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Assessment of upper tropospheric HOx sources over the tropical Pacific based on NASA GTE/PEM data: Net effect on HOx and other photochemical parameters

  • Author(s): Crawford, J
  • Davis, D
  • Olson, J
  • Chen, G
  • Liu, S
  • Gregory, G
  • Barrick, J
  • Sachse, G
  • Sandholm, S
  • Heikes, B
  • Singh, H
  • Blake, D
  • et al.
Abstract

Data for the tropical upper troposphere (8-12 km, 20° N-20° S) collected during NASA's Pacific Exploratory Missions have been used to carry out a detailed examination of the photochemical processes controlling HO (OH+HO ). Of particular significance is the availability of measurements of nonmethane hydrocarbons, oxygenated hydrocarbons (i.e., acetone, methanol, and ethanol) and peroxides (i.e., H O and CH OOH). These observations have provided constraints on model calculations permitting an assessment of the potential impact of these species on the levels of HO , CH O , CH O, as well as ozone budget parameters. Sensitivity calculations using a time-dependent photochemical box model show that when constrained by measured values of the above oxygenated species, model estimated HO levels are elevated relative to unconstrained calculations. The impact of constraining these species was found to increase with altitude, reflecting the systematic roll-off in water vapor mixing ratios with altitude. At 11-12 km, overall increases in HO approached a factor of 2 with somewhat larger increases being found for gross and net photochemical production of ozone. While significant, the impact on HO due to peroxides appears to be less than previously estimated. In particular, observations of elevated H O levels may be more influenced by local photochemistry than by convective transport. Issues related to the uncertainty in high-altitude water vapor levels and the possibility of other contributing sources of HO are discussed. Finally, it is noted that the uncertainties in gas kinetic rate coefficients at the low temperatures of the upper troposphere and as well as OH sensor calibrations should be areas of continued investigation. Copyright 1999 by the American Geophysical Union. x 2 2 2 3 x 3 2 2 x x x 2 2 x

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