Atmospheric volatile organic compounds (VOCs) measurement was carried out using gas chromatography-flame ionization detector (GC-FID) technique (Airmo VOCs online analyzer) in a typical urban area in Beijing from April 2014 to January 2015. Ambient levels, variation characteristics and influential factors contributing to the formation of near-ground-ozone and secondary organic aerosols as well as health risk assessment of VOCs were analyzed. Based on these analyses, the important VOC species that should be given more attention for pollution control were identified and the source apportionment of VOCs was made. Suggestions for VOCs pollution control countermeasures were put forward. The annual average concentration of 84 VOCs was 119 μg·m⁻³ and the hourly mean concentration was 9.11–567 μg·m⁻³. Ambient level of VOCs in Beijing has been alleviated in recent years, but is still severe compared to some other cities. VOCs with the largest proportion were alkanes in spring and halogenated hydrocarbons in summer, autumn and winter. The variation of 84 VOCs concentrations was consistent with that of the ambient air quality index, indicating that VOCs had a strong influence on ambient air quality. Influenced by the concentration and activity of VOCs, the largest contribution to ozone formation potential and secondary organic aerosol formation potential came from alkenes and aromatic hydrocarbons, respectively. Five VOCs species such as benzene pose carcinogenic risk to exposed populations. Contrary to some previous studies, benzene was found to have potential cancer risk in some urban areas in China. The main sources of VOCs in the study area were vehicle exhaust, solvent usage, and industrial processes. In order to improve air quality in Beijing and reduce the infection rate of air pollutant related diseases, it is necessary to strengthen the control the emission of VOCs from those three sources.

Environmental context: Both inorganic and organic arsenic species are toxic to the environment when labile. The Diffusive Gradients in Thin Films technique, equipped with ferrihydrite binding gel enables measurement of labile arsenic species from water and soil solutions. This study indicated that labile arsenic species are quantitatively adsorbed to the gel, and that they are stable for up to 2 weeks following deployment. Arsenic speciation was determined in the solution extracted from a ferrihydrite binding gel layer in a DGT unit (FB-DGT) deployed in water using coupled high-performance liquid chromatography and hydride generation atomic fluorescence spectrometry (HPLC-HG-AFS). However, the extent of change in arsenic speciation during the extraction process is unknown. By identifying the arsenic species in the FB-DGT gel directly, using X-ray absorption near edge spectroscopy (XANES) fitting with model arsenic compounds, we obtain a better understanding of the ability of FB-DGT to measure labile arsenic species in solution. The results presented herein confirm that FB-DGT accumulated labile inorganic and methylated arsenic species. Arsenic species bound to the FB-DGT gel were stable for up to 2 weeks following deployment. However, caution should be applied when interpreting the proportion of As species measured by HPLC-HG-AFS in solution extracted from FB-DGT because the distribution of arsenic species in extracted solutions was found to be modified by the extraction process. Some (~20 %) of arsenate was converted into arsenite, and a significant amount (~25 %) of dimethylarsinic acid (DMAsV) was converted into monomethylarsonic acid (MMAsV) or arsenate (AsV). Only inorganic arsenite (iAsIII) was stable during the extraction process. These findings suggested that, based on the XANES measurement, although As species were quantitatively accumulated in the FB-DGT gel, the FB-DGT technique was still unsuitable for studying As speciation. This is because changes in arsenic speciation were observed to occur during gel extraction, prior to HPLC-HG-AFS measurement, and because the XANES technique is available for routine measurements.

Emerging research indicates that ground-level ozone (O₃) has become a leading contributor to air quality concerns in many Chinese cities, with the Yangtze River Delta (YRD) region facing particular challenges. This study investigated the characterization of air pollutants in Wujiang, which is located within the YRD demonstration zone, during the warm season (April–September) of 2022. The contributions of emission and meteorology to O₃ were identified, the O₃-NO_X-VOC sensitivities were discussed, and the VOC sources and their contributions to O₃ formation were analyzed. A random forest model revealed that the high O₃ concentration was mainly caused by a combination of increased emission intensity due to the resumption of work and production after the COVID-19 pandemic, along with adverse meteorological conditions. The results revealed more than 92% of the pollution days were related to O₃ during the warm season, and the impact of O₃ precursor emissions was slightly greater than that of the meteorological conditions. O₃ formation was in the VOC-limited regime, and emission reduction strategies targeting VOCs, particularly aromatics such as toluene and xylene, have been identified as the most effective approach for mitigating O₃ pollution. Changes in O₃-NO_X-VOC sensitivity were also observed from the VOC-limited regime to the transitional regime, which was primarily driven by variations in the NO_X concentrations. The VOC source analysis results showed that the contributions of gasoline vehicle exhaust and diesel engine exhaust (mobile source emissions) were significantly greater than those of the other sources, accounting for 20.8% and 16.5% of the total VOC emissions, respectively. This study highlights the crucial role of mobile source emission control in mitigating O₃ pollution. Furthermore, prioritizing the control of VOC emission sources with minimal NO_X contributions is highly recommended within the VOC-limited regime.

Tuberculosis (TB) remains a leading global health threat, with the rise of drug-resistant (DR-TB) strains posing a significant impediment to disease control. An increasingly recognized and complex challenge is heteroresistance, the coexistence of drug-susceptible and drug-resistant Mycobacterium tuberculosis subpopulations within a single host. This phenomenon acts as a crucial intermediate in the evolution toward fixed resistance and has been strongly associated with poor clinical prognoses, including treatment failure and the amplification of resistance. This review synthesizes the current state of knowledge regarding the screening methodologies for and the adverse outcomes associated with TB heteroresistance. The diagnostic gap creates a substantial risk of misclassifying patients and prescribing functionally inadequate therapeutic regimens. Further, the presence of heteroresistance significantly correlates with diminished treatment efficacy and an increased likelihood of unfavorable outcomes. Importantly, the precise clinical significance of low-frequency resistant variants remains a critical area of investigation, with an urgent need to establish evidence-based thresholds to guide therapy. Future research must focus on defining clinically relevant heteroresistance thresholds, standardizing advanced diagnostic platforms, and further elucidating the biological mechanisms that govern the emergence and persistence of these heteroresistance bacterial populations to ultimately improve patient outcomes and curb the spread of drug-resistant tuberculosis.

This study developed a gas chromatography–tandem mass spectrometry (GC-MS/MS) method for detecting dinotefuran residues in fruits and vegetables. The modified extraction procedure employed solvent conversion for GC-MS/MS compatibility, achieving a linear range of 0.001–2.0 mg/kg (r² > 0.999), a LOD of 0.003 mg/kg, and a LOQ of 0.01 mg/kg. Recovery rates ranged from 88.2% to 104.5% (RSD: 3.5–5.8%). The analysis of 18 commercial samples from Weifang, China, revealed the highest residues in nectarines (0.12 mg/kg) and lowest residues in cucumbers (0.02 mg/kg), with the dietary exposure risk assessment indicating hazard quotients well below safety thresholds. The literature review showed that dinotefuran has a shorter soil half-life (10–30 days) than most neonicotinoids, a low adsorption coefficient (Koc 30–50), high leaching potential, and significant toxicity to pollinators (LD₅₀ = 0.023 μg/bee). The validated method provides reliable detection across diverse matrices, while the environmental behavior analysis highlights the need for the careful management of dinotefuran applications to minimize ecological impacts despite its favorable degradation profile compared to other neonicotinoids.