scholarly journals Development of the global atmospheric general circulation-chemistry model BCC-GEOS-Chem v1.0: model description and evaluation

2019 ◽  
Author(s):  
Xiao Lu ◽  
Lin Zhang ◽  
Tongwen Wu ◽  
Michael S. Long ◽  
Jun Wang ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Tropospheric Ozone ◽  
General Circulation ◽  
Climate Models ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Circulation Model ◽  
Satellite Observations ◽  
Model Description ◽  
Atmospheric General Circulation

Abstract. Chemistry plays an indispensable role in investigations of the atmosphere, however, many climate models either ignore or greatly simplify atmospheric chemistry, limiting both their accuracy and their scope. We present the development and evaluation of the online global atmospheric chemical model BCC-GEOS-Chem v1.0, coupling the GEOS-Chem chemical transport model (CTM) as an atmospheric chemistry component in the Beijing Climate Center atmospheric general circulation model (BCC-AGCM). The GEOS-Chem atmospheric chemistry component includes detailed tropospheric HOx-NOx-VOC-ozone-bromine-aerosol chemistry and online dry and wet deposition schemes. We then demonstrate the new capabilities of BCC-GEOS-Chem v1.0 relative to the base BCC-AGCM model through a three-year (2012–2014) simulation with anthropogenic emissions from the Community Emissions Data System (CEDS) used in the Coupled Model Intercomparison Project Phase 6 (CMIP6). The model well captures the spatial distributions and seasonal variations in tropospheric ozone, with seasonal mean biases of 0.4–2.2 ppbv at 700–400 hPa compared to satellite observations and within 10 ppbv at the surface-500 hPa compared to global ozonesonde observations. The model has larger high ozone biases over the tropics which we attribute to an overestimate of ozone chemical production. It underestimates ozone in the upper troposphere which likely due to either the use of a simplified stratospheric ozone scheme and/or to biases in estimated stratosphere-troposphere exchange dynamics. The model diagnoses the global tropospheric ozone burden, OH concentration, and methane chemical lifetime to be 336 Tg, 1.16 × 106 molecule cm−3, and 8.3 years, respectively, consistent with recent multi-model assessments. The spatiotemporal distributions of NO2, CO, SO2, CH2O, and aerosols optical depth are generally in agreement with satellite observations. The development of BCC-GEOS-Chem v1.0 represents an important step for the development of fully coupled earth system models (ESMs) in China.

scholarly journals Development of the global atmospheric chemistry general circulation model BCC-GEOS-Chem v1.0: model description and evaluation

2020 ◽  
Vol 13 (9) ◽  
pp. 3817-3838
Author(s):  
Xiao Lu ◽  
Lin Zhang ◽  
Tongwen Wu ◽  
Michael S. Long ◽  
Jun Wang ◽  
...  
Keyword(s):  
General Circulation Model ◽  
Atmospheric Chemistry ◽  
Tropospheric Ozone ◽  
General Circulation ◽  
Climate Models ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Circulation Model ◽  
Satellite Observations ◽  
Model Description

Abstract. Chemistry plays an indispensable role in investigations of the atmosphere; however, many climate models either ignore or greatly simplify atmospheric chemistry, limiting both their accuracy and their scope. We present the development and evaluation of the online global atmospheric chemical model BCC-GEOS-Chem v1.0, coupling the GEOS-Chem chemical transport model (CTM) as an atmospheric chemistry component in the Beijing Climate Center atmospheric general circulation model (BCC-AGCM). The GEOS-Chem atmospheric chemistry component includes detailed tropospheric HOx–NOx–volatile organic compounds–ozone–bromine–aerosol chemistry and online dry and wet deposition schemes. We then demonstrate the new capabilities of BCC-GEOS-Chem v1.0 relative to the base BCC-AGCM model through a 3-year (2012–2014) simulation with anthropogenic emissions from the Community Emissions Data System (CEDS) used in the Coupled Model Intercomparison Project Phase 6 (CMIP6). The model captures well the spatial distributions and seasonal variations in tropospheric ozone, with seasonal mean biases of 0.4–2.2 ppbv at 700–400 hPa compared to satellite observations and within 10 ppbv at the surface to 500 hPa compared to global ozonesonde observations. The model has larger high-ozone biases over the tropics which we attribute to an overestimate of ozone chemical production. It underestimates ozone in the upper troposphere which is likely due either to the use of a simplified stratospheric ozone scheme or to biases in estimated stratosphere–troposphere exchange dynamics. The model diagnoses the global tropospheric ozone burden, OH concentration, and methane chemical lifetime to be 336 Tg, 1.16×106 molecule cm−3, and 8.3 years, respectively, which is consistent with recent multimodel assessments. The spatiotemporal distributions of NO2, CO, SO2, CH2O, and aerosol optical depth are generally in agreement with satellite observations. The development of BCC-GEOS-Chem v1.0 represents an important step for the development of fully coupled earth system models (ESMs) in China.

scholarly journals Evaluation of ACCMIP outgoing longwave radiation from tropospheric ozone using TES satellite observations

2013 ◽  
Vol 13 (8) ◽  
pp. 4057-4072 ◽  
Author(s):  
K. W. Bowman ◽  
D. T. Shindell ◽  
H. M. Worden ◽  
J.F. Lamarque ◽  
P. J. Young ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Tropospheric Ozone ◽  
Outgoing Longwave Radiation ◽  
Radiative Forcing ◽  
Climate Models ◽  
Climate Model ◽  
Longwave Radiation ◽  
Satellite Observations ◽  
Ensemble Mean ◽  
High Bias

Abstract. We use simultaneous observations of tropospheric ozone and outgoing longwave radiation (OLR) sensitivity to tropospheric ozone from the Tropospheric Emission Spectrometer (TES) to evaluate model tropospheric ozone and its effect on OLR simulated by a suite of chemistry-climate models that participated in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The ensemble mean of ACCMIP models show a persistent but modest tropospheric ozone low bias (5–20 ppb) in the Southern Hemisphere (SH) and modest high bias (5–10 ppb) in the Northern Hemisphere (NH) relative to TES ozone for 2005–2010. These ozone biases have a significant impact on the OLR. Using TES instantaneous radiative kernels (IRK), we show that the ACCMIP ensemble mean tropospheric ozone low bias leads up to 120 mW m−2 OLR high bias locally but zonally compensating errors reduce the global OLR high bias to 39 ± 41 m Wm−2 relative to TES data. We show that there is a correlation (R2 = 0.59) between the magnitude of the ACCMIP OLR bias and the deviation of the ACCMIP preindustrial to present day (1750–2010) ozone radiative forcing (RF) from the ensemble ozone RF mean. However, this correlation is driven primarily by models whose absolute OLR bias from tropospheric ozone exceeds 100 m Wm−2. Removing these models leads to a mean ozone radiative forcing of 394 ± 42 m Wm−2. The mean is about the same and the standard deviation is about 30% lower than an ensemble ozone RF of 384 ± 60 m Wm−2 derived from 14 of the 16 ACCMIP models reported in a companion ACCMIP study. These results point towards a profitable direction of combining satellite observations and chemistry-climate model simulations to reduce uncertainty in ozone radiative forcing.

Parameterization of PBL Processes in an Atmospheric General Circulation Model: Description and Preliminary Assessment

2009 ◽  
Vol 137 (3) ◽  
pp. 1061-1082 ◽  
Author(s):  
Celal S. Konor ◽  
Gabriel Cazes Boezio ◽  
Carlos R. Mechoso ◽  
Akio Arakawa
Keyword(s):  
General Circulation Model ◽  
General Circulation ◽  
Atmospheric General Circulation Model ◽  
Potential Temperature ◽  
Circulation Model ◽  
Surface Fluxes ◽  
Shortwave Radiation ◽  
Model Description ◽  
Atmospheric General Circulation ◽  
Seasonal And Diurnal Variations

Abstract This paper presents the basic features of a newly developed planetary boundary layer (PBL) parameterization, and the performance assessment of a version of the University of California, Los Angeles (UCLA), Atmospheric General Circulation Model (AGCM) to which the parameterization is incorporated. The UCLA AGCM traditionally uses a framework in which a sigma-type vertical coordinate for the PBL shares a coordinate surface with the free atmosphere at the PBL top. This framework facilitates an explicit representation of processes concentrated near the PBL top, which is crucially important especially for predicting PBL clouds. In the new framework, multiple layers are introduced between the PBL top and earth’s surface, allowing for predictions of the vertical profiles of potential temperature, total water mixing ratio, and horizontal winds within the PBL. The vertically integrated “bulk” turbulent kinetic energy (TKE) is also predicted for the PBL. The PBL-top mass entrainment is determined through an equation including the effects of TKE and the radiative and evaporative cooling processes concentrated near the PBL top. The surface fluxes are determined from an aerodynamic formula in which the velocity scale depends both on the square root of TKE and the grid-scale PBL velocity at the lowermost model layer. The turbulent fluxes within the PBL are determined through an approach that includes the effects of both large convective and small diffusive eddies. AGCM simulations with the new formulation of PBL are analyzed with a focus on the seasonal and diurnal variations. The simulated seasonal cycle of stratocumulus over the eastern oceans is realistic, as are the diurnal cycles of the PBL depth and precipitation over land. The simulated fluxes of latent heat, momentum, and shortwave radiation at the ocean surface and baroclinic activity in the middle latitudes show significant improvements over the previous versions of the AGCM based on the single-layer PBL.

scholarly journals Consistent simulation of bromine chemistry from the marine boundary layer to the stratosphere – Part 1: Model description, sea salt aerosols and pH

2008 ◽  
Vol 8 (19) ◽  
pp. 5899-5917 ◽  
Author(s):  
A. Kerkweg ◽  
P. Jöckel ◽  
A. Pozzer ◽  
H. Tost ◽  
R. Sander ◽  
...  
Keyword(s):  
Size Distribution ◽  
Atmospheric Chemistry ◽  
General Circulation ◽  
Circulation Model ◽  
Reaction Rates ◽  
Sea Salt ◽  
Aerosol Size Distribution ◽  
Model Description ◽  
Aerosol Chemistry ◽  
Coarse Mode

Abstract. This is the first article of a series presenting a detailed analysis of bromine chemistry simulated with the atmospheric chemistry general circulation model ECHAM5/MESSy. Release from sea salt is an important bromine source, hence the model explicitly calculates aerosol chemistry and phase partitioning for coarse mode aerosol particles. Many processes including chemical reaction rates are influenced by the particle size distribution, and aerosol associated water strongly affects the aerosol pH. Knowledge of the aerosol pH is important as it determines the aerosol chemistry, e.g., the efficiency of sulphur oxidation and bromine release. Here, we focus on the simulated sea salt aerosol size distribution and the coarse mode aerosol pH. A comparison with available field data shows that the simulated aerosol distributions agree reasonably well within the range of measurements. In spite of the small number of aerosol pH measurements and the uncertainty in its experimental determination, the simulated aerosol pH compares well with the observations. The aerosol pH ranges from alkaline aerosol in areas of strong production down to pH-values of 1 over regions of medium sea salt production and high levels of gas phase acids, mostly polluted regions over the oceans in the Northern Hemisphere.

scholarly journals Stratospheric lifetime ratio of CFC-11 and CFC-12 from satellite and model climatologies

2014 ◽  
Vol 14 (11) ◽  
pp. 16865-16906 ◽  
Author(s):  
L. Hoffmann ◽  
C. M. Hoppe ◽  
R. Müller ◽  
G. S. Dutton ◽  
J. C. Gille ◽  
...  
Keyword(s):  
Global Warming ◽  
Atmospheric Chemistry ◽  
Climate Model ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Michelson Interferometer ◽  
Coupled Model ◽  
Model System ◽  
Satellite Observations ◽  
The Impact

Abstract. Chlorofluorocarbons (CFCs) play a key role in stratospheric ozone loss and are strong infrared absorbers that contribute to global warming. The stratospheric lifetimes of CFCs are a measure of their global loss rates that are needed to determine global warming and ozone depletion potentials. We applied the tracer-tracer correlation approach to zonal mean climatologies from satellite measurements and model data to assess the lifetimes of CFCl3 (CFC-11) and CF2Cl2 (CFC-12). We present estimates of the CFC-11/CFC-12 lifetime ratio and the absolute lifetime of CFC-12, based on a reference lifetime of 52 yr for CFC-11. We analyzed climatologies from three satellite missions, the Atmospheric Chemistry Experiment-Fourier Transform Spectrometer (ACE-FTS), the HIgh Resolution Dynamics Limb Sounder (HIRDLS), and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS). We found a CFC-11/CFC-12 lifetime ratio of 0.47±0.08 and a CFC-12 lifetime of 111(96–132) yr for ACE-FTS, a ratio of 0.46±0.07 and a lifetime of 112(97–133) yr for HIRDLS, and a ratio of 0.46±0.08 and a lifetime of 112(96–135) yr for MIPAS. The error-weighted, combined CFC-11/CFC-12 lifetime ratio is 0.47±0.04 and the CFC-12 lifetime estimate is 112(102–123) yr. These results agree with the recent Stratosphere-troposphere Processes And their Role in Climate (SPARC) reassessment, which recommends lifetimes of 52(43–67) yr and 102(88–122) yr, respectively. Having smaller uncertainties than the results from other recent studies, our estimates can help to better constrain CFC-11 and CFC-12 lifetime recommendations in future scientific studies and assessments. Furthermore, the satellite observations were used to validate first simulation results from a new coupled model system, which integrates a Lagrangian chemistry transport model into a climate model. For the coupled model we found a CFC-11/CFC-12 lifetime ratio of 0.48±0.07 and a CFC-12 lifetime of 110(95–129) yr, based on a ten-year perpetual run. Closely reproducing the satellite observations, the new model system will likely become a useful tool to assess the impact of advective transport, mixing, and photochemistry as well as climatological variability on the stratospheric lifetimes of long-lived tracers.

scholarly journals Improved Simulation of the Antarctic Stratospheric Final Warming by Modifying the Orographic Gravity Wave Parameterization in the Beijing Climate Center Atmospheric General Circulation Model

Atmosphere ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 576
Author(s):  
Yixiong Lu ◽  
Tongwen Wu ◽  
Xin Xu ◽  
Li Zhang ◽  
Min Chu
Keyword(s):  
Gravity Wave ◽  
General Circulation Model ◽  
General Circulation ◽  
Climate Models ◽  
Atmospheric General Circulation Model ◽  
Circulation Model ◽  
Wave Drag ◽  
Atmospheric General Circulation ◽  
Stratospheric Final Warming ◽  
The Antarctic

The Antarctic stratospheric final warming (SFW) is usually simulated with a substantial delay in climate models, and the corresponding temperatures in austral spring are lower than observations, implying insufficient stratospheric wave drag. To investigate the role of orographic gravity wave drag (GWD) in modeling the Antarctic SFW, in this study the orographic GWD parameterization scheme is modified in the middle-atmosphere version of the Beijing Climate Center Atmospheric General Circulation Model. A pair of simulations are conducted to compare two orographic GWD schemes in simulating the breakdown of the stratospheric polar vortex over Antarctica. The control simulation with the default orographic GWD scheme exhibits delayed vortex breakdown and the cold-pole bias seen in most climate models. In the simulation with modified orographic GWD scheme, the simulated vortex breaks down earlier by 8 days, and the associated cold-pole bias is reduced by more than 2 K. The modified scheme provides stronger orographic GWD in the lower stratosphere, which drives an accelerated polar downwelling branch of the Brewer–Dobson circulation and, in turn, produces adiabatic warming. Our study suggests that modifying orographic GWD parameterizations in climate models would be a valid way of improving the SFW simulation over Antarctica.

scholarly journals Sensitivity of an atmospheric general circulation model to the parameterization of leads in sea ice

1997 ◽  
Vol 25 ◽  
pp. 96-101 ◽  
Author(s):  
Gregory M. Flato ◽  
David Ramsden
Keyword(s):  
Sea Ice ◽  
General Circulation Model ◽  
General Circulation ◽  
Climate Models ◽  
Atmospheric General Circulation Model ◽  
Circulation Model ◽  
Open Water ◽  
Arctic Sea Ice ◽  
Atmospheric General Circulation ◽  
Hemisphere Winter

Open-water leads in sea ice dominate the exchange of heat between the ocean and atmosphere in ice-covered regions, and so must be included in climate models. A parameterization of leads used in one such model is compared to observations and the results of a detailed Arctic sea-ice model. Such comparisons, however, are hampered by the errors in observed lead fraction, but the parameterization appears to compare better in winter than in summer. Simulations with an atmospheric general circulation model (AGCM), using prescribed sea-surface temperatures and ice extent, are used to illustrate the effect of parameterized lead fraction on atmospheric climate, and so provide some insight into the importance of improved lead-fraction parameterizations and observations. The effect of leads in the AGCM is largest in Northern Hemisphere winter, with zonal mean surface-air temperatures over ice increasing by up to 5 K when lead fraction is increased from 1% to near 5%. The effect of leads on sensible heat loss in winter is more important than the effect on radiative heat gain in summer. No significant effect on sea-level pressure, and hence on atmospheric circulation, is found, however. Indirect effects, due to feedbacks between the atmosphere and ice thickness and extent, were not included in these simulations, but could amplify the response.

scholarly journals Stratospheric lifetime ratio of CFC-11 and CFC-12 from satellite and model climatologies

2014 ◽  
Vol 14 (22) ◽  
pp. 12479-12497 ◽  
Author(s):  
L. Hoffmann ◽  
C. M. Hoppe ◽  
R. Müller ◽  
G. S. Dutton ◽  
J. C. Gille ◽  
...  
Keyword(s):  
Global Warming ◽  
Atmospheric Chemistry ◽  
Climate Model ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Michelson Interferometer ◽  
Coupled Model ◽  
Model System ◽  
Satellite Observations ◽  
The Impact

Abstract. Chlorofluorocarbons (CFCs) play a key role in stratospheric ozone loss and are strong infrared absorbers that contribute to global warming. The stratospheric lifetimes of CFCs are a measure of their stratospheric loss rates that are needed to determine global warming and ozone depletion potentials. We applied the tracer–tracer correlation approach to zonal mean climatologies from satellite measurements and model data to assess the lifetimes of CFCl3 (CFC-11) and CF2Cl2 (CFC-12). We present estimates of the CFC-11/CFC-12 lifetime ratio and the absolute lifetime of CFC-12, based on a reference lifetime of 52 years for CFC-11. We analyzed climatologies from three satellite missions, the Atmospheric Chemistry Experiment-Fourier Transform Spectrometer (ACE-FTS), the HIgh Resolution Dynamics Limb Sounder (HIRDLS), and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS). We found a CFC-11/CFC-12 lifetime ratio of 0.47±0.08 and a CFC-12 lifetime of 112(96–133) years for ACE-FTS, a ratio of 0.46±0.07 and a lifetime of 113(97–134) years for HIRDLS, and a ratio of 0.46±0.08 and a lifetime of 114(98–136) years for MIPAS. The error-weighted, combined CFC-11/CFC-12 lifetime ratio is 0.46±0.04 and the CFC-12 lifetime estimate is 113(103–124) years. These results agree with the recent Stratosphere-troposphere Processes And their Role in Climate (SPARC) reassessment, which recommends lifetimes of 52(43–67) years and 102(88–122) years, respectively. Having smaller uncertainties than the results from other recent studies, our estimates can help to better constrain CFC-11 and CFC-12 lifetime recommendations in future scientific studies and assessments. Furthermore, the satellite observations were used to validate first simulation results from a new coupled model system, which integrates a Lagrangian chemistry transport model into a climate model. For the coupled model we found a CFC-11/CFC-12 lifetime ratio of 0.48±0.07 and a CFC-12 lifetime of 110(95–129) years, based on a 10-year perpetual run. Closely reproducing the satellite observations, the new model system will likely become a useful tool to assess the impact of advective transport, mixing, and photochemistry as well as climatological variability on the stratospheric lifetimes of long-lived tracers.

scholarly journals Stratospheric SO<sub>2</sub> and sulphate aerosol, model simulations and satellite observations

2013 ◽  
Vol 13 (4) ◽  
pp. 11395-11425 ◽  
Author(s):  
C. Brühl ◽  
J. Lelieveld ◽  
M. Höpfner ◽  
H. Tost
Keyword(s):  
Atmospheric Chemistry ◽  
Radiative Forcing ◽  
General Circulation ◽  
Middle Atmosphere ◽  
Lower Boundary ◽  
Circulation Model ◽  
Volcanic Eruptions ◽  
Satellite Observations ◽  
Quasi Biennial Oscillation ◽  
Tropospheric Aerosol

Abstract. A multiyear study with the atmospheric chemistry general circulation model EMAC with the aerosol module GMXe at high altitude resolution demonstrates that the sulfur gases COS and SO2, the latter from low-latitude volcanic eruptions, predominantly control the formation of stratospheric aerosol. The model consistently uses the same parameters in the troposphere and stratosphere for 7 aerosol modes applied. Lower boundary conditions for COS and other long-lived trace gases are taken from measurement networks, while estimates of volcanic SO2 emissions are based on satellite observations. We show comparisons with satellite data for aerosol extinction (e.g. SAGE) and SO2 in the middle atmosphere (MIPAS on ENVISAT). This corroborates the interannual variability induced by the Quasi-Biennial Oscillation, which is internally generated by the model. The model also realistically simulates the radiative effects of stratospheric and tropospheric aerosol including the effects on the model dynamics. The medium strength volcanic eruptions of 2005 and 2006 exerted a nonnegligible radiative forcing of up to −0.6 W m−2 in the tropics, while the large Pinatubo eruption caused a maximum though short term tropical forcing of about −10 W m−2. The study also shows that observed upper stratospheric SO2 can be simulated accurately only when a sulphur sink on meteoritic dust is included and the photolysis of gaseous H2SO4 in the near infrared is higher than assumed previously.

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