Continuous haze monitoring was conducted from 12:00 3 April to 12:00 8 April 2016 in Beijing, China to develop a more detailed understanding of spring haze characteristics. The PM₂.₅ concentration ranged from 6.30 to 165 μg m⁻³ with an average of 63.8 μg m⁻³. Nitrate was the most abundant species, accounting for 36.4% of PM₂.₅, followed by organic carbon (21.5%), NH₄⁺ (19.3%), SO₄²⁻ (18.8%), and elemental carbon (4.10%), indicating the key role of nitrate in this haze event. Species contribution varied based on the phase of the haze event. For example, sulfate concentration was high during the haze formation phase, nitrate was high during the haze, and secondary organic carbon (SOC) had the highest contribution during the scavenging phase. The secondary transition of sulfate was influenced by SO₂, followed by relative humidity (RH) and Oₓ (O₃+NO₂). Nitrate formation occurred in two stages: through NO₂ oxidation, which was vulnerable to Oₓ; and by the partitioning of N (+5) which was susceptible to RH and temperature. SOC tended to form when Oₓ and RH were balanced. According to hourly species behavior, sulfate and nitrate were enriched during haze formation when the mixed layer height decreased. However, SOC accumulated prior to the haze event and during formation, which demonstrated the strong contribution of secondary inorganic aerosols, and the limiting contribution of SOC to this haze case. Investigating backward trajectories showed that high speed northwestern air masses following a straight path corresponded to the clear periods, while southwesterly air masses which traversed heavily polluted regions brought abundant pollutants to Beijing and stimulated the occurrence of haze pollution. Results indicate that the control of NO₂ needs to be addressed to reduce spring haze. Finally, the correlation between air mass trajectories and pollution conditions in Beijing reinforce the necessity of inter-regional cooperation and control.

Despite the efforts of the European Commission to implement measures that offset the detrimental effects of agricultural intensification, farmland bird populations continue to decline. Pesticide use has been pointed out as a major cause of decline, with growing concern about those agro-chemicals that act as endocrine disruptors. We report here on the effects of flutriafol, a ubiquitous systemic fungicide used for cereal seed treatment, on the physiology and reproduction of a declining gamebird. Captive red-legged partridges (Alectoris rufa; n = 11–13 pairs per treatment) were fed wheat treated with 0%, 20% or 100% of the flutriafol application rate during 25 days in late winter. We studied treatment effects on the reproductive performance, carotenoid-based coloration and cellular immune responsiveness of adult partridges, and their relationship with changes in oxidative stress biomarkers and plasma biochemistry. We also studied the effect of parental exposure on egg antioxidant content and on the survival, growth and cellular immune response of offspring. Exposed partridges experienced physiological effects (reduced levels of cholesterol and triglycerides), phenotypical effects (a reduction in the carotenoid-based pigmentation of their eye rings), and most importantly, severe adverse effects on reproduction: a reduced clutch size and fertile egg ratio, and an overall offspring production reduced by more than 50%. No effects on body condition or cellular immune response of either exposed adult or their surviving offspring were observed. These results, together with previous data on field exposure in wild partridges, demonstrate that seed treatment with flutriafol represents a risk for granivorous birds; they also highlight a need to improve the current regulation system used for foreseeing and preventing negative impacts of Plant Protection Products on wildlife.

Drinking water safety is continuously threatened by the emergence of numerous toxic organic pollutants (TOPs) in environmental waters. In this study, an approach integrating in vitro bioassays and chemical analyses was performed to explore toxicological profiles of representative source and drinking water from waterworks of the Yangtze River (Yz), Taihu Lake (Th), and the Huaihe River (Hh) basins in eastern China. Overall, 34 of 96 TOPs were detected in all water samples, with higher concentrations in both source and drinking water samples of Hh, and pollutant profiles also differed across different river basins. Non-specific bioassays indicated that source water samples of Hh waterworks showed higher genotoxicity and mutagenicity than samples of Yz and Th. An EROD assay demonstrated dioxin-like toxicity which was detected in 5 of 7 source water samples, with toxin concentration levels ranging from 62.40 to 115.51 picograms TCDD equivalents per liter of water (eq./L). PAHs and PCBs were not the main contributors to observed dioxin-like toxicity in detected samples. All source water samples induced estrogenic activities of 8.00–129.00 nanograms 17β-estradiol eq./L, and estrogens, including 17α-ethinylestradiol and estriol, contributed 40.38–84.15% of the observed activities in examined samples. While drinking water treatments efficiently removed TOPs and their toxic effects, and estrogenic activity was still observed in drinking water samples of Hh. Altogether, this study indicated that the representative source water in eastern China, especially that found in Hh, may negatively affect human health, a finding that demonstrates an urgent requirement for advanced drinking water treatments.

Total suspended particulate matter (TSP) was collected during the summer and winter in five Japanese cities spanning Hokkaido to Kyushu (Sapporo, Kanazawa, Tokyo, Sagamihara and Kitakyushu) from 1997 to 2014. Nine polycyclic aromatic hydrocarbons (PAHs) with four to six rings, including pyrene (Pyr) and benzo[a]pyrene (BaP), were identified using high-performance liquid chromatography (HPLC) with fluorescence detection. Two nitropolycyclic aromatic hydrocarbons (NPAHs), 1-nitropyrene (1-NP) and 6-nitrobenzo[a]pyrene (6-NBaP), were identified by HPLC with chemiluminescence detection. A comparison of PAH and NPAH concentrations and [NPAH]/[PAH] ratios such as [1-NP]/[Pyr] and [6-NBaP]/[BaP] revealed the following characteristics in the five cities: (1) In Sapporo, Kanazawa, Tokyo and Sagamihara, the concentrations of PAHs and NPAHs were high at the beginning of the sampling period and then steadily decreased, with NPAHs decreasing faster than PAHs. The large initial [1-NP]/[Pyr] ratios suggest that the major contributor was automobiles but subsequent decreases in this ratio suggest decreased automobile contributions. (2) By contrast, PAH concentrations in Kitakyushu did not decrease during the sampling period, though concentrations of NPAHs decreased. The consistently smaller [1-NP]/[Pyr] ratio and larger [6-NBaP]/[BaP] ratio in Kitakyushu suggests that the major contributor of PAHs was not automobiles but iron manufacturing which uses a large amount of coal. The sudden increase in atmospheric PAH concentrations in the winter of 2014 may also be due to iron manufacturing.

Perfluoroalkyl acids (PFAAs) are being increasingly reported as emerging contaminants in riverine and marine settings. This study investigated the contamination level and spatial distribution of 17 PFAAs within the depth profile of the Bohai and Yellow Seas using newly detected sampling data from 49 sites (June 29 to July 14, 2016). Moreover, the riverine flux of 11 selected PFAAs in 33 rivers draining into the Bohai and Yellow Seas was estimated from previous studies (2002–2014) in order to establish the relationship between riverine sources and marine sinks. The results showed that the Bohai and Yellow Seas were commonly contaminated with PFAAs: total concentrations of PFAAs in the surface, middle, and bottom zones ranged from 4.55 to 556 ng L−1, 4.61–575 ng L−1, and 4.94–572 ng L−1, respectively. The predominant compounds were PFOA (0.55–449 ng L−1), PFBA (<LOQ-34.5 ng L−1), and PFPeA (<LOQ-54.3 ng L−1), accounting for 10.1–87.0%, 5.2–59.5%, and 0.6–68.6% of the total PFAAs, respectively. In general, the ∑PFAA concentrations showed a slightly decreasing trend with sampling depth. Contamination was particularly severe in Laizhou Bay, fed by the Xiaoqing River and an industrial park known for PFAA production. The total riverine PFAA mass flux into the Bohai and Yellow Seas was estimated to be 72.2 t y−1, of which 94.8% was carried by the Yangtze and Xiaoqing Rivers. As the concentration of short-chain PFAAs begins to rise in seawater, further studies on the occurrence and fate of short-chain PFAAs with special focus on effective control measures would be very timely, particularly in the Xiaoqing River and Laizhou Bay.

PM2.5 pollution is an environmental issue caused by multiple natural and socioeconomic factors, presenting with significant spatial disparities across mainland China. However, the determinant power of natural and socioeconomic factors and their interactive impact on PM2.5 pollution is still unclear. In the study, the GeogDetector method was used to quantify nonlinear associations between PM2.5 and potential factors. This study found that natural factors, including ecological environments and climate, were more influential than socioeconomic factors, and climate was the predominant factor (q = 0.56) in influencing PM2.5 pollution. Among all interactions of the six influencing factors, the interaction of industry and climate had the largest influence (q = 0.66). Two recognized major contaminated areas were the Tarim Basin in the northwest region and the eastern plain region; the former was mainly influenced by the warm temperate arid climate and desert, and the latter was mainly influenced by the warm temperate semi-humid climate and multiple socioeconomic factors. The findings provided an interpretation of the influencing mechanisms of PM2.5 pollution, which can contribute to more specific policies aimed at successful PM2.5 pollution control and abatement.

Foodstuffs may be contaminated by organophosphate esters (OPEs) and become an important source of human exposure since OPEs are ubiquitous in the environment. In the present study, 10 OPEs were analyzed in various food matrices collected from a city in Eastern China including chicken, pork, fishes, vegetables, tofu, eggs, milk and cereals. The concentrations of Σ₁₀OPEs ranged from 1.1 to 9.6 ng g⁻¹ fresh weight (fw) in the foodstuffs. Cereals had the highest residual level of total OPEs with a mean value of 5.7 ng g⁻¹ fw. Tris(2-ethylhexyl) phosphate was detected in all foodstuff samples and showed the highest median residual concentration of 1.3 ng g⁻¹ fw among the OPE analogs. The daily dietary intake of OPEs was calculated as 3.6 and 2.4 μg d⁻¹ for adults and children. Cereals were identified as the major contributor to the total OPEs among different types of foodstuffs. Preliminary exposure assessment revealed that the current non-cancer health risks of OPEs via dietary intake were in the range of 10⁻⁵-10⁻³, indicating low risk levels. Moreover, the hazard index of OPEs indicated that the risk for children (3 × 10⁻³) was higher than adults (2 × 10⁻³).

Biogenic volatile organic compounds (BVOCs) are released to the atmosphere from vegetation. BVOCs aid in maintaining ecosystem sustainability via a series of functions, however, VOCs can alter tropospheric photochemistry and negatively affect biological organisms at high concentrations. Due to their critical role in ecosystem and environmental sustainability, BVOCs receive particular attention by global change biologists. To understand how plant VOC emissions affect stress responses within a dose-response context, dose responses should be evaluated. This commentary collectively documents hormetic-like responses of plant-emitted VOCs to external stimuli. Hormesis is a generalizable biphasic dose response phenomenon where the response to low doses acts in an opposite way at high doses. These collective findings suggest that ecological implications of low-level stress that may alter BVOC emissions should be considered in future studies. This commentary promotes new insights into the interface between biological systems and environmental change that influence several parts of the globe, and provide a base for advancing hazard assessment testing strategies and protocols to provide decision makers with adequate data for generating environmental standards.

The gulf of Annaba, the most important touristic and economic coastal zone located in Northeast Algeria, is contaminated by several pollutants from urban, agricultural, harbor and industrial activities. Elevated levels of heavy metals were detected in a locally prevalent edible mollusk Donax trunculus (Bivalvia, Donacidae) widely used as a sentinel species for the assessment of marine pollution. The present work aims to measure the difference between two localities, one being full of different pollutants (Sidi Salem) and the other being relatively clean (El Battah) and to evaluate the ability of D. trunculus to overcome the environmental stress during a transplantation experiment by a determination of fatty acid profile, the enzymes activities and the level of metallothioneins (MTs), a biomarker of metallic contamination. Adults of D. trunculus were collected at Sidi Salem (contaminated site) and transplanted into El Battah (reference site) for 21 days in cages (60 × 60 × 60 cm with a 2 mm mesh). Biochemical analyzes were conducted at different times (0, 7, 14 and 21 days). At 0-day experiment: the rate of the fatty acids, the enzymes activities and MT levels at the site of Sidi Salem (polluted site) were significantly different from those of El Battah. During the transplantation a gradual restoration of fatty acids rates, enzymes activities and MT levels was observed. At the end of the period of transplantation, the values are comparable to those of El Battah. A two-way ANOVA (time, site) on data revealed significant effects of time and site. Overally, D. trunculus is able to induce its detoxification system and to restore relatively rapidly the status of individuals from the reference site (El Battah).

Recently, health damage to children exposed to synthetic polyurethane (PU) running tracks has aroused social panic in China. Some possible toxic volatiles may be responsible for these damages. However, the exact cause remains unclear. We have detected a low concentration of sulfur dioxide (SO₂; 1.80–3.30 mg/m³) on the surface of the PU running track. Surprisingly, we found that SO₂ was generated from the PU running track, and even such a low concentration of SO₂ could induce severe lung inflammation with hemorrhage, inflammatory cell infiltration, and inflammatory factor secretion in mice after 2-week exposure. Prolonged exposure (5 weeks) to the SO₂ caused chronic pulmonary inflammation and pulmonary fibrosis in the mice. Peripheral hemogram results showed that platelet concentration increased significantly in the SO₂ group compared to that in the control group, and the proportion of blood neutrophils and monocytes among total leukocytes was more imbalanced in the SO₂ group (16.6%) than in the control group (8.0%). Further histopathology results of sternal marrow demonstrated that hematopoietic hyperplasia was severely suppressed with increased reticular stroma and adipocytes under SO₂ exposure. These data indicate that a low concentration of SO₂ generated spontaneously from PU running track outdoors as a secondary product is still harmful to health, as it impairs the respiratory system, hematopoiesis, and immunologic function. This indicates that the low-concentration SO₂ could be a major cause of diseases induced by air pollution, such as chronic obstructive pulmonary disease.