Diel variations of airborne microbes and antibiotic resistance genes in Response to urban PM2.5 chemical properties during the heating season.

Among the components of fine particulate matter (PM2.5), the contributions of airborne microorganisms and antibiotic resistance genes (ARGs) to health risks have been overlooked. Airborne microbial dynamics exhibit a unique diurnal cycle due to environmental influences. However, the specific roles of PM2.5 chemical properties resulting from fossil fuel combustion in driving circadian fluctuations in microbial populations and ARGs remain unclear. This study explored the interactions between toxic components and microbial communities during the heating period to understand the variations in ARGs. Bacterial and fungal communities showed a higher susceptibility to diel variations in PM2.5 compared to their chemical properties. Mantel tests revealed that chemical properties and microbial community interactions contribute differently to ARG variations, both directly and indirectly, during circadian fluctuations. Our findings highlight that, during the daytime, the enrichment of pathogenic microorganisms and ARGs increases the risk of PM2.5 toxicity. Conversely, during the nighttime, the utilization of water-soluble ions by the fungal community increased, leading to a significant increase in fungal biomass. Notably, Aspergillus exhibited a significant correlation with mobile genetic elements and ARGs, implying that this genus is a crucial driver of airborne ARGs. This study provides novel insights into the interplay between the chemical composition, microbial communities, and ARGs in PM, underscoring the urgent need for a comprehensive understanding of effective air pollution control strategies.

What is the role of interface in the catalytic elimination of multi-carbon air pollutants?

Multi-carbon air pollutants pose serious hazards to the environment and health, especially soot and volatile organic compounds (VOCs). Catalytic oxidation is one of the most effective technologies for eliminating them. The oxidation of soot and most hydrocarbon VOCs begins with C-H (or edge-CH) activation, so this commonality can be targeted to design active sites. Rationally designed interface nanostructures optimize metal-support interactions (MSIs), providing suitable active sites for C-H activation. Meanwhile, the interfacial reactant spillover facilitates the further decomposition of activated intermediates. Thus, rationally exploiting interfacial effects is critical to enhancing catalytic activity. In this review, we analyzed recent advances in the following aspects: I. Understanding of the interface effects and design; II. Optimization of the catalyst-reactant contact, metal-support interface, and MSIs; III. Design of the interfacial composition and perimeter. Based on the analysis of the advances and current status, we provided challenges and opportunities for the rational design of interface nanostructures and interface-related stability. Meanwhile, a critical outlook was given on the interfacial sites of single-atom catalysts (SACs) for specific activation and catalytic selectivity.