Severe haze episodes in cold season in Beijing have been mitigated greatly during the last decade. However, the changes in aerosol chemistry as responses to the large reductions in gaseous precursors during the two phases of clean air action, i.e., phase Ⅰ (2013–2017) and phase Ⅱ (2018–2020), are less understood. Here we characterized such changes in cold season (January–March) by using five-year real-time aerosol particle composition measurements. Our results showed consistently large reductions for all chemical species from 2013 to 2020 with the largest decreases being chloride (95%) and organics (74%) followed by sulfate (69%), while the decreases in nitrate were comparatively small (44%). However, the contributions of sulfate were fairly stable despite the increased nitrate contributions from 18% in 2013 to 30% in 2020. Organic aerosol (OA) composition also changed significantly since 2018 with large increases in the contributions of secondary OA and corresponding decreases in primary OA from fossil fuel combustion and cooking emissions. The changes in aerosol chemistry were closely related to the different reductions in gaseous precursors, e.g., SO₂ vs. NO₂, and the enhanced secondary processes, e.g., the increases in O₃, sulfur and nitrogen oxidation efficiency. Further, we found that the changes in aerosol chemistry in cold season during the phase Ⅱ of clean air action (2018–2020) started to slow down with relatively small changes in PM₂.₅ and secondary inorganic species. Our results point towards a future challenge in mitigating air pollution in cold season, and the need of more stringent and scientific strategies to control secondary aerosol pollution in an environment with enhanced oxidation capacity and high precursors.

Sodium percarbonate (SPC, 2Na₂CO₃∙3H₂O₂), is a compound that can be used under multiple environmental applications. In this work, SPC was employed as oxidant in the treatment of soil contaminated with diesel oil. The soil samples were collected during the earthmoving stage of RNEST Oil Refinery (Petrobras), Brazil. Then, the samples were air-dried, mixed and characterized. Subsequently, raw soil was contaminated with diesel and treated by photo-Fenton reaction (H₂O₂/Fe²⁺/UV). SPC played a significant role in the generation of hydroxyl radicals under the catalytic effect of ferrous ions (Fe²⁺), hydrogen peroxide (H₂O₂) and radiation. These radicals provoked the photodegradation of polycyclic aromatic hydrocarbons (PAHs), in the soil remediation. A factorial design 3³ was carried out to assess the variables which most influenced the decrease in total organic carbon (TOC). The study was performed with the following variables: initial concentration of [H₂O₂] and [Fe²⁺], between 190.0 and 950.0 mmol L⁻¹ and 0.0–14.4 mmol L⁻¹, respectively. UV radiation was supplied from sunlight, blacklight lamps, and system without radiation. All experiments were performed with 5.0 g of contaminated soil in 50.0 mL of solution. The initial concentration of Fe²⁺ showed the statistically most significant effect. The oxidation efficiency evaluated in the best condition showed a decrease from 34,765 mg kg⁻¹ to 15,801 mg kg⁻¹ in TOC and from 85.750 mg kg⁻¹ to 20.770 mg kg⁻¹ in PAHs content. Moreover, the sums of low and high molecular weight polycyclic aromatic hydrocarbons (LMW-PAHs and HMW-PAHs) were 19.537 mg kg⁻¹ and 1.233 mg kg⁻¹, respectively. Both values are within the limits recommended by the United Sates Environmental Protection Agency (USEPA) and evidenced the satisfactory removal of PAHs from contaminated soil, being an alternative to classic oxidation protocols.

Pollutants in wastewater and exhaust gas bring out serious concerns to public health and the environment. Biochar can be developed as a sustainable adsorbent originating from abundant bio-wastes, such as agricultural waste, forestry residue, food waste and human waste. Here we highlight the state-of-the-art research progress on pyrochar and hydrochar for the sorption of pollutants (heavy metal, organics, gas, etc) in wastewater and exhaust gases. The adsorption performance of pyrochar and hydrochar are compared and discussed in-depth, including preparation procedures (carbonization and activation), sorption possible mechanisms, and physiochemical properties. Challenges and perspective for designing efficient and environmental benign biochar-based adsorbents are finally addressed.

Potato (Solanum tuberosum L.) production in irrigated coarse-textured soils requires intensive nitrogen (N) fertilization which may increase reactive N losses. Biological soil additives including N-fixing microbes (NFM) have been promoted as a means to increase crop N use efficiency, though few field studies have evaluated their effects, and none have examined the combined use of NFM with microbial inhibitors. A 2-year study (2018–19) in an irrigated loamy sand quantified the effects of the urease inhibitor NBPT, the nitrification inhibitor DMPSA, NFM, and the additive combinations DMPSA + NBPT and DMPSA + NFM on potato performance and growing season nitrous oxide (N₂O) emissions and nitrate (NO₃⁻) leaching. All treatments, except a zero-N control, received diammonium phosphate at 45 kg N ha⁻¹ and split applied urea at 280 kg N ha⁻¹. Compared with urea alone, DMPSA + NBPT reduced NO₃⁻ leaching and N₂O emissions by 25% and 62%, respectively, and increased crop N uptake by 19% in one year, although none of the additive treatments increased tuber yields. The DMPSA and DMPSA + NBPT treatments had greater soil ammonium concentration, and all DMPSA-containing treatments consistently reduced N₂O emissions, compared to urea-only. Use of NBPT by itself reduced NO₃⁻ leaching by 21% across growing seasons and N₂O emissions by 37% in 2018 relative to urea-only. In contrast to the inhibitors, NFM by itself increased N₂O by 23% in 2019; however, co-applying DMPSA with NFM reduced N₂O emissions by ≥ 50% compared to urea alone. These results demonstrate that DMPSA can mitigate N₂O emissions in potato production systems and that DMPSA + NBPT can reduce both N₂O and NO₃⁻ losses and increase the N supply for crop uptake. This is the first study to show that combining a nitrification inhibitor with NFM can result in decreased N₂O emissions in contrast to unintended increases in N₂O emissions that can occur when NFM is applied by itself.

Iron-bearing nanoparticles (IBNPs) were abundant in particulate matter (PM). Due to their high reactivity, IBNPs were considered hazardous to human health, however, their toxic mode-of-action(s) are highly unclear. Ferroptosis is a novel programmed cell death (PCD) that highly associated with intracellular iron. However, the pro-ferroptotic effect of IBNPs has not been characterized. To this end, we ought to investigate whether and how IBNPs (synthetic γ-Fe₂O₃ and Fe₃O₄ NPs were selected as the model compounds) are involved in ferroptosis. We found that human umbilical vein endothelial cells (HUVECs) phagocytized large qualities of γ-Fe₂O₃ and Fe₃O₄ NPs, resulting in increased intracellular iron level. We further observed the disrupted cystine/glutamate reverse transporter (System Xc⁻) and glutathione peroxidase 4 (GPX4) signaling in γ-Fe₂O₃ and Fe₃O₄ NPs-challenged HUVECs. γ-Fe₂O₃ and Fe₃O₄ NPs could also cause mitochondrial fusion and fission dysregulation, activate lipid peroxidation and iron metabolism-related genes in a P53-dependent manner. Together, the ferroptotic activity of IBNPs should be acknowledged for the risk assessment of PM associated health effects.

6:2 Cl-PFESA is a polyfluoroalkyl ether with high environmental persistence that has been confirmed to have significant adverse effects on animals. In this study, 6-week-old female C57BL/6 mice were exposed to 0, 1, 3 and 10 μg/L 6:2 Cl-PFESA for 10 weeks to estimate the hepatotoxicity of 6:2 Cl-PFESA and explore its underlying molecular mechanism. The results indicated that 6:2 Cl-PFESA preferentially bioaccumulated in the liver and induced hepatic cytoplasmic vacuolation and hepatomegaly in mice. In addition, serum metabolic profiling showed that 6:2 Cl-PFESA exposure caused an abnormal increase in amino acids and an abnormal decrease in acyl-carnitine, which interfered with fatty acid transport and increased the risk of metabolic diseases. Further experiments showed that 6:2 Cl-PFESA formed more hydrogen bonds with PPAR-γ than PFOS, Rosi and GW9662, and the binding affinity of 6:2 Cl-PFESA toward PPAR-γ was the highest among the ligands. 6:2 Cl-PFESA promoted the differentiation of 3T3-L1 cells by increasing PPAR-γ expression. Therefore, our results showed that 6:2 Cl-PFESA has the potential to induce liver damage and dysfunction in female mice, and this effect was achieved through PPAR-γ. This study is the first to reveal the hepatic toxicity of 6:2 Cl-PFESA in female mammals and provides new insights for subsequent in-depth research.

Arsenic (As) exposure is a global public health concern affecting millions worldwide and stems from drinking water and foods containing As. Here, we assessed how agronomic practices and postharvest fermentation techniques influence As concentrations in rice bran, and calculated health risks from consumption. A global suite of 53 rice brans were tested for total As and speciation. Targeted quantification of inorganic As (iAs) concentrations in rice bran were used to calculate Target Hazard Quotient (THQ) and Lifetime Cancer Risk (LCR) across the lifespan. Mean iAs was highest in Thailand rice bran samples (0.619 mg kg⁻¹) and lowest in Guatemala (0.017 mg kg⁻¹) rice bran samples. When comparing monosodium-methanearsonate (MSMA) treated and the Native-soil counterpart under the irrigation technique Alternate Wetting and Drying (AWD) management, the MSMA treatment had significantly higher total As (p = 0.022), and iAs (p = 0.016). No significant differences in As concentrations were found between conventional and organic production, nor between fermented and non-fermented rice bran. Health risk assessment calculations for the highest iAs-rice bran dosage scenario for adults, children and infants exceeded THQ and LCR thresholds, and LCR was above threshold for median iAs-rice bran. This environmental exposure investigation into rice bran provides novel information with food safety guidance for an emerging global ingredient.

Historical mining activities cause widespread, long-term trace metal contamination of freshwater ecosystems. However, measuring trace metal bioavailability has proven difficult, because it depends on many factors, not least concentrations in water, sediment and habitat. Simple tools are needed to assess bioavailabilities. The use of biomonitors has been widely advocated to provide a realistic measure. To date there have been few attempts to identify ubiquitous patterns of trace metal accumulation within and between freshwater biomonitors at geographical scales relevant to trace metal contamination. Here we address this through a nationwide collection of freshwater biomonitors (species of Gammarus, Leuctra, Baetis, Rhyacophila, Hydropsyche) from 99 English and Welsh stream sites spanning a gradient of high to low trace metal loading. The study tested for inter-biomonitor variation in trace metal body burden, and for congruence amongst accumulations of trace metals within taxa and between taxa across the gradient. In general, significant differences in trace metal body burden occurred between taxa: Gammarus sp. was the most different compared with insect biomonitors. Bivariate relationships between trace metals within biomonitors reflected trace metal profiles in the environment. Strong correlations between some trace metals suggested accumulation was also influenced by physiological pathways. Bivariate relationships between insect biomonitors for body burdens of As, Cu, Mn and Pb were highly consistent. Our data show that irrespective of taxonomic or ecological differences, there is a commonality of response amongst insect taxa, indicating one or more could provide consistent measures of trace metal bioavailability.

The Carbon Offsetting and Reduction Scheme for International Aviation (CORSIA) is the first programme to tackle carbon dioxide (CO₂) emissions from a single industry at the global level, to realize the carbon-neutral growth of international flights from 2020 onwards. However, the COVID-19 pandemic has caused a drastic decline in the global aviation industry. The International Civil Aviation Organization (ICAO) has adjusted the CORSIA by removing 2020 emissions from the baseline, which now will only be based on 2019 emissions. We estimate that the total carbon dioxide (CO₂) emissions from global international flights decreased by 70 % from February to July 2020 compared to those in 2019. Our analysis suggests that the annual CO₂ emissions from international flights during the pilot stage of CORSIA (2021–2023) will be far below the revised baseline even if the global aviation industry could embrace an optimistic recovery. The major airline companies will have very limited motivations due to the CORSIA scheme to implement mitigation actions proactively. Therefore, more progressive actions are needed to align the industry recovery of global aviation and climate change mitigation during the post-COVID-19 period.

In this work, the novel technology was used to remove heavy metal from sludge. The coupled with biodegradable ethylenediamine disuccinic acid (EDDS) and approaching anode electrokinetic (AA-EK) technique was used to enhance heavy metal removing from sludge. Electric current, sludge and electrolyte characteristics, heavy metal removal efficiency and residual content distribution, and heavy metal fractions percentage of variation were evaluated during the electrokinetic remediation process. Results demonstrated that the coupled with EDDS and AA-EK technique obtain a predominant heavy metal removal efficiency, and promote electric current increasing during the enhanced electrokinetic remediation process. The catholyte electrical conductivity was higher than the anolyte, and electrical conductivity of near the cathode sludge achieved a higher value than anode sludge during the coupled with EDDS and AA-EK remediation process. AA-EK technique can produce a great number of H⁺, which caused the sludge acidification and pH decrease. Cu, Zn, Cr, Pb, Ni and Mn obtain the highest extraction efficiency after the coupled with EDDS and AA-EK remediation, which were 52.2 ± 2.57%, 56.8 ± 3.62%, 60.4 ± 3.62%, 47.2 ± 2.35%, 53.0 ± 3.48%, 54.2 ± 3.43%, respectively. Also, heavy metal fractions analysis demonstrated that the oxidizable fraction percentage decreased slowly after the coupled with EDDS and AA-EK remediation.