1,3,5-Trimethylbeneze (TMB) is an important constituent of anthropogenic volatile organic compounds that contributes to the formation of secondary organic aerosol (SOA). A series of chamber experiments were performed to probe the effects of NOₓ and SO₂ on SOA formation from TMB photooxidation. The molecular composition of TMB SOA was investigated by ultra-high performance liquid chromatography/electrospray ionization high-resolution quadrupole time-of-flight mass spectrometry (UPLC/ESI-HR-Q-TOFMS). We found that the SOA yield increases notably with elevated NOₓ concentrations under low-NOₓ condition ([TMB]₀/[NOₓ]₀ > 10 ppbC ppb⁻¹), while an opposite trend is observed in high-NOₓ experiments ([TMB]₀/[NOₓ]₀ < 10 ppbC ppb⁻¹). The increase in SOA yield in low-NOₓ regime is attributed to the increase of NOₓ-induced OH concentrations. The formation of low-volatility species might be suppressed, thereby leading to a lower SOA yield in high-NOₓ conditions. Moreover, SOA formation was promoted in experiment with SO₂ addition. Multifunctional products containing carbonyl, acid, alcohol, and nitrate functional groups were characterized in TMB/NOₓ photooxidation, whereas several organosulfates (OSs) and nitrooxy organosulfates were identified in TMB/NOₓ/SO₂ photooxidation based on HR-Q-TOFMS analysis. The formation mechanism relevant to the detected compounds in SOA were proposed. Based on our measurements, the photooxidation of TMB in the presence of SO₂ may be a new source of OSs in the atmosphere. The results presented here also deepen the understanding of SOA formation under relatively complex polluted environments.

The residual characteristics and the adsorption-desorption behaviors of azoxystrobin (AZO) as well as the soil ecological effects in the individual repeated treatments of AZO and its combination with chlorothalonil (CTL), chlortetracycline (CTC) and ciprofloxacin (CIP) were systematically studied in organic manure (OM)-amended soil under laboratory conditions. The presence of CTL, CTC, and CIP, both individually and combined, decreased the sorption affinity of AZO with the Freundlich adsorption and desorption coefficient decreasing by 0.3–24.2%, and CTC and CIP exhibited greater adverse effects than CTL. AZO dissipated slowly and the residues significantly accumulated during ten repeated treatments. The dissipation of AZO was inhibited to different degrees in the combined treatments. Biolog analysis revealed that the soil microbial functional diversity in the OM-soil + AZO and OM-soil + AZO + CTL treatments was higher than that in the OM-soil treatment during the former three repeated treatments, but which was inhibited during the latter seven repeated treatments. The soil microbial functional diversity in the OM-soil + AZO + CTC, OM-soil + AZO + CIP and OM-soil + AZO + CTL + CTC + CIP treatments was inhibited during the ten repeated treatments compared with OM-soil treatment. Metagenomic results showed that all repeated treatments significantly increased the relative abundance of Actinobacteria, but significantly decreased that of Proteobacteria and Firmicutes during the ten repeated treatments. Furthermore, the relative abundance of soil dominant bacterial genera Rhodococcus, Mycobacterium and Arthrobacter in all the repeated treatments significantly increased by 1.5–1283.9% compared with the OM-soil treatment. It is concluded that coexistence of CTL, CTC and CIP, both individually and combined, with AZO can inhibit the dissipation of AZO, reduce the adsorption affinity of AZO on soil, and alter the soil microbial community structure and functional diversity.

We utilized volcanic CO₂ vents at Castello Aragonese off Ischia Island as a natural laboratory to investigate the effect of lowered pH/elevated CO₂ on the bioactivities of extracts from fleshy brown algae Sargassum vulgare C. Agardh. We analysed the carbohydrate levels, antioxidant capacity, antibacterial, antifungal, antiprotozoal, anticancer properties and antimutagenic potential of the algae growing at the acidified site (pH ∼ 6.7) and those of algae growing at the nearby control site Lacco Ameno (pH∼8.1). The results of the present study show that the levels of polysaccharides fucoidan and alginate were higher in the algal population at acidified site. In general, extracts for the algal population from the acidified site showed a higher antioxidant capacity, antilipidperoxidation, antibacterial, antifungal, antiprotozoal, anticancer activities and antimutagenic potential compared to the control population. The increased bioactivity in acidified population could be due to elevated levels of bioactive compounds of algae and/or associated microbial communities. In this snapshot study, we performed bioactivity assays but did not characterize the chemistry and source of presumptive bioactive compounds. Nevertheless, the observed improvement in the medicinal properties of S. vulgare in the acidified oceans provides a promising basis for future marine drug discovery.

This study investigates the influence of meteorology, land use, built environment, and traffic characteristics on near-road ultrafine particle (UFP) concentrations. To achieve this objective, minute-level UFP concentrations were measured at various locations along a major arterial road in the Greater Toronto Area (GTA) between February and May 2019. Each location was visited five times, at least once in the morning, mid-day, and afternoon. Each visit lasted for 30 min, resulting in 2.5 h of minute-level data collected at each location. Local traffic information, including vehicle class and turning movements, were processed using computer vision techniques. The number of fast-food restaurants, cafes, trees, traffic signals, and building footprint, were found to have positive impacts on the mean UFP, while distance to the closest major road was negatively associated with UFP. We employed the Extreme Gradient Boosting (XGBoost) method to develop prediction models for UFP concentrations. The Shapley additive explanation (SHAP) measures were used to capture the influence of each feature on model output. The model results demonstrated that minute-level counts of local traffic from different directions had significant impacts on near-road UFP concentrations, model performance was robust under random cross-validation as coefficients of determination (R²) ranged from 0.63 to 0.69, but it revealed weaknesses when data at specific locations were eliminated from the training dataset. This result indicates that proper cross-validation techniques should be developed to better evaluate machine learning models for air quality predictions.

This study developed a process of genetically engineered bacteria Rhodococcus erythropolis expressing Nirs and AMO combined with membrane bioreactor (MBR), nanofiltration (NF) and reverse osmosis (RO) membrane (pRho-NA-MNR) for advanced treatment of landfill leachate. Results demonstrated that pRho-NA-MNR presented higher removal rate of chemical oxygen demand (COD), biological oxygen demand (BOD), ammonia nitrogen (N–NH₄), total nitrogen (TN) and total organic carbon (TOC) than activated sludge (AS-MNR) system. Administration of pRho-NA increased nitrification by converting N–NH₄ to nitrite (N–NO₂) and Nitrate (N–NO₃), and promoting denitrification by converting N–NO₂ to nitrogen (N₂) in the landfill leachate treatment, promoted the pH control, increased sludge activity and effluent yield, shortened phase length adaptation under alternating aerobic-anoxic conditions. pRho-NA increased the nitration and denitrifying rate in the aerobic and anaerobic stage in the system by increasing Cyt cd1 and Cyt c expression in the activated sludge. Nitrogen removal by nitrification and denitrification was positively correlated to the concentration of Nirs and AMO expression. Treatment with pRho-NA promoted pollutant removal efficiency of membrane bioreactor, nanofiltration and reverse osmosis membrane processes in landfill leachate. In conclusion, data suggest that pRho-NA-MNR facilitates the formation of granular sludge and enhances comparable removal of nitrogen and organic compounds, indicating the practice of this process should be considered in landfill leachate treatment system.

To highlight the levels and distributions and to assess the risk of human exposure of chlorinated paraffins (CPs) in PM₂.₅ in China, the concentrations and homologue patterns of short−chain chlorinated paraffins (SCCPs) and medium−chain chlorinated paraffins (MCCPs) in PM₂.₅ from 10 cities in China were studied in 2013 and 2014. The mean concentrations of ΣSCCPs and ΣMCCPs were 19.9 ± 41.1 ng m⁻³ and 15.6 ± 18.6 ng m⁻³, respectively. Unexpectedly, the highest pollution levels occurred in two central cities (Xinxiang and Taiyuan) rather than in well−known eastern megacities such as Beijing, Nanjing, Shanghai, and Guangzhou. By comparing with earlier research, it has indicated the trend of CPs industry shifting from large eastern cities to small and medium-sized cities in central China to some extent. In addition, the composition pattern of SCCPs demonstrated an obviously differences from previous studies, with C₁₁ and Cl₇ predominating and accounting for 45.1% and 24.9%, respectively. Meanwhile, the ratio of MCCPs/SCCPs in most cities was less than 1.00 except for Guangzhou (1.92), Shanghai (1.29), and Taiyuan (1.11). Combined with the results of correlation analysis and principal component analysis, the observed pollution characteristics of CPs in PM₂.₅ had similar sources, which were more influenced by the ratio of MCCPs/SCCPs than by organic carbon, elemental carbon, temperature, population, and gross domestic product. Overall, the composition of CPs reflected the characteristics of local industrial production and consumption, and also implied efforts of Chinese enterprises to reduce the content of short carbon groups of CPs production. The CPs mainly deposited in head airways during the process of entering the human respiratory system. However, at the present levels, there was no significant carcinogenic effect for human health.

Distinct cropland acidification has been reported in China due to nitrogen (N) fertilizer overuse. However, the impacts on food production and thereby on food security are largely unknown. Yield losses in the period 1980–2050 were therefore assessed by simulating soil pH changes combined with derived pH-yield relationships for wheat, maize and rice. If the N fertilizer input continues to increase at 1% annually, the predicted average soil pH decline is about one unit and relative yield losses are expected to increase from approximately 4%–24% during 2010–2050. If the N fertilizer increase stops in 2020 (N2020), the expected losses are approximately 16% in 2050, which is comparable to a scenario of 100% crop residue return (100%RR). However, if 30% of the N fertilizer is replaced by manure N (30%MR), the losses reduce to near 5% in 2050. Soil acidification was predicted to reverse and expected losses are only 2.5% in 2050 in a combined scenario of N2020, 100%RR and 30%MR. Our results illustrate the potential food insecurity induced by cropland acidification and address the necessity of mitigation.

This study aims to use ultraviolet (UV) irradiation to decompose polybrominated diphenyl ethers (PBDEs) in the elutes and then reuse the surfactants. The results indicate that UV can remove 2,2′,4,4′-tetrabrominated diphenyl ether (BDE-47) from surfactant eluents and Triton X series surfactants also can remove BDE-47 from the soil. Triton X-100 (TX-100) is the most promising surfactant during the washing and photodegradation processes. Quench experiments suggest that both ¹O₂ and OH• were involved in the TX-100 decomposition but only ¹O₂ is responsible for the degradation of BDE-47. In analysis of the photoproducts of BDE-47 by Gas Chromatography Mass Spectrum (GC-MS) and Liquid Chromatography High Resolution Mass Spectrometry (LC-HRMS), BDE-47 was mainly debrominated to the lower-brominated BDEs and then oxidized to ring-opening products. The little loss of TX-100 can mainly be attributed to the breakage of polyethylene oxide (PEO) chain. Nevertheless, the washing wastes treated by UV light can exhibit higher solubility for BDE-47 than before, indicating they can be reused for BDE-47 removal from soil. The toxicity assessment experiments were performed using Escherichia coli (E.coli) as an indicator. The results indicate that the removal of BDE-47 by UV irradiation can reduce the toxicity of eluent.

The seasonal variation and distribution among different matrices of endocrine-disrupting chemicals (EDCs) were investigated in the eutrophic water ecosystem of the Pearl River Delta, Guangdong, China. The chlorophyll a (Chl a) levels were generally higher in summer than in spring; however, the concentrations of 4-tert-octylphenol (OP), 4-nonylphenol (NP), and bisphenol A (BPA) in surface water were generally higher in spring (oligotrophic) than in summer (eutrophic). The levels of EDCs in SPM were lower in spring than in summer, a pattern seen in the seasonal variation of Chl a and particulate organic carbon (POC). The seasonal variations of EDCs in water bodies with different levels of eutrophication were analyzed in several dimensions including sediment, POC, algae and fish bile. The log Kₒc for SPM/water was higher in summer than in spring. The log Kₒc values for NP, OP, and BPA exhibited the following trends between matrices: colloid/water > sediment/water > SPM/water > algae/water, colloid/water > sediment/water > algae/water > SPM/water, and colloid/water > algae/water > sediment/water > SPM/water. The EDCs levels were different in fish tissues with the order bile > liver > muscle, with the concentrations being an order of magnitude higher in bile than in liver and an order of magnitude higher in liver than in muscle. The sequence of the bioconcentration factor (log BCF) for bile/water and liver/water was NP < OP < BPA in eutrophic conditions, but NP > OP > BPA in oligotrophic conditions. The order in eutrophic conditions was the same as the log BCF and log Kₒc for algae/water, indicating that the accumulation of EDCs in water bodies could be affected by algae, which could be one of the reasons of the seasonal variation of EDCs in water.

In recent years, numerous studies paid more attention to the molecular mechanisms associated with fluoride toxicity. However, the detailed mechanisms of fluoride immunotoxicity in bovine neutrophils remain unclear. Neutrophil extracellular traps (NETs) is a novel immune mechanism of neutrophils. We hypothesized that sodium fluoride (NaF) can trigger NETs activation and release, and investigate the related molecular mechanisms during the process. We exposed peripheral blood neutrophils to 1 mM NaF for 120 min in bovine neutrophils. The results showed that NaF exposure triggered NET-like structures decorated with histones and granule proteins. Quantitative measurement of NETs content correlated positively with the concentration of NaF. Mechanistically, NaF exposure increased reactive oxygen species (ROS) levels and phosphorylation levels of ERK, p38, whereas inhibiting the activities of superoxide dismutase (SOD) and catalase (CAT) compared with control neutrophils. NETs formation is induced by NaF and this effect was inhibited by the inhibitors diphenyleneiodonium chloride (DPI), U0126 and SB202190. Our findings described the potential importance of NaF-triggered NETs related molecules, which might help to extend the current understanding of NaF immunotoxicity.