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Major influence of BrO on the NOx and nitrate budgets in the Arctic spring, inferred from Δ17O(NO3-) measurements during ozone depletion events

  • S. Morin
  • , J. Savarino
  • , S. Bekki
  • , A. Cavender
  • , P. B. Shepson
  • , J. W. Bottenheim
  • CNRS
  • Purdue University
  • Environment and Climate Change Canada

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

The triple oxygen isotopic composition of atmospheric inorganic nitrate was measured in samples collected in the Arctic in springtime at Alert, Nunavut and Barrow, Alaska. The isotope anomaly of nitrate (?17O ≤ ? 17O 0.52?18O) was used to probe the influence of ozone (O3), bromine oxide (BrO), and peroxy radicals (RO2) in the oxidation of NO to NO2, and to identify the dominant pathway that leads to the production of atmospheric nitrate. Isotopic measurements confirm that the hydrolysis of bromine nitrate (BrONO2) is a major source of nitrate in the context of ozone depletion events (ODEs), when brominated compounds primarily originating from sea salt catalytically destroy boundary layer ozone. They also show a case when BrO is the main oxidant of NO into NO2.

Original languageEnglish
Pages (from-to)238-241
Number of pages4
JournalEnvironmental Chemistry
Volume4
Issue number4
DOIs
StatePublished - 2007

Keywords

  • Atmospheric chemistry
  • Halogen compounds
  • Isotopes
  • Nitrates
  • Ozone depletion events.

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