TY - JOUR
T1 - Nocturnal Ozone Enhancement Reshapes Urban Fine-Particle Chemistry
AU - Yang, Ke
AU - Zhang, Antai
AU - Zeng, Yaling
AU - Yang, Xin
AU - Xing, Chunbo
AU - Cai, Baohua
AU - Shi, Shao
AU - Yuan, Xin
AU - Zhang, Baixin
AU - Zhai, Jinghao
AU - Zhang, Yin
AU - Hou, Ziting
AU - Shen, Zhenxing
AU - Fu, Tzung May
AU - Zhu, Lei
AU - Shen, Huizhong
AU - Ye, Jianhuai
AU - Wang, Chen
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/6/9
Y1 - 2026/6/9
N2 - Nocturnal ozone enhancement (NOE) extends ozone exposure and may exacerbate risks to human health and ecosystem, yet its impacts on fine-particle matter (PM2.5) chemistry remain poorly constrained. We characterized NOE occurrence across four Chinese megacities (Beijing, Shanghai, Guangzhou, and Shenzhen; 2019–2024) and integrated year-long in-field observations in Shenzhen with nontarget ultrahigh-resolution mass spectrometry and statistical analysis to examine NOE events. Here we show that NOE events in a megacity occurred with an average frequency ranging from 9.82 to12.37%. In Shenzhen, NOE events were associated with stronger mixing signatures and elevated nocturnal oxidizing capacity. Secondary aerosol components were enhanced and dominated the PM2.5 response, as indicated by a more than 2-fold increase in the nitrate oxidation ratio, higher organic carbon/elemental carbon(OC/EC) ratio, and elevated particle oxidative potential. Importantly, these oxidizing and aerosol enhancements persisted into the subsequent daytime. At the molecular level, water-soluble organic matter shifted toward highly oxidized, carboxyl-bearing CHO species, and we identified 11 NOE-characteristic compounds dominated by CHO formulas. These results link nocturnal ozone dynamics to particle chemistry and highlight nighttime ozone as a lever for joint control of urban O3 and PM2.5.
AB - Nocturnal ozone enhancement (NOE) extends ozone exposure and may exacerbate risks to human health and ecosystem, yet its impacts on fine-particle matter (PM2.5) chemistry remain poorly constrained. We characterized NOE occurrence across four Chinese megacities (Beijing, Shanghai, Guangzhou, and Shenzhen; 2019–2024) and integrated year-long in-field observations in Shenzhen with nontarget ultrahigh-resolution mass spectrometry and statistical analysis to examine NOE events. Here we show that NOE events in a megacity occurred with an average frequency ranging from 9.82 to12.37%. In Shenzhen, NOE events were associated with stronger mixing signatures and elevated nocturnal oxidizing capacity. Secondary aerosol components were enhanced and dominated the PM2.5 response, as indicated by a more than 2-fold increase in the nitrate oxidation ratio, higher organic carbon/elemental carbon(OC/EC) ratio, and elevated particle oxidative potential. Importantly, these oxidizing and aerosol enhancements persisted into the subsequent daytime. At the molecular level, water-soluble organic matter shifted toward highly oxidized, carboxyl-bearing CHO species, and we identified 11 NOE-characteristic compounds dominated by CHO formulas. These results link nocturnal ozone dynamics to particle chemistry and highlight nighttime ozone as a lever for joint control of urban O3 and PM2.5.
KW - nocturnal ozone enhancement
KW - PMchemical composition
KW - secondary aerosol formation
KW - urban nighttime chemistry
UR - https://www.scopus.com/pages/publications/105041266961
U2 - 10.1021/acs.est.6c04333
DO - 10.1021/acs.est.6c04333
M3 - 文章
C2 - 42118138
AN - SCOPUS:105041266961
SN - 0013-936X
VL - 60
SP - 16068
EP - 16079
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 22
ER -