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A study of ozone in the Colorado mountains
Authors:F C Fehsenfeld  M J Bollinger  S C Liu  D D Parrish  M McFarland  M Trainer  D Kley  P C Murphy  D L Albritton  D H Lenschow
Institution:(1) Present address: Aeronomy Laboratory, Environmental Research Laboratories, National Oceanic and Atmospheric Administration, 80303 Boulder, CO, U.S.A.;(2) Cooperative Institute for Research in Environmental Sciences, University of Colorado/NOAA, 80309 Boulder, CO, U.S.A.;(3) Department of Chemistry, University of Colorado, 80309 CO, Boulder, U.S.A.;(4) Rocky Mountain Analytical Laboratory, 5530 Marshall, 80002 CO, Denver, U.S.A.;(5) Department of Chemistry, Metropolitan State College, 80204 Denver, CO, U.S.A.;(6) Institut für Chemie 3: Atmosphärische Chemie, Kernforschungsanlage Jülich, Postfach 1913, D-5170 Jülich, Federal Republic of Germany;(7) National Center for Atmospheric Research, 80307 Boulder, CO, U.S.A.
Abstract:The seasonal and diurnal variations of ozone mixing ratios have been observed at Niwot Ridge. Colorado. The ozone mixing ratios have been correlated with the NO x (NO+NO2) mixing ratios measured concurrently at the site. The seasonal and diurnal variations in O3 can be reasonably well understood by considering photochemistry and transport. In the winter there is no apparent systematic diurnal variation in the O3 mixing ratio because there is little diurnal change of transport and a slow photochemistry. In the summer, the O3 levels at the site are suppressed at night due to the presence of a nocturnal inversion layer that isolated ozone near the surface, where it is destroyed. Ozone is observed to increase in the summer during the day. The increases in ozone correlate with increasing NO x levels, as well as with the levels of other compounds of anthropogenic origin. We interpret this correlation as in-situ or in-transit photochemical production of ozone from these precursors that are transported to our site. The levels of ozone recorded approach 100 ppbv at NO x mixing ratios of approximately 3 ppbv. Calculations made using a simple clean tropospheric chemical model are consistent with the NO x -related trend observed for the daytime ozone mixing ratio. However, the chemistry, which does not include nonmethane hydrocarbon photochemistry, underestimates the observed O3 production.
Keywords:Tropospheric ozone  ozone precursors  photochemistry  nitrogen oxides  rural ozone
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