Effect of Marine and Land Convection on Wet Scavenging of Ozone Precursors Observed During a SEAC4RS Case Study

Abstract

AbstractConvective clouds are important for both the vertical redistribution of tropospheric trace gases and the removal, via microphysical scavenging, of soluble trace gas precursors of ozone. We investigate wet scavenging of formaldehyde (CH2O), hydrogen peroxide (H2O2), and methyl hydrogen peroxide (CH3OOH) in quasi‐marine and land convective storms over Texas, USA observed on 18 September 2013 during the 2013 SEAC4RS campaign. Cloud‐resolving simulations using the Weather Research and Forecasting model with Chemistry (WRF‐Chem) were performed to understand the effect of entrainment, scavenging efficiency (SE), and ice physics processes on these trace gases with varying solubility. While marine and land convection can have distinctly different microphysical properties, we did not find significant differences in the SEs of CH2O, H2O2, or CH3OOH. The SEs of 44%–53% for CH2O and 85%–90% for H2O2 are consistent with our previous studies from SEAC4RS and the 2012 DC3 field experiment storms. Using WRF‐Chem simulations, the ice retention factor (rf) for CH2O was determined to be 0.5–0.9, which is higher than found in previous studies. We show that the CH2O rf is higher in airmass and multicell storms than in severe storms and hypothesize that ice shattering may affect CH2O rf values. The CH3OOH SEs (39%–73%) were higher than expected from Henry's Law equilibrium. While recent studies suggest that CH3OOH measurements have interference due to methane diol, we find that this interference cannot fully explain the higher‐than‐expected CH3OOH SEs determined here and during DC3, suggesting further research is needed to understand CH3OOH vertical redistribution.