338 research outputs found

    Trajectory model simulations of ozone (O<sub>3</sub>) and carbon monoxide (CO) in the lower stratosphere

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    A domain-filling, forward trajectory model originally developed for simulating stratospheric water vapor is used to simulate ozone (O3) and carbon monoxide (CO) in the lower stratosphere. Trajectories are initialized in the upper troposphere, and the circulation is based on reanalysis wind fields. In addition, chemical production and loss rates along trajectories are included using calculations from the Whole Atmosphere Community Climate Model (WACCM). The trajectory model results show good overall agreement with satellite observations from the Aura Microwave Limb Sounder (MLS) and the Atmospheric Chemistry Experiment Fourier Transform Spectrometer (ACE-FTS) in terms of spatial structure and seasonal variability. The trajectory model results also agree well with the Eulerian WACCM simulations. Analysis of the simulated tracers shows that seasonal variations in tropical upwelling exerts strong influence on O3 and CO in the tropical lower stratosphere, and the coupled seasonal cycles provide a useful test of the transport simulations. Interannual variations in the tracers are also closely coupled to changes in upwelling, and the trajectory model can accurately capture and explain observed changes during 2005–2011. This demonstrates the importance of variability in tropical upwelling in forcing chemical changes in the tropical lower stratosphere

    Trajectory model simulations of ozone (O 3) and carbon monoxide (CO) in the lower stratosphere

    Get PDF
    A domain-filling, forward trajectory model originally developed for simulating stratospheric water vapor is used to simulate ozone (O3) and carbon monoxide (CO) in the lower stratosphere. Trajectories are initialized in the upper troposphere, and the circulation is based on reanalysis wind fields. In addition, chemical production and loss rates along trajectories are included using calculations from the Whole Atmosphere Community Climate Model (WACCM). The trajectory model results show good overall agreement with satellite observations from the Aura Microwave Limb Sounder (MLS) and the Atmospheric Chemistry Experiment Fourier Transform Spectrometer (ACE-FTS) in terms of spatial structure and seasonal variability. The trajectory model results also agree well with the Eulerian WACCM simulations. Analysis of the simulated tracers shows that seasonal variations in tropical upwelling exerts strong influence on O3 and CO in the tropical lower stratosphere, and the coupled seasonal cycles provide a useful test of the transport simulations. Interannual variations in the tracers are also closely coupled to changes in upwelling, and the trajectory model can accurately capture and explain observed changes during 2005–2011. This demonstrates the importance of variability in tropical upwelling in forcing chemical changes in the tropical lower stratosphere

    Bulk Properties of Isentropic Mixing into the Tropics in the Lower Stratosphere

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    Timescales for mixing of midlatitude air into the tropical lower stratosphere are deduced from observations of long-lived tracers N2O and CCl3F. Bulk mixing between tropical and midlatitude regions is assumed to be isentropic and relatively slow compared with local mixing within each region. The mean value of the mixing timescale ranges from 12 to 18 months near 20 km. There is a tendency for shorter mixing times at higher and lower altitudes, although vertical profiles of mixing cannot be definitively established by the data. A more robust quantity is given by the fraction of midlatitude air entrained into the tropical upwelling region. Implied mixing fractions exceed 50% above 22 km

    The distribution of hydrogen, nitrogen, and chlorine radicals in the lower stratosphere: Implications for changes in O_3 due to emission of NO_y from supersonic aircraft

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    In situ measurements of hydrogen, nitrogen, and chlorine radicals obtained in the lower stratosphere during SPADE are compared to results from a photochemical model that assimilates measurements of radical precursors and environmental conditions. Models allowing for heterogeneous hydrolysis of N_2O_5 agree well with measured concentrations of NO and ClO, but concentrations of HO_2 and OH are underestimated by 10 to 25%, concentrations of NO_2 are overestimated by 10 to 30%, and concentrations of HCl are overestimated by a factor of 2. Discrepancies for [OH] and [HO_2] are reduced if we allow for higher yields of O(^1D) from O_3 photolysis and for heterogeneous production of HNO_2. The data suggest more efficient catalytic removal of O_3 by hydrogen and halogen radicals relative to nitrogen oxide radicals than predicted by models using recommended rates and cross sections. Increases in [O_3] in the lower stratosphere may be larger in response to inputs of NO_y from supersonic aircraft than estimated by current assessment models

    The diurnal variation of hydrogen, nitrogen, and chlorine radicals: implications for the heterogeneous production of HNO_2

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    In situ measurements of hydrogen, nitrogen, and chlorine radicals obtained through sunrise and sunset in the lower stratosphere during SPADE are compared to results from a photochemical model constrained by observed concentrations of radical precursors and environmental conditions. Models allowing for heterogeneous hydrolysis of N_(2)O_(5) on sulfate aerosols agree with measured concentrations of NO, NO_(2), and ClO throughout the day, but fail to account for high concentrations of OH and HO_(2) observed near sunrise and sunset. The morning burst of [OH] and [HO_(2)] coincides with the rise of [NO] from photolysis of NO_(2), suggesting a new source of HO_(x) that photolyzes in the near UV (350 to 400 nm) spectral region. A model that allows for the heterogeneous production of HNO_(2) results in an excellent simulation of the diurnal variations of [OH] and [HO_(2)]
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