This study explores the generation of ultrafine particle emissions, measured in particle number (PN), based on a portable emissions measurement system (PEMS) in the City of Toronto between October and December 2019. Two driving routes were designed to include busy arterial roads and highways. All measurements were conducted between 10 a.m. and 4 p.m. Altogether, emissions from 31 drives were collected, leading to approximately 200,000 s of data. A spike detection algorithm was employed to isolate PN spikes in time series data. A sensitivity analysis was also conducted to identify the most optimum method for spike detection. The results indicate that the average emission rate during a PN spike is approximately 8 times the emission rate along the rest of the drive. In each test trip, about 25% of the duration was attributed to spike events, contributing 75% of total PN emissions. A Pearson correlation of 0.45 was estimated between the number of PN spikes and the number of sharp accelerations (above 8.5 km/h/s). The Pearson correlation between the occurrence of high engine torque (above 65.0 Nm) and the number of PN spikes was estimated at 0.80. The number of PN spikes was highest on arterial roads where the vehicle speed was relatively low, but with high variability, and including a high number of sharp accelerations. This pattern of UFP emissions leads to high UFP concentrations along arterial roads in the inner city core.

Solutions of technical polychlorinated naphthalene (PCN) Halowax formulations (Halowax 1014 and Halowax 1051) diluted with Milli-Q water and sealed in the Pyrex glass tubes and quartz tubes were subjected to artificial solar and natural solar irradiation under different time intervals and field conditions. In particular, the results of several field irradiation experiments have shown increased PCN photodegradation as altitude increases above sea level. Irradiation in artificial solar conditions caused a substantial change in the PCN congener profiles of Halowax 1014 and Halowax 1051 test solutions. Interestingly, in long-term experiments, the relative abundance of congeners that contribute to dioxin-like activity, i.e. the compounds such as 1,2,3,5,7- and 1,2,4,6,7-PentaCN (PeCNs #52/60), 1,2,3,4,6,7- and 1,2,3,5,6,7-HexaCN (HxCNs #66/67), and 1,2,3,4,5,6,7-HeptaCN (HpCN #73), temporally increased substantially. In the field photodegradation experiments, the PCNs #52/60 and #66/67 were formed, while a relative persistence of PCN #73 was evident. Highest chlorinated octachloronaphthalene (OcCN #75), exposed to strong UV radiation at high altitude, was much less stable than lower molecular mass PCNs. Photodegradation of the technical PCN formulations produced also an unidentified aromatic compound. We conclude, that photodegradation of PCNs, which are considered as a widespread anthropogenic pollutants, is not restricted to any specific environmental condition. It can also be observed at low altitudes.

The accumulation of cadmium (Cd) in rice grains is closely associated with the content of mineral nutrients and amino acid metabolism, but the causal link among them is unclear. Profiles of amino acids (AAs) and quantities of essential nutrients in grains from early and late rice cultivars grown at four sites with different Cd levels were analyzed in the present study. Hazard quotients (HQs) for consumers by intake of rice from late cultivars were much higher than that from early cultivars at sites with soil Cd content of 0.25, 0.61 and 0.84 mg kg⁻¹. Cadmium accumulation in grains resulted in a sharp reduction of total essential AAs and non-essential AAs in both early and late rice cultivars. High-Cd-accumulating (HCA) cultivars had significantly higher level of glutamate (Glu) than low-Cd-accumulating (LCA) cultivars when rice Cd content was less than 0.20 mg kg⁻¹. However, Glu level in grains dramatically declined with the accumulation of Cd, which subsequently leaded to the reduction of other AAs. Cadmium content was well predicted by five amino acids (i.e., Glu, Alanine, Phenylalanine, Glycine and Threonine) or four essential elements (Ca, Fe, Mn and Zn) when rice Cd was less than 0.80 mg kg⁻¹. Amino acids played more important roles than nutrients in Cd accumulation. When Cd content was in the range of 0.40–1.16 mg kg⁻¹, the Mn content in rice increased significantly with the increase of Cd content, while the Glu content dropped down synchronously. Remarkably, the ratio between Mn and Glu displayed the highest direct path coefficient on Cd accumulation than any single cation or amino acid. These results indicate that high capacity in synthesizing Glu and concentrating Mn is the determinant factor for Cd accumulation in rice grains, and abundant Glu in aleurone layer may alleviate Cd toxicity by forming Glu-Cd complex.

This article has been retracted: please see Elsevier Policy on Article Withdrawal (https://www.elsevier.com/about/our-business/policies/article-withdrawal).This article has been retracted at the request of the Editors-in-Chief and Authors. The corresponding author informed the journal that full permission had not been obtained to use all the samples documented in the study. The authors apologise for any inconvenience caused.

Significant progress has been made in reducing emissions of air pollutants in the San Joaquin Valley in California. Nevertheless, from May to October, the valley still experiences numerous exceedances of the ozone health standard. As the standards are tightened, it is becoming harder to design policies to attain them. To better understand historical emissions reductions in the context of necessary future control efforts, we analyze 25 years of hourly measurements of ozone and nitrogen oxides concentrations for the hottest one third of days in Fresno using multiple linear regression analysis. We then analyze the changing dynamics of the weekend effect over the years in order to evaluate the growing importance of day-to-day carryover on ozone concentrations. A simplified model of the day-of-week pattern of ozone concentrations is used to explore the impact of same-day and previous-day concentrations. In addition to ozone, Oₓ (O₃ + NO₂) is used to distinguish reductions of atmospheric oxidants from short-duration exchanges between O₃ and NO₂. The analysis shows that there has been a significant increase in the importance of day-to-day carryover on ozone levels, and that consequently the ozone weekend effect in Fresno has changed over the last 25 years. In the 1990s, lower NOₓ on the weekend led to increased ozone on Saturdays and Sundays but levels of Oₓ remained constant. In the 2010s, lower weekend NOₓ led to reduced ozone on Saturdays, Sundays and Mondays showing that reductions in primary pollutants are sufficient to yield immediate decreases in secondary pollutants. Overall, the photochemical regime in the atmosphere has evolved such that carryover and regional pollution will be increasingly important in determining local ozone concentrations. Policies will therefore need to pay greater attention to regional emissions as local reductions may not be sufficient to meet the health standard.

China is one of the largest coastal countries in the world, which have all kinds of marginal systems. Studies have reported the sedimentary Polycyclic aromatic hydrocarbons (PAHs) pollution status, including their concentrations, sources and risks, in localized marginal systems, which showed significant differences. Thus, a comprehensive understanding of their pollution in marginal systems along China Mainland is urgently needed on a national scale. In the present study, the concentrations of 16 priority PAHs in surface sediments from 62 different marginal systems along China Mainland were reviewed. Their sources were identified and apportioned, and the health risks and ecological risks were also evaluated. As a result, the total sedimentary PAHs varied in a wide range of 4–3700 ng/g, with the lowest values observed in Kenting National Park in East China Sea and the highest values observed in Daliao River estuary in Bohai Sea. Their concentrations suggested that they were not contaminated-weakly contaminated in most study areas, but were contaminated-heavily contaminated in some pollution hot-spots. Source identification and apportion suggested that the sedimentary PAHs were mainly originated from coal combustion, vehicular emission, natural gas combustion and petrogenic source, but the coal combustion and vehicular emission contributed most to their emission (>90%). Risk assessment suggested that the carcinogenic risks were lower than the upper limit of the acceptable range (10⁻⁴), which were acceptable at a large spatial scale. However, for sediments from Qinhuangdao coastal wetland, Daliao River estuary and Yangpu Bay, their carcinogenic risks were higher than 10⁻⁴, which will pose high carcinogenic risks for adults. The non-carcinogenic risks were acceptable in all marginal systems with values lower than the safety guideline (<1). In the ecological risk assessment, their concentrations in some pollution hot-spots were higher than the safety guidelines (effects range low, ERL), suggesting a higher potential ecological risk.

Phytoextraction using Celosia argentea Linn. can potentially decontaminate Cd-contaminated soils. However, most earlier studies have been conducted at laboratory scale and for a relatively short remediation period. To evaluate the phytoextraction efficiency of C. argentea combined with different soil amendments (ammonium chloride, Bacillus megaterium, and citric acid), an 18-month field experiment was carried out in a farmland soil contaminated with 3.68 mg kg⁻¹ Cd by mine tailings in southern China. Soil Cd concentrations were decreased by 6.34 ± 0.73% after the three harvestings (with no amendments), which was 2.27 times that of the no-planting control (p < 0.05). Application of ammonium chloride, B. megaterium, and citric acid increased the overall Cd reduction rate in soil by 40.5%, 46.1%, and 105%, respectively. The application of citric acid decreased total Cd in soil by up to 16.9% in the rhizosphere soil and 13.0% in the bulk soil. The highest annual shoot biomass yield and Cd extraction amount reached 8.79 t ha⁻¹ and 273 g ha⁻¹. Acid-soluble Cd fraction in the rhizosphere was significantly lower compared to that in the bulk soil (p < 0.05), which indicates that mobile Cd in the rhizosphere was taken up by the roots vastly. C. argentea phytoextraction also improved soil metabolic functions by increasing the activities of soil enzymes (urease, invertase, phosphatase, and catalase). These findings demonstrate that Cd phytoextraction using C. argentea with the application of soil amendments can greatly improve the quality of Cd-contaminated soils.

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.

The atmospheric circulation plays a critical role in the global transport and deposition of atmospheric pollutants such as mercury (Hg). Desert dust emissions contribute to nearly 60–95% of the global dust budget and thus, desert dust may facilitate atmospheric Hg transport and deposition to the downwind regions worldwide. The role of desert dust in biogeochemical cycling of Hg, however, has not been well recognized by the Hg research community. In this study, we measured the concentration of particulate bound Hg (HgP) in total suspended particulate (TSP) collected from China’s largest desert, Taklimakan Desert, between 2013 and 2017. The results show that HgP concentrations over the Taklimakan Desert atmosphere are remarkably higher than those observed from background sites in China and are even comparable to those measured in most of the Chinese metropolitan cities. Moreover, HgP concentrations in the Taklimakan Desert exhibit a distinct seasonal pattern peaking during dust storm outbreak periods in spring and summer (March to August). A preliminary estimation demonstrates that export of total Hg associated with atmospheric dust from the Taklimakan Desert could be 59.7 ± 60.3 (1SD) Mg yr⁻¹. The unexpectedly high HgP concentrations during duststorms, together with consistent seasonal pattern of Hg revealed from the snow/ice, clearly demonstrate that Asian desert dust could act as a significant carrier of atmospheric Hg to the cryosphere of Western China and even can have further global reach.