Particulate matter (PM) deposited on canopy surfaces could be washed off and carried in throughfall to the ground. This would help plants recapture airborne PM on their canopy surfaces and then develop a PM purification capacity. Sixteen commonly greening plant species in north China (including 13 arbor species and 3 shrub species) were selected to investigate the washing process of plant-deposited PM during precipitation events. We measured the PM wash-off mass in throughfall under canopies of 16 plant species and in atmospheric precipitation during 14 precipitation events through field positioning experiments in 2015, compared the seasonal changes and species differences in PM wash-off mass, and discussed the predominant factors resulting in the variation. The results showed that plant-deposited PM was largely washed off by precipitation. The average wash-off mass of total suspended particulate (TSP) in throughfall was 1.3 times higher than that in precipitation, at 18.3 ± 0.7 kg hm−2 and 7.9 ± 0.9 kg hm−2, respectively. There were significant seasonal differences in TSP wash-off mass. The value was higher in summer at 22.3 ± 1.0 kg hm−2, followed by that of winter (10.8 ± 0.6 kg hm−2) and spring (8.9 ± 1.0 kg hm−2). TSP wash-off mass in throughfall greatly varied among plant species (F = 9.542, n = 627, p < 0.001). Of the 16 selected species, Platanus acerifolia (38.0 ± 5.8 kg hm−2) showed the largest difference from that of Liriodendron chinese (8.9 ± 0.6 kg hm−2) (n = 80, p < 0.001). PM wash-off mass of different particle sizes in throughfall increased with the increase of event-based precipitation. This study enhanced the quantitative understanding of plant-deposited PM washed-off by natural precipitation among plant species and seasons. The results could provide significant guidelines for the selection and allocation of plant species to improve the PM retention capacity of urban greening plants.

F-53B (6:2 chlorinated polyfluorinated ether sulfonate) is currently recognized as a safe alternative to long-chain PFASs in China. However, an increasing number of studies have recently authenticated its biotoxicological effects. In this study, for evaluating the gut toxicity of F-53B in mammals, both female and male mice were orally exposed to 0, 1, 3, or 10 μg/L F-53B for 10 weeks. Our results showed that F-53B significantly accumulated in the colon, ileum and serum when exposed to 10 μg/L F-53B for 10 weeks. F-53B exposure not only increased the transcriptional levels of ion transport-related genes but could also interact with the CFTR protein directly. Interestingly, subchronic F-53B exposure also increased the transcription of mucus secretion-related genes, but the protein level of Muc2 decreased after F-53B exposure, indicating that there was a compensatory phenomenon after mucus barrier injury. Furthermore, F-53B exposure also induced colonic inflammation associated with gut microbiota dysbiosis in the colon. Taken together, our results indicated that the potential gut toxicity of F-53B and almost all of the changed parameters were significantly affected in both female and male mice, suggesting that F-53B could disturb the gut barrier without sex dependence in mice.

Marine fish are considered a source of high quality proteins and fatty acids. However, the consumption of fish may pose a health risk as it may have potentially toxic elements in high concentrations. In this study we quantify the multielemental composition of muscle and fins for three species of commercial marine fish from Brazil: Sphyraena guachancho (Barracuda), Priacantus arenatus (Common bigeye) and Genidens genidens (Guri sea catfish). We then assessed the potential risk of fish consumption by means of a Provisional Hazard Indices. Amongst the elements detected in fish tissue were potentially toxic elements such as Ag, Ba, Cd, Cr and Hg. Concentration differences were species-specific, and affected by the species trophic level, morphological characteristics and feeding habits. Results suggest the higher the trophic level of the fish, the higher the risk of consumption. Caution is recommended for the frequent ingestion of high trophic level fish species in Brazil.

The increased applications and production of graphene oxide (GO) make the necessity to study information on the interaction of GO with minerals. In this work, adsorption and desorption were used to study the reversibility of interaction between GO and goethite/kaolinite. Result showed that the pH value, ionic strength, and temperature had significant effects on the adsorption and desorption behavior of GO. Interaction force was stronger between GO and goethite than that of kaolinite. The interaction may be attributed to the electrostatic, hydrogen-bonding, and Lewis acid base interactions. The irreversible interaction between GO and minerals may be a main mechanism for the observed desorption hysteresis. These results are important for evaluating the fate and health risk of GO in the environment.

Diesel exhaust (DE) contributes to air pollution, an important risk factor for cardiovascular diseases. However, the mechanisms by which DE exposure induces cardiovascular dysfunction remain unknown and there is still debate on the contribution of the primary particulate matter (PM) fraction compared to the gaseous phase. Although the mitochondria play a key role in the events leading to cardiovascular diseases, their role in DE-induced cardiovascular effects has not been investigated. The aim of this study was to highlight cardiac and mitochondrial events that could be disrupted following acute and/or repeated DE exposures and the contribution of gaseous pollutants to these effects. To address this question, Wistar rats were exposed to DE generated under strictly controlled and characterized conditions and extracted upstream or downstream of the diesel particulate filter (DPF). Evaluation of the cardiac function after acute DE exposure showed a disturbance in echocardiographic parameters, which persisted and worsened after repeated exposures. The presence of the DPF did not modify the cardiovascular dysfunction revealing an important implication of the gas phase in this response. Surprisingly, redox parameters were not altered by DE exposures while an alteration in mitochondrial oxidative capacity was observed. Exploration of the mitochondrial function demonstrated a more specific alteration in complex I of the respiratory chain after repeated exposures, which was further confirmed by transcriptional analysis of left ventricular (LV) tissue. In conclusion, this work provides new insights into cardiovascular effects induced by DE, demonstrating a cardiac mitochondrial impairment associated with the gaseous phase. These effects suggest deleterious consequences in terms of cardiac function for vulnerable populations with underlying energy deficit such as patients with heart failure or the elderly.

Air pollution exposure characterization has been shaped by many constraints. These include technologies that lead to insufficient coverage across space and/or time in order to characterize individual or community-level exposures with sufficient accuracy and precision. However, there is now capacity for continuous monitoring of many air pollutants using comparatively inexpensive, real-time sensors. Crucial questions remain regarding whether or not these sensors perform adequately for various potential end uses and whether performance varies over time or across ambient conditions. Performance scrutiny of sensors via lab- and field-testing and calibration across their lifetime is necessary for interpretation of data, and has important implications for end users including cost effectiveness and ease of use. We developed a comparatively lower-cost, portable, in-home air sampling platform and a guiding development and maintenance workflow that achieved our goal of characterizing some key indoor pollutants with high sensitivity and reasonable accuracy. Here we describe the process of selecting, validating, calibrating, and maintaining our platform – the Environmental Multi-pollutant Monitoring Assembly (EMMA) – over the course of our study to-date. We highlight necessary resources and consider implications for communities or researchers interested in developing such platforms, focusing on PM₂.₅, NO, and NO₂ sensors. Our findings emphasize that lower-cost sensors should be deployed with caution, given financial and resource costs that greatly exceed sensor costs, but that selected community objectives could be supported at lesser cost and community-based participatory research strategies could be used for more wide-ranging goals.

Ammonia (NH3) emission from agricultural sources has contributed significantly to air pollution, soil acidification, water eutrophication, biodiversity loss, and declining human health. Although there are numerous strategies for reducing NH3 emission from agricultural systems, the effectiveness of these measures is highly variable. Furthermore, the integrated assessment of measures to reduce NH3 emission both from livestock production and cropping systems based on animal and crop type is lacking. Therefore, we conducted a global meta-analysis and integrated assessment of measures to reduce NH3 emission from agricultural systems. Most of the studied mitigation strategies were effective in reducing NH3 emission. In the livestock production system, dietary additive, urease inhibitor (UI), manure acidification and deep manure placement have the highest mitigation potential relative to other mitigation strategies, with reduction ranges of 35.1–54.2%, 24.3–68.7%, 88.8–95.0%, and 93.8–99.7%, respectively, relative to the control, while manure storage management could significantly reduce NH3 emission by 70.0–82.1%. In the cropping system, fertilizer source, use of enhanced efficiency fertilizers, and method of field application are most effective for reducingNH3 emission. The use of ammonium nitrate, controlled release fertilizer (CRF), and deep placement of fertilizers could reduce NH3 emission by 88.3, 56.8, and 48.0%, respectively. Choosing a proper fertilizer is critical for decreasing NH3 emission from cropping systems. We conclude that carefully planned and adopted strategies suited for local conditions are promising for minimizing NH3 emission from agricultural systems on a global scale, while possible effects of those mitigation measures on the emission of greenhouse gases should be studied in the future.

Previous studies of solid fuel emissions in household stoves focused more on emission measurements of the overall combustion process instead of the dynamic burning rate and its connection to the emissions. This study put forward a measurement system to monitor the dynamic fuel burning rate and emission rate directly, and explored their relationships during different combustion phases. Experiments were conducted using two types of wood charcoal consumed in a small open pan (i.e. fire basin) used commonly for space heating in rural China. The measured real-time CO emission rate (ERCO), fuel burning rate (BRF), and calculated carbon burning rate (BRC) all rose and then subsided as the combustion progressed. The relationships between ERCO and BRF and between ERCO and BRC were different for the two charcoals during a phase with rising carbon content in the combusted fuel (Phase I), likely because moisture evaporation and volatile matter release were the dominant processes and the reaction was complex during this phase. ERCO and BRF or BRC had linear relationships during a phase with stable carbon content in the combusted fuel (Phase II) for the two charcoals, which may be generalized to other solid fuels, because this phase is associated to fixed carbon dominating phase which usually exist during solid fuel combustion. The study presented a novel measurement approach to the combustion properties of solid fuels. The results implied that a complex relationship between the combustion and pollutant emissions existed in Phase I, and presented the possibility of estimating the fuel burning rate based on emission measurements in Phase II, or vice versa.

The removals of arsenic and selenium pollutants are always urgent desires for the water security. In this study, both sorption and catalysis strategies were combined for the effective removals of As(V) and Se(VI) over magnetic graphene oxide sheets (GOs)-oxidized carbon nanotubes (OCNTs) hydrogels. The sorption behavior facilitated the operation of catalysis reactions, meanwhile, the catalytic reduction promoted the release of occupied sorption sites and then restarted a new sorption-catalysis cycle. The synergic effect of sorption and catalysis realized 258.2 mg g⁻¹ for As(V) enrichment capacity on MPG2T1, and ultra-fast sorption and catalysis equilibriums were identified within 9 min. In the case of Se(VI), a moderate enrichment performance was observed to be 46.2 mg g⁻¹. Similarly, the ultra-fast sorption and reduction of Se(VI) were realized within 2 min. In the competition experiments, only SO₄²⁻, SO₃²⁻, and HPO₄²⁻ showed interference for As(V) and Se(VI) removals. These results testified the superiority of the synergy effect of sorption and catalysis, and the feasibility of 3D magnetic GOs-OCNTs hydrogel in practical implementations.

A novel self-assembly method was developed to prepare a γ-Fe₂O₃/graphene oxide (GO) heterogeneous catalyst that showed excellent synergy between photocatalysis and Fenton-like reactions. The γ-Fe₂O₃/GO catalyst prepared on the iron plates demonstrated efficient and reproducible catalytic activities for water treatment. It takes only 80 min to degrade 50 mg L⁻¹ methylene (MB) completely, which is the main non-biodegradable dye in wastewater from the textile industry. The heterogeneous catalyst is stable over a wide range of pH (from 2.0 to 10.2) for MB degradation, and can be easily extracted from solution and repeatedly used with little loss of catalytic activity. The high activity and stability of the catalyst system can be attributed to charge separation between γ-Fe₂O₃ and GO, which could accelerate Fenton-like process and photocatalysis. In addition, the dominant reactive oxidant species responsible for the MB degradation, including the hydroxyl radicals (•OH) and holes (h⁺), were trapped on the surface of the γ-Fe₂O₃/GO composite, as proved by a free-radical quenching experiment. The γ-Fe₂O₃/GO heterogeneous catalyst could potentially provide a solution for removal of non-biodegradable dyes from wastewater in the textile industry.