Acid Deposition Monitoring Research Articles

Navigating environmental cooperation on air pollution amid political competition in East Asia

Abstract East Asian countries have recently upgraded their regional cooperation for clean air through the Acid Deposition Monitoring Network in East Asia, with elaborate arrangements for monitoring and capacity-building assistance for multiple pollutants. This represents a departure from the earlier informal regimes with vague arrangements on acid deposition. However, despite this notable shift, this formalization in the regional governance for clean air remains largely unexplored in the existing literature. This study fills this gap by analysing the dynamics of formalization through aid from theories of regime complexity and legalization. It focuses on the decade from 2012 to 2021, employing documentary analysis and interviews. The results reveal that governments actively pursue their state interests by adjusting institutional arrangements through regime competition and selection that drive formalization. Sharing cognition of the hazardousness of multiple pollutants achieved through interactions between regional and global institutions serves as a catalyst for reaching an agreement on the arrangements.

Implementation of the ISORROPIA-lite aerosol thermodynamics model into the EMAC chemistry climate model (based on MESSy v2.55): implications for aerosol composition and acidity

Abstract. This study explores the differences in performance and results by various versions of the ISORROPIA thermodynamic module implemented within the ECHAM/MESSy Atmospheric Chemistry (EMAC) model. Three different versions of the module were used, ISORROPIA II v1, ISORROPIA II v2.3, and ISORROPIA-lite. First, ISORROPIA II v2.3 replaced ISORROPIA II v1 in EMAC to improve pH predictions close to neutral conditions. The newly developed ISORROPIA-lite has been added to EMAC alongside ISORROPIA II v2.3. ISORROPIA-lite is more computationally efficient and assumes that atmospheric aerosols exist always as supersaturated aqueous (metastable) solutions, while ISORROPIA II includes the option to allow for the formation of solid salts at low RH conditions (stable state). The predictions of EMAC by employing all three aerosol thermodynamic models were compared to each other and evaluated against surface measurements from three regional observational networks in the polluted Northern Hemisphere (Interagency Monitoring of Protected Visual Environments (IMPROVE), European Monitoring and Evaluation Programme (EMEP), and Acid Deposition Monitoring Network of East Asia (EANET)). The differences between ISORROPIA II v2.3 and ISORROPIA-lite were minimal in all comparisons with the normalized mean absolute difference for the concentrations of all major aerosol components being less than 11 % even when different phase state assumptions were used. The most notable differences were lower aerosol concentrations predicted by ISORROPIA-lite in regions with relative humidity in the range of 20 % to 60 % compared to the predictions of ISORROPIA II v2.3 in stable mode. The comparison against observations yielded satisfactory agreement especially over the USA and Europe but higher deviations over East Asia, where the overprediction of EMAC for nitrate was as high as 4 µg m−3 (∼20 %). The mean annual aerosol pH predicted by ISORROPIA-lite was on average less than a unit lower than ISORROPIA II v2.3 in stable mode, mainly for coarse-mode aerosols over the Middle East. The use of ISORROPIA-lite accelerated EMAC by nearly 5 % compared to the use of ISORROPIA II v2.3 even if the aerosol thermodynamic calculations consume a relatively small fraction of the EMAC computational time. ISORROPIA-lite can therefore be a reliable and computationally efficient alternative to the previous thermodynamic module in EMAC.

Patterns and drivers of atmospheric inorganic nitrogen deposition in Northeast Asia

Elevated nitrogen (N) deposition due to intensified emissions of NH3 and NOx is a global problem with profound consequences on living organisms and the environment. Although N emission rates are currently considered to be high in East Asia, reports on the current N deposition level and composition are still limited, especially in northeastern China, where official N deposition monitoring sites are unavailable. This limits our understanding of the spatio-temporal N deposition patterns and their influencing factors at regional to continental scales. Here, we used data collected mostly during 2019 at 38 sites, comprising 7 sites in northeastern China and 31 EANET (Acid Deposition Monitoring Network in East Asia) sites in middle and east Russia, Mongolia, central and southern China, South Korea and Japan to explore the spatial-seasonal variations and drivers of ammonium and nitrate deposition across the Northeast Asia. Total bulk inorganic N (TIN) deposition was 3.7–24.5 kg N ha−1 yr−1 and NH4+-N/NO3−-N ratio in the TIN was 0.8–2.8 in northeastern China. The bulk/wet TIN deposition averaged 7.5 kg N ha−1 yr−1 (predominantly in the form of ammonium-N: NH4+-N/NO3−-N = 1.4) over the Northeast Asia region, with the highest rates being observed in northeastern China (11.6), as well as central and southern China (10.7), followed by east Russia, South Korea and Japan (5.6), and the lowest in middle Russia and Mongolia (1.5). This regional bulk/wet TIN deposition level is about twice of the wet TIN deposition level in Europe and the United States. The TIN deposition in summer and spring was 45–467% higher than in autumn and winter. Out of the ten land uses considered, only agricultural and urban land uses significantly positively correlated with NH4+-N and NO3−-N deposition rates across all monitored sites. This study suggests that the ongoing agricultural and urban expansions are likely to enhance N deposition and its associated effects across global ecosystems.

Inter-comparison of measurements of inorganic chemical components in precipitation from NADP and CAPMoN at collocated sites in the USA and Canada during 1986–2019

Wet deposition monitoring is a critical part of the long-term monitoring of acid deposition, which aims to assess the ecological impact of anthropogenic emissions of SO2 and NOx. In North America, long-term wet deposition has been monitored through two national networks: the Canadian Air and Precipitation Monitoring Network (CAPMoN) and the US National Atmospheric Deposition Program (NADP), for Canada and the USA, respectively. In order to assess the comparability of measurements from the two networks, collocated measurements have been made at two sites, one in each country, since 1986 (Sirois et al., in Environmental Monitoring and Assessment, 62, 273–303, 2000; Wetherbee et al., in Environmental Monitoring and Assessment, 1995–2004, 2010). In this study, we compared the measurements from NADP and CAPMoN instrumentation at the collocated sites at the Pennsylvania State University (Penn State), USA, from 1989 to 2016, and Frelighsburg, Quebec, Canada, from 2002 to 2019. We also included in the study the collocated daily-vs-weekly measurements by the CAPMoN network during 1999–2001 and 2016–2017 in order to evaluate the differences in wet concentration of ions due to sampling frequency alone. The study serves as an extension to two previous CAPMoN-NADP inter-comparisons by Sirois et al. (Environmental Monitoring and Assessment, 62, 273–303, 2000) and Wetherbee et al., in (Environmental Monitoring and Assessment, 1995–2004, 2010). At the Penn State University site, for 1986–2019, CAPMoN was higher than NADP for all ions, in terms of weekly concentration, precipitation-weighted annual mean concentration, and annual wet deposition. The precipitation-weighted annual mean concentrations were higher for SO42− (2%), NO3− (12%), NH4+ (16%), H+ (6%), and base cations and Cl− (11–15%). For annual wet deposition, CAPMoN was higher for SO4−2, NO3−, NH4+ and H+ (5–17%), and base cations and Cl− (12–17%) during 1986–2019. At the Frelighsburg site, NADP changed the sample collector in October 2011. For 2002–2011, the relative differences at the Frelighsburg site were positive and similar in magnitude to those at the Penn State site. For 2012–2019, the precipitation-weighted annual mean concentrations were 5–27% lower than NADP, except for H+, which was 23% higher. The change in sample collector by NADP had the largest effect on between-network biases. The comparisons of daily-vs-weekly measurements conducted by the CAPMoN network during 1999–2001 and 2016–2017 show that the weekly measurements were higher than the daily measurements by 1–3% for SO42−, NO3−, and NH4+; 3–9% for Ca2+, Mg2+, Na+, and Cl−; 10–24% for K+; and lower for H+ by 8–30% in terms of precipitation-weighted mean concentration. Thus, differences in sampling frequencies did not contribute to the systematically higher CAPMoN measurements. Understanding the biases in the data for these networks is important for interpretation of continental scale deposition models and transboundary comparison of wet deposition trends.

Implementation of HONO into the chemistry–climate model CHASER (V4.0): roles in tropospheric chemistry

Abstract. Nitrous acid (HONO) is an important atmospheric gas given its contribution to the cycles of NOx and HOx, but its role in global atmospheric photochemistry is not fully understood. This study implemented three pathways of HONO formation in the chemistry–climate model CHASER (MIROC-ESM) to explore three physical phenomena: gas-phase kinetic reactions (GRs), direct emission (EM), and heterogeneous reactions on cloud and aerosol particles (HRs). We evaluated the simulations by the atmospheric aircraft-based measurements from EMeRGe-Asia-2018 (Effect of Megacities on the Transport and Transformation of Pollutants on the Regional to Global Scales), ATom-1 (atmospheric tomography), observations from the ship R/V Mirai, EANET (Acid Deposition Monitoring Network in eastern Asia)/EMEP (European Monitoring and Evaluation Programme) ground-based stationary observations, and the OMI (Ozone Monitoring Instrument). We showed that the inclusion of the HONO chemistry in the modelling process reduced the model bias against the measurements for PM2.5, NO3-/HNO3, NO2, OH, HO2, O3, and CO, especially in the lower troposphere and the North Pacific (NP) region. We found that the retrieved global abundance of tropospheric HONO was 1.4 TgN. Of the three source pathways, HRs and EM contributed 63 % and 26 % to the net HONO production, respectively. We also observed that reactions on the aerosol surfaces contributed larger amounts of HONO (51 %) than those on the cloud surfaces (12 %). The model exhibited significant negative biases for daytime HONO in the Asian off-the-coast region, compared with the airborne measurements by EMeRGe-Asia-2018, indicating the existence of unknown daytime HONO sources. Strengthening of aerosol uptake of NO2 near the surface and in the middle troposphere, cloud uptake, and direct HONO emission were all potential yet-unknown HONO sources. The most promising daytime source for HONO found in this study was the combination of enhanced aerosol uptake of NO2 and surface-catalysed HNO3 photolysis (maxST+JANO3-B case), which could also remedy the model bias for NO2 and O3 during EMeRGe. We also found that the simulated HONO abundance and its impact on NOx–O3 chemistry were sensitive to the yield of the heterogeneous conversion of NO2 to HONO (vs. HNO3). Inclusion of HONO reduced global tropospheric NOx (NO + NO2) levels by 20.4 %, thereby weakening the tropospheric oxidizing capacity (OH, O3) occurring for NOx-deficit environments (remote regions and upper altitudes), which in turn increased CH4 lifetime (13 %) and tropospheric CO abundance (8 %). The calculated reduction effect on the global ozone level reduced the model overestimates for tropospheric column ozone against OMI spaceborne observations for a large portion of the North Hemisphere. HRs on the surfaces of cloud particles, which have been neglected in previous modelling studies, were the main drivers of these impacts. This effect was particularly salient for the substantial reductions of levels of OH (40 %–67 %) and O3 (30 %–45 %) in the NP region during summer, given the significant reduction of the NOx level (50 %–95 %). In contrast, HRs on aerosol surfaces in China (Beijing) enhanced OH and O3 winter mean levels by 600 %–1700 % and 10 %–33 %, respectively, with regards to their minima in winter. Furthermore, sensitivity simulations revealed that the heterogeneous formation of HONO from NO2 and heterogenous photolysis of HNO3 coincided in the real atmosphere. Nevertheless, the global effects calculated in the combined case (enhancing aerosol uptakes of NO2 and implementing heterogeneous photolysis of HNO3), which most captured the measured daytime HONO level, still reduced the global tropospheric oxidizing capacity. Overall, our findings suggest that a global model that does not consider HONO heterogeneous mechanisms (especially photochemical heterogeneous formations) may erroneously predict the effect of HONO in remote areas and polluted regions.

Assessing critical loads and exceedances for acidification and eutrophication in the forests of East and Southeast Asia: A comparison with EANET monitoring data

Spatial variations in sulfur (S) and nitrogen (N) deposition have changed in East and Southeast Asia in recent decades. Nevertheless, in this region, including the tropics, regional-scale assessments of the long-term risk of acidification and eutrophication (N saturation) for terrestrial ecosystems using a critical load approach have not been updated since 2001. To evaluate future risks, maps of critical loads and exceedances were updated using recently acquired spatial datasets of soil properties, soil minerals, climate, tree plantations, and the annual S and N depositions estimated using the Community Multiscale Air Quality (CMAQ) model. The resulting maps were verified using data on long-term trends in soil pH and nitrate concentration in surface water acquired by the Acid Deposition Monitoring Network in East Asia (EANET). It was found that N deposition exceeded the critical load for eutrophication not only in East Asia but also in some parts of the tropical monsoon and humid regions in Southeast Asia, whereas S deposition partly exceeded the critical load for soil acidification in China and small parts of the tropical monsoon region. The high-risk areas for eutrophication coincided well with the EANET sites, where the increase in nitrate concentration in the surface water was significant over the last 20 years. Hence, the estimated map of the critical load exceedance for eutrophication is more plausible for assessing the risk in East and Southeast Asia than that for acidification, although the critical load exceedance for acidification would be sufficiently significant as an updated risk map based on the latest input values. This update also suggests that increased N deposition around megacities, water discharge, and tree plantations may play an important role in the spatial variability of eutrophication risks in the tropics of Southeast Asia.

Development of science and policy related to acid deposition in East Asia over 30years.

Scientific and public interest in acid deposition and its ecological impacts have increased throughout 1990s in East Asia (Northeast and Southeast Asia). After being established in 2001, the Acid Deposition Monitoring Network in East Asia (EANET) celebrates the 20th anniversary in 2021, and is now being expanded in scope reflecting the shifting social concern from acid deposition to broader air quality and climate change in recent years. This paper reviews the past 30years of development of scientific research and policy related to acid deposition in East Asia. Since the onset of the twenty-first century, East Asia has had the highest SO2 and NOx emissions in the world by continents, with substantial economic developmental inequality among countries. An overview of studies on sulfur and nitrogen deposition, the acidification of inland water and forest soil, and forest decline reveal that although limited acidification of inland water and forest soils have been documented, no decline in the populations of fish and other aquatic biota has been reported in East Asia. After a review of policy-oriented modeling studies on source receptor relationships and the critical loads of sulfur and nitrogen in East Asia, the history of EANET and its success and challenges are discussed. Finally, the importance of epistemic communities as the interface between science and policy in the region is discussed. Regional governance and cooperation are essential for reducing the emission of greenhouse gases, especially short-lived climate pollutants and atmospheric pollutants to realize the co-benefits of global climate change mitigation and improved air quality.

Incorporation of volcanic SO<sub>2</sub> emissions in the Hemispheric CMAQ (H-CMAQ) version 5.2 modeling system and assessing their impacts on sulfate aerosol over the Northern Hemisphere

Abstract. The state-of-the-science Community Multiscale Air Quality (CMAQ) Modeling System has recently been extended for hemispheric-scale modeling applications (referred to as H-CMAQ). In this study, satellite-constrained estimation of the degassing SO2 emissions from 50 volcanoes over the Northern Hemisphere is incorporated into H-CMAQ, and their impact on tropospheric sulfate aerosol (SO42-) levels is assessed for 2010. The volcanic degassing improves predictions of observations from the Acid Deposition Monitoring Network in East Asia (EANET), the United States Clean Air Status and Trends Network (CASTNET), and the United States Integrated Monitoring of Protected Visual Environments (IMPROVE). Over Asia, the increased SO42- concentrations were seen to correspond to the locations of volcanoes, especially over Japan and Indonesia. Over the USA, the largest impacts that occurred over the central Pacific were caused by including the Hawaiian Kilauea volcano, while the impacts on the continental USA were limited to the western portion during summertime. The emissions of the Soufrière Hills volcano located on the island of Montserrat in the Caribbean Sea affected the southeastern USA during the winter season. The analysis at specific sites in Hawaii and Florida also confirmed improvements in regional performance for modeled SO42- by including volcanoes SO2 emissions. At the edge of the western USA, monthly averaged SO42- enhancements greater than 0.1 µg m−3 were noted within the boundary layer (defined as surface to 750 hPa) during June–September. Investigating the change on SO42- concentration throughout the free troposphere revealed that although the considered volcanic SO2 emissions occurred at or below the middle of free troposphere (500 hPa), compared to the simulation without the volcanic source, SO42- enhancements of more than 10 % were detected up to the top of the free troposphere (250 hPa). Our model simulations and comparisons with measurements across the Northern Hemisphere indicate that the degassing volcanic SO2 emissions are an important source and should be considered in air quality model simulations assessing background SO42- levels and their source attribution.

Trends of sulfur and nitrogen deposition from 2003 to 2017 in Japanese remote areas

Emissions of sulfur (S) and nitrogen (N) compounds in East Asia has drastically changed over the last two decades. To assess the influence of the drastic changes in air pollution on ecosystems in Japan, we investigated the trends of S and N deposition during 2003–2017 at remote sites of Acid Deposition Monitoring Network in East Asia (EANET). We measured wet deposition and inferentially estimated dry deposition of S and N using monitoring data from 2003 to 2017 at eight sites. We estimated dry deposition using the inferential method with an updated parameterization for gaseous surface resistance. The linear regression method and nonparametric Mann–Kendall test was used to analyze the temporal trends based on the monthly data sets. High S and N deposition amounts over 10 kg ha−1 year−1 were frequently found at most sites. There were significant increase trends in N deposition to S deposition (N/S) ratio at all sites throughout the 15-year period. Some trends were significantly found when the 15-year period was divided into three: 2003–2007, 2008–2012, and 2013–2017. S deposition had significantly decreased over a wide area in Japan, especially at Sado-seki, Happo, Oki, Hedo, and Ogasawara, in 2013–2017. Significant decreases in oxidized N deposition at Sado-seki and Oki were also found in 2013–2017. Because of almost flat N deposition mainly contributed by reduced N deposition, the N/S ratio clearly increased. These trends were associated with the recent reductions in SO2 and NOx emissions in China. The NOx emission reduction of China has not caught up with that of SO2, and NH3 emissions have not been reduced. This caused the significant increases in the N/S ratio not only in 2013–2017 but also in 2003–2017.

Insights into seasonal variation of wet deposition over southeast Asia via precipitation adjustment from the findings of MICS-Asia III

Abstract. Asia has attracted research attention because it has the highest anthropogenic emissions in the world, and the Model Inter-Comparison Study for Asia (MICS-Asia) phase III was carried out to foster our understanding of the status of air quality over Asia. This study analyzed wet deposition in southeast Asian countries (Myanmar, Thailand, Lao People's Democratic Republic (PDR), Cambodia, Vietnam, the Philippines, Malaysia, and Indonesia) with the aim of providing insights into the seasonal variation of wet deposition. Southeast Asia was not fully considered in MICS-Asia phase II due to a lack of observational data; however, the analysis period of MICS-Asia III, namely the year 2010, is covered by ground observations of the Acid Deposition Monitoring Network in East Asia (EANET), and the coordinated simulation domain was extended to cover these observation sites. The analyzed species are wet depositions of S (sulfate aerosol, sulfur dioxide (SO2), and sulfuric acid (H2SO4)), N (nitrate aerosol, nitrogen monoxide (NO), nitrogen dioxide (NO2), and nitric acid (HNO3)), and A (ammonium aerosol and ammonia (NH3)). The wet deposition simulated with seven models driven by a unified meteorological model in MICS-Asia III was used with the ensemble approach, which effectively modulates the differences in performance among models. By comparison with EANET observations, although the seven models generally captured the wet depositions of S, N, and A, there were difficulties capturing these in some cases. Considering the model performance for ambient aerosol concentrations over southeast Asia, this failure of models is considered to be related to the difficulty in capturing the precipitation in southeast Asia, especially during the dry and wet seasons. Generally, meteorological fields overestimate the precipitation during the dry season, which leads to the overestimation of wet deposition during this season. To overcome this, a precipitation-adjusted approach that scaled the modeled precipitation to the observed value was applied, and it was demonstrated that the model performance was improved. Satellite measurements were also used to adjust for precipitation data, which adequately accounted for the spatiotemporal precipitation patterns, especially in the dry season. As the statistical scores were mostly improved by this adjustment, the estimation of wet deposition with precipitation adjustment was considered to be superior. To utilize satellite measurements, the spatial distribution of wet deposition was revised. Based on this revision, it was found that Vietnam, Malaysia, and Indonesia were upward corrected, and Myanmar, Thailand, Lao PDR, Cambodia, and the Philippines were downward-corrected; these corrections were up to ±40 %. The improved accuracy of precipitation amount was key to estimating wet deposition in this study. These results suggest that the precipitation-adjusted approach has the potential to obtain accurate estimates of wet deposition through the fusion of models and observations.

Rainwater chemistry observation in a karst city: variations, influence factors, sources and potential environmental effects.

The rainwater chemistry and related air contaminants are used to investigate the rainwater ions sources, variations, and influence factors from 2012 to 2014 in Guiyang city (the typical karst urban area of Southwest China). According to temporal rainwater ion concentrations, the obvious variations were presented in the study period, such as Ca2+ (125∼6,652 μeq L−1) and SO42− (11∼4,127 μeq L−1). Consequently, Ca2+, Mg2+, SO42− and Cl− are considered as the leading ions. Three critical influencing factors of rainwater ions concentrations, including sources variations, rainfall amount and long-distance migration (rainfall amount > 100 mm) are identified. Based on the typical ionic ratios, source identification suggested that anthropogenic inputs mainly contributed to F−, NO3− and SO42−, while the dusts (crustal sources) are the primary sources of Mg2+, Ca2+ and K+. Cl− Enrichment in long-distance transport is the main contributor of Cl−. According to the observation of high level of total wet acid deposition, the more detailed spatio-temporal monitoring of rainfall-related acid deposition (particularly sulfur deposition) is required to understand its potential environmental effects in the aquatic ecosystem of the earth surface.

Model Inter-Comparison Study for Asia (MICS-Asia) phase III: multimodel comparison of reactive nitrogen deposition over China

Abstract. Atmospheric nitrogen deposition in China has attracted public attention in recent years due to the increasing anthropogenic emission of reactive nitrogen (Nr) and its impacts on the terrestrial and aquatic ecosystems. However, limited long-term and multisite measurements have restrained the understanding of the mechanism of the Nr deposition and the chemical transport model (CTM) improvement. In this study, the performance of the simulated wet and dry deposition for different Nr species, i.e., particulate NO3- and NH4+, gaseous NOx, HNO3 and NH3 have been conducted using the framework of Model Inter-Comparison Study for Asia (MICS-Asia) phase III. A total of nine models, including five Weather Research and Forecasting models coupled with the Community Multiscale Air Quality (WRF-CMAQ) models, two self-developed regional models, a global model and a Regional Atmospheric Modeling System coupled with the Community Multiscale Air Quality (RAMS-CMAQ) model have been selected for the comparison. For wet deposition, observation data from 83 measurement sites from the East Asia Acid Deposition Monitoring Network (EANET), Chinese Ecosystem Research Network (CERN), China Agricultural University Deposition Network (CAUDN), National Acid Deposition Monitoring Network (NADMN) and Department of Ecological Environment (DEE) of China have been collected and normalized for comparison with model results. In general, most models show the consistent spatial and temporal variation of both oxidized N (Nox) and reduced N (Nrd) wet deposition in China, with the normalized mean error (NME) at around 50 %, which is lower than the value of 70 % based on EANET observation over Asia. Both the ratio of wet or dry deposition to the total inorganic N (TIN) deposition and the ratios of TIN to their emissions have shown consistent results with the Nationwide Nitrogen Deposition Monitoring Network (NNDMN) estimates. The performance of ensemble results (ENMs) was further assessed with satellite measurements. In different regions of China, the results show that the simulated Nox wet deposition was overestimated in northeastern China (NE) but underestimated in the south of China, namely southeastern (SE) and southwestern (SW) China, while the Nrd wet deposition was underestimated in all regions by all models. The deposition of Nox has larger uncertainties than the Nrd, especially in northern China (NC), indicating the chemical reaction process is one of the most important factors affecting the model performance. Compared to the critical load (CL) value, the Nr deposition in NC, SE and SW reached or exceeded reported CL values and resulted in serious ecological impacts. The control of Nrd in NC and SW and Nox in SE would be an effective mitigation measure for TIN deposition in these regions. The Nr deposition in the Tibetan Plateau (TP) with a high ratio of TIN ∕ emission (∼3.0), indicates a significant transmission from outside. Efforts to reduce these transmissions ought to be paramount due the climatic importance of the Tibetan region to the sensitive ecosystems throughout China.

Chemical Composition of Atmospheric Aerosol in the Arctic Region and Adjoining Seas along the Routes of Marine Expeditions in 2018–2019

We consider the chemical composition (ions, elements, and polycyclic aromatic hydrocarbons) of atmospheric aerosol in different regions of the North Atlantic, European and Russian parts of the Arctic Ocean, and northern latitude and Far East seas. The studies were carried out onboard marine ships along their cruising routes (RV Akademik Tryoshnikov, RV Akademik Mstislav Keldysh, and RV Professor Multanovsky). The air samples were collected using the method accepted in the international networks operating under the Acid Deposition Monitoring Network in East Asia (EANET) and European Monitoring and Evaluation Programme (EMEP). The average sum of ion concentrations and the concentrations of individual ions in the aerosol over the seas in the North Atlantic and in the European part of the Arctic Ocean is consistent with measurements in the Laptev and Kara Seas in 2018 and 2019. The high concnetrations of PAHs in aerosol in seas and the Arctic Ocean in the central part of the Russian Arctic coincide with high concentrations of ions and trace elements in the aerosol composition. A difference is noted in the distribution of concentrations of trace elements in aerosol composition between seas of the North Atlantic and central region of the Russian Arctic, which possibly points to different sources of these components.

MICS-Asia III: overview of model intercomparison and evaluation of acid deposition over Asia

Abstract. The Model Inter-Comparison Study for Asia (MICS-Asia) phase III was conducted to promote understanding of regional air quality and climate change in Asia, which have received growing attention due to the huge amount of anthropogenic emissions worldwide. This study provides an overview of acid deposition. Specifically, dry and wet deposition of the following species was analyzed: S (sulfate aerosol, sulfur dioxide (SO2), and sulfuric acid (H2SO4)), N (nitrate aerosol, nitrogen monoxide (NO), nitrogen dioxide (NO2), and nitric acid (HNO3)), and A (ammonium aerosol and ammonia (NH3)). The wet deposition simulated by a total of nine models was analyzed and evaluated using ground observation data from the Acid Deposition Monitoring Network in East Asia (EANET). In the phase III study, the number of observation sites was increased from 37 in the phase II study to 54, and southeast Asian countries were newly added. Additionally, whereas the analysis period was limited to representative months of each season in MICS-Asia phase II, the phase III study analyzed the full year of 2010. The scope of this overview mainly focuses on the annual accumulated deposition. In general, models can capture the observed wet deposition over Asia but underestimate the wet deposition of S and A, and show large differences in the wet deposition of N. Furthermore, the ratio of wet deposition to the total deposition (the sum of dry and wet deposition) was investigated in order to understand the role of important processes in the total deposition. The general dominance of wet deposition over Asia and attributions from dry deposition over land were consistently found in all models. Then, total deposition maps over 13 countries participating in EANET were produced, and the balance between deposition and anthropogenic emissions was calculated. Excesses of deposition, rather than of anthropogenic emissions, were found over Japan, northern Asia, and southeast Asia, indicating the possibility of long-range transport within and outside of Asia, as well as other emission sources. To improve the ability of models to capture the observed wet deposition, two approaches were attempted, namely, ensemble and precipitation adjustment. The ensemble approach was effective at modulating the differences in performance among models, and the precipitation-adjusted approach demonstrated that the model performance for precipitation played a key role in better simulating wet deposition. Finally, the lessons learned from the phase III study and future perspectives for phase IV are summarized.

Pollution and Deposition Characteristics of Precipitation and Its Source Apportionment in Xi'an City

Chemical and deposition characteristics as well as potential sources of precipitation in Xi'an from 2000 to 2017 were analyzed based on the acid deposition monitoring network in East Asia (EANET). The pH of precipitation showed increasing trends, whereas the conductivity of precipitation showed decreasing trends between 2000 and 2017 in Xi'an. The decreasing order of ion concentration in precipitation was as follows:SO42- > Ca2+ > NH4+ > NO3- > Na+ > Cl- > Mg2+ > K+. The percentage of SO42- in the total ion concentration decreased from 38.6% in 2000 to 27.9% in 2017. The ratio of SO42- to NO3- in recent years indicated that the type of pollutant in Xi'an changed from the coal-burning type to the mixed type. The deposition of SO42- in precipitation had a declining trend, which was consistent with the results of the Mann-Kendall test. Nitrogen and sulphur depositions in precipitation were 16.89 kg·(hm2·a)-1 and 33.52 kg·(hm2·a)-1, respectively, and ammonium nitrogen (NH4+-N) was the main deposition component of atmospheric active nitrogen in the precipitation of Xi'an. Vehicle emissions were the major contributors to SO42- (15.43%) and NO3- (72.99%). NH4+ originated mainly from agriculture sources, and the percentage reached up to 75.47%.

Introduction to the virtual special issue monitoring ecological responses to air quality and atmospheric deposition in the Athabasca Oil Sands region the wood Buffalo environmental Association's Forest health monitoring program

The expansion of oil sands resource development in the Athabasca Oil Sands Region in the early 1990's led to concerns regarding the potential ecological and health effects of increased emissions and deposition of acidic substances. Conditions attached to a 1994 approval for an oil sands facility expansion led to the creation of the Wood Buffalo Environmental Association, and its Terrestrial Environmental Effects Monitoring committee. This multi-stakeholder body was tasked with development and operation of an environmental (forest health) monitoring program for the detection of ecological responses to atmospheric emissions and deposition. Initially focused on acid deposition monitoring, jack pine forest, growing on sandy soils with limited acid buffering capacity, was selected as the receptor system. An initial set of 10 monitoring locations was established using the Canadian Acid Rain Network Early Warning System methodology (since increased to 27, with three lost to development). Ecological monitoring is on a 6-year cycle, with concurrent measures of soil, needle and lichen chemistry, and tree and understory condition, together with ongoing measurements of air quality and atmospheric deposition. Because jack pine forest edges facing the emissions sources were expected to be more exposed to acidic emissions, evaluation of stand edge monitoring locations began in 2008. Monitoring of a targeted suite of indicators began in 2012 at 25 jack pine stand edge monitoring sites. This special issue presents the results derived from biophysical sampling campaigns (1998 to 2013), coupled with ongoing ambient atmospheric, deposition and epiphytic lichen monitoring (data through 2017) and source apportionment studies, as well as papers contributed by others engaged in regional research and monitoring programs. The Forest Health Monitoring Program provides data supportive of regulatory and stakeholder evaluations of environmental quality, and is adaptive to new needs, extreme environmental events and technological development while providing continuity of monitoring.

Facilitating International Cooperation on Air Pollution in East Asia: Fragmentation of the Epistemic Communities

AbstractTo tackle transboundary air pollution in East Asia, international schemes for environmental cooperation have been introduced, including the Acid Deposition Monitoring Network in East Asia (EANET), Long‐Range Transboundary Pollution of China, Japan and Korea (LTP), and the North‐East Asian Subregional Programme for Environmental Cooperation (NEASPEC). These programs, however, have not been successful in establishing robust regimes for effectively reducing transboundary air pollution in the region. This paper aims to examine the process of forming epistemic communities through these programs in East Asia. A bibliometric data on the scientific articles and reports produced were analyzed to examine the network structure of the scientific activities through EANET. The fragmentation of expert groups within EANET and among the major international schemes on air pollution in East Asia contributed to discouraging solid formation of an epistemic community covering air pollution comprehensively in the region. That makes it difficult to reach a consensus based on the current state of scientific knowledge on air pollution for providing effective advice and recommendations for the development of policies and regulations.

The distributions and direct radiative effects of marine aerosols over East Asia in springtime

The characteristics, distributions, and direct radiative effects (DRE) of marine aerosols in the western Pacific Ocean over East Asia during the period from 17 March to 22 April 2014 were investigated by an online-coupled regional atmospheric chemistry/aerosol-climate model RIEMS-Chem (Regional Integrated Environmental Model System with Chemistry). The emissions and relevant processes of sea salt, marine primary organic aerosol (MPOA), sulfate and Methyl sulfonic acid (MSA) produced from dimethylsulfide (DMS) were parameterized and coupled with RIEMS-Chem. The model results for total aerosol masses (PM10 and PM2.5), inorganic and carbonaceous aerosols, gas precursors, and aerosol optical depth (AOD) were compared with various observational data sets including a research cruise Dongfanghong II from the Yellow Sea to the open oceans, near-surface aerosol and gas concentrations from the Acid Deposition Monitoring Network in East Asia (EANET) and China National Environmental Monitoring Center (CNEMC), and AOD from the Aerosol Robotic Network (AERONET). Model comparisons demonstrated a generally good skill of the RIEMS-Chem in representing the temporal and spatial variations of these variables. The distributions of marine aerosols were characterized by the maximum sea salt concentration up to 70 μg m−3 in the ocean northeast of Japan, the maximum concentration of MPOA >2 μg m−3 in the East China Sea and in portions of the northwest Pacific (NWP) region, and the maximum DMS-produced aerosol concentration >0.3 μg m−3 in the southern parts of the ocean. It was noteworthy that marine aerosols can be easily transported to the inland areas of south China. The clear-sky DREs by sea salt ranging from −9 to −17 W/m2 occurred in the open oceans northeast of Japan, comparable to the DREs of −10 ~ −20 W/m2 by anthropogenic aerosols, whereas the DREs by MPOA were strongest (up to −1.3 Wm−2) in the East China Sea and the oceans northeast of Japan due to active phytoplankton blooms there and comparable in magnitude to the DREs by sea salt (around −3 Wm−2) in the East China Sea. The maximum DRE by the DMS-produced aerosols was −0.4 Wm−2 mainly in the northern parts of the South China Sea. Sea salt exhibited an increasing radiative importance from the China marginal seas to the open oceans, accounting for 10% and 33% of the DREs by all aerosols, respectively. Under all-sky conditions, the sum of DREs by all the marine aerosols were estimated to be −2.2 W/m2, −3.5 W/m2, −2.3 W/m2, and −4.3 W/m2 averaged over the entire domain, ocean, East China Sea, and the NWP region, accounting for 20%, 27%, 13%, and 36% of the DREs by all aerosols, respectively, which demonstrated the important role of marine aerosols in modulating shortwave radiation in springtime in the western Pacific Ocean which was just downwind of the Asian continent with large amounts of anthropogenic and dust emissions.

Air quality and climate change, Topic 3 of the Model Inter-Comparison Study for Asia Phase III (MICS-Asia III) – Part 1: Overview and model evaluation

Abstract. Topic 3 of the Model Inter-Comparison Study for Asia (MICS-Asia) Phase III examines how online coupled air quality models perform in simulating high aerosol pollution in the North China Plain region during wintertime haze events and evaluates the importance of aerosol radiative and microphysical feedbacks. A comprehensive overview of the MICS-Asia III Topic 3 study design, including descriptions of participating models and model inputs, the experimental designs, and results of model evaluation, are presented. Six modeling groups from China, Korea and the United States submitted results from seven applications of online coupled chemistry–meteorology models. Results are compared to meteorology and air quality measurements, including data from the Campaign on Atmospheric Aerosol Research Network of China (CARE-China) and the Acid Deposition Monitoring Network in East Asia (EANET). The correlation coefficients between the multi-model ensemble mean and the CARE-China observed near-surface air pollutants range from 0.51 to 0.94 (0.51 for ozone and 0.94 for PM2.5) for January 2010. However, large discrepancies exist between simulated aerosol chemical compositions from different models. The coefficient of variation (SD divided by the mean) can reach above 1.3 for sulfate in Beijing and above 1.6 for nitrate and organic aerosols in coastal regions, indicating that these compositions are less consistent from different models. During clean periods, simulated aerosol optical depths (AODs) from different models are similar, but peak values differ during severe haze events, which can be explained by the differences in simulated inorganic aerosol concentrations and the hygroscopic growth efficiency (affected by varied relative humidity). These differences in composition and AOD suggest that future models can be improved by including new heterogeneous or aqueous pathways for sulfate and nitrate formation under hazy conditions, a secondary organic aerosol (SOA) formation chemical mechanism with new volatile organic compound (VOCs) precursors, yield data and approaches, and a more detailed evaluation of the dependence of aerosol optical properties on size distribution and mixing state. It was also found that using the ensemble mean of the models produced the best prediction skill. While this has been shown for other conditions (for example, the prediction of high-ozone events in the US (McKeen et al., 2005)), this is to our knowledge the first time it has been shown for heavy haze events.

A 15-year record (2001–2015) of the ratio of nitrate to non-sea-salt sulfate in precipitation over East Asia

Abstract. Acidifying species in precipitation can have severe impacts on ecosystems. The chemical composition of precipitation is directly related to the amount of precipitation; accordingly, it is difficult to identify long-term variation in chemical concentrations. The ratio of the nitrate (NO3−) to non-sea-salt sulfate (nss-SO42−) concentration in precipitation on an equivalent basis (hereinafter, Ratio) is a useful index to investigate the relative contributions of these acidifying species. To identify the long-term record of acidifying species in precipitation over East Asia, the region with the highest emissions worldwide, we compiled ground-based observations of the chemical composition of precipitation over China, Korea, and Japan from 2001 to 2015 based on the Acid Deposition Monitoring Network in East Asia (EANET). The spatial coverage was limited, but additional monitoring data for Japan, southern China, and northern China around Beijing were utilized. The period of analysis was divided into three phases: Phase I (2001–2005), Phase II (2006–2010), and Phase III (2011–2015). The behaviors of NO3− and nss-SO42− concentrations and hence the Ratio in precipitation were related to these precursors. The anthropogenic NOx and SO2 emissions and the NOx ∕ SO2 emission ratio were analyzed. Further, satellite observations of the NO2 and SO2 column density to capture the variation in emissions were applied. We found that the long-term trend in the NO3− concentration in precipitation was not related to the variation in NOx emission and the NO2 column. In comparison, the nss-SO42− concentration in precipitation over China, Korea, and Japan was partially connected to the changes in SO2 emissions from China, but the trends were not significant. The long-term trends of Ratio over China, Korea, and Japan were nearly flat during Phase I, increased significantly during Phase II, and were essentially flat again during Phase III. This variation in Ratio in East Asia clearly corresponded to the NOx ∕ SO2 emission ratio and the NO2 ∕ SO2 column ratio in China. The initial flat trend during Phase I was due to increases in both NOx and SO2 emissions in China, the significantly increasing trend during Phase II was triggered by the increase in NOx emissions and decrease in SO2 emissions in China, and the return to a flat trend during Phase III was caused by declines in both NOx and SO2 emissions in China. These results suggest that emissions in China had a significant impact not only on China but also on downwind precipitation chemistry during the 15-year period of 2001–2015. In terms of wet deposition, the NO3− wet deposition over China, Korea, and Japan did not change dramatically, but the nss-SO42− wet deposition declined over China, Korea, and Japan from Phase II to III. These declines were caused by a strong decrease in the nss-SO42− concentration in precipitation accompanied by a reduction in SO2 emission from China, which counteracted the increase in precipitation. These findings indicated that the acidity of precipitation shifted from sulfur to nitrogen.