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Commercial chemicals, such as synthetic musks, are of global concern, but data on their occurrence and spatial distribution in aquatic environments of large scale are scarce. Two sampling campaigns were conducted in the present study to measure freely dissolved synthetic musks in freshwaters across China using passive samplers, along with biological coexposure at selected sites. Polycyclic musks (PCMs) dominated synthetic musks, with a detection frequency of 95%. Higher concentrations of PCMs were observed in densely populated Mid, East, and South China compared to less populated regions, indicating the significance of anthropogenic activities for synthetic musks in water. The concentration ratios of galaxolide (HHCB)/tonalide (AHTN) were significantly higher in low-latitude areas than in high-latitude areas from June to September, suggesting that solar radiation played an important role in the degradation of HHCB/AHTN. Significant correlations were found between dissolved concentrations of HHCB and AHTN and their lipid-normalized concentrations in coexposed fish and clam. The estimated hazard quotients for HHCB and AHTN in freshwater fish consumed by humans were less than 0.01 at all sampling sites except the Yangtze River Basin. These results help to understand the environmental fate and ecological risks of synthetic musks on a large geographical scale.

The negative effects of air pollution, especially fine particulate matter (PM 2.5 , particles with an aerodynamic diameter of ≤2.5 μm), on human health, climate, and ecosystems are causing significant concern. Nevertheless, little is known about the contributions of emerging pollutants such as plastic particles to PM 2.5 due to the lack of continuous measurements and characterization methods for atmospheric plastic particles. Here, we investigated the levels of fine plastic particles (FPPs) in PM 2.5 collected in urban Shanghai at a 2 h resolution by using a novel versatile aerosol concentration enrichment system that concentrates ambient aerosols up to 10-fold. The FPPs were analyzed offline using the combination of spectroscopic and microscopic techniques that distinguished FPPs from other carbon-containing particles. The average FPP concentrations of 5.6 μg/m 3 were observed, and the ratio of FPPs to PM 2.5 was 13.2% in this study. The FPP sources were closely related to anthropogenic activities, which pose a potential threat to ecosystems and human health. Given the dramatic increase in plastic production over the past 70 years, this study calls for better quantification and control of FPP pollution in the atmosphere.

Quantifying the threat that climate change poses to fine particle (PM 2.5 ) pollution is hampered by large uncertainties in the relationship between PM 2.5 and meteorology. To constrain the impact of climate change on PM 2.5 , statistical models are often employed in a different manner than physical-chemical models to reduce the requirement of input data. A majority of statistical models predict PM 2.5 concentration (often log-transformed) as a simple function of meteorology, which could be biased due to the conversion of precursor gases to PM 2.5 . We reduced this bias by developing a unique statistic model where the sum of PM 2.5 and the weighted precursor gases, rather than the PM 2.5 alone, was predicted as a function of meteorology and a proxy of primary emissions, where the input data of PM 10 , CO, O 3 , NO x , and SO 2 were obtained from routine measurements. This modification, without losing the simplicity of statistical models, reduced the mean-square error from 27 to 17% and increased the coefficient of determination from 47 to 67% in the model cross-validation using daily PM 2.5 observations during 2013-2018 for 74 cities over China. We found a previously unrecognized mechanism that synoptic climate change in the past half-century might have increased low quantiles of PM 2.5 more strenuously than the upper quantiles in large cities over China. Climate change during 1971-2018 was projected to increase the annual mean concentration of PM 2.5 at a degree that could be comparable with the toughest-ever clean air policy during 2013-2018 had counteracted it, as inferred from the decline in the daily concentration of carbon monoxide as an inert gas. Our estimate of the impact of climate change on PM 2.5 is higher than previous statistical models, suggesting that aerosol chemistry might play a more important role than previously thought in the interaction between climate change and air pollution. Our result indicated that air quality might degrade if the future synoptic climate change could continue interacting with aerosol chemistry as it had occurred in the past half-century.