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Quasi-Lagrangian investigation into dimethyl sulfide oxidation in maritime air using a combination of measurements and model.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

  • J. D. James
  • Roy M. Harrison
  • N. H. Savage
  • A. G. Allen
  • J. L. Grenfell
  • B. J. Allan
  • J. M. C. Plane
  • CN Hewitt
  • B. Davison
  • L. Robertson
<mark>Journal publication date</mark>2000
<mark>Journal</mark>Journal of Geophysical Research: Atmospheres
Issue numberD21
Number of pages14
Pages (from-to)26379-26392
Publication StatusPublished
<mark>Original language</mark>English


Using a combination of field measurement data and a modified photochemical box model, strong evidence is presented to suggest that the rate of daytime oxidation of dimethyl sulfide (DMS) by OH radicals is insufficient to describe the measured conversion. Quasi-Lagrangian measurements were made at two sites in the eastern Atlantic (Research Vessel and Mace Head Research Station, Ireland) as part of the Atmospheric Chemistry Studies in the Oceanic Environment (ACSOE) program. Periods of connected flow between the two sites were identified, air parcel transit times were estimated, and measurements of the main DMS oxidation products (MSA, SO2, and nss-SO4 2−) were compared with model predictions to establish whether the model's chemical mechanism could account for observed changes. The main finding was that during daytime periods with maritime air masses, the model failed to predict a sufficient increase in DMS oxidation products during the estimated transit time. This was despite a tendency to overprediction of the progress of nitrogen chemistry during air mass advection, and independent checks on the model estimates of hydroxyl radical concentrations through measurements. In the light of this, the involvement of halogen species (most probably halogen oxides) or heterogeneous oxidation processes is tentatively suggested as the cause of enhanced daytime DMS oxidation in the marine boundary layer (MBL). Increasing the rate constant for the OH + DMS reaction by a factor of 3.3 (as a crude way of simulating parallel channels of DMS oxidation) permitted model results to reproduce the measurements very much more closely.