scholarly journals Multi-model mean nitrogen and sulfur deposition from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP): evaluation historical and projected changes

2013 ◽  
Vol 13 (3) ◽  
pp. 6247-6294 ◽  
Author(s):  
J.-F. Lamarque ◽  
F. Dentener ◽  
J. McConnell ◽  
C.-U. Ro ◽  
M. Shaw ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Wet Deposition ◽  
Climate Model ◽  
Ice Core ◽  
The United States ◽  
Time Slice ◽  
Model Intercomparison ◽  
Deposition Fluxes ◽  
Continental Scale ◽  
Intercomparison Project

Abstract. We present multi-model global datasets of nitrogen and sulfate deposition covering time periods from 1850 to 2100, calculated within the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The computed deposition fluxes are compared to surface wet deposition and ice-core measurements. We use a new dataset of wet deposition for 2000–2002 based on critical assessment of the quality of existing regional network data. We show that for present-day (year 2000 ACCMIP time-slice), the ACCMIP results perform similarly to previously published multi-model assessments. For this time slice, we find a multi-model mean deposition of 50 Tg(N) yr−1 from nitrogen oxide emissions, 60 Tg(N) yr−1 from ammonia emissions, and 83 Tg(S) yr−1 from sulfur emissions. The analysis of changes between 1980 and 2000 indicates significant differences between model and measurements over the United States but less so over Europe. This difference points towards misrepresentation of 1980 NH3 emissions over North America. Based on ice-core records, the 1850 deposition fluxes agree well with Greenland ice cores but the change between 1850 and 2000 seems to be overestimated in the Northern Hemisphere for both nitrogen and sulfur species. Using the Representative Concentration Pathways to define the projected climate and atmospheric chemistry related emissions and concentrations, we find large regional nitrogen deposition increases in 2100 in Latin America, Africa and parts of Asia under some of the scenarios considered. Increases in South Asia are especially large, and are seen in all scenarios, with 2100 values more than double 2000 in some scenarios and reaching > 1300 mg(N) m−2 yr−1 averaged over regional to continental scale regions in RCP 2.6 and 8.5, ~30–50 % larger than the values in any region currently (2000). The new ACCMIP deposition dataset provides novel, consistent and evaluated global gridded deposition fields for use in a wide range of climate and ecological studies.

scholarly journals Multi-model mean nitrogen and sulfur deposition from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP): evaluation of historical and projected future changes

2013 ◽  
Vol 13 (16) ◽  
pp. 7997-8018 ◽  
Author(s):  
J.-F. Lamarque ◽  
F. Dentener ◽  
J. McConnell ◽  
C.-U. Ro ◽  
M. Shaw ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Wet Deposition ◽  
Climate Model ◽  
Ice Core ◽  
The United States ◽  
Time Slice ◽  
Sulfur Deposition ◽  
Model Intercomparison ◽  
Deposition Fluxes ◽  
Intercomparison Project

Abstract. We present multi-model global datasets of nitrogen and sulfate deposition covering time periods from 1850 to 2100, calculated within the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The computed deposition fluxes are compared to surface wet deposition and ice core measurements. We use a new dataset of wet deposition for 2000–2002 based on critical assessment of the quality of existing regional network data. We show that for present day (year 2000 ACCMIP time slice), the ACCMIP results perform similarly to previously published multi-model assessments. For this time slice, we find a multi-model mean deposition of approximately 50 Tg(N) yr−1 from nitrogen oxide emissions, 60 Tg(N) yr−1 from ammonia emissions, and 83 Tg(S) yr−1 from sulfur emissions. The analysis of changes between 1980 and 2000 indicates significant differences between model and measurements over the United States but less so over Europe. This difference points towards a potential misrepresentation of 1980 NH3 emissions over North America. Based on ice core records, the 1850 deposition fluxes agree well with Greenland ice cores, but the change between 1850 and 2000 seems to be overestimated in the Northern Hemisphere for both nitrogen and sulfur species. Using the Representative Concentration Pathways (RCPs) to define the projected climate and atmospheric chemistry related emissions and concentrations, we find large regional nitrogen deposition increases in 2100 in Latin America, Africa and parts of Asia under some of the scenarios considered. Increases in South Asia are especially large, and are seen in all scenarios, with 2100 values more than double their 2000 counterpart in some scenarios and reaching > 1300 mg(N) m−2 yr−1 averaged over regional to continental-scale regions in RCP 2.6 and 8.5, ~ 30–50% larger than the values in any region currently (circa 2000). However, sulfur deposition rates in 2100 are in all regions lower than in 2000 in all the RCPs. The new ACCMIP multi-model deposition dataset provides state-of-the-science, consistent and evaluated time slice (spanning 1850–2100) global gridded deposition fields for use in a wide range of climate and ecological studies.

scholarly journals Preindustrial to present-day changes in tropospheric hydroxyl radical and methane lifetime from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)

2013 ◽  
Vol 13 (10) ◽  
pp. 5277-5298 ◽  
Author(s):  
V. Naik ◽  
A. Voulgarakis ◽  
A. M. Fiore ◽  
L. W. Horowitz ◽  
J.-F. Lamarque ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Hydroxyl Radical ◽  
Atmospheric Chemistry ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Regional Distribution ◽  
Model Intercomparison ◽  
Intercomparison Project ◽  
Concentration Changes ◽  
Global Mean

Abstract. We have analysed time-slice simulations from 17 global models, participating in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), to explore changes in present-day (2000) hydroxyl radical (OH) concentration and methane (CH4) lifetime relative to preindustrial times (1850) and to 1980. A comparison of modeled and observation-derived methane and methyl chloroform lifetimes suggests that the present-day global multi-model mean OH concentration is overestimated by 5 to 10% but is within the range of uncertainties. The models consistently simulate higher OH concentrations in the Northern Hemisphere (NH) compared with the Southern Hemisphere (SH) for the present-day (2000; inter-hemispheric ratios of 1.13 to 1.42), in contrast to observation-based approaches which generally indicate higher OH in the SH although uncertainties are large. Evaluation of simulated carbon monoxide (CO) concentrations, the primary sink for OH, against ground-based and satellite observations suggests low biases in the NH that may contribute to the high north–south OH asymmetry in the models. The models vary widely in their regional distribution of present-day OH concentrations (up to 34%). Despite large regional changes, the multi-model global mean (mass-weighted) OH concentration changes little over the past 150 yr, due to concurrent increases in factors that enhance OH (humidity, tropospheric ozone, nitrogen oxide (NOx) emissions, and UV radiation due to decreases in stratospheric ozone), compensated by increases in OH sinks (methane abundance, carbon monoxide and non-methane volatile organic carbon (NMVOC) emissions). The large inter-model diversity in the sign and magnitude of preindustrial to present-day OH changes (ranging from a decrease of 12.7% to an increase of 14.6%) indicate that uncertainty remains in our understanding of the long-term trends in OH and methane lifetime. We show that this diversity is largely explained by the different ratio of the change in global mean tropospheric CO and NOx burdens (ΔCO/ΔNOx, approximately represents changes in OH sinks versus changes in OH sources) in the models, pointing to a need for better constraints on natural precursor emissions and on the chemical mechanisms in the current generation of chemistry-climate models. For the 1980 to 2000 period, we find that climate warming and a slight increase in mean OH (3.5 ± 2.2%) leads to a 4.3 ± 1.9% decrease in the methane lifetime. Analysing sensitivity simulations performed by 10 models, we find that preindustrial to present-day climate change decreased the methane lifetime by about four months, representing a negative feedback on the climate system. Further, we analysed attribution experiments performed by a subset of models relative to 2000 conditions with only one precursor at a time set to 1860 levels. We find that global mean OH increased by 46.4 ± 12.2% in response to preindustrial to present-day anthropogenic NOx emission increases, and decreased by 17.3 ± 2.3%, 7.6 ± 1.5%, and 3.1 ± 3.0% due to methane burden, and anthropogenic CO, and NMVOC emissions increases, respectively.

scholarly journals EC-Earth3-AerChem, a global climate model with interactive aerosols and atmospheric chemistry participating in CMIP6

2020 ◽  
Author(s):  
Twan van Noije ◽  
Tommi Bergman ◽  
Philippe Le Sager ◽  
Declan O'Donnell ◽  
Risto Makkonen ◽  
...  
Keyword(s):  
20Th Century ◽  
Southern Hemisphere ◽  
Air Temperature ◽  
Atmospheric Chemistry ◽  
Climate Model ◽  
Global Climate ◽  
Global Climate Model ◽  
Surface Air Temperature ◽  
Model Intercomparison ◽  
Intercomparison Project

Abstract. This paper documents the global climate model EC-Earth3-AerChem, one of the members of the EC-Earth3 family of models participating in the Coupled Model Intercomparison Project phase 6 (CMIP6). EC-Earth3-AerChem has interactive aerosols and atmospheric chemistry and contributes to the Aerosols and Chemistry Model Intercomparison Project (AerChemMIP). In this paper, we give an overview of the model and describe in detail how it differs from the other EC-Earth3 configurations, and what the new features are compared to the previously documented version of the model (EC-Earth 2.4). We explain how the model was tuned and spun up under pre-industrial conditions and characterize the model's general performance on the basis of a selection of coupled simulations conducted for CMIP6. The mean energy imbalance at the top of the atmosphere in the pre-industrial control simulation is −0.10 ± 0.25 W m−2 and shows no significant drift. The corresponding mean global surface air temperature is 14.05 ± 0.16 °C, with a small drift of −0.075 ± 0.009 °C per century. The model's effective equilibrium climate sensitivity is estimated at 3.9 °C and its transient climate response at 2.1 °C. The CMIP6 historical simulation displays spurious interdecadal variability in Northern Hemisphere temperatures, resulting in a large spread among ensemble members and a tendency to underestimate observed annual surface temperature anomalies from the early 20th century onwards. The observed warming of the Southern Hemisphere is well reproduced by the model. Compared to the ERA5 reanalysis of the European Centre for Medium-Range Weather Forecasts, the ensemble mean surface air temperature climatology for 1995–2014 has an average bias of −0.86 ± 0.35 °C in the Northern Hemisphere and 1.29 ± 0.05 °C in the Southern Hemisphere. The Southern Hemisphere warm bias is largely caused by errors in shortwave cloud radiative effects over the Southern Ocean, a deficiency of many climate models. Changes in the emissions of near-term climate forcers (NTCFs) have significant climate effects from the 20th century onwards. For the SSP3-7.0 shared socio-economic pathway, the model gives a global warming at the end of the 21st century (2091–2100) of 4.9 °C above the pre-industrial mean. A 0.5 °C stronger warming is obtained for the AerChemMIP scenario with reduced emissions of NTCFs. With concurrent reductions of future methane concentrations, the warming is projected to be reduced by 0.5 °C.

Snow Mass over North America: Observations and Results from the Second Phase of the Atmospheric Model Intercomparison Project

2005 ◽  
Vol 6 (5) ◽  
pp. 681-695 ◽  
Author(s):  
Allan Frei ◽  
Ross Brown ◽  
James A. Miller ◽  
David A. Robinson
Keyword(s):  
North America ◽  
Large Scale ◽  
Atmospheric Model ◽  
The United States ◽  
Second Phase ◽  
Model Intercomparison ◽  
Continental Scale ◽  
Intercomparison Project ◽  
Atmospheric Model Intercomparison Project ◽  
Snow Mass

Abstract Eighteen global atmospheric general circulation models (AGCMs) participating in the second phase of the Atmospheric Model Intercomparison Project (AMIP-2) are evaluated for their ability to simulate the observed spatial and temporal variability in snow mass, or water equivalent (SWE), over North America during the AMIP-2 period (1979–95). The evaluation is based on a new gridded SWE dataset developed from objective analysis of daily snow depth observations from Canada and the United States with snow density estimated from a simple snowpack model. Most AMIP-2 models simulate the seasonal timing and the relative spatial patterns of continental-scale SWE fairly well. However, there is a tendency to overestimate the rate of ablation during spring, and significant between-model variability is found in every aspect of the simulations, and at every spatial scale analyzed. For example, on the continental scale, the peak monthly SWE integrated over the North American continent in AMIP-2 models varies between ±50% of the observed value of ∼1500 km3. The volume of water in the snowpack, and the magnitudes of model errors, are significant in comparison to major fluxes in the continental water balance. It also appears that the median result from the suite of models tends to do a better job of estimating climatological mean features than any individual model. Year-to-year variations in large-scale SWE are only weakly correlated to observed variations, indicating that sea surface temperatures (specified from observations as boundary conditions) do not drive interannual variations of SWE in these models. These results have implications for simulations of the large-scale hydrologic cycle and for climate change impact assessments.

scholarly journals Pre-industrial to end 21st century projections of tropospheric ozone from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)

2013 ◽  
Vol 13 (4) ◽  
pp. 2063-2090 ◽  
Author(s):  
P. J. Young ◽  
A. T. Archibald ◽  
K. W. Bowman ◽  
J.-F. Lamarque ◽  
V. Naik ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Tropospheric Ozone ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Climate Projections ◽  
Model Intercomparison ◽  
Ensemble Mean ◽  
Intercomparison Project ◽  
High Bias ◽  
Ozone Precursor

Abstract. Present day tropospheric ozone and its changes between 1850 and 2100 are considered, analysing 15 global models that participated in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The ensemble mean compares well against present day observations. The seasonal cycle correlates well, except for some locations in the tropical upper troposphere. Most (75 %) of the models are encompassed with a range of global mean tropospheric ozone column estimates from satellite data, but there is a suggestion of a high bias in the Northern Hemisphere and a low bias in the Southern Hemisphere, which could indicate deficiencies with the ozone precursor emissions. Compared to the present day ensemble mean tropospheric ozone burden of 337 ± 23 Tg, the ensemble mean burden for 1850 time slice is ~30% lower. Future changes were modelled using emissions and climate projections from four Representative Concentration Pathways (RCPs). Compared to 2000, the relative changes in the ensemble mean tropospheric ozone burden in 2030 (2100) for the different RCPs are: −4% (−16%) for RCP2.6, 2% (−7%) for RCP4.5, 1% (−9%) for RCP6.0, and 7% (18%) for RCP8.5. Model agreement on the magnitude of the change is greatest for larger changes. Reductions in most precursor emissions are common across the RCPs and drive ozone decreases in all but RCP8.5, where doubled methane and a 40–150% greater stratospheric influx (estimated from a subset of models) increase ozone. While models with a high ozone burden for the present day also have high ozone burdens for the other time slices, no model consistently predicts large or small ozone changes; i.e. the magnitudes of the burdens and burden changes do not appear to be related simply, and the models are sensitive to emissions and climate changes in different ways. Spatial patterns of ozone changes are well correlated across most models, but are notably different for models without time evolving stratospheric ozone concentrations. A unified approach to ozone budget specifications and a rigorous investigation of the factors that drive tropospheric ozone is recommended to help future studies attribute ozone changes and inter-model differences more clearly.

scholarly journals The Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP): overview and description of models, simulations and climate diagnostics

2013 ◽  
Vol 6 (1) ◽  
pp. 179-206 ◽  
Author(s):  
J.-F. Lamarque ◽  
D. T. Shindell ◽  
B. Josse ◽  
P. J. Young ◽  
I. Cionni ◽  
...  
Keyword(s):  
Zonal Wind ◽  
Atmospheric Chemistry ◽  
Radiative Forcing ◽  
Model Comparison ◽  
Climate Model ◽  
Atmospheric Composition ◽  
Specific Humidity ◽  
Model Intercomparison ◽  
Wide Range ◽  
Intercomparison Project

Abstract. The Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) consists of a series of time slice experiments targeting the long-term changes in atmospheric composition between 1850 and 2100, with the goal of documenting composition changes and the associated radiative forcing. In this overview paper, we introduce the ACCMIP activity, the various simulations performed (with a requested set of 14) and the associated model output. The 16 ACCMIP models have a wide range of horizontal and vertical resolutions, vertical extent, chemistry schemes and interaction with radiation and clouds. While anthropogenic and biomass burning emissions were specified for all time slices in the ACCMIP protocol, it is found that the natural emissions are responsible for a significant range across models, mostly in the case of ozone precursors. The analysis of selected present-day climate diagnostics (precipitation, temperature, specific humidity and zonal wind) reveals biases consistent with state-of-the-art climate models. The model-to-model comparison of changes in temperature, specific humidity and zonal wind between 1850 and 2000 and between 2000 and 2100 indicates mostly consistent results. However, models that are clear outliers are different enough from the other models to significantly affect their simulation of atmospheric chemistry.

scholarly journals Evaluation of preindustrial to present-day black carbon and its albedo forcing from ACCMIP (Atmospheric Chemistry and Climate Model Intercomparison Project)

2012 ◽  
Vol 12 (8) ◽  
pp. 21713-21778 ◽  
Author(s):  
Y. H. Lee ◽  
J.-F. Lamarque ◽  
M. G. Flanner ◽  
C. Jiao ◽  
D. T. Shindell ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Climate Model ◽  
Monsoon Season ◽  
Ice Core ◽  
Ice Cores ◽  
The Arctic ◽  
Surface Mass ◽  
Intercomparison Project ◽  
The Alps ◽  
Former Ussr

Abstract. As part of the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), we evaluate the historical black carbon (BC) aerosols simulated by 8 ACCMIP models against observations including 12 ice core records, long-term surface mass concentrations and recent Arctic BC snowpack measurements. We also estimate BC albedo forcing by performing additional simulations using offline models with prescribed meteorology from 1996–2000. We evaluated the vertical profile of BC snow concentrations from these offline simulations using the recent BC snowpack measurements. Despite using the same BC emissions, the global BC burden differs by approximately a factor of 3 among models due to differences in aerosol removal parameterizations and simulated meteorology: 34 Gg to 103 Gg in 1850 and 82 Gg to 315 Gg in 2000. However, the global BC burden from preindustrial to present-day increases by 2.5–3 times with little variation among models, roughly matching the 2.5-fold increase in total BC emissions during the same period. We find a large divergence among models at both Northern Hemisphere (NH) and Southern Hemisphere (SH) high latitude regions for BC burden and at SH high latitude regions for deposition fluxes. The ACCMIP simulations match the observed BC surface mass concentrations well in Europe and North America except at Jungfraujoch and Ispra. However, the models fail to predict the Arctic BC seasonality due to severe underestimations during winter and spring. The simulated vertically resolved BC snow concentrations are, on average, within a factor of 2–3 of the BC snowpack measurements except for Greenland and the Arctic Ocean. For the ice core evaluation, models tend to capture both the observed temporal trends and the magnitudes well at Greenland sites. However, models fail to predict the decreasing trend of BC depositions/ice-core concentrations from the 1950s to the 1970s in most Tibetan Plateau ice cores. The distinct temporal trend at the Tibetan Plateau ice cores indicates a strong influence from Western Europe, but the modeled BC increases in that period are consistent with the emission changes in Eastern Europe, the Middle East, South and East Asia. At the Alps site, the simulated BCsuggests a strong influence from Europe, which agrees with the Alps ice core observations. Models successfully simulate higher BC concentrations observed at Zuoqiupu during the non-monsoon season than monsoon season, but models underpredict BC in both seasons. Despite a large divergence in BC deposition at two Antarctic ice core sites, models are able to capture the relative increase from preindustrial to present-day seen in the ice cores. In 2000 relative to 1850, globally annually averaged BC surface albedo forcing from the offline simulations ranges from 0.014 to 0.019 W m−2 among the ACCMIP models. Comparing offline and online BC albedo forcings computed by some of the same models, we find that the global annual mean can vary by up to a factor of two because of different aerosol models or different BC-snow parameterizations and snow cover. The spatial distributions of the offline BC albedo forcing in 2000 show especially high BC forcing (i.e. over 0.1 W m−2) over Manchuria, Karakoram, and most of the Former USSR. Models predict the highest global annual mean BC forcing in 1980 rather than 2000, mostly driven by the high fossil fuel and biofuel emissions in the Former USSR in 1980.

scholarly journals Tropospheric ozone changes, radiative forcing and attribution to emissions in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)

2013 ◽  
Vol 13 (6) ◽  
pp. 3063-3085 ◽  
Author(s):  
D. S. Stevenson ◽  
P. J. Young ◽  
V. Naik ◽  
J.-F. Lamarque ◽  
D. T. Shindell ◽  
...  
Keyword(s):  
Climate Change ◽  
Atmospheric Chemistry ◽  
Tropospheric Ozone ◽  
Climate Model ◽  
Anthropogenic Emissions ◽  
Model Intercomparison ◽  
A Value ◽  
Intercomparison Project ◽  
Column Ozone ◽  
Global Mean

Abstract. Ozone (O3) from 17 atmospheric chemistry models taking part in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) has been used to calculate tropospheric ozone radiative forcings (RFs). All models applied a common set of anthropogenic emissions, which are better constrained for the present-day than the past. Future anthropogenic emissions follow the four Representative Concentration Pathway (RCP) scenarios, which define a relatively narrow range of possible air pollution emissions. We calculate a value for the pre-industrial (1750) to present-day (2010) tropospheric ozone RF of 410 mW m−2. The model range of pre-industrial to present-day changes in O3 produces a spread (±1 standard deviation) in RFs of ±17%. Three different radiation schemes were used – we find differences in RFs between schemes (for the same ozone fields) of ±10%. Applying two different tropopause definitions gives differences in RFs of ±3%. Given additional (unquantified) uncertainties associated with emissions, climate-chemistry interactions and land-use change, we estimate an overall uncertainty of ±30% for the tropospheric ozone RF. Experiments carried out by a subset of six models attribute tropospheric ozone RF to increased emissions of methane (44±12%), nitrogen oxides (31 ± 9%), carbon monoxide (15 ± 3%) and non-methane volatile organic compounds (9 ± 2%); earlier studies attributed more of the tropospheric ozone RF to methane and less to nitrogen oxides. Normalising RFs to changes in tropospheric column ozone, we find a global mean normalised RF of 42 mW m−2 DU−1, a value similar to previous work. Using normalised RFs and future tropospheric column ozone projections we calculate future tropospheric ozone RFs (mW m−2; relative to 1750) for the four future scenarios (RCP2.6, RCP4.5, RCP6.0 and RCP8.5) of 350, 420, 370 and 460 (in 2030), and 200, 300, 280 and 600 (in 2100). Models show some coherent responses of ozone to climate change: decreases in the tropical lower troposphere, associated with increases in water vapour; and increases in the sub-tropical to mid-latitude upper troposphere, associated with increases in lightning and stratosphere-to-troposphere transport. Climate change has relatively small impacts on global mean tropospheric ozone RF.

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