need for joint mitigation, such as the Jing-Jin-Ji region (Beijing, Tianjin, and Hebei) and the Yangtze River Delta. Transferring advanced technology from developed regions to their developing trade partners would be an effective measure to mitigate China's Hg pollution. Our findings are relevant to interprovincial efforts to reduce trans-boundary Hg pollution in China.

As a globally transported pollutant, mercury (Hg) released from human activity and methylmercury (MeHg) in the food web are global concerns due to their increasing presence in the environment. In this study, we found that Hg released from municipal sewage into the environment in China is a substantial anthropogenic source based on mass sampling throughout China. In total, 160 Mg (140-190 Mg, from the 20th percentile to the 80th percentile) of Hg (THg) and 280 kg (240-330 kg) of MeHg were released from municipal sewage in China in 2015. The quantities of released THg and MeHg were the most concentrated in the coastal regions, especially in the East, North and South China regions. However, the per capita release of THg and MeHg was the highest in the Tibetan region, which is recognized as the cleanest region in China. THg released into aquatic environments was mitigated from 2001 to 2015 in China, but the amounts released into other sinks increased. This study provides the first picture of the release of Hg from municipal sewage into various sinks in China, and policy makers should pay more attention to the diversity and complexity of the sources and transport of Hg, which can lead to Hg accumulation in the food web and can threaten human health.

Growing concern about the risk associated with increasing environmental mercury (Hg) concentrations has resulted in a focus on the relationships between intercontinental emitted and accumulated Hg. We use a global biogeochemical Hg model with 8 continental regions and a global ocean to evaluate the legacy impacts of historical anthropogenic releases (2000BCE to 2008AD) on global source-receptor relationships of Hg. Legacy impacts of historical anthropogenic releases are confirmed to be significant on the source-receptor relationships according to our results. Historical anthropogenic releases from Asia account for 8% of total soil Hg in North America, which is smaller than the proportion (~17%) from previous studies. The largest contributors to the global oceanic Hg are historical anthropogenic releases from North America (26%), Asia (16%), Europe (14%) and South America (14%). Although anthropogenic releases from Asia have exceeded North America since the 1970s, source contributions to global Hg receptors from Asia have not exceeded North America so far. Future projections indicate that if Hg emissions are not effectively controlled, Asia will exceed North America as the largest contributor to the global ocean in 2019 and this has a long-term adverse impact on the future environment. For the Arctic Ocean, historical anthropogenic release from North America contributes most to the oceanic Hg reservoir and future projections reveal that the legacy impacts of historical releases from mid-latitudes would lead to the potential of rising Hg in the Arctic Ocean in the future decades, which calls for more effective Hg controls on mid-latitude releases., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Identifying the sanitation efficacy in reducing contaminations entering the environment is an important step for water pollution controls and developing management strategies to further improve sanitation conditions. With continuous efforts in sanitation improvement during the past decade, reductions in discharges of aquatic nutrients are expected in China. In this study, we estimated the aquatic nitrogen discharges from human excreta in 31 provinces in China during 2006-2014. The results indicated that the nitrogen discharges entering the environment from human excreta are largely determined by both local population and sanitation conditions. In 2014, the nitrogen discharges from human excreta in the rural areas (2118(1219-3140) Gg per year) (median and 95% confidence interval) are higher than those in the urban areas (1485(626-2495) Gg per year). The significant relationship (R 2 =0.38, n=29) between the total nitrogen concentrations in lakes and corresponding local nitrogen discharges indicated that, the lakes might be potentially affected by the contaminant inputs from human excreta. The further calculations under two policy scenarios showed that through sanitation improvement, further reduction of nitrogen discharges from human excreta in the developed regions might be limited. The sanitation improvement in the less-developed regions, such as Tibet, Qinghai, and Ningxia, should be considered a priority due to the larger reduction potentials., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Based on a time-series dataset and the mass balance method, the contributions of various sources to the nutrient discharges from the Yangtze River to the East China Sea are identified. The results indicate that the nutrient concentrations vary considerably among different sections of the Yangtze River. Non-point sources are an important source of nutrients to the Yangtze River, contributing about 36% and 63% of the nitrogen and phosphorus discharged into the East China Sea, respectively. Nutrient inputs from non-point sources vary among the sections of the Yangtze River, and the contributions of non-point sources increase from upstream to downstream. Considering the rice growing patterns in the Yangtze River Basin, the synchrony of rice tillering and the wet seasons might be an important cause of the high nutrient discharge from the non-point sources. Based on our calculations, a reduction of 0.99Tg per year in total nitrogen discharges from the Yangtze River would be needed to limit the occurrences of harmful algal blooms in the East China Sea to 15 times per year. The extensive construction of sewage treatment plants in urban areas may have only a limited effect on reducing the occurrences of harmful algal blooms in the future., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Risk assessments for human health have been conducted for municipal solid waste incinerators (MSWIs) in many western countries, whereas only a few risk assessments have been performed for MSWIs in developing countries such as China where the use of waste incineration is increasing rapidly. To assess the mercury exposure risks of a population living near the largest MSWI in South China, we combined internal exposure and external exposure assessment with an individual-specific questionnaire. The mercury concentrations in air, soil, and locally collected food around the MSWI were assessed. The total mercury (T-Hg) and methylmercury (MeHg) of 447 blood samples from a control group, residential exposure group, and MSWI workers were measured. The internal and external exposures of the subject population were analyzed. Significant difference in MeHg concentrations was observed between the control group and the exposed group, between the control group and the MSWI workers, and between the exposed group and the MSWI workers (median levels: 0.70 μg/L, 0.81 μg/L, and 1.02 μg/L for the control group, exposed group, and MSWI workers, respectively). The MeHg/T-Hg ratio was 0.51 ± 0.19, 0.59 ± 0.17 and 0.58 ± 0.25, respectively. Multiple linear regression analysis indicated that MeHg concentrations were positively correlated with the gaseous mercury in the air. Combining internal and external exposure assessment showed that the direct contribution of MSWI emissions was minor compared with the dietary contribution. The external and internal exposures were well matched with each other. This study also suggested that an integrated method combining internal and external exposure assessment with an individual-specific questionnaire is feasible to assess the risks for a population living near a MSWI., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Based on an analysis of measured data and distribution factors, we developed the China Aquatic Mercury Release (CAMR) model, which we used to calculate an inventory of mercury (Hg) that was released to aquatic environments from primary anthropogenic sources in China. We estimated a total release of 98 tons of Hg in 2012, including coal-fired power plants (17%), nonferrous metal smelting (33%), coal mining and washing (25%), domestic sewage (17%), and other sectors (8.3%). The total primary anthropogenic Hg released to aquatic environments in China decreased at an annual average rate of 1.7% between 2001 and 2012, even though GDP grew at an annual average rate of 10% during this period. In addition to the Hg that was released to aquatic environments in China's provinces, we estimated the Hg release amounts and intensities (in g/km(2)·yr) for China's 58 secondary river basins. The highest aquatic Hg release intensities in China were associated with industrial wastewater on the North China Plain and domestic sewage in eastern China and southern China. We found that the overall uncertainty of our inventory ranges from -22% to 32%. We suggest that the inventory provided by this study can help establish a more accurate map of regional and global Hg cycling; it also has implications for water quality management in China.

Exports from mainland China are a significant source of mercury (Hg) in the adjacent seas (Bohai Sea, Yellow Sea, East China Sea, and South China Sea) near China. A total of 240 ± 23 Mg was contributed in 2012 (30% from natural sources and 70% from anthropogenic sources), including Hg from rivers, industrial wastewater, domestic sewage, groundwater, nonpoint sources, and coastal erosion. Among the various sources, the Hg from rivers amounts to 160 ± 21 Mg and plays a dominant role. The Hg that is exported from mainland China increased from 1984 to 2013; the contributions from rivers, industrial wastewater, domestic sewage and groundwater increased, and the contributions from nonpoint sources and coastal erosion remained stable. A box model is constructed to simulate the mass balance of Hg in these seas and quantify the sources, sinks and Hg biogeochemical cycle in the seas. In total, 160 Mg of Hg was transported to the Pacific Ocean and other oceans from these seas through oceanic currents in 2012, which could have negative impacts on the marine ecosystem. A prediction of the changes in Hg exportation through 2030 shows that the impacts of terrestrial export might worsen without effective pollution reduction measures and that the Hg load in these seas will increase, especially in the seawater of the Bohai Sea, Yellow Sea, and East China Sea and in the sea margin sediments of the Bohai Sea and East China Sea.