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Title: Improvements to the WRF-Chem 3.5.1 model for quasi-hemispheric simulations of aerosols and ozone in the Arctic

Journal Article · · Geoscientific Model Development (Online)
 [1]; ORCiD logo [2];  [2]; ORCiD logo [3];  [3];  [3];  [3];  [2]
  1. Inst. Pierre Simon Laplace, Paris (France). Lab. Atmospheres, Environments, Spatial Observations (LATMOS); Total S.A., Paris (France)
  2. Inst. Pierre Simon Laplace, Paris (France). Lab. Atmospheres, Environments, Spatial Observations (LATMOS)
  3. Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

In this study, the WRF-Chem regional model is updated to improve simulated short-lived pollutants (e.g., aerosols, ozone) in the Arctic. Specifically, we include in WRF-Chem 3.5.1 (with SAPRC-99 gas-phase chemistry and MOSAIC aerosols) (1) a correction to the sedimentation of aerosols, (2) dimethyl sulfide (DMS) oceanic emissions and gas-phase chemistry, (3) an improved representation of the dry deposition of trace gases over seasonal snow, and (4) an UV-albedo dependence on snow and ice cover for photolysis calculations. We also (5) correct the representation of surface temperatures over melting ice in the Noah Land Surface Model and (6) couple and further test the recent KF-CuP (Kain–Fritsch + Cumulus Potential) cumulus parameterization that includes the effect of cumulus clouds on aerosols and trace gases. The updated model is used to perform quasi-hemispheric simulations of aerosols and ozone, which are evaluated against surface measurements of black carbon (BC), sulfate, and ozone as well as airborne measurements of BC in the Arctic. The updated model shows significant improvements in terms of seasonal aerosol cycles at the surface and root mean square errors (RMSEs) for surface ozone, aerosols, and BC aloft, compared to the base version of the model and to previous large-scale evaluations of WRF-Chem in the Arctic. These improvements are mostly due to the inclusion of cumulus effects on aerosols and trace gases in KF-CuP (improved RMSE for surface BC and BC profiles, surface sulfate, and surface ozone), the improved surface temperatures over sea ice (surface ozone, BC, and sulfate), and the updated trace gas deposition and UV albedo over snow and ice (improved RMSE and correlation for surface ozone). DMS emissions and chemistry improve surface sulfate at all Arctic sites except Zeppelin, and correcting aerosol sedimentation has little influence on aerosols except in the upper troposphere.

Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (United States); Inst. Pierre Simon Laplace, Paris (France)
Sponsoring Organization:
USDOE Office of Science (SC), Biological and Environmental Research (BER); National Association of Research and Technology (ANRT) (France); French National Center for Scientific Research (CNRS)
Grant/Contract Number:
AC05-76RL01830
OSTI ID:
1430725
Report Number(s):
PNNL-SA-125184
Journal Information:
Geoscientific Model Development (Online), Vol. 10, Issue 10; ISSN 1991-9603
Publisher:
European Geosciences UnionCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 21 works
Citation information provided by
Web of Science

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Cited By (3)

Accuracy of current Arctic springtime water vapour estimates, assessed by Raman lidar
  • Totems, Julien; Chazette, Patrick; Raut, Jean‐Christophe
  • Quarterly Journal of the Royal Meteorological Society, Vol. 145, Issue 720 https://doi.org/10.1002/qj.3492
journal March 2019
Springtime aerosol load as observed from ground-based and airborne lidars over northern Norway journal January 2018
Dimethyl sulfide and its role in aerosol formation and growth in the Arctic summer – a modelling study journal January 2019

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