Japan receives nitrogenous air pollutants via long-range transport from China. However, emissions of nitrogenous air pollutants in China have stabilized or decreased in recent years. This study examined both the long-term trends in atmospheric nitrogen (N) deposition from the 1990s to the 2010s and the response of stream water nitrate (NO₃⁻) leaching from forested areas in western Japan. A long-term (1992–2018) temporal analysis of atmospheric N deposition in Fukuoka (western Japan) was conducted. Atmospheric bulk N deposition was collected at forested sites in a suburban forest (Swₑₛₜ) and a rural forest (Rwₑₛₜ) in western Japan during 2009–2018. Stream water samples were also collected from four locations at sites Swₑₛₜ and Rwₑₛₜ during the same period. Results showed that atmospheric N deposition in Fukuoka started to decrease from the mid-2000s at an annual rate of −2.5% yr⁻¹. The decrease in atmospheric N deposition was attributable mainly to decreased atmospheric ammonium (NH₄⁺) deposition, which caused greater contribution of NO₃⁻ deposition to atmospheric N deposition. Concentrations of NO₃⁻ in the stream water samples from three of the four locations decreased significantly at an annual rate of −3.7 to −0.7% yr⁻¹. However, stream water NO₃⁻ concentrations increased in one watershed where understory vegetation has been deteriorating owing to the increased deer population. This might weaken the recovery of N leaching from forested areas.

Agricultural activities often lead to nutrient enrichment and habitat modification in rivers, possibly altering macroinvertebrate assemblages and hence ecosystem functioning. For the sake of environmental management and conservation, therefore, assessing the impacts of agricultural activities becomes indispensable, especially when these activities are predicted to be intensified in the future. In this study, the plain river network in the Lake Chaohu Basin was chosen to examine how agricultural activities influence the functioning of rivers by assessing land use, water quality, habitat condition and macroinvertebrate assemblages, followed by calculating the macroinvertebrate-based multimetric index (MMI) to indicate overall ecosystem health of the rivers. We found that agricultural activities lowered the diversity of macroinvertebrates (e.g. total number of taxa and Simpson index) primarily due to elevated ammonium concentrations in water and reduced microhabitat types, thereby impairing the habitat integrity and nutrient cycling of rivers. The macroinvertebrate-based MMI was positively correlated with increasing habitat quality but negatively with increasing nutrient concentrations, suggesting its high reliability for indicating the impacts of agricultural activities, which was further substantiated by classification and regression tree (CART) analysis. We recommend analyzing macroinvertebrate assemblages using both multivariate and multimetric approaches to offer a more comprehensive evaluation of the impacts of agricultural activities on ecosystem health. Some environmental (CODMₙ, NH₄⁺-N and PO₄³⁻-P) and biological parameters (total number of taxa), however, can be used as good proxies for MMI, when time and resources for gathering information to develop MMI are limited.

The impacts of atmospheric nitrogen (N) deposition amount on plant communities have been extensively explored. However, the responses of plant communities to the ratio of reduced (NH₄⁺–N) and oxidized (NO₃⁻–N) forms remain unclear in natural ecosystems. A field N enrichment experiment using different NH₄⁺–N/NO₃⁻–N ratios was conducted in a natural semi-arid grassland in northern China from 2014 to 2019. Nitrogen addition tended to reduce plant species richness and significantly enhanced plant community aboveground net primary productivity (ANPP). Neither plant species richness nor plant ANPP at species and community levels was significantly affected by NH₄⁺–N/NO₃⁻–N ratios. At the plant functional group level, ANPP of grasses was not significantly affected by the NH₄⁺–N/NO₃⁻–N ratios examined, whereas ANPP of forbs was significantly increased at 1:1 NH₄⁺–N/NO₃⁻–N. Regardless of N supplied using the different ratios of NH₄⁺–N/NO₃⁻–N examined, plant community ANPP was positively associated with growing season precipitation. Unexpectedly, 1:1 NH₄⁺–N/NO₃⁻–N (NH₄NO₃) significantly improved the positive response of plant community ANPP to precipitation (it had the biggest slope value). Our results suggest that precipitation was the main determinant of the influence of NH₄⁺–N/NO₃⁻–N ratios on plant community ANPP. Therefore, the results of our study showed that without referring to NH₄⁺–N/NO₃⁻–N ratios and precipitation, models using NH₄NO₃ enrichment may overestimate the positive effect of atmospheric N deposition on ecosystem ANPP in semi-arid ecozones.

One of the strategies to realize a nitrogen cycle society, we attempted to recover ammonium ions from industrial wastewater, especially sewage water with adsorbent materials. We have developed an adsorbent with high ammonium selectivity based on copper hexacyanoferrate and granulated it as pellets. Using a compact column system filled with this granule adsorbent, ammonium ions were recovered from sewage containing 1000–1500 mg-NH₄⁺/L ammonium ions. Despite the coexistence of many metal ions, the adsorbent selectively and stably adsorbed ammonium ions. Furthermore, it was shown that the saturated adsorbent can be regenerated by flowing a potassium ion solution through a column adsorbent to desorb ammonium ions. In other words, the column can be used repeatedly, and there was almost little deterioration in adsorption even after 250 cycles. In addition, it was shown that by increasing the number of stages of this column, it is possible to sufficiently reduce the ammonium in the adsorbent solution and recover the concentrated ammonium solution.

Marine atmospheric aerosols play important roles in the global radiation balance and climate change. Hence, measuring physiochemical aerosol properties is essential to better understand their formation, aging processes, and source origins. However, high temporal resolution measurements of submicron particles are currently scarce in the northern South China Sea (SCS). In this study, we conducted a ship-based cruise campaign with a scanning mobility particle sizer and an online time of flight aerosol chemical speciation monitor to measure the particle number size distribution (PNSD) and the chemical composition of submicron particles over the northern SCS during summer 2018. The mean concentration of non-refractory submicron particulate matter (NR-PM₁) was generally 9.11 ± 4.86 μg m⁻³; sulfate was the most abundant component, followed by organics, ammonium, nitrate, and chloride. Positive matrix factorization (PMF) analysis was applied to the PNSD (size PMF) and organic aerosols (OA PMF) and further investigated the source apportionment of the submicron particles. The size PMF identified four factors, including ship exhaust, ship influencing marine primary, continent affected marine secondary, and mixed accumulation aerosols. The most abundant particles in the number concentration were associated with ship emissions, which accounted for approximately 44 %. The submicron organic aerosols were highly oxidized and composed of low-volatility oxygenated OA (LV-OOA, 68 %), semi-volatile OOA (SV-OOA, 21 %), and hydrocarbon-like OA (HOA, 11 %). The backward trajectory of air masses showed that the northern SCS was most frequently (64.7 %) influenced by air masses from the Indo-Chinese Peninsula (ICP) during the campaign, implying that pollutants from ICP have a significant impact on the atmosphere of the northern SCS during summer. Thus, in situ ship-based cruise measurements can provide valuable data on the physiochemical characteristics of marine atmospheric aerosols to better understand their source origins.

Emerging per-/polyfluoroalkyl substances (PFASs), such as chlorinated polyfluorinated ether sulfonates (Cl-PFESAs), have been detected in human samples, yet investigation on their occurrence in pregnant women remains limited. Herein, ten legacy PFASs, branched perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA), two Cl-PFESAs, perfluoro-2-propoxypropanoic acid (HFPO-DA), and ammonium 4,8-dioxa-3H-perfluorononanoate (ADONA) were detected in serum samples from 480 pregnant women in Tianjin, China. The influencing effects of age, body mass index, gravidity, and parity were also evaluated. PFOS [geographic mean (GM): 7.05 ng/mL], 6:2Cl-PFESA (GM: 5.31 ng/mL), and PFOA (GM: 2.82 ng/mL) were the dominant PFASs in the serum of pregnant women, while neither HFPO-DA nor ADONA was detectable in any serum. The serum concentration of Cl-PFESAs and 6:2Cl-PFESA/PFOS ratio in the present study were 2–5 times higher than that in previous studies of pregnant women in China. Serum concentrations of Cl-PFESAs were significantly correlated with all detected PFAAs (Spearman’s Rho: 0.15–0.69, p < 0.01) excepting perfluoropentanesulfonate (PFPeS), indicating common exposure sources for Cl-PFESAs and PFAAs and some particular exposure source for PFPeS. Younger age and multi-parity were associated with lower serum concentrations of PFOS and several perfluoroalkyl sulfonates but not associated with Cl-PFESAs or PFOA, suggesting an increasing exposure to Cl-PFESAs and PFOA which neutralized the impact of age and parity. Overall, this study indicated a relatively high exposure level and composition of 6:2Cl-PFESA in pregnant women in the north coast of China, which highlights the need to investigate the exposure sources in this area.

Coastal sediments, where microplastics (MPs) accumulate, support benthic microalgae (BMA) that contribute to ecosystem functions such as primary production, nutrient recycling and sediment biostabilization. The potential interactions between MPs, BMA and associated properties and functions remain poorly understood. To examine these interactions, a survey of 22 intertidal sites was conducted. MP abundance, size and a suite of MP diversity indices (based on color and shape) were determined from surface sediments alongside biochemical and physical properties. MPs were detected at all sites and dominated by polypropylene (34%), polyester (18%) and polyethylene (11%). Fragment and fiber dominance (16–92% and 6–81% respectively) and color-shape category diversity varied significantly by site. Distance-based linear models demonstrated that estuary-wide, mean grain size and mud were the best predictors of MP abundance-diversity matrices, but variance explained was low (9%). Relationships were improved when the data was split into sandy and muddy habitats. In sandy habitats (<8% mud), physical properties of the bed (mean grain size, mud content and distance from the estuary mouth) were still selected as predictors of MP abundance-diversity (14% variance explained); but a number of bivariate relationships were detected with biochemical properties such as BMA associated pigments and organic matter. In muddy habitats (>8% mud), porewater ammonium was lower when fiber abundance and overall MP diversity were higher. The inclusion of porewater ammonium, organic matter content and pheophytins alongside physical properties explained a greater percentage of the variance in MP abundance-diversity for muddy habitats (21%). The results highlight the importance of examining plastic shapes and MP categories in addition to abundance and emphasize that functionally different habitats should be examined separately to increase our understanding of MP-biota-function relationships.

Multiphase chemistry of chlorine is coupled into a 3D regional air quality model (CMAQv5.0.1) to investigate the impacts on the atmospheric oxidation capacity, ozone (O₃), as well as fine particulate matter (PM₂.₅) and its major components over the Yangtze River Delta (YRD) region. The developed model has significantly improved the simulated hydrochloric acid (HCl), particulate chloride (PCl), and hydroxyl (OH) and hydroperoxyl (HO₂) radicals. O₃ is enhanced in the high chlorine emission regions by up to 4% and depleted in the rest of the region. PM₂.₅ is enhanced by 2–6%, mostly due to the increases in PCl, ammonium, organic aerosols, and sulfate. Nitrate exhibits inhomogeneous variations, by up to 8% increase in Shanghai and 2–5% decrease in most of the domain. Radicals show different responses to the inclusion of the multiphase chlorine chemistry during the daytime and nighttime. Both OH and HO₂ are increased throughout the day, while nitrate radicals (NO₃) and organic peroxy radicals (RO₂) show an opposite pattern during the daytime and nighttime. Higher HCl and PCl emissions can further enhance the atmospheric oxidation capacity, O₃, and PM₂.₅. Therefore, the anthropogenic chlorine emission inventory must be carefully evaluated and constrained.

The Clean Air Action implemented by the Chinese government in 2013 has greatly improved air quality in the North China Plain (NCP). In this work, we report changes in the chemical components of atmospheric fine particulate matter (PM₂.₅) at four NCP sampling sites from 2012/2013 to 2017 to investigate the impacts and drivers of the Clean Air Action on aerosol chemistry, especially for secondary inorganic aerosols (SIA). During the observation period, the concentrations of PM₂.₅ and its chemical components (especially SIA, organic carbon (OC), and elemental carbon (EC)) and the frequency of polluted days (daily PM₂.₅ concentration ≥ 75 μg m⁻³) in the NCP, declined significantly at all four sites. Asynchronized reduction in SIA components (large decreases in SO₄²⁻ with stable or even increased NO₃⁻ and NH₄⁺) was observed in urban Beijing, revealing a shift of the primary form of SIA, which suggested the fractions of NO₃⁻ increased more rapidly than SO₄²⁻ during PM₂.₅ pollution episodes, especially in 2016 and 2017. In addition, unexpected increases in the sulfur oxidation ratio (SOR) and the nitrogen oxidation ratio (NOR) were observed among sites and across years in the substantially decreased PM₂.₅ levels. They were largely determined by secondary aerosol precursors (i.e. decreased SO₂ and NO₂), photochemical oxidants (e.g. increased O₃), temperature, and relative humidity via gas-phase and heterogeneous reactions. Our results not only highlight the effectiveness of the Action Plan for improving air quality in the NCP, but also suggest an increasing importance of SIA in determining PM₂.₅ concentration and composition.

Nitrate is the most common contaminant in groundwater in Korea, as well as across the world. Reduction of nitrate to ammonia is one of the options available to remediate groundwater. In this study, nitrate in groundwater was removed using a zero-valent iron (ZVI) containing biochar synthesized by co-pyrolyzing iron oxide and sawdust biomass. Among the various biogases generated during the pyrolysis of biomass, CO and H₂ act as reducing agents to transform iron oxides to ZVI. Approximately 71% of nitrate was reduced to ammonium by ZVI-biochar at initial pH 2.0, and the reduction decreased sharply by the increase in pH. The mass of nitrate-N decreased is exactly same with the mass of ammonia-N formed. However, ammonium remained in the aqueous phase after reduction by ZVI-biochar, and the total nitrogen was not lowered. Acid-washed zeolite adsorbed most ammonium reduced by the ZVI-biochar and maintained the pH to acidic condition to facilitate the reduction of nitrate. The results of this study imply that nitrate-contaminated groundwater can be properly treated within the guidelines of water quality by synthesized ZVI-containing biochar.