To prevent spreads of Coronavirus disease-2019 (COVID-19), China adopted the lockdown measures in late January 2020, providing a platform to study the response of air quality and atmospheric chemical and physical properties to strict reduced emissions. In this study, the continuous measurements of aerosol light absorption were conducted in Nanjing, east China, from January 3 to March 31, 2020. Our results showed that the contribution of black carbon (BC) to light absorption at the different wavelengths was more than 75% and the rest light absorption was contributed by brown carbon (BrC), which was mainly originated from primary emissions. Secondary BrC absorption, which was mainly produced by photochemical oxidation, constituted a minor fraction (2–7%) of the total absorption. Compared with the sampling in the pre-lockdown, the significant decreases of BC (43%) and secondary BrC absorption (31%) were found during the lockdown period, resulting in a substantial decrease of solar energy absorbance by 36% on a local scale. The control measures also changed the diurnal variations of light absorption. Due to the reduced emissions, the relative fraction of fossil fuel to BC also dropped from 78% in the pre-lockdown to 71% in the lockdown. The concentrations of BC, PM₂.₅ and NO₂ decreased 1.1 μg m⁻³, 33 μg m⁻³ and 9.1 ppb whereas O₃ concentration increased 9.0 ppb during the COVID-19 lockdown period. The decreased concentrations of BC, PM₂.₅ and NO₂ were mainly contributed by both emission reduction (51–64%) and meteorological conditions (36–49%). Our results highlighted that the balance of control measures in alleviation of particulate matter (PM) and O₃ pollution, and meteorology should be seriously considered for improvement of air quality in this urban city of China.

Transition metals (TMs) (e.g. copper (Cu) and iron (Fe)) and certain organic compounds are known active constituents causing oxidative potential (OP) by inhaled ambient fine particulate matter (PM₂.₅) in lung fluid. Humic-like substances (HULIS), isolated from atmospheric PM₂.₅, are largely metal-free and contain mixtures of organics that are capable of complexing TMs. TMs and HULIS co-exist in the water-extractable part of PM₂.₅. In this work, we used a solid phase extraction procedure to isolate the water-soluble TMs in the hydrophilic fraction (HPI) and HULIS in the hydrophobic fraction (HPO) and carried out this isolation procedure to a set of 32 real-world PM₂.₅ samples collected in Beijing and Hong Kong, China. We quantified two OP endpoints, namely hydroxyl radical formation (denoted as OP•OH) and ascorbic acid depletion (denoted as OPAA), by the two fractions separately and combined, as well as by the bulk water-soluble aerosols. OP•OH and OPAA were well-correlated in both separate fractions and their combined mixtures or bulk water-soluble aerosols. OP by HPI far exceeded that by HPO. On a per unit PM₂.₅ mass basis, the Hong Kong samples on average had a higher OPAA and OP•OH than the Beijing samples due to more water-soluble Cu. For HPI, Cu was a dominant OP•OH and OPAA contributor (>80%), although water-soluble Fe was present at a concentration approximately one order of magnitude higher. Suppression effects on OP•OH were observed through comparing the OP of the bulk water-soluble aerosol with that of HPI. Our work reveals the importance of monitoring PM₂.₅ chemical compositions (especially water-soluble redox active metals). Furthermore, we demonstrate the need to consider metal-organic interactions when evaluating the aggregate OP by PM₂.₅ from individual components or apportioning OP by PM₂.₅ to specific chemical components.

Crude oil pollution is a global environmental concern since it persists in the environment longer than most conventional carbon sources. In December 2014, the hyper-arid Evrona Nature Reserve, Israel, experienced large-scale contamination when crude oil spilled. The overarching goal of the study was to investigate the possible changes, caused by an accidental crude oil spill, in the leaf reflectance and biochemical composition of four natural habitat desert shrubs. The specific objectives were (1) to monitor the biochemical properties of dominant shrub species in the polluted and control areas; (2) to study the long-term consequences of the contamination; (3) to provide information that will assist in planning rehabilitation actions; and (4) to explore the feasibility of vegetation indices (VIs), along with the machine learning (ML) technique, for detecting stressed shrubs based on the full spectral range. Four measurement campaigns were conducted in 2018 and 2019. Along with the various stress indicators, field spectral measurements were performed in the range of 350–2500 nm. A regression analysis to examine the relation of leaf reflectance to biochemical contents was carried out, to reveal the relevant wavelengths in which polluted and control plants differ. Vegetation indices applied in previous studies were found to be less sensitive for indirect detection of long-term oil contamination. A novel spectral index, based on indicative spectral bands, named the “normalized blue-green stress index” (NBGSI), was established. The NBGSI distinguished significantly between shrubs located in the polluted and in the control areas. The NBGSI showed a strong linear correlation with pheophytin a. Machine learning classification algorithms obtained high overall prediction accuracy in distinguishing between shrubs located in the oil-polluted and the control sites, indicating internal component differences. The findings of this study demonstrate the efficacy of indirect and non-destructive spectral tools for detecting and monitoring oil pollution stress in shrubs.

Arsenic (As) is a toxic metalloid and its widespread contamination in agricultural soils along with soil salinization has become a serious concern for human health and food security. In the present study, the effect of cotton shell biochar (CSBC) in decreasing As-induced phytotoxicity and human health risks in quinoa (Chenopodium quinoa Willd.) grown on As-spiked saline and non-saline soils was evaluated. Quinoa plants were grown on As contaminated (0, 15 and 30 mg kg⁻¹) saline and non-saline soils amended with 0, 1 and 2% CSBC. Results showed that plant growth, grain yield, stomatal conductance and chlorophyll contents of quinoa showed more decline on As contaminated saline soil than non-saline soil. The application of 2% CSBC particularly enhanced plant growth, leaf relative water contents, stomatal conductance, pigment contents and limited the uptake of As and Na as compared to soil without CSBC. Salinity in combination with As trigged the production of H₂O₂ and caused lipid peroxidation of cell membranes. Biochar ameliorated the oxidative stress by increasing the activities of antioxidant enzymes (SOD, POD, CAT). Carcinogenic and non-carcinogenic human health risks were greatly decreased in the presence of biochar. Application of 2% CSBC showed promising results in reducing human health risks and As toxicity in quinoa grown on As contaminated non-saline and saline soils. Further research is needed to evaluate the role of biochar in minimizing As accumulation in other crops on normal as well as salt affected soils under field conditions.

Paraquat (PQ) is one of the most widely used herbicides in the world due to its excellent weed control effects. Accumulating evidence has revealed that long-term exposure to PQ can significantly increase the risk of Parkinson’s disease (PD). However, the underlying molecular mechanisms are yet to be fully understood. Hence, we investigated the potential role of reactive oxygen species (ROS) and dynamin-related protein 1 (DRP1) in PQ-induced mitophagy, aiming to elaborate on possible molecular mechanisms involved in PQ-triggered neurotoxicity. Our results showed that ROS were increased, mitochondrial membrane potential was decreased at 100, 200, and 300 μM PQ concentrations, and autophagy pathways were activated at a concentration of 100 μM in neuronal cells. In addition, excessive mitophagy was observed in neurons exposed to 300 μM PQ for 24 h. Then, ROS-mediated mitochondrial fission was found to contribute to PQ-induced excessive mitophagy. Moreover, all aforementioned changes were significantly ameliorated by mdivi-1. Thus, our findings provide a novel neurotoxic mechanism and reveal the DRP1-mitochondrial fission pathway as a potential target for treatments of PQ-induced excessive mitophagy, serving as an alternative target for the prevention and treatment of Parkinson’s disease. Because harmful substances are transmitted and enriched in the food chain, the toxic effect of environmental paraquat is nonnegligible, and more investigations are needed.

High concentrations of ground-level ozone affect human health, plants, and animals. Reducing ozone pollution in rural regions, where local emissions are already low, poses challenge. We use meteorological back-trajectories, air quality model sensitivity analysis, and satellite remote sensing data to investigate the ozone sources in Yuma, Arizona and find strong international influences from Northern Mexico on 12 out of 16 ozone exceedance days. We find that such exceedances could not be mitigated by reducing emissions in Arizona; complete removal of state emissions would reduce the maximum daily 8-h average (MDA8) ozone in Yuma by only 0.7% on exceeding days. In contrast, emissions in Mexico are estimated to contribute to 11% of the ozone during these exceedances, and their reduction would reduce MDA8 ozone in Yuma to below the standard. Using satellite-based remote sensing measurements, we find that emissions of nitrogen oxides (NOₓ, a key photochemical precursor of ozone) increase slightly in Mexico from 2005 to 2016, opposite to decreases shown in the bottom-up inventory. In comparison, a decrease of NOₓ emissions in the US and meteorological factors lead to an overall of summer mean and annual MDA8 ozone in Yuma (by ∼1–4% and ∼3%, respectively). Analysis of meteorological back-trajectories also shows similar transboundary transport of ozone at the US-Mexico border in California and New Mexico, where strong influences from Northern Mexico coincide with 11 out of 17 and 6 out of 8 ozone exceedances. 2020 is the final year of the U.S.-Mexico Border 2020 Program, which aimed to reduce pollution at border regions of the US and Mexico. Our results indicate the importance of sustaining a substantial cooperative program to improve air quality at the border area.

Cadmium (Cd) is a heavy metal toxicant as a common pollutant derived from many agricultural and industrial sources. The absorption of Cd takes place primarily through Cd-contaminated food and water and, to a significant extent, via inhalation of Cd-contaminated air and cigarette smoking. Epidemiological data suggest that occupational or environmental exposure to Cd increases the health risk for osteoporosis and spontaneous fracture such as itai-itai disease. However, the direct effects and underlying mechanism(s) of Cd exposure on bone damage are largely unknown. We used primary bone marrow-derived mesenchymal stromal cells (BMMSCs) and found that Cd significantly induced BMMSC cellular senescence through over-activation of NF-κB signaling pathway. Increased cell senescence was determined by production of senescence-associated secretory phenotype (SASP), cell cycle arrest and upregulation of p21/p53/p16ᴵᴺᴷ⁴ᵃ protein expression. Additionally, Cd impaired osteogenic differentiation and increased adipogenesis of BMMSCs, and significantly induced cellular senescence-associated defects such as mitochondrial dysfunction and DNA damage. Sprague-Dawley (SD) rats were chronically exposed to Cd to verify that Cd significantly increased adipocyte number, and decreased mineralization tissues of bone marrow in vivo. Interestingly, we observed that Cd exposure remarkably retarded bone repair and regeneration after operation of skull defect. Notably, pretreatment of melatonin is able to partially prevent Cd-induced some senescence-associated defects of BMMSCs including mitochondrial dysfunction and DNA damage. Although Cd activated mammalian target of rapamycin (mTOR) pathway, rapamycin only partially ameliorated Cd-induced cell apoptosis rather than cellular senescence phenotypes of BMMSCs. In addition, a selective NF-κB inhibitor moderately alleviated Cd-caused the senescence-related defects of the BMMSCs. The study shed light on the action and mechanism of Cd on osteoporosis and bone ageing, and may provide a novel option to ameliorate the harmful effects of Cd exposure.

The present research used zebrafish (5–28 days post-fertilization; dpf) as a model organism to investigate the effects of chronic exposure to environmentally relevant sub-lethal concentrations of waterborne (261 μg/L) and dietary zinc (Zn) (1500 mg Zn/kg dw), either independently or simultaneously, during development. The results showed that whole body contents of Zn were increased in all Zn treatment groups, with the highest accumulation of Zn observed in larvae simultaneously exposed to elevated waterborne and dietary Zn. In addition, exposure to elevated levels of Zn, either through the water or the diet, led to a decrease in whole body calcium (Ca) contents at 28 dpf. The findings also suggested that exposure to elevated levels of Zn resulted in a significant reduction in whole body manganese (Mn) contents. More importantly, the magnitude of decrease in Mn contents by Zn exposure was markedly higher than that in Ca and appeared to mirror the increases in whole body Zn accumulation. These results indicate that Mn regulation is more sensitive than Ca to disruption by Zn exposure in developing fish. Further examination of the Zrt-Irt-Like Protein (ZIP) family of transporters using droplet digital PCR technologies revealed that several zip transporters exhibited temporal and exposure route-specific changes following Zn exposure. In particular, the level of zip4 was influenced by Zn exposure regardless of the exposure routes, while changes in zip7 and zip8 levels were predominantly driven by waterborne exposure. Overall, our findings demonstrated that zebrafish during the developmental periods are sensitive to elevated levels of Zn seen in the environment, particularly following co-exposures to waterborne and dietary Zn. Future toxicological assessment of elevated Zn exposure should consider both the exposure routes and the life stages of fish.

Light-absorbing organic aerosols, also known as brown carbon (BrC), enhance the warming effect of the Earth’s atmosphere. The seasonal and spatial variability of BrC absorption properties is poorly constrained and accounted for in the climate models resulting in a substantial underestimation of their radiative forcing estimates. This study reports seasonal and spatial variability of absorption properties and simple forcing efficiency of light-absorbing water-soluble organic carbon (WSOC, SFEWSOC) by utilizing current and previous field-based measurements reported mostly from Asia along with a few observations from Europe, the USA, and the Amazon rainforest. The absorption coefficient of WSOC at 365 nm (bₐbₛ₋₃₆₅) and the concentrations of carbonaceous species at Kanpur were about an order of magnitude higher during winter than in the monsoon season owing to differences in the boundary layer height, active sources and their strengths, and amount of seasonal wet precipitation. The WSOC aerosols during winter exhibited ∼1.6 times higher light absorption capacity than in the monsoon season at Kanpur site. The assessment of spatial variability of the imaginary component of the refractive index spectrum (kλ) across South Asia has revealed that it varies from ∼1 to 2 orders of magnitude and light absorption capacity of WSOC ranges from 3 to 21 W/g. The light absorption capacity of WSOC aerosols exhibited less spatial variability across East Asia (5–13 W/g) when compared to that in the South Asia. The photochemical aging of WSOC aerosols, indicated by the enhancement in WSOC/OC ratio, was linked to degradation in their light absorption capacity, whereas the absorption Ångström exponent (AAE) remained unaffected. This study recommends the adoption of refined climate models where sampling regime specific absorption properties are calculated separately, such that these inputs can better constrain the model estimates of the global effects of BrC.

Water pollution is an urgent problem that needs to be controlled via green transformation and the development of the Yangtze River Economic Belt (YREB). Based on the water pollutant discharge and socio-economic database of prefecture-level cities in the YREB from 2011 to 2015, this study explores the spatiotemporal variations in water pollutant discharge in the YREB via two main indicators: chemical oxygen demand (COD) and ammonia nitrogen (NH₃–N). Further, the spatial effects and determinants of water pollutant discharge are quantitatively estimated. The results show that (1) the water pollutant discharge in the YREB has decreased significantly, with the COD and NH₃–N discharge reduced by 10.46% and 10.79%, respectively, and the discharge reduction in the lower reaches was the most prominent; (2) the spatial pattern of water pollutant discharge in the YREB was generally stable and partially improved, and cities with a high rate of water pollutant reduction in the YREB were distributed in the main stream region of the Yangtze River and the intersection of the main stream and tributaries; (3) spatial effects had a significant impact on water pollutant discharge in the YREB, with regional cooperation and economic radiation through environmental management and control initially showing a combined reduction trend in regional water pollutants; and (4) determinants of population size and agricultural economic share declined to varying degrees at the end of the study period, although the urbanization level continued to increase, indicating that urbanization in the YREB occurred too quickly and that water pollutant discharge reduction was limited. However, economic development leading to the deterioration of the water environment was alleviated. In addition, foreign direct investment (FDI) inflows and rapid industrialization processes must be monitored to increase the reduction in characteristic water pollutants.