Atmospheric Chemistry Signatures of an Equatorially Symmetric Matsuno–Gill Circulation Pattern

Matsuno–Gill circulations have been widely studied in tropical meteorology, but their impact on stratospheric chemistry has seldom been explicitly evaluated. This study demonstrates that, in a model nudged to reanalysis, anticyclonic Rossby wave gyres that form near the tropopause as a result of equatorially symmetric heating in the troposphere provide a dynamical mechanism to influence tropical and subtropical atmospheric chemistry during near-equinox months. The anticyclonic flow entrains extratropical air from higher latitudes into the deep tropics of both hemispheres and induces cooling in the already cold upper-troposphere/lower-stratosphere (UTLS) region. Both of these aspects of the circulation allow heterogeneous chlorine activation on sulfuric acid aerosols to proceed rapidly, primarily via the HCl + ClONO2 reaction. Precipitation rates and heating rates from reanalysis are shown to be consistent with these heating and circulation response patterns in the months of interest. This study analyzes specified dynamics simulations from the Whole Atmosphere Community Climate Model (SD-WACCM) with and without tropical heterogeneous chemistry to demonstrate that these circulations influence substantially the distributions of, for example, NO2 and ClO in the UTLS tropics and subtropics of both hemispheres. This provides a previously unrecognized dynamical influence on the spatial structures of atmospheric composition changes in the UTLS during near-equinox months.

New Connections Between Tropical Dynamics and Lower Stratospheric Chemistry

<p>Matsuno-Gill circulations arising from tropospheric heating have been widely studied in tropical meteorology, but their impact on stratospheric chemistry and composition has seldom been explicitly evaluated. We show how anticyclonic Rossby wave gyres that form near the tropopause due to equatorially-symmetric Matsuno-Gill heating in near-equinox months provide a mechanism to influence chemistry in the tropical and subtropical upper-troposphere/lower-stratosphere (UTLS). This heating both generates anticyclonic flow in the lower stratosphere, which entrains extratropical air from higher latitudes deeper into the tropics of both hemispheres, and induces cooling in this already cold region. These two aspects of the circulation combine to allow heterogeneous chlorine activation on the surface of sulfuric acid aerosols to proceed rapidly. We use reanalysis to show that these Matsuno-Gill heating and wind response patterns are present in the months of interest, and then demonstrate that, in the WACCM model, they can substantially influence the distributions of species related to chlorine activation such as ClO and NO<sub>2</sub>. This provides a potential target for future tropical UTLS observation campaigns, and demonstrates a previously unrecognized mechanism in near-equinox months for dynamical influences on the spatial structures of atmospheric composition changes in this region. </p>

On the consistency of HNO₃ and NO₂ in the Aleutian High region from the Nimbus 7 LIMS Version 6 data set

This study uses photochemical calculations along kinematic trajectories in conjunction with Limb Infrared Monitor of the Stratosphere (LIMS) observations to examine the changes in HNO3 and NO2 near 30 hPa in the region of the Aleutian High (AH) during the minor warming event of January 1979. An earlier analysis of Version 5 (V5) LIMS data indicated increases in HNO3 without a corresponding decrease in NO2 in that region and a quasi-wave 2 signature in the zonal distribution of HNO3, unlike the wave 1 signal in ozone and other tracers. Version 6 (V6) LIMS also shows an increase of HNO3 in that region, but NO2 is smaller than from V5. The focus here is to convey that V6 HNO3 and NO2 are of good quality, as shown by a re-examination of their mutual changes in the AH region. Photochemical model calculations initialized with LIMS V6 data show increases of about 2 ppbv in HNO3 over 10 days along trajectories terminating in the AH region on 28 January. Those increases are mainly a result of the nighttime heterogeneous conversion of N2O5 on background stratospheric sulfuric acid aerosols. Changes in the composition of the air parcels depend on the extent of exposure to sunlight and, hence, on the dynamically controlled history of the trajectories. Trajectories that begin in low latitudes and traverse to across the North Pole in a short time lead to the low HNO3 in the region separating the anticyclone from the polar vortex, both of which contain higher HNO3. These findings help to explain the observed seasonal evolution and areal extent of both species. V6 HNO3 and NO2 are suitable, within their errors, for the validation of stratospheric chemistry–climate models.

On the consistency of HNO₃ and NO₂ in the Aleutian High reigon from the Nimbus 7 LIMS version 6 dataset

This study uses photochemical calculations along kinematic trajectories in conjunction with Limb Infrared Monitor of the Stratosphere (LIMS) observations to examine the changes in HNO3 and NO2 near 30 hPa in the region of the Aleutian High (AH) during the minor warming event of January 1979. An earlier analysis of Version 5 (V5) LIMS data indicated increases in HNO3 without a corresponding decrease in NO2 in that region and a wave-2 signature in the zonal distribution of HNO3, unlike the wave-1 signal in ozone and other tracers. Version 6 (V6) LIMS also shows an increase of HNO3 in that region, but NO2 is smaller than from V5. The focus here is to convey that both V6 HNO3 and NO2 are of better quality than from V5, as shown here by a re-examination of their mutual changes in the AH region. Photochemical model calculations initialized with LIMS V6 data show increases of about 2 ppbv in HNO3 over 10 days along trajectories terminating in the AH region on 28 January. Those increases are mainly a result of the nighttime heterogeneous conversion of N2O5 on background stratospheric sulfuric acid aerosols. Changes in the composition of the air parcels depend on the extent of exposure to sunlight and, hence, on the dynamically controlled history of the trajectories. Trajectories that begin in low latitudes and traverse to across the Pole in a short time lead to the low HNO3 in the region separating the anticyclone from the polar vortex, both of which contain higher HNO3. These findings help to explain the observed seasonal evolution and areal extent of both species. V6 HNO3 and NO2 are suitable, within their errors, for the validation of stratospheric chemistry/climate models.