scholarly journals Climatic effects of 1950–2050 changes in US anthropogenic aerosols – Part 2: Climate response

2012 ◽  
Vol 12 (7) ◽  
pp. 3349-3362 ◽  
Author(s):  
E. M. Leibensperger ◽  
L. J. Mickley ◽  
D. J. Jacob ◽  
W.-T. Chen ◽  
J. H. Seinfeld ◽  
...  
Keyword(s):  
Air Quality ◽  
Radiative Forcing ◽  
General Circulation ◽  
Transport Model ◽  
Circulation Model ◽  
Climate Response ◽  
Anthropogenic Aerosols ◽  
Anthropogenic Aerosol ◽  
The Us ◽  
Aerosol Sources

Abstract. We investigate the climate response to changing US anthropogenic aerosol sources over the 1950–2050 period by using the NASA GISS general circulation model (GCM) and comparing to observed US temperature trends. Time-dependent aerosol distributions are generated from the GEOS-Chem chemical transport model applied to historical emission inventories and future projections. Radiative forcing from US anthropogenic aerosols peaked in 1970–1990 and has strongly declined since due to air quality regulations. We find that the regional radiative forcing from US anthropogenic aerosols elicits a strong regional climate response, cooling the central and eastern US by 0.5–1.0 °C on average during 1970–1990, with the strongest effects on maximum daytime temperatures in summer and autumn. Aerosol cooling reflects comparable contributions from direct and indirect (cloud-mediated) radiative effects. Absorbing aerosol (mainly black carbon) has negligible warming effect. Aerosol cooling reduces surface evaporation and thus decreases precipitation along the US east coast, but also increases the southerly flow of moisture from the Gulf of Mexico resulting in increased cloud cover and precipitation in the central US. Observations over the eastern US show a lack of warming in 1960–1980 followed by very rapid warming since, which we reproduce in the GCM and attribute to trends in US anthropogenic aerosol sources. Present US aerosol concentrations are sufficiently low that future air quality improvements are projected to cause little further warming in the US (0.1 °C over 2010–2050). We find that most of the warming from aerosol source controls in the US has already been realized over the 1980–2010 period.

scholarly journals Climatic effects of 1950–2050 changes in US anthropogenic aerosols – Part 2: Climate response

2011 ◽  
Vol 11 (8) ◽  
pp. 24127-24164 ◽  
Author(s):  
E. M. Leibensperger ◽  
L. J. Mickley ◽  
D. J. Jacob ◽  
W.-T. Chen ◽  
J. H. Seinfeld ◽  
...  
Keyword(s):  
Air Quality ◽  
Radiative Forcing ◽  
General Circulation ◽  
Transport Model ◽  
Circulation Model ◽  
Climate Response ◽  
Anthropogenic Aerosols ◽  
Anthropogenic Aerosol ◽  
The Us ◽  
Aerosol Sources

Abstract. We investigate the climate response to US anthropogenic aerosol sources over the 1950 to 2050 period by using the NASA GISS general circulation model (GCM) and comparing to observed US temperature trends. Time-dependent aerosol distributions are generated from the GEOS-Chem chemical transport model applied to historical emission inventories and future projections. Radiative forcing from US anthropogenic aerosols peaked in 1970–1990 and has strongly declined since due to air quality regulations. We find that the regional radiative forcing from US anthropogenic aerosols elicits a strong regional climate response, cooling the central and eastern US by 0.5–1.0 °C on average during 1970–1990, with the strongest effects on maximum daytime temperatures in summer and autumn. Aerosol cooling reflects comparable contributions from direct and indirect (cloud-mediated) radiative effects. Absorbing aerosol (mainly black carbon) has negligible warming effect. Aerosol cooling reduces surface evaporation and thus decreases precipitation along the US east coast, but also increases the southerly flow of moisture from the Gulf of Mexico resulting in increased cloud cover and precipitation in the central US. Observations over the eastern US show a lack of warming in 1960–1980 followed by very rapid warming since, which we reproduce in the GCM and attribute to trends in US anthropogenic aerosol sources. Present US aerosol concentrations are sufficiently low that future air quality improvements are projected to cause little further warming in the US (0.1 °C over 2010–2050). We find that most of the potential warming from aerosol source controls in the US has already been realized over the 1980–2010 period.

scholarly journals Climatic effects of 1950–2050 changes in US anthropogenic aerosols – Part 1: Aerosol trends and radiative forcing

2011 ◽  
Vol 11 (8) ◽  
pp. 24085-24125 ◽  
Author(s):  
E. M. Leibensperger ◽  
L. J. Mickley ◽  
D. J. Jacob ◽  
W.-T. Chen ◽  
J. H. Seinfeld ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
General Circulation ◽  
Transport Model ◽  
Circulation Model ◽  
Anthropogenic Sources ◽  
So2 Emissions ◽  
Anthropogenic Aerosols ◽  
Climatic Effects ◽  
Anthropogenic Aerosol ◽  
Direct Forcing

Abstract. We use the GEOS-Chem chemical transport model combined with the GISS general circulation model to calculate the aerosol direct and indirect (warm cloud) radiative forcings from US anthropogenic sources over the 1950–2050 period, based on historical emission inventories and future projections from the IPCC A1B scenario. The aerosol simulation is evaluated with observed spatial distributions and 1980–2010 trends of aerosol concentrations and wet deposition in the contiguous US. The radiative forcing from US anthropogenic aerosols is strongly localized over the eastern US. We find that it peaked in 1970–1990, with values over the eastern US (east of 100° W) of −2.0 W m−2 for direct forcing including contributions from sulfate (−2.0 W m−2), nitrate (−0.2 W m−2), organic carbon (−0.2 W m−2), and black carbon (+0.4 W m−2). The aerosol indirect effect is of comparable magnitude to the direct forcing. We find that the forcing declined sharply from 1990 to 2010 (by 0.8 W m−2 direct and 1.0 W m−2 indirect), mainly reflecting decreases in SO2 emissions, and project that it will continue declining post-2010 but at a much slower rate since US SO2 emissions have already declined by almost 60 % from their peak. This suggests that much of the warming effect of reducing US anthropogenic aerosol sources may have already been realized by 2010, however some additional warming is expected through 2020. The small positive radiative forcing from US BC emissions (+0.3 W m−2 over the eastern US in 2010) suggests that an emission control strategy focused on BC would have only limited climate benefit.

scholarly journals Climatic effects of 1950–2050 changes in US anthropogenic aerosols – Part 1: Aerosol trends and radiative forcing

2012 ◽  
Vol 12 (7) ◽  
pp. 3333-3348 ◽  
Author(s):  
E. M. Leibensperger ◽  
L. J. Mickley ◽  
D. J. Jacob ◽  
W.-T. Chen ◽  
J. H. Seinfeld ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
General Circulation ◽  
Circulation Model ◽  
Radiative Properties ◽  
Anthropogenic Sources ◽  
So2 Emissions ◽  
Anthropogenic Aerosols ◽  
Climatic Effects ◽  
Anthropogenic Aerosol ◽  
Direct Forcing

Abstract. We calculate decadal aerosol direct and indirect (warm cloud) radiative forcings from US anthropogenic sources over the 1950–2050 period. Past and future aerosol distributions are constructed using GEOS-Chem and historical emission inventories and future projections from the IPCC A1B scenario. Aerosol simulations are evaluated with observed spatial distributions and 1980–2010 trends of aerosol concentrations and wet deposition in the contiguous US. Direct and indirect radiative forcing is calculated using the GISS general circulation model and monthly mean aerosol distributions from GEOS-Chem. The radiative forcing from US anthropogenic aerosols is strongly localized over the eastern US. We find that its magnitude peaked in 1970–1990, with values over the eastern US (east of 100° W) of −2.0 W m−2 for direct forcing including contributions from sulfate (−2.0 W m−2), nitrate (−0.2 W m−2), organic carbon (−0.2 W m−2), and black carbon (+0.4 W m−2). The uncertainties in radiative forcing due to aerosol radiative properties are estimated to be about 50%. The aerosol indirect effect is estimated to be of comparable magnitude to the direct forcing. We find that the magnitude of the forcing declined sharply from 1990 to 2010 (by 0.8 W m−2 direct and 1.0 W m−2 indirect), mainly reflecting decreases in SO2 emissions, and project that it will continue declining post-2010 but at a much slower rate since US SO2 emissions have already declined by almost 60% from their peak. This suggests that much of the warming effect of reducing US anthropogenic aerosol sources has already been realized. The small positive radiative forcing from US BC emissions (+0.3 W m−2 over the eastern US in 2010; 5% of the global forcing from anthropogenic BC emissions worldwide) suggests that a US emission control strategy focused on BC would have only limited climate benefit.

scholarly journals Meteorological modes of variability for fine particulate matter (PM2.5) air quality in the United States: implications for PM2.5 sensitivity to climate change

2012 ◽  
Vol 12 (6) ◽  
pp. 3131-3145 ◽  
Author(s):  
A. P. K. Tai ◽  
L. J. Mickley ◽  
D. J. Jacob ◽  
E. M. Leibensperger ◽  
L. Zhang ◽  
...  
Keyword(s):  
Climate Change ◽  
General Circulation ◽  
Transport Model ◽  
Circulation Model ◽  
Multiple Linear Regression Model ◽  
The United States ◽  
Chemical Transport Model ◽  
Modes Of Variability ◽  
The Us ◽  
Cyclone Frequency

Abstract. We applied a multiple linear regression model to understand the relationships of PM2.5 with meteorological variables in the contiguous US and from there to infer the sensitivity of PM2.5 to climate change. We used 2004–2008 PM2.5 observations from ~1000 sites (~200 sites for PM2.5 components) and compared to results from the GEOS-Chem chemical transport model (CTM). All data were deseasonalized to focus on synoptic-scale correlations. We find strong positive correlations of PM2.5 components with temperature in most of the US, except for nitrate in the Southeast where the correlation is negative. Relative humidity (RH) is generally positively correlated with sulfate and nitrate but negatively correlated with organic carbon. GEOS-Chem results indicate that most of the correlations of PM2.5 with temperature and RH do not arise from direct dependence but from covariation with synoptic transport. We applied principal component analysis and regression to identify the dominant meteorological modes controlling PM2.5 variability, and show that 20–40% of the observed PM2.5 day-to-day variability can be explained by a single dominant meteorological mode: cold frontal passages in the eastern US and maritime inflow in the West. These and other synoptic transport modes drive most of the overall correlations of PM2.5 with temperature and RH except in the Southeast. We show that interannual variability of PM2.5 in the US Midwest is strongly correlated with cyclone frequency as diagnosed from a spectral-autoregressive analysis of the dominant meteorological mode. An ensemble of five realizations of 1996–2050 climate change with the GISS general circulation model (GCM) using the same climate forcings shows inconsistent trends in cyclone frequency over the Midwest (including in sign), with a likely decrease in cyclone frequency implying an increase in PM2.5. Our results demonstrate the need for multiple GCM realizations (because of climate chaos) when diagnosing the effect of climate change on PM2.5, and suggest that analysis of meteorological modes of variability provides a computationally more affordable approach for this purpose than coupled GCM-CTM studies.

scholarly journals Contrasting the direct radiative effect and direct radiative forcing of aerosols

2014 ◽  
Vol 14 (11) ◽  
pp. 5513-5527 ◽  
Author(s):  
C. L. Heald ◽  
D. A. Ridley ◽  
J. H. Kroll ◽  
S. R. H. Barrett ◽  
K. E. Cady-Pereira ◽  
...  
Keyword(s):  
Energy Balance ◽  
Radiative Forcing ◽  
Transport Model ◽  
Radiative Transfer Model ◽  
Transfer Model ◽  
Radiative Effect ◽  
Chemical Transport Model ◽  
Anthropogenic Aerosols ◽  
Anthropogenic Aerosol ◽  
Direct Radiative Forcing

Abstract. The direct radiative effect (DRE) of aerosols, which is the instantaneous radiative impact of all atmospheric particles on the Earth's energy balance, is sometimes confused with the direct radiative forcing (DRF), which is the change in DRE from pre-industrial to present-day (not including climate feedbacks). In this study we couple a global chemical transport model (GEOS-Chem) with a radiative transfer model (RRTMG) to contrast these concepts. We estimate a global mean all-sky aerosol DRF of −0.36 Wm−2 and a DRE of −1.83 Wm−2 for 2010. Therefore, natural sources of aerosol (here including fire) affect the global energy balance over four times more than do present-day anthropogenic aerosols. If global anthropogenic emissions of aerosols and their precursors continue to decline as projected in recent scenarios due to effective pollution emission controls, the DRF will shrink (−0.22 Wm−2 for 2100). Secondary metrics, like DRE, that quantify temporal changes in both natural and anthropogenic aerosol burdens are therefore needed to quantify the total effect of aerosols on climate.

scholarly journals Atmospheric impact of the 1783–1784 Laki Eruption: Part II Climatic effect of sulphate aerosol

2003 ◽  
Vol 3 (4) ◽  
pp. 1177-1189 ◽  
Author(s):  
E.-J. Highwood ◽  
D. S. Stevenson
Keyword(s):  
Northern Hemisphere ◽  
Radiative Forcing ◽  
General Circulation ◽  
Model Simulation ◽  
Circulation Model ◽  
Climate Response ◽  
Sulphate Aerosol ◽  
Cold Temperatures ◽  
Direct Radiative Forcing ◽  
The Impact

Abstract. The long 1783-1784 eruption of Laki in southern Iceland, was one of the first eruptions to have been linked to an observed climate anomaly, having been held responsible for cold temperatures over much of the Northern Hemisphere in the period 1783-1785. Results from the first climate model simulation of the impact of a similar eruption to that of 1783-1784 are presented. Using sulphate aerosol fields produced in a companion chemical transport model simulation by Stevenson et al. (2003), the radiative forcing and climate response due to the aerosol are calculated here using the Reading Intermediate General Circulation Model (IGCM). The peak Northern Hemisphere mean direct radiative forcing is -5.5 Wm-2 in August 1783. The radiative forcing dies away quickly as the emissions from the volcano decrease; however, a small forcing remains over the Mediterranean until March 1784. There is little forcing in the Southern Hemisphere. There is shown to be an uncertainty of at least 50% in the direct radiative forcing due to assumptions concerning relative humidity and the sophistication of the radiative transfer code used. The indirect effects of the Laki aerosol are potentially large but essentially unquantifiable at the present time. In the IGCM at least, the aerosol from the eruption produces a climate response that is spatially very variable. The Northern Hemisphere mean temperature anomaly averaged over the whole of the calendar year containing most of the eruption is -0.21 K, statistically significant at the 95% level and in reasonable agreement with the available observations of the temperature during 1783.

scholarly journals Comparison of Climate Response to Anthropogenic Aerosol versus Greenhouse Gas Forcing: Distinct Patterns

2016 ◽  
Vol 29 (14) ◽  
pp. 5175-5188 ◽  
Author(s):  
Hai Wang ◽  
Shang-Ping Xie ◽  
Qinyu Liu
Keyword(s):  
Northern Hemisphere ◽  
Radiative Forcing ◽  
Climate Model ◽  
East Asian Monsoon ◽  
Climate Response ◽  
Anthropogenic Aerosols ◽  
Anthropogenic Aerosol ◽  
Asian Monsoon Region ◽  
Surface Temperature Change ◽  
Aerosol Forcing

Abstract Spatial patterns of climate response to changes in anthropogenic aerosols and well-mixed greenhouse gases (GHGs) are investigated using climate model simulations for the twentieth century. The climate response shows both similarities and differences in spatial pattern between aerosol and GHG runs. Common climate response between aerosol and GHG runs tends to be symmetric about the equator. This work focuses on the distinctive patterns that are unique to the anthropogenic aerosol forcing. The tropospheric cooling induced by anthropogenic aerosols is locally enhanced in the midlatitude Northern Hemisphere with a deep vertical structure around 40°N, anchoring a westerly acceleration in thermal wind balance. The aerosol-induced negative radiative forcing in the Northern Hemisphere requires a cross-equatorial Hadley circulation to compensate interhemispheric energy imbalance in the atmosphere. Associated with a southward shift of the intertropical convergence zone, this interhemispheric asymmetric mode is unique to aerosol forcing and absent in GHG runs. Comparison of key climate response pattern indices indicates that the aerosol forcing dominates the interhemispheric asymmetric climate response in historical all-forcing simulations, as well as regional precipitation change such as the drying trend over the East Asian monsoon region. While GHG forcing dominates global mean surface temperature change, its effect is on par with and often opposes the aerosol effect on precipitation, making it difficult to detect anthropogenic change in rainfall from historical observations.

scholarly journals Prognostic precipitation with three liquid water classes in the ECHAM5-HAM GCM

2015 ◽  
Vol 15 (5) ◽  
pp. 7783-7836
Author(s):  
V. Sant ◽  
R. Posselt ◽  
U. Lohmann
Keyword(s):  
Liquid Water ◽  
Radiative Forcing ◽  
General Circulation ◽  
Large Scale ◽  
Circulation Model ◽  
Liquid Water Path ◽  
Anthropogenic Aerosol ◽  
Global Circulation Models ◽  
Aerosol Forcing ◽  
Ice Phase

Abstract. In order to improve the global representation of rain formation in marine stratiform clouds a new parameterization with three prognostic liquid water classes was implemented into the general circulation model ECHAM5 with the aerosol module HAM. The additionally introduced drizzle class improves the physical representation of the droplet spectrum and more importantly, improves the microphysical processes relevant for precipitation formation compared to the standard parameterization. In order to avoid a mismatch of the liquid and ice phase, the prognostic treatment of snow has been introduced too. This has a significant effect on the amount and altitude of ice clouds, which in turn does not only affect in- and outgoing radiation, but also the parameterized collection rates. With the introduction of a prognostic precipitation scheme a more realistic representation of both liquid and ice phase large-scale precipitation is achieved compared to a diagnostic treatment. An encouraging finding is that the sensitivity of the liquid water path to the anthropogenic aerosol forcing with the prognostic treatment is reduced by about 25%. Although the total net radiative forcing is increased from 1.4±0.4 to 1.6±0.4 W m−2 from the control to the prognostic model version, the difference is within the interannual variability. Altogether the results suggest that the treatment of precipitation in global circulation models has a significant influence on the phase and lifetime of clouds, but also hints towards the uncertainties related to a prognostic precipitation scheme.

scholarly journals Competing Atmospheric and Surface-Driven Impacts of Absorbing Aerosols on the East Asian Summertime Climate

2017 ◽  
Vol 30 (22) ◽  
pp. 8929-8949 ◽  
Author(s):  
Geeta G. Persad ◽  
David J. Paynter ◽  
Yi Ming ◽  
V. Ramaswamy
Keyword(s):  
Land Surface ◽  
Radiative Forcing ◽  
General Circulation ◽  
Asian Summer Monsoon ◽  
Regional Climate ◽  
East Asian ◽  
Circulation Model ◽  
Anthropogenic Aerosols ◽  
Atmospheric Heating ◽  
Absorbing Aerosols

East Asia has some of the largest concentrations of absorbing aerosols globally, and these, along with the region’s scattering aerosols, have both reduced the amount of solar radiation reaching Earth’s surface regionally (solar dimming) and increased shortwave absorption within the atmosphere, particularly during the peak months of the East Asian summer monsoon (EASM). This study analyzes how atmospheric absorption and surface solar dimming compete in driving the response of regional summertime climate to anthropogenic aerosols, which dominates, and why—issues of particular importance for predicting how East Asian climate will respond to projected changes in absorbing and scattering aerosol emissions in the future. These questions are probed in a state-of-the-art general circulation model using a combination of realistic and novel idealized aerosol perturbations that allow analysis of the relative influence of absorbing aerosols’ atmospheric and surface-driven impacts on regional circulation and climate. Results show that even purely absorption-driven dimming decreases EASM precipitation by cooling the land surface, counteracting climatological land–sea contrast and reducing ascending atmospheric motion and onshore winds, despite the associated positive top-of-the-atmosphere regional radiative forcing. Absorption-driven atmospheric heating does partially offset the precipitation and surface evaporation reduction from surface dimming, but the overall response to aerosol absorption more closely resembles the response to its surface dimming than to its atmospheric heating. These findings provide a novel decomposition of absorbing aerosol’s impacts on regional climate and demonstrate that the response cannot be expected to follow the sign of absorption’s top-of-the-atmosphere or even atmospheric radiative perturbation.

scholarly journals Concentrations and radiative forcing of anthropogenic aerosols from 1750–2014 simulated with the OsloCTM3 and CEDS emission inventory

2018 ◽  
Author(s):  
Marianne T. Lund ◽  
Gunnar Myhre ◽  
Amund S. Haslerud ◽  
Ragnhild B. Skeie ◽  
Jan Griesfeller ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
Emission Inventory ◽  
Transport Model ◽  
Model Performance ◽  
Anthropogenic Aerosols ◽  
Anthropogenic Aerosol ◽  
Emission Data ◽  
Sensitivity Tests ◽  
Emission Changes ◽  
New Community

Abstract. We document the ability of the new generation Oslo chemistry-transport model, OsloCTM3, to accurately simulate present-day aerosol distributions. The model is then used with the new Community Emission Data System (CEDS) historical emission inventory to provide updated time series of anthropogenic aerosol concentrations and consequent direct radiative forcing (RFari) from 1750 to 2014. Overall, the OsloCTM3 performs well compared with measurements of surface concentrations and remotely sensed aerosol optical depth. Concentrations are underestimated in Asia, but the higher emissions in CEDS than previous inventories result in improvements compared to observations. The black carbon (BC) treatment in OsloCTM3 gives better agreement with observed vertical BC profiles relative to the predecessor OsloCTM2. However, Arctic wintertime BC concentrations remain underestimated, and a range of sensitivity tests indicate that better physical understanding of processes associated with atmospheric BC processing is required to simultaneously reproduce both the observed features. Uncertainties in model input data, resolution and scavenging affects the distribution of all aerosols species, especially at high latitudes and altitudes. However, we find no evidence of consistently better model performance across all observables and regions in the sensitivity tests than in the baseline configuration. Using CEDS, we estimate a total net RFari in 2014 relative to 1750 of −0.17 W m−2, significantly weaker than the IPCC AR5 2010–1750 estimate. Differences are attributable to several factors, including stronger absorption by organic aerosol, updated parameterization of BC absorption, and reduced sulfate cooling. The trend towards a weaker RFari over recent years is more pronounced than in the IPCC AR5, illustrating the importance of capturing recent regional emission changes.

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