This study provides the first estimate of dry deposition fluxes of criteria air pollutants (SO2 and NOx) across the Three Northern Regions Shelter Forest (TNRSF) region in Northern China and their long-term trends from 1982 to 2010 using the inferential method. Dry deposition velocities of SO2 and NOx increased in many places of the TNRSF up to 118.2% for SO2 and 112.1% for NOx over the last three decades due to the increased vegetation coverage over the TNRSF. The highest atmospheric deposition fluxes of SO2 and NOx were found in the Central-North China region, followed by the Northeast and the Northwest China regions of the TNRSF. A total of 820,000 t SO2 and 218,000 t NOx was estimated to be removed from the atmosphere through dry deposition process over the TNRSF from 1982 to 2010. About 50% of the total removal occurred in the Central-North China region. The estimated total SO2 and NOx dry deposition fluxes from 1982 to 2010 between a TNRSF site in this region and an adjacent farmland outside the TNRSF showed that the fluxes of these two chemicals at the TNRSF site were the factors of 2–3 greater than their fluxes in the farmland.

Few studies on size-specific health effects of particulate matter have been conducted in Asia. We examined the association between both fine and coarse particles (PM2.5 and PM10−2.5) and mortality across 11 East Asian cities from 4 countries (Korea, Japan, Taiwan, and China). We performed a two-stage analysis: we generated city-specific estimates using a time-series analysis with a generalized additive model (Quasi-Poisson distribution), and estimated the overall effects by conducting a meta-analysis. Each 10−μg/m3 increase in PM2.5 (lag01) was associated with an increase of 0.38% (95% confidence interval = 0.21%–0.55%) in all causes mortality, 0.96% (0.46%–1.46%) in cardiovascular mortality, and 1% (0.23%–1.78%) in respiratory mortality. Each 10−μg/m3 increase in PM10−2.5 (lag01) was associated with cardiovascular mortality (0.69%, [0.05%–1.33%]), although this association attenuated after controlling for other pollutants, especially PM2.5. Increased mortality was associated with increasing PM2.5 and PM10−2.5 concentrations over 11 East Asian cities.

This study aims to identify and apportion multi-source and multi-phase heavy metal pollution from natural and anthropogenic inputs using ensemble models that include stochastic gradient boosting (SGB) and random forest (RF) in agricultural soils on the local scale. The heavy metal pollution sources were quantitatively assessed, and the results illustrated the suitability of the ensemble models for the assessment of multi-source and multi-phase heavy metal pollution in agricultural soils on the local scale. The results of SGB and RF consistently demonstrated that anthropogenic sources contributed the most to the concentrations of Pb and Cd in agricultural soils in the study region and that SGB performed better than RF.

Land application of biosolids or compost constitutes an important route of soil contamination by emerging contaminants such as acetaminophen and sulfamethoxazole. Using 14C labeling, we evaluated the influence of biosolids and compost on individual fate processes of acetaminophen and sulfamethoxazole in soil. The amendment of biosolids or compost consistently inhibited the mineralization of both compounds but simultaneously enhanced the dissipation of their extractable residues or parent form. Immediately after treatment, the majority of 14C-residue became non-extractable, reaching 80.3–92.3% of the applied amount at the end of 84-d incubation. Addition of biosolids or compost appreciably accelerated the formation of bound residue, likely due to the fact that the organic material provided additional sites for binding interactions or introduced exogenous microorganisms facilitating chemical transformations. This effect of biosolids or compost should be considered in risk assessment of these and other emerging contaminants.

We investigated the association between hourly differences in air pollution and asthma exacerbation in Korea using asthma-related emergency department data and verified seasonality and demographic modifiers with an hourly temporal resolution. We applied time-stratified case-crossover adjusted for weather and influenza; the lag was stratified as 1–6, 7–12, 13–18, 19–24, 25–48, and49–72 h. Odds ratios (95% confidence interval) per interquartile range increase were 1.05 (1.00–1.11) after 1–6 h for PM10–2.5 and 1.10 (1.04–1.16) after 19–24 h for O3. Effect size was 1.14 (1.06–1.22) at a 1–6 h lag in spring for PM10–2.5, and 1.25 (1.03–1.51) at a 25–48 h lag in winter for O3. O3 effects were age- and low socio-economic status-modified at a 7–12 h lag [1.25 (1.04–1.51)]. Increased PM10–2.5 and O3 increased the risk of asthma exacerbation; the effect of PM10–2.5 was most immediate.

Six micro/nano-Cu2O crystals evolved from cubes to corner-truncated cubes, vertex-truncated octahedrons and ultimately to octahedrons were synthesized in this work, and the chronic toxicity of these crystal suspensions (10 μg L−1) for Daphnia magna was investigated over a 30-day period. Our results indicated that the octahedrons had the most evident toxic effect, but the cubes were minimally toxic. The mortality rate of the octahedral treatment was as high as 86.7%, whereas that of the cubic treatment was only 6.7%. Significant inhibitions in growth and reproduction were observed under octahedral exposure, with reduced impacts from vertex-truncated octahedrons, corner-truncated cubes, and cubic crystals. The chronic effects of different micro/nano-Cu2O crystals were related to their solubility in the gut of the organisms. The solubility of micro/nano-Cu2O crystals was influenced by surface atomic arrangement and diverse surface activity. Thus, the structure and intestinal solubility of nanocrystals should be evaluated for long-term toxicity.

Knowledge is limited about the bioaccumulation of persistent halogenated compounds (PHCs) in terrestrial wildlife. Several PHCs, including dichlorodiphenyltrichloroethane (DDT) and its metabolites (designated as DDTs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), decabromodiphenylethane (DBDPE) and 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE), and stable isotopes (δ15N and δ13C) were analyzed in the muscle of four terrestrial passerines, Parus major, Copsychus saularis, Pycnonotus sinensis and Pycnonotus jocosus, from a nature reserve in South China. P. major had the highest PHC concentrations, with median values of 1060, 401, 92, 25 and 0.3 ng/g lipid weight for DDTs, PCBs, PBDEs, DBDPE and BTBPE, respectively. Fractions of DDT in P. jocosus and PCBs 153, 118 and 180 in C. saularis were higher compared with the other species. The inter-species differences in PHC concentrations and profiles could be attributed to the differences in trophic level, diet, living habits and metabolic capacity among the birds.

Selective serotonin re-uptake inhibitors (SSRIs) antidepressants are amongst the most prescribed pharmaceutical active substances throughout the world. Their presence, already described in different environmental compartments such as wastewaters, surface, ground and drinking waters, and sediments, and their remarkable effects on non-target organisms justify the growing concern about these emerging environmental pollutants. A comprehensive review of the literature data with focus on their footprint in the aquatic biota, namely their uptake, bioaccumulation and both acute and chronic ecotoxicology is presented. Long-term multigenerational exposure studies, at environmental relevant concentrations and in mixtures of related compounds, such as oestrogenic endocrine disruptors, continue to be sparse and are imperative to better know their environmental impact.

Using enriched stable 201Hg injections into intact sediment cores, we provide the first reported Hg methylation potential rate constants (km) in prairie wetland ponds (0.016–0.17 d−1). Our km values were similar to other freshwater wetlands and did not differ in ponds categorized with high compared to low surface water concentrations of sulphate. Sites with high sulphate had higher proportions of methylmercury (MeHg) in sediment (2.9 ± 1.6% vs. 1.0 ± 0.3%) and higher surface water MeHg concentrations (1.96 ± 1.90 ng L−1vs. 0.56 ± 0.55 ng L−1). Sediment-porewater partitioning coefficients were small, and likely due to high ionic activity. Our work suggests while km measurements are useful for understanding mercury cycling processes, they are less important than surface water MeHg concentrations for assessing MeHg risks to biota. Significant differences in MeHg concentrations between sites with high and low sulphate concentrations may also inform management decisions concerning wetland remediation and creation.

Transformation products (TPs) of emerging organic contaminates (EOCs) in water are still rarely considered in environmental risk assessment, although some have been found to be concern. OH is believed as an important reactive species both in indirect phototransformation and advanced oxidation technology. Thus, eco-toxicity and human estrogenic exposure risks of four phthalates and TPs during the OH-initiated photochemical process were investigated using computational approach. Four phthalates can be degraded through OH-addition and H-transfer pathways. The OH-addition TPs were predominant for dimethyl phthalates, while H-transfer TPs were predominant for other three phthalates. Compared with phthalates, OH-addition TPs (o-OH-phthalates) were one level more toxic to aquatic organisms, and m-OH-phthalates exhibit higher estrogenic activity. Although H-transfer TPs were less harmful than OH-addition TPs, some of them still have aquatic toxicity and estrogenic activity. Therefore, more attentions should be paid to photochemical TPs and original EOCs, particularly those exhibiting high estrogenic activity to humans.