Emissions reductions in upwind areas can influence the PM₂.₅ concentrations in downwind areas via long-range transport. However, few studies have assessed the impact of upwind PM₂.₅ precursor controls on changes in downwind PM₂.₅ concentrations. In this study, we analyzed the overall impact of PM₂.₅ precursor emission controls in upwind areas on PM₂.₅ in downwind areas with two types of impacts: “direct impact” and “cross impact.” The former refers to PM₂.₅ changes in downwind areas due to the transported PM₂.₅ itself, whereas the latter represents PM₂.₅ changes due to reactions between the transported gaseous precursors and intermediates (i.e., HNO₃) originating from upwind areas and locally emitted precursors (i.e. NH₃) in the downwind areas. As a case study, we performed air quality modeling for Northeast Asia for January 15–17, 2016 by setting China and South Korea as the upwind and downwind areas, respectively. To account for potential spatiotemporal variations in NH₃ emissions in downwind areas, we considered two NH₃ conditions. When NOx emissions in China were reduced by 35%, in downwind areas the PM₂.₅ concentrations decreased by 2.2 μg/m³ under NH₃-rich conditions, while PM₂.₅ concentrations increased by 2.3 μg/m³ under NH₃-poor conditions. The direct impact increased by 4.0 μg/m³ in both cases due to upwind NOₓ disbenefit effects. However, the cross impacts led to a PM₂.₅ decrease of 6.2 μg/m³ under NH₃-rich conditions versus a PM₂.₅ increase of 1.7 μg/m³ under NH₃-poor conditions. We noted that PM₂.₅ concentrations in the downwind areas may not improve unless a cross impact outweighs a direct impact. This may be one of the reasons why South Korea PM₂.₅ concentrations have not declined despite efforts by China to reduce their PM₂.₅ precursor emissions.

Perfluoroalkyl acids (PFAAs) are a focus of scientific and regulatory attention nowadays. However, PFAAs dynamics in the environment and the factors that determine wildlife exposure are still not well understood. In this study we examined PFAAs exposure in chicks of a generalist seabird species, the lesser black-backed gull (Larus fuscus), breeding 49 km away of a PFAAs hotspot (a fluorochemical plant in Antwerp, Belgium). In order to study the pathways of PFAAs exposure, we measured how chicks’ PFAAs burden varied with age, sex, and body condition. In addition, we related PFAA concentrations to chicks’ diet using stable isotope signatures. For this purpose, we studied plasma PFAA concentrations in 1-week and 4-week-old gull chicks. Only 4 (PFOS, PFOA, PFDA and PFNA) out of the 13 target PFAA compounds were detected. Measured concentrations of PFOS and PFOA were generally high compared to other seabird species but were highly variable between individuals. Furthermore, our results suggest that maternal transfer plays a significant role in determining chicks’ PFAAs burden, and that there are variable sources of exposure for PFOS and PFOA during post-hatching development. The association between PFOS and specific stable isotopes (i.e. δ¹⁵N and δ¹³C) suggests a higher exposure to PFOS in birds with a predominantly marine diet. We also found that males’ condition was positively associated with PFOS plasmatic concentration, probably due to the indirect effect of being fed a high quality (marine) diet which appears PFOS rich. Yet, exact exposure source(s) for PFOA remain(s) unclear. Given that PFOS concentrations measured in some chicks surpassed the toxicity reference value calculated for top avian predators, continued monitoring of exposure and health of this gull population, and other wildlife populations inhabiting the area, is highly recommended.

Antibiotic resistance genes (ARGs) are emerging contaminants in the environment and have been highlighted as a worldwide environmental and health concern. As important participants in the biogeochemical cycles, mangrove ecosystems are subject to various anthropogenic disturbances, and its microbiota may be affected by various contaminants such as ARGs. This study selected 13 transects of mangrove-covered areas in Hainan, China for sediment sample collection. The abundance and diversity of ARGs and mobile genetic elements (MGEs) were investigated using high-throughput quantitative polymerase chain reaction (HT-qPCR), and high-throughput sequencing was used to study microbial structure and diversity. A total of 179 ARGs belonging to 9 ARG types were detected in the study area, and the detection rates of vanXD and vatE-01 were 100%. The abundance of ARGs was 8.30 × 10⁷–6.88 × 10⁸ copies per g sediment (1.27 × 10⁻²–3.39 × 10⁻² copies per 16S rRNA gene), which was higher than similar studies, and there were differences in the abundance of ARGs in these sampling transects. The multidrug resistance genes (MRGs) accounted for the highest proportion (69.0%), which indicates that the contamination of ARGs in the study area was very complicated. The ARGs significantly positively correlated with MGEs, which showed that the high level of ARGs was related to its self-enhancement. The dominant bacteria at the genus level were Desulfococcus, Clostridium, Rhodoplanes, Bacillus, Vibrio, Enterococcus, Sedimentibacter, Pseudoalteromonas, Paracoccus, Oscillospira, Mariprofundus, Sulfurimonas, Aminobacterium, and Novosphingobium. There was a significant positive correlation between 133 bacterial genera and some ARGs. Chthoniobacter, Flavisolibacter, Formivibrio, Kaistia, Moryella, MSBL3, Perlucidibaca, and Zhouia were the main potential hosts of ARGs in the sediments of Hainan mangrove area, and many of these bacteria are important participants in biogeochemical cycles. The results contribute to our understanding of the distribution and potential hosts of ARGs and provide a scientific basis for the protection and management of Hainan mangrove ecosystem.

While local anthropogenic emission sources contribute largely to deteriorate metro air quality, long range transport can also play a significant role in influencing levels of pollutants, particularly carbon monoxide (CO) that has a relatively long life span. A nationwide lockdown of two months imposed across India amid COVID-19 led to a dramatic decline in major sources of emissions except for household, mainly from cooking. This initially led to declined levels of CO in two of the largest megacities of India, Delhi and Mumbai under stable weather conditions, followed by a distinctly different variability under the influence of prevailing mesoscale circulation. We hereby trace the sources of CO from local emissions to transport pathways and interpret the observed variability in CO using the interactive WRF-Chem model and back trajectory analysis. For this purpose, COVID-19 emission inventory of CO has been estimated. Model results indicate a significant contribution from externally generated CO in Delhi from surrounding regions and an unusual peak on 17th May amid lockdown due to long range transport from the source region of biofuel emissions in central India. However, the oceanic winds played a larger role in keeping CO levels in check in a coastal megacity Mumbai which otherwise has high CO emissions from household sources due to a larger share of urban slums. Keeping track of evolving carbon-intensive pathways can help inform government responses to the COVID-19 pandemic to prioritize controls of emissions sources.

Mycotoxins are increasingly considered as micropollutants in the environment. Fumonisins, as one of the most important mycotoxins, cause potential health threats to humans and animals due to their ubiquitous contamination on cereals, fruit, vegetables and other environmental samples around the world. However, the contribution of fumonisins to the interaction of fungi with plant hosts is not still fully understood. Here, we investigated the effect of fumonisin B1 (FB1) on the infection of Fusarium proliferatum on banana fruit and the underlying mechanisms from the host perspective. Our results found that FB1 treatment increased the aggressiveness of F. proliferatum on banana fruit and inhibited the defense ability of banana fruit via decreasing phenylalanine ammonia lyase (PAL), β-1,3-glucanase (GLU) and chitinase (CHI) activities. Meanwhile, FB1 accelerated cell death, indicated by higher relative conductivity, MDA content and higher transcripts of cell death-related genes. FB1 treatment resulted in higher hydrogen peroxide (H₂O₂) content possibly due to MaRBOHs induction. These consequences accelerated the ROS-dependent cell death, which subsequently result in reduction of disease resistance of banana fruit. Additionally, energy metabolism and MaDORN1s-mediated eATP signaling might involve in FB1-meidiated suppression of banana defense responses. Collectively, results of the current study indicated that FB1 contamination triggered the cell death of banana peel, subsequently instigating the invasion and growth of F. proliferatum on banana fruit. In summary, for the first time, we demonstrated a previously unidentified role of fumonisins as a potential virulence factor of F. proliferatum in modulating fruit defense response, which provides new insight on the biological roles of fumonisins.

Focusing on 27 rare filter-feeding megamouth sharks (Megachasma pelagios) captured as a by-catch of drift gillnet fishery in the Pacific Ocean to the east of Taiwan, this study analyzes the concentrations of 24 elements in their muscle, discusses the bioaccumulation of each element and the correlation between different elements, and assesses the potential health risks of consuming megamouth shark muscle. Among the 24 elements, mean concentrations of Ga, Ag, Li, Bi, Hg, Co, and Cd were relatively low ranging from 10⁻³ to 10⁻¹ mg/kg, those of Pb, Ba, Mn, Ni, As, Cr, B, Sr, Cu, and Zn ranged from 10⁻¹–10¹ mg/kg, and those of Fe, Ca, Al, K, Mg, Ti, and Na were relatively high ranging from 10¹ to 10³ mg/kg. The toxic element content index was most significantly correlated with the concentration of Cu. Hence, this study recommends that the concentration of Cu could be used as an indicator of metal accumulation in megamouth shark muscle. The log bioconcentration factor (BCF) ranged from less than 0 to 7.85 in shark muscle. For elements with a concentration of less than 100 μg/L in seawater, the log BCF was inversely proportional to their concentration in seawater. According to the correlation analysis, the accumulation of elements in muscle of megamouth sharks is primarily affected by the concentrations of dissolved elements in seawater, except that the accumulation of Hg, As, Cu, Ti, Al, and Fe appears to be mainly affected by feeding behaviors. The assessment of the health risk of consuming megamouth shark muscle showed that its total hazard index was greater than 1. This suggests that the long-term or high-frequency consumption of megamouth shark muscle may cause health hazards due to the accumulation of trace elements, particularly those with a large contribution of health risk, including As, Hg, and Cu.

The sorption behavior of phthalate additives in plastic and microplastic litter is an important process controlling the exposure, net health risk and ecotoxicity of these co-occurring pollutants. Plastic crystallinity and particle morphology are hypothesized to be important variables for microplastics sorption behavior, but to date there have been few direct studies to explicitly test for the influence of these parameters. To address this, in this study we explored the sorption of dibutyl phthalate (DBP) as a probe molecule to diverse polyethylene microplastics including irregularly-shaped pure polyethylene microplastics (IPPM), black plastic film microplastics (BPFM), white plastic film microplastics (WPFM), and commercial microspheres (CM), which had crystallinities ranging from 17 to 99%. Sorption kinetics for all materials could be well represented with both a pseudo-first-order (R² = 0.87–0.93) and pseudo-second-order model (R² = 0.87–0.93). Further, sorption was highly linear in the concentration range of 0.5–10 mg L⁻¹, with no greater performance from a linear sorption model (R² = 0.96–0.99) than the non-linear Freundlich or Temkin sorption models. The partition coefficient (Kd) of DBP sorption onto IPPM, BPFM, WPFM and CMs were 1974.55 L kg⁻¹, 1483.85 L kg⁻¹, 1477.45 L kg⁻¹ and 509.37 L kg⁻¹, respectively, showing a significant decrease with increasing crystallinity (r² = 0.98). The particle size of microplastics (27–1000 μm) is, however, an indecisive factor affecting their sorption behavior for DBP in this study. This study provides new insight that crystallinity plays a governing role on the sorption of phthalate from microplastic. This should be considered in future exposure studies and assessments of phthalates from plastics and microplastics.

Plant leaf cuticles play a critical role in the accumulation and transport of atmospheric polycyclic aromatic hydrocarbons (PAHs). The relationship between the distribution and retained amount of PAHs on the leaf cuticles and the leaves micro-zone structures is still unclear. In this study, a confocal microscopic fluorescence spectral analysis (CMFSA) system with a spatial resolution of 200 nm was established as a direct and noninvasive means to determine the microscopic distribution and quantify the retained amount of benzo[a]pyrene (B[a]P) at Aegiceras corniculatum (Ac), Kandelia obovata (Ko) and Avicennia marina (Am) leaf cuticle micro-zones (0.096 mm²). The linear ranges for the established method were 10–1900 ng spot⁻¹ for Ac, 15–1700 ng spot⁻¹ for Ko and 30–1800 ng spot⁻¹ for Am, and the detection limits were 0.06 ng spot⁻¹ for Ac, 0.06 ng spot⁻¹ for Ko and 0.07 ng spot⁻¹ for Am. Notably, B[a]P formed clusters and unevenly distributed at the leaf cuticles. On the adaxial cuticles, B[a]P was mainly accumulated unevenly along the epidermis cell wall, and it was also distinctively distributed in the secretory cells around salt glands for Ac and Am. On the abaxial leaf cuticles, B[a]P was concentrated in the salt glands and stomata apart from being unevenly distributed in the epidermis cell wall. Moreover, the amount of B[a]P retained presented a negative correlation with the polarity of leaf cuticles, which resulted in the amount of B[a]P retained on the adaxial leaf cuticles being significantly higher than that on abaxial leaf cuticles. Our results provide a potential in situ method for investigating the distribution and retained amount of PAHs at plant leaf surface micro-zones, which would contribute to further studying and understanding the mechanism of migration and transformation of PAHs by plant leaves from a microscopic perspective.

The rapid development of China's industrial economy and implementation of air pollution controls have led to great changes in sulfur (S), nitrogen (N) and base cation (BC) deposition in the past three decades. We estimated China's anthropogenic BC emissions and simulated BC deposition from 1985 to 2015 with a five-year interval using a multilayer Eulerian model. Deposition of S and N from 2000 to 2015 with a five-year interval was simulated with the EMEP MSC-W model and the Multi-resolution Emission Inventory of China (MEIC). The critical load (CL) and its exceedance were then calculated to evaluate the potential long-term acidification risks. From 1985 to 2005, the BC deposition in China was estimated to have increased by 16 % and then decreased by 33 % till 2015. S deposition was simulated to increase by 49 % from 2000 to 2005 and then decrease by 44 % in 2015, while N deposition increased by 32 % from 2000 to 2010 with a limited reduction afterward. The maximum CL of S was found to increase in 67 % of mainland China areas from 1985 to 2005 and to decline in 55 % of the areas from 2005 to 2015, attributed largely to the changed BC deposition. Consistent with the progress of national controls on SO₂ and NOX emissions, the CL exceedance of S increased from 2.9 to 4.6 Mt during 2000–2005 and then decreased to 2.5 Mt in 2015, while that of N increased from 0.4 in 2000 to 1.2 Mt in 2010 and then decreased to 1.1 Mt in 2015. The reduced BC deposition due to particle emission controls partially offset the benefit of SO₂ control on acidification risk reduction in the past decade. It demonstrates the need for a comprehensive strategy for multi-pollutant control against soil acidification.

Biogas slurry (BS) and bio-waste hydrothermal carbonization aqueous phase (HP) are nutrient-rich wastewater. To prevent environment contamination, transforming BS and HP into synthetic fertilizers in the agricultural field can potentially realize resource utilization. We hypothesized that acidic HP could neutralize alkaline BS, adjusting floodwater pH from 6.88 to 8.00 and mitigating ammonia (NH₃) volatilization from the paddy soil. In this soil column study, the mixture of BS and HP was applied to paddy soil to substitute 50%, 75%, and 100% to urea. With a low (L) or high (H) ratio of HP, treatments were labeled as BCL50, BCL75, BCL100, BCH50, BCH75, and BCH100. Results showed that microbial byproduct- and fulvic acid-like substance were the main components in BS and HP using 3D-EEM analysis, respectively. Co-application of BS and HP mitigated the NH₃ volatilization by 4.2%–65.5% compared with CKU. BCL100 and BCH100 treatments significantly (P < 0.05) mitigated NH₃ volatilization by 65.5% and 56.8%, which also significantly (P < 0.05) mitigated the yield-scale NH₃ volatilization by 49.6% and 42.3%, compared with CKU. The low NH₄⁺-N concentration and pH value in floodwater were the main reason explained the NH₃ mitigation. Therefore, this study demonstrated that BS and HP co-application can substitute the urea as a valuable N fertilizer in a rational rate and meanwhile mitigate the NH₃ volatilization. This study will provide new ideas for the utilization of BS and HP resources in the context of ammonia mitigation.