scholarly journals ENSO and Pacific Decadal Variability in the Community Earth System Model Version 2

2020 ◽  
Vol 12 (12) ◽  
Author(s):  
A. Capotondi ◽  
C. Deser ◽  
A. S. Phillips ◽  
Y. Okumura ◽  
S. M. Larson
2019 ◽  
Vol 46 (14) ◽  
pp. 8329-8337 ◽  
Author(s):  
A. Gettelman ◽  
C. Hannay ◽  
J. T. Bacmeister ◽  
R. B. Neale ◽  
A. G. Pendergrass ◽  
...  

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):  
Sarah L Bradley ◽  
Michele Petrini ◽  
Raymond Sellevold ◽  
Miren Vizcaino ◽  
William H. Lipscomb ◽  
...  

<p>The last deglaciation provides as unique a framework to investigate the processes of ice sheet and climate interaction during periods of mass loss as in the current climate. Here we simulate the Last Glacial Maximum (LGM) northern hemisphere ice sheets climate, surface mass balance (SMB), and dynamics with the Community Earth System Model version 2 (CESM2, Danabasoglu et al., 2020)) and the Community Ice Sheet Model version 2 (CISM2, Lipscomb et al., 2019). This LGM simulation will be later used as starting point for coupled CESM2-CISM2 simulations of the last deglaciation.</p><p> </p><p>CESM2 is run at the nominal resolution used for IPCC-type projections (approx. 1 degree for all components). The model includes an advanced snow/firn and SMB calculation (van Kampenhout et al, 2019; Sellevold et al, 2019) the land component (CLM, cite) that has been evaluated and applied to the simulation of the future Greenland melt (van Kampenhout et al, 2020, Muntjewerf et al., 2020a,b, Sellevold & Vizcaino, 2020).</p><p> </p><p>Our analysis examines how the global, Arctic, and North Atlantic climate result in the simulated radiative and turbulent heat fluxes over the ice sheets, and the mass fluxes from precipitation, refreezing, runoff, and sublimation. We also examine the simulated ice streams in CISM2, which is run at 8 km under a higher-order approximation for ice flow.</p>


2021 ◽  
Author(s):  
Amélie Desmarais ◽  
Bruno Tremblay

AbstractUncertainties in the timing of a seasonal ice cover in the Arctic Ocean depend on model physics and parameterizations, natural variability at decadal timescales and uncertainties in climate scenarios and forcings. We use the Gridded Monthly Sea-Ice Extent and Concentration, 1850 Onward product to assess the simulated decadal variability from the Community Earth System Model – Large Ensemble (CESM-LE) in the Pacific, Eurasian and Atlantic sector of the Arctic where a longer observational record exists. Results show that sea-ice decadal (8-16 years) variability in CESM-LE is in agreement with the observational record in the Pacific sector of the Arctic, underestimated in the Eurasian sector of the Arctic, specifically in the East-Siberian Sea, and slightly overestimated in the Atlantic sector of the Arctic, specifically in the Greenland Sea. Results also show an increase in variability at decadal timescales in the Eurasian and Pacific sectors during the transition to a seasonally ice-free Arctic, in agreement with the observational record although this increase is delayed by 10-20 years. If the current sea-ice retreat in the Arctic continues to be Pacific-centric, results from the CESM-LE suggest that uncertainty in the timing of an ice-free Arctic associated with natural variability is realistic, but that a seasonal ice cover may occur earlier than projected.


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>


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