A012-0001
Assessing the vertical structure of Arctic aerosols using tethered-balloon-borne measurements

Monday, 7 December 2020
Poster
Hagen Telg, CIRES/University of Colorado/NOAA/GML, Boulder, CO, United States, Jessie Creamean, Colorado State University, Fort Collins, CO, United States, Fan Mei, Pacific Northwest National Laboratory, Richland, WA, United States, Darielle Dexheimer, Sandia National Laboratories, Org 8863, Albuquerque, NM, United States, Gijs de Boer, CIRES/University of Colorado/NOAA/PSL, Boulder, CO, United States, Matthew Shupe, CIRES/University of Colorado/NOAA PSL, Boulder, CO, United States, Amy Solomon, Cooperative Institute for Research in Environmental Sciences, Boulder, CO, United States and Allison C McComiskey, Brookhaven National Laboratory, Upton, NY, United States
Abstract:
The rapidly-warming Arctic is sensitive to perturbations in the surface energy budget, which can be caused by clouds and aerosols. However, the interactions between clouds and aerosols are poorly quantified in the Arctic, in part due to: (1) limited observations of vertical structure of aerosols relative to clouds and (2) ground-based observations often being inadequate for assessing aerosol impacts on cloud formation in the characteristically stratified Arctic atmosphere. Here, we present a novel evaluation of Arctic aerosol vertical distributions using 3 years’ worth of tethered balloon system (TBS) measurements spanning multiple seasons. The TBS was deployed at the U.S. Department of Energy Atmospheric Radiation Measurement program’s facility at Oliktok Point, Alaska. Aerosols were examined in tandem with atmospheric stability and ground-based remote sensing of cloud macrophysical properties to specifically address the representativeness of near-surface aerosols to those at cloud base. Based on a statistical analysis of the TBS profiles, ground-based aerosol number concentrations were unequal to those at cloud base 68% of the time. Intermittent aerosol layers were observed 27% of the time due to poorly mixed below-cloud environments, mostly in the spring, causing a decoupling of the surface from the cloud layer. A uniform distribution of aerosol below cloud was observed 32% of the time due to a well-mixed below-cloud environment, mostly during the fall. The fall was also particularly susceptible to precipitation scavenging affecting total aerosol number concentrations. Results such as these could be used to improve future parameterizations of aerosols and their impacts on Arctic cloud formation and radiative properties.