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Concentrations of OH and HO2 radicals during NAMBLEX: measurements and steady state analysis

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Author(s)

  • J.D. Lee
  • G.P. Johnson
  • T. Ingham
  • S.C. Smith
  • W.J. Bloss
  • D.E. Heard

Department/unit(s)

Publication details

JournalAtmospheric Chemistry and Physics
DatePublished - Jul 2005
Issue number5
Volume6
Number of pages19
Pages (from-to)1435-1453
Original languageEnglish

Abstract

OH and HO2 concentrations were measured simultaneously at the Mace Head Atmospheric Research Station in the summer of 2002 during the NAMBLEX ( North Atlantic Marine Boundary Layer EXperiment) field campaign. OH was measured by laser-induced fluorescence employing the FAGE ( Fluorescence Assay by Gas Expansion) technique, with a mean daytime detection limit of 2.7 x 10(5) molecule cm(-3) (5 min acquisition period; signal-to-noise ratio = 1). HO2 was detected as OH following its chemical conversion through addition of NO, with a mean detection limit of 4.4 x 10(6) molecule cm(-3). The diurnal variation of OH was measured on 24 days, and that of HO2 on 17 days. The local solar noon OH concentrations ranged between ( 3 8) x 10(6) molecule cm(-3), with a 24 h mean concentration of 9.1 x 10(5) molecule cm(-3). The local solar noon HO2 concentrations were (0.9 - 2.1) x 10(8) molecule cm(-3) (3.5 - 8.2 pptv), with a 24 h mean concentration of 4.2 x 10(7) molecule cm(-3) (1.6 pptv). HO2 radicals in the range (2 - 3) x 10(7) molecule cm(-3) were observed at night. During NAMBLEX, a comprehensive suite of supporting measurements enabled a detailed study of the behaviour of HOx radicals under primarily clean marine conditions. Steady state expressions are used to calculate OH and HO2 concentrations and to evaluate the effect of different free-radical sources and sinks. The diurnally averaged calculated to measured OH ratio was 1.04 +/- 0.36, but the ratio displays a distinct diurnal variation, being less than 1 during the early morning and late afternoon/ evening, and greater than 1 in the middle of the day. For HO2 there was an overprediction, with the agreement between calculated and measured concentrations improved by including reaction with measured IO and BrO radicals and uptake to aerosols. Increasing the concentration of IO radicals included in the calculations to above that measured by a DOAS instrument with an absorption path located mainly over the ocean, reflecting the domination of the inter-tidal region as an iodine source at Mace Head, led to further improvement. The results are compared with previous measurements at Mace Head, and elsewhere in the remote marine boundary layer.

Bibliographical note

© Author(s) 2005. This work is licensed under a Creative Commons License.

    Research areas

  • LASER-INDUCED FLUORESCENCE, MARINE BOUNDARY-LAYER, TROPOSPHERIC OH, RO2 RADICALS, MACE HEAD, FIELD-MEASUREMENTS, OZONE PHOTOLYSIS, PEROXY-RADICALS, SOUTHERN-OCEAN, MODELING OH

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