Signal Transductions of BEAS-2B Cells in Response to Carcinogenic PM2.5 Exposure Based on a Microfluidic System.

PM2.5 (particulate matter less than 2.5 µm in diameter) is considered as a harmful carcinogen. Determining the precise relationship between the chemical constituents of PM2.5 in the air and cancer progression could aid the treatment of environment related disease and establishing risk reduction strategies. Herein, we used transcriptomics (RNA-seq) and an integrated microfluidic system to identify the global gene expression and differential target proteins expression induced by ambient fine particles collected from the heavy haze in China. The results clearly indicated that cancer related pathways exhibited the strongest dysregulation. The ambient fine particles could be uptaken into the cells by pinocytosis, mainly promoting the PI3K-Akt pathway, FGF/FGFR/MAPK/VEGF signaling, and the JAK-STAT pathway, leading to evading apoptosis, sustained angiogenesis, and cell proliferation, which are the most important hallmarks of cancer. And fine particles also have been demonstrated to create intracellular reactive oxygen species (ROS) and mitochondrial ROS, change intracellular free Ca2+, and induce apoptosis, which are all key players in mediating cancer progression. It was observed by transmission electron microscopy (TEM) that the particles from the haze could enter the mitochondria, resulting in disturbance of the mitochondrial membrane and disruption of the mitochondria, and these particles can even enter inside the nucleus. It was also found in our study of organics (OC, PAHs) and metals (Zn, As, V) that compounds of fine particles were more closely associated with the exacerbation of cancer and secondary aerosols generated by traffic had the largest impact on cancer related signal transductions.

A comprehensive exploration of characteristics and source attribution of carbonaceous aerosols in PM2.5 in an East China megacity.

A total of 84 PM2.5 (fine particulate matter) aerosol samples were collected between October 2020 and August 2021 within an urban site in Hangzhou, an East China megacity. Chemical species, such as organic carbon (OC), elemental carbon (EC), as well as char, soot, and n-alkanes, were analyzed to determine their pollution characteristics and source contributions. The mean yearly concentrations of OC, EC, char, soot, and total n-alkanes (∑n-alkane) were 8.76 ± 3.61 µg/m3, 1.44 ± 0.76 µg/m3, 1.21 ± 0.69 µg/m3, 0.3 ± 0.1 µg/m3, and 24.2 ± 10.6 ng/m3. The OC, EC, and ∑n-alkanes were found in the highest levels during winter and lowest during summer. There were strong correlations between OC and EC in both winter and spring, suggesting similar potential sources for these carbonaceous components in both seasons. There were poor correlations among the target pollutants due to summertime secondary organic carbon formation. Potential source contribution functions analysis showed that local pollution levels in winter and autumn were likely influenced by long-range transportation from the Plain of North China. Source index and positive matrix factorization models provided insights into the complex sources of n-alkanes in Hangzhou. Their major contributors were identified as terrestrial plant releases (32.7%), traffic emissions (28.8%), coal combustion (27.3%), and microbial activity (11.2%). Thus, controlling vehicular emissions and coal burning could be key measures to alleviate n-alkane concentrations in the atmosphere of Hangzhou, as well as other Chinese urban centers.

Chemical composition characteristics and source analysis of PM2.5 in Jiaxing, China: insights into the effect of COVID-19 outbreak.

Jiaxing is a medium-sized city in the Yangtze River Delta (YRD), which showed complex local and surrounding pollution sources. To study the COVID-19 impact on the ambient PM2.5 in Jiaxing, we collected the PM2.5 samples from 2 January to 25 April 2020 and analysed their chemical compositions (including carbon components, water-soluble ions (WSIs), and inorganic elements). The concentration of PM2.5 was 83.13 ± 30.93 µg/m3 before COVID-19 pandemic and then remarkably decreased with COVID-19 outbreak due to the suspension of mobility and industrial activities. Meanwhile, the concentrations of main chemical species (carbon components, water-soluble ions and inorganic elements) of PM2.5 all decreased from period A (2-20 January 2020) to period B (23 January to 10 February 2020). Moreover, Trajectory clustering analysis showed that close-range transport was one of the dominant factors throughout all the periods, except for period D (1-25 April 2020). In addition, the PSCF model indicated that the COVID-19 outbreak resulted in a significant decrease of WPSCF value. This study highlighted the differences in chemical compositions and sources of PM2.5 since COVID-19 pandemic was reported and provided a better understanding of its outbreak on PM2.5.

PM2.5-bound polycyclic aromatic hydrocarbons of a megacity in eastern China: Source apportionment and cancer risk assessment.

Ninety-six fine particulate matter (PM2.5) samples covering four seasons from October 2020 to August 2021 were collected at a 'super' site in Hangzhou, a megacity in eastern China. These samples were analyzed to determine the sources and potential cancer risks to humans of 16 United States Environmental Protection Agency priority polycyclic aromatic hydrocarbons (PAHs). The average concentrations of the PAHs in PM2.5 in autumn, winter, spring, and summer were 8.35 ± 4.90, 27.9 ± 13.6, 8.3 ± 5.97, and 1.05 ± 0.50 ng/m3, respectively, and with an annual average of 11.9 ± 13.2 ng/m3. The source apportionment by positive matrix factorization analysis indicated that, based on the yearly average, the major sources of PAHs were traffic emissions (38.2 %), coal combustion (28.9 %), coke (21.7 %), and volatilization (11.1 %). Strong correlations between high concentrations of carbonaceous aerosols and high-molecular-weight PAHs in winter could be attributed to incomplete combustion. Long-range transport of air from the sea to the southeast resulted in low concentrations of carbonaceous aerosols and low-molecular-weight PAHs in summer. Trajectory clustering and the potential source contribution function both indicated that the Yangtze River Delta was the main source region of PAHs for PM2.5 in Hangzhou in spring and summer. In autumn and winter, it was dominated by long-range transport from northern China. Lifetime lung cancer risk assessment revealed that the PAHs in PM2.5 impose moderate human health risks in Hangzhou due to traffic emissions. The results of this study provide important information for policymakers to establish abatement strategies to reduce PAH emissions in Hangzhou, and perhaps other urban centers across China.

Insights into the characteristics and sources of primary and secondary organic carbon: High time resolution observation in urban Shanghai.

There is growing evidence suggesting that organic aerosols play an important role in the evolution of severe haze episodes. However, long-term investigations of the different characteristics of carbonaceous aerosols during haze and non-haze days are insufficient. In this work, hourly measurements of organic carbon (OC) and elemental carbon (EC) in PM2.5 were conducted in Shanghai, a megacity in Eastern China, over the course of a year from July 2013 to June 2014. Both OC and EC exhibited a bimodal diel pattern and were highly dependent on the wind speed and direction. The concentration-weighted trajectory (CWT) analysis illustrated that primary OC (POC) and EC were largely associated with regional and long-range transport. Secondary OC (SOC) formation was the strongest during the harvest season owing to significant biomass burning emissions from the adjacent Yangtze River Delta and farther agricultural regions. Compared to OC (6.7 µg m-3) and EC (2.0 µg m-3) in the non-haze days, higher levels of both OC (15.6 µg m-3) and EC (7.7 µg m-3) were observed in the haze days as expected, but with lower OC/EC ratios in the haze days (2.4) than in non-haze days (4.6). The proportion of POC and EC in PM2.5 remained relatively constant as a function of PM2.5 mass loadings, while that of SOC significantly decreased on the highly polluted days. It is concluded that the haze pollution in urban Shanghai was influenced more by the primary emissions (POC and EC), while the role of SOC in triggering haze was limited.

First long-term detection of paleo-oceanic signature of dust aerosol at the southern marginal area of the Taklimakan Desert.

We firstly conducted a long-term in-situ field measurement at a marginal area (Hotan) of the southern Taklimakan Desert covering all four seasons. Detailed chemical characterization of dust aerosol over Hotan showed several unconventional features, including (1) ubiquity of high Na+ and Cl- abundances in the Taklimakan dust aerosol and its Cl-/Na+ ratio close to seawater; (2) high Ca content in the Taklimakan dust (7.4~8.0%) which was about two times of that in the natural crust; (3) high abundance of soluble sulfate concentrations and strong correlations between sulfate and Na+ and Cl- as well as typical mineral tracers such as Al and Ca. Our results collectively indicated that the dust aerosol from the Taklimakan Desert was characterized of evident paelo-oceanic signature as the Taklimakan Desert was found as an ocean in the ancient times from the perspective of paleogeology. It was estimated that primary sources dominated the total abundances of sulfate during the dust seasons while previous climate modeling works had seldom considered the cooling effects of sulfate from the Taklimakan Desert.

Mixing of dust with pollution on the transport path of Asian dust--revealed from the aerosol over Yulin, the north edge of Loess Plateau.

Both PM(2.5) and TSP were monitored in the spring from 2006 to 2008 in an intensive ground monitoring network of five sites (Tazhong, Yulin, Duolun, Beijing, and Shanghai) along the pathway of Asian dust storm across China to investigate the mixing of dust with pollution on the pathway of the long-range transport of Asian dust. Mineral was found to be the most loading component of aerosols both in dust event days and non-dust days. The concentrations of those pollution elements, As, Cd, Pb, Zn, and S in aerosol were much higher than their mean abundances in the crust even in dust event days. The high concentration of SO(4)(2-) could be from both sources: one from the transformation of the local emitted SO(2) and the other from the sulfate that existed in primary dust, which was transported to Yulin. Na(+), Ca(2+), and Mg(2+) were mainly from the crustal source, while NO(3)(-) and NH(4)(+) were from the local pollution sources. The mixing of dust with pollution aerosol over Yulin in dust event day was found to be ubiquitous, and the mixing extent could be expressed by the ratio of NO(3)(-)/Al in dust aerosol. The ratio of Ca/Al was used as a tracer to study the dust source. The comparison of the ratios of Ca/Al together with back trajectory analysis indicated that the sources of the dust aerosol that invaded Yulin could be from the northwestern desert in China and Mongolia Gobi.