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Interpreting Geostationary Environment Monitoring Spectrometer (GEMS) geostationary satellite observations of the diurnal variation in nitrogen dioxide (NO2) over East Asia

  • Laura Hyesung Yang
  • , Daniel J. Jacob
  • , Ruijun Dang
  • , Yujin J. Oak
  • , Haipeng Lin
  • , Jhoon Kim
  • , Shixian Zhai
  • , Nadia K. Colombi
  • , Drew C. Pendergrass
  • , Ellie Beaudry
  • , Viral Shah
  • , Xu Feng
  • , Robert M. Yantosca
  • , Heesung Chong
  • , Junsung Park
  • , Hanlim Lee
  • , Won Jin Lee
  • , Soontae Kim
  • , Eunhye Kim
  • , Katherine R. Travis
  • James H. Crawford, Hong Liao
  • Harvard University
  • Yonsei University
  • The University of Hong Kong
  • NASA Goddard Space Flight Center
  • Science Systems and Applications, Inc.
  • Center for Astrophysics | Harvard & Smithsonian
  • Pukyong National University
  • National Institute of Environmental Research
  • Ajou University
  • NASA Langley Research Center
  • Nanjing University of Information Science & Technology

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Nitrogen oxide radicals (NOx≡ NO+NO2) emitted by fuel combustion are important precursors of ozone and particulate matter pollution, and NO2 itself is harmful to public health. The Geostationary Environment Monitoring Spectrometer (GEMS), launched in space in 2020, now provides hourly daytime observations of NO2 columns over East Asia. This diurnal variation offers unique information on the emission and chemistry of NO2, but it needs to be carefully interpreted. Here we investigate the drivers of the diurnal variation in NO2 observed by GEMS during winter and summer over Beijing and Seoul. We place the GEMS observations in the context of ground-based column observations (Pandora instruments) and GEOS-Chem chemical transport model simulations. We find good agreement between the diurnal variations in NO2 columns in GEMS, Pandora, and GEOS-Chem, and we use GEOS-Chem to interpret these variations. NO2 emissions are 4 times higher in the daytime than at night, driving an accumulation of NO2 over the course of the day, offset by losses from chemistry and transport (horizontal flux divergence). For the urban core, where the Pandora instruments are located, we find that NO2 in winter increases throughout the day due to high daytime emissions and increasing NO2/NOX ratio from entrainment of ozone, partly balanced by loss from transport and with a negligible role of chemistry. In summer, by contrast, chemical loss combined with transport drives a minimum in the NO2 column at 13:00-14:00 local time (LT). Segregation of the GEMS data by wind speed further demonstrates the effect of transport, with NO2 in winter accumulating throughout the day at low winds but flat at high winds. The effect of transport can be minimized in summer by spatially averaging observations over the broader metropolitan scale, under which conditions the diurnal variation in NO2 reflects a dynamic balance between emission and chemical loss.

Original languageEnglish
Pages (from-to)7027-7039
Number of pages13
JournalAtmospheric Chemistry and Physics
Volume24
Issue number12
DOIs
StatePublished - Jun 18 2024
Externally publishedYes

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