The Role of Vegetation in Flash Drought Occurrence - A Sensitivity Study using Community Earth System Model version 2

Author(s):  
Liang Chen ◽  
Trent W. Ford ◽  
Priyanka Yadav

AbstractFlash droughts are noted by their unusually rapid rate of onset or intensification, which makes it difficult to anticipate and prepare for them, thus resulting in severe impacts. Although the development of flash drought can be associated with certain atmospheric conditions, vegetation also plays a role in propagating flash drought. This study examines the climatology of warm season (Mar–Sep) flash drought occurrence in the United States (US) between 1979-2014, and quantifies the possible impacts of vegetation on flash drought based on a set of sensitivity experiments using the Community Earth System Model version 2 (CESM). With atmospheric nudging, CESM well captures historical flash drought. Compared with NASA's Modern-Era Retrospective Analysis for Research and Applications version 2 (MERRA-2) and National Climate Assessment - Land Data Assimilation System (NCA-LDAS), CESM shows agreement on the high flash drought frequency in the Great Plains and southeastern US, but overestimates flash drought occurrence in the Midwest. The vegetation sensitivity experiments suggest that vegetation greening can significantly increase the flash drought frequency in the Great Plains and the western US during the warm seasons through enhanced evapotranspiration. However, flash drought occurrence is not significantly affected by vegetation phenology in the eastern US and Midwest due to weak land-atmosphere coupling. In response to vegetation greening, the extent of flash drought also increases, but the duration of flash drought is not sensitive to greening. This study highlights the importance of vegetation in flash drought development, and provides insights for improving flash drought monitoring and early warning.

2020 ◽  
Author(s):  
Yaman Liu ◽  
Xinyi Dong ◽  
Minghuai Wang ◽  
Louisa K. Emmons ◽  
Yawen Liu ◽  
...  

Abstract. Organic aerosol (OA) has been considered as one of the most important uncertainties in climate modeling due to the complexity in presenting its chemical production and depletion mechanisms. To better understand the capability of climate models and probe into the associated uncertainties in simulating OA, we evaluate the Community Earth System Model version 2.1 (CESM2.1) configured with the Community Atmosphere Model version 6 (CAM6) with comprehensive tropospheric and stratospheric chemistry representation (CAM6-Chem), through a long-term simulation (1988–2019) with observations collected from multiple datasets in the United States. We find that CESM generally reproduces the inter-annual variation and seasonal cycle of OA mass concentration at surface layer with correlation of 0.40 as compared to ground observations, and systematically overestimates (69 %) in summer and underestimates (−19 %) in winter. Through a series of sensitivity simulations, we reveal that modeling bias is primarily related to the dominant fraction of monoterpene-formed secondary organic aerosol (SOA), and a strong positive correlation of 0.67 is found between monoterpene emission and modeling bias in eastern US during summer. In terms of vertical profile, the model prominently underestimates OA and monoterpene concentrations by 37–99 % and 82–99 % respectively in the upper air (> 500 m) as validated against aircraft observations. Our study suggests that the current Volatility Basis Set (VBS) scheme applied in CESM might be parameterized with too high monoterpene SOA yields which subsequently result in strong SOA production near emission source area. We also find that the model has difficulty in reproducing the decreasing trend of surface OA in southeast US, probably because of employing pure gas VBS to represent isoprene SOA which is in reality mainly formed through multiphase chemistry, thus the influence of aerosol acidity and sulfate particle change on isoprene SOA formation has not been fully considered in the model. This study reveals the urgent need to improve the SOA modeling in climate models.


2021 ◽  
Author(s):  
Yaman Liu ◽  
Xinyi Dong ◽  
Minghuai Wang ◽  
Louisa Emmons ◽  
Yawen Liu ◽  
...  

<p>Organic aerosol (OA) has been considered as one of the most important uncertainties in climate modeling due to the complexity in presenting its chemical production and depletion mechanisms. To better understand the capability of climate models and probe into the associated uncertainties in simulating OA, we evaluate the Community Earth System Model version 2.1 (CESM2.1) configured with the Community Atmosphere Model version 6 (CAM6) with comprehensive tropospheric and stratospheric chemistry representation (CAM6-Chem), through a long-term simulation (1988–2019) with observations collected from multiple datasets in the United States. We find that CESM generally reproduces the inter-annual variation and seasonal cycle of OA mass concentration at surface layer with correlation of 0.40 as compared to ground observations, and systematically overestimates (69 %) in summer and underestimates (-19 %) in winter. Through a series of sensitivity simulations, we reveal that modeling bias is primarily related to the dominant fraction of monoterpene-formed secondary organic aerosol (SOA), and a strong positive correlation of 0.67 is found between monoterpene emission and modeling bias in eastern US during summer. In terms of vertical profile, the model prominently underestimates OA and monoterpene concentrations by 37–99 % and 82–99 % respectively in the upper air (>500 m) as validated against aircraft observations. Our study suggests that the current Volatility Basis Set (VBS) scheme applied in CESM might be parameterized with too high monoterpene SOA yields which subsequently result in strong SOA production near emission source area. We also find that the model has difficulty in reproducing the decreasing trend of surface OA in southeast US, probably because of employing pure gas VBS to represent isoprene SOA which is in reality mainly formed through multiphase chemistry, thus the influence of aerosol acidity and sulfate particle change on isoprene SOA formation has not been fully considered in the model. This study reveals the urgent need to improve the SOA modeling in climate models.</p>


2021 ◽  
Vol 21 (10) ◽  
pp. 8003-8021
Author(s):  
Yaman Liu ◽  
Xinyi Dong ◽  
Minghuai Wang ◽  
Louisa K. Emmons ◽  
Yawen Liu ◽  
...  

Abstract. Organic aerosol (OA) has been considered as one of the most important uncertainties in climate modeling due to the complexity in presenting its chemical production and depletion mechanisms. To better understand the capability of climate models and probe into the associated uncertainties in simulating OA, we evaluate the Community Earth System Model version 2.1 (CESM2.1) configured with the Community Atmosphere Model version 6 (CAM6) with comprehensive tropospheric and stratospheric chemistry representation (CAM6-Chem) through a long-term simulation (1988–2019) with observations collected from multiple datasets in the United States. We find that CESM generally reproduces the interannual variation and seasonal cycle of OA mass concentration at surface layer with a correlation of 0.40 compared to ground observations and systematically overestimates (69 %) in summer and underestimates (−19 %) in winter. Through a series of sensitivity simulations, we reveal that modeling bias is primarily related to the dominant fraction of monoterpene-formed secondary organic aerosol (SOA), and a strong positive correlation of 0.67 is found between monoterpene emission and modeling bias in the eastern US during summer. In terms of vertical profile, the model prominently underestimates OA and monoterpene concentrations by 37 %–99 % and 82 %–99 %, respectively, in the upper air (> 500 m) as validated against aircraft observations. Our study suggests that the current volatility basis set (VBS) scheme applied in CESM might be parameterized with monoterpene SOA yields that are too high, which subsequently results in strong SOA production near the emission source area. We also find that the model has difficulty in reproducing the decreasing trend of surface OA in the southeastern US probably because of employing pure gas VBS to represent isoprene SOA which is in reality mainly formed through multiphase chemistry; thus, the influence of aerosol acidity and sulfate particle change on isoprene SOA formation has not been fully considered in the model. This study reveals the urgent need to improve the SOA modeling in climate models.


2019 ◽  
Vol 46 (14) ◽  
pp. 8329-8337 ◽  
Author(s):  
A. Gettelman ◽  
C. Hannay ◽  
J. T. Bacmeister ◽  
R. B. Neale ◽  
A. G. Pendergrass ◽  
...  

2012 ◽  
Vol 5 (2) ◽  
pp. 369-411 ◽  
Author(s):  
J.-F. Lamarque ◽  
L. K. Emmons ◽  
P. G. Hess ◽  
D. E. Kinnison ◽  
S. Tilmes ◽  
...  

Abstract. We discuss and evaluate the representation of atmospheric chemistry in the global Community Atmosphere Model (CAM) version 4, the atmospheric component of the Community Earth System Model (CESM). We present a variety of configurations for the representation of tropospheric and stratospheric chemistry, wet removal, and online and offline meteorology. Results from simulations illustrating these configurations are compared with surface, aircraft and satellite observations. Major biases include a negative bias in the high-latitude CO distribution, a positive bias in upper-tropospheric/lower-stratospheric ozone, and a positive bias in summertime surface ozone (over the United States and Europe). The tropospheric net chemical ozone production varies significantly between configurations, partly related to variations in stratosphere-troposphere exchange. Aerosol optical depth tends to be underestimated over most regions, while comparison with aerosol surface measurements over the United States indicate reasonable results for sulfate , especially in the online simulation. Other aerosol species exhibit significant biases. Overall, the model-data comparison indicates that the offline simulation driven by GEOS5 meteorological analyses provides the best simulation, possibly due in part to the increased vertical resolution (52 levels instead of 26 for online dynamics). The CAM-chem code as described in this paper, along with all the necessary datasets needed to perform the simulations described here, are available for download at www.cesm.ucar.edu.


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