4.7 Article

Inferring vertical variability and diurnal evolution of O3 formation sensitivity based on the vertical distribution of summertime HCHO and NO2 in Guangzhou, China

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 827, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.154045

关键词

Ozone formation sensitivity; Formaldehyde; Nitrogen oxides; MAX-DOAS; TROPOMI

资金

  1. Natural Science Fund of Jiangsu Province [BK20210485]
  2. China Postdoctoral Science Foundation [2021M701453]
  3. Research Fund Program of Guangdong-Hongkong-Macau Joint Laboratory of Collaborative Innovation for Environmental Quality [GHML2021-102]
  4. Presidential Foundation of the Hefei Institutes of Physical Science, CAS, China [YZJJ2021QN06]
  5. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA23020301]
  6. National Natural Science Foundation of China [41977184, 41941011, 51778596]
  7. Major Projects of High Resolution Earth Observation Systems of National Science and Technology [202104i07020002]
  8. Youth Innovation Promotion Association of CAS [05-Y30B01-9001-19/20-3]
  9. Young Talent Project of the Center for Excellence in Regional Atmospheric Environment, CAS [2021443]
  10. [CERAE202004]

向作者/读者索取更多资源

In Guangzhou, China, it was found that vertical profiles of formaldehyde and aerosol are more sensitive to O3 pollution in the late afternoon and at noon at higher altitudes, while the vertical profile of nitrogen dioxide exhibits an exponential decreasing shape, indicating lower sensitivity to O3 pollution.
The vertical distributions of formaldehyde (HCHO) and nitrogen dioxide (NO2) and their indicative roles in ozone (O-3) sensitivity are important for designing O-3 mitigation strategies. Using hyperspectral remote sensing observations, tropospheric vertical profiles of HCHO, NO2, and aerosol extinction were investigated in Guangzhou, China from July to September 2019. On both O3 non-exceedance and polluted days, the HCHO and aerosol vertical profiles exhibited similar Gaussian shapes, but the NO2 profile exhibited an exponential decreasing shape. HCHO and aerosol were especially sensitive to O-3 pollution, with higher values generally occurring at approximately noon and late afternoon at higher altitudes. We attempted to study the diurnal evolution of O-3 sensitivity at different altitudes based on the HCHO to NO2 ratio (FNR) vertical profile. The FNR thresholds marking the transition regime (2.5 < FNR < 4.0) were derived from the relationship between the increase in O-3 (delta O-3) and FNR. Our results showed that O-3 sensitivity tends to be VOC-limited both at lower (below approximately 0.4 km) and higher (above approximately 1.8 km) altitudes throughout the daytime. In the middle altitudes, the photochemical formation of O-3 was mainly in the transition/NOx-limited regime in the morning and afternoon but in the VOC-limited regime at noontime. The relationship between TROPOMI column FNR and near-surface O-3 sensitivity was further investigated. Compared with the MAX-DOAS near-surface FNR, slightly higher values of column FNR would increase the number of days classified as transition regimes, which was mainly caused by the inhomogeneous vertical distribution of HCHO and NO2 in the lower troposphere. This study provides an improved understanding of vertical variability and diurnal evolution of O-3 formation sensitivity.

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