Science.gov

Sample records for aerosol climate effects

  1. Aerosol indirect effect on biogeochemical cycles and climate.

    PubMed

    Mahowald, Natalie

    2011-11-11

    The net effect of anthropogenic aerosols on climate is usually considered the sum of the direct radiative effect of anthropogenic aerosols, plus the indirect effect of these aerosols through aerosol-cloud interactions. However, an additional impact of aerosols on a longer time scale is their indirect effect on climate through biogeochemical feedbacks, largely due to changes in the atmospheric concentration of CO(2). Aerosols can affect land and ocean biogeochemical cycles by physical forcing or by adding nutrients and pollutants to ecosystems. The net biogeochemical effect of aerosols is estimated to be equivalent to a radiative forcing of -0.5 ± 0.4 watts per square meter, which suggests that reaching lower carbon targets will be even costlier than previously estimated.

  2. Aerosol effects on deep convection in a multi-scale aerosol-climate model

    NASA Astrophysics Data System (ADS)

    Wang, M.; Ghan, S. J.; Morrison, H.

    2012-12-01

    Aerosols have been demonstrated to affect convective clouds and precipitation in observations, process models, and regional climate models. However, examining aerosol effects on convective clouds and precipitation in global climate models has been extremely challenging, as until recently the treatments in the few global climate models that include aerosol effects on convective clouds have used conventional cumulus parameterizations and hence have been quite crude. We have recently built a multi-scale aerosol-climate model, PNNL-MMF, which is an extension of a multi-scale modeling framework (MMF) model. The extended model explicitly treats aerosol effects on deep convection using a two-moment cloud microphysics scheme in the cloud-resolving model component of the MMF. In this presentation, we examine aerosol effects on convective clouds at the global scale using the PNNL-MMF model. Our results show that the frequency of precipitation occurrence at a given liquid water path increases with increasing aerosol loading for deep clouds with surface precipitation rate larger than 10 mm/day. This relationship is particularly evident during the summer time, when convection activity is strong, and may indicate invigoration of deep convection by aerosols. The modeled relationship of aerosols, clouds and precipitation is further compared with observations from the ARM long-term sites (e.g., SGP). The causes of the modeled relationship of aerosols, clouds and precipitations are examined by using a pair of 5-year MMF simulations with and without anthropogenic aerosols.

  3. Climate Effects of Black Carbon Aerosols in China and India

    NASA Astrophysics Data System (ADS)

    Menon, Surabi; Hansen, James; Nazarenko, Larissa; Luo, Yunfeng

    2002-09-01

    In recent decades, there has been a tendency toward increased summer floods in south China, increased drought in north China, and moderate cooling in China and India while most of the world has been warming. We used a global climate model to investigate possible aerosol contributions to these trends. We found precipitation and temperature changes in the model that were comparable to those observed if the aerosols included a large proportion of absorbing black carbon (``soot''), similar to observed amounts. Absorbing aerosols heat the air, alter regional atmospheric stability and vertical motions, and affect the large-scale circulation and hydrologic cycle with significant regional climate effects.

  4. Potential Climate Effects of Dust Aerosols' over West Africa

    NASA Astrophysics Data System (ADS)

    JI, Z.; Wang, G.; Pal, J. S.; Yu, M.

    2014-12-01

    Climate in West Africa is under the influence of the West African monsoon circulation and mineral dust emitted from the Sahara desert (which is the world's largest source of mineral dust emission). Dust aerosols alter the atmospheric radiative fluxes and act as cloud condensation nuclei in the process of emission, transportation and deposition. However, our understanding regarding how dust aerosols influence the present-day and future climate of West Africa is very limited. In this study, a regional climate model RegCM4.3.4-CLM4.5 is used to investigate the potential climatic effects of dust aerosols both in present (1981-2000) and future (2081-2100) periods over WA. First, the model performance and dust climatic effects are evaluated. The contribution of dust climatic effects under RCP8.5 scenario and their confounding effects with land use change are assessed. Our results indicate that the model can reproduce with reasonable accuracy the spatial and temporal distribution of climatology, aerosol optical depth and surface concentration over WA. The shortwave radiative forcing of dust is negative in the surface and positive in the atmosphere, with greater changes in JJA and MAM compared to those in SON and DJF. Over most of West Africa, cooling is the dominant effect on temperature. Their impact on precipitation features a dipole pattern, with decrease in the north and increase in the south of West Africa. Despite the dust-induced decrease of precipitation amount, dusts cause extreme precipitation to increase. To evaluate the uncertainties surrounding our modeling results, sensitivity experiments driven by ICBC from MIROC-ESM and CESM and their dynamic downscaling results are used for comparisons. Results from these sensitivity experiments indicate that the impact of dust aerosols on present and future climate is robust.

  5. Revisiting Aerosol Effects in Global Climate Models Using an Aerosol Lidar Simulator

    NASA Astrophysics Data System (ADS)

    Ma, P. L.; Chepfer, H.; Winker, D. M.; Ghan, S.; Rasch, P. J.

    2015-12-01

    Aerosol effects are considered a major source of uncertainty in global climate models and the direct and indirect radiative forcings have strong model dependency. These forcings are routinely evaluated (and calibrated) against observations, among them satellite retrievals are greatly used for their near-global coverage. However, the forcings calculated from model output are not directly comparable with those computed from satellite retrievals since sampling and algorithmic differences (such as cloud screening, noise reduction, and retrieval) between models and observations are not accounted for. It is our hypothesis that the conventional model validation procedures for comparing satellite observations and model simulations can mislead model development and introduce biases. Hence, we have developed an aerosol lidar simulator for global climate models that simulates the CALIOP lidar signal at 532nm. The simulator uses the same algorithms as those used to produce the "GCM-oriented CALIPSO Aerosol Product" to (1) objectively sample lidar signal profiles; and (2) derive aerosol fields (e.g., extinction profile, aerosol type, etc) from lidar signals. This allows us to sample and derive aerosol fields in the model and real atmosphere in identical ways. Using the Department of Energy's ACME model simulations, we found that the simulator-retrieved aerosol distribution and aerosol-cloud interactions are significantly different from those computed from conventional approaches, and that the model is much closer to satellite estimates than previously believed.

  6. Modeling the Relationships Between Aerosol Properties and the Direct and Indirect Effects of Aerosols on Climate

    NASA Technical Reports Server (NTRS)

    Toon, Owen B.

    1994-01-01

    Aerosols may affect climate directly by scattering and absorbing visible and infrared energy, They may also affect climate indirectly by modifying the properties of clouds through microphysical processes, and by altering abundances of radiatively important gases through heterogeneous chemistry. Researchers understand which aerosol properties control the direct effect of aerosols on the radiation budget. Unfortunately, despite an abundance of data on certain types of aerosols, much work remains to be done to determine the values of these properties. For instance we have little idea about the global distribution, seasonal variation, or interannual variability of the aerosol optical depth. Also we do not know the visible light absorption properties of tropical aerosols which may contain much debris from slash and burn agriculture. A positive correlation between aerosol concentrations and albedos of marine stratus clouds is observed, and the causative microphysics is understood. However, models suggest that it is difficult to produce new particles in the marine boundary layer. Some modelers have suggested that the particles in the marine boundary layer may originate in the free troposphere and be transported into the boundary layer. Others argue that the aerosols are created in the marine boundary layer. There are no data linking aerosol concentration and cirrus cloud albedo, and models suggest cirrus properties may not be very sensitive to aerosol abundance. There is clear evidence of a radiatively significant change in the global lower stratospheric ozone abundance during the past few decades. These changes are caused by heterogeneous chemical reactions occurring on the surfaces of particles. The rates of these reactions depend upon the chemical composition of the particles. Although rapid advances in understanding heterogeneous chemistry have been made, much remains to be done.

  7. BAECC Biogenic Aerosols - Effects on Clouds and Climate

    SciTech Connect

    Petäjä, Tuukka; Moisseev, Dmitri; Sinclair, Victoria; O'Connor, Ewan J.; Manninen, Antti J.; Levula, Janne; Väänänen, Riikka; Heikkinen, Liine; Äijälä, Mikko; Aalto, Juho; Bäck, Jaana

    2015-11-01

    “Biogenic Aerosols - Effects on Clouds and Climate (BAECC)”, featured the U.S. Department of Energy’s Atmospheric Radiation Measurement (ARM) Program’s 2nd Mobile Facility (AMF2) in Hyytiälä, Finland. It operated for an 8-month intensive measurement campaign from February to September 2014. The main research goal was to understand the role of biogenic aerosols in cloud formation. One of the reasons to perform BAECC study in Hyytiälä was the fact that it hosts SMEAR-II (Station for Measuring Forest Ecosystem-Atmosphere Relations), which is one of the world’s most comprehensive surface in-situ observation sites in a boreal forest environment. The station has been measuring atmospheric aerosols, biogenic emissions and an extensive suite of parameters relevant to atmosphere-biosphere interactions continuously since 1996. The BAECC enables combining vertical profiles from AMF2 with surface-based in-situ SMEAR-II observations and allows the processes at the surface to be directly related to processes occurring throughout the entire tropospheric column. With the inclusion of extensive surface precipitation measurements, and intensive observation periods involving aircraft flights and novel radiosonde launches, the complementary observations of AMF2 and SMEAR-II provide a unique opportunity for investigating aerosol-cloud interactions, and cloud-to-precipitation processes. The BAECC dataset will initiate new opportunities for evaluating and improving models of aerosol sources and transport, cloud microphysical processes, and boundary-layer structures.

  8. Effect of Aerosol and Ocean Representation on Simulated Climate Responses

    NASA Astrophysics Data System (ADS)

    Dallafior, Tanja; Folini, Doris; Knutti, Reto; Wild, Martin

    2016-04-01

    It is still debated to what extent anthropogenic aerosols shaped 20th century surface temperatures, especially sea surface temperatures (SSTs), through alteration of surface solar radiation (SSR). SSTs, in turn, are crucial in the context of atmospheric circulation and ocean heat uptake. Uncertainty considering anthropogenic aerosol forcing thus translates into uncertainty regarding ocean heat uptake and, ultimately, climate responses towards anthropogenic influences. We use the global climate model ECHAM to analyse the 20th century climate response towards either anthropogenic aerosols or well-mixed greenhouse gases or both with different representations of ocean and aerosols: atmosphere-only with prescribed SSTs and interactive aerosols; mixed-layer ocean and interactive or prescribed aerosols; fully coupled with prescribed aerosols. For interactive aerosols we use the Hamburg Aerosol Module (HAM). Our results suggest that up to 15% of global ocean surfaces undergo an SSR reduction of at least -4W/m² in the year 2000, due to anthropogenic aerosols. The area affected depends on how aerosols are represented and whether clear sky or all sky SSR is considered. In MLO equilibria with interactive aerosols, anthropogenic aerosols clearly shape surface temperature response patterns. This is to a lesser degree the case for the transient fully coupled case. Additivity of global mean temperature responses towards single forcings - an assumption often made in the literature - is not fulfilled for the MLO experiments, but for the fully coupled experiments. While some of these differences can be attributed to the differing ocean representation, it is implied that differing aerosol representation may play an even more relevant role. Thus, our results corroborate not only the relevance of anthropogenic aerosols for surface temperature responses, but also highlight the relevance of choice of aerosol representation.

  9. Aerosol Indirect Effects on Cirrus Clouds in Global Aerosol-Climate Models

    NASA Astrophysics Data System (ADS)

    Liu, X.; Zhang, K.; Wang, Y.; Neubauer, D.; Lohmann, U.; Ferrachat, S.; Zhou, C.; Penner, J.; Barahona, D.; Shi, X.

    2015-12-01

    Cirrus clouds play an important role in regulating the Earth's radiative budget and water vapor distribution in the upper troposphere. Aerosols can act as solution droplets or ice nuclei that promote ice nucleation in cirrus clouds. Anthropogenic emissions from fossil fuel and biomass burning activities have substantially perturbed and enhanced concentrations of aerosol particles in the atmosphere. Global aerosol-climate models (GCMs) have now been used to quantify the radiative forcing and effects of aerosols on cirrus clouds (IPCC AR5). However, the estimate uncertainty is very large due to the different representation of ice cloud formation and evolution processes in GCMs. In addition, large discrepancies have been found between model simulations in terms of the spatial distribution of ice-nucleating aerosols, relative humidity, and temperature fluctuations, which contribute to different estimates of the aerosol indirect effect through cirrus clouds. In this presentation, four GCMs with the start-of-the art representations of cloud microphysics and aerosol-cloud interactions are used to estimate the aerosol indirect effects on cirrus clouds and to identify the causes of the discrepancies. The estimated global and annual mean anthropogenic aerosol indirect effect through cirrus clouds ranges from 0.1 W m-2 to 0.3 W m-2 in terms of the top-of-the-atmosphere (TOA) net radiation flux, and 0.5-0.6 W m-2 for the TOA longwave flux. Despite the good agreement on global mean, large discrepancies are found at the regional scale. The physics behind the aerosol indirect effect is dramatically different. Our analysis suggests that burden of ice-nucleating aerosols in the upper troposphere, ice nucleation frequency, and relative role of ice formation processes (i.e., homogeneous versus heterogeneous nucleation) play key roles in determining the characteristics of the simulated aerosol indirect effects. In addition to the indirect effect estimate, we also use field campaign

  10. Climate effects of anthropogenic aerosols over East Asia based on modeling study

    NASA Astrophysics Data System (ADS)

    Mukai, Makiko

    The increasing emission of anthropogenic aerosols causes serious air pollution episodes and various effects on the climate by the aerosols interacting with the radiation budget by directly absorbing and scattering the solar radiation, and by them indirectly modifying the optical properties and lifetimes of clouds. In East Asia anthropogenic aerosol concentrations are rapidly increasing. It is therefore necessary to evaluate the sensitivity of anthropogenic aerosols upon the radiative forcing in this region. For this purpose we utilize an atmospheric general circulation model (AGCM) with an aerosol transport and radiation model and an ocean mixed-layer model. The model in this study was a three-dimensional aerosol transport-radiation model (SPRINTARS), driven by the AGCM developed by CCSR (Center for Climate System Research), NIES (National Institute for Environmental Studies), and FRCGC (Frontier Research Center for Global Change). This model incorporates sulfate, carbonaceous, sea salt, and mineral dust aerosols, the first three of which are assumed to acts as cloud condensation nuclei that generate cloud droplets whose number increases with the number of nuclei. We assumed sulfate and carbonaceous aerosol from fuel burning for anthropogenic aerosol. And the model simulations of equilibrium experiments were performed to investigate the impact of anthropogenic aerosols based on present-day emission data and the preindustrial-era emission data. Our simulation results showed that copious anthropogenic aerosol loading causes significant decrease in the surface downward shortwave radiation flux (SDSWRF), which indicates that a direct effect of aerosols has the greatest influence on the surface radiation. It is found from our model simulations that low-level clouds increase but convective clouds decrease due to reduced convective activity caused by surface cooling when anthropogenic aerosol increases. It was also found that the contributions of aerosols to the radiation

  11. The importance of aerosol water for air pollution effects on weather and climate

    NASA Astrophysics Data System (ADS)

    Metzger, S.; Lelieveld, J.

    2007-12-01

    We apply a new concept to study air pollution effects on weather and climate, which is based on thermodynamic principles that explain hydration and osmosis - including the required transformation of laboratory based concepts to atmospheric conditions. Under ambient conditions the equilibrium relative humidity (ERH) determines the saturation molality, solute and solvent activities (and activity coefficients), and the aerosol associated water mass, sine the water content is fixed by ERH for a given aerosol concentration and type. As a consequence, aerosol water drives the gas/liquid/solid aerosol partitioning, ambient aerosol size-distributions and directly links aerosol hygroscopic growth into fog, haze and clouds. Various modeling results indicate that a) our new concept is not limited to dilute binary solutions, b) sensitive aerosol properties such as the pH of binary and mixed inorganic/organic salt solutions up to saturation can be computed accurately, and c) that anthropogenic emissions can be directly linked to visibility reduction, cloud formation and climate forcing, if we explicitly account for the aerosol water mass. Our new concept is more explicit than the traditional CCN concept as it abandons the use of ambiguous terms such as "marine" and "continental" aerosols, and refines lumped categories such as mineral dust, biomass burning, sea salt, organic or sulfate aerosols currently used in atmospheric modeling. Despite, our concept is computationally very efficient as it allows solving the whole gas/liquid/solid aerosol partitioning analytically without numerical iterations. It is therefore especially suited for regional high resolution, or global climate applications.

  12. Regional climate effects of aerosols on precipitation and snowpack in California

    NASA Astrophysics Data System (ADS)

    Wu, L.; Su, H.; Jiang, J. H.; Zhao, C.; Qian, Y.; Painter, T. H.

    2015-12-01

    Water sources in California are derived predominantly from precipitation (mostly during the winter time) and storage in the snowpack in the Sierra Nevada. With California facing one of the most severe droughts on record, it is important to understand the factors influencing precipitation and snowpack for water management and hydropower operation. Recent observational and numerical modeling studies have shown that aerosol pollutants can substantially change precipitation and snowpack in the Sierra Nevada. However, previous studies focused only on one of the aerosol effects or just focus on a single event. A complete view on regional climate effects of aerosol on precipitation and snowpack in California is not delivered yet. In this study, we use a fully coupled aerosol-meteorology-snowpack model (WRF-Chem-SNICAR) to investigate aerosol impacts on regional climate in California, with a focus on precipitation and snowpack. We will evaluate the performance of the WRF-Chem-SNICAR model on simulating regional climate in California. Sensitivity experiments will be conducted to disentangle the relative roles of each aerosol effect, such as aerosol radiation interaction vs. aerosol cloud interaction and aerosol snowpack interaction, local emission vs. long-range transport etc.

  13. Stratospheric aerosols and climatic change

    NASA Technical Reports Server (NTRS)

    Toon, O. B.; Pollack, J. B.

    1978-01-01

    Stratospht1ic sulfuric acid particles scatter and absorb sunlight and they scatter, absorb and emit terrestrial thermal radiation. These interactions play a role in the earth's radiation balance and therefore affect climate. The stratospheric aerosols are perturbed by volcanic injection of SO2 and ash, by aircraft injection of SO2, by rocket exhaust of Al2O3 and by tropospheric mixing of particles and pollutant SO2 and COS. In order to assess the effects of these perturbations on climate, the effects of the aerosols on the radiation balance must be understood and in order to understand the radiation effects the properties of the aerosols must be known. The discussion covers the aerosols' effect on the radiation balance. It is shown that the aerosol size distribution controls whether the aerosols will tend to warm or cool the earth's surface. Calculations of aerosol properties, including size distribution, for various perturbation sources are carried out on the basis of an aerosol model. Calculations are also presented of the climatic impact of perturbed aerosols due to volcanic eruptions and Space Shuttle flights.

  14. Uncertainties in global aerosols and climate effects due to biofuel emissions

    NASA Astrophysics Data System (ADS)

    Kodros, J. K.; Scott, C. E.; Farina, S. C.; Lee, Y. H.; L'Orange, C.; Volckens, J.; Pierce, J. R.

    2015-08-01

    Aerosol emissions from biofuel combustion impact both health and climate; however, while reducing emissions through improvements to combustion technologies will improve health, the net effect on climate is largely unconstrained. In this study, we examine sensitivities in global aerosol concentration, direct radiative climate effect, and cloud-albedo aerosol indirect climate effect to uncertainties in biofuel emission factors, optical mixing state, and model nucleation and background secondary organic aerosol (SOA). We use the Goddard Earth Observing System global chemical-transport model (GEOS-Chem) with TwO Moment Aerosol Sectional (TOMAS) microphysics. The emission factors include amount, composition, size, and hygroscopicity, as well as optical mixing-state properties. We also evaluate emissions from domestic coal use, which is not biofuel but is also frequently emitted from homes. We estimate the direct radiative effect assuming different mixing states (homogeneous, core-shell, and external) with and without absorptive organic aerosol (brown carbon). We find the global-mean direct radiative effect of biofuel emissions ranges from -0.02 to +0.06 W m-2 across all simulation/mixing-state combinations with regional effects in source regions ranging from -0.2 to +0.8 W m-2. The global-mean cloud-albedo aerosol indirect effect (AIE) ranges from +0.01 to -0.02 W m-2 with regional effects in source regions ranging from -1.0 to -0.05 W m-2. The direct radiative effect is strongly dependent on uncertainties in emissions mass, composition, emissions aerosol size distributions, and assumed optical mixing state, while the indirect effect is dependent on the emissions mass, emissions aerosol size distribution, and the choice of model nucleation and secondary organic aerosol schemes. The sign and magnitude of these effects have a strong regional dependence. We conclude that the climate effects of biofuel aerosols are largely unconstrained, and the overall sign of the aerosol

  15. Guidelines for the aerosol climatic effects special study: An element of the NASA climate research program

    NASA Technical Reports Server (NTRS)

    1979-01-01

    Research to help develop better understanding of the role of aerosols in the Earth's radiative balance is summarized. Natural volcanic injections of aerosols into the stratosphere to understand and model any resultant evidence of climate change are considered. The approach involves: (1) measurements from aircraft, balloon and ground based platforms which complement and enhance the aerosol information derived from satellite data; (2) development of instruments required for some of these measurements; (3) theoretical and laboratory work to aid in interpreting and utilizing space based and in situ data; and (4) preparation for and execution of concentrated observations of stratospheric aerosols following a future large volcanic eruption.

  16. Assessing the effects of anthropogenic aerosols on Pacific storm track using a multiscale global climate model.

    PubMed

    Wang, Yuan; Wang, Minghuai; Zhang, Renyi; Ghan, Steven J; Lin, Yun; Hu, Jiaxi; Pan, Bowen; Levy, Misti; Jiang, Jonathan H; Molina, Mario J

    2014-05-13

    Atmospheric aerosols affect weather and global general circulation by modifying cloud and precipitation processes, but the magnitude of cloud adjustment by aerosols remains poorly quantified and represents the largest uncertainty in estimated forcing of climate change. Here we assess the effects of anthropogenic aerosols on the Pacific storm track, using a multiscale global aerosol-climate model (GCM). Simulations of two aerosol scenarios corresponding to the present day and preindustrial conditions reveal long-range transport of anthropogenic aerosols across the north Pacific and large resulting changes in the aerosol optical depth, cloud droplet number concentration, and cloud and ice water paths. Shortwave and longwave cloud radiative forcing at the top of atmosphere are changed by -2.5 and +1.3 W m(-2), respectively, by emission changes from preindustrial to present day, and an increased cloud top height indicates invigorated midlatitude cyclones. The overall increased precipitation and poleward heat transport reflect intensification of the Pacific storm track by anthropogenic aerosols. Hence, this work provides, for the first time to the authors' knowledge, a global perspective of the effects of Asian pollution outflows from GCMs. Furthermore, our results suggest that the multiscale modeling framework is essential in producing the aerosol invigoration effect of deep convective clouds on a global scale.

  17. Assessing the effects of anthropogenic aerosols on Pacific storm track using a multiscale global climate model.

    PubMed

    Wang, Yuan; Wang, Minghuai; Zhang, Renyi; Ghan, Steven J; Lin, Yun; Hu, Jiaxi; Pan, Bowen; Levy, Misti; Jiang, Jonathan H; Molina, Mario J

    2014-05-13

    Atmospheric aerosols affect weather and global general circulation by modifying cloud and precipitation processes, but the magnitude of cloud adjustment by aerosols remains poorly quantified and represents the largest uncertainty in estimated forcing of climate change. Here we assess the effects of anthropogenic aerosols on the Pacific storm track, using a multiscale global aerosol-climate model (GCM). Simulations of two aerosol scenarios corresponding to the present day and preindustrial conditions reveal long-range transport of anthropogenic aerosols across the north Pacific and large resulting changes in the aerosol optical depth, cloud droplet number concentration, and cloud and ice water paths. Shortwave and longwave cloud radiative forcing at the top of atmosphere are changed by -2.5 and +1.3 W m(-2), respectively, by emission changes from preindustrial to present day, and an increased cloud top height indicates invigorated midlatitude cyclones. The overall increased precipitation and poleward heat transport reflect intensification of the Pacific storm track by anthropogenic aerosols. Hence, this work provides, for the first time to the authors' knowledge, a global perspective of the effects of Asian pollution outflows from GCMs. Furthermore, our results suggest that the multiscale modeling framework is essential in producing the aerosol invigoration effect of deep convective clouds on a global scale. PMID:24733923

  18. Aerosol Effects on Radiation and Climate: Column Closure Experiments with Towers, Aircraft, and Satellites

    NASA Technical Reports Server (NTRS)

    Russell, Philip B.

    1994-01-01

    Many theoretical studies have shown that anthropogenic aerosol particles can change the radiation balance in an atmospheric column and might thereby exert a significant effect on the Earth's climate. In particular, recent calculations have shown that sulfate particles from anthropogenic combustion may already exert a cooling influence on the Earth that partially offsets the warming caused by the greenhouse gases from the same combustion. Despite the potential climatic importance of anthropogenic aerosols, simultaneous measurements of anthropogenic aerosol properties and their effect on atmospheric radiation have been very rare. Successful comparisons of measured radiation fields with those calculated from aerosol measurements - now referred to as column closure comparisons - are required to improve the accuracy and credibility of climate predictions. This paper reviews the column closure experiment performed at the Mt. Sutro Tower in San Francisco in 1975, in which elevated radiometers measured the change in Earth-plus-atmosphere albedo caused by an aerosol layer, while a lidar, sunphotometer, nephelometer, and other radiometers measured properties of the responsible aerosol. The time-dependent albedo calculated from the measured aerosol properties agreed with that measured by the tower radiometers. Also presented are designs for future column closure studies using radiometers and aerosol instruments on the ground, aircraft, and satellites. These designs draw upon algorithms and experience developed in the Sutro Tower study, as well as more recent experience with current measurement and analysis capabilities.

  19. AEROSOL, CLOUDS, AND CLIMATE CHANGE

    SciTech Connect

    SCHWARTZ, S.E.

    2005-09-01

    Earth's climate is thought to be quite sensitive to changes in radiative fluxes that are quite small in absolute magnitude, a few watts per square meter, and in relation to these fluxes in the natural climate. Atmospheric aerosol particles exert influence on climate directly, by scattering and absorbing radiation, and indirectly by modifying the microphysical properties of clouds and in turn their radiative effects and hydrology. The forcing of climate change by these indirect effects is thought to be quite substantial relative to forcing by incremental concentrations of greenhouse gases, but highly uncertain. Quantification of aerosol indirect forcing by satellite- or ground-based remote sensing has proved quite difficult in view of inherent large variation in the pertinent observables such as cloud optical depth, which is controlled mainly by liquid water path and only secondarily by aerosols. Limited work has shown instances of large magnitude of aerosol indirect forcing, with local instantaneous forcing upwards of 50 W m{sup 66}-2. Ultimately it will be necessary to represent aerosol indirect effects in climate models to accurately identify the anthropogenic forcing at present and over secular time and to assess the influence of this forcing in the context of other forcings of climate change. While the elements of aerosol processes that must be represented in models describing the evolution and properties of aerosol particles that serve as cloud condensation particles are known, many important components of these processes remain to be understood and to be represented in models, and the models evaluated against observation, before such model-based representations can confidently be used to represent aerosol indirect effects in climate models.

  20. Sensitivity studies for incorporating the direct effect of sulfate aerosols into climate models

    NASA Astrophysics Data System (ADS)

    Miller, Mary Rawlings Lamberton

    2000-09-01

    Aerosols have been identified as a major element of the climate system known to scatter and absorb solar and infrared radiation, but the development of procedures for representing them is still rudimentary. This study addresses the need to improve the treatment of sulfate aerosols in climate models by investigating how sensitive radiative particles are to varying specific sulfate aerosol properties. The degree to which sulfate particles absorb or scatter radiation, termed the direct effect, varies with the size distribution of particles, the aerosol mass density, the aerosol refractive indices, the relative humidity and the concentration of the aerosol. This study develops 504 case studies of altering sulfate aerosol chemistry, size distributions, refractive indices and densities at various ambient relative humidity conditions. Ammonium sulfate and sulfuric acid aerosols are studied with seven distinct size distributions at a given mode radius with three corresponding standard deviations implemented from field measurements. These test cases are evaluated for increasing relative humidity. As the relative humidity increases, the complex index of refraction and the mode radius for each distribution correspondingly change. Mie theory is employed to obtain the radiative properties for each case study. The case studies are then incorporated into a box model, the National Center of Atmospheric Research's (NCAR) column radiation model (CRM), and NCAR's community climate model version 3 (CCM3) to determine how sensitive the radiative properties and potential climatic effects are to altering sulfate properties. This study found the spatial variability of the sulfate aerosol leads to regional areas of intense aerosol forcing (W/m2). These areas are particularly sensitive to altering sulfate properties. Changes in the sulfate lognormal distribution standard deviation can lead to substantial regional differences in the annual aerosol forcing greater than 2 W/m 2. Changes in the

  1. Assessing the Effects of Anthropogenic Aerosols on Pacific Storm Track Using a Multiscale Global Climate Model

    SciTech Connect

    Wang, Yuan; Wang, Minghuai; Zhang, Renyi; Ghan, Steven J.; Lin, Yun; Hu, Jiaxi; Pan, Bowen; Levy, Misti; Jiang, Jonathan; Molina, Mario J.

    2014-05-13

    Atmospheric aerosols impact weather and global general circulation by modifying cloud and precipitation processes, but the magnitude of cloud adjustment by aerosols remains poorly quantified and represents the largest uncertainty in estimated forcing of climate change. Here we assess the impacts of anthropogenic aerosols on the Pacific storm track using a multi-scale global aerosol-climate model (GCM). Simulations of two aerosol scenarios corresponding to the present day and pre-industrial conditions reveal long-range transport of anthropogenic aerosols across the north Pacific and large resulting changes in the aerosol optical depth, cloud droplet number concentration, and cloud and ice water paths. Shortwave and longwave cloud radiative forcing at the top of atmosphere are changed by - 2.5 and + 1.3 W m-2, respectively, by emission changes from pre-industrial to present day, and an increased cloud-top height indicates invigorated mid-latitude cyclones. The overall increased precipitation and poleward heat transport reflect intensification of the Pacific storm track by anthropogenic aerosols. Hence, this work provides for the first time a global perspective of the impacts of Asian pollution outflows from GCMs. Furthermore, our results suggest that the multi-scale modeling framework is essential in producing the aerosol invigoration effect of deep convective clouds on the global scale.

  2. Assessing the effects of anthropogenic aerosols on Pacific storm track using a multiscale global climate model

    PubMed Central

    Wang, Yuan; Wang, Minghuai; Zhang, Renyi; Ghan, Steven J.; Lin, Yun; Hu, Jiaxi; Pan, Bowen; Levy, Misti; Jiang, Jonathan H.; Molina, Mario J.

    2014-01-01

    Atmospheric aerosols affect weather and global general circulation by modifying cloud and precipitation processes, but the magnitude of cloud adjustment by aerosols remains poorly quantified and represents the largest uncertainty in estimated forcing of climate change. Here we assess the effects of anthropogenic aerosols on the Pacific storm track, using a multiscale global aerosol–climate model (GCM). Simulations of two aerosol scenarios corresponding to the present day and preindustrial conditions reveal long-range transport of anthropogenic aerosols across the north Pacific and large resulting changes in the aerosol optical depth, cloud droplet number concentration, and cloud and ice water paths. Shortwave and longwave cloud radiative forcing at the top of atmosphere are changed by −2.5 and +1.3 W m−2, respectively, by emission changes from preindustrial to present day, and an increased cloud top height indicates invigorated midlatitude cyclones. The overall increased precipitation and poleward heat transport reflect intensification of the Pacific storm track by anthropogenic aerosols. Hence, this work provides, for the first time to the authors’ knowledge, a global perspective of the effects of Asian pollution outflows from GCMs. Furthermore, our results suggest that the multiscale modeling framework is essential in producing the aerosol invigoration effect of deep convective clouds on a global scale. PMID:24733923

  3. Aerosol effect on climate extremes in Europe under different future scenarios

    NASA Astrophysics Data System (ADS)

    Sillmann, J.; Pozzoli, L.; Vignati, E.; Kloster, S.; Feichter, J.

    2013-05-01

    This study investigates changes in extreme temperature and precipitation events under different future scenarios of anthropogenic aerosol emissions (i.e., SO2 and black and organic carbon) simulated with an aerosol-climate model (ECHAM5-HAM) with focus on Europe. The simulations include a maximum feasible aerosol reduction (MFR) scenario and a current legislation emission (CLEmod) scenario where Europe implements the MFR scenario, but the rest of the world follows the current legislation scenario and a greenhouse gas scenario. The strongest changes relative to the year 2000 are projected for the MFR scenario, in which the global aerosol reduction greatly enforces the general warming effect due to greenhouse gases and results in significant increases of temperature and precipitation extremes in Europe. Regional warming effects can also be identified from aerosol reductions under the CLEmodscenario. This becomes most obvious in the increase of the hottest summer daytime temperatures in Northern Europe.

  4. Climate forcing by anthropogenic aerosols.

    PubMed

    Charlson, R J; Schwartz, S E; Hales, J M; Cess, R D; Coakley, J A; Hansen, J E; Hofmann, D J

    1992-01-24

    Although long considered to be of marginal importance to global climate change, tropospheric aerosol contributes substantially to radiative forcing, and anthropogenic sulfate aerosol in particular has imposed a major perturbation to this forcing. Both the direct scattering of shortwavelength solar radiation and the modification of the shortwave reflective properties of clouds by sulfate aerosol particles increase planetary albedo, thereby exerting a cooling influence on the planet. Current climate forcing due to anthropogenic sulfate is estimated to be -1 to -2 watts per square meter, globally averaged. This perturbation is comparable in magnitude to current anthropogenic greenhouse gas forcing but opposite in sign. Thus, the aerosol forcing has likely offset global greenhouse warming to a substantial degree. However, differences in geographical and seasonal distributions of these forcings preclude any simple compensation. Aerosol effects must be taken into account in evaluating anthropogenic influences on past, current, and projected future climate and in formulating policy regarding controls on emission of greenhouse gases and sulfur dioxide. Resolution of such policy issues requires integrated research on the magnitude and geographical distribution of aerosol climate forcing and on the controlling chemical and physical processes.

  5. Climate Forcing by Anthropogenic Aerosols

    NASA Astrophysics Data System (ADS)

    Charlson, R. J.; Schwartz, S. E.; Hales, J. M.; Cess, R. D.; Coakley, J. A., Jr.; Hansen, J. E.; Hofmann, D. J.

    1992-01-01

    Although long considered to be of marginal importance to global climate change, tropospheric aerosol contributes substantially to radiative forcing, and anthropogenic sulfate aerosol in particular has imposed a major perturbation to this forcing. Both the direct scattering of short-wavelength solar radiation and the modification of the shortwave reflective properties of clouds by sulfate aerosol particles increase planetary albedo, thereby exerting a cooling influence on the planet. Current climate forcing due to anthropogenic sulfate is estimated to be -1 to -2 watts per square meter, globally averaged. This perturbation is comparable in magnitude to current anthropogenic greenhouse gas forcing but opposite in sign. Thus, the aerosol forcing has likely offset global greenhouse warming to a substantial degree. However, differences in geographical and seasonal distributions of these forcings preclude any simple compensation. Aerosol effects must be taken into account in evaluating anthropogenic influences on past, current, and projected future climate and in formulating policy regarding controls on emission of greenhouse gases and sulfur dioxide. Resolution of such policy issues requires integrated research on the magnitude and geographical distribution of aerosol climate forcing and on the controlling chemical and physical processes.

  6. Climate forcing by anthropogenic aerosols

    NASA Technical Reports Server (NTRS)

    Charlson, R. J.; Schwartz, S. E.; Hales, J. M.; Cess, R. D.; Coakley, J. A., Jr.; Hansen, J. E.; Hofmann, D. J.

    1992-01-01

    Although long considered to be of marginal importance to global climate change, tropospheric aerosol contributes substantially to radiative forcing, and anthropogenic sulfate aerosol, in particular, has imposed a major perturbation to this forcing. Both the direct scattering of short-wavelength solar radiation and the modification of the shortwave reflective properties of clouds by sulfate aerosol particles increase planetary albedo, thereby exerting a cooling influence on the planet. Current climate forcing due to anthropogenic sulfate is estimated to be -1 to -2 watts per square meter, globally averaged. This perturbation is comparable in magnitude to current anthropogenic greenhouse gas forcing but opposite in sign. Thus, the aerosol forcing has likely offset global greenhouse warming to a substantial degree. However, differences in geographical and seasonal distributions of these forcings preclude any simple compensation. Aerosol effects must be taken into account in evaluating anthropogenic influences on past, current, and projected future climate and in formulating policy regarding controls on emission of greenhouse gases and sulfur dioxide. Resolution of such policy issues requires integrated research on the magnitude and geographical distribution of aerosol climate forcing and on the controlling chemical and physical processes.

  7. Quantification of regional radiative impacts and climate effects of tropical fire aerosols

    NASA Astrophysics Data System (ADS)

    Tosca, M. G.; Zender, C. S.; Randerson, J. T.

    2011-12-01

    Regionally expansive smoke clouds originating from deforestation fires in Indonesia can modify local precipitation patterns via direct aerosol scattering and absorption of solar radiation (Tosca et al., 2010). Here we quantify the regional climate impacts of fire aerosols for three tropical burning regions that together account for about 70% of global annual fire emissions. We use the Community Atmosphere Model, version 5 (CAM5) coupled to a slab ocean model (SOM) embedded within the Community Earth System Model (CESM). In addition to direct aerosol radiative effects, CAM5 also quantifies indirect, semi-direct and cloud microphysical aerosol effects. Climate impacts are determined using regionally adjusted emissions data that produce realistic aerosol optical depths in CAM5. We first analyzed a single 12-year transient simulation (1996-2007) forced with unadjusted emissions estimates from the Global Fire Emissions Database, version 3 (GFEDv3) and compared the resulting aerosol optical depths (AODs) for 4 different burning regions (equatorial Asia, southern Africa, South America and boreal North America) to observed MISR and MODIS AODs for the same period. Based on this analysis we adjusted emissions for each burning region between 150 and 300% and forced a second simulation with the regionally adjusted emissions. Improved AODs from this simulation are compared to AERONET observations available at 15 stations throughout the tropics. We present here two transient simulations--one with the adjusted fire emissions and one without fires--to quantify the cumulative fire aerosol climate impact for three major tropical burning regions (equatorial Asia, southern Africa and South America). Specifically, we quantify smoke effects on radiation, precipitation, and temperature. References Tosca, M.G., J.T. Randerson, C.S. Zender, M.G. Flanner and P.J. Rasch (2010), Do biomass burning aerosols intensify drought in equatorial Asia during El Nino?, Atmos. Chem. Phys., 10, 3515

  8. Aerosol climate effects and air quality impacts from 1980 to 2030

    SciTech Connect

    Menon, Surabi; Menon, Surabi; Unger, Nadine; Koch, Dorothy; Francis, Jennifer; Garrett, Tim; Sednev, Igor; Shindell, Drew; Streets, David

    2007-11-26

    We investigate aerosol effects on climate for 1980, 1995 (meant to reflect present-day) and 2030 using the NASA Goddard Institute for Space Studies climate model coupled to an on-line aerosol source and transport model with interactive oxidant and aerosol chemistry. Aerosols simulated include sulfates, organic matter (OM), black carbon (BC), sea-salt and dust and additionally, the amount of tropospheric ozone is calculated, allowing us to estimate both changes to air quality and climate for different time periods and emission amounts. We include both the direct aerosol effect and indirect aerosol effects for liquid-phase clouds. Future changes for the 2030 A1B scenario are examined, focusing on the Arctic and Asia, since changes are pronounced in these regions. Our results for the different time periods include both emission changes and physical climate changes. We find that the aerosol indirect effect (AIE) has a large impact on photochemical processing, decreasing ozone amount and ozone forcing, especially for the future (2030-1995). Ozone forcings increase from 0 to 0.12 Wm{sup -2} and the total aerosol forcing increases from -0.10 Wm{sup -2} to -0.94 Wm{sup -2} (AIE increases from -0.13 to -0.68 Wm{sup -2}) for 1995-1980 versus 2030-1995. Over the Arctic we find that compared to ozone and the direct aerosol effect, the AIE contributes the most to net radiative flux changes. The AIE, calculated for 1995-1980, is positive (1.0 Wm{sup -2}), but the magnitude decreases (-0.3Wm{sup -2}) considerably for the future scenario. Over Asia, we evaluate the role of biofuel and transportation-based emissions (for BC and OM) via a scenario (2030A) that includes a projected increase (factor of two) in biofuel and transport-based emissions for 2030 A1B over Asia. Projected changes from present-day due to the 2030A emissions versus 2030 A1B are a factor of 4 decrease in summertime precipitation in Asia. Our results are sensitive to emissions used. Uncertainty in present

  9. Simulation of the radiative effect of black carbon aerosols and the regional climate responses over China

    NASA Astrophysics Data System (ADS)

    Wu, Jian; Jiang, Weimei; Fu, Congbin; Su, Bingkai; Liu, Hongnian; Tang, Jianping

    2004-08-01

    As part of the development work of the Chinese new regional climate model (RIEMS), the radiative process of black carbon (BC) aerosols has been introduced into the original radiative procedures of RIEMS, and the transport model of BC aerosols has also been established and combined with the RIEMS model. Using the new model system, the distribution of black carbon aerosols and their radiative effect over the China region are investigated. The influences of BC aerosole on the atmospheric radiative transfer and on the air temperature, land surface temperature, and total rainfall are analyzed. It is found that BC aerosols induce a positive radiative forcing at the top of the atmosphere (TOA), which is dominated by shortwave radiative forcing. The maximum radiative forcing occurs in North China in July and in South China in April. At the same time, negative radiative forcing is observed on the surface. Based on the radiative forcing comparison between clear sky and cloudy sky, it is found that cloud can enforce the TOA positive radiative forcing and decrease the negative surface radiative forcing. The responses of the climate system in July to the radiative forcing due to BC aerosols are the decrease in the air temperature in the middle and lower reaches of the Changjiang River and Huaihe area and most areas of South China, and the weak increase or decrease in air temperature over North China. The total rainfall in the middle and lower reaches of the Changjiang River area is increased, but it decreased in North China in July.

  10. Multi-Decadal Variation of Aerosols: Sources, Transport, and Climate Effects

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Diehl, Thomas; Bian, Huisheng; Streets, David

    2008-01-01

    We present a global model study of multi-decadal changes of atmospheric aerosols and their climate effects using a global chemistry transport model along with the near-term to longterm data records. We focus on a 27-year time period of satellite era from 1980 to 2006, during which a suite of aerosol data from satellite observations, ground-based measurements, and intensive field experiments have become available. We will use the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model, which involves a time-varying, comprehensive global emission dataset that we put together in our previous investigations and will be improved/extended in this project. This global emission dataset includes emissions of aerosols and their precursors from fuel combustion, biomass burning, volcanic eruptions, and other sources from 1980 to the present. Using the model and satellite data, we will analyze (1) the long-term global and regional aerosol trends and their relationship to the changes of aerosol and precursor emissions from anthropogenic and natural sources, (2) the intercontinental source-receptor relationships controlled by emission, transport pathway, and climate variability.

  11. Climatic Effects of 1950-2050 Changes in US Anthropogenic Aerosols. Part 1; Aerosol Trends and Radiative Forcing

    NASA Technical Reports Server (NTRS)

    Leibensperger, E. M.; Mickley, L. J.; Jacob, D. J.; Chen, W.-T.; Seinfeld, J. H.; Nenes, A.; Adams, P. J.; Streets, D. G.; Kumar, N.; Rind, D.

    2012-01-01

    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 deg W) of -2.0Wm(exp-2 for direct forcing including contributions from sulfate (-2.0Wm-2), nitrate (-0.2Wm(exp-2), organic carbon (-0.2Wm(exp-2), and black carbon (+0.4Wm(exp-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 0.8Wm(exp-2) direct and 1.0Wm(exp-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 (+0.3Wm(exp-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.

  12. Modeling the direct and indirect climatic effects of tropospheric sulfate aerosols

    NASA Astrophysics Data System (ADS)

    Cox, Stephen J.

    2000-10-01

    Modeling studies of the climatic effects of tropospheric sulfate aerosols are presented. Both the direct scattering by the aerosols and the indirect effect of enhanced cloud albedo from increased aerosol numbers are addressed, in separate studies. The direct effect study uses aerosol mass concentrations from the MOGUNTIA chemical transport model. A parameterization is developed to model the radiative forcing due to direct shortwave scattering by the aerosols in the NCAR Community Climate Model, an atmospheric general circulation model. Aerosol layer optical properties are folded into the direct and diffuse surface albedo. The aerosol forcing is similar in magnitude, but opposite in sign, to the longwave forcing by anthropogenic greenhouse gases such as CO 2, CH4, N2O, CF2CL2, and CFCL3. CCM1 is run for thirty-five years with equal and opposite global annual mean aerosol and greenhouse forcings, and the results compared to a control run with no forcing. It is determined that the global mean temperate responds to the forcings equally, with a global sensitivity of 1.25 K/(W m -2), but the regional temperature response shows marked variation, which could not be predicted simply from the forcing pattern. The aerosol forcing is concentrated in the industrial continental areas of the Northern Hemisphere midlatitudes, yet a strong cooling response is noted in regions thousands of kilometers away (for instance, western Canada) from centers of aerosol concentration. The indirect effect is studied with more recent sulfate estimates, from the Oslo Chemical Transport Model. Field studies are used to relate sulfate mass concentration to cloud droplet number concentration, and subsequently to cloud droplet effective radius. The indirect parameterization is incorporated into NCAR CCM3, along with a new shortwave parameterization which allows the full vertical distribution of the aerosols to be accounted for. The indirect radiative forcing is found to be a cooling of 0.47 W m-2

  13. Long range climate effect of carbon dioxide and sulfate aerosols

    SciTech Connect

    Washington, Warren M.; Meehl, Gerald A.

    2002-09-16

    The program has led to better climate model components, has developed new and more efficient methods of solving climate model equations and has taken advantage of the new computing technologies thus providing more reliable estimates of potential climate change. The CHAMMP sponsored and the NCAR-CSM (Climate System Model) are complimentary efforts and under this leadership are developing state-of-the-art, high resolution, computationally efficient components thus providing a more realistic simulation.

  14. Direct and semi-direct aerosol radiative effect on the Mediterranean climate variability using a coupled regional climate system model

    NASA Astrophysics Data System (ADS)

    Nabat, Pierre; Somot, Samuel; Mallet, Marc; Sevault, Florence; Chiacchio, Marc; Wild, Martin

    2015-02-01

    A fully coupled regional climate system model (CNRM-RCSM4) has been used over the Mediterranean region to investigate the direct and semi-direct effects of aerosols, but also their role in the radiation-atmosphere-ocean interactions through multi-annual ensemble simulations (2003-2009) with and without aerosols and ocean-atmosphere coupling. Aerosols have been taken into account in CNRM-RCSM4 through realistic interannual monthly AOD climatologies. An evaluation of the model has been achieved, against various observations for meteorological parameters, and has shown the ability of CNRM-RCSM4 to reproduce the main patterns of the Mediterranean climate despite some biases in sea surface temperature (SST), radiation and cloud cover. The results concerning the aerosol radiative effects show a negative surface forcing on average because of the absorption and scattering of the incident radiation. The SW surface direct effect is on average -20.9 Wm-2 over the Mediterranean Sea, -14.7 Wm-2 over Europe and -19.7 Wm-2 over northern Africa. The LW surface direct effect is weaker as only dust aerosols contribute (+4.8 Wm-2 over northern Africa). This direct effect is partly counterbalanced by a positive semi-direct radiative effect over the Mediterranean Sea (+5.7 Wm-2 on average) and Europe (+5.0 Wm-2) due to changes in cloud cover and atmospheric circulation. The total aerosol effect is consequently negative at the surface and responsible for a decrease in land (on average -0.4 °C over Europe, and -0.5 °C over northern Africa) and sea surface temperature (on average -0.5 °C for the Mediterranean SST). In addition, the latent heat loss is shown to be weaker (-11.0 Wm-2) in the presence of aerosols, resulting in a decrease in specific humidity in the lower troposphere, and a reduction in cloud cover and precipitation. Simulations also indicate that dust aerosols warm the troposphere by absorbing solar radiation, and prevent radiation from reaching the surface, thus

  15. On the characteristics of aerosol indirect effect based on dynamic regimes in global climate models

    DOE PAGES

    Zhang, Shipeng; Wang, Minghuai; Ghan, Steven J.; Ding, Aijun; Wang, Hailong; Zhang, Kai; Neubauer, David; Lohmann, Ulrike; Ferrachat, Sylvaine; Takeamura, Toshihiko; et al

    2016-03-04

    Aerosol–cloud interactions continue to constitute a major source of uncertainty for the estimate of climate radiative forcing. The variation of aerosol indirect effects (AIE) in climate models is investigated across different dynamical regimes, determined by monthly mean 500 hPa vertical pressure velocity (ω500), lower-tropospheric stability (LTS) and large-scale surface precipitation rate derived from several global climate models (GCMs), with a focus on liquid water path (LWP) response to cloud condensation nuclei (CCN) concentrations. The LWP sensitivity to aerosol perturbation within dynamic regimes is found to exhibit a large spread among these GCMs. It is in regimes of strong large-scale ascentmore » (ω500  <  −25 hPa day−1) and low clouds (stratocumulus and trade wind cumulus) where the models differ most. Shortwave aerosol indirect forcing is also found to differ significantly among different regimes. Shortwave aerosol indirect forcing in ascending regimes is close to that in subsidence regimes, which indicates that regimes with strong large-scale ascent are as important as stratocumulus regimes in studying AIE. It is further shown that shortwave aerosol indirect forcing over regions with high monthly large-scale surface precipitation rate (> 0.1 mm day−1) contributes the most to the total aerosol indirect forcing (from 64 to nearly 100 %). Results show that the uncertainty in AIE is even larger within specific dynamical regimes compared to the uncertainty in its global mean values, pointing to the need to reduce the uncertainty in AIE in different dynamical regimes.« less

  16. Climate impact of biofuels in shipping: global model studies of the aerosol indirect effect.

    PubMed

    Righi, Mattia; Klinger, Carolin; Eyring, Veronika; Hendricks, Johannes; Lauer, Axel; Petzold, Andreas

    2011-04-15

    Aerosol emissions from international shipping are recognized to have a large impact on the Earth's radiation budget, directly by scattering and absorbing solar radiation and indirectly by altering cloud properties. New regulations have recently been approved by the International Maritime Organization (IMO) aiming at progressive reductions of the maximum sulfur content allowed in marine fuels from current 4.5% by mass down to 0.5% in 2020, with more restrictive limits already applied in some coastal regions. In this context, we use a global bottom-up algorithm to calculate geographically resolved emission inventories of gaseous (NO(x), CO, SO(2)) and aerosol (black carbon, organic matter, sulfate) species for different kinds of low-sulfur fuels in shipping. We apply these inventories to study the resulting changes in radiative forcing, attributed to particles from shipping, with the global aerosol-climate model EMAC-MADE. The emission factors for the different fuels are based on measurements at a test bed of a large diesel engine. We consider both fossil fuel (marine gas oil) and biofuels (palm and soy bean oil) as a substitute for heavy fuel oil in the current (2006) fleet and compare their climate impact to that resulting from heavy fuel oil use. Our simulations suggest that ship-induced surface level concentrations of sulfate aerosol are strongly reduced, up to about 40-60% in the high-traffic regions. This clearly has positive consequences for pollution reduction in the vicinity of major harbors. Additionally, such reductions in the aerosol loading lead to a decrease of a factor of 3-4 in the indirect global aerosol effect induced by emissions from international shipping.

  17. Climate impact of biofuels in shipping: global model studies of the aerosol indirect effect.

    PubMed

    Righi, Mattia; Klinger, Carolin; Eyring, Veronika; Hendricks, Johannes; Lauer, Axel; Petzold, Andreas

    2011-04-15

    Aerosol emissions from international shipping are recognized to have a large impact on the Earth's radiation budget, directly by scattering and absorbing solar radiation and indirectly by altering cloud properties. New regulations have recently been approved by the International Maritime Organization (IMO) aiming at progressive reductions of the maximum sulfur content allowed in marine fuels from current 4.5% by mass down to 0.5% in 2020, with more restrictive limits already applied in some coastal regions. In this context, we use a global bottom-up algorithm to calculate geographically resolved emission inventories of gaseous (NO(x), CO, SO(2)) and aerosol (black carbon, organic matter, sulfate) species for different kinds of low-sulfur fuels in shipping. We apply these inventories to study the resulting changes in radiative forcing, attributed to particles from shipping, with the global aerosol-climate model EMAC-MADE. The emission factors for the different fuels are based on measurements at a test bed of a large diesel engine. We consider both fossil fuel (marine gas oil) and biofuels (palm and soy bean oil) as a substitute for heavy fuel oil in the current (2006) fleet and compare their climate impact to that resulting from heavy fuel oil use. Our simulations suggest that ship-induced surface level concentrations of sulfate aerosol are strongly reduced, up to about 40-60% in the high-traffic regions. This clearly has positive consequences for pollution reduction in the vicinity of major harbors. Additionally, such reductions in the aerosol loading lead to a decrease of a factor of 3-4 in the indirect global aerosol effect induced by emissions from international shipping. PMID:21428387

  18. A Climate Process Team focused on better representation of aerosol indirect effects in climate models through improved cloud macrophysical parameterization

    NASA Astrophysics Data System (ADS)

    Wood, R.; Larson, V. E.; Donner, L.; Golaz, J.; Guo, H.; Gettelman, A.; Morrison, H.; Bogenschutz, P.; Feingold, G.; Yamaguchi, T.; Lee, S.; Stephens, G. L.; Lebsock, M. D.; Kubar, T. L.; Grosvenor, D. P.

    2011-12-01

    The representation of aerosol indirect effects (AIEs) in climate models is hampered in part by a poor representation of cloud macrophysical processes. Accurate representation of AIEs involves a complex interplay between cloud microphysics, turbulent dynamics, and radiation. This presentation describes the goals, progress, and future activities of a NSF/NOAA Climate Process Team focused on the improved representation of cloud macrophysical processes through the incorporation of a unified cloud and turbulence scheme into two of the leading US climate models (NCAR CAM, GFDL AM3). We describe how a combination of process modeling, field observations, and single column modeling can be used to improve model physics. We then describe progress in the implementation of the scheme in the full climate model. We describe observational metrics from satellites that the team is using to establish the fidelity of the model results and guide future model development.

  19. CHASER: An Innovative Satellite Mission Concept to Measure the Effects of Aerosols on Clouds and Climate

    NASA Astrophysics Data System (ADS)

    Renno, N.; Williams, E.; Rosenfeld, D.; Fischer, D.; Fischer, J.; Kremic, T.; Agrawal, A.; Andreae, M.; Bierbaum, R.; Blakeslee, R.; Boerner, A.; Bowles, N.; Christian, H.; Dunion, J.; Horvath, A.; Huang, X.; Khain, A.; Kinne, S.; Lemos, M.-C.; Penner, J.

    2012-04-01

    The formation of cloud droplets on aerosol particles, technically known as the activation of cloud condensation nuclei (CCN), is the fundamental process driving the interactions of aerosols with clouds and precipitation. Knowledge of these interactions is foundational to our understanding of weather and climate. The Intergovernmental Panel on Climate Change (IPCC) and the Decadal Survey (NRC 2007) indicate that the uncertainty in how clouds adjust to aerosol perturbations dominates the uncertainty in the overall quantification of the radiative forcing attributable to human activities. The Clouds, Hazards, and Aerosols Survey for Earth Researchers (CHASER) mission concept responds to the IPCC and Decadal Survey concerns by studying the activation of CCN and their interactions with clouds and storms. CHASER proposes to revolutionize our understanding of the interactions of aerosols with clouds by making the first global measurements of the fundamental physical entity linking them: activated cloud condensation nuclei. The CHASER mission was conceptualized to measure all quantities necessary for determining the interactions of aerosols with clouds and storms. Measurements by current satellites allow the determination of crude profiles of cloud particle size but not of the activated CCN that seed them. CHASER uses a new technique (Freud et al. 2011; Rosenfeld et al. 2012) and high-heritage instruments to produce the first global maps of activated CCN and the properties of the clouds associated with them. CHASER measures the CCN concentration and cloud thermodynamic forcing simultaneously, allowing their effects to be distinguished. Changes in the behavior of a group of weather systems in which only one of the quantities varies (a partial derivative of the intensity with the desirable quantity) allow the determination of each effect statistically. The high uncertainties of current climate predictions limit their much-needed use in decision-making. CHASER mitigates this

  20. Nonlinear effects of anthropogenic aerosol and urban land surface forcing on spring climate in eastern China

    NASA Astrophysics Data System (ADS)

    Deng, Jiechun; Xu, Haiming; Zhang, Leying

    2016-05-01

    Anthropogenic aerosols and urban land cover change induce opposite thermal effects on the atmosphere near surface as well as in the troposphere. One can think of these anthropogenic effects as composed of two parts: the individual effect due to an individual anthropogenic forcing and the nonlinear effects resulting from the coexistence of two forcing factors. In this study, we explored the role of such nonlinear effects in affecting East Asian climate, as well as individual forcing effects, using the Community Atmosphere Model version 5.1 coupled with the Community Land Model version 4. Atmospheric responses were simulated by including anthropogenic aerosol emission only, urban cover only, or the combination of the two, over eastern China. Results showed that nonlinear responses were different from any effects by an individual forcing or the linear combination of individual responses. The nonlinear interaction could generate cold horizontal temperature advection to cool the troposphere, which induced anomalous subsidence along the Yangtze River Valley (YRV). This anomalous vertical motion, together with a weakened low-level southwesterly, favored below-normal (above-normal) rainfall over the YRV (southern China), shifting the spring rain belt southward. The resultant diabatic cooling, in turn, amplified the anomalous descent and further decreased tropospheric temperature over the YRV, forming a positive feedback loop to maintain the nonlinear effects. Consequently, the nonlinear effects acted to reduce the climate anomalies from a simple linear combination of two individual effects and played an important role in regional responses to one anthropogenic forcing when the other is prescribed.

  1. Direct Radiative Forcing and Regional Climatic Effects of Anthropogenic Aerosols Over East Asia: A Regional Coupled Climate-Chemistry/Aerosol Model Study

    SciTech Connect

    Giorgi, Filippo; Bi, Xunqiang; Qian, Yun )

    2002-09-01

    We present a series of regional climate model simulations aimed at assessing the radiative forcing and surface climatic effects of anthropogenic sulfate and fossil fuel soot over east Asia. The simulations are carried out with a coupled regional climate-chemistry/aerosol model for the 5-year period of 1993-1997 using published estimates of sulfur emissions for the period. Anthropogenic sulfate induces a negative radiative forcing spatially varying from -1 to -8 W/m2 in the winter to -1 to -15 W/m2 in the summer, with maxima over the Sichan Basin of southwest China and over some areas of east and northeast China. This forcing induces a surface cooling in the range of -0.1 to -0.7 K. Fossil fuel soot exerts a positive atmospheric radiative forcing of 0.5 to 2 W/m2 and enhances the surface cooling by a few tenths of K due to increased surface shielding from solar radiation. Doubling of sulfur emissions induces a substantial increase in radiative forcing (up to -7 to -8 W/m2) and associated surface cooling. With doubled sulfur emissions, the surface cooling exceeds -1 K and is statistically significant at the 90% confidence level over various areas of China. The aerosol forcing and surface cooling tend to inhibit precipitation over the region, although this effect is relatively small in the simulations. Some features of the simulated aerosol-induced cooling are consistent with temperature trends observed in recent decades over different regions of China.

  2. Science Plan Biogenic AerosolsEffects on Clouds and Climate (BAECC)

    SciTech Connect

    Petäjä, T

    2013-12-01

    Atmospheric aerosol particles impact human health in urban environments, while on regional and global scales they can affect climate patterns, the hydrological cycle, and the intensity of radiation that reaches the Earth’s surface. In spite of recent advances in the understanding of aerosol formation processes and the links between aerosol dynamics and biosphere-atmosphere-climate interactions, great challenges remain in the analysis of related processes on a global scale. Boreal forests, situated in a circumpolar belt in the northern latitudes throughout the United States, Canada, Russia and Scandinavia, are among the most active areas of atmospheric aerosol formation among all biomes. The formation of aerosol particles and their growth to the sizes of cloud condensation nuclei in these areas are associated with biogenic volatile organic emissions from vegetation and soil.

  3. Influence of aerosol vertical distribution on radiative budget and climate

    NASA Astrophysics Data System (ADS)

    Nabat, Pierre; Michou, Martine; Saint-Martin, David; Watson, Laura

    2016-04-01

    Aerosols interact with shortwave and longwave radiation with ensuing consequences on radiative budget and climate. Aerosols are represented in climate models either using an interactive aerosol scheme including prognostic aerosol variables, or using climatologies, such as monthly aerosol optical depth (AOD) fields. In the first case, aerosol vertical distribution can vary rapidly, at a daily or even hourly scale, following the aerosol evolution calculated by the interactive scheme. On the contrary, in the second case, a fixed aerosol vertical distribution is generally imposed by climatological profiles. The objective of this work is to study the impact of aerosol vertical distribution on aerosol radiative forcing, with ensuing effects on climate. Simulations have thus been carried out using CNRM-CM, which is a global climate model including an interactive aerosol scheme representing the five main aerosol species (desert dust, sea-salt, sulfate, black carbon and organic matter). Several multi-annual simulations covering the past recent years are compared, including either the prognostic aerosol variables, or monthly AOD fields with different aerosol vertical distributions. In the second case, AOD fields directly come from the first simulation, so that all simulations have the same integrated aerosol loads. The results show that modifying the aerosol vertical distribution has a significant impact on radiative budget, with consequences on global climate. These differences, highlighting the importance of aerosol vertical distribution in climate models, probably come from the modification of atmospheric circulation induced by changes in the heights of the different aerosols. Besides, nonlinear effects in the superposition of aerosol and clouds reinforce the impact of aerosol vertical distribution, since aerosol radiative forcing depends highly upon the presence of clouds, and upon the relative vertical position of aerosols and clouds.

  4. The effect of aerosols and sea surface temperature on China's climate over the late twentieth century

    NASA Astrophysics Data System (ADS)

    Folini, Doris; Wild, Martin

    2015-04-01

    Focusing on China in the second half of the twentieth century, we examine the relative role of aerosols and prescribed, observation based sea surface temperatures (SSTs) for the evolution of surface solar radiation (SSR), surface air temperature (SAT), and precipitation in ensembles of transient (1870 - 2005) sensitivity experiments with the global climate model ECHAM5-HAM. Observations and simulations with transient SSTs and aerosol emissions agree reasonably well in eastern China in terms of SSR dimming (-6 +/- 2 W/m2/decade, 1960 - 2000), statistically non-significant JJA SAT trend (1950 - 2000), and drying in JJA from 1950 to 1990 (-2.5% to -3.5% per decade, essentially via reduction of convective precipitation). Other major observed features are not reproduce by the model, e.g. precipitation increase in the 1990s in the Yangtze valley, the strong warming in winter in northern parts of China and Mongolia, or SSR dimming in western China. For the model results, SO2 emissions are more relevant than emissions of black and organic carbon. Aerosol effects are less pronounced at higher model resolution. Transient SSTs are found to be crucial for decadal scale SAT variability over land, especially the strong warming in the 1990s, and, via SST forced reduction of cloud cover, for the ceasing of SSR dimming around the year 2000. Unforced cloud variability leads to relevant scatter (up to +/- 2 W/m2/decade) of modeled SSR trends at individual observation sites.

  5. Climate Engineering with Stratospheric Aerosols and Associated Engineering Parameters

    SciTech Connect

    Kravitz, Benjamin S.

    2013-02-12

    Climate engineering with stratospheric aerosols, an idea inspired by large volcaniceruptions, could cool the Earth’s surface and thus alleviate some of the predicted dangerous impacts of anthropogenic climate change. However, the effectiveness of climate engineering to achieve a particular climate goal, and any associated side effects, depend on certain aerosol parameters and how the aerosols are deployed in the stratosphere. Through the examples of sulfate and black carbon aerosols, this paper examines "engineering" parameters-aerosol composition, aerosol size, and spatial and temporal variations in deployment-for stratospheric climate engineering. The effects of climate engineering are sensitive to these parameters, suggesting that a particle could be found ordesigned to achieve specific desired climate outcomes. This prospect opens the possibility for discussion of societal goals for climate engineering.

  6. Simulation of bulk aerosol direct radiative effects and its climatic feedbacks in South Africa using RegCM4

    NASA Astrophysics Data System (ADS)

    Tesfaye, M.; Botai, J.; Sivakumar, V.; Mengistu Tsidu, G.; Rautenbach, C. J. deW.; Moja, Shadung J.

    2016-05-01

    In this study, 12 year runs of the Regional Climate Model (RegCM4) have been used to analyze the bulk aerosol radiative effects and its climatic feedbacks in South Africa. Due to the geographical locations where the aerosol potential source regions are situated and the regional dynamics, the South African aerosol spatial-distribution has a unique feature. Across the west and southwest areas, desert dust particles are dominant. However, sulfate and carbonaceous aerosols are primarily distributed over the east and northern regions of the country. Analysis of the Radiative Effects (RE) shows that in South Africa the bulk aerosols play a role in reducing the net radiation absorbed by the surface via enhancing the net radiative heating in the atmosphere. Hence, across all seasons, the bulk aerosol-radiation-climate interaction induced statistically significant positive feedback on the net atmospheric heating rate. Over the western and central parts of South Africa, the overall radiative feedbacks of bulk aerosol predominantly induces statistically significant Cloud Cover (CC) enhancements. Whereas, over the east and southeast coastal areas, it induces minimum reductions in CC. The CC enhancement and RE of aerosols jointly induce radiative cooling at the surface which in turn results in the reduction of Surface Temperature (ST: up to -1 K) and Surface Sensible Heat Flux (SSHF: up to -24 W/m2). The ST and SSHF decreases cause a weakening of the convectively driven turbulences and surface buoyancy fluxes which lead to the reduction of the boundary layer height, surface pressure enhancement and dynamical changes. Throughout the year, the maximum values of direct and semi-direct effects of bulk aerosol were found in areas of South Africa which are dominated by desert dust particles. This signals the need for a strategic regional plan on how to reduce the dust production and monitoring of the dust dispersion as well as it initiate the need of further research on different

  7. Stratospheric aerosols and climatic change

    NASA Technical Reports Server (NTRS)

    Baldwin, B.; Pollack, J. B.; Summers, A.; Toon, O. B.; Sagan, C.; Van Camp, W.

    1976-01-01

    Generated primarily by volcanic explosions, a layer of submicron silicate particles and particles made of concentrated sulfuric acids solution is present in the stratosphere. Flights through the stratosphere may be a future source of stratospheric aerosols, since the effluent from supersonic transports contains sulfurous gases (which will be converted to H2SO4) while the exhaust from Space Shuttles contains tiny aluminum oxide particles. Global heat balance calculations have shown that the stratospheric aerosols have made important contributions to some climatic changes. In the present paper, accurate radiative transfer calculations of the globally-averaged surface temperature (T) are carried out to estimate the sensitivity of the climate to changes in the number of stratospheric aerosols. The results obtained for a specified model atmosphere, including a vertical profile of the aerosols, indicate that the climate is unlikely to be affected by supersonic transports and Space Shuttles, during the next decades.

  8. Direct and indirect effects of anthropogenic aerosols as simulated by SP-CAM global climate model with superparameterization of clouds

    NASA Astrophysics Data System (ADS)

    Khairoutdinov, M.; Grabowski, W.; Morrison, H.

    2010-12-01

    Direct and indirect effects of aerosols on radiative forcing are among major uncertainties of the climate change simulated by global climate models (GCMs). Traditional GCMs have grid spacing that is too coarse to resolve individual clouds; instead, clouds are represented using cloud parameterizations. Accordingly, the interactions between parameterized clouds and aerosols need also to be parameterized. Recently, it became practical to apply a new kind of GCM, a Multiscale Modeling Framework (MMF) to the aerosol-cloud-radiation problem. In SP-CAM MMF, the cloud and convection parameterizations are replaced with a small-domain coarse-resolution cloud-system-resolving model (CRM), often called in this context a "superparameterization". The CRM subcycles within the GCM's time step, explicitly simulating evolution of clouds in each GCM's grid cell in response to large-scale (GCM) dynamics. The CRM computes the precipitation rates, cloud statistics, large-scale tendencies due to cloud processes, and radiative heating rates. Recently, the single-moment bulk microphysics scheme used by the CRM in SP-CAM has been upgraded to a more sophisticated two-moment bulk microphysics scheme. The new bulk scheme's prognostic variables include not only water content, but also number concentration for all liquid and solid water species such as cloud liquid and ice water, rain, snow and graupel. The effect of aerosols on simulated clouds can be modeled through specified globally and monthly varying fields of cloud-condensation nuclei (CCN) derived from several species of prescribed aerosol climatology. The cloud drop concentration is modeled using the local CCN count and updraft vertical velocity at cloud bases. In this study, the results of global climate simulations using current and pre-industrial aerosol distributions are contrasted. The presence of anthropogenic sulfate aerosols tends to increase the strength of the meridional circulation such as the Hadley cell, redistributing

  9. Toward understanding the climatic effects of aerosols under hazy environments: an overview of field observations in China

    NASA Astrophysics Data System (ADS)

    Li, Zhanqing

    2009-03-01

    Due to its fast economical growth and high density of population, China presents a unique environment to study the direct and indirect effects of heavy aerosol loadings on regional and global climates. Thanks to the East Asian Study of Tropospheric Aerosols: an International Regional Experiment (EAST-AIRE) (Li et al. 2007a), much knowledge has been gained concerning the temporal and spatial distributions of aerosol loading and single scattering albedo, their radiative effects and transportation mechanisms, among others. Deployment of the ARM Mobile Facility in China (AMF-China) in 2008 and enhancement of the EAST-AIRE observation capability will further help tackle with the effects of aerosols on cloud microphysics, precipitation, atmospheric adiabatic heating rate and circulation, especially on the Asian monsoon system. An overview is presented of the EAST-AIRE routine measurements and AMF intensive field campaign in 2008 in China.

  10. A satellite view of aerosols in the climate system

    NASA Technical Reports Server (NTRS)

    Kaufman, Yoram J.; Tanre, Didier; Boucher, Olivier

    2002-01-01

    Anthropogenic aerosols are intricately linked to the climate system and to the hydrologic cycle. The net effect of aerosols is to cool the climate system by reflecting sunlight. Depending on their composition, aerosols can also absorb sunlight in the atmosphere, further cooling the surface but warming the atmosphere in the process. These effects of aerosols on the temperature profile, along with the role of aerosols as cloud condensation nuclei, impact the hydrologic cycle, through changes in cloud cover, cloud properties and precipitation. Unravelling these feedbacks is particularly difficult because aerosols take a multitude of shapes and forms, ranging from desert dust to urban pollution, and because aerosol concentrations vary strongly over time and space. To accurately study aerosol distribution and composition therefore requires continuous observations from satellites, networks of ground-based instruments and dedicated field experiments. Increases in aerosol concentration and changes in their composition, driven by industrialization and an expanding population, may adversely affect the Earth's climate and water supply.

  11. A reduced-form approach to characterizing sulfate aerosol effects on climate in integrated assessment models. Final report

    SciTech Connect

    Wigley, T.M.L.

    1996-04-01

    The objective of this study was to devise a methodology for estimating the spatial patterns of future climate change accounting for the effects of both greenhouse gases and sulfate aerosols under a wide range of emissions scenarios, using the results of General Circulation Models.

  12. Aerosol Radiative Effects: Expected Variations in Optical Depth Spectra and Climate Forcing, with Implications for Closure Experiment Strategies

    NASA Technical Reports Server (NTRS)

    Russell, Philip B.; Stowe, L. L.; Hobbs, P. V.; Podolske, James R. (Technical Monitor)

    1995-01-01

    We examine measurement strategies for reducing uncertainties in aerosol direct radiative forcing by focused experiments that combine surface, air, and space measurements. Particularly emphasized are closure experiments, which test the degree of agreement among different measurements and calculations of aerosol properties and radiative effects. By combining results from previous measurements of large-scale smokes, volcanic aerosols, and anthropogenic aerosols with models of aerosol evolution, we estimate the spatial and temporal variability in optical depth spectra to be expected in the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX, planned for summer 1996 off the Eastern U.S. seaboard). In particular, we examine the expected changes in the wavelength dependence of optical depth as particles evolve through nucleation, growth by condensation and coagulation, and removal via sedimentation. We then calculate the expected radiative climate forcing (i.e. change in net radiative flux) for typical expected aerosols and measurement conditions (e.g. solar elevations, surface albedos, radiometer altitudes). These calculations use new expressions for flux and albedo changes, which account not only for aerosol absorption, but also for instantaneous solar elevation angles and the dependence of surface albedo on solar elevation. These factors, which are usually ignored or averaged in calculations of global aerosol effects, can have a strong influence on fluxes measured in closure experiments, and hence must be accounted for in calculations if closure is to be convincingly tested. We compare the expected measurement signal to measurement uncertainties expected for various techniques in various conditions. Thereby we derive recommendations for measurement strategies that combine surface, airborne, and spaceborne measurements.

  13. The climate impact of aviation aerosols

    NASA Astrophysics Data System (ADS)

    Gettelman, A.; Chen, C.

    2013-06-01

    A comprehensive general circulation model (GCM) is used to estimate the climate impact of aviation emissions of black carbon (BC) and sulfate (SO4) aerosols. Aviation BC is found not to exert significant radiative forcing impacts, when BC nucleating efficiencies in line with observations are used. Sulfate emissions from aircraft are found to alter liquid clouds at altitudes below emission (˜200 hPa); contributing to shortwave cloud brightening through enhanced liquid water path and drop number concentration in major flight corridors, particularly in the N. Atlantic. Global averaged sulfate direct and indirect effects on liquid clouds of 46 mWm-2are larger than the warming effect of aviation induced cloudiness of 16 mWm-2. The net result of including contrail cirrus and aerosol effects is a global averaged cooling of -21±11 mWm-2. These aerosol forcings should be considered with contrails in evaluating the total global impact of aviation on climate.

  14. Characterization of Atmospheric Aerosol Behavior and Climatic Effects by Analysis of SAGE 2 and Other Space, Air, and Ground Measurements

    NASA Technical Reports Server (NTRS)

    Livingston, John M.

    1999-01-01

    This report documents the research performed under NASA Ames Cooperative Agreement NCC 2-991, which covered the period 1 April 1997 through 31 March 1999. Previously, an interim technical report (Technical Report No. 1, 20 March 1998) summarized the work completed during the period 1 April 1997 through 31 March 1998. The objective of the proposed research was to advance our understanding of atmospheric aerosol behavior, aerosol-induced climatic effects, and the remote measurement and retrieval capabilities of spaceborne sensors such as SAGE II by combining and comparing data from these instruments and from airborne and ground-based instruments.

  15. Investigation of mineral aerosols radiative effects over High Mountain Asia in 1990-2009 using a regional climate model

    NASA Astrophysics Data System (ADS)

    Ji, Zhenming; Kang, Shichang; Zhang, Qianggong; Cong, Zhiyuan; Chen, Pengfei; Sillanpää, Mika

    2016-09-01

    Mineral aerosols scatter and absorb incident solar radiation in the atmosphere, and play an important role in the regional climate of High Mountain Asia (the domain includes the Himalayas, Tibetan Plateau, Pamir, Hindu-kush, Karakorum and Tienshan Mountains). Dust deposition on snow/ice can also change the surface albedo, resulting in perturbations in the surface radiation balance. However, most studies that have made quantitative assessments of the climatic effect of mineral aerosols over the High Mountain Asia region did not consider the impact of dust on snow/ice at the surface. In this study, a regional climate model coupled with an aerosol-snow/ice feedback module was used to investigate the emission, distribution, and deposition of dust and the climatic effects of aerosols over High Mountain Asia. Two sets of simulations driven by a reanalysis boundary condition were performed, i.e., with and without dust-climate feedback. Results indicated that the model captured the spatial and temporal features of the climatology and aerosol optical depth (AOD). High dust emission fluxes were simulated in the interior of the Tibetan Plateau (TP) and the Yarlung Tsangpo Valley in March-April-May (MAM), with a decreasing trend during 1990-2009. Dry deposition was controlled by the topography, and its spatial and seasonal features agreed well with the dust emission fluxes. The maximum wet deposition occurred in the western (southern and central) TP in MAM (JJA). A positive surface radiative forcing was induced by dust, including aerosol-snow/ice feedback, resulting in 2-m temperature increases of 0.1-0.5 °C over the western TP and Kunlun Mountains in MAM. Mineral dust also caused a decrease of 5-25 mm in the snow water equivalent (SWE) over the western TP, Himalayas, and Pamir Mountains in DJF and MAM. The long-term regional mean radiative forcing via dust deposition on snow showed an rising trend during 1990-2009, which suggested the contribution of aerosols surface

  16. Sources, Transport, and Climate Impacts of Biomass Burning Aerosols

    NASA Technical Reports Server (NTRS)

    Chin, Mian

    2010-01-01

    In this presentation, I will first talk about fundamentals of modeling of biomass burning emissions of aerosols, then show the results of GOCART model simulated biomass burning aerosols. I will compare the model results with observations of satellite and ground-based network in terms of total aerosol optical depth, aerosol absorption optical depth, and vertical distributions. Finally the long-range transport of biomass burning aerosols and the climate effects will be addressed. I will also discuss the uncertainties associated with modeling and observations of biomass burning aerosols

  17. Premonsoon Aerosol Characterization and Radiative Effects Over the Indo-Gangetic Plains: Implications for Regional Climate Warming

    NASA Technical Reports Server (NTRS)

    Gautam, Ritesh; Hsu, N. Christina; Lau, K.-M.

    2010-01-01

    The Himalayas have a profound effect on the South Asian climate and the regional hydrological cycle, as it forms a barrier for the strong monsoon winds and serves as an elevated heat source, thus controlling the onset and distribution of precipitation during the Indian summer monsoon. Recent studies have suggested that radiative heating by absorbing aerosols, such as dust and black carbon over the Indo-Gangetic Plains (IGP) and slopes of the Himalayas, may significantly accelerate the seasonal warming of the Hindu Kush-Himalayas-Tibetan Plateau (HKHT) and influence the subsequent evolution of the summer monsoon. This paper presents a detailed characterization of aerosols over the IGP and their radiative effects during the premonsoon season (April-May-June) when dust transport constitutes the bulk of the regional aerosol loading, using ground radiometric and spaceborne observations. During the dust-laden period, there is a strong response of surface shortwave flux to aerosol absorption indicated by the diurnally averaged forcing efficiency of -70 W/sq m per unit optical depth. The simulated aerosol single-scattering albedo, constrained by surface flux and aerosol measurements, is estimated to be 0.89+/- 0.01 (at approx.550 nm) with diurnal mean surface and top-of-atmosphere forcing values ranging from -11 to -79.8 W/sq m and +1.4 to +12 W/sq m, respectively, for the premonsoon period. The model-simulated solar heating rate profile peaks in the lower troposphere with enhanced heating penetrating into the middle troposphere (5-6 km), caused by vertically extended aerosols over the IGP with peak altitude of approx.5 km as indicated by spaceborne Cloud-Aerosol Lidar with Orthogonal Polarization observations. On a long-term climate scale, our analysis, on the basis of microwave satellite measurements of tropospheric temperatures from 1979 to 2007, indicates accelerated annual mean warming rates found over the Himalayan-Hindu Kush region (0.21 C/decade+/-0.08 C

  18. Sensitivity of modelled sulfate aerosol and its radiative effect on climate to ocean DMS concentration and air-sea flux

    NASA Astrophysics Data System (ADS)

    Tesdal, Jan-Erik; Christian, James R.; Monahan, Adam H.; von Salzen, Knut

    2016-09-01

    Dimethylsulfide (DMS) is a well-known marine trace gas that is emitted from the ocean and subsequently oxidizes to sulfate in the atmosphere. Sulfate aerosols in the atmosphere have direct and indirect effects on the amount of solar radiation reaching the Earth's surface. Thus, as a potential source of sulfate, ocean efflux of DMS needs to be accounted for in climate studies. Seawater concentration of DMS is highly variable in space and time, which in turn leads to high spatial and temporal variability in ocean DMS emissions. Because of sparse sampling (in both space and time), large uncertainties remain regarding ocean DMS concentration. In this study, we use an atmospheric general circulation model with explicit aerosol chemistry (CanAM4.1) and several climatologies of surface ocean DMS concentration to assess uncertainties about the climate impact of ocean DMS efflux. Despite substantial variation in the spatial pattern and seasonal evolution of simulated DMS fluxes, the global-mean radiative effect of sulfate is approximately linearly proportional to the global-mean surface flux of DMS; the spatial and temporal distribution of ocean DMS efflux has only a minor effect on the global radiation budget. The effect of the spatial structure, however, generates statistically significant changes in the global-mean concentrations of some aerosol species. The effect of seasonality on the net radiative effect is larger than that of spatial distribution and is significant at global scale.

  19. Improvement and Application of Atmospheric Radiative Transfer Models for Prediction of the Climatic Effects of Aerosol

    NASA Technical Reports Server (NTRS)

    Bergstrom, Robert W.; Mlawer, Eli J.; Sokolik, Irina N.; Clough, Shepard A.; Toon, Owen B.

    1998-01-01

    This paper presents a radiative transfer model that has been developed to accurately predict the atmospheric radiant flux in both the infrared and the solar spectrum with a minimum of computational effort. The model is designed to be included in numerical climate models. To assess the accuracy of the model, the results are compared to other more detailed models for several standard cases in the solar and thermal spectrum. As the thermal spectrum has been treated in other publications, we focus here on the solar part of the spectrum. We perform several example calculations focussing on the question of absorption of solar radiation by gases and aerosols.

  20. Improvement and Application of Atmospheric Radiative Transfer Models for Prediction of the Climatic Effects of Aerosol

    NASA Technical Reports Server (NTRS)

    Bergstrom, Robert W.

    1998-01-01

    This paper presents a radiative transfer model that has been developed to accurately predict the atmospheric radiant flux in both the infrared and the solar spectrum with a minimum of computational effort. The model is designed to be included in numerical climate models. To assess the accuracy of the model, the results are compared to other more detailed models for several standard cases in the solar and thermal spectrum. As the thermal spectrum has been treated in other publications we focus here on the solar part of the spectrum. We perform several example calculations focussing on the question of absorption of solar radiation by gases and aerosols.

  1. Medieval Loess Constraints On the Climate Effect of Dust Aerosols In the Great Plains of North America

    NASA Astrophysics Data System (ADS)

    Miller, R. L.; Cook, B. I.; Seager, R.; Mason, J. A.

    2011-12-01

    Loess deposits in the Great Plains of North America, together with tree ring records, suggest the occurrence of medieval megadroughts within the past millenium when rainfall was below average over several decades. Loess results from the deposition of dust aerosols, created by wind erosion, perhaps following vegetation loss after extended drought. Dust aerosols have been previously shown to exacerbate the absence of rainfall during the twentieth century Dust Bowl, reinforcing the drought and loss of vegetation. Ocean temperatures in the equatorial Pacific make the predominant contribution to hydroclimate variability in this region, but dust may have had an amplifying effect during the medieval drought once the vegetation loss was sufficiently extensive. Here, we describe GCM experiments with dust aerosols created by wind erosion over medieval sources within North America. Our goal is twofold: first, to calculate the climate effect of dust, which is believed to reduce precipitation during the Dust Bowl. Second, we calculate dust deposition for comparison to the observed thickness of loess deposits. This comparison serves as a constraint upon the total dust mobilization and the aerosol effect upon precipitation, both of which depend upon the incompletely known source extent and its productivity.

  2. Climate implications of carbonaceous aerosols: An aerosol microphysical study using the GISS/MATRIX climate model

    SciTech Connect

    Bauer, Susanne E.; Menon, Surabi; Koch, Dorothy; Bond, Tami; Tsigaridis, Kostas

    2010-04-09

    Recently, attention has been drawn towards black carbon aerosols as a likely short-term climate warming mitigation candidate. However the global and regional impacts of the direct, cloud-indirect and semi-direct forcing effects are highly uncertain, due to the complex nature of aerosol evolution and its climate interactions. Black carbon is directly released as particle into the atmosphere, but then interacts with other gases and particles through condensation and coagulation processes leading to further aerosol growth, aging and internal mixing. A detailed aerosol microphysical scheme, MATRIX, embedded within the global GISS modelE includes the above processes that determine the lifecycle and climate impact of aerosols. This study presents a quantitative assessment of the impact of microphysical processes involving black carbon, such as emission size distributions and optical properties on aerosol cloud activation and radiative forcing. Our best estimate for net direct and indirect aerosol radiative forcing change is -0.56 W/m{sup 2} between 1750 and 2000. However, the direct and indirect aerosol effects are very sensitive to the black and organic carbon size distribution and consequential mixing state. The net radiative forcing change can vary between -0.32 to -0.75 W/m{sup 2} depending on these carbonaceous particle properties. Assuming that sulfates, nitrates and secondary organics form a coating shell around a black carbon core, rather than forming a uniformly mixed particles, changes the overall net radiative forcing from a negative to a positive number. Black carbon mitigation scenarios showed generally a benefit when mainly black carbon sources such as diesel emissions are reduced, reducing organic and black carbon sources such as bio-fuels, does not lead to reduced warming.

  3. Impact of Black Carbon Aerosols on Regional Climate

    NASA Astrophysics Data System (ADS)

    Menon, S.; Hansen, J.; Nazarenko, L.; Luo, Y.

    2002-12-01

    We have evaluated the effect of anthropogenic aerosols on the regional climates of China and India: regions where aerosol emissions have been increasing at an alarming rate. We use the Goddard Institute for Space Studies (GISS) climate model to perform simulations that investigate recent trends in summer precipitation observed over China - North drought, South flooding - considered to be the largest observed in several decades. We perform several simulations to differentiate between the climate effects of sulfate and black carbon aerosols and use realistic aerosol distributions obtained from measurements over China, India and the Indian Ocean. The trends in precipitation as well as the summer time surface cooling over China and India have been captured by using aerosols that have a low single scatter albedo (0.85), i.e., by assuming that the aerosols are mostly absorbing. Since black carbon aerosols are absorbing aerosols and cause surface cooling with heating at the top of the atmosphere and in the lower troposphere, the change in the vertical temperature profile causes changes in the large-scale vertical velocity fields, latent heating, convective activity and cloud cover. This change in the large-scale circulation may explain some of the changes in the precipitation and temperature trends observed over China and India in recent decades. Our results suggest that black carbon aerosols can have a significant influence on regional climate through changes in the hydrological cycle and large-scale circulation.

  4. Impacts of Aerosol Direct Effects on the South Asian Climate: Assessment of Radiative Feedback Processes Using Model Simulations and Satellite/Surface Measurements

    NASA Technical Reports Server (NTRS)

    Wang, Sheng-Hsiang; Gautam, Ritesh; Lau, William K. M.; Tsay, Si-Chee; Sun, Wen-Yih; Kim, Kyu-Myong; Chern, Jiun-Dar; Hsu, Christina; Lin, Neng-Huei

    2011-01-01

    Current assessment of aerosol radiative effect is hindered by our incomplete knowledge of aerosol optical properties, especially absorption, and our current inability to quantify physical and microphysical processes. In this research, we investigate direct aerosol radiative effect over heavy aerosol loading areas (e.g., Indo-Gangetic Plains, South/East Asia) and its feedbacks on the South Asian climate during the pre-monsoon season (March-June) using the Purdue Regional Climate Model (PRCM) with prescribed aerosol data derived by the NASA Goddard Earth Observing System Model (GEOS-5). Our modeling domain covers South and East Asia (60-140E and 0-50N) with spatial resolutions of 45 km in horizontal and 28 layers in vertical. The model is integrated from 15 February to 30 June 2008 continuously without nudging (i.e., only forced by initial/boundary conditions). Two numerical experiments are conducted with and without the aerosol-radiation effects. Both simulations are successful in reproducing the synoptic patterns on seasonal-to-interannual time scales and capturing a pre-monsoon feature of the northward rainfall propagation over Indian region in early June which shown in Tropical Rainfall Measuring Mission (TRMM) observation. Preliminary result suggests aerosol-radiation interactions mainly alter surface-atmosphere energetics and further result in an adjustment of the vertical temperature distribution in lower atmosphere (below 700 hPa). The modifications of temperature and associated rainfall and circulation feedbacks on the regional climate will be discussed in the presentation.

  5. Atmospheric Aerosol Properties and Climate Impacts

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Kahn, Ralph A.; Remer, Lorraine A.; Yu, Hongbin; Rind, David; Feingold, Graham; Quinn, Patricia K.; Schwartz, Stephen E.; Streets, David G.; DeCola, Phillip; Halthore, Rangasayi

    2009-01-01

    This report critically reviews current knowledge about global distributions and properties of atmospheric aerosols, as they relate to aerosol impacts on climate. It assesses possible next steps aimed at substantially reducing uncertainties in aerosol radiative forcing estimates. Current measurement techniques and modeling approaches are summarized, providing context. As a part of the Synthesis and Assessment Product in the Climate Change Science Program, this assessment builds upon recent related assessments, including the Fourth Assessment Report of the Intergovernmental Panel on Climate Change (IPCC AR4, 2007) and other Climate Change Science Program reports. The objectives of this report are (1) to promote a consensus about the knowledge base for climate change decision support, and (2) to provide a synthesis and integration of the current knowledge of the climate-relevant impacts of anthropogenic aerosols for policy makers, policy analysts, and general public, both within and outside the U.S government and worldwide.

  6. Atmospheric Carbon Dioxide and Aerosols: Effects of Large Increases on Global Climate

    ERIC Educational Resources Information Center

    Science, 1971

    1971-01-01

    Mathematical models indicate increasing atmospheric carbon dioxide causes an increase in surface temperature at a decreasing rate, and the rate of temperature decrease caused by increasing aerosols increases with aerosol concentration. (AL)

  7. OCS, stratospheric aerosols and climate

    NASA Astrophysics Data System (ADS)

    Turco, R. P.; Whitten, R. C.; Toon, O. B.; Pollack, J. B.; Hamill, P.

    1980-01-01

    Carbonyl sulphide (OCS) is found to be the predominant sulphur-bearing compound in our atmosphere1-3. It contributes to the formation of stratospheric sulphate aerosol particles4, which affect the Earth's radiation balance and climate5-7. Using recently obtained data, we estimate that OCS has a global source of ~5 tg per year (tg = 1012 g) and a lifetime of roughly 1 yr. We calculate that increasing anthropogenic emissions of OCS could cause measurable climate alterations within the next century. Numerous sources of OCS have been identified (see Fig. 1). Crutzen et al.8 estimate that natural and agricultural fires contribute 0.2-0.3 tg of OCS to the atmosphere each year. Adams et al.9 measured average OCS emission rates for a variety of common soils of about 0.004 g m-2 yr-1, which may be extrapolated to a global OCS source of nearly 0.5 tg yr-1. Adams et al.9 also noted OCS emissions several thousand times greater than average above saline marshes. Carbonyl sulphide has been detected near cattle feedlots in concentrations as high as 6,000 p.p.b.v.10. Volcanoes and fumaroles seem to represent a minor source of OCS (refs 11,12). We estimate that the direct contributions of biospheric processes to the OCS budget may be ~1 tg yr-1.

  8. A New Approach to Modeling Aerosol Effects on East Asian Climate: Parametric Uncertainties Associated with Emissions, Cloud Microphysics and their Interactions

    SciTech Connect

    Yan, Huiping; Qian, Yun; Zhao, Chun; Wang, Hailong; Wang, Minghuai; Yang, Ben; Liu, Xiaohong; Fu, Qiang

    2015-09-16

    In this study, we adopt a parametric sensitivity analysis framework that integrates the quasi-Monte Carlo parameter sampling approach and a surrogate model to examine aerosol effects on the East Asian Monsoon climate simulated in the Community Atmosphere Model (CAM5). A total number of 256 CAM5 simulations are conducted to quantify the model responses to the uncertain parameters associated with cloud microphysics parameterizations and aerosol (e.g., sulfate, black carbon (BC), and dust) emission factors and their interactions. Results show that the interaction terms among parameters are important for quantifying the sensitivity of fields of interest, especially precipitation, to the parameters. The relative importance of cloud-microphysics parameters and emission factors (strength) depends on evaluation metrics or the model fields we focused on, and the presence of uncertainty in cloud microphysics imposes an additional challenge in quantifying the impact of aerosols on cloud and climate. Due to their different optical and microphysical properties and spatial distributions, sulfate, BC, and dust aerosols have very different impacts on East Asian Monsoon through aerosol-cloud-radiation interactions. The climatic effects of aerosol do not always have a monotonic response to the change of emission factors. The spatial patterns of both sign and magnitude of aerosol-induced changes in radiative fluxes, cloud, and precipitation could be different, depending on the aerosol types, when parameters are sampled in different ranges of values. We also identify the different cloud microphysical parameters that show the most significant impact on climatic effect induced by sulfate, BC and dust, respectively, in East Asia.

  9. Dust aerosol effect on semi-arid climate over Northwest China detected from A-Train satellite measurements

    NASA Astrophysics Data System (ADS)

    Huang, J.; Minnis, P.; Yan, H.; Yi, Y.; Chen, B.; Zhang, L.; Ayers, J. K.

    2010-07-01

    The impact of dust aerosols on the semi-arid climate of Northwest China is analyzed by comparing aerosol and cloud properties derived over the China semi-arid region (hereafter, CSR) and the United States semi-arid region (hereafter, USR) using several years of surface and A-Train satellite observations during active dust event seasons. These regions have similar climatic conditions, but aerosol concentrations are greater over the CSR. Because the CSR is close to two major dust source regions (Taklamakan and Gobi deserts), the aerosols over the CSR not only contain local anthropogenic aerosols (agricultural dust, black carbon and other anthropogenic aerosols), but also include natural dust transported from the source regions. The aerosol optical depth, averaged over a 3-month period, derived from MODIS for the CSR is 0.27, which is 47% higher than that over the USR (0.19). Although transported natural dust only accounts for 53% of this difference, it is a major contributor to the average absorbing aerosol index, which is 27% higher in the CSR (1.07) than in the USR (0.84). During dust event periods, liquid water cloud particle size, optical depth and liquid water path are smaller by 9%, 30% and 33% compared to dust-free conditions, respectively.

  10. Dust aerosol effect on semi-arid climate over Northwest China detected from A-Train satellite measurements

    NASA Astrophysics Data System (ADS)

    Huang, J.; Minnis, P.; Yan, H.; Yi, Y.; Chen, B.; Zhang, L.; Ayers, J. K.

    2010-05-01

    The impact of dust aerosols on the semi-arid climate of Northwest China is analyzed by comparing aerosol and cloud properties derived over the China semi-arid region (hereafter, CSR) and the United States semi-arid region (hereafter, USR) using several years of surface and A-Train satellite observations during active dust event seasons. These regions have similar climatic conditions, but aerosol concentrations are greater over the CSR. Because the CSR is close to two major dust source regions (Taklamakan and Gobi deserts), the aerosols over the CSR not only contain local anthropogenic aerosols (agricultural dust, black carbon and other anthropogenic aerosols), but also include natural dust transported from the source regions. The aerosol optical depth, averaged over a 3-month period, derived from MODIS for the CSR is 0.27, which is 47% higher than that over the USR (0.19). Although transported natural dust only accounts for 53% of this difference, it is a major contributor to the average absorbing aerosol index, which is 27% higher in the CSR (1.07) than in the USR (0.84). During dust event periods, liquid water cloud particle size, optical depth and liquid water path are smaller by 9%, 30% and 33% compared to dust-free conditions, respectively.

  11. The contribution of carbonaceous aerosols to climate change

    SciTech Connect

    Penner, J.E. |; Chuang, C.C.; Liousse, C.

    1996-04-01

    Contribution of aerosols to climate change results from two effects: clear-sky and cloudy-sky forcing. The clear-sky climate forcing by carbonaceous aerosols from biomass burning and fossil fuel burning depends on the relative contribution of scattering and absorption by the aerosols which in turn depends on the fraction of aerosol mass associated with black carbon and its size distribution. This paper reviews estimates for the emission of carbonaceous aerosols, placing these estimates in the context of estimates for the emissions of anthropogenic and natural sulfate aerosols and natural sources of organic particulate matter. The cloudy-sky forcing from carbonaceous aerosols is difficult to estimate because, among other factors, it depends on the amount of absorption by the aerosols in the cloud. It is also highly sensitive to the assumed pre-existing, natural aerosol abundance. An upper limit for this cloudy-sky forcing is -4.4 W/m{sup 2}, but may range as low as -2.4 W/m{sup 2}, depending on background aerosol concentrations. These estimates do not yet account for absorption of radiation by black carbon associated with cloud or the presence of pre-existing dust particles.

  12. Global-mean temperature change from shipping toward 2050: improved representation of the indirect aerosol effect in simple climate models.

    PubMed

    Lund, Marianne Tronstad; Eyring, Veronika; Fuglestvedt, Jan; Hendricks, Johannes; Lauer, Axel; Lee, David; Righi, Mattia

    2012-08-21

    We utilize a range of emission scenarios for shipping to determine the induced global-mean radiative forcing and temperature change. Ship emission scenarios consistent with the new regulations on nitrogen oxides (NO(x)) and sulfur dioxide (SO(2)) from the International Maritime Organization and two of the Representative Concentration Pathways are used as input to a simple climate model (SCM). Based on a complex aerosol-climate model we develop and test new parametrizations of the indirect aerosol effect (IAE) in the SCM that account for nonlinearities in radiative forcing of ship-induced IAE. We find that shipping causes a net global cooling impact throughout the period 1900-2050 across all parametrizations and scenarios. However, calculated total net global-mean temperature change in 2050 ranges from -0.03[-0.07,-0.002]°C to -0.3[-0.6,-0.2]°C in the A1B scenario. This wide range across parametrizations emphasizes the importance of properly representing the IAE in SCMs and to reflect the uncertainties from complex global models. Furthermore, our calculations show that the future ship-induced temperature response is likely a continued cooling if SO(2) and NO(x) emissions continue to increase due to a strong increase in activity, despite current emission regulations. However, such cooling does not negate the need for continued efforts to reduce CO(2) emissions, since residual warming from CO(2) is long-lived.

  13. Global-mean temperature change from shipping toward 2050: improved representation of the indirect aerosol effect in simple climate models.

    PubMed

    Lund, Marianne Tronstad; Eyring, Veronika; Fuglestvedt, Jan; Hendricks, Johannes; Lauer, Axel; Lee, David; Righi, Mattia

    2012-08-21

    We utilize a range of emission scenarios for shipping to determine the induced global-mean radiative forcing and temperature change. Ship emission scenarios consistent with the new regulations on nitrogen oxides (NO(x)) and sulfur dioxide (SO(2)) from the International Maritime Organization and two of the Representative Concentration Pathways are used as input to a simple climate model (SCM). Based on a complex aerosol-climate model we develop and test new parametrizations of the indirect aerosol effect (IAE) in the SCM that account for nonlinearities in radiative forcing of ship-induced IAE. We find that shipping causes a net global cooling impact throughout the period 1900-2050 across all parametrizations and scenarios. However, calculated total net global-mean temperature change in 2050 ranges from -0.03[-0.07,-0.002]°C to -0.3[-0.6,-0.2]°C in the A1B scenario. This wide range across parametrizations emphasizes the importance of properly representing the IAE in SCMs and to reflect the uncertainties from complex global models. Furthermore, our calculations show that the future ship-induced temperature response is likely a continued cooling if SO(2) and NO(x) emissions continue to increase due to a strong increase in activity, despite current emission regulations. However, such cooling does not negate the need for continued efforts to reduce CO(2) emissions, since residual warming from CO(2) is long-lived. PMID:22830995

  14. Advancing Solar Irradiance Measurement for Climate-Related Studies: Accurate Constraint on Direct Aerosol Radiative Effect (DARE)

    NASA Technical Reports Server (NTRS)

    Tsay, Si-Chee; Ji, Q. Jack

    2011-01-01

    Earth's climate is driven primarily by solar radiation. As summarized in various IPCC reports, the global average of radiative forcing for different agents and mechanisms, such as aerosols or CO2 doubling, is in the range of a few W/sq m. However, when solar irradiance is measured by broadband radiometers, such as the fleet of Eppley Precision Solar Pyranometers (PSP) and equivalent instrumentation employed worldwide, the measurement uncertainty is larger than 2% (e.g., WMO specification of pyranometer, 2008). Thus, out of the approx. 184 W/sq m (approx.263 W/sq m if cloud-free) surface solar insolation (Trenberth et al. 2009), the measurement uncertainty is greater than +/-3.6 W/sq m, overwhelming the climate change signals. To discern these signals, less than a 1 % measurement uncertainty is required and is currently achievable only by means of a newly developed methodology employing a modified PSP-like pyranometer and an updated calibration equation to account for its thermal effects (li and Tsay, 2010). In this talk, we will show that some auxiliary measurements, such as those from a collocated pyrgeometer or air temperature sensors, can help correct historical datasets. Additionally, we will also demonstrate that a pyrheliometer is not free of the thermal effect; therefore, comparing to a high cost yet still not thermal-effect-free "direct + diffuse" approach in measuring surface solar irradiance, our new method is more economical, and more likely to be suitable for correcting a wide variety of historical datasets. Modeling simulations will be presented that a corrected solar irradiance measurement has a significant impact on aerosol forcing, and thus plays an important role in climate studies.

  15. Climate Implications of the Heterogeneity of Anthropogenic Aerosol Forcing

    NASA Astrophysics Data System (ADS)

    Persad, Geeta Gayatri

    Short-lived anthropogenic aerosols are concentrated in regions of high human activity, where they interact with radiation and clouds, causing horizontally heterogeneous radiative forcing between polluted and unpolluted regions. Aerosols can absorb shortwave energy in the atmosphere, but deplete it at the surface, producing opposite radiative perturbations between the surface and atmosphere. This thesis investigates climate and policy implications of this horizontal and vertical heterogeneity of anthropogenic aerosol forcing, employing the Geophysical Fluid Dynamics Laboratory's AM2.1 and AM3 models, both at a global scale and using East Asia as a regional case study. The degree of difference between spatial patterns of climate change due to heterogeneous aerosol forcing versus homogeneous greenhouse gas forcing deeply impacts the detection, attribution, and prediction of regional climate change. This dissertation addresses a gap in current understanding of these two forcings' response pattern development, using AM2.1 historical forcing simulations. The results indicate that fast atmospheric and land-surface processes alone substantially homogenize the global pattern of surface energy flux response to heterogeneous aerosol forcing. Aerosols' vertical redistribution of energy significantly impacts regional climate, but is incompletely understood. It is newly identified here, via observations and historical and idealized forcing simulations, that increased aerosol-driven atmospheric absorption may explain half of East Asia's recent surface insolation decline. Further, aerosols' surface and atmospheric effects counteract each other regionally---atmospheric heating enhances summer monsoon circulation, while surface dimming suppresses it---but absorbing aerosols' combined effects reduce summer monsoon rainfall. This thesis constitutes the first vertical decomposition of aerosols' impacts in this high-emissions region and elucidates the monsoonal response to aerosols

  16. Aerosols-cloud-climate -interactions in the Norwegian Earth System Model (NorESM). Importance of biogenic particles for cloud properties and anthropogenic indirect effect.

    NASA Astrophysics Data System (ADS)

    Seland, Ø.; Iversen, T.; Kirkevâg, A.

    2012-04-01

    According to the 4th assessment report of IPCC, major sources of uncertainty in anthropogenic climate change projections are inaccurate model description and weak knowledge of aerosols and their interactions with radiation and clouds, as well as the cloud feedback to radiative forcing. One important aspect of the associated uncertainty is the natural atmosphere. Anthropogenic climate change is an increment caused by anthropogenic emissions relative to the properties of the climate system untouched by man. This is crucial for the direct and indirect effects of aerosols, since the amount, size and physical properties of natural background particles strongly influence the same properties of the anthropogenic aerosol components. In many climate models where CDNC is calculated explicitly, CDNC is constrained by prescribing a lower bound below which calculated values are not allowed. This is done in order to keep the aerosol in-direct effect within estimated values. The rationale for using such a lower bound is to keep the aerosol radiative forcing constrained by the forcing of green-house gases and 20th century climate.We hypothesize this lower bound can be removed or made less strict by including aerosols of biogenic origin. We will present results and sensitivity studies from simulations with the NorESM where we have added contributions from organic carbon of natural origin both from vegetation and oceanic sources. By including aerosols of biogenic origin we obtain close to the median indirect radiative forcing reported by IPCC AR4, as well as reproducing the temperature increase in the 20th century. NorESM is based on the Earth system model CCSM4.0 from NCAR, but is using CAM4-Oslo instead of CAM4 as atmosphere model and an updated version of MICOM from the Bergen Climate Model (BCM) instead of the ocean model POP2. The aerosol module includes sea-salt, dust, sulphate, black carbon (BC) and particulate organic matter (OM). Primary aerosol size-distributions are

  17. The effect of aerosols and sea surface temperature on China's climate in the late twentieth century from ensembles of global climate simulations

    NASA Astrophysics Data System (ADS)

    Folini, D.; Wild, M.

    2015-03-01

    Over the late twentieth century, China has seen a strong increase in aerosol emissions, whose quantitative role for observed changes in surface solar radiation (SSR), surface air temperature (SAT), and precipitation remains debated. We use ensembles of transient sensitivity experiments with the global climate model ECHAM5 from the Max Planck Institute for Meteorology, Hamburg, Germany, combined with the Hamburg Aerosol Module to examine the effect of aerosols and prescribed, observation-based sea surface temperatures (SSTs) on the above variables. Observations and control experiments agree reasonably well in eastern China in terms of SSR dimming (-6 ± 2 W/m2/decade, 1960-2000; stronger than in models of the Coupled Model Intercomparison Project Phase 5, CMIP5), statistically nonsignificant summer SAT trend (1950-2005), and drying in summer from 1950 to 1990 (-2.5% to -3.5% per decade, essentially via reduction of convective precipitation). Other observed features are not reproduced by the model, e.g., precipitation increase in the 1990s in the Yangtze River valley or, from the 1960s onward, the strong winter warming in northern China and Mongolia and SSR dimming in western China. Aerosol effects are stronger for sulfur dioxide than for black and organic carbon and are more pronounced at lower model resolution. Transient SSTs are crucial for decadal-scale SAT variability over land, especially the strong warming in the 1990s, and, via SST forced reduction of cloud cover, for the ceasing of SSR dimming around the year 2000. Unforced cloud variability leads to relevant scatter (up to ±2 W/m2/decade) of modeled SSR trends at individual observation sites.

  18. Global Distribution and Climate Forcing of Marine Organic Aerosol - Part 2: Effects on Cloud Properties and Radiative Forcing

    SciTech Connect

    Gantt, Brett; Xu, Jun; Meskhidze, N.; Zhang, Yang; Nenes, Athanasios; Ghan, Steven J.; Liu, Xiaohong; Easter, Richard C.; Zaveri, Rahul A.

    2012-07-25

    A series of simulations with the Community Atmosphere Model version 5 (CAM5) with a 7-mode Modal Aerosol Model were conducted to assess the changes in cloud microphysical properties and radiative forcing resulting from marine organic aerosols. Model simulations show that the anthropogenic aerosol indirect forcing (AIF) predicted by CAM5 is decreased in absolute magnitude by up to 0.09 Wm{sup -2} (7 %) when marine organic aerosols are included. Changes in the AIF from marine organic aerosols are associated with small global increases in low-level incloud droplet number concentration and liquid water path of 1.3 cm{sup -3} (1.5 %) and 0.22 gm{sup -2} (0.5 %), respectively. Areas especially sensitive to changes in cloud properties due to marine organic aerosol include the Southern Ocean, North Pacific Ocean, and North Atlantic Ocean, all of which are characterized by high marine organic emission rates. As climate models are particularly sensitive to the background aerosol concentration, this small but non-negligible change in the AIF due to marine organic aerosols provides a notable link for ocean-ecosystem marine low-level cloud interactions and may be a candidate for consideration in future earth system models.

  19. On the Feasibility of Studying Shortwave Aerosol Radiative Forcing of Climate Using Dual-Wavelength Aerosol Backscatter Lidar

    NASA Technical Reports Server (NTRS)

    Redemann, Jens; Russell, Philip B.; Winker, David M.; McCormick, M. Patrick; Hipskind, R. Stephen (Technical Monitor)

    2000-01-01

    The current low confidence in the estimates of aerosol-induced perturbations of Earth's radiation balance is caused by the highly non-uniform compositional, spatial and temporal distributions of tropospheric aerosols on a global scale owing to their heterogeneous sources and short lifetimes. Nevertheless, recent studies have shown that the inclusion of aerosol effects in climate model calculations can improve agreement with observed spatial and temporal temperature distributions. In light of the short lifetimes of aerosols, determination of their global distribution with space-borne sensors seems to be a necessary approach. Until recently, satellite measurements of tropospheric aerosols have been approximate and did not provide the full set of information required to determine their radiative effects. With the advent of active aerosol remote sensing from space (e.g., PICASSO-CENA), the applicability fo lidar-derived aerosol 180 deg -backscatter data to radiative flux calculations and hence studies of aerosol effects on climate needs to be investigated.

  20. Simulation of Climate Forcing by Aerosols

    SciTech Connect

    Ghan, Steven J.; Bian, Xindi; Chapman, Elaine G.; Easter, Richard C.; Fann, George I.; Kothari, Suraj C.; Zaveri, Rahul A.; Zhang, Yang

    2004-05-03

    The largest source of uncertainty in estimates of the radiative forcing governing climate change is in the radiative forcing due to anthropogenic aerosols. Current estimates of the global mean of the aerosol radiative forcing range from –0.3 to –3.0 watts per square meter (Wm-2 ) which is opposite in sign and possibly comparable in magnitude to the +2 Wm-2 forcing due to increasing greenhouse gases. We have developed a global aerosol and climate modeling system that provides arguably the most detailed treatment of aerosols and their impact on the planetary radiation balance of any model, but our estimates of radiative forcing have been hindered by our lack of access to high performance computing resources. We propose to use the MSCF to conduct a series of simulations with and without emissions of a variety of aerosol particles and aerosol precursors. These extensive simulations will enable us to produce much more refined estimates of the impact of anthropogenic emissions on radiative forcing of climate change. To take full advantage of the parallelism available on the MSCF MPP1, we will apply the Global Array Toolkit to dynamically load balance the reactive chemistry component of our model. We will adapt our modifications of the serial NCAR Community Climate Model CCM2 to the parallel NCAR CCM3.10.

  1. Future vegetation-climate interactions in Eastern Siberia: an assessment of the competing effects of CO2 and secondary organic aerosols

    NASA Astrophysics Data System (ADS)

    Arneth, Almut; Makkonen, Risto; Olin, Stefan; Paasonen, Pauli; Holst, Thomas; Kajos, Maija K.; Kulmala, Markku; Maximov, Trofim; Miller, Paul A.; Schurgers, Guy

    2016-04-01

    Disproportional warming in the northern high latitudes and large carbon stocks in boreal and (sub)arctic ecosystems have raised concerns as to whether substantial positive climate feedbacks from biogeochemical process responses should be expected. Such feedbacks occur when increasing temperatures lead, for example, to a net release of CO2 or CH4. However, temperature-enhanced emissions of biogenic volatile organic compounds (BVOCs) have been shown to contribute to the growth of secondary organic aerosol (SOA), which is known to have a negative radiative climate effect. Combining measurements in Eastern Siberia with model-based estimates of vegetation and permafrost dynamics, BVOC emissions, and aerosol growth, we assess here possible future changes in ecosystem CO2 balance and BVOC-SOA interactions and discuss these changes in terms of possible climate effects. Globally, the effects of changes in Siberian ecosystem CO2 balance and SOA formation are small, but when concentrating on Siberia and the Northern Hemisphere the negative forcing from changed aerosol direct and indirect effects become notable - even though the associated temperature response would not necessarily follow a similar spatial pattern. While our analysis does not include other important processes that are of relevance for the climate system, the CO2 and BVOC-SOA interplay serves as an example for the complexity of the interactions between emissions and vegetation dynamics that underlie individual terrestrial processes and highlights the importance of addressing ecosystem-climate feedbacks in consistent, process-based model frameworks.

  2. Aerosol Climate Time Series Evaluation In ESA Aerosol_cci

    NASA Astrophysics Data System (ADS)

    Popp, T.; de Leeuw, G.; Pinnock, S.

    2015-12-01

    Within the ESA Climate Change Initiative (CCI) Aerosol_cci (2010 - 2017) conducts intensive work to improve algorithms for the retrieval of aerosol information from European sensors. By the end of 2015 full mission time series of 2 GCOS-required aerosol parameters are completely validated and released: Aerosol Optical Depth (AOD) from dual view ATSR-2 / AATSR radiometers (3 algorithms, 1995 - 2012), and stratospheric extinction profiles from star occultation GOMOS spectrometer (2002 - 2012). Additionally, a 35-year multi-sensor time series of the qualitative Absorbing Aerosol Index (AAI) together with sensitivity information and an AAI model simulator is available. Complementary aerosol properties requested by GCOS are in a "round robin" phase, where various algorithms are inter-compared: fine mode AOD, mineral dust AOD (from the thermal IASI spectrometer), absorption information and aerosol layer height. As a quasi-reference for validation in few selected regions with sparse ground-based observations the multi-pixel GRASP algorithm for the POLDER instrument is used. Validation of first dataset versions (vs. AERONET, MAN) and inter-comparison to other satellite datasets (MODIS, MISR, SeaWIFS) proved the high quality of the available datasets comparable to other satellite retrievals and revealed needs for algorithm improvement (for example for higher AOD values) which were taken into account for a reprocessing. The datasets contain pixel level uncertainty estimates which are also validated. The paper will summarize and discuss the results of major reprocessing and validation conducted in 2015. The focus will be on the ATSR, GOMOS and IASI datasets. Pixel level uncertainties validation will be summarized and discussed including unknown components and their potential usefulness and limitations. Opportunities for time series extension with successor instruments of the Sentinel family will be described and the complementarity of the different satellite aerosol products

  3. Future vegetation-climate interactions in Eastern Siberia: an assessment of the competing effects of CO2 and secondary organic aerosols

    NASA Astrophysics Data System (ADS)

    Arneth, A.; Makkonen, R.; Olin, S.; Paasonen, P.; Holst, T.; Kajos, M. K.; Kulmala, M.; Maximov, T.; Miller, P. A.; Schurgers, G.

    2015-10-01

    Disproportional warming in the northern high latitudes, and large carbon stocks in boreal and (sub)arctic ecosystems have raised concerns as to whether substantial positive climate feedbacks from biogeochemical process responses should be expected. Such feedbacks occur if increasing temperatures lead to e.g. a net release of CO2 or CH4. However, temperature-enhanced emissions of biogenic volatile organic compounds (BVOC) have been shown to contribute to the growth of secondary organic aerosol (SOA) which is known to have a negative radiative climate effect. Combining measurements in Eastern Siberia with model-based estimates of vegetation and permafrost dynamics, BVOC emissions and aerosol growth, we assess here possible future changes in ecosystem CO2 balance and BVOC-SOA interactions, and discuss these changes in terms of possible climate effects. On global level, both are very small but when concentrating on Siberia and the northern hemisphere the negative forcing from changed aerosol direct and indirect effects become notable - even though the associated temperature response would not necessarily follow a similar spatial pattern. While our analysis does not include other important processes that are of relevance for the climate system, the CO2 and BVOC-SOA interplay used serves as an example of the complexity of the interactions between emissions and vegetation dynamics that underlie individual terrestrial feedbacks and highlights the importance of addressing ecosystem-climate feedbacks in consistent, process-based model frameworks.

  4. Smoke and pollution aerosol effect on cloud cover.

    PubMed

    Kaufman, Yoram J; Koren, Ilan

    2006-08-01

    Pollution and smoke aerosols can increase or decrease the cloud cover. This duality in the effects of aerosols forms one of the largest uncertainties in climate research. Using solar measurements from Aerosol Robotic Network sites around the globe, we show an increase in cloud cover with an increase in the aerosol column concentration and an inverse dependence on the aerosol absorption of sunlight. The emerging rule appears to be independent of geographical location or aerosol type, thus increasing our confidence in the understanding of these aerosol effects on the clouds and climate. Preliminary estimates suggest an increase of 5% in cloud cover.

  5. Smoke and Pollution Aerosol Effect on Cloud Cover

    NASA Technical Reports Server (NTRS)

    Kaufman, Yoram J.; Koren, Ilan

    2006-01-01

    Pollution and smoke aerosols can increase or decrease the cloud cover. This duality in the effects of aerosols forms one of the largest uncertainties in climate research. Using solar measurements from Aerosol Robotic Network sites around the globe, we show an increase in cloud cover with an increase in the aerosol column concentration and an inverse dependence on the aerosol absorption of sunlight. The emerging rule appears to be independent of geographical location or aerosol type, thus increasing our confidence in the understanding of these aerosol effects on the clouds and climate. Preliminary estimates suggest an increase of 5% in cloud cover.

  6. Radiative Effects of Aerosols

    NASA Technical Reports Server (NTRS)

    Valero, Francisco P. J.

    1997-01-01

    During the Atlantic Stratocumulus Transition Experiment (ASTEX) in June 1992, two descents in cloud-free regions allowed comparison of the change in aerosol optical depth as determined by an onboard total-direct-diffuse radiometer (TDDR) to the change calculated from measured size resolved aerosol microphysics and chemistry. Both profiles included pollution haze layer from Europe but the second also included the effect of a Saharan dust layer above the haze. The separate contributions of supermicrometer (coarse) and submicrometer (fine) aerosol were determined and thermal analysis of the pollution haze indicated that the fine aerosol was composed primarily of a sulfate/water mixture with a refractory soot-like core.

  7. Clays as mineral dust aerosol: An integrated approach to studying climate, atmospheric chemistry, and biogeochemical effects of atmospheric clay minerals in an undergraduate research laboratory

    NASA Astrophysics Data System (ADS)

    Hatch, C. D.; Crane, C. C.; Harris, K. J.; Thompson, C. E.; Miles, M. K.; Weingold, R. M.; Bucuti, T.

    2011-12-01

    Entrained mineral dust aerosol accounts for 45% of the global annual atmospheric aerosol load and can have a significant influence on important environmental issues, including climate, atmospheric chemistry, cloud formation, biogeochemical processes, visibility, and human health. 70% of all mineral aerosol mass originating from Africa consists of layered aluminosilicates, including illite, kaolinite, and montmorillonite clays. Clay minerals are a largely neglected component of mineral aerosol, yet they have unique physiochemical properties, including a high reactive surface area, large cation exchange capacities, small particle sizes, and a relatively large capacity to take up adsorbed water, resulting in expansion of clay layers (and a larger reactive surface area for heterogeneous interactions) in some cases. An integrated laboratory research approach has been implemented at Hendrix College, a Primarily Undergraduate Institution, in which undergraduate students are involved in independent and interdisciplinary research projects that relate the chemical aging processes (heterogeneous chemistry) of clay minerals as a major component of mineral aerosol to their effects on climate (water adsorption), atmospheric chemistry (trace gas uptake), and biogeochemistry (iron dissolution and phytoplankton biomarker studies). Preliminary results and future directions will be reported.

  8. Impact of Asia Dust Aerosols on Regional Environment and Climate

    NASA Astrophysics Data System (ADS)

    Huang, J.

    2015-12-01

    East Asia is a major dust source in the world and has great impacts on regional climate in Asia, where the large arid and semi-arid regions are. In this study, the typical transport paths of East Asia dust, which affect regional and global climates, are demonstrated and numerous effects of dust aerosols on clouds and precipitation primarily over East Asian arid and semi-arid regions are discussed. Compared with the dust aerosols of Saharan, those of East Asian are more absorptive of solar radiation, and can influence the cloud properties not only by acting as cloud condensation nuclei and ice nuclei but also through changing the relative humidity and stability of the atmosphere (via semi-direct effect). Converting visible light to thermal energy, dust aerosols can burn clouds to produce a warming effect on climate, which is opposite to the first and second indirect effects of aerosols. Over Asia arid and semi-arid regions, the positive feedback in the aerosol-cloud-precipitation interaction may aggravate drought in its inner land. Impact of Asia dust on regional environment, especially on haze weather, are also presented in this talk.

  9. Stratospheric aerosol forcing for climate modeling: 1850-1978

    NASA Astrophysics Data System (ADS)

    Arfeuille, Florian; Luo, Beiping; Thomason, Larry; Vernier, Jean-Paul; Peter, Thomas

    2016-04-01

    We present here a stratospheric aerosol dataset produced using the available aerosol optical depth observations from the pre-satellite period. The scarce atmospheric observations are supplemented by additional information from an aerosol microphysical model, initialized by ice-core derived sulfur emissions. The model is used to derive extinctions at all altitudes, latitudes and times when sulfur injections are known for specific volcanic eruptions. The simulated extinction coefficients are then scaled to match the observed optical depths. In order to produce the complete optical properties at all wavelengths (and the aerosol surface area and volume densities) needed by climate models, we assume a lognormal size distribution of the aerosols. Correlations between the extinctions in the visible and the effective radius and distribution width parameters are taken from the better constrained SAGE II period. The aerosol number densities are then fitted to match the derived extinctions in the 1850-1978 period. From these aerosol size distributions, we then calculate extinction coefficients, single scattering albedos and asymmetry factors at all wavelengths using the Mie theory. The aerosol surface area densities and volume densities are also provided.

  10. Ship-Track Clouds, Aerosol, and Ship Dynamic Effects; A Climate Perspective from Ship-Based Measurements

    SciTech Connect

    Porch, W.M.

    1998-10-13

    Ship-track clouds are marine boundary layer clouds that form behind ocean ships and are observed from satellites in the visible and near infrared. Ship-track clouds provide a rare opportunity to connect aerosol cloud condensation nuclei (CCN) emissions and observable changes in marine stratiform clouds. A very small change in the reflectivity of these eastern Pacific and Atlantic clouds (about 4%) provides a climate feedback of similar magnitude to doubling CO{sub 2} (increasing cloud reflectivity corresponds to global cooling). The Department of Energy sponsored research from 1991 to 1995 to study ship-track clouds including two ocean-based experiments in the summers of 1991 and 1994. These experiments showed that ship-track cloud properties were often more complex those related to a reduction of droplet size with an increase in number associated with increasing CCN from the ship's plume. The clouds showed evidence of morphological changes more likely to be associated with cloud dynamic effects either initiated by the increased CCN or directly by the ship's heat output or turbulent air wake. The fact that marine stratiform clouds, that are susceptible to ship track formation, are starved for both CCN and convective turbulence complicates the separation of the two effects.

  11. On COBACC (COntinental Biosphere-Aerosol-Cloud-Climate) feedback

    NASA Astrophysics Data System (ADS)

    Kulmala, Markku

    2016-04-01

    Anthropogenic emissions of GHGs have increased substantially during the past century. Elevated concentrations of CO2 and methane are the most important forcing agents causing global warming. However, it is not straightforward to attribute or predict the climate change in detail, as the internal variability of climate is only partially understood, aerosol forcings are still highly uncertain, and there are many feedback mechanisms that are difficult to quantify. It has been recognized for decades that the biosphere plays an important role in climate. For example, Kulmala et al. (2004) suggested a negative climate feedback mechanism whereby higher temperatures and CO2-levels boost continental biomass production, leading to increased biogenic secondary organic aerosol (BSOA) and cloud condensation nuclei (CCN) concentrations, tending to cause cooling. This COBACC (COntinental Biosphere-Aerosol-Cloud-Climate) feedback is similar to the so-called CLAW-hypothesis by Charlson et al. (1987) which connects the ocean biochemistry and climate via a negative feedback loop involving CCN production due to sulphur emissions from plankton. The first quantification of the COBACC feedback loop (Kulmala et al. 2014) was based on continuous comprehensive observations at SMEAR II (Station for Measuring Forest Ecosystem-Atmosphere Relations) station in Hyytiälä, Finland, and showed that a 10 ppm increase in atmospheric CO2 concentration leads to a significant (several percent) increase in both carbon sink and aerosol source. These effects operate through changes in gross primary production, volatile organic compound (VOC) emissions and secondary aerosol formation associated with atmospheric oxidation of VOCs. Here we will describe the present knowledge from processes level understanding to whole COBACC feedback including some hints on biogenic and anthropogenic contributions to global aerosol number load. References: Charlson, R. J. et al. Nature 326, 655 1987 Kulmala, M. et al. Atmos

  12. Aerosol impacts on climate and environment over East Asia

    NASA Astrophysics Data System (ADS)

    Nakata, M.; Sano, I.; Mukai, S.

    2014-12-01

    It is well known that the aerosol distribution in East Asia is complex due to both the increasing emissions of the anthropogenic aerosols associated with economic growth and the behavior of natural dusts. Therefore, detailed observations of atmospheric particles in East Asian are important. It is concerned about the change of concentration of aerosols causes various effects on the climate by directly and indirectly modifying the optical properties and lifetimes of cloud. In addition to radiation budget change, aerosol has a significant potential to change cloud and precipitation. These circulation fields change influence on emission of natural aerosols such as dust aerosols and sea salt aerosols. Also, air pollution in megacities in East Asia has become a serious problem. Especially problematic are fine particles called PM2.5, whose diameter is 2.5 mm or less. Particulate matter (PM) pollution as indicated by high PM2.5 readings will cause a spike in the mortality rate of patients suffering from heart and lung diseases. Because fine particles are much smaller than inhalable coarse particles, the can penetrate deeper into the lungs and cause more severe effects on human health. Anthropogenic sources of PM2.5 include automobiles, factories, coal-burning power plants, and heaters in homes. It is well known that the size of dust particles decreases during long-range transport via westerly winds, and the resulting dust storms can contain high concentrations of fine particles. Accordingly, PM2.5 concentrations correspond well to both anthropogenic and dust aerosols. This work intends to investigate impacts of aerosol on regional climate change and environment over East Asia using observations and model simulations.

  13. Radiative Effects of Aerosols

    NASA Technical Reports Server (NTRS)

    Valero, Francisco P. J.

    1996-01-01

    During the Atlantic Stratocumulus Transition Experiment (ASTEX) in June 1992, two descents in cloud-free regions allowed comparison of the change in aerosol optical depth as determined by an onboard total-direct-diffuse radiometer (TDDR) to the change calculated from measured size-resolved aerosol microphysics and chemistry. Both profiles included a pollution haze from Europe but the second also included the effect of a Saharan dust layer above the haze. The separate contributions of supermicrometer (coarse) and submicrometer (fine) aerosol were determined and thermal analysis of the pollution haze indicated that the fine aerosol was composed primarily of a sulfate/water mixture with a refractory soot-like core. The soot core increased the calculated extinction by about 10% in the most polluted drier layer relative to a pure sulfate aerosol but had significantly less effect at higher humidities. A 3 km descent through a boundary layer air mass dominated by pollutant aerosol with relative humidities (RH) 10-77% yielded a close agreement between the measured and calculated aerosol optical depths (550 nm) of 0.160 (+/- 0.07) and 0. 157 (+/- 0.034) respectively. During descent the aerosol mass scattering coefficient per unit sulfate mass varied from about 5 to 16 m(exp 2)/g and primarily dependent upon ambient RH. However, the total scattering coefficient per total fine mass was far less variable at about 4+/- 0.7 m(exp 2)/g. A subsequent descent through a Saharan dust layer located above the pollution aerosol layer revealed that both layers contributed similarly to aerosol optical depth. The scattering per unit mass of the coarse aged dust was estimated at 1.1 +/- 0.2 m(exp 2)/g. The large difference (50%) in measured and calculated optical depth for the dust layer exceeded measurements.

  14. The effect of interactive gas-phase chemistry and aerosols on climate simulations over the last millennium

    NASA Astrophysics Data System (ADS)

    Tsigaridis, K.; LeGrande, A. N.; Healy, R. J.; Schmidt, G. A.

    2013-12-01

    Significant computational resources are required for long transient simulations using coupled atmosphere-ocean general circulation models. Individual simulations from the NINT version of GISS ModelE-R (part of the CMIP5 archive) of the last millennium, from year 850 to 2005, enabled with only 3 water isotopologue tracers, required ~9 months of computational time on the state-of-the-art parallel computing cluster of NCCS. The additional requirements of the full chemistry module would increase this by a factor of ~3. And yet, it is well known that chemistry and aerosols are very important on climate, both regional and global. Therefore, we have designed a set of experiments where the ocean and sea ice boundary conditions of the coupled model, paired with the land surface, greenhouse gases, insolation, and total solar irradiance (TSI) forcing from the PMIP3 protocol are applied to a series of full-chemistry GISS ModelE snap-shots each 50-years through the last millennium. We will present results from atmosphere-only model simulations with the GISS ModelE, which includes interactive gas-phase chemistry and aerosols at decadal-scale time slices, driven by millennial-length simulations performed with the same model when coupled with an ocean model. The boundary conditions for the transient simulations follow the last millennium coordinated PMIP3 experiment protocol. This experiment directly links in with other pre-industrial experiments being completed as part of IPCC AR5, using the same model and resolution as in GISS IPCC AR5. The impact of the presence of short-lived gases and aerosols on the simulated climate is studied. The role of previously omitted forcing mechanisms will be performed during the whole simulated period. The results presented are the initial runs from a larger set of experiments that will assess the climate impact of changes to dust, sea-salt, and ocean-derived sulfate, biomass burning ozone-precursors and aerosols, organic carbon, wetland methane

  15. Aerosol Climate Time Series in ESA Aerosol_cci

    NASA Astrophysics Data System (ADS)

    Popp, Thomas; de Leeuw, Gerrit; Pinnock, Simon

    2016-04-01

    Within the ESA Climate Change Initiative (CCI) Aerosol_cci (2010 - 2017) conducts intensive work to improve algorithms for the retrieval of aerosol information from European sensors. Meanwhile, full mission time series of 2 GCOS-required aerosol parameters are completely validated and released: Aerosol Optical Depth (AOD) from dual view ATSR-2 / AATSR radiometers (3 algorithms, 1995 - 2012), and stratospheric extinction profiles from star occultation GOMOS spectrometer (2002 - 2012). Additionally, a 35-year multi-sensor time series of the qualitative Absorbing Aerosol Index (AAI) together with sensitivity information and an AAI model simulator is available. Complementary aerosol properties requested by GCOS are in a "round robin" phase, where various algorithms are inter-compared: fine mode AOD, mineral dust AOD (from the thermal IASI spectrometer, but also from ATSR instruments and the POLDER sensor), absorption information and aerosol layer height. As a quasi-reference for validation in few selected regions with sparse ground-based observations the multi-pixel GRASP algorithm for the POLDER instrument is used. Validation of first dataset versions (vs. AERONET, MAN) and inter-comparison to other satellite datasets (MODIS, MISR, SeaWIFS) proved the high quality of the available datasets comparable to other satellite retrievals and revealed needs for algorithm improvement (for example for higher AOD values) which were taken into account for a reprocessing. The datasets contain pixel level uncertainty estimates which were also validated and improved in the reprocessing. For the three ATSR algorithms the use of an ensemble method was tested. The paper will summarize and discuss the status of dataset reprocessing and validation. The focus will be on the ATSR, GOMOS and IASI datasets. Pixel level uncertainties validation will be summarized and discussed including unknown components and their potential usefulness and limitations. Opportunities for time series extension

  16. Aerosol-Cloud-Precipitation Interactions in the Climate System

    NASA Astrophysics Data System (ADS)

    Andreae, M. O.

    2015-12-01

    Aerosols serve as cloud condensation nuclei (CCN) and thus have a powerful effect on cloud properties. Increased aerosol concentrations resulting from pollution lead to higher cloud droplet concentrations, but smaller droplet sizes. This in turn affects the physical processes inside clouds that lead to the initiation of precipitation. Depending on a number of factors, including aerosol composition, atmospheric stability, and cloud water content, increasing CCN concentrations may either decrease or increase rainfall. In convective clouds, early rain formation is suppressed, which makes more water and energy available to rise higher in the atmosphere and form ice particles. This may invigorate the dynamics of convection, encourage the formation of hail and lightning, and enhance the transport of materials to the upper troposphere. In turn, cloud processing also affects the concentrations, composition, and distribution of atmospheric aerosols. In order to understand and quantify the effects of air pollution on climate, and precipitation in particular, knowledge of natural abundance and characteristics of aerosols is as essential as the observation of perturbed conditions. I will present recent advances in the conceptual understanding of aerosol-precipitation interactions, as well as results of measurements on aerosol and cloud characteristics in pristine and polluted conditions.

  17. Distinguishing Aerosol Impacts on Climate Over the Past Century

    SciTech Connect

    Koch, Dorothy; Menon, Surabi; Del Genio, Anthony; Ruedy, Reto; Alienov, Igor; Schmidt, Gavin A.

    2008-08-22

    Aerosol direct (DE), indirect (IE), and black carbon-snow albedo (BAE) effects on climate between 1890 and 1995 are compared using equilibrium aerosol-climate simulations in the Goddard Institute for Space Studies General Circulation Model coupled to a mixed layer ocean. Pairs of control(1890)-perturbation(1995) with successive aerosol effects allow isolation of each effect. The experiments are conducted both with and without concurrent changes in greenhouse gases (GHG's). A new scheme allowing dependence of snow albedo on black carbon snow concentration is introduced. The fixed GHG experiments global surface air temperature (SAT) changed -0.2, -1.0 and +0.2 C from the DE, IE, and BAE. Ice and snow cover increased 1.0% from the IE and decreased 0.3% from the BAE. These changes were a factor of 4 larger in the Arctic. Global cloud cover increased by 0.5% from the IE. Net aerosol cooling effects are about half as large as the GHG warming, and their combined climate effects are smaller than the sum of their individual effects. Increasing GHG's did not affect the IE impact on cloud cover, however they decreased aerosol effects on SAT by 20% and on snow/ice cover by 50%; they also obscure the BAE on snow/ice cover. Arctic snow, ice, cloud, and shortwave forcing changes occur mostly during summer-fall, but SAT, sea level pressure, and long-wave forcing changes occur during winter. An explanation is that aerosols impact the cryosphere during the warm-season but the associated SAT effect is delayed until winter.

  18. CARES: Carbonaceous Aerosol and Radiative Effects Study Science Plan

    SciTech Connect

    Zaveri, RA; Shaw, WJ; Cziczo, DJ

    2010-05-27

    Carbonaceous aerosol components, which include black carbon (BC), urban primary organic aerosols (POA), biomass burning aerosols, and secondary organic aerosols (SOA) from both urban and biogenic precursors, have been previously shown to play a major role in the direct and indirect radiative forcing of climate. The primary objective of the CARES 2010 intensive field study is to investigate the evolution of carbonaceous aerosols of different types and their effects on optical and cloud formation properties.

  19. Assessment of climate sensitivity to the representation of aerosols in a coupled ocean-atmosphere model

    NASA Astrophysics Data System (ADS)

    Watson, Laura; Michou, Martine; Nabat, Pierre; Saint-Martin, David

    2016-04-01

    Atmospheric aerosols can significantly affect the Earth's radiative balance due to absorption, scattering, and indirect effects upon the climate system. Although our understanding of aerosol properties has improved over recent decades, aerosol radiative forcing remains as one of the largest uncertainties when projecting future climate change. A coupled ocean-atmosphere general circulation model was used to perform sensitivity tests in order to investigate how the representation of aerosols within the model can affect decadal climate variability. These tests included looking at the difference between using constant emissions versus using emissions that evolve over a period of thirty years; examining the impacts of including indirect effects from sea salt and organics; altering the aerosol optical properties; and using an interactive aerosol scheme versus using 2-D climatologies. The results of these sensitivity tests show how modifying certain aspects of the aerosol scheme can significantly modify radiative flux and global surface temperature.

  20. The Aerosol-Monsoon Climate System of Asia

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.; Kyu-Myong, Kim

    2012-01-01

    In Asian monsoon countries such as China and India, human health and safety problems caused by air-pollution are worsening due to the increased loading of atmospheric pollutants stemming from rising energy demand associated with the rapid pace of industrialization and modernization. Meanwhile, uneven distribution of monsoon rain associated with flash flood or prolonged drought, has caused major loss of human lives, and damages in crop and properties with devastating societal impacts on Asian countries. Historically, air-pollution and monsoon research are treated as separate problems. However a growing number of recent studies have suggested that the two problems may be intrinsically intertwined and need to be studied jointly. Because of complexity of the dynamics of the monsoon systems, aerosol impacts on monsoons and vice versa must be studied and understood in the context of aerosol forcing in relationship to changes in fundamental driving forces of the monsoon climate system (e.g. sea surface temperature, land-sea contrast etc.) on time scales from intraseasonal variability (weeks) to climate change ( multi-decades). Indeed, because of the large contributions of aerosols to the global and regional energy balance of the atmosphere and earth surface, and possible effects of the microphysics of clouds and precipitation, a better understanding of the response to climate change in Asian monsoon regions requires that aerosols be considered as an integral component of a fully coupled aerosol-monsoon system on all time scales. In this paper, using observations and results from climate modeling, we will discuss the coherent variability of the coupled aerosol-monsoon climate system in South Asia and East Asia, including aerosol distribution and types, with respect to rainfall, moisture, winds, land-sea thermal contrast, heat sources and sink distributions in the atmosphere in seasonal, interannual to climate change time scales. We will show examples of how elevated

  1. Aerosols, climate, and the hydrological cycle.

    PubMed

    Ramanathan, V; Crutzen, P J; Kiehl, J T; Rosenfeld, D

    2001-12-01

    Human activities are releasing tiny particles (aerosols) into the atmosphere. These human-made aerosols enhance scattering and absorption of solar radiation. They also produce brighter clouds that are less efficient at releasing precipitation. These in turn lead to large reductions in the amount of solar irradiance reaching Earth's surface, a corresponding increase in solar heating of the atmosphere, changes in the atmospheric temperature structure, suppression of rainfall, and less efficient removal of pollutants. These aerosol effects can lead to a weaker hydrological cycle, which connects directly to availability and quality of fresh water, a major environmental issue of the 21st century.

  2. Stronger constraints on the anthropogenic indirect aerosol effect.

    PubMed

    Lohmann, Ulrike; Lesins, Glen

    2002-11-01

    The anthropogenic indirect aerosol effects of modifying cloud albedo and cloud lifetime cannot be deduced from observations alone but require a modeling component. Here we validate a climate model, with and without indirect aerosol effects, by using satellite observations. The model agrees better with observations when both indirect aerosol effects are included. However, the simulated clouds are more susceptible to aerosols than the observed clouds from the POLDER satellite, thus overestimating the indirect aerosol effect. By taking the difference in susceptibilities into account, the global mean total anthropogenic aerosol effect is reduced from -1.4 to -0.85 watts per square meter.

  3. Air pollution and climate response to aerosol direct radiative effects: A modeling study of decadal trends across the northern hemisphere

    EPA Science Inventory

    Decadal hemispheric Weather Research and Forecast-Community Multiscale Air Quality simulations from 1990 to 2010 were conducted to examine the meteorology and air quality responses to the aerosol direct radiative effects. The model's performance for the simulation of hourly surfa...

  4. Aerosol climate time series from ESA Aerosol_cci (Invited)

    NASA Astrophysics Data System (ADS)

    Holzer-Popp, T.

    2013-12-01

    Within the ESA Climate Change Initiative (CCI) the Aerosol_cci project (mid 2010 - mid 2013, phase 2 proposed 2014-2016) has conducted intensive work to improve algorithms for the retrieval of aerosol information from European sensors AATSR (3 algorithms), PARASOL, MERIS (3 algorithms), synergetic AATSR/SCIAMACHY, OMI and GOMOS. Whereas OMI and GOMOS were used to derive absorbing aerosol index and stratospheric extinction profiles, respectively, Aerosol Optical Depth (AOD) and Angstrom coefficient were retrieved from the other sensors. Global datasets for 2008 were produced and validated versus independent ground-based data and other satellite data sets (MODIS, MISR). An additional 17-year dataset is currently generated using ATSR-2/AATSR data. During the three years of the project, intensive collaborative efforts were made to improve the retrieval algorithms focusing on the most critical modules. The team agreed on the use of a common definition for the aerosol optical properties. Cloud masking was evaluated, but a rigorous analysis with a pre-scribed cloud mask did not lead to improvement for all algorithms. Better results were obtained using a post-processing step in which sudden transitions, indicative of possible occurrence of cloud contamination, were removed. Surface parameterization, which is most critical for the nadir only algorithms (MERIS and synergetic AATSR / SCIAMACHY) was studied to a limited extent. The retrieval results for AOD, Ångström exponent (AE) and uncertainties were evaluated by comparison with data from AERONET (and a limited amount of MAN) sun photometer and with satellite data available from MODIS and MISR. Both level2 and level3 (gridded daily) datasets were validated. Several validation metrics were used (standard statistical quantities such as bias, rmse, Pearson correlation, linear regression, as well as scoring approaches to quantitatively evaluate the spatial and temporal correlations against AERONET), and in some cases

  5. Arctic climate response to geoengineering with stratospheric sulfate aerosols

    NASA Astrophysics Data System (ADS)

    McCusker, K. E.; Battisti, D. S.; Bitz, C. M.

    2010-12-01

    Recent warming and record summer sea-ice area minimums have spurred expressions of concern for arctic ecosystems, permafrost, and polar bear populations, among other things. Geoengineering by stratospheric sulfate aerosol injections to deliberately cancel the anthropogenic temperature rise has been put forth as a possible solution to restoring Arctic (and global) climate to modern conditions. However, climate is particularly sensitive in the northern high latitudes, responding easily to radiative forcing changes. To that end, we explore the extent to which tropical injections of stratospheric sulfate aerosol can accomplish regional cancellation in the Arctic. We use the Community Climate System Model version 3 global climate model to execute simulations with combinations of doubled CO2 and imposed stratospheric sulfate burdens to investigate the effects on high latitude climate. We further explore the sensitivity of the polar climate to ocean dynamics by running a suite of simulations with and without ocean dynamics, transiently and to equilibrium respectively. We find that, although annual, global mean temperature cancellation is accomplished, there is over-cooling on land in Arctic summer, but residual warming in Arctic winter, which is largely due to atmospheric circulation changes. Furthermore, the spatial extent of these features and their concurrent impacts on sea-ice properties are modified by the inclusion of ocean dynamical feedbacks.

  6. Effect of Terrestrial and Marine Organic Aerosol on Regional and Global Climate: Model Development, Application, and Verification with Satellite Data

    SciTech Connect

    Meskhidze, Nicholas; Zhang, Yang; Kamykowski, Daniel

    2012-03-28

    In this DOE project the improvements to parameterization of marine primary organic matter (POM) emissions, hygroscopic properties of marine POM, marine isoprene derived secondary organic aerosol (SOA) emissions, surfactant effects, new cloud droplet activation parameterization have been implemented into Community Atmosphere Model (CAM 5.0), with a seven mode aerosol module from the Pacific Northwest National Laboratory (PNNL)'s Modal Aerosol Model (MAM7). The effects of marine aerosols derived from sea spray and ocean emitted biogenic volatile organic compounds (BVOCs) on microphysical properties of clouds were explored by conducting 10 year CAM5.0-MAM7 model simulations at a grid resolution 1.9° by 2.5° with 30 vertical layers. Model-predicted relationship between ocean physical and biological systems and the abundance of CCN in remote marine atmosphere was compared to data from the A-Train satellites (MODIS, CALIPSO, AMSR-E). Model simulations show that on average, primary and secondary organic aerosol emissions from the ocean can yield up to 20% increase in Cloud Condensation Nuclei (CCN) at 0.2% Supersaturation, and up to 5% increases in droplet number concentration of global maritime shallow clouds. Marine organics were treated as internally or externally mixed with sea salt. Changes associated with cloud properties reduced (absolute value) the model-predicted short wave cloud forcing from -1.35 Wm-2 to -0.25 Wm-2. By using different emission scenarios, and droplet activation parameterizations, this study suggests that addition of marine primary aerosols and biologically generated reactive gases makes an important difference in radiative forcing assessments. All baseline and sensitivity simulations for 2001 and 2050 using global-through-urban WRF/Chem (GU-WRF) were completed. The main objective of these simulations was to evaluate the capability of GU-WRF for an accurate representation of the global atmosphere by exploring the most accurate configuration of

  7. Aerosol Properties and Processes: A Path from Field and Laboratory Measurements to Global Climate Models

    SciTech Connect

    Ghan, Steven J.; Schwartz, Stephen E.

    2007-07-01

    Aerosols exert a substantial influence on climate and climate change through a variety of complex mechanisms. Consequently there is a need to represent aerosol effects in global climate models, and models have begun to include representations of these effects. However, the treatment of aerosols in current global climate models is presently highly simplified, omitting many important processes and feedbacks. Consequently there is need for substantial improvement. Here we describe the U. S. Department of Energy strategy for improving the treatment of aerosol properties and processes in global climate models. The strategy begins with a foundation of field and laboratory measurements that provide the basis for modules of selected aerosol properties and processes. These modules are then integrated in regional aerosol models, which are evaluated by comparing with field measurements. Issues of scale are then addressed so that the modules can be applied to global aerosol models, which are evaluated by comparing with global satellite measurements. Finally, the validated set of modules are applied to global climate models for multi-century simulations. This strategy can be applied to successive generations of global climate models.

  8. Evaluating the potential impact of marine organic aerosols on climate assessments

    NASA Astrophysics Data System (ADS)

    Meskhidze, N.; Gantt, B.; Xu, J.

    2011-12-01

    Natural aerosols influence clouds and the hydrological cycle by their ability to act as cloud condensation nuclei (CCN). Because the anthropogenic contribution to climate forcing represents the difference between the total forcing and that from natural aerosols, understanding background aerosols is necessary to evaluate the influences of anthropogenic aerosols on cloud reflectivity and persistence (so-called indirect radiative forcing) and on precipitation. The effects of marine organic aerosols on microphysical properties of shallow clouds are explored using the NCAR Community Atmosphere Model (CAM5.0), coupled with the PNNL Modal Aerosol Model. Organic enrichment of sea spray is estimated using newly developed wind speed dependent size-resolved source function, while production of secondary organic aerosol of marine origin is inferred from the ocean emissions of biogenic trace gases. Model-predicted abundance of CCN in remote marine atmosphere is compared to satellite and in-situ data. Simulations show that over biologically productive ocean waters organic aerosols of marine origin can contribute up to 20% increase in CCN (at a supersaturation of 0.2%) number concentrations. Corresponding changes associated with cloud properties (liquid water path and droplet number) can reduce global annual mean indirect radiative forcing of anthropogenic aerosol by 0.1 Wm-2 or 8%. This study suggests that neglecting the effects of marine organic aerosol in climate models could result in overprediction of aerosol indirect effect.

  9. Global aerosol effects on convective clouds

    NASA Astrophysics Data System (ADS)

    Wagner, Till; Stier, Philip

    2013-04-01

    Atmospheric aerosols affect cloud properties, and thereby the radiation balance of the planet and the water cycle. The influence of aerosols on clouds is dominated by increase of cloud droplet and ice crystal numbers (CDNC/ICNC) due to enhanced aerosols acting as cloud condensation and ice nuclei. In deep convective clouds this increase in CDNC/ICNC is hypothesised to increase precipitation because of cloud invigoration through enhanced freezing and associated increased latent heat release caused by delayed warm rain formation. Satellite studies robustly show an increase of cloud top height (CTH) and precipitation with increasing aerosol optical depth (AOD, as proxy for aerosol amount). To represent aerosol effects and study their influence on convective clouds in the global climate aerosol model ECHAM-HAM, we substitute the standard convection parameterisation, which uses one mean convective cloud for each grid column, with the convective cloud field model (CCFM), which simulates a spectrum of convective clouds, each with distinct values of radius, mixing ratios, vertical velocity, height and en/detrainment. Aerosol activation and droplet nucleation in convective updrafts at cloud base is the primary driver for microphysical aerosol effects. To produce realistic estimates for vertical velocity at cloud base we use an entraining dry parcel sub cloud model which is triggered by perturbations of sensible and latent heat at the surface. Aerosol activation at cloud base is modelled with a mechanistic, Köhler theory based, scheme, which couples the aerosols to the convective microphysics. Comparison of relationships between CTH and AOD, and precipitation and AOD produced by this novel model and satellite based estimates show general agreement. Through model experiments and analysis of the model cloud processes we are able to investigate the main drivers for the relationship between CTH / precipitation and AOD.

  10. Global observations of aerosol-cloud-precipitation-climate interactions

    NASA Astrophysics Data System (ADS)

    Rosenfeld, Daniel; Andreae, Meinrat O.; Asmi, Ari; Chin, Mian; Leeuw, Gerrit; Donovan, David P.; Kahn, Ralph; Kinne, Stefan; Kivekäs, Niku; Kulmala, Markku; Lau, William; Schmidt, K. Sebastian; Suni, Tanja; Wagner, Thomas; Wild, Martin; Quaas, Johannes

    2014-12-01

    Cloud drop condensation nuclei (CCN) and ice nuclei (IN) particles determine to a large extent cloud microstructure and, consequently, cloud albedo and the dynamic response of clouds to aerosol-induced changes to precipitation. This can modify the reflected solar radiation and the thermal radiation emitted to space. Measurements of tropospheric CCN and IN over large areas have not been possible and can be only roughly approximated from satellite-sensor-based estimates of optical properties of aerosols. Our lack of ability to measure both CCN and cloud updrafts precludes disentangling the effects of meteorology from those of aerosols and represents the largest component in our uncertainty in anthropogenic climate forcing. Ways to improve the retrieval accuracy include multiangle and multipolarimetric passive measurements of the optical signal and multispectral lidar polarimetric measurements. Indirect methods include proxies of trace gases, as retrieved by hyperspectral sensors. Perhaps the most promising emerging direction is retrieving the CCN properties by simultaneously retrieving convective cloud drop number concentrations and updraft speeds, which amounts to using clouds as natural CCN chambers. These satellite observations have to be constrained by in situ observations of aerosol-cloud-precipitation-climate (ACPC) interactions, which in turn constrain a hierarchy of model simulations of ACPC. Since the essence of a general circulation model is an accurate quantification of the energy and mass fluxes in all forms between the surface, atmosphere and outer space, a route to progress is proposed here in the form of a series of box flux closure experiments in the various climate regimes. A roadmap is provided for quantifying the ACPC interactions and thereby reducing the uncertainty in anthropogenic climate forcing.

  11. Stratospheric Aerosol--Observations, Processes, and Impact on Climate

    NASA Technical Reports Server (NTRS)

    Kresmer, Stefanie; Thomason, Larry W.; von Hobe, Marc; Hermann, Markus; Deshler, Terry; Timmreck, Claudia; Toohey, Matthew; Stenke, Andrea; Schwarz, Joshua P.; Weigel, Ralf; Fueglistaler, Stephan; Prata, Fred J.; Vernier, Jean-Paul; Schlager, Hans; Barnes, John E.; Antuna-Marrero, Juan-Carlos; Fairlie, Duncan; Palm, Mathias; Mahieu, Emmanuel; Notholt, Justus; Rex, Markus; Bingen, Christine; Vanhellemont, Filip; Bourassa, Adam; Plane, John M. C.; Klocke, Daniel; Carn, Simon A.; Clarisse, Lieven; Trickl, Thomas; Neeley, Ryan; James, Alexander D.; Rieger, Landon; Wilson, James C.; Meland, Brian

    2016-01-01

    Interest in stratospheric aerosol and its role in climate have increased over the last decade due to the observed increase in stratospheric aerosol since 2000 and the potential for changes in the sulfur cycle induced by climate change. This review provides an overview about the advances in stratospheric aerosol research since the last comprehensive assessment of stratospheric aerosol was published in 2006. A crucial development since 2006 is the substantial improvement in the agreement between in situ and space-based inferences of stratospheric aerosol properties during volcanically quiescent periods. Furthermore, new measurement systems and techniques, both in situ and space based, have been developed for measuring physical aerosol properties with greater accuracy and for characterizing aerosol composition. However, these changes induce challenges to constructing a long-term stratospheric aerosol climatology. Currently, changes in stratospheric aerosol levels less than 20% cannot be confidently quantified. The volcanic signals tend to mask any nonvolcanically driven change, making them difficult to understand. While the role of carbonyl sulfide as a substantial and relatively constant source of stratospheric sulfur has been confirmed by new observations and model simulations, large uncertainties remain with respect to the contribution from anthropogenic sulfur dioxide emissions. New evidence has been provided that stratospheric aerosol can also contain small amounts of nonsulfatematter such as black carbon and organics. Chemistry-climate models have substantially increased in quantity and sophistication. In many models the implementation of stratospheric aerosol processes is coupled to radiation and/or stratospheric chemistry modules to account for relevant feedback processes.

  12. Evidence of Aerosol's Influence on Climate from Beijing Olympics

    NASA Astrophysics Data System (ADS)

    Chen, S.; Fu, Q.; Huang, J.; Ge, J.; Su, J.

    2009-12-01

    Air pollution is a difficult problem during the process of industrialization in most developing countries. In China, the main air pollutants are inhaled aerosol particles. Because of the extremely high loading and rapid development, Beijing became a heavily polluted city, with a population of more than 16 million. The 2008 Olympic Summer Games provided a unique opportunity for the study of climate effects of aerosols due to many measurements taken to fight pollution caused by industrialization and economic growth.Surface temperature is the most intuitive meteorological factor and easy to get. Therefore, aerosol’s radiative effects on regional climate can be known by studying the relationship between aerosols and surface temperature in Beijing city in August 2008. However, many factors can affect the surface temperature and cloud is considered as a very important meteorological element in radiation balance. In order to remove the impact of clouds on surface temperature, here the ground temperature in clear sky days (when cloud cover is less than 2) are selected. Aerosol data from the MODerate resolution Imaging Spectroradiometer (MODIS) onboard the Earth Observing System (EOS) Aqua shows that aerosol concentration decreased significantly in the area of Olympic venues in August 2008. Meanwhile, the ground-based observation data shows the surface temperature during the day (14LT) and night (02LT) in August 2008 is higher and lower than the mean temperature in August from 2002 to 2008, respectively. It is discovered that the distribution of satellite-retrieved aerosol optical Depth (AOD) in the whole area of Beijing in August of 2003 and 2004 is similar to that in 2008. We chosen four meteorological stations to analyze surface temperature and found that the diurnal changes of surface temperature are consistent with that in August of 2003, 2004 and 2008. Meanwhile, the decrease of AOD in the area of Olympic venues in August 2008 leads to the increase of precipitation

  13. Climate-aerosol interactions over the Mediterranean region: a regional coupled modelling approach

    NASA Astrophysics Data System (ADS)

    Nabat, Pierre; Somot, Samuel; Mallet, Marc

    2015-04-01

    in the atmospheric model ALADIN-Climate in order to better understand aerosol processes at the daily scale. This scheme shows its ability to represent correctly the aerosol patterns over the Mediterranean, especially with regards to dust outbreaks that were measured during the ChArMEx/TRAQA field campaign. Moreover, the use of a prognostic aerosol scheme instead of a monthly climatology enables to better reproduce the daily variations of surface radiation and temperature and related extremes. This also leads to changes in the mean climate, insofar as aerosol variations and their effects depend on weather regimes and cloud cover.

  14. Aerosol Forcing of Climate Change and Anomalous Atmospheric Absorption

    NASA Technical Reports Server (NTRS)

    Hansen, James E.

    2000-01-01

    The forcings that drive long-term climate change are not known with an accuracy sufficient to define future climate change, Anthropogenic greenhouse gases (GHGs), which are well-measured, cause a strong positive (warming) forcing. But other, poorly measured, anthropogenic forcings, especially changes of atmospheric aerosols, clouds, and land-use patterns, cause a negative forcing that tends to offset greenhouse warming. We will focus on the role of aerosols as a climate forcing mechanism and the contribution that aerosols might make to the so-called "anomalous" atmospheric absorption that has been inferred from some atmospheric measurements.

  15. Aerosol Forcing of Climate Change and "Anomalous" Atmospheric Absorption

    NASA Technical Reports Server (NTRS)

    Hansen, James E.

    1999-01-01

    The forcings that drive long-term climate change are not known with an accuracy sufficient to define future climate change. Anthropogenic greenhouse gases (GHGs), which are well-measured, cause a strong positive (warming) forcing. But other, poorly measured, anthropogenic forcings, especially changes of atmospheric aerosols, clouds, and land-use patterns, cause a negative forcing that tends to offset greenhouse warming. We will focus on the role of aerosols as a climate forcing mechanism and the contribution that aerosols might make to the so- called "anomalous" atmospheric absorption that has been inferred from some atmospheric measurements.

  16. Aerosols and clouds in chemical transport models and climate models.

    SciTech Connect

    Lohmann,U.; Schwartz, S. E.

    2008-03-02

    Clouds exert major influences on both shortwave and longwave radiation as well as on the hydrological cycle. Accurate representation of clouds in climate models is a major unsolved problem because of high sensitivity of radiation and hydrology to cloud properties and processes, incomplete understanding of these processes, and the wide range of length scales over which these processes occur. Small changes in the amount, altitude, physical thickness, and/or microphysical properties of clouds due to human influences can exert changes in Earth's radiation budget that are comparable to the radiative forcing by anthropogenic greenhouse gases, thus either partly offsetting or enhancing the warming due to these gases. Because clouds form on aerosol particles, changes in the amount and/or composition of aerosols affect clouds in a variety of ways. The forcing of the radiation balance due to aerosol-cloud interactions (indirect aerosol effect) has large uncertainties because a variety of important processes are not well understood precluding their accurate representation in models.

  17. Boreal forests, aerosols and the impacts on clouds and climate.

    PubMed

    Spracklen, Dominick V; Bonn, Boris; Carslaw, Kenneth S

    2008-12-28

    Previous studies have concluded that boreal forests warm the climate because the cooling from storage of carbon in vegetation and soils is cancelled out by the warming due to the absorption of the Sun's heat by the dark forest canopy. However, these studies ignored the impacts of forests on atmospheric aerosol. We use a global atmospheric model to show that, through emission of organic vapours and the resulting condensational growth of newly formed particles, boreal forests double regional cloud condensation nuclei concentrations (from approx. 100 to approx. 200 cm(-3)). Using a simple radiative model, we estimate that the resulting change in cloud albedo causes a radiative forcing of between -1.8 and -6.7 W m(-2) of forest. This forcing may be sufficiently large to result in boreal forests having an overall cooling impact on climate. We propose that the combination of climate forcings related to boreal forests may result in an important global homeostasis. In cold climatic conditions, the snow-vegetation albedo effect dominates and boreal forests warm the climate, whereas in warmer climates they may emit sufficiently large amounts of organic vapour modifying cloud albedo and acting to cool climate.

  18. Time Series of Aerosol Column Optical Depth at the Barrow, Alaska, ARM Climate Research Facility for 2008 Fourth Quarter 2009 ARM and Climate Change Prediction Program Metric Report

    SciTech Connect

    C Flynn; AS Koontz; JH Mather

    2009-09-01

    The uncertainties in current estimates of anthropogenic radiative forcing are dominated by the effects of aerosols, both in relation to the direct absorption and scattering of radiation by aerosols and also with respect to aerosol-related changes in cloud formation, longevity, and microphysics (See Figure 1; Intergovernmental Panel on Climate Change, Assessment Report 4, 2008). Moreover, the Arctic region in particular is especially sensitive to changes in climate with the magnitude of temperature changes (both observed and predicted) being several times larger than global averages (Kaufman et al. 2009). Recent studies confirm that aerosol-cloud interactions in the arctic generate climatologically significant radiative effects equivalent in magnitude to that of green house gases (Lubin and Vogelmann 2006, 2007). The aerosol optical depth is the most immediate representation of the aerosol direct effect and is also important for consideration of aerosol-cloud interactions, and thus this quantity is essential for studies of aerosol radiative forcing.

  19. Aerosol direct radiative effect over China estimated with visibility measurements

    NASA Astrophysics Data System (ADS)

    Ye, K.; Lin, J.

    2012-12-01

    As a short-lived climate forcer, aerosols exhibit strong radiative effects that vary significantly across the space and time. Current understanding of the long-term variability of aerosol climate forcings is however very poor due to lack of relevant atmospheric measurements. Historic records for visibility measurements from thousands of ground meteorological stations offer a plausible tool to study the decadal and multi-decadal variability of aerosol radiative effects. As a first step, this study presents a method to estimate aerosol direct radiative effect over China based on visibility data for 2006. Visibility data from about 400 ground stations are converted to near-surface aerosol extinction coefficients, which are converted then to aerosol optical depth (AOD) based on spatially and temporally varying vertical distributions of aerosol optical properties simulated by the widely used chemical transport model GEOS-Chem. The resulting AOD data are consistent with direct measurements from the China Aerosol Remote Sensing Network (CARSNET) and the Aerosol Robotic Network (AERONET) in regions where visibility and AOD measurement sites are close in distance. Next, the visibility-derived AOD data are combined with other aerosol optical properties adopted from GEOS-Chem, cloud data from ground stations and surface albedo data from moderate-resolution imaging spectroradiometer (MODIS) to derive the direct radiative effect, by employing the Santa Barbara DISORT Atmospheric Radiative Transfer model (SBDART). Spatial and monthly variations of aerosol radiative effects are examined.

  20. Exploiting Representation of the Aerosol-Radiation interactions in Climate Systems: Observation-based Analyses and Global Climate Modeling

    NASA Astrophysics Data System (ADS)

    Chen, Y. C.; Li, J.; Lee, W. L.; Diner, D. J.; Garay, M. J.; Kalashnikova, O. V.

    2015-12-01

    Aerosols affect the Earth's climate by perturbing the radiation budget through scattering and absorption of solar radiation and emitting thermal infrared radiation (defined and referred to as aerosol direct effect). At first order, it is essential for a model to realistically represent the distributions of clouds, convection, aerosol profiles and their associated radiative properties (cloud fraction and effective radius), which are critical for simulating Earth's surface energy and water budgets. The representation of aerosols and their radiative properties remains problematic both in retrieval and modeling. Up to now, the representation of aerosol optical depth (AOD) in GCMs is still far from agreement with the observation. We evaluate the aerosol simulations from the 20th century CMIP5 simulations, and investigate the biases in aerosol loadings against observations. AOD and retrieved aerosol types (e.g., sea salt, organic matter, sulfate) from MISR, MODIS, and CALIPSO satellite observations are utilized to compare with model simulated aerosols. The impacts of the biases of modeled AOD and cloud fraction on aerosol direct effects in GCMs will be presented.

  1. The Spatial and Temporal Heterogeneity of Precipitation and Aerosol-Cloud Radiative Forcing Uncertainty in Climatically Important Regions

    NASA Astrophysics Data System (ADS)

    Regayre, L.; Pringle, K.; Lee, L.; Booth, B.; Browse, J.; Mann, G.; Woodhouse, M. T.; Reddington, C.; Carslaw, K. S.; Rap, A.

    2015-12-01

    Aerosol-cloud radiative forcing and precipitation sensitivities are quantified within climatically important regions, where surface temperatures and moisture availability are thought to influence large-scale climatic effects. The sensitivity of precipitation and the balance of incoming and outgoing radiation to uncertain historical aerosol emission fluxes and aerosol-cloud parametrisations are quantified and their climatic importance considered. The predictability of monsoon onset and intensity, position of the inter-tropical convergence zone, tropical storm frequency and intensity, heat transport to the Arctic and changes in the mode of the El Niño Southern Oscillation are all limited by the parametric uncertainties examined here. Precipitation and aerosol-cloud radiative forcing sensitivities are found to be both spatially and temporally heterogeneous. Statistical analysis highlights aspects of aerosol-climate research and model development that should be prioritised in order to reduce the impact of uncertainty in regional precipitation and aerosol-cloud forcing on near-term climate projections.

  2. Projected effect of 2000-2050 changes in climate and emissions on aerosol levels in China and associated transboundary transport

    EPA Science Inventory

    We investigate projected 2000–2050 changes in concentrations of aerosols in China and the associated transboundary aerosol transport by using the chemical transport model GEOS-Chem driven by the Goddard Institute for Space Studies (GISS) general circulation model (GCM) 3 at 4° × ...

  3. The relative roles of sulfate aerosols and greenhouse gases in climate forcing

    NASA Technical Reports Server (NTRS)

    Kiehl, J. T.; Briegleb, B. P.

    1993-01-01

    Calculations of the effects of both natural and anthropogenic tropospheric sulfate aerosols indicate that the aerosol climate forcing is sufficiently large in a number of regions of the Northern Hemisphere to reduce significantly the positive forcing from increased greenhouse gases. Summer sulfate aerosol forcing in the Northern Hemisphere completely offsets the greenhouse forcing over the eastern United States and central Europe. Anthropogenic sulfate aerosols contribute a globally averaged annual forcing of -0.3 watt per square meter as compared with +2.1 watts per square meter for greenhouse gases. Sources of the difference in magnitude with the previous estimate of Charlson et al. (1992) are discussed.

  4. Radiative forcing and climate response to projected 21st century aerosol decreases

    NASA Astrophysics Data System (ADS)

    Westervelt, D. M.; Horowitz, L. W.; Naik, V.; Golaz, J.-C.; Mauzerall, D. L.

    2015-11-01

    It is widely expected that global emissions of atmospheric aerosols and their precursors will decrease strongly throughout the remainder of the 21st century, due to emission reduction policies enacted to protect human health. For instance, global emissions of aerosols and their precursors are projected to decrease by as much as 80 % by the year 2100, according to the four Representative Concentration Pathway (RCP) scenarios. The removal of aerosols will cause unintended climate consequences, including an unmasking of global warming from long-lived greenhouse gases. We use the Geophysical Fluid Dynamics Laboratory Coupled Climate Model version 3 (GFDL CM3) to simulate future climate over the 21st century with and without the aerosol emission changes projected by each of the RCPs in order to isolate the radiative forcing and climate response resulting from the aerosol reductions. We find that the projected global radiative forcing and climate response due to aerosol decreases do not vary significantly across the four RCPs by 2100, although there is some mid-century variation, especially in cloud droplet effective radius, that closely follows the RCP emissions and energy consumption projections. Up to 1 W m-2 of radiative forcing may be unmasked globally from 2005 to 2100 due to reductions in aerosol and precursor emissions, leading to average global temperature increases up to 1 K and global precipitation rate increases up to 0.09 mm day-1. However, when using a version of CM3 with reduced present-day aerosol radiative forcing (-1.0 W m-2), the global temperature increase for RCP8.5 is about 0.5 K, with similar magnitude decreases in other climate response parameters as well. Regionally and locally, climate impacts can be much larger than the global mean, with a 2.1 K warming projected over China, Japan, and Korea due to the reduced aerosol emissions in RCP8.5, as well as nearly a 0.2 mm day-1 precipitation increase, a 7 g m-2 LWP decrease, and a 2 μm increase in

  5. Desert dust and anthropogenic aerosol interactions in the Community Climate System Model coupled-carbon-climate model

    SciTech Connect

    Mahowald, Natalie; Rothenberg, D.; Lindsay, Keith; Doney, Scott C.; Moore, Jefferson Keith; Randerson, James T.; Thornton, Peter E; Jones, C. D.

    2011-02-01

    Coupled-carbon-climate simulations are an essential tool for predicting the impact of human activity onto the climate and biogeochemistry. Here we incorporate prognostic desert dust and anthropogenic aerosols into the CCSM3.1 coupled carbon-climate model and explore the resulting interactions with climate and biogeochemical dynamics through a series of transient anthropogenic simulations (20th and 21st centuries) and sensitivity studies. The inclusion of prognostic aerosols into this model has a small net global cooling effect on climate but does not significantly impact the globally averaged carbon cycle; we argue that this is likely to be because the CCSM3.1 model has a small climate feedback onto the carbon cycle. We propose a mechanism for including desert dust and anthropogenic aerosols into a simple carbon-climate feedback analysis to explain the results of our and previous studies. Inclusion of aerosols has statistically significant impacts on regional climate and biogeochemistry, in particular through the effects on the ocean nitrogen cycle and primary productivity of altered iron inputs from desert dust deposition.

  6. Sensitivity of remote aerosol distributions to representation of cloud-aerosol interactions in a global climate model

    NASA Astrophysics Data System (ADS)

    Wang, H.; Easter, R. C.; Rasch, P. J.; Wang, M.; Liu, X.; Ghan, S. J.; Qian, Y.; Yoon, J.-H.; Ma, P.-L.; Velu, V.

    2013-01-01

    Many global aerosol and climate models, including the widely used Community Atmosphere Model version 5 (CAM5), have large biases in predicting aerosols in remote regions such as upper troposphere and high latitudes. In this study, we conduct CAM5 sensitivity simulations to understand the role of key processes associated with aerosol transformation and wet removal affecting the vertical and horizontal long-range transport of aerosols to the remote regions. Improvements are made to processes that are currently not well represented in CAM5, which are guided by surface and aircraft measurements together with results from a multi-scale aerosol-climate model (PNNL-MMF) that explicitly represents convection and aerosol-cloud interactions at cloud-resolving scales. We pay particular attention to black carbon (BC) due to its importance in the Earth system and the availability of measurements. We introduce into CAM5 a new unified scheme for convective transport and aerosol wet removal with explicit aerosol activation above convective cloud base. This new implementation reduces the excessive BC aloft to better simulate observed BC profiles that show decreasing mixing ratios in the mid- to upper-troposphere. After implementing this new unified convective scheme, we examine wet removal of submicron aerosols that occurs primarily through cloud processes. The wet removal depends strongly on the sub-grid scale liquid cloud fraction and the rate of conversion of liquid water to precipitation. These processes lead to very strong wet removal of BC and other aerosols over mid- to high latitudes during winter months. With our improvements, the Arctic BC burden has a10-fold (5-fold) increase in the winter (summer) months, resulting in a much better simulation of the BC seasonal cycle as well. Arctic sulphate and other aerosol species also increase but to a lesser extent. An explicit treatment of BC aging with slower aging assumptions produces an additional 30-fold (5-fold) increase in

  7. Global climate forcing of aerosols embodied in international trade

    NASA Astrophysics Data System (ADS)

    Lin, Jintai; Tong, Dan; Davis, Steven; Ni, Ruijing; Tan, Xiaoxiao; Pan, Da; Zhao, Hongyan; Lu, Zifeng; Streets, David; Feng, Tong; Zhang, Qiang; Yan, Yingying; Hu, Yongyun; Li, Jing; Liu, Zhu; Jiang, Xujia; Geng, Guannan; He, Kebin; Huang, Yi; Guan, Dabo

    2016-10-01

    International trade separates regions consuming goods and services from regions where goods and related aerosol pollution are produced. Yet the role of trade in aerosol climate forcing attributed to different regions has never been quantified. Here, we contrast the direct radiative forcing of aerosols related to regions' consumption of goods and services against the forcing due to emissions produced in each region. Aerosols assessed include black carbon, primary organic aerosol, and secondary inorganic aerosols, including sulfate, nitrate and ammonium. We find that global aerosol radiative forcing due to emissions produced in East Asia is much stronger than the forcing related to goods and services ultimately consumed in that region because of its large net export of emissions-intensive goods. The opposite is true for net importers such as Western Europe and North America: global radiative forcing related to consumption is much greater than the forcing due to emissions produced in these regions. Overall, trade is associated with a shift of radiative forcing from net importing to net exporting regions. Compared to greenhouse gases such as carbon dioxide, the short atmospheric lifetimes of aerosols cause large localized differences between consumption- and production-related radiative forcing. International efforts to reduce emissions in the exporting countries will help alleviate trade-related climate and health impacts of aerosols while lowering global emissions.

  8. Potential Impact of South Asian Anthropogenic Aerosols on Northern Hemisphere Climate

    NASA Astrophysics Data System (ADS)

    Bollasina, M. A.; Ming, Y.; Ramaswamy, V.

    2014-12-01

    South Asia has one of the world's highest aerosol loading due to the dramatic increase of anthropogenic emissions from the 1950s associated with rapid urbanization and population growth. The possible large-scale impact of the late 20th century increase of South Asian aerosol emissions on climate away from the source regions was studied by means of historical ensemble experiments with a state-of-the-art coupled climate model with fully interactive aerosols and a representation of both direct and indirect aerosol effects. The key characteristics of the northern hemisphere responses are examined separately for winter and summer, and show that regional aerosols induce significant planetary-scale teleconnection patterns. In both seasons, the large-scale aerosol imprint originates from substantial changes in the regional precipitation distribution. During the winter, in response to anomalous surface cooling in the northern Indian Ocean, aerosols cause a westward shift of convection over the eastern Indian Ocean and compensating subsidence to the west and over the Maritime continent. During the summer, aerosols are collocated with rainfall, and cause a widespread drying over South Asia mostly by indirect effects. In both cases, the impact of the regional diabatic heating anomaly propagates remotely by exciting a northern hemisphere wave-train which, enhanced by regional feedbacks, leads to remarkable changes in near-surface climate, including circulation and temperature, over Eurasia, the northern Pacific and North America. Depending on the region, the induced anomalies may have opposite signs between the two seasons, and may thus contribute to reinforcing or dampening those due greenhouse gases. These results underscore the potential influence of Asian aerosols on global climate, which is a compelling problem as regional aerosol loading will continue to be large in the coming decades.

  9. The role of aerosols in cloud drop parameterizations and its applications in global climate models

    SciTech Connect

    Chuang, C.C.; Penner, J.E.

    1996-04-01

    The characteristics of the cloud drop size distribution near cloud base are initially determined by aerosols that serve as cloud condensation nuclei and the updraft velocity. We have developed parameterizations relating cloud drop number concentration to aerosol number and sulfate mass concentrations and used them in a coupled global aerosol/general circulation model (GCM) to estimate the indirect aerosol forcing. The global aerosol model made use of our detailed emissions inventories for the amount of particulate matter from biomass burning sources and from fossil fuel sources as well as emissions inventories of the gas-phase anthropogenic SO{sub 2}. This work is aimed at validating the coupled model with the Atmospheric Radiation Measurement (ARM) Program measurements and assessing the possible magnitude of the aerosol-induced cloud effects on climate.

  10. Enhanced research program on the long-range climatic effects of increased atmospheric carbon dioxide and sulfate aerosols. Final report

    SciTech Connect

    Washington, W.M.; Meehl, G.A.

    1997-04-01

    Consistent with the objectives to extract as much as possible from existing models on the role of the oceans in the greenhouse effect and to improve various aspects of the coupled system, the authors made significant progress in three areas. (1) In a series of manuscripts, they documented how the El Nino-Southern Oscillation operates in the model and how it is enhanced with increased carbon dioxide. (2) In studies with collaborators Branstator, Karoly, and Karl, they explored the possible carbon dioxide ``fingerprint`` in zonal mean temperatures, the effects of changes in extratropical teleconnections, and the regional effects of low-frequency variability and climate change. (3) They experimented with an advanced version of the NCAR community climate model (CCM0) that also includes the Ramanathan and Collins cirrus albedo feedback mechanism. This model was run with a mixed layer and was tested with the 1{degree} 20-level Semtner and Chervin ocean model. The latter includes the Arctic Ocean and dynamic sea ice, both showing realistic results. The authors completed the coupling of the advanced models. The dynamic ocean model was a 1{degree}x1{degree} version of the Semtner-Chervin 1/2{degree}x1/2{degree} ocean model with 20 vertical levels. The 1{degree}x1{degree} version of the Semtner-Chervin model used in this research explicitly resolved some aspects of the mesoscale eddies as did the parent model. The new coupled model system for greenhouse gas simulations on climate change was tested on multidecadal runs.

  11. Evaluating aerosol indirect effect through marine stratocumulus clouds

    SciTech Connect

    Kogan, Z.N.; Kogan, Y.L.; Lilly, D.K.

    1996-04-01

    During the last decade much attention has been focused on anthropogenic aerosols and their radiative influence on the global climate. Charlson et al. and Penner et al. have demonstrated that tropospheric aerosols and particularly anthropogenic sulfate aerosols may significantly contribute to the radiative forcing exerting a cooling influence on climate (-1 to -2 W/m{sup 2}) which is comparable in magnitude to greenhouse forcing, but opposite in sign. Aerosol particles affect the earth`s radiative budget either directly by scattering and absorption of solar radiation by themselves or indirectly by altering the cloud radiative properties through changes in cloud microstructure. Marine stratocumulus cloud layers and their possible cooling influence on the atmosphere as a result of pollution are of special interest because of their high reflectivity, durability, and large global cover. We present an estimate of thet aerosol indirect effect, or, forcing due to anthropogenic sulfate aerosols.

  12. Role of Climate Change in Global Predictions of Future Tropospheric Ozone and Aerosols

    NASA Technical Reports Server (NTRS)

    Liao, Hong; Chen, Wei-Ting; Seinfeld, John H.

    2006-01-01

    A unified tropospheric chemistry-aerosol model within the Goddard Institute for Space Studies general circulation model II is applied to simulate an equilibrium CO2-forced climate in the year 2100 to examine the effects of climate change on global distributions of tropospheric ozone and sulfate, nitrate, ammonium, black carbon, primary organic carbon, secondary organic carbon, sea salt, and mineral dust aerosols. The year 2100 CO2 concentration as well as the anthropogenic emissions of ozone precursors and aerosols/aerosol precursors are based on the Intergovernmental Panel on Climate Change Special Report on Emissions Scenarios (SRES) A2. Year 2100 global O3 and aerosol burdens predicted with changes in both climate and emissions are generally 5-20% lower than those simulated with changes in emissions alone; as exceptions, the nitrate burden is 38% lower, and the secondary organic aerosol burden is 17% higher. Although the CO2-driven climate change alone is predicted to reduce the global O3 concentrations over or near populated and biomass burning areas because of slower transport, enhanced biogenic hydrocarbon emissions, decomposition of peroxyacetyl nitrate at higher temperatures, and the increase of O3 production by increased water vapor at high NOx levels. The warmer climate influences aerosol burdens by increasing aerosol wet deposition, altering climate-sensitive emissions, and shifting aerosol thermodynamic equilibrium. Climate change affects the estimates of the year 2100 direct radiative forcing as a result of the climate-induced changes in burdens and different climatological conditions; with full gas-aerosol coupling and accounting for ozone and direct radiative forcings by the O2, sulfate, nitrate, black carbon, and organic carbon are predicted to be +0.93, -0.72, -1.0, +1.26, and -0.56 W m(exp -2), respectively, using present-day climate and year 2100 emissions, while they are predicted to be +0.76, -0.72, 0.74, +0.97, and -0.58 W m(exp -2

  13. Sensitivity of Remote Aerosol Distributions to Representation of Cloud-Aerosol Interactions in a Global Climate Model

    SciTech Connect

    Wang, Hailong; Easter, Richard C.; Rasch, Philip J.; Wang, Minghuai; Liu, Xiaohong; Ghan, Steven J.; Qian, Yun; Yoon, Jin-Ho; Ma, Po-Lun; Vinoj, V.

    2013-06-05

    Many global aerosol and climate models, including the widely used Community Atmosphere Model version 5 (CAM5), have large biases in predicting aerosols in remote regions such as upper troposphere and high latitudes. In this study, we conduct CAM5 sensitivity simulations to understand the role of key processes associated with aerosol transformation and wet removal affecting the vertical and horizontal long-range transport of aerosols to the remote regions. Improvements are made to processes that are currently not well represented in CAM5, which are guided by surface and aircraft measurements together with results from a multi-scale aerosol-climate model (PNNL-MMF) that explicitly represents convection and aerosol-cloud interactions at cloud-resolving scales. We pay particular attention to black carbon (BC) due to its importance in the Earth system and the availability of measurements. We introduce into CAM5 a new unified scheme for convective transport and aerosol wet removal with explicit aerosol activation above convective cloud base. This new implementation reduces the excessive BC aloft to better simulate observed BC profiles that show decreasing mixing ratios in the mid- to upper-troposphere. After implementing this new unified convective scheme, we examine wet removal of submicron aerosols that occurs primarily through cloud processes. The wet removal depends strongly on the sub-grid scale liquid cloud fraction and the rate of conversion of liquid water to precipitation. These processes lead to very strong wet removal of BC and other aerosols over mid- to high latitudes during winter months. With our improvements, the Arctic BC burden has a10-fold (5-fold) increase in the winter (summer) months, resulting in a much better simulation of the BC seasonal cycle as well. Arctic sulphate and other aerosol species also increase but to a lesser extent. An explicit treatment of BC aging with slower aging assumptions produces an additional 30-fold (5-fold) increase in

  14. Two Hundred Fifty Years of Aerosols and Climate: The End of the Age of Aerosols

    SciTech Connect

    Smith, Steven J.; Bond, Tami C.

    2014-01-20

    Carbonaceous and sulfur aerosols have a substantial global and regional influence on climate in addition to their impact on health and ecosystems. The magnitude of this influence has changed substantially over the past and is expected to continue to change into the future. An integrated picture of the changing climatic influence of black carbon, organic carbon and sulfate over the period 1850 through 2100, focusing on uncertainty, is presented using updated historical inventories and a coordinated set of emission projections. While aerosols have had a substantial impact on climate over the past century, by the end of the 21st century aerosols will likely be only a minor contributor to radiative forcing due to increases in greenhouse gas forcing and a global decrease in pollutant emissions. This outcome is even more certain under a successful implementation of a policy to limit greenhouse gas emissions as low-carbon energy technologies that do not emit appreciable aerosol or SO2 are deployed.

  15. Addition of Tropospheric Chemistry and Aerosols to the NCAR Community Climate System Model

    SciTech Connect

    Cameron-Smith, P; Lamarque, J; Connell, P; Chuang, C; Rotman, D; Taylor, J

    2005-11-14

    Atmospheric chemistry and aerosols have several important roles in climate change. They affect the Earth's radiative balance directly: cooling the earth by scattering sunlight (aerosols) and warming the Earth by trapping the Earth's thermal radiation (methane, ozone, nitrous oxide, and CFCs are greenhouse gases). Atmospheric chemistry and aerosols also impact many other parts of the climate system: modifying cloud properties (aerosols can be cloud condensation nuclei), fertilizing the biosphere (nitrogen species and soil dust), and damaging the biosphere (acid rain and ozone damage). In order to understand and quantify the effects of atmospheric chemistry and aerosols on the climate and the biosphere in the future, it is necessary to incorporate atmospheric chemistry and aerosols into state-of-the-art climate system models. We have taken several important strides down that path. Working with the latest NCAR Community Climate System Model (CCSM), we have incorporated a state-of-the-art atmospheric chemistry model to simulate tropospheric ozone. Ozone is not just a greenhouse gas, it damages biological systems including lungs, tires, and crops. Ozone chemistry is also central to the oxidizing power of the atmosphere, which destroys a lot of pollutants in the atmosphere (which is a good thing). We have also implemented a fast chemical mechanism that has high fidelity with the full mechanism, for significantly reduced computational cost (to facilitate millennium scale simulations). Sulfate aerosols have a strong effect on climate by reflecting sunlight and modifying cloud properties. So in order to simulate the sulfur cycle more fully in CCSM simulations, we have linked the formation of sulfate aerosols to the oxidizing power of the atmosphere calculated by the ozone mechanisms, and to dimethyl sulfide emissions from the ocean ecosystem in the model. Since the impact of sulfate aerosols depends on the relative abundance of other aerosols in the atmosphere, we also

  16. Unexpected Benefits of Reducing Aerosol Cooling Effects.

    PubMed

    Xing, Jia; Wang, Jiandong; Mathur, Rohit; Pleim, Jonathan; Wang, Shuxiao; Hogrefe, Christian; Gan, Chuen-Meei; Wong, David C; Hao, Jiming

    2016-07-19

    Impacts of aerosol cooling are not limited to changes in surface temperature since modulation of atmospheric dynamics resulting from the increased stability can deteriorate local air quality and impact human health. Health impacts from two manifestations of the aerosol direct effects (ADE) are estimated in this study: (1) the effect on surface temperature and (2) the effect on air quality through atmospheric dynamics. Average mortalities arising from the enhancement of surface PM2.5 concentration due to ADE in East Asia, North America and Europe are estimated to be 3-6 times higher than reduced mortality from decreases of temperature due to ADE. Our results suggest that mitigating aerosol pollution is beneficial in decreasing the impacts of climate change arising from these two manifestations of ADE health impacts. Thus, decreasing aerosol pollution gets direct benefits on health, and indirect benefits on health through changes in local climate and not offsetting changes associated only with temperature modulations as traditionally thought. The modulation of air pollution due to ADE also translates into an additional human health dividend in regions (e.g., U.S. Europe) with air pollution control measures but a penalty for regions (e.g., Asia) witnessing rapid deterioration in air quality. PMID:27310144

  17. Linearity of Climate Response to Increases in Black Carbon Aerosols

    SciTech Connect

    Mahajan, Salil; Evans, Katherine J.; Hack, James J.; Truesdale, John

    2013-04-19

    The impact of absorbing aerosols on global climate are not completely understood. Here, we present results of idealized experiments conducted with the Community Atmosphere Model (CAM4) coupled to a slab ocean model (CAM4-SOM) to simulate the climate response to increases in tropospheric black carbon aerosols (BC) by direct and semi-direct effects. CAM4-SOM was forced with 0, 1x, 2x, 5x and 10x an estimate of the present day concentration of BC while maintaining their estimated present day global spatial and vertical distribution. The top of the atmosphere (TOA) radiative forcing of BC in these experiments is positive (warming) and increases linearly as the BC burden increases. The total semi-direct effect for the 1x experiment is positive but becomes increasingly negative for higher BC concentrations. The global average surface temperature response is found to be a linear function of the TOA radiative forcing. The climate sensitivity to BC from these experiments is estimated to be 0.42 K $ W^{-1} m^{2}$ when the semi-direct effects are accounted for and 0.22 K $ W^{-1} m^{2}$ with only the direct effects considered. Global average precipitation decreases linearly as BC increases, with a precipitation sensitivity to atmospheric absorption of 0.4 $\\%$ $W^{-1}m^{2}$ . The hemispheric asymmetry of BC also causes an increase in southward cross-equatorial heat transport and a resulting northward shift of the inter-tropical convergence zone in the simulations at a rate of 4$^{\\circ}$N $ PW^{-1}$. Global average mid- and high-level clouds decrease, whereas the low-level clouds increase linearly with BC. The increase in marine stratocumulus cloud fraction over the south tropical Atlantic is caused by increased BC-induced diabatic heating of the free troposphere.

  18. Aerosol physical properties and their impact on climate change processes

    NASA Astrophysics Data System (ADS)

    Strzalkowska, Agata; Zielinski, Tymon; Petelski, Tomasz; Makuch, Przemyslaw; Pakszys, Paulina; Markuszewski, Piotr; Piskozub, Jacek; Drozdowska, Violetta; Gutowska, Dorota; Rozwadowska, Anna

    2013-04-01

    Characterizing aerosols involves the specification of not only their spatial and temporal distributions but their multi-component composition, particle size distribution and physical properties as well. Due to their light attenuation and scattering properties, aerosols influence radiance measured by satellite for ocean color remote sensing. Studies of marine aerosol production and transport are important for many earth sciences such as cloud physics, atmospheric optics, environmental pollution studies, and interaction between ocean and atmosphere. It was one of the reasons for the growth in the number of research programs dealing with marine aerosols. Sea salt aerosols are among the most abundant components of the atmospheric aerosol, and thus it exerts a strong influence on radiation, cloud formation, meteorology and chemistry of the marine atmosphere. An accurate understanding and description of these mechanisms is crucial to modeling climate and climate change. This work provides information on combined aerosol studies made with lidars and sun photometers onboard the ship and in different coastal areas. We concentrate on aerosol optical thickness and its variations with aerosol advections into the study area. We pay special attention to the problem of proper data collection and analyses techniques. We showed that in order to detect the dynamics of potential aerosol composition changes it is necessary to use data from different stations where measurements are made using the same techniques. The combination of such information with air mass back-trajectories and data collected at stations located on the route of air masses provides comprehensive picture of aerosol variations in the study area both vertically and horizontally. Acknowledgements: The support for this study was provided by the project Satellite Monitoring of the Baltic Sea Environment - SatBałtyk founded by European Union through European Regional Development Fund contract No. POIG 01

  19. Inter-annual Tropospheric Aerosol Variability in Late Twentieth Century and its Impact on Tropical Atlantic and West African Climate by Direct and Semi-direct Effects

    SciTech Connect

    Evans, Katherine J; Hack, James J; Truesdale, John; Mahajan, Salil; Lamarque, J-F

    2012-01-01

    A new high-resolution (0.9$^{\\circ}$x1.25$^{\\circ}$ in the horizontal) global tropospheric aerosol dataset with monthly resolution is generated using the finite-volume configuration of Community Atmosphere Model (CAM4) coupled to a bulk aerosol model and forced with recent estimates of surface emissions for the latter part of twentieth century. The surface emissions dataset is constructed from Coupled Model Inter-comparison Project (CMIP5) decadal-resolution surface emissions dataset to include REanalysis of TROpospheric chemical composition (RETRO) wildfire monthly emissions dataset. Experiments forced with the new tropospheric aerosol dataset and conducted using the spectral configuration of CAM4 with a T85 truncation (1.4$^{\\circ}$x1.4$^{\\circ}$) with prescribed twentieth century observed sea surface temperature, sea-ice and greenhouse gases reveal that variations in tropospheric aerosol levels can induce significant regional climate variability on the inter-annual timescales. Regression analyses over tropical Atlantic and Africa reveal that increasing dust aerosols can cool the North African landmass and shift convection southwards from West Africa into the Gulf of Guinea in the spring season in the simulations. Further, we find that increasing carbonaceous aerosols emanating from the southwestern African savannas can cool the region significantly and increase the marine stratocumulus cloud cover over the southeast tropical Atlantic ocean by aerosol-induced diabatic heating of the free troposphere above the low clouds. Experiments conducted with CAM4 coupled to a slab ocean model suggest that present day aerosols can shift the ITCZ southwards over the tropical Atlantic and can reduce the ocean mixed layer temperature beneath the increased marine stratocumulus clouds in the southeastern tropical Atlantic.

  20. Aerosols implicated as a prime driver of twentieth-century North Atlantic climate variability.

    PubMed

    Booth, Ben B B; Dunstone, Nick J; Halloran, Paul R; Andrews, Timothy; Bellouin, Nicolas

    2012-04-04

    Systematic climate shifts have been linked to multidecadal variability in observed sea surface temperatures in the North Atlantic Ocean. These links are extensive, influencing a range of climate processes such as hurricane activity and African Sahel and Amazonian droughts. The variability is distinct from historical global-mean temperature changes and is commonly attributed to natural ocean oscillations. A number of studies have provided evidence that aerosols can influence long-term changes in sea surface temperatures, but climate models have so far failed to reproduce these interactions and the role of aerosols in decadal variability remains unclear. Here we use a state-of-the-art Earth system climate model to show that aerosol emissions and periods of volcanic activity explain 76 per cent of the simulated multidecadal variance in detrended 1860-2005 North Atlantic sea surface temperatures. After 1950, simulated variability is within observational estimates; our estimates for 1910-1940 capture twice the warming of previous generation models but do not explain the entire observed trend. Other processes, such as ocean circulation, may also have contributed to variability in the early twentieth century. Mechanistically, we find that inclusion of aerosol-cloud microphysical effects, which were included in few previous multimodel ensembles, dominates the magnitude (80 per cent) and the spatial pattern of the total surface aerosol forcing in the North Atlantic. Our findings suggest that anthropogenic aerosol emissions influenced a range of societally important historical climate events such as peaks in hurricane activity and Sahel drought. Decadal-scale model predictions of regional Atlantic climate will probably be improved by incorporating aerosol-cloud microphysical interactions and estimates of future concentrations of aerosols, emissions of which are directly addressable by policy actions.

  1. Sensitivity of the climate response to regional aerosol emissions

    NASA Astrophysics Data System (ADS)

    Kasoar, Matthew; Voulgarakis, Apostolos; Shindell, Drew; Lamarque, Jean-Francois; Shawki, Dilshad

    2015-04-01

    Short-lived emissions like aerosols and their precursors have inhomogeneous distributions in the atmosphere. As a result, aerosol radiative forcing of the climate is highly uneven, and depends on both the location of emission as well as circulation patterns. Unlike well-mixed greenhouse gases such as CO2, the climate response to aerosol forcing may therefore be very dependent on the source region, and so understanding how the sensitivity of the climate varies with emission and forcing location has implications for the design of policy regarding short-lived climate forcers, as well as for understanding the coupling between radiative forcing and climate response. Using the UK Met Office's HadGEM3 composition-climate model, we have performed a series of experiments to investigate the climate response to aerosol species from different key anthropogenic emission regions, in particular East Asia, South Asia, the USA, and the whole northern mid-latitude band. Recent results from these simulations will be presented, focusing in particular on the patterns of climate forcing due to Asian anthropogenic emissions, and the resulting responses in surface temperature and precipitation. Large-scale circulation changes, driven by regional temperature gradients, are found to play an important role in explaining the observed climate responses, which can be substantial even in in parts of the world far from the location of the forcing. The correct magnitude of aerosol forcing remains, however, one of the greatest uncertainties in our current understanding of anthropogenic influences on climate. Aerosol radiative forcing varies considerably between different composition-climate models, and to explore the implications of this for climate responses we use the GISS Model-E2 and NCAR CESM1 models in addition to HadGEM3. These reveal a remarkable variation in the simulated climate response as a result of differences in the radiative forcing from identical perturbations to regional sulphate

  2. Studies of the aerosol indirect effect from sulfate and black carbon aerosols

    NASA Astrophysics Data System (ADS)

    Kristjánsson, Jón Egill

    2002-08-01

    The indirect effect of anthropogenic aerosols is investigated using the global climate model National Center for Atmospheric Research Community Climate Model Version 3 (NCAR CCM3). Two types of anthropogenic aerosols are considered, i.e., sulfate and black carbon aerosols. The concentrations and horizontal distributions of these aerosols were obtained from simulations with a life-cycle model incorporated into the global climate model. They are then combined with size-segregated background aerosols. The aerosol size distributions are subjected to condensation, coagulation, and humidity swelling. By making assumptions on supersaturation, we determine cloud droplet number concentrations in water clouds. Cloud droplet sizes and top of atmosphere (TOA) radiative fluxes are in good agreement with satellite observations. Both components of the indirect effect, i.e., the radius and lifetime effects, are computed as pure forcing terms. Using aerosol data for 2000 from the Intergovernmental Panel on Climate Change (IPCC), we find, globally averaged, a 5% decrease in cloud droplet radius and a 5% increase in cloud water path due to anthropogenic aerosols. The largest changes are found over SE Asia, followed by the North Atlantic, Europe, and the eastern United States. This is also the case for the radiative forcing (``indirect effect''), which has a global average of -1.8 W m-2. When the experiment is repeated using data for 2100 from the IPCC A2 scenario, an unchanged globally averaged radiative forcing is found, but the horizontal distribution has been shifted toward the tropics. Sensitivity experiments show that the radius effect is ~3 times as important as the lifetime effect and that black carbon only contributes marginally to the overall indirect effect.

  3. Introducing the aerosol-climate model MAECHAM5-SAM2

    NASA Astrophysics Data System (ADS)

    Hommel, R.; Timmreck, C.; Graf, H. F.

    2009-04-01

    We are presenting a new global aerosol model MAECHAM5-SAM2 to study the aerosol dynamics in the UTLS under background and volcanic conditions. The microphysical core modul SAM2 treats the formation, the evolution and the transport of stratospheric sulphuric acid aerosol. The aerosol size distribution and the weight percentage of the sulphuric acid solution is calculated dependent on the concentrations of H2SO4 and H2O, their vapor pressures, the atmospheric temperature and pressure. The fixed sectional method is used to resolve an aerosol distribution between 1 nm and 2.6 micron in particle radius. Homogeneous nucleation, condensation and evaporation, coagulation, water-vapor growth, sedimentation and sulphur chemistry are included. The module is applied in the middle-atmosphere MAECHAM5 model, resolving the atmosphere up to 0.01 hPa (~80 km) in 39 layers. It is shown here that MAECHAM5-SAM2 well represents in-situ measured size distributions of stratospheric background aerosol in the northern hemisphere mid-latitudes. Distinct differences can be seen when derived integrated aerosol parameters (surface area, effective radius) are compared with aerosol climatologies based on the SAGE II satellite instrument (derived by the University of Oxford and the NASA AMES laboratory). The bias between the model and the SAGE II data increases as the moment of the aerosol size distribution decreases. Thus the modeled effective radius show the strongest bias, followed by the aerosol surface area density. Correspondingly less biased are the higher moments volume area density and the mass density of the global stratospheric aerosol coverage. This finding supports the key finding No. 2 of the SPARC Assessment of Stratospheric Aerosol Properties (2006), where it was shown that during periods of very low aerosol load in the stratosphere, the consistency between in-situ and satellite measurements, which exist in a volcanically perturbed stratosphere, breaks down and significant

  4. Volcanic aerosols: Chemistry, evolution, and effects

    NASA Technical Reports Server (NTRS)

    Turco, Richard

    1991-01-01

    Stratospheric aerosols have been the subject of scientific speculation since the 1880s, when the powerful eruption of Krakatoa attracted worldwide attention to the upper atmosphere through spectacular optical displays. The presence of a permanent tenuous dust layer in the lower stratosphere was postulated in the 1920s following studies of the twilight glow. Junge collected the first samples of these 'dust' particles and demonstrated that they were actually composed of sulfates, most likely concentrated sulfuric acid (Junge and Manson, 1961; Junge, 1963). Subsequent research has been spurred by the realization that stratospheric particles can influence the surface climate of earth through their effects on atmospheric radiation. Such aerosols can also influence, through chemical and physical effects, the trace composition of the atmosphere, ozone concentrations, and atmospheric electrical properties. The properties of stratospheric aerosols (both the background particles and those enhanced by volcanic eruptions) were measured in situ by balloon ascents and high altitude aircraft sorties. The aerosols were also observed remotely from the ground and from satellites using both active (lidar) and passive (solar occultation) techniques (remote sensing instruments were carried on aircraft and balloon platforms as well). In connection with the experimental work, models were developed to test theories of particle formation and evolution, to guide measurement strategies, to provide a means of connecting laboratory and field data, and to apply the knowledge gained to answer practical questions about global changes in climate, depletion of the ozone layer, and related environmental problems.

  5. Improving our fundamental understanding of the role of aerosol-cloud interactions in the climate system.

    PubMed

    Seinfeld, John H; Bretherton, Christopher; Carslaw, Kenneth S; Coe, Hugh; DeMott, Paul J; Dunlea, Edward J; Feingold, Graham; Ghan, Steven; Guenther, Alex B; Kahn, Ralph; Kraucunas, Ian; Kreidenweis, Sonia M; Molina, Mario J; Nenes, Athanasios; Penner, Joyce E; Prather, Kimberly A; Ramanathan, V; Ramaswamy, Venkatachalam; Rasch, Philip J; Ravishankara, A R; Rosenfeld, Daniel; Stephens, Graeme; Wood, Robert

    2016-05-24

    The effect of an increase in atmospheric aerosol concentrations on the distribution and radiative properties of Earth's clouds is the most uncertain component of the overall global radiative forcing from preindustrial time. General circulation models (GCMs) are the tool for predicting future climate, but the treatment of aerosols, clouds, and aerosol-cloud radiative effects carries large uncertainties that directly affect GCM predictions, such as climate sensitivity. Predictions are hampered by the large range of scales of interaction between various components that need to be captured. Observation systems (remote sensing, in situ) are increasingly being used to constrain predictions, but significant challenges exist, to some extent because of the large range of scales and the fact that the various measuring systems tend to address different scales. Fine-scale models represent clouds, aerosols, and aerosol-cloud interactions with high fidelity but do not include interactions with the larger scale and are therefore limited from a climatic point of view. We suggest strategies for improving estimates of aerosol-cloud relationships in climate models, for new remote sensing and in situ measurements, and for quantifying and reducing model uncertainty.

  6. Improving our fundamental understanding of the role of aerosol-cloud interactions in the climate system.

    PubMed

    Seinfeld, John H; Bretherton, Christopher; Carslaw, Kenneth S; Coe, Hugh; DeMott, Paul J; Dunlea, Edward J; Feingold, Graham; Ghan, Steven; Guenther, Alex B; Kahn, Ralph; Kraucunas, Ian; Kreidenweis, Sonia M; Molina, Mario J; Nenes, Athanasios; Penner, Joyce E; Prather, Kimberly A; Ramanathan, V; Ramaswamy, Venkatachalam; Rasch, Philip J; Ravishankara, A R; Rosenfeld, Daniel; Stephens, Graeme; Wood, Robert

    2016-05-24

    The effect of an increase in atmospheric aerosol concentrations on the distribution and radiative properties of Earth's clouds is the most uncertain component of the overall global radiative forcing from preindustrial time. General circulation models (GCMs) are the tool for predicting future climate, but the treatment of aerosols, clouds, and aerosol-cloud radiative effects carries large uncertainties that directly affect GCM predictions, such as climate sensitivity. Predictions are hampered by the large range of scales of interaction between various components that need to be captured. Observation systems (remote sensing, in situ) are increasingly being used to constrain predictions, but significant challenges exist, to some extent because of the large range of scales and the fact that the various measuring systems tend to address different scales. Fine-scale models represent clouds, aerosols, and aerosol-cloud interactions with high fidelity but do not include interactions with the larger scale and are therefore limited from a climatic point of view. We suggest strategies for improving estimates of aerosol-cloud relationships in climate models, for new remote sensing and in situ measurements, and for quantifying and reducing model uncertainty. PMID:27222566

  7. Final Report for LDRD Project ''A New Era of Research in Aerosol/Cloud/Climate Interactions at LLNL''

    SciTech Connect

    Chuang, C; Bergman, D J; Dignon, J E; Connell, P S

    2002-01-31

    Observations of global temperature records seem to show less warming than predictions of global warming brought on by increasing concentrations of CO{sub 2} and other greenhouse gases. One of the reasonable explanations for this apparent inconsistency is that the increasing concentrations of anthropogenic aerosols may be partially counteracting the effects of greenhouse gases. Aerosols can scatter or absorb the solar radiation, directly change the planetary albedo. Aerosols, unlike CO{sub 2}, may also have a significant indirect effect by serving as cloud condensation nuclei (CCN). Increases in CCN can result in clouds with more but smaller droplets, enhancing the reflection of solar radiation. Aerosol direct and indirect effects are a strong function of the distributions of all aerosol types and the size distribution of the aerosol in question. However, the large spatial and temporal variabilities in the concentration, chemical characteristics, and size distribution of aerosols have made it difficult to assess the magnitude of aerosol effects on atmospheric radiation. These variabilities in aerosol characteristics as well as their effects on clouds are the leading sources of uncertainty in predicting future climate variation. Inventory studies have shown that the present-day anthropogenic emissions contribute more than half of fine particle mass primarily due to sulfate and carbonaceous aerosols derived from fossil fuel combustion and biomass burning. Parts of our earlier studies have been focused on developing an understanding of global sulfate and carbonaceous aerosol abundances and investigating their climate effects [Chuang et al., 1997; Penner et al., 1998]. We have also modeled aerosol optical properties to account for changes in the refractive indices with relative humidity and dry aerosol composition [Grant et al., 1999]. Moreover, we have developed parameterizations of cloud response to aerosol abundance for use in global models to evaluate the importance

  8. The impact of aerosols on the climate and its changes in China

    NASA Astrophysics Data System (ADS)

    Li, Z.

    2013-05-01

    Heavy and widespread presence of aerosols could impinge significantly on regional and global climate depending on aerosol distribution, transport and evolution of optical, physical and chemical properties. To unravel the impact and interactions between aerosols and climate of China, several field experiments have been conducted in the region. Besides, numerous studies are being carried out using the long-term (up to 50 years) routine meteorological measurements. Findings will be summarized from two China-US joint experiments: the East Asian Study of Tropospheric Aerosols: an International Regional Experiment (EAST-AIRE) in 2005 and the Atmospheric Radiation Measurements (ARM) Mobile Facility deployment in 2008 (AMF-China), as well as from analyses of routine data. The experiments have produced a wealth of measurements pertaining to aerosol properties, meteorological regimes, cloud, radiation and precipitation in order to gain insights into the potential mechanism by which aerosols affect and interact with the monsoon regime. By taking advantage of the field observation data, many evidences of aerosol's direct, indirect and semi-direct effects are revealed, with the bulk published in two special sections of the J. Geophy. Res. In addition, some features of the impact of increasing aerosols on the long-term trends of temperature, rainfall, wind and storms emerge from careful analyses of general meteorological data.

  9. Improving Aerosol Simulation over South Asia for Climate and Air Quality Studies

    NASA Technical Reports Server (NTRS)

    Pan, Xiaohua; Chin, Mian; Bian, Huisheng; Gautam, Ritesh

    2014-01-01

    Atmospheric pollution over South Asia attracts special attention due to its effects on regional climate, the water cycle, and human health. These effects are potentially growing owing to rising trends of anthropogenic aerosol emissions found there. However, it has been proved quite challenging to adequately represent the aerosol spatial distribution and magnitude over this critical region in global models (Pan et al. 2014), with the surface concentrations, aerosol optical depth (AOD), and absorbing AOD (AAOD) significantly underestimated, especially in October-January when the agricultural waste burning and anthropogenic aerosol dominate over dust aerosol. In this study, we aim to investigate the causes for such discrepancy in winter by conducting sets of model experiments with NASA's GEOS-5 in terms of (1) spatial resolution, (2) emission amount, and (3) meteorological fields.

  10. Radiative forcing and climate response to projected 21st century aerosol decreases

    NASA Astrophysics Data System (ADS)

    Westervelt, D. M.; Horowitz, L. W.; Naik, V.; Mauzerall, D. L.

    2015-03-01

    It is widely expected that global emissions of atmospheric aerosols and their precursors will decrease strongly throughout the remainder of the 21st century, due to emission reduction policies enacted to protect human health. For instance, global emissions of aerosols and their precursors are projected to decrease by as much as 80% by the year 2100, according to the four Representative Concentration Pathway (RCP) scenarios. The removal of aerosols will cause unintended climate consequences, including an unmasking of global warming from long-lived greenhouse gases. We use the Geophysical Fluid Dynamics Laboratory Climate Model version 3 (GFDL CM3) to simulate future climate over the 21st century with and without the aerosol emission changes projected by each of the RCPs in order to isolate the radiative forcing and climate response resulting from the aerosol reductions. We find that the projected global radiative forcing and climate response due to aerosol decreases do not vary significantly across the four RCPs by 2100, although there is some mid-century variation, especially in cloud droplet effective radius, that closely follows the RCP emissions and energy consumption projections. Up to 1 W m-2 of radiative forcing may be unmasked globally from 2005 to 2100 due to reductions in aerosol and precursor emissions, leading to average global temperature increases up to 1 K and global precipitation rate increases up to 0.09 mm d-1. Regionally and locally, climate impacts can be much larger, with a 2.1 K warming projected over China, Japan, and Korea due to the reduced aerosol emissions in RCP8.5, as well as nearly a 0.2 mm d-1 precipitation increase, a 7 g m-2 LWP decrease, and a 2 μm increase in cloud droplet effective radius. Future aerosol decreases could be responsible for 30-40% of total climate warming by 2100 in East Asia, even under the high greenhouse gas emissions scenario (RCP8.5). The expected unmasking of global warming caused by aerosol reductions will

  11. Aerosols and Clouds: In Cahoots to Change Climate

    SciTech Connect

    Berg, Larry

    2014-03-29

    Key knowledge gaps persist despite advances in the scientific understanding of how aerosols and clouds evolve and affect climate. The Two-Column Aerosol Project, or TCAP, was designed to provide a detailed set of observations to tackle this area of unknowns. Led by PNNL atmospheric scientist Larry Berg, ARM's Climate Research Facility was deployed in Cape Cod, Massachusetts for the 12-month duration of TCAP, which came to a close in June 2013. "We are developing new tools to look at particle chemistry, like our mass spectrometer used in TCAP that can tell us the individual chemical composition of an aerosol," said Berg. "Then, we'll run our models and compare it with the data that we have to make sure we're getting correct answers and make sure our climate models are reflecting the best information."

  12. Aerosols and Clouds: In Cahoots to Change Climate

    ScienceCinema

    Berg, Larry

    2016-07-12

    Key knowledge gaps persist despite advances in the scientific understanding of how aerosols and clouds evolve and affect climate. The Two-Column Aerosol Project, or TCAP, was designed to provide a detailed set of observations to tackle this area of unknowns. Led by PNNL atmospheric scientist Larry Berg, ARM's Climate Research Facility was deployed in Cape Cod, Massachusetts for the 12-month duration of TCAP, which came to a close in June 2013. "We are developing new tools to look at particle chemistry, like our mass spectrometer used in TCAP that can tell us the individual chemical composition of an aerosol," said Berg. "Then, we'll run our models and compare it with the data that we have to make sure we're getting correct answers and make sure our climate models are reflecting the best information."

  13. Estimating the influence of the secondary organic aerosols on present climate using ECHAM5-HAM

    NASA Astrophysics Data System (ADS)

    O'Donnell, D.; Tsigaridis, K.; Feichter, J.

    2011-01-01

    In recent years, several field measurement campaigns have highlighted the importance of the organic fraction of aerosol mass, and with such spatial diversity that one may assert that these aerosols are ubiquitous in the troposphere, with particular importance in continental areas. Investigation of the chemical composition of organic aerosol remains a work in progress, but it is now clear that a significant portion of the total organic mass is composed of secondary organic material, that is, aerosol chemically formed from gaseous volatile organic carbon (VOC) precursors. A number of such precursors, of both biogenic and anthropogenic origin, have been identified. Experimental, inventory building and modelling studies have followed. Laboratory studies have yielded information on the chemical pathways that lead to secondary organic aerosol (SOA) formation, and provided the means to estimate the aerosol yields from a given precursor-oxidant reaction. Global inventories of anthropogenic VOC emissions, and of biogenic VOC emitter species distribution and their emission potential have been constructed. Models have been developed that provide global estimates of precursor VOC emissions, SOA formation and atmospheric burdens of these species. This paper estimates the direct and indirect effects of these aerosols using the global climate-aerosol model ECHAM5-HAM. For year 2000 conditions, we estimate a global annual mean shortwave (SW) aerosol direct effect due to SOA of -0.3 W m-2. The model predicts a positive SW indirect effect due to SOA amounting to +0.23 W m-2, arising from enlargement of particles due to condensation of SOA, together with an enhanced coagulation sink for small particles. Longwave effects are small. Finally, we indicate of areas of research into SOA that are required in order to better constrain our estimates of the influence of aerosols on the climate system.

  14. Secondary aerosol formation from stress-induced biogenic emissions and possible climate feedbacks

    NASA Astrophysics Data System (ADS)

    Mentel, Th. F.; Kleist, E.; Andres, S.; Dal Maso, M.; Hohaus, T.; Kiendler-Scharr, A.; Rudich, Y.; Springer, M.; Tillmann, R.; Uerlings, R.; Wahner, A.; Wildt, J.

    2013-09-01

    Atmospheric aerosols impact climate by scattering and absorbing solar radiation and by acting as ice and cloud condensation nuclei. Biogenic secondary organic aerosols (BSOAs) comprise an important component of atmospheric aerosols. Biogenic volatile organic compounds (BVOCs) emitted by vegetation are the source of BSOAs. Pathogens and insect attacks, heat waves and droughts can induce stress to plants that may impact their BVOC emissions, and hence the yield and type of formed BSOAs, and possibly their climatic effects. This raises questions of whether stress-induced changes in BSOA formation may attenuate or amplify effects of climate change. In this study we assess the potential impact of stress-induced BVOC emissions on BSOA formation for tree species typical for mixed deciduous and Boreal Eurasian forests. We studied the photochemical BSOA formation for plants infested by aphids in a laboratory setup under well-controlled conditions and applied in addition heat and drought stress. The results indicate that stress conditions substantially modify BSOA formation and yield. Stress-induced emissions of sesquiterpenes, methyl salicylate, and C17-BVOCs increase BSOA yields. Mixtures including these compounds exhibit BSOA yields between 17 and 33%, significantly higher than mixtures containing mainly monoterpenes (4-6% yield). Green leaf volatiles suppress SOA formation, presumably by scavenging OH, similar to isoprene. By classifying emission types, stressors and BSOA formation potential, we discuss possible climatic feedbacks regarding aerosol effects. We conclude that stress situations for plants due to climate change should be considered in climate-vegetation feedback mechanisms.

  15. Secondary aerosol formation from stress-induced biogenic emissions and possible climate feedbacks

    NASA Astrophysics Data System (ADS)

    Mentel, Th. F.; Kleist, E.; Andres, S.; Maso, M. D.; Hohaus, T.; Kiendler-Scharr, A.; Rudich, Y.; Springer, M.; Tillmann, R.; Uerlings, R.; Wahner, A.; Wildt, J.

    2013-03-01

    Atmospheric aerosols impact climate by scattering and absorbing solar radiation and by acting as ice and cloud condensation nuclei. Secondary organic aerosols (SOA) comprise an important component of atmospheric aerosols. Biogenic volatile organic compounds (BVOC) emitted by vegetation are a major source of SOA. Pathogens and insect attacks, heat waves and droughts can induce stress to plants that may impact their BVOC emissions, and hence the yield and type of formed SOA, and possibly their climatic effects. This raises questions whether stress-induced changes in SOA formation may attenuate or amplify effects of climate change. In this study we assess the potential impact of stress-induced BVOC emissions on SOA formation for tree species typical for mixed deciduous and Boreal Eurasian forests. We studied the photochemical SOA formation for infested plants in a laboratory setup under well-controlled conditions and applied in addition heat and drought stress. The results indicate that stress conditions substantially modify SOA formation. While sesquiterpenes, methyl salicylate, and C17-BVOC increase SOA yield, green leaf volatiles suppress SOA formation. By classifying emission types, stressors and SOA formation potential, we propose possible climatic feedbacks regarding aerosol effects. We conclude that stress situations for plants due to climate change should be considered in climate-vegetation feedback mechanisms.

  16. Aerosol-Water Cycle Interaction: A New Challenge in Monsoon Climate Research

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.

    2006-01-01

    Long recognized as a major environmental hazard, aerosol is now known to have strong impacts on both regional and global climate. It has been estimated that aerosol may reduce by up to 10% of the seasonal mean solar radiation reaching the earth surface, producing a global cooling effect that opposes global warming (Climate Change 2001). This means that the potential perils that humans have committed to global warming may be far greater than what we can detect at the present. As a key component of the Earth climate system, the water cycle is profoundly affected by the presence of aerosols in the atmosphere. Through the so-called direct effect , aerosol scatters and/or absorbs solar radiation, thus cooling the earth surface and changing the horizontal and vertical radiational heating contrast in the atmosphere. The heating contrast drives anomalous atmospheric circulation, resulting in changes in convection, clouds, and rainfall. Another way aerosol can affect the water cycle is through the so-called indirect effects, whereby aerosol increases the number of cloud condensation nuclei, prolongs life time of clouds, and inhibits the growth of cloud drops to raindrops. This leads to more clouds, and increased reflection of solar radiation, and further cooling at the earth surface. In monsoon regions, the response of the water cycle to aerosol forcing is especially complex, not only because of presence of diverse mix of aerosol species with vastly different radiative properties, but also because the monsoon is strongly influenced by ocean and land surface processes, land use, land change, as well as regional and global greenhouse warming effects. Thus, sorting out the impacts of aerosol forcing, and interaction with the monsoon water cycle is a very challenging problem. In this talk, I will offer some insights into how aerosols may impact the Asian monsoon based on preliminary results from satellite observations and climate model experiments. Specifically, I will discuss

  17. Aerosol-Water Cycle Interaction: A New Challenge in Monsoon Climate Research

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.

    2006-01-01

    Long recognized as a major environmental hazard, aerosol is now known to have strong impacts on both regional and global climate. It has been estimated that aerosol may reduce by up to 10% of the seasonal mean solar radiation reaching the earth surface, producing a global cooling effect that opposes global warming (Climate Change 2001). This means that the potential perils that humans have committed to global warming may be far greater than what we can detect at the present. As a key component of the Earth climate system, the water cycle is profoundly affected by the presence of aerosols in the atmosphere. Through the so-called "direct effect", aerosol scatters and/or absorbs solar radiation, thus cooling the earth surface and changing the horizontal and vertical radiational heating contrast in the atmosphere. The heating contrast drives anomalous atmospheric circulation, resulting in changes in convection, clouds, and rainfall. Another way aerosol can affect the water cycle is through the so-called "indirect effects", whereby aerosol increases the number of cloud condensation nuclei, prolongs life time of clouds, and inhibits the growth of cloud drops to raindrops. This leads to more clouds, and increased reflection of solar radiation, and further cooling at the earth surface. In monsoon regions, the response of the water cycle to aerosol forcing is especially complex, not only because of presence of diverse mix of aerosol species with vastly different radiative properties, but also because the monsoon is strongly influenced by ocean and land surface processes, land use, land change, as well as regional and global greenhouse warming effects. Thus, sorting out the impacts of aerosol forcing, and interaction with the monsoon water cycle is a very challenging problem. In this talk, I will offer some insights into how aerosols may impact the Asian monsoon based on preliminary results from satellite observations and climate model experiments. Specifically, I will

  18. Growing up MODIS: Towards a mature aerosol climate data record

    NASA Astrophysics Data System (ADS)

    Levy, Robert C.

    2013-05-01

    Aerosols are major players within the Earth's climate system, affecting the radiation budget, clouds and the hydrological cycle. In high concentrations near the surface, aerosols (or particulate matter, PM) affect visibility, impact air quality, and can contribute to poor health. Among others, Yoram Kaufman recognized the importance of aerosols to climate, and helped to design new instrumentation and algorithms to retrieve and quantify global aerosol properties. One instrument, known as the Moderate Imaging Resolution Spectro-radiometer (MODIS), was deployed on the AM-1 satellite (later known as Terra), part of NASA's Earth Observing System (EOS). In 1998, armed with an M.S. and job experience in neither aerosols nor satellites, I was looking for a new job. I somehow found my way to the MODIS Aerosol team. It was only a year before Terra launch, and most major decisions about the MODIS aerosol retrieval algorithms had been finalized. Since then, we worked through launch, initial evaluation of the product with AERONET and field deployments, and continued efforts to understand the product and refine retrieval algorithms. I have had opportunities to participate in field experiments, write papers, and earn my PhD. The "second generation" algorithm for aerosol retrieval over land has been hugely successful. We have collected nearly a half-million collocations with AERONET and other dataseis, made new discoveries, and have contributed to research and operational projects globally. Due to the dedication of the entire team, the MODIS aerosol product now is one of the highlights of NASA's EOS program. It is used for climate research and air quality forecasting, as well for applications not even considered before the MODIS era. More recently, a focus is on stitching the MODIS aerosol product into the "climate data record" (CDR) for global aerosol, determining whether the product has sufficient length, consistency and continuity to determine climate variability and change

  19. Dust Aerosol Impact on North Africa Climate: A GCM Investigation of Aerosol-Cloud-Radiation Interactions Using A-Train Satellite Data

    SciTech Connect

    Gu, Y.; Liou, K. N.; Jiang, Jonathan; Su, Hui; Liu, Xiaohong

    2012-02-15

    The climatic effects of dust aerosols in North Africa have been investigated using the atmospheric general circulation model (AGCM) developed at the University of California, Los Angeles (UCLA). The model includes an efficient and physically based radiation parameterization scheme developed specifically for application to clouds and aerosols. Parameterization of the effective ice particle size in association with the aerosol indirect effect based on cloud and aerosol data retrieved from A-Train satellite observations have been employed in the climate model simulations. Offline simulations reveal that the direct solar, IR, and net forcings by dust aerosols generally increase with increasing aerosol optical depth (AOD). When the dust semi-direct effect is included with the presence of ice clouds, positive IR radiative forcing is enhanced, since ice clouds trap substantial IR radiation, while the positive solar forcing with dust aerosols alone has been changed to negative values due to the strong reflection of solar radiation by clouds, indicating that cloud forcing could exceed aerosol forcing. With the aerosol indirect effect, the net cloud forcing is generally reduced for ice water path (IWP) larger than 20 g m-2. The magnitude of the reduction increases with IWP. AGCM simulations show that the reduced ice crystal mean effective size due to the aerosol first indirect effect result in less OLR and net solar flux at the top of the atmosphere over the cloudy area of the North Africa region because ice clouds with smaller size trap more IR radiation and reflect more solar radiation. The precipitation in the same area, however, increases due to the aerosol indirect effect on ice clouds, corresponding to the enhanced convection as indicated by reduced OLR. The increased precipitation seems to be associated with enhanced ice water contents in this region. The 200 mb radiative heating rate shows more cooling with the aerosol indirect effect since greater cooling is

  20. Untangling aerosol effects on clouds and precipitation in a buffered system.

    PubMed

    Stevens, Bjorn; Feingold, Graham

    2009-10-01

    It is thought that changes in the concentration of cloud-active aerosol can alter the precipitation efficiency of clouds, thereby changing cloud amount and, hence, the radiative forcing of the climate system. Despite decades of research, it has proved frustratingly difficult to establish climatically meaningful relationships among the aerosol, clouds and precipitation. As a result, the climatic effect of the aerosol remains controversial. We propose that the difficulty in untangling relationships among the aerosol, clouds and precipitation reflects the inadequacy of existing tools and methodologies and a failure to account for processes that buffer cloud and precipitation responses to aerosol perturbations.

  1. The contribution of aerosol hygroscopic growth to the modeled aerosol radiative effect

    NASA Astrophysics Data System (ADS)

    Kokkola, Harri; Kühn, Thomas; Kirkevåg, Alf; Romakkaniemi, Sami; Arola, Antti

    2016-04-01

    The hygroscopic growth of atmospheric aerosols can have a significant effect on the direct radiative effect of atmospheric aerosol. However, there are significant uncertainties concerning how much of the radiative forcing is due to different chemical compounds, especially water. For example, modeled optical depth of water in global aerosol-climate models varies by more than a factor of two. These differences can be attributed to differences in modeled 1) hygroscopicity, 2) ambient relative humidity, and/or 3) aerosol size distribution. In this study, we investigate which of these above-mentioned factors cause the largest variability in the modeled optical depth of water. In order to do this, we have developed a tool that calculates aerosol extinction using interchangeable global 3D data of aerosol composition, relative humidity, and aerosol size distribution fields. This data is obtained from models that have taken part in the open international initiative AeroCom (Aerosol Comparisons between Observations and Models). In addition, we use global 3D data for relative humidity from the Atmospheric Infrared Sounder (AIRS) flying on board NASA's Aqua satellite and the National Centers for Environmental Prediction (NCEP) reanalysis data. These observations are used to evaluate the modeled relative humidity fields. In the first stage of the study, we made a detailed investigation using the aerosol-chemistry-climate model ECHAM-HAMMOZ in which most of the aerosol optical depth is caused by water. Our results show that the model significantly overestimates the relative humidity over the oceans while over land, the overestimation is lower or it is underestimated. Since this overestimation occurs over the oceans, the water optical depth is amplified as the hygroscopic growth is very sensitive to changes in high relative humidities. Over land, error in modeled relative humidity is unlikely to cause significant errors in water optical depth as relative humidities are generally

  2. Steps Toward an Aerosol-Type Global Climate Data Record

    NASA Astrophysics Data System (ADS)

    Kahn, R. A.

    2015-12-01

    Earth-observing satellites have produced a global record of aerosol optical depth approaching two decades in length. However a global record of aerosol properties at the level-of-detail required for constraining aerosol radiative forcing, aerosol-cloud interaction assessments, and many air quality applications is as yet lacking. Some aerosol-type information is derived from surface-based photometers, and qualitative classification is possible under favorable conditions from MISR, POLDER, and CALIPSO. More detailed particle microphysical properties are obtained from in situ measurements, but sampling is poor, and the suite of coincident measurements required for many applications is rarely acquired. Aerosol transport models can connect remote-sensing and in situ observations to specific aerosol sources, and extrapolate limited observational sampling in space and time. The biggest challenges to producing a global aerosol-type data record are filling gaps in detailed observations, maintaining global observing capabilities, and putting the pieces together. Obtaining detailed particle properties is probably the leading observational gap. One simplifying factor is that, for a given aerosol source and season, aerosol amounts can vary, but the particle properties tend to be repeatable. So an aircraft payload designed and deployed frequently enough to acquire the PDFs of the key variables could fill this gap; the SAM-CAAM (Systematic Aircraft Measurements to Characterize Aerosol Air Masses) concept aims at meeting this objective. Such data would add value to the entire satellite data record, improving the aerosol property assumptions in retrievals, and providing quantitative mass extinction efficiencies to translate between remote-sensing optical constraints and the aerosol mass book-kept in climate models. This will also help putting the pieces together in other ways, by improving the connection between remote-sensing particle types and those defined in models. The

  3. Carbonaceous aerosol tracers in ice-cores record multi-decadal climate oscillations

    PubMed Central

    Seki, Osamu; Kawamura, Kimitaka; Bendle, James A. P.; Izawa, Yusuke; Suzuki, Ikuko; Shiraiwa, Takayuki; Fujii, Yoshiyuki

    2015-01-01

    Carbonaceous aerosols influence the climate via direct and indirect effects on radiative balance. However, the factors controlling the emissions, transport and role of carbonaceous aerosols in the climate system are highly uncertain. Here we investigate organic tracers in ice cores from Greenland and Kamchatka and find that, throughout the period covered by the records (1550 to 2000 CE), the concentrations and composition of biomass burning-, soil bacterial- and plant wax- tracers correspond to Arctic and regional temperatures as well as the warm season Arctic Oscillation (AO) over multi-decadal time-scales. Specifically, order of magnitude decreases (increases) in abundances of ice-core organic tracers, likely representing significant decreases (increases) in the atmospheric loading of carbonaceous aerosols, occur during colder (warmer) phases in the high latitudinal Northern Hemisphere. This raises questions about causality and possible carbonaceous aerosol feedback mechanisms. Our work opens new avenues for ice core research. Translating concentrations of organic tracers (μg/kg-ice or TOC) from ice-cores, into estimates of the atmospheric loading of carbonaceous aerosols (μg/m3) combined with new model constraints on the strength and sign of climate forcing by carbonaceous aerosols should be a priority for future research. PMID:26411576

  4. Aerosol radiative effects over BIMSTEC regions

    NASA Astrophysics Data System (ADS)

    Kumar, Sumit; Kar, S. C.; Mupparthy, Raghavendra S.

    Aerosols can have variety of shapes, composition, sizes and other properties that influence their optical characteristics and thus the radiative impact. The visible impact of aerosol is the formation of haze, a layer of particles from vehicular, industrial emissions and biomass burning. The characterization of these fine particles is important for regulators and researchers because of their potential impact on human health, their ability to travel thousands of kilometers crossing international borders, and their influence on climate forcing and global warming. The Bay of Bengal Initiative for Multi-Sectoral Technical and Economic Cooperation (BIMSTEC) with Member Countries Bangladesh, Bhutan, India, Myanmar, Nepal, Sri Lanka and Thailand has emerged as an important regional group for technical and economic Cooperation. Continuing the quest for a deeper understanding of BIMSTEC countries weather and climate, in this paper we focused on aerosols and their direct radiative effects. Because of various contrasts like geophysical, agricultural practices, heterogeneous land/ocean surface, population etc these regions present an excellent natural laboratory for studying aerosol-meteorology interactions in tropical to sub-tropical environments. We exploited data available on multiple platforms (such as MISR, MODIS etc) and models (OPAC, SBDART etc) to compute the results. Ten regions were selected with different surface characteristics, also having considerable differences in the long-term trends and seasonal distribution of aerosols. In a preliminary analysis pertaining to pre-monsoon (March-April-May) of 2013, AOD _{555nm} is found to be maximum over Bangladesh (>0.52) and minimum over Bhutan (0.22), whereas other regions have intermediate values. Concurrent to these variability of AOD we found a strong reduction in incoming flux at surface of all the regions (> -25 Wm (-2) ), except Bhutan and Sri Lanka (< -18Wm (-2) ). The top of the atmosphere (TOA) forcing values are

  5. Climate Change Science Program Synthesis and Assessment Reports: Aerosol Properties and Their Impacts on Climate

    NASA Astrophysics Data System (ADS)

    Decola, P.; Moss, R.

    2004-12-01

    The Climate Change Science Program (CCSP) is developing and extending its research activities to support policymaking and adaptive management. The program includes a set of "Synthesis and Assessment Products," active participation in international assessments such as those of the Intergovernmental Panel on Climate Change, improvements in modeling and other resources to facilitate comparison of response options, and development, with users, of tools to support adaptive management and planning. These efforts are building on substantial ongoing efforts of agencies and departments participating in the CCSP. One of the products focuses on aerosol properties and their impact on climate. The very complex mixture of aerosol types and their spatial distributions provide diverse warming and cooling influences on climate, and impact the formation of both water droplets and ice crystals in clouds. Our poor understanding of aerosol properties and distributions results in large uncertainties about the net impact of aerosols on climate and impairs our ability to project climate changes. The product will be produced in two phases: Phase-I aims for a few explicit and focused scientific "review nuggets" in the near term that would be not only stand alone as CCSP-facilitated products, but that would also be useful input to community-wide activities like the IPCC and Phase-II that would connect and focus the new (2006/7) level of community-wide understanding of climate change (and aerosol-climate inclusively) to explicit decision-support information and tools. In this light, we have embarked on Phase I of a synthesis product entitled, "Aerosol properties and their impacts on climate," which addresses Goal 2, "Improve quantification of the forces bringing about changes in the Earth's climate and related systems," under the Strategic Plan of the CCSP. We present here the status of this first phase of work, which is focused on new assessment and synthesis information stimulated by the

  6. Transient Climate Impacts for Scenarios of Aerosol Emissions from Asia: A Story of Coal versus Gas

    NASA Astrophysics Data System (ADS)

    Grandey, B. S.; Cheng, H.; Wang, C.

    2014-12-01

    Projections of anthropogenic aerosol emissions are uncertain. In Asia, it is possible that emissions may increase if business continues as usual, with economic growth driving an increase in coal burning. But it is also possible that emissions may decrease rapidly due to the widespread adoption of cleaner technology or a shift towards non-coal fuels, such as natural gas. In this study, the transient climate impacts of three aerosol emissions scenarios are investigated: an RCP4.5 (Representative Concentration Pathway 4.5) control; a scenario with reduced Asian anthropogenic aerosol emissions; and a scenario with enhanced Asian anthropogenic aerosol emissions. A coupled atmosphere-ocean configuration of CESM (Community Earth System Model), including CAM5 (Community Atmosphere Model version 5), is used. Enhanced Asian aerosol emissions are found to delay global mean warming by one decade at the end of the century. Aerosol-induced suppression of the East Asian and South Asian summer monsoon precipitation occurs. The enhanced Asian aerosol emissions also remotely impact precipitation in other parts of the world: over the Sahel, West African monsoon precipitation is suppressed; and over Australia, austral summer monsoon precipitation is enhanced. These remote impacts on precipitation are associated with a southward shift of the ITCZ. The aerosol-induced sea surface temperature (SST) response appears to play an important role in the precipitation changes over South Asia and Australia, but not over East Asia. These results indicate that energy production in Asia, through the consequent aerosol emissions and associated radiative effects, might significantly influence future climate both locally and globally.

  7. Aerosol and Earth's Climate: A Perspective from Energy and Water Cycles

    NASA Astrophysics Data System (ADS)

    Li, Z.

    2014-12-01

    Aerosol particles can affect virtually all meteorological variables due to their direct and indirect effects by altering Earth's energy and water cycles. Heavy loading of aerosols reduce the amount of solar radiation reaching ground, that could lower surface temperature, reduce ocean-land contrast and thus affect monsoon system, whereas solar energy absorbed by aerosols alters atmospheric stability to have a feedback effect on atmospheric dynamics. By altering cloud microphysics and macrophysics, aerosols can also change cloud properties and precipitation frequency and amount. All of these can influence regional weather and climate in a dramatically. We have analyzed ample data from long-term routine measurements, intensive field experiments and global satellite products to study, together with some modeling studies, to study the impact of aerosol on global and regional climate. Particular attention will be given to the findings from our experiments as EAST-AIRE and EAST-AIRC, and DOE ARM Mobile Facility deployment in China where severe air pollution seems to have significantly impeded upon the regional climate and its long-term changes in terms of temperature, precipitation, thunderstorm, fog, atmospheric circulation, etc.

  8. Climate response of the South Asian monsoon system to anthropogenic aerosols

    SciTech Connect

    Ganguly, Dilip; Rasch, Philip J.; Wang, Hailong; Yoon, Jin-Ho

    2012-07-13

    The equilibrium climate response to the total effects (direct, indirect and semi-direct effects) of aerosols arising from anthropogenic and biomass burning emissions on the South Asian summer monsoon system is studied using a coupled atmosphere-slab ocean model. Our results suggest that anthropogenic and biomass burning aerosols generally induce a reduction in mean summer monsoon precipitation over most parts of the Indian subcontinent, strongest along the western coastline of the Indian peninsula and eastern Nepal region, but modest increases also occur over the north western part of the subcontinent. While most of the noted reduction in precipitation is triggered by increased emissions of aerosols from anthropogenic activities, modest increases in the north west are mostly associated with decreases in local emissions of aerosols from forest fire and grass fire sources. Anthropogenic aerosols from outside Asia also contribute to the overall reduction in precipitation but the dominant contribution comes from aerosol sources within Asia. Local emissions play a more important role in the total rainfall response to anthropogenic aerosol sources during the early monsoon period, whereas both local as well as remote emissions of aerosols play almost equally important roles during the later part of the monsoon period. While precipitation responses are primarily driven by local aerosol forcing, regional surface temperature changes over the region are strongly influenced by anthropogenic aerosols from sources further away (non-local changes). Changes in local anthropogenic organic and black carbon emissions by as much as a factor of two (preserving their ratio) produce the same basic signatures in the model's summer monsoon temperature and precipitation responses.

  9. Simulation of South Asian aerosols for regional climate studies

    NASA Astrophysics Data System (ADS)

    Nair, Vijayakumar S.; Solmon, Fabien; Giorgi, Filippo; Mariotti, Laura; Babu, S. Suresh; Moorthy, K. Krishna

    2012-02-01

    Extensive intercomparison of columnar and near-surface aerosols, simulated over the South Asian domain using the aerosol module included in the regional climate model (RegCM4) of the Abdus Salam International Centre for Theoretical Physics (ICTP) have been carried out using ground-based network of Sun/sky Aerosol Robotic Network (AERONET) radiometers, satellite sensors such as Moderate Resolution Imaging Spectroradiometer (MODIS) and Multiangle Imaging Spectroradiometer (MISR), and ground-based black carbon (BC) measurements made at Aerosol Radiative Forcing over India (ARFI) network stations. In general, RegCM4 simulations reproduced the spatial and seasonal characteristics of aerosol optical depth over South Asia reasonably well, particularly over west Asia, where mineral dust is a major contributor to the total aerosol loading. In contrast, RegCM4 simulations drastically underestimated the BC mass concentrations over most of the stations, by a factor of 2 to 5, with a large spatial variability. Seasonally, the discrepancy between the measured and simulated BC tended to be higher during winter and periods when the atmospheric boundary layer is convectively stable (such as nighttime and early mornings), while during summer season and during periods when the boundary layer is convectively unstable (daytime) the discrepancies were much lower, with the noontime values agreeing very closely with the observations. A detailed analysis revealed that the model does not reproduce the nocturnal high in BC, observed at most of the Indian sites especially during winter, because of the excessive vertical transport of aerosols under stable boundary layer conditions. As far as the vertical distribution was concerned, the simulated vertical profiles of BC agreed well with airborne measurements during daytime. This comprehensive validation exercise reveals the strengths and weaknesses of the model in simulating the spatial and temporal heterogeneities of the aerosol fields over

  10. Indian monsoon and the elevated-heat-pump mechanism in a coupled aerosol-climate model

    NASA Astrophysics Data System (ADS)

    D'Errico, Miriam; Cagnazzo, Chiara; Fogli, Pier Giuseppe; Lau, William K. M.; Hardenberg, Jost; Fierli, Federico; Cherchi, Annalisa

    2015-09-01

    A coupled aerosol-atmosphere-ocean-sea ice climate model is used to explore the interaction between aerosols and the Indian summer monsoon precipitation on seasonal-to-interannual time scales. Results show that when increased aerosol loading is found on the Himalayas slopes in the premonsoon period (April-May), intensification of early monsoon rainfall over India and increased low-level westerly flow follow, in agreement with the elevated-heat-pump mechanism. The increase in rainfall during the early monsoon season has a cooling effect on the land surface. In the same period, enhanced surface cooling may also be amplified through solar dimming by more cloudiness and aerosol loading, via increased dust transported by low-level westerly flow. The surface cooling causes subsequent reduction in monsoon rainfall in July-August over India. The time-lagged nature of the reasonably realistic response of the model to aerosol forcing suggests that absorbing aerosols, besides their potential key roles in impacting monsoon water cycle and climate, may influence the seasonal variability of the Indian summer monsoon.

  11. Aerosol-cloud-precipitation interactions in warm clouds in the PNNL-MMF multi-scale aerosol-climate model

    NASA Astrophysics Data System (ADS)

    Wang, M.; Ghan, S.; Liu, X.; Ovchinnikov, M.; Chand, D.; Qian, Y.; Easter, R. C.; Morrison, H.; Marchand, R.

    2011-12-01

    Aerosol-cloud-precipitation interactions in warm clouds are examined in the multi-scale aerosol-climate model PNNL-MMF, which is an extension of a multi-scale modeling framework (MMF) model. The extended model treats aerosol-cloud-precipitation interactions using a two-moment cloud microphysics scheme in the cloud-resolving model component of the MMF at much finer spatial and temporal scales than in conventional global climate models. The dependence of the probability of precipitation (POP) on liquid water path (LWP) and aerosol loading in the MMF model is in reasonable agreement with the satellite observations. In contrast, the dependence of POP on aerosol loading in a global model with a conventional cloud parameterization (Community Atmosphere Model Version 5, or CAM5) is much stronger than in the MMF and in the satellite observations. The stronger dependence of POP on aerosol loading in CAM5 is consistent with the much larger role played by autoconversion in rain production in CAM5 (48%) than that in the MMF model (3.2%). The better agreement in the dependence of POP on aerosol loading between the MMF model and the satellite observations suggests that the smaller indirect forcing in the MMF is more realistic. Rain susceptibility is further examined to explore how surface rain rate may depend on cloud droplet number concentration (CDNC) and aerosol loading. It is found that the rain susceptibility strongly depends on the relative contribution of autoconversion and accretion in rain production. In tropical marine clouds, surface rain rate is positively correlated with cloud-top droplet effective radius, consistent with satellite observations. However, surface rain rate and column-mean CDNC are not strongly correlated, as the relative contribution of autoconversion is small in these clouds. In mid-latitude marine clouds, autoconversion plays a more important role in rain production in the MMF model, especially at the intermediate LWPs (200-400 g m-2), which

  12. A Strategy to Assess Aerosol Direct Radiative Forcing of Climate Using Satellite Radiation Measurements

    NASA Technical Reports Server (NTRS)

    Kaufman, Yoram J.; Tanre, Didier; Einaudi, Franco (Technical Monitor)

    2001-01-01

    Atmospheric aerosols have a complex internal chemical composition and optical properties. Therefore it is difficult to model their impact on redistribution and absorption of solar radiation, and the consequent impact on atmospheric dynamics and climate. The use in climate models of isolated aerosol parameters retrieved from satellite data (e.g. optical thickness) may result in inconsistent calculations, if the model assumptions differ from these of the satellite retrieval schemes. Here we suggest a strategy to assess the direct impact of aerosol on the radiation budget at the top and bottom of the atmosphere using satellite and ground based measurements of the spectral solar radiation scattered by the aerosol. This method ensures consistent use of the satellite data and increases its accuracy. For Kaufman and Tanre: Strategy for aerosol direct forcing anthropogenic aerosol in the fine mode (e.g. biomass burning smoke and urban pollution) consistent use of satellite derived optical thickness can yield the aerosol impact on the spectral solar flux with accuracy an order of magnitude better than the optical thickness itself. For example, a simulated monthly average smoke optical thickness of 0.5 at 0.55 microns (forcing of 40-50 W/sq m) derived with an error of 20%, while the forcing can be measured directly with an error of only 0-2 W/sq m. Another example, the effect of large dust particles on reflection of solar flux can be derived three times better than retrievals of optical thickness. Since aerosol impacts not only the top of the atmosphere but also the surface irradiation, a combination of satellite and ground based measurements of the spectral flux, can be the most direct mechanism to evaluate the aerosol effect on climate and assimilate it in climate models. The strategy is applied to measurements from SCAR-B and the Tarfox experiments. In SCAR-B aircraft spectral data are used to derive the 24 hour radiative forcing of smoke at the top of the atmosphere of

  13. Impact of anthropogenic aerosols on regional climate change in Beijing, China

    NASA Astrophysics Data System (ADS)

    Zhao, B.; Liou, K. N.; He, C.; Lee, W. L.; Gu, Y.; Li, Q.; Leung, L. R.

    2015-12-01

    Anthropogenic aerosols affect regional climate significantly through radiative (direct and semi-direct) and indirect effects, but the magnitude of these effects over megacities are subject to large uncertainty. In this study, we evaluated the effects of anthropogenic aerosols on regional climate change in Beijing, China using the online-coupled Weather Research and Forecasting/Chemistry Model (WRF/Chem) with the Fu-Liou-Gu radiation scheme and a spatial resolution of 4km. We further updated this radiation scheme with a geometric-optics surface-wave (GOS) approach for the computation of light absorption and scattering by black carbon (BC) particles in which aggregation shape and internal mixing properties are accounted for. In addition, we incorporated in WRF/Chem a 3D radiative transfer parameterization in conjunction with high-resolution digital data for city buildings and landscape to improve the simulation of boundary-layer, surface solar fluxes and associated sensible/latent heat fluxes. Preliminary simulated meteorological parameters, fine particles (PM2.5) and their chemical components agree well with observational data in terms of both magnitude and spatio-temporal variations. The effects of anthropogenic aerosols, including BC, on radiative forcing, surface temperature, wind speed, humidity, cloud water path, and precipitation are quantified on the basis of simulation results. With several preliminary sensitivity runs, we found that meteorological parameters and aerosol radiative effects simulated with the incorporation of improved BC absorption and 3-D radiation parameterizations deviate substantially from simulation results using the conventional homogeneous/core-shell configuration for BC and the plane-parallel model for radiative transfer. Understanding of the aerosol effects on regional climate change over megacities must consider the complex shape and mixing state of aerosol aggregates and 3D radiative transfer effects over city landscape.

  14. An overview of geoengineering of climate using stratospheric sulphate aerosols.

    PubMed

    Rasch, Philip J; Tilmes, Simone; Turco, Richard P; Robock, Alan; Oman, Luke; Chen, Chih-Chieh; Stenchikov, Georgiy L; Garcia, Rolando R

    2008-11-13

    We provide an overview of geoengineering by stratospheric sulphate aerosols. The state of understanding about this topic as of early 2008 is reviewed, summarizing the past 30 years of work in the area, highlighting some very recent studies using climate models, and discussing methods used to deliver sulphur species to the stratosphere. The studies reviewed here suggest that sulphate aerosols can counteract the globally averaged temperature increase associated with increasing greenhouse gases, and reduce changes to some other components of the Earth system. There are likely to be remaining regional climate changes after geoengineering, with some regions experiencing significant changes in temperature or precipitation. The aerosols also serve as surfaces for heterogeneous chemistry resulting in increased ozone depletion. The delivery of sulphur species to the stratosphere in a way that will produce particles of the right size is shown to be a complex and potentially very difficult task. Two simple delivery scenarios are explored, but similar exercises will be needed for other suggested delivery mechanisms. While the introduction of the geoengineering source of sulphate aerosol will perturb the sulphur cycle of the stratosphere signicantly, it is a small perturbation to the total (stratosphere and troposphere) sulphur cycle. The geoengineering source would thus be a small contributor to the total global source of 'acid rain' that could be compensated for through improved pollution control of anthropogenic tropospheric sources. Some areas of research remain unexplored. Although ozone may be depleted, with a consequent increase to solar ultraviolet-B (UVB) energy reaching the surface and a potential impact on health and biological populations, the aerosols will also scatter and attenuate this part of the energy spectrum, and this may compensate the UVB enhancement associated with ozone depletion. The aerosol will also change the ratio of diffuse to direct energy

  15. An overview of geoengineering of climate using stratospheric sulphate aerosols

    SciTech Connect

    Rasch, Philip J.; Tilmes, S.; Turco, Richard P.; Robock, Alan; Oman, Luke; Chen, Chih-Chieh; Stenchikov, Georgiy; Garcia, Rolando R.

    2010-01-01

    We provide an overview of geoengineering by stratospheric sulphate aerosols. The state of understanding about this topic as of early 2008 is reviewed, summarizing the past 30 years of work in the area, highlighting some very recent studies using climate models, and discussing methods used to deliver sulphur species to the stratosphere. The studies reviewed here suggest that sulphate aerosols can counteract the globally averaged temperature increase associated with increasing greenhouse gases, and reduce changes to some other components of the Earth system. There are likely to be remaining regional climate changes after geoengineering, with some regions experiencing significant changes in temperature or precipitation. The aerosols also serve as surfaces for heterogeneous chemistry resulting in increased ozone depletion. The delivery of sulphur species to the stratosphere in a way that will produce particles of the right size is shown to be a complex and potentially very difficult task. Two simple delivery scenarios are explored, but similar exercises will be needed for other suggested delivery mechanisms. While the introduction of the geoengineering source of sulphate aerosol will perturb the sulphur cycle of the stratosphere signicantly, it is a small perturbation to the total (stratosphere and troposphere) sulphur cycle. The geoengineering source would thus be a small contributor to the total global source of ‘acid rain’ that could be compensated for through improved pollution control of anthropogenic tropospheric sources. Some areas of research remain unexplored. Although ozone may be depleted, with a consequent increase to solar ultraviolet-B (UVB) energy reaching the surface and a potential impact on health and biological populations, the aerosols will also scatter and attenuate this part of the energy spectrum, and this may compensate the UVB enhancement associated with ozone depletion. The aerosol will also change the ratio of diffuse to direct energy

  16. Aerosol-Induced Changes of Convective Cloud Anvils Produce Strong Climate Warming

    NASA Technical Reports Server (NTRS)

    Koren, I.; Remer, L. A.; Altaratz, O.; Martins, J. V.; Davidi, A.

    2010-01-01

    The effect of aerosol on clouds poses one of the largest uncertainties in estimating the anthropogenic contribution to climate change. Small human-induced perturbations to cloud characteristics via aerosol pathways can create a change in the top-of-atmosphere radiative forcing of hundreds of Wm(exp-2) . Here we focus on links between aerosol and deep convective clouds of the Atlantic and Pacific Intertropical Convergence Zones, noting that the aerosol environment in each region is entirely different. The tops of these vertically developed clouds consisting of mostly ice can reach high levels of the atmosphere, overshooting the lower stratosphere and reaching altitudes greater than 16 km. We show a link between aerosol, clouds and the free atmosphere wind profile that can change the magnitude and sign of the overall climate radiative forcing. We find that increased aerosol loading is associated with taller cloud towers and anvils. The taller clouds reach levels of enhanced wind speeds that act to spread and thin the anvi1 clouds, increasing areal coverage and decreasing cloud optical depth. The radiative effect of this transition is to create a positive radiative forcing (warming) at top-of-atmosphere. Furthermore we introduce the cloud optical depth (r), cloud height (Z) forcing space and show that underestimation of radiative forcing is likely to occur in cases of non homogenous clouds. Specifically, the mean radiative forcing of towers and anvils in the same scene can be several times greater than simply calculating the forcing from the mean cloud optical depth in the scene. Limitations of the method are discussed, alternative sources of aerosol loading are tested and meteorological variance is restricted, but the trend of taller clouds; increased and thinner anvils associated with increased aerosol loading remains robust through all the different tests and perturbations.

  17. Aerosol optical properties and their radiative effects in northern China

    NASA Astrophysics Data System (ADS)

    Li, Zhanqing; Xia, Xiangao; Cribb, Maureen; Mi, Wen; Holben, Brent; Wang, Pucai; Chen, Hongbin; Tsay, Si-Chee; Eck, T. F.; Zhao, Fengsheng; Dutton, E. G.; Dickerson, R. E.

    2007-11-01

    As a fast developing country covering a large territory, China is experiencing rapid environmental changes. High concentrations of aerosols with diverse properties are emitted in the region, providing a unique opportunity for understanding the impact of environmental changes on climate. Until very recently, few observational studies were conducted in the source regions. The East Asian Study of Tropospheric Aerosols: An International Regional Experiment (EAST-AIRE) attempts to characterize the physical, optical and chemical properties of the aerosols and their effects on climate over China. This study presents some preliminary results using continuous high-quality measurements of aerosol, cloud and radiative quantities made at the first EAST-AIRE baseline station at Xianghe, about 70 km east of Beijing over a period of one year (September 2004 to September 2005). It was found that the region is often covered by a thick layer of haze (with a yearly mean aerosol optical depth equal to 0.82 at 500 nm and maximum greater than 4) due primarily to anthropogenic emissions. An abrupt "cleanup" of the haze often took place in a matter of one day or less because of the passage of cold fronts. The mean single scattering albedo is approximately 0.9 but has strong day-to-day variations with maximum monthly averages occurring during the summer. Large aerosol loading and strong absorption lead to a very large aerosol radiative effect at the surface (the annual 24-hour mean values equals 24 W m-2), but a much smaller aerosol radiative effect at the top of the atmosphere (one tenth of the surface value). The boundary atmosphere is thus heated dramatically during the daytime, which may affect atmospheric stability and cloud formation. In comparison, the cloud radiative effect at the surface is only moderately higher (-41 W m-2) than the aerosol radiative effect at the surface.

  18. A Simple Model of Global Aerosol Indirect Effects

    NASA Technical Reports Server (NTRS)

    Ghan, Steven J.; Smith, Steven J.; Wang, Minghuai; Zhang, Kai; Pringle, Kirsty; Carslaw, Kenneth; Pierce, Jeffrey; Bauer, Susanne; Adams, Peter

    2013-01-01

    Most estimates of the global mean indirect effect of anthropogenic aerosol on the Earth's energy balance are from simulations by global models of the aerosol lifecycle coupled with global models of clouds and the hydrologic cycle. Extremely simple models have been developed for integrated assessment models, but lack the flexibility to distinguish between primary and secondary sources of aerosol. Here a simple but more physically based model expresses the aerosol indirect effect (AIE) using analytic representations of cloud and aerosol distributions and processes. Although the simple model is able to produce estimates of AIEs that are comparable to those from some global aerosol models using the same global mean aerosol properties, the estimates by the simple model are sensitive to preindustrial cloud condensation nuclei concentration, preindustrial accumulation mode radius, width of the accumulation mode, size of primary particles, cloud thickness, primary and secondary anthropogenic emissions, the fraction of the secondary anthropogenic emissions that accumulates on the coarse mode, the fraction of the secondary mass that forms new particles, and the sensitivity of liquid water path to droplet number concentration. Estimates of present-day AIEs as low as 5 W/sq m and as high as 0.3 W/sq m are obtained for plausible sets of parameter values. Estimates are surprisingly linear in emissions. The estimates depend on parameter values in ways that are consistent with results from detailed global aerosol-climate simulation models, which adds to understanding of the dependence on AIE uncertainty on uncertainty in parameter values.

  19. Indirect aerosol effect increases CMIP5 models projected Arctic warming

    DOE PAGES

    Chylek, Petr; Vogelsang, Timothy J.; Klett, James D.; Hengartner, Nicholas; Higdon, Dave; Lesins, Glen; Dubey, Manvendra K.

    2016-02-20

    Phase 5 of the Coupled Model Intercomparison Project (CMIP5) climate models’ projections of the 2014–2100 Arctic warming under radiative forcing from representative concentration pathway 4.5 (RCP4.5) vary from 0.9° to 6.7°C. Climate models with or without a full indirect aerosol effect are both equally successful in reproducing the observed (1900–2014) Arctic warming and its trends. However, the 2014–2100 Arctic warming and the warming trends projected by models that include a full indirect aerosol effect (denoted here as AA models) are significantly higher (mean projected Arctic warming is about 1.5°C higher) than those projected by models without a full indirect aerosolmore » effect (denoted here as NAA models). The suggestion is that, within models including full indirect aerosol effects, those projecting stronger future changes are not necessarily distinguishable historically because any stronger past warming may have been partially offset by stronger historical aerosol cooling. In conclusion, the CMIP5 models that include a full indirect aerosol effect follow an inverse radiative forcing to equilibrium climate sensitivity relationship, while models without it do not.« less

  20. Impacts of Snow Darkening by Absorbing Aerosols on Eurasian Climate

    NASA Technical Reports Server (NTRS)

    Kim, Kyu-Myong; Lau, William K M.; Yasunari, Teppei J.; Kim, Maeng-Ki; Koster, Randal D.

    2016-01-01

    The deposition of absorbing aerosols on snow surfaces reduces snow-albedo and allows snowpack to absorb more sunlight. This so-called snow darkening effect (SDE) accelerates snow melting and leads to surface warming in spring. To examine the impact of SDE on weather and climate during late spring and early summer, two sets of NASA GEOS-5 model simulations with and without SDE are conducted. Results show that SDE-induced surface heating is particularly pronounced in Eurasian regions where significant depositions of dust transported from the North African deserts, and black carbon from biomass burning from Asia and Europe occur. In these regions, the surface heating due to SDE increases surface skin temperature by 3-6 degrees Kelvin near the snowline in spring. Surface energy budget analysis indicates that SDE-induced excess heating is associated with a large increase in surface evaporation, subsequently leading to a significant reduction in soil moisture, and increased risks of drought and heat waves in late spring to early summer. Overall, we find that rainfall deficit combined with SDE-induced dry soil in spring provide favorable condition for summertime heat waves over large regions of Eurasia. Increased frequency of summer heat waves with SDE and the region of maximum increase in heat-wave frequency are found along the snow line, providing evidence that early snowmelt by SDE may increase the risks of extreme summer heat wave. Our results suggest that climate models that do not include SDE may significantly underestimate the effect of global warming over extra-tropical continental regions.

  1. Chapter 3: Evaluating the impacts of carbonaceous aerosols on clouds and climate

    SciTech Connect

    Menon, Surabi; Del Genio, Anthony D.

    2007-09-03

    Any attempt to reconcile observed surface temperature changes within the last 150 years to changes simulated by climate models that include various atmospheric forcings is sensitive to the changes attributed to aerosols and aerosol-cloud-climate interactions, which are the main contributors that may well balance the positive forcings associated with greenhouse gases, absorbing aerosols, ozone related changes, etc. These aerosol effects on climate, from various modeling studies discussed in Menon (2004), range from +0.8 to -2.4 W m{sup -2}, with an implied value of -1.0 W m{sup -2} (range from -0.5 to -4.5 W m{sup -2}) for the aerosol indirect effects. Quantifying the contribution of aerosols and aerosol-cloud interactions remain complicated for several reasons some of which are related to aerosol distributions and some to the processes used to represent their effects on clouds. Aerosol effects on low lying marine stratocumulus clouds that cover much of the Earth's surface (about 70%) have been the focus of most of prior aerosol-cloud interaction effect simulations. Since cumulus clouds (shallow and deep convective) are short lived and cover about 15 to 20% of the Earth's surface, they are not usually considered as radiatively important. However, the large amount of latent heat released from convective towers, and corresponding changes in precipitation, especially in biomass regions due to convective heating effects (Graf et al. 2004), suggest that these cloud systems and aerosol effects on them, must be examined more closely. The radiative heating effects for mature deep convective systems can account for 10-30% of maximum latent heating effects and thus cannot be ignored (Jensen and Del Genio 2003). The first study that isolated the sensitivity of cumulus clouds to aerosols was from Nober et al. (2003) who found a reduction in precipitation in biomass burning regions and shifts in circulation patterns. Aerosol effects on convection have been included in other

  2. Global Atmospheric Aerosol Modeling

    NASA Technical Reports Server (NTRS)

    Hendricks, Johannes; Aquila, Valentina; Righi, Mattia

    2012-01-01

    Global aerosol models are used to study the distribution and properties of atmospheric aerosol particles as well as their effects on clouds, atmospheric chemistry, radiation, and climate. The present article provides an overview of the basic concepts of global atmospheric aerosol modeling and shows some examples from a global aerosol simulation. Particular emphasis is placed on the simulation of aerosol particles and their effects within global climate models.

  3. Spatial patterns of substantial climate impact from anthropogenic aerosols in the early instrumental period

    NASA Astrophysics Data System (ADS)

    Undorf, Sabine; Bollasina, Massimo; Hegerl, Gabriele

    2016-04-01

    While many aspects of climate variation in the early instrumental period (1860-1950) are still unexplained, for instance the early twentieth-century warming from the 1910s to the 1940s, the role of anthropogenic aerosols in this period has been overlooked. Yet, the period is also an interesting case study to isolate aerosol impacts since it is characterised by the increase of North American and especially European aerosol emissions concurrently with negligible Asian emissions and relatively low carbon dioxide concentrations. We thus analyse the spatial and temporal patterns of aerosol impact for this period in available observations (NOAA 20th-century reanalysis, etc.) and historical single-forcing and all-forcing experiments with state-of-the-art CMIP5 models. We make use of coupled empirical orthogonal functions (EOFs) applied to surface temperature -the most reliable variable in observations- and different aerosol indicating variables such as aerosol optical depth and short-wave downward radiation, some of which include aerosol indirect effects. The principal components of the most important EOFs are then regressed onto sea level pressure, winds, and other variables to identify associated circulation patterns. A decomposition into multi-decadal and longer time scales is performed by filtering the data prior to the analysis. Our analysis reveals both statistically significant local and non-local aerosol impact and identifies circulation states associated with the temperature response. The results are consistent across different aerosol variables, and show a strong non-local response as well as specific differences between time scales. We find a distinctive circulation pattern which strongly resembles observations and might explain the observed early twentieth century warming in the Arctic.

  4. The Joint Aerosol-Monsoon Experiment: A New Challenge to Monsoon Climate Research

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.

    2008-01-01

    Aerosol and monsoon related droughts and floods are two of the most serious environmental hazards confronting more than 60% of the population of the world living in the Asian monsoon countries. In recent years, thanks to improved satellite and in-situ observations, and better models, great strides have been made in aerosol, and monsoon research respectively. There is now a growing body of evidence suggesting that interaction of aerosol forcing with water cycle dynamics in monsoon regions may substantially alter the redistribution of energy at the earth surface and in the atmosphere, and therefore significantly impact monsoon rainfall variability and long term trends. In this talk, I will describe issues related to societal needs, scientific background, and challenges in studies of aerosol-water cycle interaction in Asian monsoon regions. As a first step towards addressing these issues, the authors call for an integrated observation and modeling research approach aimed at the interactions between aerosol chemistry and radiative effects and monsoon dynamics of the coupled ocean-atmosphere-land system. A Joint Aerosol-Monsoon Experiment (JAMEX) is proposed for 2007-2011, with an enhanced observation period during 2008-09, encompassing diverse arrays of observations from surface, aircraft, unmanned aerial vehicles, and satellites of physical and chemical properties of aerosols, long range aerosol transport as well as meteorological and oceanographic parameters in the Indo-Pacific Asian monsoon region. JAMEX will leverage on coordination among many ongoing and planned national programs on aerosols and monsoon research in China, India, Japan, Nepal, Italy, US, as well as international research programs of the World Climate Research Program (WCRP) and the World Meteorological Organization (WMO).

  5. Quantifying the uncertainties of aerosol indirect effects and impacts on decadal-scale climate variability in NCAR CAM5 and CESM1

    SciTech Connect

    Park, Sungsu

    2014-12-12

    The main goal of this project is to systematically quantify the major uncertainties of aerosol indirect effects due to the treatment of moist turbulent processes that drive aerosol activation, cloud macrophysics and microphysics in response to anthropogenic aerosol perturbations using the CAM5/CESM1. To achieve this goal, the P.I. hired a postdoctoral research scientist (Dr. Anna Fitch) who started her work from the Nov.1st.2012. In order to achieve the project goal, the first task that the Postdoc. and the P.I. did was to quantify the role of subgrid vertical velocity variance on the activation and nucleation of cloud liquid droplets and ice crystals and its impact on the aerosol indirect effect in CAM5. First, we analyzed various LES cases (from dry stable to cloud-topped PBL) to check whether this isotropic turbulence assumption used in CAM5 is really valid. It turned out that this isotropic turbulence assumption is not universally valid. Consequently, from the analysis of LES, we derived an empirical formulation relaxing the isotropic turbulence assumption used for the CAM5 aerosol activation and ice nucleation, and implemented the empirical formulation into CAM5/CESM1, and tested in the single-column and global simulation modes, and examined how it changed aerosol indirect effects in the CAM5/CESM1. These results were reported in the poster section in the 18th Annual CESM workshop held in Breckenridge, CO during Jun.17-20.2013. While we derived an empirical formulation from the analysis of couple of LES from the first task, the general applicability of that empirical formulation was questionable, because it was obtained from the limited number of LES simulations. The second task we did was to derive a more fundamental analytical formulation relating vertical velocity variance to TKE using other information starting from basic physical principles. This was a somewhat challenging subject, but if this could be done in a successful way, it could be directly

  6. Geo-Engineering Climate Change with Sulfate Aerosol

    NASA Astrophysics Data System (ADS)

    Rasch, P. J.; Crutzen, P. J.

    2006-12-01

    We explore the impact of injecting a precursor of sulfate aerosols into the middle atmosphere where they would act to increase the planetary albedo and thus counter some of the effects of greenhouse gase forcing. We use an atmospheric general circulation model (CAM, the Community Atmosphere Model) coupled to a slab ocean model for this study. Only physical effects are examined, that is we ignore the biogeochemical and chemical implications of changes to greenhouse gases and aerosols, and do not explore the important ethical, legal, and moral issues that are associated with deliberate geo-engineering efforts. The simulations suggest that the sulfate aerosol produced from the SO2 source in the stratosphere is sufficient to counterbalance most of the warming associated with the greenhouse gas forcing. Surface temperatures return to within a few tenths of a degree(K) of present day levels. Sea ice and precipitation distributions are also much closer to their present day values. The polar region surface temperatures remain 1-3 degrees warm in the winter hemisphere than present day values. This study is very preliminary. Only a subset of the relevant effects have been explored. The effect of such an injection of aerosols on middle atmospheric chemistry, and the effect on cirrus clouds are obvious missing components that merit scrutiny. There are probably others that should be considered. The injection of such aerosols cannot help in ameliorating the effects of CO2 changes on ocean PH, or other effects on the biogeochemistry of the earth system.

  7. Biotic stress accelerates formation of climate-relevant aerosols in boreal forests

    NASA Astrophysics Data System (ADS)

    Joutsensaari, J.; Yli-Pirilä, P.; Korhonen, H.; Arola, A.; Blande, J. D.; Heijari, J.; Kivimäenpää, M.; Mikkonen, S.; Hao, L.; Miettinen, P.; Lyytikäinen-Saarenmaa, P.; Faiola, C. L.; Laaksonen, A.; Holopainen, J. K.

    2015-11-01

    Boreal forests are a major source of climate-relevant biogenic secondary organic aerosols (SOAs) and will be greatly influenced by increasing temperature. Global warming is predicted to not only increase emissions of reactive biogenic volatile organic compounds (BVOCs) from vegetation directly but also induce large-scale insect outbreaks, which significantly increase emissions of reactive BVOCs. Thus, climate change factors could substantially accelerate the formation of biogenic SOAs in the troposphere. In this study, we have combined results from field and laboratory experiments, satellite observations and global-scale modelling in order to evaluate the effects of insect herbivory and large-scale outbreaks on SOA formation and the Earth's climate. Field measurements demonstrated 11-fold and 20-fold increases in monoterpene and sesquiterpene emissions respectively from damaged trees during a pine sawfly (Neodiprion sertifer) outbreak in eastern Finland. Laboratory chamber experiments showed that feeding by pine weevils (Hylobius abietis) increased VOC emissions from Scots pine and Norway spruce seedlings by 10-50 fold, resulting in 200-1000-fold increases in SOA masses formed via ozonolysis. The influence of insect damage on aerosol concentrations in boreal forests was studied with a global chemical transport model GLOMAP and MODIS satellite observations. Global-scale modelling was performed using a 10-fold increase in monoterpene emission rates and assuming 10 % of the boreal forest area was experiencing outbreak. Results showed a clear increase in total particulate mass (local max. 480 %) and cloud condensation nuclei concentrations (45 %). Satellite observations indicated a 2-fold increase in aerosol optical depth over western Canada's pine forests in August during a bark beetle outbreak. These results suggest that more frequent insect outbreaks in a warming climate could result in substantial increase in biogenic SOA formation in the boreal zone and, thus

  8. Biotic stress accelerates formation of climate-relevant aerosols in boreal forests

    NASA Astrophysics Data System (ADS)

    Joutsensaari, J.; Yli-Pirilä, P.; Korhonen, H.; Arola, A.; Blande, J. D.; Heijari, J.; Kivimäenpää, M.; Mikkonen, S.; Hao, L.; Miettinen, P.; Lyytikäinen-Saarenmaa, P.; Faiola, C. L.; Laaksonen, A.; Holopainen, J. K.

    2015-04-01

    Boreal forests are a major source of climate-relevant biogenic secondary organic aerosols (SOA) and will be greatly influenced by increasing temperature. Global warming is predicted to increase emissions of reactive biogenic volatile organic compounds (BVOC) from vegetation directly, but will also induce large-scale insect outbreaks, which significantly increase emissions of reactive BVOC. Thus, climate change factors could substantially accelerate the formation of biogenic SOA in the troposphere. In this study, we have combined results from field and laboratory experiments, satellite observations and global scale modelling in order to evaluate the effects of insect herbivory and large-scale outbreaks on SOA formation and the Earth's climate. Field measurements demonstrated 11-fold and 20-fold increases in monoterpene and sesquiterpene emissions, respectively, from damaged trees during a pine sawfly (Neodiprion sertifer) outbreak in eastern Finland. Laboratory chamber experiments showed that feeding by pine weevils (Hylobius abietis) increased VOC emissions from Scots pine and Norway spruce seedlings by 10-50 fold resulting in 200-1000 fold increases in SOA masses formed via ozonolysis. The influence of insect damage on aerosol concentrations in boreal forests was studied with a global chemical transport model GLOMAP and MODIS satellite observations. Global scale modelling was performed using a 10-fold increase in monoterpene emission rates and assuming 10% of the boreal forest area was experiencing outbreak. Results showed a clear increase in total particulate mass (local max. 480%) and cloud condensation nuclei concentrations (45%). Satellite observations indicated a two-fold increase in aerosol optical depth (AOD) over western Canada's pine forests in August during a bark beetle outbreak. These results suggest that more frequent insect outbreaks in a warming climate could result in substantial increase in biogenic SOA formation in the boreal zone and, thus

  9. Aerosol-climate interactions over southern Africa: the ENSO signal and interannual variability

    NASA Astrophysics Data System (ADS)

    Tummon, Fiona

    2010-05-01

    Southern Africa is a region that experiences high interannual climatic variability. It is also a region that, in general is poorly developed, has a high population growth rate and is at times politically unstable. As a whole, the region is extremely vulnerable to climatic changes, with a large proportion of the population depending on rain-fed agriculture as a source of income and subsistence. It is well known that the El-Nino/La-Nina oscillation contributes significantly to the climate variability over much of southern Africa; with El-Nino years generally being dry and warm in the southeastern parts and unusually wet in the eastern equatorial regions, whilst La-Nina years are generally wet and cool in the southeast, but dry in the eastern tropics. This in turn effects vegetation growth, and as a result the extent of biomass burning in the following dry season; with above-average wet seasons leading to increased burning, and drier than average seasons being followed by less extensive burning. The savannas of Africa experience some of the most extensive burning in the world, and contribute a very significant portion of the aerosol loading over southern Africa during the dry austral winter season, from June through October. At present, however, the climatic impact of aerosols over southern Africa is poorly understood, particularly in terms of the interannual variability of these impacts. The regional climate model RegCM3 is used to investigate the climatic impacts of the aerosol burden over southern African further, with particular focus on interannual variability and the role of ENSO. Preliminary results indicate that the impacts of the direct and semi-direct aerosol-effects on regional temperature, precipitation and circulation patterns vary between dry (El-Nino) and wet (La-Nina) years. There is a strong seasonality to these effects, with significant impacts occurring only during the austral winter, when biomass burning peaks throughout the southern Africa

  10. Future Climate Impacts of Direct Radiative Forcing Anthropogenic Aerosols, Tropospheric Ozone, and Long-lived Greenhouse Gases

    NASA Technical Reports Server (NTRS)

    Chen, Wei-Ting; Liao, Hong; Seinfeld, John H.

    2007-01-01

    Long-lived greenhouse gases (GHGs) are the most important driver of climate change over the next century. Aerosols and tropospheric ozone (O3) are expected to induce significant perturbations to the GHG-forced climate. To distinguish the equilibrium climate responses to changes in direct radiative forcing of anthropogenic aerosols, tropospheric ozone, and GHG between present day and year 2100, four 80-year equilibrium climates are simulated using a unified tropospheric chemistry-aerosol model within the Goddard Institute for Space Studies (GISS) general circulation model (GCM) 110. Concentrations of sulfate, nitrate, primary organic (POA) carbon, secondary organic (SOA) carbon, black carbon (BC) aerosols, and tropospheric ozone for present day and year 2100 are obtained a priori by coupled chemistry-aerosol GCM simulations, with emissions of aerosols, ozone, and precursors based on the Intergovernmental Panel on Climate Change (IPCC) Special Report on Emissions Scenario (SRES) A2. Changing anthropogenic aerosols, tropospheric ozone, and GHG from present day to year 2100 is predicted to perturb the global annual mean radiative forcing by +0.18 (considering aerosol direct effects only), +0.65, and +6.54 W m(sup -2) at the tropopause, and to induce an equilibrium global annual mean surface temperature change of +0.14, +0.32, and +5.31 K, respectively, with the largest temperature response occurring at northern high latitudes. Anthropogenic aerosols, through their direct effect, are predicted to alter the Hadley circulation owing to an increasing interhemispheric temperature gradient, leading to changes in tropical precipitation. When changes in both aerosols and tropospheric ozone are considered, the predicted patterns of change in global circulation and the hydrological cycle are similar to those induced by aerosols alone. GHG-induced climate changes, such as amplified warming over high latitudes, weakened Hadley circulation, and increasing precipitation over the

  11. Global Aerosol Direct Radiative Effect From CALIOP and C3M

    NASA Technical Reports Server (NTRS)

    Winker, Dave; Kato, Seiji; Tackett, Jason

    2015-01-01

    Aerosols are responsible for the largest uncertainties in current estimates of climate forcing. These uncertainties are due in part to the limited abilities of passive sensors to retrieve aerosols in cloudy skies. We use a dataset which merges CALIOP observations together with other A-train observations to estimate aerosol radiative effects in cloudy skies as well as in cloud-free skies. The results can be used to quantify the reduction of aerosol radiative effects in cloudy skies relative to clear skies and to reduce current uncertainties in aerosol radiative effects.

  12. International Workshop on Stratospheric Aerosols: Measurements, Properties, and Effects

    NASA Technical Reports Server (NTRS)

    Pueschel, Rudolf F. (Editor)

    1991-01-01

    Following a mandate by the International Aerosol Climatology Program under the auspices of International Association of Meteorology and Atmospheric Physics International Radiation Commission, 45 scientists from five nations convened to discuss relevant issues associated with the measurement, properties, and effects of stratospheric aerosols. A summary is presented of the discussions on formation and evolution, transport and fate, effects on climate, role in heterogeneous chemistry, and validation of lidar and satellite remote sensing of stratospheric aerosols. Measurements are recommended of the natural (background) and the volcanically enhanced aerosol (sulfuric acid and silica particles), the exhaust of shuttle, civil aviation and supersonic aircraft operations (alumina, soot, and ice particles), and polar stratospheric clouds (ice, condensed nitric and hydrochloric acids).

  13. The impact of residential combustion emissions on atmospheric aerosol, human health and climate

    NASA Astrophysics Data System (ADS)

    Butt, E. W.; Rap, A.; Schmidt, A.; Reddington, C.; Scott, C.; Pringle, K.; Woodhouse, M.; Spracklen, D. V.

    2015-12-01

    Combustion of fuels in the residential sector for cooking and heating, results in the emission of aerosol and aerosol precursors that effect air quality, human health and climate. Residential emissions are dominated by the combustion of solid fuels which are the primary energy source for nearly half the world's population. Despite this importance, residential emissions are poorly quantified, as are their impacts on air quality and climate. We used a global aerosol microphysics model to simulate the impact of residential emissions on atmospheric aerosol in the year 2000, and evaluated simulated concentrations against surface observations of aerosol mass and number. Residential emissions make the largest contributions to surface particulate matter (PM2.5) concentrations in East Asia, South Asia and Eastern Europe, matching regions of greatest emissions. We used concentration response functions to estimate a global annual excess adult (> 30 years of age) premature mortality due to residential emissions of between 113, 300 and 827, 000 when uncertainties in both residential emissions and health effects of PM2.5 were accounted for. Premature mortality was greatest in Asia, with China and India accounting for 50% of simulated global excess mortality. Using an offline radiative transfer model, we show that residential emissions exerted a global annual mean direct radiative effect of between -66 mW m-2 and +21 mW m-2, accounting for uncertainties in emissions flux and assumed ratio of carbonaceous and sulphur emissions. Residential emissions exerted a negative global annual mean first aerosol indirect effect of between -52 mW m-2 and -16 mW m-2, which was found to be sensitive to the assumed size distribution of carbonaceous emissions. Our results demonstrate that reducing residential combustion emissions would have substantial benefits for human health through reductions in ambient PM2.5 concentrations.

  14. Direct and semidirect aerosol effects of southern African biomass burning aerosol

    NASA Astrophysics Data System (ADS)

    Sakaeda, Naoko; Wood, Robert; Rasch, Philip J.

    2011-06-01

    southern Sahel. The changes are consistent with the low-level aerosol-forced cooling pattern. The results highlight the importance of semidirect radiative effects and precipitation responses for determining the climatic effects of aerosols in the African region.

  15. Direct and semidirect aerosol effects of Southern African biomass burning aerosol

    SciTech Connect

    Sakaeda, Naoko; Wood, Robert; Rasch, Philip J.

    2011-06-21

    importance of semi-direct radiative effects and precipitation responses for determining the climatic effects of aerosols in the African region.

  16. Modeling of aerosol properties related to direct climate forcing

    NASA Astrophysics Data System (ADS)

    Koloutsou-Vakakis, Sotiria; Rood, Mark J.; Nenes, Athanasios; Pilinis, Christodoulos

    1998-07-01

    A long-term local experiment was designed with the purpose to accurately quantify aerosol parameters needed in order to estimate aerosol climate forcing at an anthropogenically perturbed continental site. Total light-scattering σλ,sp and backscattering σλ,bsp coefficients at wavelength λ, the hygroscopic growth factors with respect to scattering, ƒ(RH)λ,s, and the backscatter ratio bλ are the parameters considered in the paper. Reference and controlled relative humidity nephelometry measurements were taken at a ground level field sampling station, located near Bondville Illinois (40°03'12″N, W 88°22'19″W). Aerosol particle chemical composition and mass particle size distributions were also measured. The target parameters were also estimated from models. The modeling approach involved a two-step process. In the first step, aerosol properties were parameterized with an approach that made use of a modified thermodynamic equilibrium model, published laboratory measurements of single hygroscopic particle properties, and empirical mixing rules. In the second step, the parameterized aerosol properties were used as inputs into a code that calculate σλ,sp and σλ,bsp as functions of λ, RH, particle size, and composition. Comparison between the measured and the modeled results showed that depending on the assumptions, the differences between the modeled and observed results were within 5 to 28% for ƒ(RH)λ,s and within 22-35% for bλ at low RH and 0-20% for bλ at high RH. The temporal variation of the particle size distribution, the equilibrium state of the particles, and the hygroscopicity of the material characterized as residual were the major factors limiting the predictive ability of the models.

  17. Constraining cloud lifetime effects of aerosols using A-Train satellite observations

    SciTech Connect

    Wang, Minghuai; Ghan, Steven J.; Liu, Xiaohong; Ecuyer, Tristan L.; Zhang, Kai; Morrison, H.; Ovchinnikov, Mikhail; Easter, Richard C.; Marchand, Roger; Chand, Duli; Qian, Yun; Penner, Joyce E.

    2012-08-15

    Aerosol indirect effects have remained the largest uncertainty in estimates of the radiative forcing of past and future climate change. Observational constraints on cloud lifetime effects are particularly challenging since it is difficult to separate aerosol effects from meteorological influences. Here we use three global climate models, including a multi-scale aerosol-climate model PNNL-MMF, to show that the dependence of the probability of precipitation on aerosol loading, termed the precipitation frequency susceptibility (S{sub pop}), is a good measure of the liquid water path response to aerosol perturbation ({lambda}), as both Spop and {lambda} strongly depend on the magnitude of autoconversion, a model representation of precipitation formation via collisions among cloud droplets. This provides a method to use satellite observations to constrain cloud lifetime effects in global climate models. S{sub pop} in marine clouds estimated from CloudSat, MODIS and AMSR-E observations is substantially lower than that from global climate models and suggests a liquid water path increase of less than 5% from doubled cloud condensation nuclei concentrations. This implies a substantially smaller impact on shortwave cloud radiative forcing (SWCF) over ocean due to aerosol indirect effects than simulated by current global climate models (a reduction by one-third for one of the conventional aerosol-climate models). Further work is needed to quantify the uncertainties in satellite-derived estimates of S{sub pop} and to examine S{sub pop} in high-resolution models.

  18. Constraining cloud lifetime effects of aerosols using A-Train satellite observations

    NASA Astrophysics Data System (ADS)

    Wang, Minghuai; Ghan, Steven; Liu, Xiaohong; L'Ecuyer, Tristan S.; Zhang, Kai; Morrison, Hugh; Ovchinnikov, Mikhail; Easter, Richard; Marchand, Roger; Chand, Duli; Qian, Yun; Penner, Joyce E.

    2012-08-01

    Aerosol indirect effects have remained the largest uncertainty in estimates of the radiative forcing of past and future climate change. Observational constraints on cloud lifetime effects are particularly challenging since it is difficult to separate aerosol effects from meteorological influences. Here we use three global climate models, including a multi-scale aerosol-climate model PNNL-MMF, to show that the dependence of the probability of precipitation on aerosol loading, termed the precipitation frequency susceptibility (Spop), is a good measure of the liquid water path response to aerosol perturbation (λ), as both Spop and λ strongly depend on the magnitude of autoconversion, a model representation of precipitation formation via collisions among cloud droplets. This provides a method to use satellite observations to constrain cloud lifetime effects in global climate models. Spop in marine clouds estimated from CloudSat, MODIS and AMSR-E observations is substantially lower than that from global climate models and suggests a liquid water path increase of less than 5% from doubled cloud condensation nuclei concentrations. This implies a substantially smaller impact on shortwave cloud radiative forcing over ocean due to aerosol indirect effects than simulated by current global climate models (a reduction by one-third for one of the conventional aerosol-climate models). Further work is needed to quantify the uncertainties in satellite-derived estimates of Spop and to examine Spop in high-resolution models.

  19. Impact on aerosol emissions in China and India on local and global climate

    NASA Astrophysics Data System (ADS)

    Kühn, Thomas; Partanen, Antti-Ilari; Henriksson, Svante V.; Bergman, Tommi; Laakso, Anton; Kokkola, Harri; Romakkaniemi, Sami; Laaksonen, Ari

    2013-04-01

    Existing surface temperature records show warming in the beginning of last century, followed by cooling starting from 1940 and again strong heating from 1975 until recent years. This behaviour has been attributed to increase in the greenhouse gas and aerosol emission as well as to natural variability of climate. Making a difference between these is crucial as climate predictions and international policy related to emission reductions are based on the models that are mainly evaluated against the historical temperature records. While in Europe and North America the aerosol emissions have decreased since the late 1970s, the emissions in China and India have started to increase dramatically at about the same time and have only recently started to stagnate due to new regulations in China. Here we use emission scenarios from the years 1996 through 2010 to assess the effect that these emissions have on local aerosol properties and climate as well as on the global climate. We use the aerosol-climate model ECHAM5-HAM [Roeckner2003, Roeckner2004] to simulate the local aerosol properties in China and India in the years 1996 through 2010, and their impact on local as well as global climate. For anthropogenic aerosol greenhouse gas emissions we use the ACCMIP-MACCity Aerocom emissions (Aerocom 2) [Lamarque2010] in combination with the emissions for China and India after Lu et. al [Lu2011] for the mentioned period of time. To assess the effect of anthropogenic aerosol emissions on earth's climate is assessed using the ECHAM-HAM model coupled to a mixed layer ocean on a T42L19 grid. The model is run with fixed yearly emissions for several emission scenarios (e.g. for the years 1996 and 2010), with data derived from 100-year averages. Additionally we run a number of transient simulations (i.e. with varying yearly emissions) from 1996 to 2010 in the attempt to extract a climate trend for the given period. References [Roeckner2003] Roeckner, E., Bäuml, R., Bonaventura, L., Brokopf

  20. Advancing Models and Evaluation of Cumulus, Climate and Aerosol Interactions

    SciTech Connect

    Gettelman, Andrew

    2015-10-27

    This project was successfully able to meet its’ goals, but faced some serious challenges due to personnel issues. Nonetheless, it was largely successful. The Project Objectives were as follows: 1. Develop a unified representation of stratifom and cumulus cloud microphysics for NCAR/DOE global community models. 2. Examine the effects of aerosols on clouds and their impact on precipitation in stratiform and cumulus clouds. We will also explore the effects of clouds and precipitation on aerosols. 3. Test these new formulations using advanced evaluation techniques and observations and release

  1. Estimation of Aerosol Direct Radiative Effects from Satellite and In Situ Measurements

    NASA Technical Reports Server (NTRS)

    Bergstrom, Robert W.; Russell, Philip B.; Schmid, Beat; Redemann, Jens; McIntosh, Dawn

    2000-01-01

    Ames researchers have combined measurements from satellite, aircraft, and the surface to estimate the effect of airborne particles (aerosols) on the solar radiation over the North Atlantic region. These aerosols (which come from both natural and pollution sources) can reflect solar radiation, causing a cooling effect that opposes the warming caused by carbon dioxide. Recently, increased attention has been paid to aerosol effects to better understand the Earth climate system.

  2. Integrating biomass, sulphate and sea-salt aerosol responses into a microphysical chemical parcel model: implications for climate studies.

    PubMed

    Ghosh, S; Smith, M H; Rap, A

    2007-11-15

    Aerosols are known to influence significantly the radiative budget of the Earth. Although the direct effect (whereby aerosols scatter and absorb solar and thermal infrared radiation) has a large perturbing influence on the radiation budget, the indirect effect (whereby aerosols modify the microphysical and hence the radiative properties and amounts of clouds) poses a greater challenge to climate modellers. This is because aerosols undergo chemical and physical changes while in the atmosphere, notably within clouds, and are removed largely by precipitation. The way in which aerosols are processed by clouds depends on the type, abundance and the mixing state of the aerosols concerned. A parametrization with sulphate and sea-salt aerosol has been successfully integrated within the Hadley Centre general circulation model (GCM). The results of this combined parametrization indicate a significantly reduced role, compared with previous estimates, for sulphate aerosol in cloud droplet nucleation and, consequently, in indirect radiative forcing. However, in this bicomponent system, the cloud droplet number concentration, N(d) (a crucial parameter that is used in GCMs for radiative transfer calculations), is a smoothly varying function of the sulphate aerosol loading. Apart from sea-salt and sulphate aerosol particles, biomass aerosol particles are also present widely in the troposphere. We find that biomass smoke can significantly perturb the activation and growth of both sulphate and sea-salt particles. For a fixed salt loading, N(d) increases linearly with modest increases in sulphate and smoke masses, but significant nonlinearities are observed at higher non-sea-salt mass loadings. This non-intuitive N(d) variation poses a fresh challenge to climate modellers.

  3. What We Can Say About the Roles of Natural and Anthropogenic Aerosols in Climate Change

    NASA Astrophysics Data System (ADS)

    Kahn, Ralph

    2016-07-01

    Although particles from natural sources dominate the globally averaged aerosol load, it is widely understood that human activity has added significantly to the atmospheric aerosol inventory in many regions. Anthropogenic contributions include pollution particles from industrial activity, transportation, cook-stoves, and other combustion sources, smoke from agricultural fires and those wildfires that result from land-management practices, soil and mineral dust mobilized in regions where overgrazing, severe tilling, or overuse of surface water resources have occurred, and biogenic particles from vegetation planted and maintained by the populance. The history of human influence is complex - in the 18th and 19th centuries agricultural burning tended to dominate the anthropogenic component in most places, whereas more recently, fossil fuel combustion leads the human contribution is many areas. However, identifying and quantifying the anthropogenic aerosol component on global scales is a challenging endeavor at present. Most estimates of the anthropogenic component come from aerosol transport models that are initialized with aerosol and precursor-gas source locations, emission strengths, and injection heights. The aerosol is then advected based on meteorological modeling, possibly modified chemically or physically, and removed by parameterized wet or dry deposition processes. Aerosol effects on clouds are also represented in some climate models, but with even greater uncertainty than the direct aerosol effects on Earth's radiation balance. Even for present conditions, aerosol source inventories are deduced from whatever constraints can be found, along with much creativity and many assumptions. Aerosol amount (i.e., aerosol optical depth) is routinely measured globally from space, but observational constraints on the anthropogenic component require some knowledge of the aerosol type as well, a much more difficult quantity to derive. As large-swath, multi-spectral, single

  4. Stratospheric aerosol modification by supersonic transport operations with climate implications

    NASA Technical Reports Server (NTRS)

    Toon, O. B.; Turco, R. P.; Pollack, J. B.; Whitten, R. C.; Poppoff, I. G.; Hamill, P.

    1980-01-01

    The potential effects on stratospheric aerosois of supersonic transport emissions of sulfur dioxide gas and submicron size soot granules are estimated. An interactive particle-gas model of the stratospheric aerosol is used to compute particle changes due to exhaust emissions, and an accurate radiation transport model is used to compute the attendant surface temperature changes. It is shown that a fleet of several hundred supersonic aircraft, operating daily at 20 km, could produce about a 20% increase in the concentration of large particles in the stratosphere. Aerosol increases of this magnitude would reduce the global surface temperature by less than 0.01 K.

  5. Toward a New Era of Research in Aerosol/Cloud/Climate Interactions at LLNL

    SciTech Connect

    Chuang, C,; Dignon, J.; Grant, K.; Connell, P.; Bergman, D.; Rotman, D.; Wright, D.; McGraw, R.; Schwartz, S.

    2000-09-27

    One of the largest uncertainties in simulations of climate change over the industrial period is the impact of anthropogenic aerosols on the Earth's radiation budget. Much of this uncertainty arises from the limited capability for either precisely linking precursor gases to the formation and size distribution of the aerosols or quantitatively describing the existing levels of global aerosol loading. This project builds on our aerosol and chemistry expertise to address each of these uncertainties in a more quantitative fashion than is currently possible. With the current LDRD support, we are in the process to implement an aerosol microphysics module into our global chemistry model to more fundamentally and completely describe the processes that determine the distribution of atmospheric aerosols. Using this new modeling capability, in conjunction with the most current version of NCAR climate model, we will examine the influence of these processes on aerosol direct and indirect climate forcing.

  6. Total Volcanic Stratospheric Aerosol Optical Depths and Implications for Global Climate Change

    NASA Technical Reports Server (NTRS)

    Ridley, D. A.; Solomon, S.; Barnes, J. E.; Burlakov, V. D.; Deshler, T.; Dolgii, S. I.; Herber, A. B.; Nagai, T.; Neely, R. R., III; Nevzorov, A. V.; Ritter, C.; Sakai, T.; Santer, B. D.; Sato, M.; Schmidt, A.; Uchino, O.; Vernier, J. P.

    2014-01-01

    Understanding the cooling effect of recent volcanoes is of particular interest in the context of the post-2000 slowing of the rate of global warming. Satellite observations of aerosol optical depth above 15 km have demonstrated that small-magnitude volcanic eruptions substantially perturb incoming solar radiation. Here we use lidar, Aerosol Robotic Network, and balloon-borne observations to provide evidence that currently available satellite databases neglect substantial amounts of volcanic aerosol between the tropopause and 15 km at middle to high latitudes and therefore underestimate total radiative forcing resulting from the recent eruptions. Incorporating these estimates into a simple climate model, we determine the global volcanic aerosol forcing since 2000 to be 0.19 +/- 0.09W/sq m. This translates into an estimated global cooling of 0.05 to 0.12 C. We conclude that recent volcanic events are responsible for more post-2000 cooling than is implied by satellite databases that neglect volcanic aerosol effects below 15 km.

  7. Total volcanic stratospheric aerosol optical depths and implications for global climate change

    NASA Astrophysics Data System (ADS)

    Ridley, D. A.; Solomon, S.; Barnes, J. E.; Burlakov, V. D.; Deshler, T.; Dolgii, S. I.; Herber, A. B.; Nagai, T.; Neely, R. R.; Nevzorov, A. V.; Ritter, C.; Sakai, T.; Santer, B. D.; Sato, M.; Schmidt, A.; Uchino, O.; Vernier, J. P.

    2014-11-01

    Understanding the cooling effect of recent volcanoes is of particular interest in the context of the post-2000 slowing of the rate of global warming. Satellite observations of aerosol optical depth above 15 km have demonstrated that small-magnitude volcanic eruptions substantially perturb incoming solar radiation. Here we use lidar, Aerosol Robotic Network, and balloon-borne observations to provide evidence that currently available satellite databases neglect substantial amounts of volcanic aerosol between the tropopause and 15 km at middle to high latitudes and therefore underestimate total radiative forcing resulting from the recent eruptions. Incorporating these estimates into a simple climate model, we determine the global volcanic aerosol forcing since 2000 to be -0.19 ± 0.09 Wm-2. This translates into an estimated global cooling of 0.05 to 0.12°C. We conclude that recent volcanic events are responsible for more post-2000 cooling than is implied by satellite databases that neglect volcanic aerosol effects below 15 km.

  8. Global profiles of the direct aerosol effect using vertically resolved aerosol data

    NASA Astrophysics Data System (ADS)

    Korras Carraca, Marios Bruno; Pappas, Vasilios; Matsoukas, Christos; Hatzianastassiou, Nikolaos; Vardavas, Ilias

    2014-05-01

    Atmospheric aerosols, both natural and anthropogenic, can cause climate change through their direct, indirect, and semi-direct effects on the radiative energy budget of the Earth-atmosphere system. In general, aerosols cause cooling of the surface and the planet, while they warm the atmosphere due to scattering and absorption of incoming solar radiation. The importance of vertically resolved direct radiative effect (DRE) and heating/cooling effects of aerosols is strong, while large uncertainties still lie with their magnitudes. In order to be able to quantify them throughout the atmosphere, a detailed vertical profile of the aerosol effect is required. Such data were made available recently by the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) on board the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) satellite. CALIOP is the first polarization lidar to fly in space and has been acquiring unique data on aerosols and clouds since June 2006. The aim of this study is to investigate both the vertically resolved geographic and seasonal variation of the DRE due to aerosols. The vertical profile of DRE under all-sky and clear-sky conditions is computed using the deterministic spectral radiative transfer model FORTH. From the DRE, the effect on atmospheric heating/cooling rate profiles due to aerosols can also be derived. We use CALIOP Level 2-Version 3 Layer aerosol optical depth data as input to our radiation transfer model, for a period of 3 complete years (2007-2009). These data are provided on a 5 km horizontal resolution and in up to 8 vertical layers and have been regridded on our model horizontal and vertical resolutions. We use cloud data from the International Satellite Cloud Climatology Project (ISCCP), while the aerosol asymmetry factor and single scattering albedo are taken from the Global Aerosol Data Set (GADS). The model computations are performed on a monthly, 2.5°× 2.5° resolution on global scale, at 40

  9. Aerosol indirect effect on tropospheric ozone via lightning

    NASA Astrophysics Data System (ADS)

    Yuan, Tianle; Remer, Lorraine A.; Bian, Huisheng; Ziemke, Jerald R.; Albrecht, Rachel; Pickering, Kenneth E.; Oreopoulos, Lazaros; Goodman, Steven J.; Yu, Hongbin; Allen, Dale J.

    2012-09-01

    Tropospheric ozone (O3) is a pollutant and major greenhouse gas and its radiative forcing is still uncertain. Inadequate understanding of processes related to O3 production, in particular those natural ones such as lightning, contributes to this uncertainty. Here we demonstrate a new effect of aerosol particles on O3production by affecting lightning activity and lightning-generated NOx (LNOx). We find that lightning flash rate increases at a remarkable rate of 30 times or more per unit of aerosol optical depth. We provide observational evidence that indicates the observed increase in lightning activity is caused by the influx of aerosols from a volcano. Satellite data analyses show O3is increased as a result of aerosol-induced increase in lightning and LNOx, which is supported by modle simulations with prescribed lightning change. O3production increase from this aerosol-lightning-ozone link is concentrated in the upper troposphere, where O3 is most efficient as a greenhouse gas. In the face of anthropogenic aerosol increase our findings suggest that lightning activity, LNOx and O3, especially in the upper troposphere, have all increased substantially since preindustrial time due to the proposed aerosol-lightning-ozone link, which implies a stronger O3 historical radiative forcing. Aerosol forcing therefore has a warming component via its effect on O3 production and this component has mostly been ignored in previous studies of climate forcing related to O3and aerosols. Sensitivity simulations suggest that 4-8% increase of column tropospheric ozone, mainly in the tropics, is expected if aerosol-lighting-ozone link is parameterized, depending on the background emission scenario. We note, however, substantial uncertainties remain on the exact magnitude of aerosol effect on tropospheric O3 via lightning. The challenges for obtaining a quantitative global estimate of this effect are also discussed. Our results have significant implications for understanding past and

  10. Aerosols, Clouds, and Precipitation as Scale Interactions in the Climate System and Controls on Climate Change

    NASA Astrophysics Data System (ADS)

    Donner, Leo

    Clouds are major regulators of atmospheric energy flows. Their character depends on atmospheric composition, dynamics, and thermodynamic state. Clouds can assume organized structures whose scales are planetary, while processes important for determining basic properties occur on the scale of microns. The range of processes, scales, and interactions among them has precluded the development of concise theories for the role of clouds in climate, and limitations in modeling clouds in complex climate models remain among the key uncertainties in understanding and projecting climate change. The distribution function of vertical velocities (updraft speeds) in clouds is an important control on climate forcing by clouds and possibly a strong correlate with climate sensitivity. (Climate forcing refers to the change in Earth's energy balance as atmospheric composition changes, in particular, due to human activity. Climate sensitivity is defined here as the equilibrium change in globally averaged annual surface temperature as a result of doubled carbon dioxide.) Vertical velocities are central because they determine the thermodynamic environment governing phase changes of water, with both equilibrium and non-equilibrium phenomena important. The spatial and temporal spectra of relevant vertical velocities includes scales both numerically resolved by climate models and below their resolution limit. The latter implies a requirement to parameterize these smaller scale motions in models. The scale dependence of vertical velocities and emerging observational constraints on their distribution provide new opportunities for representing aerosols, clouds, and precipitation in climate models. Success in doing so could provide important breakthroughs in understanding both climate forcing and sensitivity.

  11. Coupled Aerosol-Chemistry-Climate Twentieth-Century Transient Model Investigation: Trends in Short-Lived Species and Climate Responses

    NASA Technical Reports Server (NTRS)

    Koch, Dorothy; Bauer, Susanne E.; Del Genio, Anthony; Faluvegi, Greg; McConnell, Joseph R.; Menon, Surabi; Miller, Ronald L.; Rind, David; Ruedy, Reto; Schmidt, Gavin A.; Shindell, Drew

    2011-01-01

    The authors simulate transient twentieth-century climate in the Goddard Institute for Space Studies (GISS) GCM, with aerosol and ozone chemistry fully coupled to one another and to climate including a full dynamic ocean. Aerosols include sulfate, black carbon (BC), organic carbon, nitrate, sea salt, and dust. Direct and BC snow-albedo radiative effects are included. Model BC and sulfur trends agree fairly well with records from Greenland and European ice cores and with sulfur deposition in North America; however, the model underestimates the sulfur decline at the end of the century in Greenland. Global BC effects peak early in the century (1940s); afterward the BC effects decrease at high latitudes of the Northern Hemisphere but continue to increase at lower latitudes. The largest increase in aerosol optical depth occurs in the middle of the century (1940s-80s) when sulfate forcing peaks and causes global dimming. After this, aerosols decrease in eastern North America and northern Eurasia leading to regional positive forcing changes and brightening. These surface forcing changes have the correct trend but are too weak. Over the century, the net aerosol direct effect is -0.41 Watts per square meter, the BC-albedo effect is -0.02 Watts per square meter, and the net ozone forcing is +0.24 Watts per square meter. The model polar stratospheric ozone depletion develops, beginning in the 1970s. Concurrently, the sea salt load and negative radiative flux increase over the oceans around Antarctica. Net warming over the century is modeled fairly well; however, the model fails to capture the dynamics of the observedmidcentury cooling followed by the late century warming.Over the century, 20% of Arctic warming and snow ice cover loss is attributed to the BC albedo effect. However, the decrease in this effect at the end of the century contributes to Arctic cooling. To test the climate responses to sulfate and BC pollution, two experiments were branched from 1970 that removed

  12. Global Observations of Aerosols and Clouds from Combined Lidar and Passive Instruments to Improve Radiation Budget and Climate Studies

    NASA Technical Reports Server (NTRS)

    Winker, David M.

    1999-01-01

    Current uncertainties in the effects of clouds and aerosols on the Earth radiation budget limit our understanding of the climate system and the potential for global climate change. Pathfinder Instruments for Cloud and Aerosol Spaceborne Observations - Climatologie Etendue des Nuages et des Aerosols (PICASSO-CENA) is a recently approved satellite mission within NASA's Earth System Science Pathfinder (ESSP) program which will address these uncertainties with a unique suite of active and passive instruments. The Lidar In-space Technology Experiment (LITE) demonstrated the potential benefits of space lidar for studies of clouds and aerosols. PICASSO-CENA builds on this experience with a payload consisting of a two-wavelength polarization-sensitive lidar, an oxygen A-band spectrometer (ABS), an imaging infrared radiometer (IIR), and a wide field camera (WFC). Data from these instruments will be used to measure the vertical distributions of aerosols and clouds in the atmosphere, as well as optical and physical properties of aerosols and clouds which influence the Earth radiation budget. PICASSO-CENA will be flown in formation with the PM satellite of the NASA Earth Observing System (EOS) to provide a comprehensive suite of coincident measurements of atmospheric state, aerosol and cloud optical properties, and radiative fluxes. The mission will address critical uncertainties iin the direct radiative forcing of aerosols and clouds as well as aerosol influences on cloud radiative properties and cloud-climate radiation feedbacks. PICASSO-CENA is planned for a three year mission, with a launch in early 2003. PICASSO-CENA is being developed within the framework of a collaboration between NASA and CNES.

  13. East Asian Studies of Tropospheric Aerosols and their Impact on Regional Climate (EAST-AIRC): An Overview

    SciTech Connect

    Li, Zhanqing; Li, C.; Chen, H.; Tsay, S. C.; Holben, B. N.; Huang, J.; Li, B.; Maring, H.; Qian, Yun; Shi, Guangyu; Xia, X.; Yin, Y.; Zheng, Y.; Zhuang, G.

    2011-02-01

    As the most populated region of the world, Asia is a major source of aerosols with potential large impact over vast downstream areas. Papers published in this special section describe the variety of aerosols observed in China and their effects and interactions with the regional climate as part of the East Asian Study of Tropospheric Aerosols and Impact on Regional Climate (EAST-AIRC). The majority of the papers are based on analyses of observations made under three field projects, namely, the Atmospheric Radiation Measurements (ARM) Mobile Facility mission in China (AMF10 China), the East Asian Study of Tropospheric Aerosols: an International Regional Experiment (EAST-AIRE), and the Atmospheric Aerosols of China and their Climate Effects (AACCE). The former two are US-China collaborative projects and the latter is a part of the China’s National Basic Research program (or often referred to as “973 project”). Routine meteorological data of China are also employed in some studies. The wealth of general and specialized measurements lead to extensive and close-up investigations of the optical, physical and chemical properties of anthropogenic, natural, and mixed aerosols; their sources, formation and transport mechanisms; horizontal, vertical and temporal variations; direct and indirect effects and interactions with the East Asian monsoon system. Particular efforts are made to advance our understanding of the mixing and interaction between dust and anthropogenic pollutants during transport. Several modeling studies were carried out to simulate aerosol impact on radiation budget, temperature, precipitation, wind and atmospheric circulation, fog, etc. In addition, impacts of the Asian monsoon system on aerosol loading are also simulated.

  14. East Asian Studies of Tropospheric Aerosols and their Impact on Regional Climate (EAST-AIRC): An overview

    NASA Astrophysics Data System (ADS)

    Li, Zhanqing; Li, C.; Chen, H.; Tsay, S.-C.; Holben, B.; Huang, J.; Li, B.; Maring, H.; Qian, Y.; Shi, G.; Xia, X.; Yin, Y.; Zheng, Y.; Zhuang, G.

    2011-04-01

    As the most populated region of the world, Asia is a major source of aerosols with potential large impact over vast downstream areas. Papers published in this special section describe the variety of aerosols observed in China and their effects and interactions with the regional climate as part of the East Asian Study of Tropospheric Aerosols and their Impact on Regional Climate (EAST-AIRC). The majority of the papers are based on analyses of observations made under three field projects, namely, the Atmospheric Radiation Measurements (ARM) Mobile Facility mission in China (AMF-China), the East Asian Study of Tropospheric Aerosols: An International Regional Experiment (EAST-AIRE), and the Atmospheric Aerosols of China and their Climate Effects (AACCE). The former two are U.S.-China collaborative projects, and the latter is a part of the China's National Basic Research program (or often referred to as "973 project"). Routine meteorological data of China are also employed in some studies. The wealth of general and specialized measurements lead to extensive and close-up investigations of the optical, physical, and chemical properties of anthropogenic, natural, and mixed aerosols; their sources, formation, and transport mechanisms; horizontal, vertical, and temporal variations; direct and indirect effects; and interactions with the East Asian monsoon system. Particular efforts are made to advance our understanding of the mixing and interaction between dust and anthropogenic pollutants during transport. Several modeling studies were carried out to simulate aerosol impact on radiation budget, temperature, precipitation, wind and atmospheric circulation, fog, etc. In addition, impacts of the Asian monsoon system on aerosol loading are also simulated.

  15. Effect of Increasing Temperature on Carbonaceous Aerosol Direct Radiative Effect over Southeastern US

    NASA Astrophysics Data System (ADS)

    Mielonen, Tero; Kokkola, Harri; Hienola, Anca; Kühn, Thomas; Merikanto, Joonas; Korhonen, Hannele; Arola, Antti; Kolmonen, Pekka; Sogacheva, Larisa; de Leeuw, Gerrit

    2016-04-01

    Aerosols are an important regulator of the Earth's climate. They scatter and absorb incoming solar radiation and thus cool the climate by reducing the amount of energy reaching the atmospheric layers and the surface below (direct effect). A certain subset of the particles can also act as initial formation sites for cloud droplets and thereby modify the microphysics, dynamics, radiative properties and lifetime of clouds (indirect effects). The magnitude of aerosol radiative effects remains the single largest uncertainty in current estimates of anthropogenic radiative forcing. One of the key quantities needed for accurate estimates of anthropogenic radiative forcing is an accurate estimate of the radiative effects from natural unperturbed aerosol. The dominant source of natural aerosols over Earth's vast forested regions are biogenic volatile organic compounds (BVOC) which, following oxidation in the atmosphere, can condense onto aerosol particles to form secondary organic aerosol (SOA) and significantly modify the particles' properties. In accordance with the expected positive temperature dependence of BVOC emissions, several previous studies have shown that some aerosol properties, such as mass concentration and ability to act as cloud condensation nuclei (CCN), also correlate positively with temperature at many forested sites. There is conflicting evidence as to whether the aerosol direct effects have a temperature dependence due to increased BVOC emissions. The main objective of this study is to investigate the causes of the observed effect of increasing temperatures on the aerosol direct radiative effect, and to provide a quantitative estimate of this effect and of the resulting negative feedback in a warming climate. More specifically, we will investigate the causes of the positive correlation between aerosol optical depth (AOD) and land surface temperature (LST) over southeastern US where biogenic emissions are a significant source of atmospheric particles. In

  16. Global climate impacts of country-level primary carbonaceous aerosol from solid-fuel cookstove emissions

    NASA Astrophysics Data System (ADS)

    Lacey, Forrest; Henze, Daven

    2015-11-01

    Cookstove use is globally one of the largest unregulated anthropogenic sources of primary carbonaceous aerosol. While reducing cookstove emissions through national-scale mitigation efforts has clear benefits for improving indoor and ambient air quality, and significant climate benefits from reduced green-house gas emissions, climate impacts associated with reductions to co-emitted black (BC) and organic carbonaceous aerosol are not well characterized. Here we attribute direct, indirect, semi-direct, and snow/ice albedo radiative forcing (RF) and associated global surface temperature changes to national-scale carbonaceous aerosol cookstove emissions. These results are made possible through the use of adjoint sensitivity modeling to relate direct RF and BC deposition to emissions. Semi- and indirect effects are included via global scaling factors, and bounds on these estimates are drawn from current literature ranges for aerosol RF along with a range of solid fuel emissions characterizations. Absolute regional temperature potentials are used to estimate global surface temperature changes. Bounds are placed on these estimates, drawing from current literature ranges for aerosol RF along with a range of solid fuel emissions characterizations. We estimate a range of 0.16 K warming to 0.28 K cooling with a central estimate of 0.06 K cooling from the removal of cookstove aerosol emissions. At the national emissions scale, countries’ impacts on global climate range from net warming (e.g., Mexico and Brazil) to net cooling, although the range of estimated impacts for all countries span zero given uncertainties in RF estimates and fuel characterization. We identify similarities and differences in the sets of countries with the highest emissions and largest cookstove temperature impacts (China, India, Nigeria, Pakistan, Bangladesh and Nepal), those with the largest temperature impact per carbon emitted (Kazakhstan, Estonia, and Mongolia), and those that would provide the

  17. Environment, Health and Climate: Impact of African aerosols

    NASA Astrophysics Data System (ADS)

    Liousse, C.; Doumbia, T.; Assamoi, E.; Galy-Lacaux, C.; Baeza, A.; Penner, J. E.; Val, S.; Cachier, H.; Xu, L.; Criqui, P.

    2012-12-01

    Fossil fuel and biofuel emissions of particles in Africa are expected to significantly increase in the near future, particularly due to rapid growth of African cities. In addition to biomass burning emissions prevailing in these areas, air quality degradation is then expected with important consequences on population health and climatic/radiative impact. In our group, we are constructing a new integrated methodology to study the relations between emissions, air quality and their impacts. This approach includes: (1) African combustion emission characterizations; (2) joint experimental determination of aerosol chemistry from ultrafine to coarse fractions and health issues (toxicology and epidemiology). (3) integrated environmental, health and radiative modeling. In this work, we show some results illustrating our first estimates of African anthropogenic emission impacts: - a new African anthropogenic emission inventory adapted to regional specificities on traffic, biofuel and industrial emissions has been constructed for the years 2005 and 2030. Biomass burning inventories were also improved in the frame of AMMA (African Monsoon) program. - carbonaceous aerosol radiative impact in Africa has been modeled with TM5 model and Penner et al. (2011) radiative code for these inventories for 2005 and 2030 and for two scenarios of emissions : a reference scenario, with no further emission controls beyond those achieved in 2003 and a ccc* scenario including planned policies in Kyoto protocol and regulations as applied to African emission specificities. In this study we will show that enhanced heating is expected with the ccc* scenarios emissions in which the OC fraction is relatively lower than in the reference scenario. - results of short term POLCA intensive campaigns in Bamako and Dakar in terms of aerosol chemical characterization linked to specific emissions sources and their inflammatory impacts on the respiratory tract through in vitro studies. In this study, organic

  18. Thermal blanketing: a case for aerosol-induced climatic alteration.

    PubMed

    Idso, S B

    1974-10-01

    Long-term temperature records at Phoenix, Arizona, indicate the existence of a post-1946 warming trend that may be attributed to the buildup of pollution in the lower layers of the atmosphere. The causative mechanism appears to be an enhancement of the so-called "greenhouse effect," induced by the inter-action of aerosol with long-wavelength thermal radiation in the lower atmosphere.

  19. Effects of aerosol on evaporation, freezing and precipitation in a multiple cloud system

    NASA Astrophysics Data System (ADS)

    Lee, Seoung Soo; Kim, Byung-Gon; Yum, Seong Soo; Seo, Kyong-Hwan; Jung, Chang-Hoon; Um, Jun Shik; Li, Zhanqing; Hong, JinKyu; Chang, Ki-Ho; Jeong, Jin-Yim

    2016-04-01

    Aerosol effects on clouds and precipitation account for a large portion of uncertainties in the prediction of the future course of global hydrologic circulations and climate. As a process of a better understanding of interactions between aerosol, clouds and precipitation, simulations are performed for a mixed-phase convective multiple-cloud system over the tropics. Studies on single-cloud systems have shown that aerosol-induced increases in freezing, associated increases in parcel buoyancy and thus the intensity of clouds (or updrafts) are a main mechanism which controls aerosol-cloud-precipitation interactions in convective clouds. However, in the multiple-cloud system that plays much more important roles in global hydrologic circulations and thus climate than single-cloud systems, aerosol effects on condensation play the most important role in aerosol-induced changes in the intensity of clouds and the effects on freezing play a negligible role in those changes. Aerosol-induced enhancement in evaporation intensifies gust fronts and increases the number of subsequently developing clouds, which leads to the substantial increases in condensation and associated intensity of convection. Although aerosol-induced enhancement in freezing takes part in the increases in condensation by inducing stronger convergence around cloud bottom, the increases in condensation are ~one order of magnitude larger than those in freezing. It is found that while aerosol-induced increases in freezing create intermittent extremely heavy precipitation, aerosol-induced increases in evaporation enhance light and medium precipitation in the multiple-cloud system here. This increase in light and medium precipitation makes it possible that cumulative precipitation increases with increasing aerosol concentration, although the increase is small. It is interesting that the altitude of the maximum of the time- and domain-averaged hydrometeor mass densities is quite robust to increases in aerosol

  20. Global impact of smoke aerosols from landscape fires on climate and the Hadley circulation

    NASA Astrophysics Data System (ADS)

    Tosca, M. G.; Randerson, J. T.; Zender, C. S.

    2013-05-01

    Each year landscape fires across the globe emit black and organic carbon smoke particles that can last in the atmosphere for days to weeks. We characterized the climate response to these aerosols using an Earth system model. We used remote sensing observations of aerosol optical depth (AOD) and simulations from the Community Atmosphere Model, version 5 (CAM5) to optimize satellite-derived smoke emissions for high biomass burning regions. Subsequent global simulations using the adjusted fire emissions produced AODs that were in closer agreement with surface and space-based measurements. We then used CAM5, which included radiative aerosol effects, to evaluate the climate response to the fire-aerosol forcing. We conducted two 52 yr simulations, one with four sets of monthly cycling 1997-2009 fire emissions and one without. Fire emissions increased global mean annual AOD by 10% (+0.02) and decreased net all-sky surface radiation by 1% (1.3 W m-2). Elevated AODs reduced global surface temperatures by 0.13 ± 0.01 °C. Though global precipitation declined only slightly, patterns of precipitation changed, with large reductions near the Equator offset by smaller increases north and south of the intertropical convergence zone (ITCZ). A combination of increased tropospheric heating and reduced surface temperatures increased equatorial subsidence and weakened the Hadley circulation. As a consequence, precipitation decreased over tropical forests in South America, Africa and equatorial Asia. These results are consistent with the observed correlation between global temperatures and the strength of the Hadley circulation and studies linking tropospheric heating from black carbon aerosols with tropical expansion.

  1. Global impact of contemporary smoke aerosols from landscape fires on climate and the Hadley circulation

    NASA Astrophysics Data System (ADS)

    Tosca, M. G.; Randerson, J. T.; Zender, C. S.

    2012-10-01

    Each year landscape fires across the globe emit black and organic carbon smoke particles that can last in the atmosphere for days to weeks. We characterized the climate response to these aerosols using a global Earth system model. We used remote sensing observations of aerosol optical depth (AOD) and global simulations from the Community Atmosphere Model, version 5 (CAM5) to optimize satellite-derived smoke emissions for high biomass burning regions. Subsequent global simulations using the adjusted fire emissions produced AODs that were in closer agreement with surface and space-based measurements. We then used CAM5, which included radiative aerosol effects, to evaluate the climate response to the fire-aerosol forcing. We conducted two 52 yr simulations, one with four sets of monthly cycling 1997-2009 fire emissions and one without. Fire emissions increased global annual mean AOD by 10% (+0.02) and decreased net all-sky surface radiation by 1% (1.3 W m-2). Elevated AODs reduced global surface temperatures by 0.13 ± 0.01 °C. Though global precipitation declined only slightly, patterns of precipitation changed, with large reductions near the Equator offset by smaller increases north and south of the intertropical convergence zone (ITCZ). A combination of increased tropospheric heating and reduced surface temperatures increased equatorial subsidence and weakened the Hadley circulation. As a consequence, precipitation decreased over tropical forests in South America, Africa and equatorial Asia. These results are consistent with the observed correlation between global temperatures and the strength of the Hadley circulation and studies linking tropospheric heating from black carbon aerosols with tropical expansion.

  2. Tropospheric Aerosol Climate Forcing in Clear-Sky Satellite Observations over the Oceans.

    PubMed

    Haywood; Ramaswamy; Soden

    1999-02-26

    Tropospheric aerosols affect the radiative forcing of Earth's climate, but their variable concentrations complicate an understanding of their global influence. Model-based estimates of aerosol distributions helped reveal spatial patterns indicative of the presence of tropospheric aerosols in the satellite-observed clear-sky solar radiation budget over the world's oceans. The results show that, although geographical signatures due to both natural and anthropogenic aerosols are manifest in the satellite observations, the naturally occurring sea-salt is the leading aerosol contributor to the global-mean clear-sky radiation balance over oceans. PMID:10037595

  3. Asian aerosols: current and year 2030 distributions and implications to human health and regional climate change.

    PubMed

    Carmichael, Gregory R; Adhikary, Bhupesh; Kulkarni, Sarika; D'Allura, Alessio; Tang, Youhua; Streets, David; Zhang, Qiang; Bond, Tami C; Ramanathan, Veerabhadran; Jamroensan, Aditsuda; Marrapu, Pallavi

    2009-08-01

    Aerosol distributions in Asia calculated over a 4-year period and constrained by satellite observations of aerosol optical depth (AOD) are presented. Vast regions in Asia that include > 80% of the population have PM2.5 concentrations that exceed on an annual basis the WHO guideline of 10 microg/m3, often by factors of 2 to 4. These high aerosol loadings also have important radiative effects, causing a significant dimming at the surface, and mask approximately 45% of the warming by greenhouse gases. Black carbon (BC) concentrations are high throughout Asia, representing 5-10% of the total AOD, and contributing significantly to atmospheric warming (its warming potential is approximately 55% of that due to CO2). PM levels and AODs in year 2030, estimated based on simulations that consider future changes in emissions, are used to explore opportunities for win-win strategies built upon addressing air quality and climate change together. It is found that in 2030 the PM2.5 levels in significant parts of Asia will increase and exacerbate health impacts; but the aerosols will have a larger masking effect on radiative forcing, due to a decrease in BC and an increase in SO2 emissions.

  4. Black carbon reduction will weaken the aerosol net cooling effect

    NASA Astrophysics Data System (ADS)

    Wang, Z. L.; Zhang, H.; Zhang, X. Y.

    2014-12-01

    Black carbon (BC), a distinct type of carbonaceous material formed from the incomplete combustion of fossil and biomass based fuels under certain conditions, can interact with solar radiation and clouds through its strong light-absorption ability, thereby warming the Earth's climate system. Some studies have even suggested that global warming could be slowed down in a short term by eliminating BC emission due to its short lifetime. In this study, we estimate the influence of removing some sources of BC and other co-emitted species on the aerosol radiative effect by using an aerosol-climate coupled model BCC_AGCM2.0.1_CUACE/Aero, in combination with the aerosol emissions from the Representative Concentration Pathways (RCPs) scenarios. We find that the global annual mean aerosol net cooling effect at the top of the atmosphere (TOA) will be enhanced by 0.12 W m-2 compared with present-day conditions if the BC emission is reduced exclusively to the level projected for 2100 based on the RCP2.6 scenario. This will be beneficial for the mitigation of global warming. However, the global annual mean aerosol net cooling effect at the TOA will be weakened by 1.7-2.0 W m-2 relative to present-day conditions if emissions of BC and co-emitted sulfur dioxide and organic carbon are simultaneously reduced as the most close conditions to the actual situation to the level projected for 2100 in different ways based on the RCP2.6, RCP4.5, and RCP8.5 scenarios. Because there are no effective ways to remove the BC exclusively without influencing the other co-emitted components, our results therefore indicate that a reduction in BC emission can lead to an unexpected warming on the Earth's climate system in the future.

  5. Aerosol and ozone changes as forcing for climate evolution between 1850 and 2100

    NASA Astrophysics Data System (ADS)

    Szopa, Sophie; Balkanski, Y.; Schulz, M.; Bekki, S.; Cugnet, D.; Fortems-Cheiney, A.; Turquety, S.; Cozic, A.; Déandreis, C.; Hauglustaine, D.; Idelkadi, A.; Lathière, J.; Lefevre, F.; Marchand, M.; Vuolo, R.; Yan, N.; Dufresne, J.-L.

    2013-05-01

    Global aerosol and ozone distributions and their associated radiative forcings were simulated between 1850 and 2100 following a recent historical emission dataset and under the representative concentration pathways (RCP) for the future. These simulations were used in an Earth System Model to account for the changes in both radiatively and chemically active compounds, when simulating the climate evolution. The past negative stratospheric ozone trends result in a negative climate forcing culminating at -0.15 W m-2 in the 1990s. In the meantime, the tropospheric ozone burden increase generates a positive climate forcing peaking at 0.41 W m-2. The future evolution of ozone strongly depends on the RCP scenario considered. In RCP4.5 and RCP6.0, the evolution of both stratospheric and tropospheric ozone generate relatively weak radiative forcing changes until 2060-2070 followed by a relative 30 % decrease in radiative forcing by 2100. In contrast, RCP8.5 and RCP2.6 model projections exhibit strongly different ozone radiative forcing trajectories. In the RCP2.6 scenario, both effects (stratospheric ozone, a negative forcing, and tropospheric ozone, a positive forcing) decline towards 1950s values while they both get stronger in the RCP8.5 scenario. Over the twentieth century, the evolution of the total aerosol burden is characterized by a strong increase after World War II until the middle of the 1980s followed by a stabilization during the last decade due to the strong decrease in sulfates in OECD countries since the 1970s. The cooling effects reach their maximal values in 1980, with -0.34 and -0.28 W m-2 respectively for direct and indirect total radiative forcings. According to the RCP scenarios, the aerosol content, after peaking around 2010, is projected to decline strongly and monotonically during the twenty-first century for the RCP8.5, 4.5 and 2.6 scenarios. While for RCP6.0 the decline occurs later, after peaking around 2050. As a consequence the relative

  6. Efficient formation of stratospheric aerosol for climate engineering by emission of condensible vapor from aircraft

    NASA Astrophysics Data System (ADS)

    Pierce, Jeffrey R.; Weisenstein, Debra K.; Heckendorn, Patricia; Peter, Thomas; Keith, David W.

    2010-09-01

    Recent analysis suggests that the effectiveness of stratospheric aerosol climate engineering through emission of non-condensable vapors such as SO2 is limited because the slow conversion to H2SO4 tends to produce aerosol particles that are too large; SO2 injection may be so inefficient that it is difficult to counteract the radiative forcing due to a CO2 doubling. Here we describe an alternate method in which aerosol is formed rapidly in the plume following injection of H2SO4, a condensable vapor, from an aircraft. This method gives better control of particle size and can produce larger radiative forcing with lower sulfur loadings than SO2 injection. Relative to SO2 injection, it may reduce some of the adverse effects of geoengineering such as radiative heating of the lower stratosphere. This method does not, however, alter the fact that such a geoengineered radiative forcing can, at best, only partially compensate for the climate changes produced by CO2.

  7. The Impact of humidity above stratiform clouds on indirect aerosol climate forcing

    SciTech Connect

    Ackerman, A S; Kirkpatrick, M P; Stevens, D E; Toon, O B

    2004-12-20

    Some of the global warming effect of anthropogenic greenhouse gases is offset by increased solar reflection from clouds with smaller droplets that form on increased numbers of cloud condensation nuclei in polluted air. The global magnitude of the resulting indirect aerosol climate forcing is estimated to be comparable (and opposed) to the anthropogenic carbon dioxide forcing, but estimates are highly uncertain because of complexities in characterizing the physical process that determine global aerosol and cloud populations and their interactions. Beyond reflecting sunlight more effectively, smaller droplets are less efficient at producing precipitation, and decreased precipitation is expected to result in increased cloud water and cloud cover, further increasing the indirect forcing. Yet polluted marine boundary-layer clouds are not generally observed to hold more water. Here we use model simulations of stratocumulus clouds to show that suppression of precipitation from increased droplet concentrations leads to increased cloud water only when sufficient precipitation reaches the surface, a condition favored when the overlying air is moist. Otherwise, aerosol induced suppression of precipitation enhances entrainment of overlying dry air, thereby reducing cloud water and diminishing the indirect climate forcing.

  8. Efficient Formation of Stratospheric Aerosol for Climate Engineering by Emission of Condensible Vapor from Aircraft

    NASA Technical Reports Server (NTRS)

    Pierce, Jeffrey R.; Weisenstein, Debra K.; Heckendorn, Patricia; Peter. Thomas; Keith, David W.

    2010-01-01

    Recent analysis suggests that the effectiveness of stratospheric aerosol climate engineering through emission of non-condensable vapors such as SO2 is limited because the slow conversion to H2SO4 tends to produce aerosol particles that are too large; SO2 injection may be so inefficient that it is difficult to counteract the radiative forcing due to a CO2 doubling. Here we describe an alternate method in which aerosol is formed rapidly in the plume following injection of H2SO4, a condensable vapor, from an aircraft. This method gives better control of particle size and can produce larger radiative forcing with lower sulfur loadings than SO2 injection. Relative to SO2 injection, it may reduce some of the adverse effects of geoengineering such as radiative heating of the lower stratosphere. This method does not, however, alter the fact that such a geoengineered radiative forcing can, at best, only partially compensate for the climate changes produced by CO2.

  9. Incorporation of advanced aerosol activation treatments into CESM/CAM5: model evaluation and impacts on aerosol indirect effects

    NASA Astrophysics Data System (ADS)

    Gantt, B.; He, J.; Zhang, X.; Zhang, Y.; Nenes, A.

    2014-07-01

    One of the greatest sources of uncertainty in the science of anthropogenic climate change is from aerosol-cloud interactions. The activation of aerosols into cloud droplets is a direct microphysical linkage between aerosols and clouds; parameterizations of this process link aerosol with cloud condensation nuclei (CCN) and the resulting indirect effects. Small differences between parameterizations can have a large impact on the spatiotemporal distributions of activated aerosols and the resulting cloud properties. In this work, we incorporate a series of aerosol activation schemes into the Community Atmosphere Model version 5.1.1 within the Community Earth System Model version 1.0.5 (CESM/CAM5) which include factors such as insoluble aerosol adsorption and giant cloud condensation nuclei (CCN) activation kinetics to understand their individual impacts on global-scale cloud droplet number concentration (CDNC). Compared to the existing activation scheme in CESM/CAM5, this series of activation schemes increase the computation time by ~10% but leads to predicted CDNC in better agreement with satellite-derived/in situ values in many regions with high CDNC but in worse agreement for some regions with low CDNC. Large percentage changes in predicted CDNC occur over desert and oceanic regions, owing to the enhanced activation of dust from insoluble aerosol adsorption and reduced activation of sea spray aerosol after accounting for giant CCN activation kinetics. Comparison of CESM/CAM5 predictions against satellite-derived cloud optical thickness and liquid water path shows that the updated activation schemes generally improve the low biases. Globally, the incorporation of all updated schemes leads to an average increase in column CDNC of 150% and an increase (more negative) in shortwave cloud forcing of 12%. With the improvement of model-predicted CDNCs and better agreement with most satellite-derived cloud properties in many regions, the inclusion of these aerosol activation

  10. Assessing aerosol indirect effect through ice clouds in CAM5

    NASA Astrophysics Data System (ADS)

    Zhang, Kai; Liu, Xiaohong; Yoon, Jin-Ho; Wang, Minghuai; Comstock, Jennifer M.; Barahona, Donifan; Kooperman, Gabriel

    2013-05-01

    Ice clouds play an important role in regulating the Earth's radiative budget and influencing the hydrological cycle. Aerosols can act as solution droplets or ice nuclei for ice crystal formation, thus affecting the physical properties of ice clouds. Because the related dynamical and microphysical processes happen at very small spatial and temporal scales, it is a great challenge to accurately represent them in global climate models. Consequently, the aerosol indirect effect through ice clouds (ice AIE) estimated by global climate models is associated with large uncertainties. In order to better understand these processes and improve ice cloud parameterization in the Community Atmospheric Model, version 5 (CAM5), we analyze in-situ measurements from various research campaigns, and use the derived statistical information to evaluate and constrain the model [1]. We also make use of new model capabilities (prescribed aerosols and nudging) to estimate the aerosol indirect effect through ice clouds, and quantify the uncertainties associated with ice nucleation processes. In this study, a new approach is applied to separate the impact of aerosols on warm and cold clouds by using the prescribed-aerosol capability in CAM5 [2]. This capability allows a single simulation to simultaneously include up to three aerosol fields: online calculated, as well as prescribed pre-industrial (PI) and present-day conditions (PD). In a set of sensitivity simulations, we use the same aerosol fields to drive droplet activation in warm clouds, and different (PD and PI) conditions for different components of the ice nucleation parameterization in pure ice clouds, so as to investigate various ice nucleation mechanisms in an isolated manner. We also applied nudging in our simulations, which helps to increase the signal-to-noise ratio in much shorter simulation period [3] and isolate the impact of aerosols on ice clouds from other factors, such as temperature and relative humidity change. The

  11. Understanding the contributions of aerosol properties and parameterization discrepancies to droplet number variability in a global climate model

    NASA Astrophysics Data System (ADS)

    Morales Betancourt, R.; Nenes, A.

    2014-05-01

    Aerosol indirect effects in climate models strongly depend on the representation of the aerosol activation process. In this study, we assess the process-level differences across activation parameterizations that contribute to droplet number uncertainty by using the adjoints of the Abdul-Razzak and Ghan (2000) and Fountoukis and Nenes (2005) droplet activation parameterizations in the framework of the Community Atmospheric Model version 5.1 (CAM5.1). The adjoint sensitivities of Nd to relevant input parameters are used to (i) unravel the spatially resolved contribution of aerosol number, mass, and chemical composition to changes in Nd between present-day and pre-industrial simulations and (ii) identify the key variables responsible for the differences in Nd fields and aerosol indirect effect estimates when different activation schemes are used within the same modeling framework. The sensitivities are computed online at minimal computational cost. Changes in aerosol number and aerosol mass concentrations were found to contribute to Nd differences much more strongly than chemical composition effects. The main sources of discrepancy between the activation parameterizations considered were the treatment of the water uptake by coarse mode particles, and the sensitivity of the parameterized Nd accumulation mode aerosol geometric mean diameter. These two factors explain the different predictions of Nd over land and over oceans when these parameterizations are employed. Discrepancies in the sensitivity to aerosol size are responsible for an exaggerated response to aerosol volume changes over heavily polluted regions. Because these regions are collocated with areas of deep clouds, their impact on shortwave cloud forcing is amplified through liquid water path changes. The same framework is also utilized to efficiently explore droplet number uncertainty attributable to hygroscopicity parameter of organic aerosol (primary and secondary). Comparisons between the parameterization

  12. The aerosol-monsoon climate system of Asia: A new paradigm

    NASA Astrophysics Data System (ADS)

    Lau, William K. M.

    2016-02-01

    This commentary is based on a series of recent lectures on aerosol-monsoon interactions I gave at the Beijing Normal University in August 2015. A main theme of the lectures is on a new paradigm of "An Aerosol-Monsoon-Climate-System", which posits that aerosol, like rainfall, cloud, and wind, is an integral component of the monsoon climate system, influencing monsoon weather and climate on all timescales. Here, salient issues discussed in my lectures and my personal perspective regarding interactions between atmospheric dynamics and aerosols from both natural and anthropogenic sources are summarized. My hope is that under this new paradigm, we can break down traditional disciplinary barriers, advance a deeper understanding of weather and climate in monsoon regions, as well as entrain a new generation of geoscientists to strive for a sustainable future for one of the most complex and challenging human-natural climate sub-system of the earth.

  13. Satellite Remote Sensing and Mesoscale Modeling of Biomass Burning Aerosols over the Southeast Asian Maritime Continent: Climatic Implications of Smokes on Regional Energy Balance, Cloud Formations and Precipitations

    NASA Astrophysics Data System (ADS)

    Feng, N.

    2015-12-01

    The influences of anthropogenic aerosols have been suggested as an important reason for climate changes over Southeast Asia (SE Asia, 10°S~20°N and 90°E~135°E). Accurate observations and modelling of aerosols effects on the weather and climate patterns is crucial for a better understanding and mitigation of anthropogenic climate change. This study uses NASA satellite observations along with online-coupled Weather Research and Forecasting model with Chemistry (WRF-Chem) to evaluate aerosols impacts on climate over SE Asia. We assess the direct and semi-direct radiative effects of smoke particles over this region during September, 2009 when a significant El Niño event caused the highest biomass burning activity during the last 15 years. Quantification efforts are made to assess how changes of radiative and non radiative parameters (sensible and latent heat) due to smoke aerosols would affect regional climate process such as precipitations, clouds and planetary boundary layer process. Comparison of model simulations for the current land cover conditions against surface meteorological observations and satellite observations of precipitations and cloudiness show satisfactory performance of the model over our study area. In order to quantitatively validate the model results, several experiments will be performed to test the aerosols radiative feedback under different radiation schemes and with/without considering aerosol effects explicitly in the model. Relevant ground-based data (e.g. AERONET), along with aerosol vertical profile data from CALIPSO, will also be applied.

  14. he Impact of Primary Marine Aerosol on Atmospheric Chemistry, Radiation and Climate: A CCSM Model Development Study

    SciTech Connect

    Keene, William C.; Long, Michael S.

    2013-05-20

    marine aerosol production on the microphysical properties of aerosol populations and clouds over the ocean and the corresponding direct and indirect effects on radiative transfer; (2) atmospheric burdens of reactive halogen species and their impacts on O3, NOx, OH, DMS, and particulate non-sea-salt SO42-; and (3) the global production and influences of marine-derived particulate organic carbon. The model reproduced major characteristics of the marine aerosol system and demonstrated the potential sensitivity of global, decadal-scale climate metrics to multiphase marine-derived components of Earth's troposphere. Due to the combined computational burden of the coupled system, the currently available computational resources were the limiting factor preventing the adequate statistical analysis of the overall impact that multiphase chemistry might have on climate-scale radiative transfer and climate.

  15. A 10-year global gridded Aerosol Optical Thickness Reanalysis for climate and applied applications

    NASA Astrophysics Data System (ADS)

    Lynch, P.; Reid, J. S.; Zhang, J.; Westphal, D. L.; Campbell, J. R.; Curtis, C. A.; Hegg, D.; Hyer, E. J.; Sessions, W.; Shi, Y.; Turk, J.

    2013-12-01

    While standalone satellite and model aerosol products see wide utilization, there is a significant need of a best-available fused product on a regular grid for numerous climate and applied applications. Remote sensing and modeling technologies have now advanced to a point where aerosol data assimilation is an operational reality at numerous centers. It is inevitable that, like meteorological reanalyses, aerosol reanalyses will see heavy use in the near future. A first long term, 2003-2012 global 1x1 degree and 6-hourly aerosol optical thickness (AOT) reanalysis product has been generated. The goal of this effort is not only for climate applications, but to generate a dataset that can be used by the US Navy to understand operationally hindering aerosol events, aerosol impacts on numerical weather prediction, and application of electro-optical technologies. The reanalysis utilizes Navy Aerosol Analysis and Prediction System (NAAPS) at its core and assimilates quality controlled collection 5 Moderate Resolution Imaging Spectroradiometer (MODIS) AOD with minor corrections from Multi-angle Imaging SpectroRaditometer (MISR). A subset of this product includes Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) lidar assimilation since its launch in mid-2006. Surface aerosol sources, including dust and smoke, in the aerosol model have been regionally tuned so that fine and coarse mode AOTs best match those resolve by ground-based Aerosol Robotic Network (AERONET). The AOT difference between the model and satellite AOT is then used to adjust other aerosol processes, eg., sources, dry deposition, etc. Aerosol wet deposition is constrained with satellite-retrieved precipitation. The final AOT reanalysis is shown to exhibit good agreement with AERONET. Here we review the development of the reanalysis and consider issues particular to aerosol reanalyses that make them distinct from standard meteorological reanalyses. Considerations are also made for extending such work

  16. Detecting cross-equatorial wind change as a fingerprint of climate response to anthropogenic aerosol forcing

    NASA Astrophysics Data System (ADS)

    Wang, Hai; Xie, Shang-Ping; Tokinaga, Hiroki; Liu, Qinyu; Kosaka, Yu

    2016-04-01

    Anthropogenic aerosols are a major driver of the twetieth century climate change. In climate models, the aerosol forcing, larger in the Northern than Southern Hemispheres, induces an interhemispheric Hadley circulation. In support of the model result, we detected a robust change in the zonal mean cross-equatorial wind over the past 60 years from ship observations and reanalyses, accompanied by physically consistent changes in atmospheric pressure and marine cloud cover. Single-forcing experiments indicate that the observed change in cross-equatorial wind is a fingerprint of aerosol forcing. This zonal mean mode follows the evolution of global aerosol forcing that is distinct from regional changes in the Atlantic sector. Atmospheric simulations successfully reproduce this interhemispheric mode, indicating the importance of sea surface temperature mediation in response to anthropogenic aerosol forcing. As societies awaken to reduce aerosol emissions, a phase reversal of this interhemispheric mode is expected in the 21st century.

  17. The Effect of Aerosol Hygroscopicity and Volatility on Aerosol Optical Properties During Southern Oxidant and Aerosol Study

    NASA Astrophysics Data System (ADS)

    Khlystov, A.; Grieshop, A. P.; Saha, P.; Subramanian, R.

    2014-12-01

    Secondary organic aerosol (SOA) from biogenic sources can influence optical properties of ambient aerosol by altering its hygroscopicity and contributing to light absorption directly via formation of brown carbon and indirectly by enhancing light absorption by black carbon ("lensing effect"). The magnitude of these effects remains highly uncertain. A set of state-of-the-art instruments was deployed at the SEARCH site near Centerville, AL during the Southern Oxidant and Aerosol Study (SOAS) campaign in summer 2013 to measure the effect of relative humidity and temperature on aerosol size distribution, composition and optical properties. Light scattering and absorption by temperature- and humidity-conditioned aerosols was measured using three photo-acoustic extinctiometers (PAX) at three wavelengths (405 nm, 532 nm, and 870 nm). The sample-conditioning system provided measurements at ambient RH, 10%RH ("dry"), 85%RH ("wet"), and 200 C ("TD"). In parallel to these measurements, a long residence time temperature-stepping thermodenuder (TD) and a variable residence time constant temperature TD in combination with three SMPS systems and an Aerosol Chemical Speciation Monitor (ACSM) were used to assess aerosol volatility and kinetics of aerosol evaporation. We will present results of the on-going analysis of the collected data set. We will show that both temperature and relative humidity have a strong effect on aerosol optical properties. SOA appears to increase aerosol light absorption by about 10%. TD measurements suggest that aerosol equilibrated fairly quickly, within 2 s. Evaporation varied substantially with ambient aerosol loading and composition and meteorology.

  18. Assessing Impact of Aerosol Intercontinental Transport on Regional Air Quality and Climate: What Satellites Can Help

    NASA Technical Reports Server (NTRS)

    Yu, Hongbin

    2011-01-01

    Mounting evidence for intercontinental transport of aerosols suggests that aerosols from a region could significantly affect climate and air quality in downwind regions and continents. Current assessment of these impacts for the most part has been based on global model simulations that show large variability. The aerosol intercontinental transport and its influence on air quality and climate involve many processes at local, regional, and intercontinental scales. There is a pressing need to establish modeling systems that bridge the wide range of scales. The modeling systems need to be evaluated and constrained by observations, including satellite measurements. Columnar loadings of dust and combustion aerosols can be derived from the MODIS and MISR measurements of total aerosol optical depth and particle size and shape information. Characteristic transport heights of dust and combustion aerosols can be determined from the CALIPSO lidar and AIRS measurements. CALIPSO liar and OMI UV technique also have a unique capability of detecting aerosols above clouds, which could offer some insights into aerosol lofting processes and the importance of above-cloud transport pathway. In this presentation, I will discuss our efforts of integrating these satellite measurements and models to assess the significance of intercontinental transport of dust and combustion aerosols on regional air quality and climate.

  19. North Atlantic Aerosol Properties and Direct Radiative Effects: Key Results from TARFOX and ACE-2

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Livingston, J. M.; Schmid, B.; Bergstrom, R. A.; Hignett, P.; Hobbs, P. V.; Durkee, P. A.; Condon, Estelle (Technical Monitor)

    1998-01-01

    Aerosol effects on atmospheric radiative fluxes provide a forcing function that can change the climate in potentially significant ways. This aerosol radiative Forcing is a major source of uncertainty in understanding the observed climate change of the past century and in predicting, future climate. To help reduce this uncertainty, the International Global Atmospheric Chemistry Project (IGAC) has endorsed a series of multiplatform aerosol field campaigns. The Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX) and the second Aerosol Characterization Experiment (ACE-2) were the first IGAC campaigns to address the impact of anthropogenic aerosols. Both TARFOX and ACE-2 gathered extensive data sets on aerosol properties and radiative effects. TARFOX focused on the urban-industrial haze plume flowing from the eastern United States over the western Atlantic Ocean, whereas ACE-2 studied aerosols carried over the eastern Atlantic from both European urban/industrial and African mineral sources. These aerosols often have a marked influence on the top-of-atmosphere radiances measured by satellites, as illustrated in Figure 1. Shown there are contours of aerosol optical depth derived from radiances measured by the AVHRR sensor on the NOAA-11 satellite. The contours readily show that aerosols originating in North America, Europe, and Africa impact the radiative properties of air over the North Atlantic. However, the accurate derivation of flux chances, or radiative forcing, from the satellite-measured radiances or 'etrieved optical depths remains a difficult challenge. In this paper we summarize key Initial results from TARFOX and, to a lesser extent ACE-2, with a focus on those results that allow an improved assessment of the flux changes caused by North Atlantic aerosols at middle and high latitudes.

  20. North Atlantic Aerosol Properties and Direct Radiative Effects: Key Results from TARFOX and ACE-2

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Livingston, J. M.; Schmid, B.; Bergstrom, Robert A.; Hignett, P.; Hobbs, P. V.; Durkee, P. A.

    2000-01-01

    Aerosol effects on atmospheric radiative fluxes provide a forcing function that can change the climate In potentially significant ways. This aerosol radiative forcing is a major source of uncertainty in understanding the observed climate change of the past century and in predicting future climate. To help reduce this uncertainty, the International Global Atmospheric Chemistry Project (IGAC) has endorsed a series of multiplatform aerosol field campaigns. The Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX) and the second Aerosol Characterization Experiment (ACE-2) were the first IGAC campaigns to address the impact of anthropogenic aerosols, Both TARFOX and ACE-2 gathered extensive data sets on aerosol properties and radiative effects, TARFOX focused on the urban-industrial haze plume flowing from the eastern United States over the western Atlantic Ocean, whereas ACE-2 studied aerosols carried over the eastern Atlantic from both European urban/industrial and African mineral sources. These aerosols often have a marked influence on the top-of-atmosphere radiances measured by satellites. Shown there are contours of aerosol optical depth derived from radiances measured by the AVHRR sensor on the NOAA-11 satellite. The contours readily show that aerosols originating in North America, Europe, and Africa impact the radiative properties of air over the North Atlantic. However, the accurate derivation of flux changes, or radiative forcing, from the satellite measured radiances or retrieved optical depths remains a difficult challenge. In this paper we summarize key initial results from TARFOX and, to a lesser extent, ACE-2, with a focus on those results that allow an improved assessment of the flux changes caused by North Atlantic aerosols at middle latitudes.

  1. The impact of residential combustion emissions on atmospheric aerosol, human health and climate

    NASA Astrophysics Data System (ADS)

    Butt, E. W.; Rap, A.; Schmidt, A.; Scott, C. E.; Pringle, K. J.; Reddington, C. L.; Richards, N. A. D.; Woodhouse, M. T.; Ramirez-Villegas, J.; Yang, H.; Vakkari, V.; Stone, E. A.; Rupakheti, M.; Praveen, P. S.; van Zyl, P. G.; Beukes, J. P.; Josipovic, M.; Mitchell, E. J. S.; Sallu, S. M.; Forster, P. M.; Spracklen, D. V.

    2015-07-01

    Combustion of fuels in the residential sector for cooking and heating, results in the emission of aerosol and aerosol precursors impacting air quality, human health and climate. Residential emissions are dominated by the combustion of solid fuels. We use a global aerosol microphysics model to simulate the uncertainties in the impact of residential fuel combustion on atmospheric aerosol. The model underestimates black carbon (BC) and organic carbon (OC) mass concentrations observed over Asia, Eastern Europe and Africa, with better prediction when carbonaceous emissions from the residential sector are doubled. Observed seasonal variability of BC and OC concentrations are better simulated when residential emissions include a seasonal cycle. The largest contributions of residential emissions to annual surface mean particulate matter (PM2.5) concentrations are simulated for East Asia, South Asia and Eastern Europe. We use a concentration response function to estimate the health impact due to long-term exposure to ambient PM2.5 from residential emissions. We estimate global annual excess adult (> 30 years of age) premature mortality of 308 000 (113 300-497 000, 5th to 95th percentile uncertainty range) for monthly varying residential emissions and 517 000 (192 000-827 000) when residential carbonaceous emissions are doubled. Mortality due to residential emissions is greatest in Asia, with China and India accounting for 50 % of simulated global excess mortality. Using an offline radiative transfer model we estimate that residential emissions exert a global annual mean direct radiative effect of between -66 and +21 mW m-2, with sensitivity to the residential emission flux and the assumed ratio of BC, OC and SO2 emissions. Residential emissions exert a global annual mean first aerosol indirect effect of between -52 and -16 mW m-2, which is sensitive to the assumed size distribution of carbonaceous emissions. Overall, our results demonstrate that reducing residential

  2. Global atmospheric sulfur budget under volcanically quiescent conditions: Aerosol-chemistry-climate model predictions and validation

    NASA Astrophysics Data System (ADS)

    Sheng, Jian-Xiong; Weisenstein, Debra K.; Luo, Bei-Ping; Rozanov, Eugene; Stenke, Andrea; Anet, Julien; Bingemer, Heinz; Peter, Thomas

    2015-01-01

    The global atmospheric sulfur budget and its emission dependence have been investigated using the coupled aerosol-chemistry-climate model SOCOL-AER. The aerosol module comprises gaseous and aqueous sulfur chemistry and comprehensive microphysics. The particle distribution is resolved by 40 size bins spanning radii from 0.39 nm to 3.2 μm, including size-dependent particle composition. Aerosol radiative properties required by the climate model are calculated online from the aerosol module. The model successfully reproduces main features of stratospheric aerosols under nonvolcanic conditions, including aerosol extinctions compared to Stratospheric Aerosol and Gas Experiment II (SAGE II) and Halogen Occultation Experiment, and size distributions compared to in situ measurements. The calculated stratospheric aerosol burden is 109 Gg of sulfur, matching the SAGE II-based estimate (112 Gg). In terms of fluxes through the tropopause, the stratospheric aerosol layer is due to about 43% primary tropospheric aerosol, 28% SO2, 23% carbonyl sulfide (OCS), 4% H2S, and 2% dimethyl sulfide (DMS). Turning off emissions of the short-lived species SO2, H2S, and DMS shows that OCS alone still establishes about 56% of the original stratospheric aerosol burden. Further sensitivity simulations reveal that anticipated increases in anthropogenic SO2 emissions in China and India have a larger influence on stratospheric aerosols than the same increase in Western Europe or the U.S., due to deep convection in the western Pacific region. However, even a doubling of Chinese and Indian emissions is predicted to increase the stratospheric background aerosol burden only by 9%. In contrast, small to moderate volcanic eruptions, such as that of Nabro in 2011, may easily double the stratospheric aerosol loading.

  3. Evaluating the aerosol first indirect effect using satellite data

    NASA Astrophysics Data System (ADS)

    Shao, Hongfei

    First proposed by Twomey, the aerosol first indirect effect hypothesizes that increased aerosol concentration leads to a larger number of cloud condensation nuclei, and therefore smaller but more numerous cloud droplets, which results in greater reflection of incoming solar radiation. It is known that this phenomenon has a net effect to cool the Earth radiatively and offset a substantial amount of the warming caused by the increasing of greenhouse gases. However, the magnitude of this effect has been very uncertain. For example, discrepancies of more than a factor of 2 have been reported among various observational results. This uncertainty is a major hurdle in advancing our understanding of how humans have altered, and may in the future alter the Earth's climate. One of the difficulties in deriving the magnitude of this effect from observational data arises from the fact that the aerosol abundance often varies coherently with meteorological conditions, which makes it extremely hard to distinguish between the changes in cloud microphysical parameters caused by varying aerosol concentration and by varying meteorological conditions. Therefore, the goal of this study is to find a reliable method to extract the real strength and to narrow the uncertainty in the estimates of the indirect radiative effect of aerosols. To achieve this goal, first, a satellite visible/near-infrared algorithm is developed to retrieve cloud optical depth and effective radius simultaneously at solar wavelengths (0.63 and 1.61 mum), and a satellite microwave algorithm is developed to retrieve liquid water path in the microwave range (19 and 37 GHz). Using these algorithm we derive cloud microphysical variables in relation to the aerosol first indirect effect. Second, a drizzle index is introduced to discriminate the drizzle clouds from non-drizzle clouds from satellite, which ensures our estimation of the first indirect effect not being contaminated by precipitation related processes. Third

  4. Aerosol Types using Passive Remote Sensing: Global Distribution, Consistency Check, Total-Column Investigation and Translation into Composition Derived from Climate and Chemical Transport Model

    NASA Astrophysics Data System (ADS)

    Kacenelenbogen, M. S.; Dawson, K. W.; Johnson, M. S.; Burton, S. P.; Redemann, J.; Hasekamp, O. P.; Hair, J. W.; Ferrare, R. A.; Butler, C. F.; Holben, B. N.; Beyersdorf, A. J.; Ziemba, L. D.; Froyd, K. D.; Dibb, J. E.; Shingler, T.; Sorooshian, A.; Jimenez, J. L.; Campuzano Jost, P.; Jacob, D. J.

    2015-12-01

    To improve the predictions of aerosol composition in chemical transport models (CTMs) and global climate models (GCMs), we have developed an aerosol classification algorithm (called Specified Clustering and Mahalanobis Classification, SCMC) that assigns an aerosol type to multi-parameter retrievals by spaceborne, airborne or ground based passive remote sensing instruments [Russell et al., 2014]. The aerosol types identified by our scheme are pure dust, polluted dust, urban-industrial/developed economy, urban-industrial/developing economy, dark biomass smoke, light biomass smoke and pure marine. We apply the SCMC method to two different total-column datasets of aerosol optical properties: inversions from the ground-based AErosol RObotic NETwork (AERONET) and retrievals from the space-borne POLDER (Polarization and Directionality of Earth's Reflectances) instrument. The POLDER retrievals that we use differ from the standard POLDER retrievals [Deuzé et al., 2001] as they make full use of multi-angle, multispectral polarimetric data [Hasekamp et al., 2011]. We analyze agreement in the aerosol types inferred from both AERONET and POLDER globally. Then, we investigate how our total-column "effective" SCMC aerosol types relate to different aerosol types within the column (i.e. either a mixture of different types within one layer in the vertical or the stacking of different aerosol types within the vertical column). For that, we compare AERONET-SCMC aerosol types to collocated NASA LaRC HSRL vertically resolved aerosol types [Burton et al., 2012] during the SEAC4RS and DISCOVER-AQ airborne field experiments, mostly over Texas in Aug-Sept 2013. Finally, in order to evaluate the GEOS-Chem CTM aerosol types, we translate each of our SCMC aerosol type into a unique distribution of GEOS-Chem aerosol composition (e.g. biomass burning, dust, sulfate, sea salt). We bridge the gap between remote sensing and model-inferred aerosol types by using multiple years of collocated AERONET

  5. Global fine-mode aerosol radiative effect, as constrained by comprehensive observations

    NASA Astrophysics Data System (ADS)

    Chung, Chul E.; Chu, Jung-Eun; Lee, Yunha; van Noije, Twan; Jeoung, Hwayoung; Ha, Kyung-Ja; Marks, Marguerite

    2016-07-01

    Aerosols directly affect the radiative balance of the Earth through the absorption and scattering of solar radiation. Although the contributions of absorption (heating) and scattering (cooling) of sunlight have proved difficult to quantify, the consensus is that anthropogenic aerosols cool the climate, partially offsetting the warming by rising greenhouse gas concentrations. Recent estimates of global direct anthropogenic aerosol radiative forcing (i.e., global radiative forcing due to aerosol-radiation interactions) are -0.35 ± 0.5 W m-2, and these estimates depend heavily on aerosol simulation. Here, we integrate a comprehensive suite of satellite and ground-based observations to constrain total aerosol optical depth (AOD), its fine-mode fraction, the vertical distribution of aerosols and clouds, and the collocation of clouds and overlying aerosols. We find that the direct fine-mode aerosol radiative effect is -0.46 W m-2 (-0.54 to -0.39 W m-2). Fine-mode aerosols include sea salt and dust aerosols, and we find that these natural aerosols result in a very large cooling (-0.44 to -0.26 W m-2) when constrained by observations. When the contribution of these natural aerosols is subtracted from the fine-mode radiative effect, the net becomes -0.11 (-0.28 to +0.05) W m-2. This net arises from total (natural + anthropogenic) carbonaceous, sulfate and nitrate aerosols, which suggests that global direct anthropogenic aerosol radiative forcing is less negative than -0.35 W m-2.

  6. What does nature tell us about aerosol effects in a trade cumulus regime?

    NASA Astrophysics Data System (ADS)

    Yuan, T.; Remer, L. A.; Yu, H.; Wang, H.

    2011-12-01

    Detecting aerosol effect on cloud amount has been elusive to both observations and modeling due to potential buffering mechanisms and convolution of meteorology. Here through a natural experiment provided by long-term degassing of a low-lying volcano and use of A-Train satellite observations, we show modifications of trade cumulus cloud fields including decreased droplet size, decreased precipitation efficiency and increased cloud amount are associated with volcanic aerosols. In addition we find significantly higher cloud tops for polluted clouds. We demonstrate that the observed microphysical and macrophysical changes cannot be explained by synoptic meteorology or the orographic effect of the Hawaiian Islands. Idealized large eddy simulations reproduce some key observed features of the cloud response to aerosol perturbations, which helps us further understand the underlying mechanisms. The "total shortwave aerosol forcing", resulting from direct and indirect forcings including both cloud albedo and cloud amount, is almost an order of magnitude higher than aerosol direct forcing alone. Furthermore, the precipitation reduction associated with enhanced aerosol leads to large changes in the energetics of air-sea exchange and trade wind boundary layer. Our results represent the first observational evidence of large-scale increase of cloud amount due to aerosols in a trade cumulus regime, which can be used to constrain the representation of aerosol-cloud interactions in climate models. The findings also have implications for volcano-climate interactions and climate mitigation research.

  7. Aerosol Indirect Effect on Warm Clouds over Eastern China Using Combined CALIOP and MODIS Observations

    NASA Astrophysics Data System (ADS)

    Guo, Jianping; Wang, Fu; Huang, Jingfeng; Li, Xiaowen

    2015-04-01

    Aerosol, one of key components of the climate system, is highly variable, both temporally and spatially. It often exerts great influences on the cloud-precipitation chain processes by serving as CCN/IN, altering cloud microphysics and its life cycle. Yet, the aerosol indirect effect on clouds remains largely unknown, because the initial changes in clouds due to aerosols may be enhanced or dampened by such feedback processes as modified cloud dynamics, or evaporation of the smaller droplets due to the competition for water vapor. In this study, we attempted to quantify the aerosol effects on warm cloud over eastern China, based on near-simultaneous retrievals from MODIS/AQUA, CALIOP/CALIPSO and CPR/CLOUDSAT during the period 2006 to 2010. The seasonality of aerosol from ground-based PM10 is quite different from that estimated from MODIS AOD. This result is corroborated by lower level profile of aerosol occurrence frequency from CALIOP, indicating the significant role CALIOP could play in aerosol-cloud interaction. The combined use of CALIOP and CPR facilitate the process to exactly determine the (vertical) position of warm cloud relative to aerosol, out of six scenarios in terms of aerosol-cloud mixing status in terms of aerosol-cloud mixing status, which shows as follows: AO (Aerosol only), CO (Cloud only), SASC (Single aerosol-single cloud), SADC (single aerosol-double cloud), DASC (double aerosol-single cloud), and others. Results shows that about 54% of all the cases belong to mixed status, among all the collocated aerosol-cloud cases. Under mixed condition, a boomerang shape is observed, i.e., reduced cloud droplet radius (CDR) is associated with increasing aerosol at moderate aerosol pollution (AOD<0.4), becoming saturated at AOD of 0.5, followed by an increase in CDR with aerosol. In contrast, there is no such boomerang shape found for (aerosol-cloud) separated cases. We categorize dataset into warm-season and cold-season subsets to figure out how the

  8. Aerosol-cloud interactions: effect on precipitation

    NASA Astrophysics Data System (ADS)

    Takle, Jasmine; Maheskumar, R.

    2016-05-01

    Aerosols are tiny suspended particle in the atmosphere with high variability in time and space, play a major role in modulating the cloud properties and thereby precipitation. To understand the aerosol induced Invigoration effect predictors like aerosol optical depth, cloud optical depth, cloud top temperature, cloud effective radii, ice water path, retrieved from the Moderate resolution Imaging Spectroradiometer (MODIS) level-3 aqua satellite data were analysed for pre monsoon April-May and post monsoon October-November months over the Indian subcontinent 8 ° N to 33° N, 65 °E to 100 °E during the period 2003-2013. Apart from the above data, mesoscale dynamical parameters such as vertical wind shear of horizontal wind, relative humidity, were also considered to understand their role in invigoration. Case studies have been carried out for the regions having heavy rainfall events & minimal rainfall events during high Aerosol optical depths occasions respectively. Analysis revealed that the heavy rainfall which occurred in this region with higher optical depths might be due to invigoration effect of aerosols wherein the dynamical as well as thermodynamical parameters were also found favourable. Minimal rainfall events were also observed most probably due to the suppression of rain formation/delay in precipitation due to high amount of aerosol concentration in these regions. Prominent 36 such cases were studied all over India during Pre & Post monsoon months.

  9. Investigation of multiple scattering effects in aerosols

    NASA Technical Reports Server (NTRS)

    Deepak, A.

    1980-01-01

    The results are presented of investigations on the various aspects of multiple scattering effects on visible and infrared laser beams transversing dense fog oil aerosols contained in a chamber (4' x 4' x 9'). The report briefly describes: (1) the experimental details and measurements; (2) analytical representation of the aerosol size distribution data by two analytical models (the regularized power law distribution and the inverse modified gamma distribution); (3) retrieval of aerosol size distributions from multispectral optical depth measurements by two methods (the two and three parameter fast table search methods and the nonlinear least squares method); (4) modeling of the effects of aerosol microphysical (coagulation and evaporation) and dynamical processes (gravitational settling) on the temporal behavior of aerosol size distribution, and hence on the extinction of four laser beams with wavelengths 0.44, 0.6328, 1.15, and 3.39 micrometers; and (5) the exact and approximate formulations for four methods for computing the effects of multiple scattering on the transmittance of laser beams in dense aerosols, all of which are based on the solution of the radiative transfer equation under the small angle approximation.

  10. First Evaluation of the CCAM Aerosol Simulation over Africa: Implications for Regional Climate Modeling

    NASA Astrophysics Data System (ADS)

    Horowitz, H.; Garland, R. M.; Thatcher, M. J.; Naidoo, M.; van der Merwe, J.; Landman, W.; Engelbrecht, F.

    2015-12-01

    An accurate representation of African aerosols in climate models is needed to understand the regional and global radiative forcing and climate impacts of aerosols, at present and under future climate change. However, aerosol simulations in regional climate models for Africa have not been well-tested. Africa contains the largest single source of biomass-burning smoke aerosols and dust globally. Although aerosols are short-lived relative to greenhouse gases, black carbon in particular is estimated to be second only to carbon dioxide in contributing to warming on a global scale. Moreover, Saharan dust is exported great distances over the Atlantic Ocean, affecting nutrient transport to regions like the Amazon rainforest, which can further impact climate. Biomass burning aerosols are also exported from Africa, westward from Angola over the Atlantic Ocean and off the southeastern coast of South Africa to the Indian Ocean. Here, we perform the first extensive quantitative evaluation of the Conformal-Cubic Atmospheric Model (CCAM) aerosol simulation against monitored data, focusing on aerosol optical depth (AOD) observations over Africa. We analyze historical regional simulations for 1999 - 2012 from CCAM consistent with the experimental design of CORDEX at 50 km global horizontal resolution, through the dynamical downscaling of ERA-Interim data reanalysis data, with the CMIP5 emissions inventory (RCP8.5 scenario). CCAM has a prognostic aerosol scheme for organic carbon, black carbon, sulfate, and dust, and non-prognostic sea salt. The CCAM AOD at 550nm was compared to AOD (observed at 440nm, adjusted to 550nm with the Ångström exponent) from long-term AERONET stations across Africa. Sites strongly impacted by dust and biomass burning and with long continuous records were prioritized. In general, the model captures the monthly trends of the AERONET data. This presentation provides a basis for understanding how well aerosol particles are represented over Africa in

  11. Investigation of aviation emission impacts on global tropospheric chemistry and climate using a size-resolved aerosol-chemistry model

    NASA Astrophysics Data System (ADS)

    Kapadia, Zarashpe; Spracklen, Dominick; Arnold, Stephen; Borman, Duncan; Mann, Graham; Pringle, Kirsty; Monks, Sarah; Reddington, Carly; Rap, Alexandru; Scott, Catherine

    2014-05-01

    Aviation is responsible for 3% of global anthropogenic CO2 emissions, but 2-14% of anthropogenic induced climate warming due to contributions from short lived climate forcers. The global civil aviation fleet is projected to double by 2026 in relation to a 2006 baseline and so will play a substantial role in future climate change. Uncertainty in the net impact of aviation on climate is largely due to uncertainty in the impacts of aviation emissions on ozone and aerosol. To study the impact of aviation emissions we use the GLOMAP-mode global aerosol microphysics model coupled to the 3-D chemical transport model TOMCAT. GLOMAP-mode has been extended to include treatment of nitrate aerosol. We include a full suite of non-CO2 aviation emissions (including NOX, SO2, HCs, BC and OC) in the model. We combined the simulated changes in ozone and aerosol with a 3D radiative transfer model to quantify the radiative effect due to aviation non-CO2 emissions. We find that aviation emissions increase O3 concentrations by up to 5.3% in the upper troposphere (UT), broadly matching previous studies. Black carbon (BC) and organic carbon (OC) concentrations increase by 26.5% and 14.6% respectively in the UT, whereas nitrate aerosol is reduced in some regions due to co-emission of NOX and SO2 In the UT, aviation emissions increase both total aerosol number as well as the concentration of particles greater than 70 nm diameter (N70). Entrainment of these particles into the free troposphere results in aviation emissions also increasing N70 in the boundary layer, causing a cooling through the first aerosol indirect effect. We explore differences in these responses compared with those simulated when using the recommended aviation emissions from CMIP5 (5th Climate Model Intercomparison Project), which only include NOX and BC emissions. Our results suggest that aviation emissions of SO2 and HCs neglected by CMIP5 produce important effects on ozone, aerosol number, and N70. We suggest CMIP5

  12. Do primary marine aerosol organics play a role in the biological regulation of climate?

    NASA Astrophysics Data System (ADS)

    Quinn, P.; Bates, T. S.; Coffman, D. J.; Russell, L. M.; Modini, R. L.

    2015-12-01

    Field and laboratory observations reveal a source of primary marine organic aerosol that is emitted to the atmosphere along with inorganic sea salt during the wind-driven production of sea spray aerosol (SSA). Surface seawater processes and properties that control the amount and the composition of organics emitted to the atmosphere are not well understood. Ramifications of the emission of primary marine organic aerosol on clouds and climate have been suggested but not confirmed. An oceanic, biological impact on clouds and climate by primary marine aerosol requires that a) the organic fraction of SSA is controlled by surface ocean biological processes and b) that primary marine aerosol makes up a significant number fraction of CCN in the marine boundary layer. Generation and characterization of freshly emitted SSA in the laboratory and at sea have revealed information about the size, composition, volatility, and hygroscopicity of primary marine aerosol. It has been shown that SSA is an internal mixture of sea salt and organics with the organic fraction increasing with decreasing particle size. In addition, quantification of the enrichment of organic matter in freshly emitted SSA relative to seawater has shown that high enrichments occur in regions of both eutrophic and oligotrophic waters, indicating that enrichment can be decoupled from local biological activity. Measurements of ambient (not generated) marine aerosol number size distributions and size-segregated chemical composition can be used to estimate the number fraction of CCN attributable to primary marine aerosol. An analysis of Eastern Pacific, Northern Atlantic, and Southern Ocean marine aerosol indicates that the primary marine aerosol makes up only a small fraction of the total CCN in the marine atmosphere. This presentation will consider current evidence derived from generation of freshly emitted SSA and measurements of ambient marine aerosol to assess the role of primary marine aerosol organics in the

  13. The impact of humidity above stratiform clouds on indirect aerosol climate forcing.

    PubMed

    Ackerman, Andrew S; Kirkpatrick, Michael P; Stevens, David E; Toon, Owen B

    2004-12-23

    Some of the global warming from anthropogenic greenhouse gases is offset by increased reflection of solar radiation by clouds with smaller droplets that form in air polluted with aerosol particles that serve as cloud condensation nuclei. The resulting cooling tendency, termed the indirect aerosol forcing, is thought to be comparable in magnitude to the forcing by anthropogenic CO2, but it is difficult to estimate because the physical processes that determine global aerosol and cloud populations are poorly understood. Smaller cloud droplets not only reflect sunlight more effectively, but also inhibit precipitation, which is expected to result in increased cloud water. Such an increase in cloud water would result in even more reflective clouds, further increasing the indirect forcing. Marine boundary-layer clouds polluted by aerosol particles, however, are not generally observed to hold more water. Here we simulate stratocumulus clouds with a fluid dynamics model that includes detailed treatments of cloud microphysics and radiative transfer. Our simulations show that the response of cloud water to suppression of precipitation from increased droplet concentrations is determined by a competition between moistening from decreased surface precipitation and drying from increased entrainment of overlying air. Only when the overlying air is humid or droplet concentrations are very low does sufficient precipitation reach the surface to allow cloud water to increase with droplet concentrations. Otherwise, the response of cloud water to aerosol-induced suppression of precipitation is dominated by enhanced entrainment of overlying dry air. In this scenario, cloud water is reduced as droplet concentrations increase, which diminishes the indirect climate forcing.

  14. Remote Sensing of Aerosols from Satellites: Why Has It Been Do Difficult to Quantify Aerosol-Cloud Interactions for Climate Assessment, and How Can We Make Progress?

    NASA Technical Reports Server (NTRS)

    Kahn, Ralph A.

    2015-01-01

    The organizers of the National Academy of Sciences Arthur M. Sackler Colloquia Series on Improving Our Fundamental Understanding of the Role of Aerosol-Cloud Interactions in the Climate System would like to post Ralph Kahn's presentation entitled Remote Sensing of Aerosols from Satellites: Why has it been so difficult to quantify aerosol-cloud interactions for climate assessment, and how can we make progress? to their public website.

  15. Light absorption by secondary organic aerosol from α-pinene: Effects of oxidants, seed aerosol acidity, and relative humidity

    SciTech Connect

    Song, Chen; Gyawali, Madhu; Zaveri, Rahul A.; Shilling, John E.; Arnott, W. Patrick

    2013-10-25

    It is well known that light absorption from dust and black carbon aerosols has a warming effect on climate while light scattering from sulfate, nitrate, and sea salt aerosols has a cooling effect. However, there are large uncertainties associated with light absorption and scattering by different types of organic aerosols, especially in the near-UV and UV spectral regions. In this paper, we present the results from a systematic laboratory study focused on measuring light absorption by secondary organic aerosols (SOAs) generated from dark α-pinene + O3 and α-pinene + NOx + O3 systems in the presence of neutral and acidic sulfate seed aerosols. Light absorption was monitored using photoacoustic spectrometers at four different wavelengths: 355, 405, 532, and 870 nm. Significant light absorption at 355 and 405 nm was observed for the SOA formed from α-pinene + O3 + NO3 system only in the presence of highly acidic sulfate seed aerosols under dry conditions. In contrast, no absorption was observed when the relative humidity was elevated to greater than 27% or in the presence of neutral sulfate seed aerosols. Organic nitrates in the SOA formed in the presence of neutral sulfate seed aerosols were found to be nonabsorbing, while the light-absorbing compounds are speculated to be aldol condensation oligomers with nitroxy organosulfate groups that are formed in highly acidic sulfate aerosols. Finally and overall, these results suggest that dark α-pinene + O3 and α-pinene + NOx + O3 systems do not form light-absorbing SOA under typical atmospheric conditions.

  16. New understanding and quantification of the regime dependence of aerosol-cloud interaction for studying aerosol indirect effects

    DOE PAGES

    Chen, Jingyi; Liu, Yangang; Zhang, Minghua; Peng, Yiran

    2016-02-28

    In this study, aerosol indirect effects suffer from large uncertainty in climate models and among observations. This study focuses on two plausible factors: regime dependence of aerosol-cloud interactions and the effect of cloud droplet spectral shape. We show, using a new parcel model, that combined consideration of droplet number concentration (Nc) and relative dispersion (ε, ratio of standard deviation to mean radius of the cloud droplet size distribution) better characterizes the regime dependence of aerosol-cloud interactions than considering Nc alone. Given updraft velocity (w), ε increases with increasing aerosol number concentration (Na) in the aerosol-limited regime, peaks in the transitionalmore » regime, and decreases with further increasing Na in the updraft-limited regime. This new finding further reconciles contrasting observations in literature and reinforces the compensating role of dispersion effect. The nonmonotonic behavior of ε further quantifies the relationship between the transitional Na and w that separates the aerosol- and updraft-limited regimes.« less

  17. Aerosol interactions with African/Atlantic climate dynamics

    NASA Astrophysics Data System (ADS)

    Hosseinpour, F.; Wilcox, E. M.

    2014-07-01

    Mechanistic relationships exist between variability of dust in the oceanic Saharan air layer (OSAL) and transient changes in the dynamics of Western Africa and the tropical Atlantic Ocean. This study provides evidence of possible interactions between dust in the OSAL region and African easterly jet-African easterly wave (AEJ-AEW) system in the climatology of boreal summer, when easterly wave activity peaks. Synoptic-scale changes in instability and precipitation in the African/Atlantic intertropical convergence zone are correlated with enhanced aerosol optical depth (AOD) in the OSAL region in response to anomalous 3D overturning circulations and upstream/downstream thermal anomalies at above and below the mean-AEJ level. Upstream and downstream anomalies are referred to the daily thermal/dynamical changes over the West African monsoon region and the Eastern Atlantic Ocean, respectively. Our hypothesis is that AOD in the OSAL is positively correlated with the downstream AEWs and negatively correlated with the upstream waves from climatological perspective. The similarity between the 3D pattern of thermal/dynamical anomalies correlated with dust outbreaks and those of AEWs provides a mechanism for dust radiative heating in the atmosphere to reinforce AEW activity. We proposed that the interactions of OSAL dust with regional climate mainly occur through coupling of dust with the AEWs.

  18. Trend of surface solar radiation over Asia simulated by aerosol transport-climate model

    NASA Astrophysics Data System (ADS)

    Takemura, T.; Ohmura, A.

    2009-12-01

    Long-term records of surface radiation measurements indicate a decrease in the solar radiation between the 1950s and 1980s (“global dimming”), then its recovery afterward (“global brightening”) at many locations all over the globe [Wild, 2009]. On the other hand, the global brightening is delayed over the Asian region [Ohmura, 2009]. It is suggested that these trends of the global dimming and brightening are strongly related with a change in aerosol loading in the atmosphere which affect the climate change through the direct, semi-direct, and indirect effects. In this study, causes of the trend of the surface solar radiation over Asia during last several decades are analyzed with an aerosol transport-climate model, SPRINTARS. SPRINTARS is coupled with MIROC which is a general circulation model (GCM) developed by Center for Climate System Research (CCSR)/University of Tokyo, National Institute for Environmental Studies (NIES), and Frontier Research Center for Global Change (FRCGC) [Takemura et al., 2000, 2002, 2005, 2009]. The horizontal and vertical resolutions are T106 (approximately 1.1° by 1.1°) and 56 layers, respectively. SPRINTARS includes the transport, radiation, cloud, and precipitation processes of all main tropospheric aerosols (black and organic carbons, sulfate, soil dust, and sea salt). The model treats not only the aerosol mass mixing ratios but also the cloud droplet and ice crystal number concentrations as prognostic variables, and the nucleation processes of cloud droplets and ice crystals depend on the number concentrations of each aerosol species. Changes in the cloud droplet and ice crystal number concentrations affect the cloud radiation and precipitation processes in the model. Historical emissions, that is consumption of fossil fuel and biofuel, biomass burning, aircraft emissions, and volcanic eruptions are prescribed from database provided by the Aerosol Model Intercomparison Project (AeroCom) and the latest IPCC inventories

  19. The Role of Non-CO2 Greenhouse Gases and Aerosols in Climate Mitigation

    SciTech Connect

    Smith, Steven J.; Bond, Tami C.; Wigley, Tom M.; de la Chesnaye, Francisco; Pitcher, Hugh M.

    2003-11-17

    Forcing agents other than carbon dioxide, such as methane, nitrous oxide, halocarbons, and perhaps aerosol particles, may play a major role in mitigating climate change. Of these agents, methane is the most important greenhouse gas and has substantial mitigation potential. The role of black and organic carbon aerosols has attracted increasing interest and we explicitly include these carbonaceous aerosols in our calculations. This paper analyzes the potential role of different forcing agents in reducing future climate forcing in a multi-gas, integrated assessment model in which mitigation options compete and interact. Our framework includes all of the important atmospheric forcing agents: carbon dioxide, methane, nitrous oxide, halocarbons, sulfur dioxide, and carbonaceous aerosols along with an array of potential mitigation options. Through an integrated analysis of all available options we present a realistic portrait of the potential role of these forcing agents in limiting future climate change.

  20. Distinct Patterns of Climate Response to Anthropogenic Aerosol Versus Greenhouse Gas Forcing

    NASA Astrophysics Data System (ADS)

    WANG, H.; Xie, S. P.; Liu, Q.

    2015-12-01

    Patterns of climate response to anthropogenic aerosols and well-mixed greenhouse gas (GHG) changes are investigated using eight models from Phase 5 of the Coupled Model Intercomparison Project. In the 20th century, the principal climate response patterns show both similarities and differences between aerosol and GHG runs. This paper focuses on distinct patterns of climate response to aerosol and GHG changes, while a recent companion study discussed the similarities. The GHG induced radiative forcing gives rise to amplified warming in the tropical upper troposphere and intensified mid-latitude jets in both hemispheres. However, for the anthropogenic aerosols, they are concentrated in the Northern Hemisphere and the temperature change shows a deep cooling structure in the troposphere around 40°N. Consistent with thermal wind balance, the cooling anchors a westerly acceleration to its south in aerosol runs. The response to aerosol induced inter-hemispheric asymmetry is also interpreted in terms of an anomalous Hadley circulation across the equator. Careful comparison indicates that the aerosol forcing dominates the Northern Hemisphere response in atmospheric circulation and precipitation, including a southward shift of the Inter Tropical Convergence Zone, the drying trend over the East Asia monsoon region, the southward shift of the East Asia westerly jet and the North Pacific cooling. The GHG forcing dominates the tropical Pacific rainfall increase mediated by the sea surface temperature pattern. Several climate response pattern indices are evaluated for the relative importance of aerosol and GHG forcing. The aerosol induced inter-hemisphere thermal contrast plays a key role in inducing climate response patterns that are quite different from the results in GHG runs.

  1. Effects of aerosol emission pathways on future warming and human health

    NASA Astrophysics Data System (ADS)

    Partanen, Antti-Ilari; Matthews, Damon

    2016-04-01

    The peak global temperature is largely determined by cumulative emissions of long-lived greenhouse gases. However, anthropogenic emissions include also so-called short-lived climate forcers (SLCFs), which include aerosol particles and methane. Previous studies with simple models indicate that the timing of SLCF emission reductions has only a small effect on the rate of global warming and even less of an effect on global peak temperatures. However, these simple model analyses do not capture the spatial dynamics of aerosol-climate interactions, nor do they consider the additional effects of aerosol emissions on human health. There is therefore merit in assessing how the timing of aerosol emission reductions affects global temperature and premature mortality caused by elevated aerosol concentrations, using more comprehensive climate models. Here, we used an aerosol-climate model ECHAM-HAMMOZ to simulate the direct and indirect radiative forcing resulting from aerosol emissions. We simulated Representative Concentration Pathway (RCP) scenarios, and we also designed idealized low and high aerosol emission pathways based on RCP4.5 scenario (LOW and HIGH, respectively). From these simulations, we calculated the Effective Radiative Forcing (ERF) from aerosol emissions between 1850 and 2100, as well as aerosol concentrations used to estimate the premature mortality caused by particulate pollution. We then use the University of Victoria Earth System Climate Model to simulate the spatial and temporal pattern of climate response to these aerosol-forcing scenarios, in combination with prescribed emissions of both short and long-lived greenhouse gases according to the RCP4.5 scenario. In the RCP scenarios, global mean ERF declined during the 21st century from -1.3 W m-2 to -0.4 W m-2 (RCP8.5) and -0.2 W m-2 (RCP2.6). In the sensitivity scenarios, the forcing at the end of the 21st century was -1.6 W m-2 (HIGH) and practically zero (LOW). The difference in global mean temperature

  2. Role of aerosols on the Indian Summer Monsoon variability, as simulated by state-of-the-art global climate models

    NASA Astrophysics Data System (ADS)

    Cagnazzo, Chiara; Biondi, Riccardo; D'Errico, Miriam; Cherchi, Annalisa; Fierli, Federico; Lau, William K. M.

    2016-04-01

    Recent observational and modeling analyses have explored the interaction between aerosols and the Indian summer monsoon precipitation on seasonal-to-interannual time scales. By using global scale climate model simulations, we show that when increased aerosol loading is found on the Himalayas slopes in the premonsoon period (April-May), intensification of early monsoon rainfall over India and increased low-level westerly flow follow, in agreement with the elevated-heat-pump (EHP) mechanism. The increase in rainfall during the early monsoon season has a cooling effect on the land surface that may also be amplified through solar dimming (SD) by more cloudiness and aerosol loading with subsequent reduction in monsoon rainfall over India. We extend this analyses to a subset of CMIP5 climate model simulations. Our results suggest that 1) absorbing aerosols, by influencing the seasonal variability of the Indian summer monsoon with the discussed time-lag, may act as a source of predictability for the Indian Summer Monsoon and 2) if the EHP and SD effects are operating also in a number of state-of-the-art climate models, their inclusion could potentially improve seasonal forecasts.

  3. Regional Biases in Droplet Activation Parameterizations: Strong Influence on Aerosol Second Indirect Effect in the Community Atmosphere Model v5.

    NASA Astrophysics Data System (ADS)

    Morales, R.; Nenes, A.

    2014-12-01

    Aerosol-cloud interactions constitute one of the most uncertain aspects of anthropogenic climate change estimates. The magnitude of these interactions as represented in climate models strongly depends on the process of aerosol activation. This process is the most direct physical link between aerosols and cloud microphysical properties. Calculation of droplet number in GCMs requires the computation of new droplet formation (i.e., droplet activation), through physically based activation parameterizations. Considerable effort has been placed in ensuring that droplet activation parameterizations have a physically consistent response to changes in aerosol number concentration. However, recent analyses using an adjoint sensitivity approach showed that parameterizations can exhibit considerable biases in their response to other aerosol properties, such as aerosol modal diameter or to the aerosol chemical composition. This is a potentially important factor in estimating aerosol indirect effects since changes in aerosol properties from pre-industrial times to present day exhibit a very strong regional signature. In this work we use the Community Atmosphere Model (CAM5) to show that the regional imprint of the changes in aerosol properties during the last century interacts with the droplet activation parameterization in a way that these biases are amplified over climatically relevant regions. Two commonly used activation routines, the CAM5 default, Abdul-Razzak and Ghan parameterization, as well as the Fountoukis and Nenes parameterization are used in this study. We further explored the impacts of Nd parameterization biases in the first and second aerosol indirect effects separately, by performing simulations were droplet number was not allowed to intervene in the precipitation initiation process. The simulations performed show that an unphysical response to changes in the diameter of accumulation mode aerosol translates into extremely high Nd concentrations over South

  4. Background on health effects of acid aerosols.

    PubMed

    Lippmann, M

    1989-02-01

    This introduction to the 1987 NIEHS-EPA Symposium on the Health Effects of Acid Aerosols reviews the state of our knowledge on this topic as of the close of the 1984 NIEHS Conference on the Health Effects of Acid Precipitation (Environmental Health Perspectives, Volume 63) and the results of some key studies completed since that time. These studies, together with the results of the studies presented in the papers that follow, provide a substantial increment in our knowledge of the health effects of acid aerosols.

  5. Background on health effects of acid aerosols.

    PubMed Central

    Lippmann, M

    1989-01-01

    This introduction to the 1987 NIEHS-EPA Symposium on the Health Effects of Acid Aerosols reviews the state of our knowledge on this topic as of the close of the 1984 NIEHS Conference on the Health Effects of Acid Precipitation (Environmental Health Perspectives, Volume 63) and the results of some key studies completed since that time. These studies, together with the results of the studies presented in the papers that follow, provide a substantial increment in our knowledge of the health effects of acid aerosols. PMID:2707208

  6. Aerosol polarization effects on atmospheric correction and aerosol retrievals in ocean color remote sensing.

    PubMed

    Wang, Menghua

    2006-12-10

    The current ocean color data processing system for the Sea-viewing Wide Field-of-View Sensor (SeaWiFS) and the moderate resolution imaging spectroradiometer (MODIS) uses the Rayleigh lookup tables that were generated using the vector radiative transfer theory with inclusion of the polarization effects. The polarization effects, however, are not accounted for in the aerosol lookup tables for the ocean color data processing. I describe a study of the aerosol polarization effects on the atmospheric correction and aerosol retrieval algorithms in the ocean color remote sensing. Using an efficient method for the multiple vector radiative transfer computations, aerosol lookup tables that include polarization effects are generated. Simulations have been carried out to evaluate the aerosol polarization effects on the derived ocean color and aerosol products for all possible solar-sensor geometries and the various aerosol optical properties. Furthermore, the new aerosol lookup tables have been implemented in the SeaWiFS data processing system and extensively tested and evaluated with SeaWiFS regional and global measurements. Results show that in open oceans (maritime environment), the aerosol polarization effects on the ocean color and aerosol products are usually negligible, while there are some noticeable effects on the derived products in the coastal regions with nonmaritime aerosols.

  7. Retrieving the Vertical Structure of the Effective Aerosol Complex Index of Refraction from a Combination of Aerosol in Situ and Remote Sensing Measurements During TARFOX

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Turco, R. P.; Liou, K. N.; Russell, P. B.; Bergstrom, R. W.; Schmid, B.; Livingston, J. M.; Hobbs, P. V.; Hartley, W. S.; Ismail, S.; Ferrare, R. A.; Browell, E. V.

    2000-01-01

    The largest uncertainty in estimates of the effects of atmospheric aerosols on climate stems from uncertainties in the determination of their microphysical properties, including the aerosol complex index of refraction, which in turn determines their optical properties. A novel technique is used to estimate the aerosol complex index of refraction in distinct vertical layers from a combination of aerosol in situ size distribution and remote sensing measurements during the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX). In particular, aerosol backscatter measurements using the NASA Langley LASE (Lidar Atmospheric Sensing Experiment) instrument and in situ aerosol size distribution data are utilized to derive vertical profiles of the "effective" aerosol complex index of refraction at 815 nm (i.e., the refractive index that would provide the same backscatter signal in a forward calculation on the basis of the measured in situ particle size distributions for homogeneous, spherical aerosols). A sensitivity study shows that this method yields small errors in the retrieved aerosol refractive indices, provided the errors in the lidar-derived aerosol backscatter are less than 30% and random in nature. Absolute errors in the estimated aerosol refractive indices are generally less than 0.04 for the real part and can be as much as 0.042 for the imaginary part in the case of a 30% error in the lidar-derived aerosol backscatter. The measurements of aerosol optical depth from the NASA Ames Airborne Tracking Sunphotometer (AATS-6) are successfully incorporated into the new technique and help constrain the retrieved aerosol refractive indices. An application of the technique to two TARFOX case studies yields the occurrence of vertical layers of distinct aerosol refractive indices. Values of the estimated complex aerosol refractive index range from 1.33 to 1.45 for the real part and 0.001 to 0.008 for the imaginary part. The methodology devised in this study

  8. The effect of smoke, dust, and pollution aerosol on shallow cloud development over the Atlantic Ocean.

    PubMed

    Kaufman, Yoram J; Koren, Ilan; Remer, Lorraine A; Rosenfeld, Daniel; Rudich, Yinon

    2005-08-01

    Clouds developing in a polluted environment tend to have more numerous but smaller droplets. This property may lead to suppression of precipitation and longer cloud lifetime. Absorption of incoming solar radiation by aerosols, however, can reduce the cloud cover. The net aerosol effect on clouds is currently the largest uncertainty in evaluating climate forcing. Using large statistics of 1-km resolution MODIS (Moderate Resolution Imaging Spectroradiometer) satellite data, we study the aerosol effect on shallow water clouds, separately in four regions of the Atlantic Ocean, for June through August 2002: marine aerosol (30 degrees S-20 degrees S), smoke (20 degrees S-5 degrees N), mineral dust (5 degrees N-25 degrees N), and pollution aerosols (30 degrees N- 60 degrees N). All four aerosol types affect the cloud droplet size. We also find that the coverage of shallow clouds increases in all of the cases by 0.2-0.4 from clean to polluted, smoky, or dusty conditions. Covariability analysis with meteorological parameters associates most of this change to aerosol, for each of the four regions and 3 months studied. In our opinion, there is low probability that the net aerosol effect can be explained by coincidental, unresolved, changes in meteorological conditions that also accumulate aerosol, or errors in the data, although further in situ measurements and model developments are needed to fully understand the processes. The radiative effect at the top of the atmosphere incurred by the aerosol effect on the shallow clouds and solar radiation is -11 +/- 3 W/m2 for the 3 months studied; 2/3 of it is due to the aerosol-induced cloud changes, and 1/3 is due to aerosol direct radiative effect.

  9. The effect of smoke, dust, and pollution aerosol on shallow cloud development over the Atlantic Ocean.

    PubMed

    Kaufman, Yoram J; Koren, Ilan; Remer, Lorraine A; Rosenfeld, Daniel; Rudich, Yinon

    2005-08-01

    Clouds developing in a polluted environment tend to have more numerous but smaller droplets. This property may lead to suppression of precipitation and longer cloud lifetime. Absorption of incoming solar radiation by aerosols, however, can reduce the cloud cover. The net aerosol effect on clouds is currently the largest uncertainty in evaluating climate forcing. Using large statistics of 1-km resolution MODIS (Moderate Resolution Imaging Spectroradiometer) satellite data, we study the aerosol effect on shallow water clouds, separately in four regions of the Atlantic Ocean, for June through August 2002: marine aerosol (30 degrees S-20 degrees S), smoke (20 degrees S-5 degrees N), mineral dust (5 degrees N-25 degrees N), and pollution aerosols (30 degrees N- 60 degrees N). All four aerosol types affect the cloud droplet size. We also find that the coverage of shallow clouds increases in all of the cases by 0.2-0.4 from clean to polluted, smoky, or dusty conditions. Covariability analysis with meteorological parameters associates most of this change to aerosol, for each of the four regions and 3 months studied. In our opinion, there is low probability that the net aerosol effect can be explained by coincidental, unresolved, changes in meteorological conditions that also accumulate aerosol, or errors in the data, although further in situ measurements and model developments are needed to fully understand the processes. The radiative effect at the top of the atmosphere incurred by the aerosol effect on the shallow clouds and solar radiation is -11 +/- 3 W/m2 for the 3 months studied; 2/3 of it is due to the aerosol-induced cloud changes, and 1/3 is due to aerosol direct radiative effect. PMID:16076949

  10. Measured and modeled cloud-aerosol radiative effects in polluted cumulus clouds

    NASA Astrophysics Data System (ADS)

    Schmidt, K. S.; Feingold, G.; Pilewskie, P.; Jiang, H.; Coddington, O.

    2009-04-01

    Recent studies have emphasized the need to consider aerosol particles and clouds as an entity rather than artificially separating aerosol and cloud radiative forcing. A particularly difficult situation is that of cumulus clouds in a polluted background where radiative effects from heterogeneous clouds, aerosol particles, and surface albedo can only be distinguished by their spectral signature. We have used spectral irradiance measurements from the Gulf of Mexico Atmospheric Composition and Climate Study, and extensive three-dimensional radiative transfer calculations applied to the output of large eddy simulations, to show that measurements below clouds or cloud gaps are only reproduced when including aerosol particles in the calculations. Our technique enables the derivation of measurement-based spectral forcing and absorption of the cloud-aerosol-system. Furthermore, we present a new spectral effect caused by a combination of molecular scattering and cumulus cloud effects that is also relevant to cloud remote sensing.

  11. A perspective on SOA generated in aerosol water from glyoxal and methylglyoxal and its impacts on climate-relevant aerosol properties

    NASA Astrophysics Data System (ADS)

    Sareen, N.; McNeill, V. F.

    2011-12-01

    In recent years, glyoxal and methylglyoxal have emerged to be potentially important SOA precursors with significant implications for climate-related aerosol properties. Here we will discuss how the chemistry of these and similar organic compounds in aerosol water can affect the aerosol optical and cloud formation properties. Aqueous-phase SOA production from glyoxal and methylglyoxal is a potential source of strongly light-absorbing organics, or "brown carbon". We characterized the kinetics of brown carbon formation from these precursors in mixtures of ammonium sulfate and water using UV-Vis spectrophotometry. This mechanism has been incorporated into a photochemical box model with coupled gas phase-aqueous aerosol chemistry. Methylglyoxal and related compounds also may impact an aerosol's ability to act as a cloud condensation nucleus. We recently showed via pendant drop tensiometry and aerosol chamber studies that uptake of methylglyoxal from the gas phase driven by aqueous-phase oligomerization chemistry is a potentially significant, previously unidentified source of surface-active organic material in aerosols. Results from pendant drop tensiometry showed significantly depressed surface tension in methylglyoxal-ammonium sulfate solutions. We further found that ammonium sulfate particles exposed to gas-phase methylglyoxal in a 3.5 m3 aerosol reaction chamber activate into cloud droplets at sizes up to 15% lower at a given supersaturation than do pure ammonium sulfate particles. The observed enhancement exceeds that predicted based on Henry's Law and our measurements of surface tension depression in bulk solutions, suggesting that surface adsorption of methylglyoxal plays a role in determining CCN activity. Methylglyoxal and similar gas-phase surfactants may be an important and overlooked source of enhanced CCN activity in the atmosphere. To characterize the SOA products formed in these solutions, an Aerosol Chemical Ionization Mass Spectrometer (CIMS) was used

  12. Climatic analysis of satellite aerosol data on variations of submicron aerosols over East China

    NASA Astrophysics Data System (ADS)

    Tan, Chenghao; Zhao, Tianliang; Xu, Xiaofeng; Liu, Jane; Zhang, Lei; Tang, Lili

    2015-12-01

    Recently, haze events frequently occurred in East China. To assess the impacts of aerosols on air quality over the region, we investigate the interannual variations of the total aerosols and the submicron aerosols, in terms of the aerosol mass concentration (AMC) and Fine Mode Fraction (FMF), respectively, using the Moderate Resolution Imaging Spectrometer (MODIS) aerosol products, which can be used for regional air quality assessment, from 2003 to 2013. On average, the AMC distributes as "northern high and southern low", whereas the FMF shows a "northern low and southern high" pattern. High FMF occurs in the warm seasons, but low FMF appears in the cool seasons. During the 10 years, the AMC shows increasing trend in northern and decreasing trend in southeastern parts of the region, whereas an increasing trend in the FMF is observed over the entire East China, likely related to elevated submicron aerosols from anthropogenic sources. The East Asian summer monsoon impacts the submicron aerosols more than the total aerosols. The enhanced submicron aerosols are responsible for rapid deterioration of air quality in East China in recent years.

  13. Radiative Effects of Aerosol in the Marine Environment: Tales from the Two-Column Aerosol Project

    NASA Astrophysics Data System (ADS)

    Berg, L. K.; Fast, J. D.; Barnard, J.; Chand, D.; Chapman, E. G.; Comstock, J. M.; Ferrare, R. A.; Flynn, C. J.; Hair, J. W.; Hostetler, C. A.; Hubbe, J.; Johnson, R.; Kassianov, E.; Kluzek, C.; Laskin, A.; Lee, Y.; Mei, F.; Michalsky, J. J.; Redemann, J.; Rogers, R. R.; Russell, P. B.; Sedlacek, A. J.; Schmid, B.; Shilling, J. E.; Shinozuka, Y.; Springston, S. R.; Tomlinson, J. M.; Wilson, J. M.; Zelenyuk, A.; Berkowitz, C. M.

    2013-12-01

    There is still uncertainty associated with the direct radiative forcing by atmospheric aerosol and its representation in atmospheric models. This is particularly true in marine environments near the coast where the aerosol loading is a function of both naturally occurring and anthropogenic aerosol. These regions are also subject to variable synoptic and thermally driven flows (land-sea breezes) that transport aerosol between the continental and marine environments. The situation is made more complicated due to seasonal changes in aerosol emissions. Given these differences in emissions, we expect significant differences in the aerosol intensive and extensive properties between summer and winter and data is needed to evaluate models over the wide range of conditions. To address this issue, the recently completed Two Column Aerosol Project (TCAP) was designed to measure the key aerosol parameters in two atmospheric columns, one located over Cape Cod, Massachusetts and another approximately 200 km from the coast over the Atlantic Ocean. Measurements included aerosol size distribution, chemical composition, optical properties and vertical distribution. Several aspects make TCAP unique, including the year-long deployment of a suite of surface-based instruments by the US Department of Energy's Atmospheric Radiation Measurement (ARM) Climate Research Facility and two aircraft intensive operations periods supported by the ARM Airborne Facility, one conducted in July 2012 and a second in February 2013. The presentation will include a discussion of the impact of the aerosol optical properties and their uncertainty on simulations of the radiation budget within the TCAP domain in the context of both single column and regional scale models. Data from TCAP will be used to highlight a number of important factors, including diurnal variation in aerosol optical depth measured at the surface site, systematic changes in aerosol optical properties (including scattering, absorption, and

  14. Comparative Climate Responses of Anthropogenic Greenhouse Gases, All Major Aerosol Components, Black Carbon, and Methane, Accounting for the Evolution of the Aerosol Mixing State and of Clouds/Precipitation from Multiple Aerosol Size Distributions

    NASA Astrophysics Data System (ADS)

    Jacobson, M. Z.

    2005-12-01

    Several modeling studies to date have simulated the global climate response of anthropogenic greenhouse gases and bulk (non-size-resolved) sulfate or generic aerosol particles together, but no study has examined the climate response of greenhouse gases simultaneously with all major size- and composition resolved aerosol particle components. Such a study is important for improving our understanding of the effects of anthropogenic pollutants on climate. Here, the GATOR-GCMOM model is used to study the global climate response of (a) all major greenhouse gases and size-resolved aerosol components, (b) all major greenhouse gases alone, (c) fossil-fuel soot (black carbon, primary organic matter, sulfuric acid, bisulfate, sulfate), and (d) methane. Aerosol components treated in all simulations included water, black carbon, primary organic carbon, secondary organic carbon, sulfuric acid, bisulfate, sulfate, nitrate, chloride, ammonium, sodium, hydrogen ion, soil dust, and pollen/spores. Fossil-fuel soot (FFS) was emitted into its own size distribution. All other components, including biofuel and biomass soot, sea-spray, soil dust, etc., were emitted into a second distribution (MIX). The FFS distribution grew by condensation of secondary organic matter and sulfuric acid, hydration of water, and dissolution of nitric acid, ammonia, and hydrochloric acid. It self-coagulated and heterocoagulated with the MIX distribution, which also grew by condensation, hydration, and dissolution. Treatment of separate distributions for FFS allowed FFS to evolve from an external mixture to an internal mixture. In both distributions, black carbon was treated as a core component for optical calculations. Both aerosol distributions served as CCN during explicit size-resolved cloud formation. The resulting clouds grew by coagulation and condensation, coagulated with interstitial aerosol particles, and fell to the surface as rain and snow, carrying aerosol constituents with them. Thus, cloud

  15. EDITORIAL: Aerosol cloud interactions—a challenge for measurements and modeling at the cutting edge of cloud climate interactions

    NASA Astrophysics Data System (ADS)

    Spichtinger, Peter; Cziczo, Daniel J.

    2008-04-01

    Research in aerosol properties and cloud characteristics have historically been considered two separate disciplines within the field of atmospheric science. As such, it has been uncommon for a single researcher, or even research group, to have considerable expertise in both subject areas. The recent attention paid to global climate change has shown that clouds can have a considerable effect on the Earth's climate and that one of the most uncertain aspects in their formation, persistence, and ultimate dissipation is the role played by aerosols. This highlights the need for researchers in both disciplines to interact more closely than they have in the past. This is the vision behind this focus issue of Environmental Research Letters. Certain interactions between aerosols and clouds are relatively well studied and understood. For example, it is known that an increase in the aerosol concentration will increase the number of droplets in warm clouds, decrease their average size, reduce the rate of precipitation, and extend the lifetime. Other effects are not as well known. For example, persistent ice super-saturated conditions are observed in the upper troposphere that appear to exceed our understanding of the conditions required for cirrus cloud formation. Further, the interplay of dynamics versus effects purely attributed to aerosols remains highly uncertain. The purpose of this focus issue is to consider the current state of knowledge of aerosol/cloud interactions, to define the contemporary uncertainties, and to outline research foci as we strive to better understand the Earth's climate system. This focus issue brings together laboratory experiments, field data, and model studies. The authors address issues associated with warm liquid water, cold ice, and intermediate temperature mixed-phase clouds. The topics include the uncertainty associated with the effect of black carbon and organics, aerosol types of anthropogenic interest, on droplet and ice formation. Phases

  16. Effects of aerosol sources and chemical compositions on cloud drop sizes and glaciation temperatures

    NASA Astrophysics Data System (ADS)

    Zipori, Assaf; Rosenfeld, Daniel; Tirosh, Ofir; Teutsch, Nadya; Erel, Yigal

    2015-09-01

    The effect of aerosols on cloud properties, such as its droplet sizes and its glaciation temperatures, depends on their compositions and concentrations. In order to examine these effects, we collected rain samples in northern Israel during five winters (2008-2011 and 2013) and determined their chemical composition, which was later used to identify the aerosols' sources. By combining the chemical data with satellite-retrieved cloud properties, we linked the aerosol types, sources, and concentrations with the cloud glaciation temperatures (Tg). The presence of dust increased Tg from -26°C to -12°C already at relatively low dust concentrations. This result is in agreement with the conventional wisdom that desert dust serves as good ice nuclei (INs). With higher dust concentrations, Tg saturated at -12°C, even though cloud droplet sizes decreased as a result of the cloud condensation nucleating (CCN) activity of the dust. Marine air masses also encouraged freezing, but in this case, freezing was enhanced by the larger cloud droplet sizes in the air masses (caused by low CCN concentrations) and not by IN concentrations or by aerosol type. An increased fraction of anthropogenic aerosols in marine air masses caused a decrease in Tg, indicating that these aerosols served as poor IN. Anthropogenic aerosols reduced cloud droplet sizes, which further decreased Tg. Our results could be useful in climate models for aerosol-cloud interactions, as we investigated the effects of aerosols of different sources on cloud properties. Such parameterization can simplify these models substantially.

  17. Retrieving the Vertical Structure of the Effective Aerosol Complex Index of Refraction from a Combination of Aerosol in Situ and Remote Sensing Measurements During TARFOX

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Turco, R. P.; Liou, K. N.; Russell, P. B.; Bergstrom, R. W.; Schmid, B.; Livingston, J. M.; Hobbs, P. V.; Hartley, W. S.; Ismail, S.

    2000-01-01

    The largest uncertainty in estimates of the effects of atmospheric aerosols on climate stems from uncertainties in the determination of their microphysical properties, including the aerosol complex index of refraction, which in turn determines their optical properties. A novel technique is used to estimate the aerosol complex index of refraction in distinct vertical layers from a combination of aerosol in situ size distribution and remote sensing measurements during the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX). In particular, aerosol backscatter measurements using the NASA Langley LASE (Lidar Atmospheric Sensing Experiment) instrument and in situ aerosol size distribution data are utilized to derive vertical profiles of the 'effective' aerosol complex index of refraction at 815 nm (i.e., the refractive index that would provide the same backscatter signal in a forward calculation on the basis of the measured in situ particle size distributions for homogeneous, spherical aerosols). A sensitivity study shows that this method yields small errors in the retrieved aerosol refractive indices, provided the errors in the lidar derived aerosol backscatter are less than 30% and random in nature. Absolute errors in the estimated aerosol refractive indices are generally less than 0.04 for the real part and can be as much as 0.042 for the imaginary part in the case of a 30% error in the lidar-derived aerosol backscatter. The measurements of aerosol optical depth from the NASA Ames Airborne Tracking Sunphotometer (AATS-6) are successfully incorporated into the new technique and help constrain the retrieved aerosol refractive indices. An application of the technique to two TARFOX case studies yields the occurrence of vertical layers of distinct aerosol refractive indices. Values of the estimated complex aerosol refractive index range from 1.33 to 1.45 for the real part and 0.001 to 0.008 for the imaginary part. The methodology devised in this study

  18. Overview of the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES)

    SciTech Connect

    Zaveri, Rahul A.; Shaw, William J.; Cziczo, D. J.; Schmid, Beat; Ferrare, R.; Alexander, M. L.; Alexandrov, Mikhail; Alvarez, R. J.; Arnott, W. P.; Atkinson, D.; Baidar, Sunil; Banta, Robert M.; Barnard, James C.; Beranek, Josef; Berg, Larry K.; Brechtel, Fred J.; Brewer, W. A.; Cahill, John F.; Cairns, Brian; Cappa, Christopher D.; Chand, Duli; China, Swarup; Comstock, Jennifer M.; Dubey, Manvendra K.; Easter, Richard C.; Erickson, Matthew H.; Fast, Jerome D.; Floerchinger, Cody; Flowers, B. A.; Fortner, Edward; Gaffney, Jeffrey S.; Gilles, Mary K.; Gorkowski, K.; Gustafson, William I.; Gyawali, Madhu S.; Hair, John; Hardesty, Michael; Harworth, J. W.; Herndon, Scott C.; Hiranuma, Naruki; Hostetler, Chris A.; Hubbe, John M.; Jayne, J. T.; Jeong, H.; Jobson, Bertram T.; Kassianov, Evgueni I.; Kleinman, L. I.; Kluzek, Celine D.; Knighton, B.; Kolesar, K. R.; Kuang, Chongai; Kubatova, A.; Langford, A. O.; Laskin, Alexander; Laulainen, Nels S.; Marchbanks, R. D.; Mazzoleni, Claudio; Mei, F.; Moffet, Ryan C.; Nelson, Danny A.; Obland, Michael; Oetjen, Hilke; Onasch, Timothy B.; Ortega, Ivan; Ottaviani, M.; Pekour, Mikhail S.; Prather, Kimberly A.; Radney, J. G.; Rogers, Ray; Sandberg, S. P.; Sedlacek, Art; Senff, Christoph; Senum, Gunar; Setyan, Ari; Shilling, John E.; Shrivastava, ManishKumar B.; Song, Chen; Springston, S. R.; Subramanian, R.; Suski, Kaitlyn; Tomlinson, Jason M.; Volkamer, Rainer M.; Wallace, Hoyt A.; Wang, J.; Weickmann, A. M.; Worsnop, Douglas R.; Yu, Xiao-Ying; Zelenyuk, Alla; Zhang, Qi

    2012-08-22

    Substantial uncertainties still exist in the scientific understanding of the possible interactions between urban and natural (biogenic) emissions in the production and transformation of atmospheric aerosol and the resulting impact on climate change. The U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) program's Carbonaceous Aerosol and Radiative Effects Study (CARES) carried out in June 2010 in Central Valley, California, was a comprehensive effort designed to improve this understanding. The primary objective of the field study was to investigate the evolution of secondary organic and black carbon aerosols and their climate-related properties in the Sacramento urban plume as it was routinely transported into the forested Sierra Nevada foothills area. Urban aerosols and trace gases experienced significant physical and chemical transformations as they mixed with the reactive biogenic hydrocarbons emitted from the forest. Two heavily-instrumented ground sites - one within the Sacramento urban area and another about 40 km to the northeast in the foothills area - were set up to characterize the evolution of meteorological variables, trace gases, aerosol precursors, aerosol size, composition, and climate-related properties in freshly polluted and 'aged' urban air. On selected days, the DOE G-1 aircraft was deployed to make similar measurements upwind and across the evolving Sacramento plume in the morning and again in the afternoon. The NASA B-200 aircraft, carrying remote sensing instruments, was also deployed to characterize the vertical and horizontal distribution of aerosols and aerosol optical properties within and around the plume. This overview provides: a) the scientific background and motivation for the study, b) the operational and logistical information pertinent to the execution of the study, c) an overview of key observations and initial results from the aircraft and ground-based sampling platforms, and d) a roadmap of planned data

  19. Overview of the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES)

    SciTech Connect

    Zaveri, R. A.; Shaw, W. J.; Cziczo, D. J.; Schmid, B.; Ferrare, R. A.; Alexander, M. L.; Alexandrov, M.; Alvarez, R. J.; Arnott, W. P.; Atkinson, D. B.; Baidar, S.; Banta, R. M.; Barnard, J. C.; Beranek, J.; Berg, L. K.; Brechtel, F.; Brewer, W. A.; Cahill, J. F.; Cairns, B.; Cappa, C. D.; Chand, D.; China, S.; Comstock, J. M.; Dubey, M. K.; Easter, R. C.; Erickson, M. H.; Fast, J. D.; Floerchinger, C.; Flowers, B. A.; Fortner, E.; Gaffney, J. S.; Gilles, M. K.; Gorkowski, K.; Gustafson, W. I.; Gyawali, M.; Hair, J.; Hardesty, R. M.; Harworth, J. W.; Herndon, S.; Hiranuma, N.; Hostetler, C.; Hubbe, J. M.; Jayne, J. T.; Jeong, H.; Jobson, B. T.; Kassianov, E. I.; Kleinman, L. I.; Kluzek, C.; Knighton, B.; Kolesar, K. R.; Kuang, C.; Kubátová, A.; Langford, A. O.; Laskin, A.; Laulainen, N.; Marchbanks, R. D.; Mazzoleni, C.; Mei, F.; Moffet, R. C.; Nelson, D.; Obland, M. D.; Oetjen, H.; Onasch, T. B.; Ortega, I.; Ottaviani, M.; Pekour, M.; Prather, K. A.; Radney, J. G.; Rogers, R. R.; Sandberg, S. P.; Sedlacek, A.; Senff, C. J.; Senum, G.; Setyan, A.; Shilling, J. E.; Shrivastava, M.; Song, C.; Springston, S. R.; Subramanian, R.; Suski, K.; Tomlinson, J.; Volkamer, R.; Wallace, H. W.; Wang, J.; Weickmann, A. M.; Worsnop, D. R.; Yu, X. -Y.; Zelenyuk, A.; Zhang, Q.

    2012-01-01

    Substantial uncertainties still exist in the scientific understanding of the possible interactions between urban and natural (biogenic) emissions in the production and transformation of atmospheric aerosol and the resulting impact on climate change. The U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) program’s Carbonaceous Aerosol and Radiative Effects Study (CARES) carried out in June 2010 in Central Valley, California, was a comprehensive effort designed to improve this understanding. The primary objective of the field study was to investigate the evolution of secondary organic and black carbon aerosols and their climate-related properties in the Sacramento urban plume as it was routinely transported into the forested Sierra Nevada foothills area. Urban aerosols and trace gases experienced significant physical and chemical transformations as they mixed with the reactive biogenic hydrocarbons emitted from the forest. Two heavily-instrumented ground sites – one within the Sacramento urban area and another about 40 km to the northeast in the foothills area – were set up to characterize the evolution of meteorological variables, trace gases, aerosol precursors, aerosol size, composition, and climate-related properties in freshly polluted and “aged” urban air. On selected days, the DOE G-1 aircraft was deployed to make similar measurements upwind and across the evolving Sacramento plume in the morning and again in the afternoon. The NASA B-200 aircraft, carrying remote sensing instruments, was also deployed to characterize the vertical and horizontal distribution of aerosols and aerosol optical properties within and around the plume. This overview provides: a) the scientific background and motivation for the study, b) the operational and logistical information pertinent to the execution of the study, c) an overview of key observations and initial findings from the aircraft and ground-based sampling platforms, and d) a roadmap of

  20. Overview of the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES)

    NASA Astrophysics Data System (ADS)

    Zaveri, R. A.; Shaw, W. J.; Cziczo, D. J.; Schmid, B.; Ferrare, R. A.; Alexander, M. L.; Alexandrov, M.; Alvarez, R. J.; Arnott, W. P.; Atkinson, D. B.; Baidar, S.; Banta, R. M.; Barnard, J. C.; Beranek, J.; Berg, L. K.; Brechtel, F.; Brewer, W. A.; Cahill, J. F.; Cairns, B.; Cappa, C. D.; Chand, D.; China, S.; Comstock, J. M.; Dubey, M. K.; Easter, R. C.; Erickson, M. H.; Fast, J. D.; Floerchinger, C.; Flowers, B. A.; Fortner, E.; Gaffney, J. S.; Gilles, M. K.; Gorkowski, K.; Gustafson, W. I.; Gyawali, M.; Hair, J.; Hardesty, R. M.; Harworth, J. W.; Herndon, S.; Hiranuma, N.; Hostetler, C.; Hubbe, J. M.; Jayne, J. T.; Jeong, H.; Jobson, B. T.; Kassianov, E. I.; Kleinman, L. I.; Kluzek, C.; Knighton, B.; Kolesar, K. R.; Kuang, C.; Kubátová, A.; Langford, A. O.; Laskin, A.; Laulainen, N.; Marchbanks, R. D.; Mazzoleni, C.; Mei, F.; Moffet, R. C.; Nelson, D.; Obland, M. D.; Oetjen, H.; Onasch, T. B.; Ortega, I.; Ottaviani, M.; Pekour, M.; Prather, K. A.; Radney, J. G.; Rogers, R. R.; Sandberg, S. P.; Sedlacek, A.; Senff, C. J.; Senum, G.; Setyan, A.; Shilling, J. E.; Shrivastava, M.; Song, C.; Springston, S. R.; Subramanian, R.; Suski, K.; Tomlinson, J.; Volkamer, R.; Wallace, H. W.; Wang, J.; Weickmann, A. M.; Worsnop, D. R.; Yu, X.-Y.; Zelenyuk, A.; Zhang, Q.

    2012-08-01

    Substantial uncertainties still exist in the scientific understanding of the possible interactions between urban and natural (biogenic) emissions in the production and transformation of atmospheric aerosol and the resulting impact on climate change. The US Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) program's Carbonaceous Aerosol and Radiative Effects Study (CARES) carried out in June 2010 in Central Valley, California, was a comprehensive effort designed to improve this understanding. The primary objective of the field study was to investigate the evolution of secondary organic and black carbon aerosols and their climate-related properties in the Sacramento urban plume as it was routinely transported into the forested Sierra Nevada foothills area. Urban aerosols and trace gases experienced significant physical and chemical transformations as they mixed with the reactive biogenic hydrocarbons emitted from the forest. Two heavily-instrumented ground sites - one within the Sacramento urban area and another about 40 km to the northeast in the foothills area - were set up to characterize the evolution of meteorological variables, trace gases, aerosol precursors, aerosol size, composition, and climate-related properties in freshly polluted and "aged" urban air. On selected days, the DOE G-1 aircraft was deployed to make similar measurements upwind and across the evolving Sacramento plume in the morning and again in the afternoon. The NASA B-200 aircraft, carrying remote sensing instruments, was also deployed to characterize the vertical and horizontal distribution of aerosols and aerosol optical properties within and around the plume. This overview provides: (a) the scientific background and motivation for the study, (b) the operational and logistical information pertinent to the execution of the study, (c) an overview of key observations and initial findings from the aircraft and ground-based sampling platforms, and (d) a roadmap of planned data

  1. Overview of the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES)

    NASA Astrophysics Data System (ADS)

    Zaveri, R. A.; Shaw, W. J.; Cziczo, D. J.; Schmid, B.; Alexander, M. L.; Alexandrov, M.; Alvarez, R. J.; Arnott, W. P.; Atkinson, D. B.; Baidar, S.; Banta, R. M.; Barnard, J. C.; Beranek, J.; Berg, L. K.; Brechtel, F.; Brewer, W. A.; Cahill, J. F.; Cairns, B.; Cappa, C. D.; Chand, D.; China, S.; Comstock, J. M.; Dubey, M. K.; Easter, R. C.; Fast, J. D.; Floerchinger, C.; Flowers, B. A.; Fortner, E.; Gaffney, J. S.; Gilles, M. K.; Gorkowski, K.; Gustafson, W. I.; Gyawali, M.; Hair, J.; Hardesty, R. M.; Harworth, J. W.; Herndon, S.; Hiranuma, N.; Hostetler, C.; Hubbe, J. M.; Jayne, J. T.; Jeong, H.; Jobson, B. T.; Kleinman, L. I.; Kluzek, C.; Knighton, B.; Kolesar, K. R.; Kuang, C.; Langford, A. O.; Laskin, A.; Marchbanks, R. D.; Mazzoleni, C.; Mei, F.; Moffet, R. C.; Nelson, D.; Obland, M. D.; Oetjen, H.; Onasch, T. B.; Ortega, I.; Ottaviani, M.; Pekour, M.; Prather, K. A.; Radney, J. G.; Rogers, R. R.; Sandberg, S. P.; Sedlacek, A.; Senff, C. J.; Senum, G.; Setyan, A.; Shilling, J. E.; Shrivastava, M.; Song, C.; Springston, S. R.; Subramanian, R.; Tomlinson, J.; Volkamer, R.; Wallace, H. W.; Wang, J.; Weickmann, A. M.; Yu, X.-Y.; Zelenyuk, A.; Zhang, Q.

    2012-01-01

    Substantial uncertainties still exist in the scientific understanding of the possible interactions between urban and natural (biogenic) emissions in the production and transformation of atmospheric aerosol and the resulting impact on climate change. The US Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) program's Carbonaceous Aerosol and Radiative Effects Study (CARES) carried out in June 2010 in Central Valley, California, was a comprehensive effort designed to improve this understanding. The primary objective of the field study was to investigate the evolution of secondary organic and black carbon aerosols and their climate-related properties in the Sacramento urban plume as it was routinely transported into the forested Sierra Nevada foothills area. Urban aerosols and trace gases experienced significant physical and chemical transformations as they mixed with the reactive biogenic hydrocarbons emitted from the forest. Two heavily-instrumented ground sites - one within the Sacramento urban area and another about 40 km to the northeast in the foothills area - were set up to characterize the evolution of meteorological variables, trace gases, aerosol precursors, aerosol size, composition, and climate-related properties in freshly polluted and "aged" urban air. On selected days, the DOE G-1 aircraft was deployed to make similar measurements upwind and across the evolving Sacramento plume in the morning and again in the afternoon. The NASA B-200 aircraft, carrying remote sensing instruments, was also deployed to characterize the vertical and horizontal distribution of aerosols and aerosol optical properties within and around the plume. This overview provides: (a) the scientific background and motivation for the study, (b) the operational and logistical information pertinent to the execution of the study, (c) an overview of key observations and initial results from the aircraft and ground-based sampling platforms, and (d) a roadmap of planned data

  2. The persistently variable "background" stratospheric aerosol layer and global climate change.

    PubMed

    Solomon, S; Daniel, J S; Neely, R R; Vernier, J-P; Dutton, E G; Thomason, L W

    2011-08-12

    Recent measurements demonstrate that the "background" stratospheric aerosol layer is persistently variable rather than constant, even in the absence of major volcanic eruptions. Several independent data sets show that stratospheric aerosols have increased in abundance since 2000. Near-global satellite aerosol data imply a negative radiative forcing due to stratospheric aerosol changes over this period of about -0.1 watt per square meter, reducing the recent global warming that would otherwise have occurred. Observations from earlier periods are limited but suggest an additional negative radiative forcing of about -0.1 watt per square meter from 1960 to 1990. Climate model projections neglecting these changes would continue to overestimate the radiative forcing and global warming in coming decades if these aerosols remain present at current values or increase.

  3. A dichotomy in primary marine organic aerosol-cloud-climate system

    NASA Astrophysics Data System (ADS)

    Ceburnis, D.; Ovadnevaite, J.; Martucci, G.; Bialek, J.; Monahan, C.; Rinaldi, M.; Facchini, C.; Berresheim, H.; Worsnop, D. R.; O'Dowd, C.

    2011-12-01

    D. Ceburnis1, J. Ovadnevaite1, G. Martucci1, J. Bialek1, C. Monahan1, M. Rinaldi2, M. C. Facchini2, H. Berresheim1, D. R. Worsnop3,4 and C. D. O'Dowd1 1School of Physics & Centre for Climate and Air Pollution Studies, National University of Ireland Galway, University Road, Galway, Ireland 2Institute of Atmospheric Sciences and Climate, National Research Council, Bologna, 20129, Italy. 3 Aerodyne Research, Inc., 45 Manning Road, Billerica, MA 01821-3976, USA 4 Physics Department, University of Helsinki, P.O. Box 64, 00014, Helsinki, Finland Organic matter has been observed to significantly contribute to particulate matter in every environment including pristine remote oceans. A significant if not dominant contribution of insoluble organic matter to marine aerosol has been proved to be of biogenic origin1,2. High time resolution measurements of marine organic matter have demonstrated a dynamic system with regular organic matter plume events occurring during summer3 as well as frequent open ocean particle formation events4. High-time resolution measurements of primary marine organic sea-spray physico-chemical properties reveal an apparent dichotomous behavior in terms of water uptake: specifically sea-spray aerosol enriched in organic matter possesses a low hygroscopic Growth Factor (GF~1.25) while simultaneously having a cloud condensation nucleus/condensation nuclei (CCN/CN) activation efficiency of between 83% at 0.25% supersaturation and 100% at 0.75%5. Simultaneous retrieval of Cloud Droplet Number Concentration (CDNC) during primary organic aerosol plumes reveal CDNC concentrations of 350 cm-3 in newly formed marine stratocumulus cloud for boundary layer organic mass concentrations of 3-4 ug m-36. It is suggested that marine hydrogels are responsible for this dichotomous behavior which has profound impacts to aerosol-cloud-climate system along with a better understood process analysis of aerosol formation by sea-spray7. A hydrophobic character of organic matter

  4. Incorporation of advanced aerosol activation treatments into CESM/CAM5: model evaluation and impacts on aerosol indirect effects

    NASA Astrophysics Data System (ADS)

    Gantt, B.; He, J.; Zhang, X.; Zhang, Y.; Nenes, A.

    2013-12-01

    One of the greatest sources of uncertainty in the science of anthropogenic climate change is from aerosol-cloud interactions. The activation of aerosols into cloud droplets is a direct microphysical link between aerosols and clouds; parameterizations of this process realistically link aerosol with cloud condensation nuclei (CCN) and the resulting indirect effects. Small differences between parameterizations can have a large impact on the spatiotemporal distributions of activated aerosols and the resulting cloud properties. In this work, we incorporate a series of aerosol activation schemes into the Community Atmosphere Model version 5.1.1 within the Community Earth System Model version 1.0.5 (CESM/CAM5), which include factors such as insoluble aerosol adsorption, giant cloud condensation nuclei (CCN) activation kinetics, and entrainment to understand their individual impacts on global scale cloud droplet number concentrations (CDNCs). Compared to the existing simple activation scheme in CESM/CAM5, this series of schemes predict CDNCs that are typically in better agreement with satellite-derived and observed values. The largest changes in predicted CDNCs occur over desert and oceanic regions, owing to the enhanced activation of dust from insoluble aerosol adsorption and reductions in cloud supersaturation from the intense absorption of water vapor in regions of strong giant CCN emissions (e.g., sea-salt). Comparison of CESM/CAM5 against satellite-derived cloud optical thickness and liquid water path shows that the updated activation schemes improve the low biases in their predictions. Globally, the incorporation of all updated schemes leads to an average increase in column CDNCs of 155%, an increase in shortwave cloud forcing of 13%, and a decrease in surface shortwave radiation of 4%. In terms of meteorological impacts, these updated aerosol activation schemes result in a slight decrease in near-surface temperature of 0.9 °C and precipitation of 0.04 mm day-1

  5. Coupling Satellite and Ground-Based Instruments to Map Climate Forcing by Anthropogenic Aerosols

    NASA Technical Reports Server (NTRS)

    Charlson, Robert J.; Anderson, Theodore L.; Hostetler, Chris (Technical Monitor)

    2000-01-01

    Climate forcing by anthropogenic aerosols is a significant but highly uncertain factor in global climate change. Only satellites can offer the global coverage essential to reducing this uncertainty; however, satellite measurements must be coupled with correlative, in situ measurements both to constrain the aerosol optical properties required in satellite retrieval algorithms and to provide chemical identification of aerosol sources. This grant funded the first two years of a three-year project which seeks to develop methodologies for combining spaceborne lidar with in-situ aerosol data sets to improve estimates of direct aerosol climate forcing. Progress under this two-year grant consisted in the development and deployment of a new in-situ capability for measuring aerosol 180' backscatter and the extinction-to-backscatter ratio. This new measurement capacity allows definitive lidar/in-situ comparisons and improves our ability to interpret lidar data in terms of climatically relevant quantities such as the extinction coefficient and optical depth. Measurements were made along the coast of Washington State, in Central Illinois, over the Indian Ocean, and in the Central Pacific. Thus, this research, combined with previous measurements by others, is rapidly building toward a global data set of extinction-to-backscatter ratio for key aerosol types. Such information will be critical to interpreting lidar data from the upcoming PICASSO-CENA, or P-C, satellite mission. Another aspect of this project is to investigate innovative ways to couple the lidar-satellite signal with targeted in-situ measurements toward a direct determination of aerosol forcing. This aspect is progressing in collaboration with NASA Langley's P-C lidar simulator and radiative transfer modeling by the University of Lille, France.

  6. Coupling Satellite and Ground-Based Instruments to Map Climate Forcing by Anthropogenic Aerosol

    NASA Technical Reports Server (NTRS)

    Charlson, Robert J.; Anderson, Theodore L.; Hostetler, Chris (Technical Monitor)

    2000-01-01

    Climate forcing by anthropogenic aerosols is a significant but highly uncertain factor in global climate change. Only satellites can offer the global coverage essential to reducing this uncertainty; however, satellite measurements must be coupled with correlative, in situ measurements both to constrain the aerosol optical properties required in satellite retrieval algorithms and to provide chemical identification of aerosol sources. This grant funded the third year of a three-year project which seeks to develop methodologies for combining spaceborne lidar with in-situ aerosol data sets to improve estimates of direct aerosol climate forcing. Progress under this one-year grant consisted in analysis and publication of field studies using a new in-situ capability for measuring aerosol 180 deg backscatter and the extinction-to-backscatter ratio. This new measurement capacity allows definitive lidar/in-situ comparisons and improves our ability to interpret lidar data in terms of climatically relevant quantities such as the extinction coefficient and optical depth. Analyzed data consisted of measurements made along the coast of Washington State, in Central Illinois, over the Indian Ocean, and in the Central Pacific. Thus, this research, combined with previous measurements by others, is rapidly building toward a global data set of extinction-to-backscatter ratio for key aerosol types. Such information will be critical to interpreting lidar data from the upcoming PICASSO-CENA, or P-C, satellite mission. Another aspect of this project is to investigate innovative ways to couple the lidar-satellite signal with target in-situ measurements toward a direct determination of aerosol forcing. This aspect is progressing in collaboration with NASA Langley's P-C lidar simulator.

  7. Volcanic effects on climate

    NASA Technical Reports Server (NTRS)

    Robock, Alan

    1991-01-01

    Volcanic eruptions which inject large amounts of sulfur-rich gas into the stratosphere produce dust veils which last years and cool the earth's surface. At the same time, these dust veils absorb enough solar radiation to warm the stratosphere. Since these temperature changes at the earth's surface and in the stratosphere are both in the opposite direction of hypothesized effects from greenhouse gases, they act to delay and mask the detection of greenhouse effects on the climate system. Tantalizing recent research results have suggested regional effects of volcanic eruptions, including effects on El Nino/Southern Oscillation (ENSO). In addition, a large portion of the global climate change of the past 100 years may be due to the effects of volcanoes, but a definite answer is not yet clear. While effects of several years were demonstrated with both data studies and numerical models, long-term effects, while found in climate model calculations, await confirmation with more realistic models. Extremely large explosive prehistoric eruptions may have produced severe weather and climate effects, sometimes called a 'volcanic winter'. Complete understanding of the above effects of volcanoes is hampered by inadequacies of data sets on volcanic dust veils and on climate change. Space observations can play an increasingly important role in an observing program in the future. The effects of volcanoes are not adequately separated from ENSO events, and climate modeling of the effects of volcanoes is in its infancy. Specific suggestions are made for future work to improve the knowledge of this important component of the climate system.

  8. "Investigation of Trends in Aerosol Direct Radiative Effects over North America Using a Coupled Meteorology-Chemistry Model"

    EPA Science Inventory

    While aerosol radiative effects have been recognized as some of the largest sources of uncertainty among the forcers of climate change, there has been little effort devoted to verification of the spatial and temporal variability of the magnitude and directionality of aerosol radi...

  9. “Modeling Trends in Aerosol Direct Radiative Effects over the Northern Hemisphere using a Coupled Meteorology-Chemistry Model”

    EPA Science Inventory

    While aerosol radiative effects have been recognized as some of the largest sources of uncertainty among the forcers of climate change, the verification of the spatial and temporal variability of the magnitude and directionality of aerosol radiative forcing has remained challengi...

  10. Aerosol Absorption by Black Carbon and Dust: Implications of Climate Change and Air Quality in Asia

    NASA Technical Reports Server (NTRS)

    Chin, Mian

    2010-01-01

    Atmospheric aerosol distributions from 2000 to 2007 are simulated with the global model GOCART to attribute light absorption by aerosol to its composition and sources. We show the seasonal and interannual variations of absorbing aerosols in the atmosphere over Asia, mainly black carbon and dust. and their linkage to the changes of anthropogenic and dust emissions in the region. We compare our results with observations from satellite and ground-based networks, and estimate the importance of black carbon and dust on regional climate forcing and air quality.

  11. The Impact of Biogenic and Anthropogenic Atmospheric Aerosol on Climate in Egypt

    NASA Astrophysics Data System (ADS)

    Ibrahim, A. I.; Zakey, A.; Steiner, A. L.; Shokr, M. E.; El-Raey, M.; Ahmed, Y.; Al-Hadidi, A.; Zakey, A.

    2014-12-01

    Aerosols are indicators of air quality as they reduce visibility and adversely affect public health. Aerosol optical depth (AOD) is a measure of the radiation extinction due to interaction of radiation with aerosol particles in the atmosphere. Using this optical measure of atmospheric aerosols we explore the seasonal and annual patterns of aerosols from both anthropogenic and biogenic sources over Egypt. Here, we use an integrated environment-climate-aerosol model in conjunction with inversion technique to identify the aerosol particle size distribution over different locations in Egypt. The online-integrated Environment-Climate-Aerosol model (EnvClimA), which is based on the International Center for Theoretical Physics Regional Climate Model (ICTP-RegCM), is used to study the emission of different aerosols and their impact on climate parameters for a long-term base line simulation run over Egypt and North Africa. The global emission inventory is downscaled and remapping them over Egypt using local factors such as population, traffic and industrial activities to identify the sources of anthropogenic and biogenic emission from local emission over Egypt. The results indicated that the dominant natural aerosols over Egypt are dust emissions that frequently occur during the transitional seasons (Spring and Autumn). From the local observation we identify the number of dust and sand storm occurrences over Egypt. The Multiangle Imaging SpectroRadiometer (MISR) is used to identify the optical characterizations of different types of aerosols over Egypt. Modeled aerosol optical depth and MISR observed (at 555 nm) are compared from March 2000 through November 2013. The results identify that the MISR AOD captures the maximum peaks of AOD in March/April that coincide with the Khamasin dust storms. However, peaks in May are either due to photochemical reactions or anthropogenic activities. Note: This presentation is for a Partnerships for Enhanced Engagement in Research (PEER

  12. Future Projections of Aerosol Optical Depth, Radiative Forcing, and Climate Response Due to Declining Aerosol Emissions in the Representative Concentration Pathways

    NASA Astrophysics Data System (ADS)

    Westervelt, D. M.; Mauzerall, D. L.; Horowitz, L. W.; Naik, V.

    2014-12-01

    It is widely expected that global emissions of atmospheric aerosols and their precursors will decrease strongly throughout the remainder of the 21st century, due to emission reduction policies enacted based on human health concerns. However, the resulting decrease in atmospheric aerosol burden will have unintended climate consequences. Since aerosols generally exert a net cooling influence on the climate, their removal will lead to an unmasking of global warming as well as other changes to the climate system. Aerosol and precursor global emissions decrease by as much as 80% by the year 2100, according to projections in four Representative Concentration Pathway (RCP) scenarios. We use the Geophysical Fluid Dynamics Laboratory Climate Model version 3 (GFDL CM3) to simulate future climate over the 21st century with and without aerosol emission changes projected by the RCPs in order to isolate the radiative forcing and climate response due to the aerosol reductions. We find that up to 1 W m-2 of radiative forcing may be unmasked globally by 2100 due to reductions in aerosol and precursor emissions, leading to average global temperature increases up to 1 K and global precipitation rate increases up to 0.09 mm d-1 (3%). Regionally and locally, climate impacts are much larger, as RCP8.5 projects a 2.1 K warming over China, Japan, and Korea due to reduced aerosol emissions. Our results highlight the importance of crafting emissions control policies with both climate and air pollution benefits in mind. The expected unmasking of additional global warming from aerosol reductions highlights the importance of robust greenhouse gas mitigation policies and may require more aggressive policies than anticipated.

  13. Quantitative analysis of the direct effect of aerosols over decadal scale by using ECHAM6-standalone

    NASA Astrophysics Data System (ADS)

    Muhammad, K.; Bott, A.; Hense, A.

    2013-12-01

    The influence of aerosols on climate is an important but still highly uncertain aspect in climate research. By using atmospheric general circulation model ECHAM6 our objective is to quantify the direct effect of aerosols over decadal time scale in comparison to the variability induced by the varying sea surface temperatures (SST) and sea ice concentrations (SIC) taken by the AMIP-II data base and the inevitable internal and unpredictable climate noise. We integrated the model with prescribed SST/SIC along with observed green house gases and aerosols concentrations for ten year period 1995-2004. Two ensembles with sample size ten, each have been created by starting the integrations on January 1st, 1995 with ten different initial conditions derived from two control runs over 15-years. These ensembles differ for tropospheric aerosols (TA): the non-aerosol case (NAC) is without any TA and aerosol case (AC) is utilizing a time variable data set of aerosols optical properties for input into the solar part of the ECHAM6 radiation code (Kinne et al, 2006). This set-up allows for a quantitative estimation and separation of the stationary and transient aerosol effects, the SST/SIC induced variability and the internal variability due to large scale atmospheric instabilities and non-linearities with the help of a two-way analysis of variance. We analyzed ensemble data for top of atmosphere (TOA) energy balance and temperature at 850 hPa. In the NAC, the ensemble exhibits a global and annual mean 3 W/m2 imbalance of the TOA radiation balance whereas the AC shows only 0.6 W/m2 being much closer in radiative balance over ten year period. The aerosols increase global planetary albedo from 0.29 (non-aerosol) to 0.30 for aerosol case. Extending the analysis to regional values of annual mean TOA radiation balance components, we find that the changes in TOA solar radiation budget are highly significant for static direct aerosol effect with local contributions to the total variability

  14. A Global Modeling Study on Carbonaceous Aerosol Microphysical Characteristics and Radiative Effects

    NASA Technical Reports Server (NTRS)

    Bauer, S. E.; Menon, S.; Koch, D.; Bond, T. C.; Tsigaridis, K.

    2010-01-01

    Recently, attention has been drawn towards black carbon aerosols as a short-term climate warming mitigation candidate. However the global and regional impacts of the direct, indirect and semi-direct aerosol effects are highly uncertain, due to the complex nature of aerosol evolution and the way that mixed, aged aerosols interact with clouds and radiation. A detailed aerosol microphysical scheme, MATRIX, embedded within the GISS climate model is used in this study to present a quantitative assessment of the impact of microphysical processes involving black carbon, such as emission size distributions and optical properties on aerosol cloud activation and radiative effects. Our best estimate for net direct and indirect aerosol radiative flux change between 1750 and 2000 is -0.56 W/m2. However, the direct and indirect aerosol effects are quite sensitive to the black and organic carbon size distribution and consequential mixing state. The net radiative flux change can vary between -0.32 to -0.75 W/m2 depending on these carbonaceous particle properties at emission. Taking into account internally mixed black carbon particles let us simulate correct aerosol absorption. Absorption of black carbon aerosols is amplified by sulfate and nitrate coatings and, even more strongly, by organic coatings. Black carbon mitigation scenarios generally showed reduced radiative fluxeswhen sources with a large proportion of black carbon, such as diesel, are reduced; however reducing sources with a larger organic carbon component as well, such as bio-fuels, does not necessarily lead to a reduction in positive radiative flux.

  15. The impact of residential combustion emissions on atmospheric aerosol, human health, and climate

    NASA Astrophysics Data System (ADS)

    Butt, E. W.; Rap, A.; Schmidt, A.; Scott, C. E.; Pringle, K. J.; Reddington, C. L.; Richards, N. A. D.; Woodhouse, M. T.; Ramirez-Villegas, J.; Yang, H.; Vakkari, V.; Stone, E. A.; Rupakheti, M.; Praveen, P. S.; van Zyl, P. G.; Beukes, J. P.; Josipovic, M.; Mitchell, E. J. S.; Sallu, S. M.; Forster, P. M.; Spracklen, D. V.

    2016-01-01

    Combustion of fuels in the residential sector for cooking and heating results in the emission of aerosol and aerosol precursors impacting air quality, human health, and climate. Residential emissions are dominated by the combustion of solid fuels. We use a global aerosol microphysics model to simulate the impact of residential fuel combustion on atmospheric aerosol for the year 2000. The model underestimates black carbon (BC) and organic carbon (OC) mass concentrations observed over Asia, Eastern Europe, and Africa, with better prediction when carbonaceous emissions from the residential sector are doubled. Observed seasonal variability of BC and OC concentrations are better simulated when residential emissions include a seasonal cycle. The largest contributions of residential emissions to annual surface mean particulate matter (PM2.5) concentrations are simulated for East Asia, South Asia, and Eastern Europe. We use a concentration response function to estimate the human health impact due to long-term exposure to ambient PM2.5 from residential emissions. We estimate global annual excess adult (> 30 years of age) premature mortality (due to both cardiopulmonary disease and lung cancer) to be 308 000 (113 300-497 000, 5th to 95th percentile uncertainty range) for monthly varying residential emissions and 517 000 (192 000-827 000) when residential carbonaceous emissions are doubled. Mortality due to residential emissions is greatest in Asia, with China and India accounting for 50 % of simulated global excess mortality. Using an offline radiative transfer model we estimate that residential emissions exert a global annual mean direct radiative effect between -66 and +21 mW m-2, with sensitivity to the residential emission flux and the assumed ratio of BC, OC, and SO2 emissions. Residential emissions exert a global annual mean first aerosol indirect effect of between -52 and -16 mW m-2, which is sensitive to the assumed size distribution of carbonaceous emissions

  16. Can anthropogenic aerosol concentrations effect the snowfall rate?

    NASA Astrophysics Data System (ADS)

    Lohmann, U.; Zhang, J.; Pi, J.

    2003-04-01

    The mesoscale model GESIMA is used to simulate microphysical properties of Arctic clouds and their effect on radiation. Different case studies during the FIRE.ACE/SHEBA project show that GESIMA is able to simulate the cloud boundaries, ice and liquid water content and effective radii in good agreement with observations. For two different aerosol scenarios, the simulation results show that the anthropogenic aerosol can alter microphysical properties of Arctic clouds, and consequently modify surface precipitation. Borys et al. (2000) proposed that anthropogenically-induced decreases in cloud droplet size inhibit the riming process. On the contrary, we find that the accretion of snow crystals with cloud droplets is increased in the polluted cloud due to its higher cloud droplet number concentration. Instead the autoconversion rate of cloud droplets and accretion of drizzle by snow decreases caused by the shut-down of the collision-coalescence process in the polluted cloud. The amount of precipitation reaching the surface as snow depends crucially on the crystal shape. If aggregates are assumed, then a 10-fold increase in aerosol concentration leads to an increase in accumulated snow by 40% after 7 hours of simulation whereas the snow amount decreases by 30% when planar crystals are assumed because of the larger accretion efficiency of snow crystals with cloud droplets in case of aggregates. We will also perform climate model simulations to estimate the importance of this effect globally.

  17. Technical Note: On the use of nudging for aerosol-climate model intercomparison studies

    DOE PAGES

    Zhang, K.; Wan, H.; Liu, X.; Ghan, S. J.; Kooperman, G. J.; Ma, P.-L.; Rasch, P. J.

    2014-04-24

    Nudging is an assimilation technique widely used in the development and evaluation of climate models. Constraining the simulated wind and temperature fields using global weather reanalysis facilitates more straightforward comparison between simulation and observation, and reduces uncertainties associated with natural variabilities of the large-scale circulation. On the other hand, the forcing introduced by nudging can be strong enough to change the basic characteristics of the model climate. In the paper we show that for the Community Atmosphere Model version 5, due to the systematic temperature bias in the standard model and the sensitivity of simulated ice formation to anthropogenic aerosolmore » concentration, nudging towards reanalysis results in substantial reductions in the ice cloud amount and the impact of anthropogenic aerosols on longwave cloud forcing. In order to reduce discrepancies between the nudged and unconstrained simulations and meanwhile take the advantages of nudging, two alternative experimentation methods are evaluated. The first one constrains only the horizontal winds. The second method nudges both winds and temperature, but replaces the long-term climatology of the reanalysis by that of the model. Results show that both methods lead to substantially improved agreement with the free-running model in terms of the top-of-atmosphere radiation budget and cloud ice amount. The wind-only nudging is more convenient to apply, and provides higher correlations of the wind fields, geopotential height and specific humidity between simulation and reanalysis. This suggests nudging the horizontal winds but not temperature is a good strategy for the investigation of aerosol indirect effects through ice clouds, since it provides well-constrained meteorology without strongly perturbing the model's mean climate.« less

  18. Indirect Radiative Warming Effect in the Winter and Spring Arctic Associated with Aerosol Pollution from Mid-latitude Regions

    NASA Astrophysics Data System (ADS)

    Zhao, Chuanfeng; Garrett, Timothy

    2016-04-01

    Different from global cooling effects of aerosols and aerosol-cloud interactions, anthropogenic aerosols from mid-latitude are found to play an increased warming effect in the Arctic in later winter and early spring. Using four-year (2000-2003) observation of aerosol, cloud and radiation at North Slope of Alaska, it is found that the aerosols can increase cloud droplet effective radius 3 um for fixed liquid water path, and increase cloud thermal emissivity about 0.05-0.08. In other words, aerosols are associated with a warming of 1-1.6 degrees (3-5 W/m2) in the Arctic during late winter and early spring solely due to their first indirect effect. Further analysis indicates that total aerosol climate effects are even more significant (8-10 W/m2), with about 50% contribution from aerosol first indirect effect and another 50% contribution from complicated feedbacks. It also shows strong seasonal distribution of the aerosol indirect radiative effects, with warming effects in seasons other than in summer. However, only the significant warming effect in winter and spring passes through the significance test. The strong warming effect due to aerosol indirect effect could be further strengthened through following feedbacks involving the surface albedo (early ice melting).

  19. Understanding the contributions of aerosol properties and parameterization discrepancies to droplet number variability in a Global Climate Model

    NASA Astrophysics Data System (ADS)

    Morales Betancourt, R.; Nenes, A.

    2013-12-01

    Aerosol indirect effects in climate models strongly depend on the representation of the aerosol activation process. In this study, we assess the process level differences across activation parameterizations that contribute to droplet number uncertainty by using the adjoints of the Abdul-Razzak and Ghan (2000) and Fountoukis and Nenes (2005) droplet activation parameterizations in the framework of the Community Atmospheric Model version 5.1 (CAM5.1). The adjoint sensitivities of Nd to relevant input parameters are used to: (i) unravel the spatially resolved contribution of aerosol number, mass, and chemical composition to changes in Nd between present day and pre-industrial simulations; (ii) identify the key variables responsible for the differences in Nd fields and aerosol indirect effect estimates when different activation schemes are used within the same modeling framework. The sensitivities are computed online at minimal computational cost. Changes in aerosol number and aerosol mass concentrations were found to contribute to Nd differences much more strongly than chemical composition effects. The main sources of discrepancy between the activation parameterization considered were the treatment of the water uptake by coarse mode particles, and the sensitivity of the parameterized Nd accumulation mode aerosol geometric mean diameter. These two factors explain the different predictions of Nd over land and over oceans when these parameterizations are employed. Discrepancies in the sensitivity to aerosol size are responsible for an exaggerated response to aerosol volume changes over heavily polluted regions. Because these regions are collocated with areas of deep clouds their impact on short wave cloud forcing is amplified through liquid water path changes. Application of the adjoint-sensitivities illustrated the importance of primary organic matter emissions in controlling the droplet number concentration changes in several areas. The same framework is also utilized

  20. Distinct effects of anthropogenic aerosols on the East Asian summer monsoon between multidecadal strong and weak monsoon stages

    NASA Astrophysics Data System (ADS)

    Xie, Xiaoning; Wang, Hongli; Liu, Xiaodong; Li, Jiandong; Wang, Zhaosheng; Liu, Yangang

    2016-06-01

    Because industrial emissions of anthropogenic aerosols over East Asia have greatly increased in recent decades, the interactions between atmospheric aerosols and the East Asian summer monsoon (EASM) have attracted enormous attention. To further understand the aerosol-EASM interaction, we investigate the impacts of anthropogenic aerosols on the EASM during the multidecadal strong (1950-1977) and weak (1978-2000) EASM stages using the Community Atmospheric Model 5.1. Numerical experiments are conducted for the whole period, including the two different EASM stages, with present day (PD, year 2000) and preindustrial (PI, year 1850) aerosol emissions, as well as the observed time-varying aerosol emissions. A comparison of the results from PD and PI shows that, with the increase in anthropogenic aerosols, the large-scale EASM intensity is weakened to a greater degree (-9.8%) during the weak EASM stage compared with the strong EASM stage (-4.4%). The increased anthropogenic aerosols also result in a significant reduction in precipitation over North China during the weak EASM stage, as opposed to a statistically insignificant change during the strong EASM stage. Because of greater aerosol loading and the larger sensitivity of the climate system during weak EASM stages, the aerosol effects are more significant during these EASM stages. These results suggest that anthropogenic aerosols from the same aerosol emissions have distinct effects on the EASM and the associated precipitation between the multidecadal weak and strong EASM stages.

  1. Effectively Rebutting Climate Misinformation

    NASA Astrophysics Data System (ADS)

    Cook, J.

    2011-12-01

    Climate science faces one of the best funded misinformation campaigns in history. The challenge for climate communicators is that misinformation is extremely difficult to dislodge, even after people understand that it's incorrect. Understanding how the human brain processes information is crucial to successful rebuttal. To avoid the danger of reinforcing misinformation (known as the 'backfire effect'), emphasis should be on positive facts, not the myth. Another key to dislodging myths is replacing them with an alternate narrative. In order to provide a narrative about arguments that misrepresent climate science, a broader understanding of how these arguments mislead is required. Movements that deny a scientific consensus have 5 characteristics in common and these also apply to climate denial. The arguments against the scientific consensus involve conspiracy theories, fake experts, cherry picking, logical fallacies and misrepresentation or impossible expectations. Learning to identify these rhetorical techniques is an important tool in the climate communication toolbox. I discuss examples of misrepresentations of climate science and the rhetorical techniques employed. I demonstrate how to respond to these arguments by explaining the facts of climate science while in the process, providing an alternate narrative.

  2. Atmospheric aerosols: Their Optical Properties and Effects

    NASA Technical Reports Server (NTRS)

    1976-01-01

    Measured properties of atmospheric aerosol particles are presented. These include aerosol size frequency distribution and complex retractive index. The optical properties of aerosols are computed based on the presuppositions of thermodynamic equilibrium and of Mie-theory.

  3. A Study of Direct and Cloud-Mediated Radiative Forcing of Climate Due to Aerosols

    NASA Technical Reports Server (NTRS)

    Yu, Shao-Cai

    1999-01-01

    The Intergovernmental Panel on Climate Change (IPCC) has reported that in the southeastern US and eastern China, the general greenhouse warming due to anthropogenic gaseous emissions is dominated by the cooling effect of anthropogenic aerosols. To verify this model prediction in eastern China and southeastern US, we analyzed regional patterns of climate changes at 72 stations in eastern China during 1951- 94 (44 years), and at 52 stations in the southeastern US during 1949-94 (46 years) to detect the fingerprint of aerosol radiative forcing. It was found that the mean rates of change of annual mean daily, maximum, minimum temperatures and diurnal temperature range (DTR) in eastern China were 0.8, -0.2, 1.8, and -2.0 C/100 years respectively, while the mean rates of change of annual mean daily, maximum, minimum temperatures and DTR in the southeastern US were -0.2, -0.6, 0.2, and -0.8 C/100 years, respectively. This indicates that the high rate of increase in annual mean minimum temperature in eastern China results in a slightly warming trend of daily temperature, while the high rate of decrease in annual mean maximum temperature and low rate of increase in annual mean minimum temperature lead to the cooling trend of daily temperature in the southeastern US. We found that the warming from the longwave forcing due to both greenhouse gases and aerosols was completely counteracted by the shortwave aerosol forcing in the southeastern US in the past 46 years. A slightly overall warming trend in eastern China is evident; winters have become milder. This finding is explained by hypothesizing that increasing energy usage during the past 44 years has resulted in more coal and biomass burning, thus increasing the emission of absorbing soot and organic aerosols in eastern China. Such emissions, in addition to well-known Asia dust and greenhouse gases, may be responsible for the winter warming trend in eastern China that we have reported here. The sensitivity of aerosol

  4. Effects of Aerosol on Atmospheric Dynamics and Hydrologic Processes During Boreal Spring and Summer

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.; Kim, M. K.; Kim, K. M.; Chin, Mian

    2005-01-01

    Global and regional climate impacts of present-day aerosol loading during boreal spring are investigated using the NASA finite volume General Circulation Model (fvGCM). Three-dimensional distributions of loadings of five species of tropospheric aerosols, i.e., sulfate, black carbon, organic carbon, soil dust, and sea salt are prescribed from outputs of the Goddard Ozone Chemistry Aerosol Radiation and Transport model (GOCART). The aerosol loadings are used to calculate the extinction coefficient, single scattering albedo, and asymmetric factor at eleven spectral wavelengths in the radiative transfer code. We find that aerosol-radiative forcing during boreal spring excites a wavetrain-like pattern in tropospheric temperature and geopotential height that emanates from Northern Africa, through Eurasia, to northeastern Pacific. Associated with the teleconnection is strong surface cooling over regions with large aerosol loading, i.e., China, India, and Africa. Low-to-mid tropospheric heating due to shortwave absorption is found in regions with large loading of dust (Northern Africa, and central East Asia), and black carbon (South and East Asia). In addition pronounced surface cooling is found over the Caspian Sea and warming over Eurasian and northeastern Asia, where aerosol loadings are relatively low. These warming and cooling are components of teleconnection pattern produced primarily by atmospheric heating from absorbing aerosols, i.e., dust from North Africa and black carbon from South and East Asia. Effects of aerosols on atmospheric hydrologic cycle in the Asian monsoon region are also investigated. Results show that absorbing aerosols, i.e., black carbon and dust, induce large-scale upper-level heating anomaly over the Tibetan Plateau in April and May, ushering in an early onset of the Indian summer monsoon. Absorbing aerosols also enhance lower-level heating and anomalous ascent over northern India, intensifying the Indian monsoon. Overall, the aerosol

  5. Effects of Aerosol on Atmospheric Dynamics and Hydrologic Processes during Boreal Spring and Summer

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.; Kim, M. K.; Chin, Mian; Kim, K. M.

    2005-01-01

    Global and regional climate impacts of present-day aerosol loading during boreal spring are investigated using the NASA finite volume General Circulation Model (fvGCM). Three-dimensional distributions of loadings of five species of tropospheric aerosols, i.e., sulfate, black carbon, organic carbon, soil dust, and sea salt are prescribed from outputs of the Goddard Ozone Chemistry Aerosol Radiation and Transport model (GOCART). The aerosol loadings are used to calculate the extinction coefficient, single scattering albedo, and asymmetric factor at eleven spectral wavelengths in the radiative transfer code. We find that aerosol-radiative forcing during boreal spring excites a wavetrain-like pattern in tropospheric temperature and geopotential height that emanates from Northern Africa, through Eurasia, to northeastern Pacific. Associated with the teleconnection is strong surface cooling over regions with large aerosol loading, i.e., China, India, and Africa. Low-to-mid tropospheric heating due to shortwave absorption is found in regions with large loading of dust (Northern Africa, and central East Asia), and black carbon (South and East Asia). In addition pronounced surface cooling is found over the Caspian Sea and warming over Eurasian and northeastern Asia, where aerosol loadings are relatively low. These warming and cooling are components of teleconnection pattern produced primarily by atmospheric heating from absorbing aerosols, i.e., dust from North Africa and.black carbon from South and East Asia. Effects of aerosols on atmospheric hydrologic cycle in the Asian monsoon region are also investigated. Results show that absorbing aerosols, i.e., black carbon and dust, induce large-scale upper-level heating anomaly over the Tibetan Plateau in April and May, ushering in an early onset of the Indian summer monsoon. Absorbing aerosols also enhance lower-level heating and anomalous ascent over northern India, intensifying the Indian monsoon. Overall, the aerosol

  6. Investigating the impacts of aviation NOX, SO2 and black carbon emissions on ozone, aerosol and climate.

    NASA Astrophysics Data System (ADS)

    Kapadia, Zarashpe; Borman, Duncan; Spracklen, Dominick; Arnold, Stephen; Mann, Graham; Williams, Paul

    2013-04-01

    Aviation is currently responsible for 3% of global anthropogenic CO2 emissions, but 2-14% of anthropogenic induced warming due to the co-emission of NOX, SO2 and black carbon and formation of contrails. The impact of aviation emissions on ozone and aerosol is uncertain with recent research demonstrating the need to include atmospheric nitrate chemistry. The inclusion of nitrate chemistry may lead to a 20% reduction in aviation induced ozone forcing estimates due to the competition for atmospheric oxidants such as OH . Compounding this, uncertainties relating to the effects of NOx on ozone and methane illustrate the need for refining the understanding of aviation induced impacts. Furthermore the role of aerosol microphysics in controlling the climate impacts of aviation has not yet been explored. Here we use the TOMCAT 3-D chemical transport model coupled to the GLOMAP-mode aerosol microphysics model to quantify the impacts of aviation NOX, SO2 and BC emissions on ozone, aerosol and climate. GLOMAP-mode treats size resolved aerosol using a two-moment modal approach. We evaluate the effects of nitrate processing on the diagnosed impacts of aviation emissions on atmospheric composition including the first assessment of the impact on the global concentrations of cloud condensation nuclei. We investigate interactions between gas-phase oxidant photochemistry and aerosol microphysics in regions influenced by aircraft emissions, using fully-coupled tropospheric chemistry and multi-component aerosol treatment (BC, sulphate, nitrate). Finally, we use a 3-D radiative transfer model to quantify the ozone and aerosol direct and indirect radiative effects of aviation emissions. The work presented here is part of a wider research project which will be the first study to combine aviation NOX, SO2 and black carbon emission in a global size-resolved model which considers atmospheric nitrate chemistry, which will aim to add to the science surrounding present day aviation impacts by

  7. Overview of the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES)

    NASA Technical Reports Server (NTRS)

    Zaveri, R. A.; Shaw, W. J.; Cahill, J. F.; Cairns, Brian; Cappa, C. D.; Ottaviani, Matteo; Cziczo, D. J.; Ferrare, Richard A.; Alexander, M. L.; Alexandrov, Mikhail Dmitrievic; Alvarez, R. J.; Arnott, W. P.; Atkinson, D. B.; Schmid, B.; Chand, D.; China, S.; Comstock, J. M.; Dubey, M. K.; Easter, R. C.; Erickson, M. H.; Fast, J. D.; Flowers, B. A.; Fortner, E.; Baidar, S.; Hair, J.; Hostetler, C.; Obland, M. D.; Rogers, R. R.; Floerchinger, C.; Banta, R. M.; Barnard, J. C.; Beranek, J.; Berg, L. K.; Brechtel, F.; Brewer, W. A.

    2012-01-01

    Substantial uncertainties still exist in the scientific understanding of the possible interactions between urban and natural (biogenic) emissions in the production and transformation of atmospheric aerosol and the resulting impact on climate change. The US Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) program's Carbonaceous Aerosol and Radiative Effects Study (CARES) carried out in June 2010 in Central Valley, California, was a comprehensive effort designed to improve this understanding. The primary objective of the field study was to investigate the evolution of secondary organic and black carbon aerosols and their climate-related properties in the Sacramento urban plume as it was routinely transported into the forested Sierra Nevada foothills area. Urban aerosols and trace gases experienced significant physical and chemical transformations as they mixed with the reactive biogenic hydrocarbons emitted from the forest. Two heavily-instrumented ground sites - one within the Sacramento urban area and another about 40 km to the northeast in the foothills area - were set up to characterize the evolution of meteorological variables, trace gases, aerosol precursors, aerosol size, composition, and climaterelated properties in freshly polluted and "aged" urban air. On selected days, the DOE G-1 aircraft was deployed to make similar measurements upwind and across the evolving Sacramento plume in the morning and again in the afternoon. The NASA B-200 aircraft, carrying remote sensing instruments, was also deployed to characterize the vertical and horizontal distribution of aerosols and aerosol optical properties within and around the plume. This overview provides: (a) the scientific background and motivation for the study, (b) the operational and logistical information pertinent to the execution of the study, (c) an overview of key observations and initial findings from the aircraft and ground-based sampling platforms, and (d) a roadmap of planned data

  8. Attribution of the United States "warming hole": aerosol indirect effect and precipitable water vapor.

    PubMed

    Yu, Shaocai; Alapaty, Kiran; Mathur, Rohit; Pleim, Jonathan; Zhang, Yuanhang; Nolte, Chris; Eder, Brian; Foley, Kristen; Nagashima, Tatsuya

    2014-11-06

    Aerosols can influence the climate indirectly by acting as cloud condensation nuclei and/or ice nuclei, thereby modifying cloud optical properties. In contrast to the widespread global warming, the central and south central United States display a noteworthy overall cooling trend during the 20(th) century, with an especially striking cooling trend in summertime daily maximum temperature (Tmax) (termed the U.S. "warming hole"). Here we used observations of temperature, shortwave cloud forcing (SWCF), longwave cloud forcing (LWCF), aerosol optical depth and precipitable water vapor as well as global coupled climate models to explore the attribution of the "warming hole". We find that the observed cooling trend in summer Tmax can be attributed mainly to SWCF due to aerosols with offset from the greenhouse effect of precipitable water vapor. A global coupled climate model reveals that the observed "warming hole" can be produced only when the aerosol fields are simulated with a reasonable degree of accuracy as this is necessary for accurate simulation of SWCF over the region. These results provide compelling evidence of the role of the aerosol indirect effect in cooling regional climate on the Earth. Our results reaffirm that LWCF can warm both winter Tmax and Tmin.

  9. Attribution of the United States "warming hole": aerosol indirect effect and precipitable water vapor.

    PubMed

    Yu, Shaocai; Alapaty, Kiran; Mathur, Rohit; Pleim, Jonathan; Zhang, Yuanhang; Nolte, Chris; Eder, Brian; Foley, Kristen; Nagashima, Tatsuya

    2014-01-01

    Aerosols can influence the climate indirectly by acting as cloud condensation nuclei and/or ice nuclei, thereby modifying cloud optical properties. In contrast to the widespread global warming, the central and south central United States display a noteworthy overall cooling trend during the 20(th) century, with an especially striking cooling trend in summertime daily maximum temperature (Tmax) (termed the U.S. "warming hole"). Here we used observations of temperature, shortwave cloud forcing (SWCF), longwave cloud forcing (LWCF), aerosol optical depth and precipitable water vapor as well as global coupled climate models to explore the attribution of the "warming hole". We find that the observed cooling trend in summer Tmax can be attributed mainly to SWCF due to aerosols with offset from the greenhouse effect of precipitable water vapor. A global coupled climate model reveals that the observed "warming hole" can be produced only when the aerosol fields are simulated with a reasonable degree of accuracy as this is necessary for accurate simulation of SWCF over the region. These results provide compelling evidence of the role of the aerosol indirect effect in cooling regional climate on the Earth. Our results reaffirm that LWCF can warm both winter Tmax and Tmin. PMID:25373416

  10. Attribution of the United States “warming hole”: Aerosol indirect effect and precipitable water vapor

    NASA Astrophysics Data System (ADS)

    Yu, Shaocai; Alapaty, Kiran; Mathur, Rohit; Pleim, Jonathan; Zhang, Yuanhang; Nolte, Chris; Eder, Brian; Foley, Kristen; Nagashima, Tatsuya

    2014-11-01

    Aerosols can influence the climate indirectly by acting as cloud condensation nuclei and/or ice nuclei, thereby modifying cloud optical properties. In contrast to the widespread global warming, the central and south central United States display a noteworthy overall cooling trend during the 20th century, with an especially striking cooling trend in summertime daily maximum temperature (Tmax) (termed the U.S. ``warming hole''). Here we used observations of temperature, shortwave cloud forcing (SWCF), longwave cloud forcing (LWCF), aerosol optical depth and precipitable water vapor as well as global coupled climate models to explore the attribution of the ``warming hole''. We find that the observed cooling trend in summer Tmax can be attributed mainly to SWCF due to aerosols with offset from the greenhouse effect of precipitable water vapor. A global coupled climate model reveals that the observed ``warming hole'' can be produced only when the aerosol fields are simulated with a reasonable degree of accuracy as this is necessary for accurate simulation of SWCF over the region. These results provide compelling evidence of the role of the aerosol indirect effect in cooling regional climate on the Earth. Our results reaffirm that LWCF can warm both winter Tmax and Tmin.

  11. Attribution of the United States “warming hole”: Aerosol indirect effect and precipitable water vapor

    PubMed Central

    Yu, Shaocai; Alapaty, Kiran; Mathur, Rohit; Pleim, Jonathan; Zhang, Yuanhang; Nolte, Chris; Eder, Brian; Foley, Kristen; Nagashima, Tatsuya

    2014-01-01

    Aerosols can influence the climate indirectly by acting as cloud condensation nuclei and/or ice nuclei, thereby modifying cloud optical properties. In contrast to the widespread global warming, the central and south central United States display a noteworthy overall cooling trend during the 20th century, with an especially striking cooling trend in summertime daily maximum temperature (Tmax) (termed the U.S. “warming hole”). Here we used observations of temperature, shortwave cloud forcing (SWCF), longwave cloud forcing (LWCF), aerosol optical depth and precipitable water vapor as well as global coupled climate models to explore the attribution of the “warming hole”. We find that the observed cooling trend in summer Tmax can be attributed mainly to SWCF due to aerosols with offset from the greenhouse effect of precipitable water vapor. A global coupled climate model reveals that the observed “warming hole” can be produced only when the aerosol fields are simulated with a reasonable degree of accuracy as this is necessary for accurate simulation of SWCF over the region. These results provide compelling evidence of the role of the aerosol indirect effect in cooling regional climate on the Earth. Our results reaffirm that LWCF can warm both winter Tmax and Tmin. PMID:25373416

  12. GCM Simulations of the Aerosol Indirect Effect: Sensitivity to Cloud Parameterization and Aerosol Burden

    NASA Technical Reports Server (NTRS)

    Menon, Surabi; DelGenio, Anthony D.; Koch, Dorothy; Tselioudis, George; Hansen, James E. (Technical Monitor)

    2001-01-01

    We describe the coupling of the Goddard Institute for Space Studies (GISS) general circulation model (GCM) to an online sulfur chemistry model and source models for organic matter and sea-salt that is used to estimate the aerosol indirect effect. The cloud droplet number concentration is diagnosed empirically from field experiment datasets over land and ocean that observe droplet number and all three aerosol types simultaneously; corrections are made for implied variations in cloud turbulence levels. The resulting cloud droplet number is used to calculate variations in droplet effective radius, which in turn allows us to predict aerosol effects on cloud optical thickness and microphysical process rates. We calculate the aerosol indirect effect by differencing the top-of-the-atmosphere net cloud radiative forcing for simulations with present-day vs. pre-industrial emissions. Both the first (radiative) and second (microphysical) indirect effects are explored. We test the sensitivity of our results to cloud parameterization assumptions that control the vertical distribution of cloud occurrence, the autoconversion rate, and the aerosol scavenging rate, each of which feeds back significantly on the model aerosol burden. The global mean aerosol indirect effect for all three aerosol types ranges from -1.55 to -4.36 W m(exp -2) in our simulations. The results are quite sensitive to the pre-industrial background aerosol burden, with low pre-industrial burdens giving strong indirect effects, and to a lesser extent to the anthropogenic aerosol burden, with large burdens giving somewhat larger indirect effects. Because of this dependence on the background aerosol, model diagnostics such as albedo-particle size correlations and column cloud susceptibility, for which satellite validation products are available, are not good predictors of the resulting indirect effect.

  13. GCM Simulations of the Aerosol Indirect Effect: Sensitivity to Cloud Parameterization and Aerosol Burden

    NASA Technical Reports Server (NTRS)

    Menon, Surabi; DelGenio, Anthony D.; Koch, Dorothy; Tselioudis, George; Hansen, James E. (Technical Monitor)

    2001-01-01

    We describe the coupling of the Goddard Institute for Space Studies (GISS) general circulation model (GCM) to an online sulfur chemistry model and source models for organic matter and sea-salt that is used to estimate the aerosol indirect effect. The cloud droplet number concentration is diagnosed empirically from field experiment datasets over land and ocean that observe droplet number and all three aerosol types simultaneously; corrections are made for implied variations in cloud turbulence levels. The resulting cloud droplet number is used to calculate variations in droplet effective radius, which in turn allows us to predict aerosol effects on cloud optical thickness and microphysical process rates. We calculate the aerosol indirect effect by differencing the top-of-the-atmosphere net cloud radiative forcing for simulations with present-day vs. pre-industrial emissions. Both the first (radiative) and second (microphysical) indirect effects are explored. We test the sensitivity of our results to cloud parameterization assumptions that control the vertical distribution of cloud occurrence, the autoconversion rate, and the aerosol scavenging rate, each of which feeds back significantly on the model aerosol burden. The global mean aerosol indirect effect for all three aerosol types ranges from -1.55 to -4.36 W/sq m in our simulations. The results are quite sensitive to the pre-industrial background aerosol burden, with low pre-industrial burdens giving strong indirect effects, and to a lesser extent to the anthropogenic aerosol burden, with large burdens giving somewhat larger indirect effects. Because of this dependence on the background aerosol, model diagnostics such as albedo-particle size correlations and column cloud susceptibility, for which satellite validation products are available, are not good predictors of the resulting indirect effect.

  14. The role of Saharan dust in determining the first aerosol indirect effect

    NASA Astrophysics Data System (ADS)

    Shao, H.; Liu, G.

    2007-12-01

    Anthropogenic aerosols acting as cloud condensation nuclei affect Earth's radiative balance indirectly by changing cloud radiative properties. This so-called first aerosol indirect effect (AIE) has a potentially large but poorly quantified cooling effect. In modeling the aerosol indirect forcing, because the aerosol-cloud interaction is not resolved in global climate models (GCMs), cloud droplet number concentration is typically parameterized using an empirical relationship that directly relates droplet number concentration to aerosol number concentration based on the measurements between polluted and clean clouds. It is realized that the first AIE obtained in this way can be contaminated by the coherent variation in the pertinent variables such as cloud liquid water and the degree of entrainment mixing. However, the influence from changes in aerosol properties themselves has not received a deserved attention. Using satellite observations over eastern subtropical oceans, we show that over the north-eastern Atlantic the aerosols properties are distinct from the other regions due to the dust particles originating from Sahara desert. These dust particles may significantly reduce the efficiency of aerosols to act as cloud condensation nuclei. As a result, the locally observed first AIE from this region can be significantly deviated from global mean, even resulting in positive values. Because of the large areal fraction of this region, ignoring the influence from the northern Africa dust particles will underestimate the globally averaged first AIE approximately by half.

  15. Cloud Condensation Nuclei Prediction Error from Application of Kohler Theory: Importance for the Aerosol Indirect Effect

    NASA Technical Reports Server (NTRS)

    Sotiropoulou, Rafaella-Eleni P.; Nenes, Athanasios; Adams, Peter J.; Seinfeld, John H.

    2007-01-01

    In situ observations of aerosol and cloud condensation nuclei (CCN) and the GISS GCM Model II' with an online aerosol simulation and explicit aerosol-cloud interactions are used to quantify the uncertainty in radiative forcing and autoconversion rate from application of Kohler theory. Simulations suggest that application of Koehler theory introduces a 10-20% uncertainty in global average indirect forcing and 2-11% uncertainty in autoconversion. Regionally, the uncertainty in indirect forcing ranges between 10-20%, and 5-50% for autoconversion. These results are insensitive to the range of updraft velocity and water vapor uptake coefficient considered. This study suggests that Koehler theory (as implemented in climate models) is not a significant source of uncertainty for aerosol indirect forcing but can be substantial for assessments of aerosol effects on the hydrological cycle in climatically sensitive regions of the globe. This implies that improvements in the representation of GCM subgrid processes and aerosol size distribution will mostly benefit indirect forcing assessments. Predictions of autoconversion, by nature, will be subject to considerable uncertainty; its reduction may require explicit representation of size-resolved aerosol composition and mixing state.

  16. Quantifying the Aerosol Semi-Direct Effect in the NASA GEOS-5 AGCM

    NASA Technical Reports Server (NTRS)

    Randles, Cynthia A.; Colarco, Peter R.; daSilva, Arlindo

    2011-01-01

    Aerosols such as black carbon, dust, and some organic carbon species both scatter and absorb incoming solar radiation. This direct aerosol radiative forcing (DARF) redistributes solar energy both by cooling the surface and warming the atmosphere. As a result, these aerosols affect atmospheric stability and cloud cover (the semi-direct effect, or SDE). Furthermore, in regions with persistent high loadings of absorbing aerosols (e.g. Asia), regional circulation patterns may be altered, potentially resulting in changes in precipitation patterns. Here we investigate aerosol-climate coupling using the NASA Goddard Earth Observing System model version 5 (GEOS-5) atmospheric general circulation model (AGCM), in which we have implemented an online version of the Goddard Chemistry, Aerosol, Radiation and Transport (GOCART) model. GOCART includes representations of the sources, sinks, and chemical transformation of externally mixed dust, sea salt, sulfate, and carbonaceous aerosols. We examine a series of free-running ensemble climate simulations of the present-day period (2000-2009) forced by observed sea surface temperatures to determine the impact of aerosols on the model climate. The SDE and response of each simulation is determined by differencing with respect to the control simulation (no aerosol forcing). In a free-running model, any estimate of the SDE includes changes in clouds due both to atmospheric heating from aerosols and changes in circulation. To try and quantify the SDE without these circulation changes we then examine the DARF and SDE in GEOS-5 with prescribed meteorological analyses introduced by the MERRA analysis. By doing so, we are able to examine changes in model clouds that occur on shorter scales (six hours). In the GEOS-5 data assimilation system (DAS), the analysis is defined as the best estimate of the atmospheric state at any given time, and it is determined by optimally combining a first-guess short-term GCM forecast with all available

  17. Technical Note: Estimating Aerosol Effects on Cloud Radiative Forcing

    SciTech Connect

    Ghan, Steven J.

    2013-10-09

    Estimating anthropogenic aerosol effects on the planetary energy balance through the aerosol influence on clouds using the difference in cloud radiative forcing from simulations with and without anthropogenic emissions produces estimates that are positively biased. A more representative method is suggested using the difference in cloud radiative forcing calculated with aerosol radiative effects neglected. The method also yields an aerosol radiative forcing decomposition that includes a term quantifying the impact of changes in surface albedo. The method requires only two additional diagnostic calculations: the whole-sky and clear-sky top-of-atmosphere radiative flux with aerosol radiative effects neglected.

  18. Mixing-State Sensitivity of Aerosol Absorption in the EMAC Chemistry-Climate Model

    NASA Astrophysics Data System (ADS)

    Klingmueller, Klaus; Steil, Benedikt; Bruehl, Christoph; Tost, Holger; Lelieveld, Jos

    2014-05-01

    The modelling of aerosol radiative forcing is a major cause of uncertainty in the assessment of global and regional atmospheric energy budgets and climate change. One reason is the strong dependence of the aerosol optical properties on the mixing state of aerosol components like black carbon and sulphates. Using the atmospheric chemistry-climate model EMAC, we study the radiative transfer assuming various mixing states. The aerosol optics code we employ builds on the AEROPT submodel which assumes homogeneous internal mixing utilising the volume average refractive index mixing rule. We have extended the submodel to additionally account for external mixing, partial external mixing and multilayered particles. Furthermore, we have implemented the volume average dielectric constant and Maxwell Garnett Mixing rule. We present results from regional case studies employing a new column version of the aerosol optical properties and radiative transfer code of EMAC, considering columns over China, India and Africa. The regional results are complemented by global results from a simulation for the year 2005. Our findings corroborate much stronger absorption by internal than external mixtures. Well mixed aerosol often is a good approximation for particles with a black carbon core, whereas particles with black carbon at the surface absorb significantly less. Therefore, we conclude that it is generally recommended to take the inner structure of internally mixed particles into account.

  19. Toward a Minimal Representation of Aerosols in Climate Models: Comparative Decomposition of Aerosol Direct, Semidirect, and Indirect Radiative Forcing

    SciTech Connect

    Ghan, Steven J.; Liu, Xiaohong; Easter, Richard C.; Zaveri, Rahul A.; Rasch, Philip J.; Yoon, Jin-Ho; Eaton, Brian

    2012-10-01

    The authors have decomposed the anthropogenic aerosol radiative forcing into direct contributions from each aerosol species to the planetary energy balance through absorption and scattering of solar radiation, indirect effects of anthropogenic aerosol on solar and infrared radiation through droplet and crystal nucleation on aerosol, and semidirect effects through the influence of solar absorption on the distribution of clouds. A three-mode representation of the aerosol in version 5.1 of the Community Atmosphere Model (CAM5.1) yields global annual mean radiative forcing estimates for each of these forcing mechanisms that are within 0.1 W m–2 of estimates using a more complex seven-mode representation that distinguishes between fresh and aged black carbon and primary organic matter. Simulating fresh black carbon particles separately from internally mixed accumulation mode particles is found to be important only near fossil fuel sources. In addition to the usual large indirect effect on solar radiation, this study finds an unexpectedly large positive longwave indirect effect (because of enhanced cirrus produced by homogenous nucleation of ice crystals on anthropogenic sulfate), small shortwave and longwave semidirect effects, and a small direct effect (because of cancelation and interactions of direct effects of black carbon and sulfate). Differences between the threemode and seven-mode versions are significantly larger (up to 0.2 W m–2) when the hygroscopicity of primary organic matter is decreased from 0.1 to 0 and transfer of the primary carbonaceous aerosol to the accumulation mode in the seven-mode version requires more hygroscopic material coating the primary particles. Radiative forcing by cloudborne anthropogenic black carbon is only 20.07 W m–2.

  20. Overview of the Chemistry-Aerosol Mediterranean Experiment/Aerosol Direct Radiative Forcing on the Mediterranean Climate (ChArMEx/ADRIMED) summer 2013 campaign

    NASA Astrophysics Data System (ADS)

    Mallet, M.; Dulac, F.; Formenti, P.; Nabat, P.; Sciare, J.; Roberts, G.; Pelon, J.; Ancellet, G.; Tanré, D.; Parol, F.; Denjean, C.; Brogniez, G.; di Sarra, A.; Alados-Arboledas, L.; Arndt, J.; Auriol, F.; Blarel, L.; Bourrianne, T.; Chazette, P.; Chevaillier, S.; Claeys, M.; D'Anna, B.; Derimian, Y.; Desboeufs, K.; Di Iorio, T.; Doussin, J.-F.; Durand, P.; Féron, A.; Freney, E.; Gaimoz, C.; Goloub, P.; Gómez-Amo, J. L.; Granados-Muñoz, M. J.; Grand, N.; Hamonou, E.; Jankowiak, I.; Jeannot, M.; Léon, J.-F.; Maillé, M.; Mailler, S.; Meloni, D.; Menut, L.; Momboisse, G.; Nicolas, J.; Podvin, T.; Pont, V.; Rea, G.; Renard, J.-B.; Roblou, L.; Schepanski, K.; Schwarzenboeck, A.; Sellegri, K.; Sicard, M.; Solmon, F.; Somot, S.; Torres, B.; Totems, J.; Triquet, S.; Verdier, N.; Verwaerde, C.; Waquet, F.; Wenger, J.; Zapf, P.

    2016-01-01

    The Chemistry-Aerosol Mediterranean Experiment (ChArMEx; http://charmex.lsce.ipsl.fr) is a collaborative research program federating international activities to investigate Mediterranean regional chemistry-climate interactions. A special observing period (SOP-1a) including intensive airborne measurements was performed in the framework of the Aerosol Direct Radiative Impact on the regional climate in the MEDiterranean region (ADRIMED) project during the Mediterranean dry season over the western and central Mediterranean basins, with a focus on aerosol-radiation measurements and their modeling. The SOP-1a took place from 11 June to 5 July 2013. Airborne measurements were made by both the ATR-42 and F-20 French research aircraft operated from Sardinia (Italy) and instrumented for in situ and remote-sensing measurements, respectively, and by sounding and drifting balloons, launched in Minorca. The experimental setup also involved several ground-based measurement sites on islands including two ground-based reference stations in Corsica and Lampedusa and secondary monitoring sites in Minorca and Sicily. Additional measurements including lidar profiling were also performed on alert during aircraft operations at EARLINET/ACTRIS stations at Granada and Barcelona in Spain, and in southern Italy. Remote-sensing aerosol products from satellites (MSG/SEVIRI, MODIS) and from the AERONET/PHOTONS network were also used. Dedicated meso-scale and regional modeling experiments were performed in relation to this observational effort. We provide here an overview of the different surface and aircraft observations deployed during the ChArMEx/ADRIMED period and of associated modeling studies together with an analysis of the synoptic conditions that determined the aerosol emission and transport. Meteorological conditions observed during this campaign (moderate temperatures and southern flows) were not favorable to producing high

  1. Analysis of Atmospheric Aerosol Data Sets and Application of Radiative Transfer Models to Compute Aerosol Effects

    NASA Technical Reports Server (NTRS)

    Schmid, Beat

    2005-01-01

    The Bay Area Environmental Research Institute (BAER) scientists have worked with the NASA Ames Research Center sunphotometer group led by Dr. Philip Russell for many years researching the climatic effects of aerosol particles in the stratosphere and troposphere. We have continued to work with the NASA Ames sunphotometer group in research activities representing funded, peer-reviewed proposals to NASA, NOAA and DOE. The activities are described in those proposals and also in the documents provided to the Grants Office earlier. This is the final report from January 1,2002 - June 30, 2005. The report consists of a compilation of 41 peer-reviewed publications (published, in press or submitted) produced under this Cooperative Agreement and 43 first-authored conference presentations. To save paper, reprints are not included but will, of course, be provided upon request.

  2. Connecting Organic Aerosol Climate-Relevant Properties to Chemical Mechanisms of Sources and Processing

    SciTech Connect

    Thornton, Joel

    2015-01-26

    The research conducted on this project aimed to improve our understanding of secondary organic aerosol (SOA) formation in the atmosphere, and how the properties of the SOA impact climate through its size, phase state, and optical properties. The goal of this project was to demonstrate that the use of molecular composition information to mechanistically connect source apportionment and climate properties can improve the physical basis for simulation of SOA formation and properties in climate models. The research involved developing and improving methods to provide online measurements of the molecular composition of SOA under atmospherically relevant conditions and to apply this technology to controlled simulation chamber experiments and field measurements. The science we have completed with the methodology will impact the simulation of aerosol particles in climate models.

  3. Chemical and size effects of hygroscopic aerosols on light scattering coefficients

    NASA Astrophysics Data System (ADS)

    Tang, Ignatius N.

    1996-08-01

    The extensive thermodynamic and optical properties recently reported [Tang and Munkelwitz, 1994a] for sulfate and nitrate solution droplets are incorporated into a visibility model for computing light scattering by hygroscopic aerosols. The following aerosol systems are considered: NH4HSO4, (NH4)2SO4, (NH4)3H(SO4), NaHSO4, Na2SO4, NH4NO3, and NaNO3. In addition, H2SO4 and NaCl are included to represent freshly formed sulfate and background sea-salt aerosols, respectively. Scattering coefficients, based on 1 μg dry salt per cubic meter of air, are calculated as a function of relative humidity for aerosols of various chemical compositions and lognormal size distributions. For a given size distribution the light scattered by aerosol particles per unit dry-salt mass concentration is only weakly dependent on chemical constituents of the hygroscopic sulfate and nitrate aerosols. Sulfuric acid and sodium chloride aerosols, however, are exceptions and scatter light more efficiently than all other inorganic salt aerosols considered in this study. Both internal and external mixtures exhibit similar light-scattering properties. Thus for common sulfate and nitrate aerosols, since the chemical effect is outweighed by the size effect, it follows that observed light scattering by the ambient aerosol can be approximated, within practical measurement uncertainties, by assuming the aerosol being an external mixture. This has a definite advantage for either visibility degradation or climatic impact modeling calculations, because relevant data are now available for external mixtures but only very scarce for internal mixtures.

  4. A climatologically significant aerosol longwave indirect effect in the Arctic.

    PubMed

    Lubin, Dan; Vogelmann, Andrew M

    2006-01-26

    The warming of Arctic climate and decreases in sea ice thickness and extent observed over recent decades are believed to result from increased direct greenhouse gas forcing, changes in atmospheric dynamics having anthropogenic origin, and important positive reinforcements including ice-albedo and cloud-radiation feedbacks. The importance of cloud-radiation interactions is being investigated through advanced instrumentation deployed in the high Arctic since 1997 (refs 7, 8). These studies have established that clouds, via the dominance of longwave radiation, exert a net warming on the Arctic climate system throughout most of the year, except briefly during the summer. The Arctic region also experiences significant periodic influxes of anthropogenic aerosols, which originate from the industrial regions in lower latitudes. Here we use multisensor radiometric data to show that enhanced aerosol concentrations alter the microphysical properties of Arctic clouds, in a process known as the 'first indirect' effect. Under frequently occurring cloud types we find that this leads to an increase of an average 3.4 watts per square metre in the surface longwave fluxes. This is comparable to a warming effect from established greenhouse gases and implies that the observed longwave enhancement is climatologically significant.

  5. Aerosol radiative effects in the ultraviolet, visible, and near-infrared spectral ranges using long-term aerosol data series over the Iberian Peninsula

    NASA Astrophysics Data System (ADS)

    Mateos, D.; Antón, M.; Toledano, C.; Cachorro, V. E.; Alados-Arboledas, L.; Sorribas, M.; Costa, M. J.; Baldasano, J. M.

    2014-12-01

    A better understanding of aerosol radiative properties is a crucial challenge for climate change studies. This study aims at providing a complete characterization of aerosol radiative effects in different spectral ranges within the shortwave (SW) solar spectrum. For this purpose, long-term data sets of aerosol properties from six AERONET stations located in the Iberian Peninsula (southwestern Europe) have been analyzed in terms of climatological characterization and inter-annual changes. Aerosol information was used as input for the libRadtran model in order to determine the aerosol radiative effect (ARE) at the surface in the ultraviolet (AREUV), visible (AREVIS), near-infrared (ARENIR), and the entire SW range (ARESW) under cloud-free conditions. Over the whole Iberian Peninsula, yearly aerosol radiative effects in the different spectral ranges were found to be -1.1 < AREUV < -0.7, -5.7 < AREVIS < -3.5, -2.6 < ARENIR < -1.6, and -8.8 < ARESW < -5.7 (in W m-2). Monthly means of ARE showed a seasonal pattern with larger values in spring and summer. The aerosol forcing efficiency (AFE), ARE per unit of aerosol optical depth, has also been evaluated in the four spectral ranges. AFE exhibited a dependence on single scattering albedo as well as a weaker one on the Ångström exponent. AFE is larger (in absolute value) for small and absorbing particles. The contributions of the UV, VIS, and NIR ranges to the SW efficiency varied with the aerosol types. The predominant aerosol size determined the fractions AFEVIS/AFESW and AFENIR/AFESW. The AFEVIS was the dominant contributor for all aerosol types, although non-absorbing large particles caused more even contribution of VIS and NIR intervals. The AFEUV / AFESW ratio showed a higher value in the case of absorbing fine particles.

  6. Effect of aerosol vertical distribution on aerosol-radiation interaction: A theoretical prospect.

    PubMed

    Mishra, Amit Kumar; Koren, Ilan; Rudich, Yinon

    2015-10-01

    This study presents a theoretical investigation of the effect of the aerosol vertical distribution on the aerosol radiative effect (ARE). Four aerosol composition models (dust, polluted dust, pollution and pure scattering aerosols) with varying aerosol vertical profiles are incorporated into a radiative transfer model. The simulations show interesting spectral dependence of the ARE on the aerosol layer height. ARE increases with the aerosol layer height in the ultraviolet (UV: 0.25-0.42 μm) and thermal-infrared (TH-IR: 4.0-20.0 μm) regions, whereas it decreases in the visible-near infrared (VIS-NIR: 0.42-4.0 μm) region. Changes in the ARE with aerosol layer height are associated with different dominant processes for each spectral region. The combination of molecular (Rayleigh) scattering and aerosol absorption is the key process in the UV region, whereas aerosol (Mie) scattering and atmospheric gaseous absorption are key players in the VIS-NIR region. The longwave emission fluxes are controlled by the environmental temperature at the aerosol layer level. ARE shows maximum sensitivity to the aerosol layer height in the TH-IR region, followed by the UV and VIS-NIR regions. These changes are significant even in relatively low aerosol loading cases (aerosol optical depth ∼0.2-0.3). Dust aerosols are the most sensitive to altitude followed by polluted dust and pollution in all three different wavelength regions. Differences in the sensitivity of the aerosol type are explained by the relative strength of their spectral absorption/scattering properties. The role of surface reflectivity on the overall altitude dependency is shown to be important in the VIS-NIR and UV regions, whereas it is insensitive in the TH-IR region. Our results indicate that the vertical distribution of water vapor with respect to the aerosol layer is an important factor in the ARE estimations. Therefore, improved estimations of the water vapor profiles are needed for the further reduction in

  7. Effect of aerosol vertical distribution on aerosol-radiation interaction: A theoretical prospect.

    PubMed

    Mishra, Amit Kumar; Koren, Ilan; Rudich, Yinon

    2015-10-01

    This study presents a theoretical investigation of the effect of the aerosol vertical distribution on the aerosol radiative effect (ARE). Four aerosol composition models (dust, polluted dust, pollution and pure scattering aerosols) with varying aerosol vertical profiles are incorporated into a radiative transfer model. The simulations show interesting spectral dependence of the ARE on the aerosol layer height. ARE increases with the aerosol layer height in the ultraviolet (UV: 0.25-0.42 μm) and thermal-infrared (TH-IR: 4.0-20.0 μm) regions, whereas it decreases in the visible-near infrared (VIS-NIR: 0.42-4.0 μm) region. Changes in the ARE with aerosol layer height are associated with different dominant processes for each spectral region. The combination of molecular (Rayleigh) scattering and aerosol absorption is the key process in the UV region, whereas aerosol (Mie) scattering and atmospheric gaseous absorption are key players in the VIS-NIR region. The longwave emission fluxes are controlled by the environmental temperature at the aerosol layer level. ARE shows maximum sensitivity to the aerosol layer height in the TH-IR region, followed by the UV and VIS-NIR regions. These changes are significant even in relatively low aerosol loading cases (aerosol optical depth ∼0.2-0.3). Dust aerosols are the most sensitive to altitude followed by polluted dust and pollution in all three different wavelength regions. Differences in the sensitivity of the aerosol type are explained by the relative strength of their spectral absorption/scattering properties. The role of surface reflectivity on the overall altitude dependency is shown to be important in the VIS-NIR and UV regions, whereas it is insensitive in the TH-IR region. Our results indicate that the vertical distribution of water vapor with respect to the aerosol layer is an important factor in the ARE estimations. Therefore, improved estimations of the water vapor profiles are needed for the further reduction in

  8. Simulations of aerosols and their effects on photolysis and ozone formation in Mexico City

    NASA Astrophysics Data System (ADS)

    Li, G.; Zavala, M.; Lei, W.; Karydis, V. A.; Tsimpidi, A. P.; Pandis, S.; Molina, L. T.

    2009-04-01

    Atmospheric aerosols, formed from natural and anthropogenic sources, are believed to be associated with adverse human effects at high levels in polluted urban areas. They also play a key role in climate through direct and indirect effects. Therefore, accurate simulations of aerosol composition and distribution in the atmospheric models are important in evaluating their impact on environment and climate. In the present study, a flexible gas phase chemical module with SAPRC mechanism and the CMAQ/models3 aerosol module developed by EPA have been implemented into the WRF-CHEM model. Additionally, to further improve the aerosol, especially the secondary organic aerosol (SOA) simulations, an advanced SOA module [Tsimpidi et al., 2009] has been incorporated into the WRF-CHEM model. The new SOA module is based on the volatility basis-set approach in which both primary and secondary organic components are assumed to be semivolatile and photochemically reactive [Lane et al., 2008]. Gas phase species and aerosol simulation results are compared with the available measurements obtained during the MILAGRO 2006 campaign. When the advanced SOA mechanism is employed, the SOA simulations are significantly improved. Furthermore, the aerosol impacts on the photochemistry in Mexico City have been evaluated using the FTUV [Tie et al., 2005]. Aerosol optical properties are calculated using the Mie theory and compared with available observations in Mexico City [Paredes-Miranda et al., 2008]. Aerosols, principally black carbon, reduce the photolysis frequencies of J[O3(1D)] and J[NO2] in the planetary boundary layer and hence decrease the ground-level ozone concentration. Our study demonstrates that the impact of aerosols on photochemistry is significant in polluted urban atmosphere. References: Lane, T. E., N. M. Donahue, and S. N. Pandis (2008), Simulating secondary organic aerosol formation using the volatility basis-set approach in a chemical transport model, PMCAMx, Atmos. Environ

  9. Challenges to producing a long-term stratospheric aerosol climatology for chemistry and climate

    NASA Astrophysics Data System (ADS)

    Thomason, Larry; Vernier, Jean-Paul; Bourassa, Adam; Rieger, Landon; Luo, Beiping; Peter, Thomas; Arfeuille, Florian

    2016-04-01

    Stratospheric aerosol data sets are key inputs for climate models (GCMs, CCMs) particularly for understanding the role of volcanoes on climate and as a surrogate for understanding the potential of human-derived stratospheric aerosol as mitigation for global warming. In addition to supporting activities of individual climate models, the data sets also act as a historical input to the activities of SPARC's Chemistry-Climate Model Initiative (CCMI) and the World Climate Research Programme's Coupled Model Intercomparison Project (CMIP). One such data set was produced in 2004 as a part of the SPARC Assessment of Stratospheric Aerosol Properties (ASAP), extending from 1979 and 2004. It was primarily constructed from the Stratospheric Aerosol and Gas Experiment series of instruments but supplemented by data from other space-based sources and a number of ground-based and airborne instruments. Updates to this data set have expanded the timeframe to span from 1850 through 2014 through the inclusion of data from additional sources, such as photometer data and ice core analyses. Fundamentally, there are limitations to the reliability of the optical properties of aerosol inferred from even the most complete single instrument data sets. At the same time, the heterogeneous nature of the underlying data to this historical data set produces considerable challenges to the production of a climate data set which is both homogeneous and reliable throughout its timespan. In this presentation, we will discuss the impact of this heterogeneity showing specific examples such as the SAGE II to OSIRIS/CALIPSO transition in 2005. Potential solutions to these issues will also be discussed.

  10. Evaluation of Present-day Aerosols over China Simulated from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)

    NASA Astrophysics Data System (ADS)

    Liao, H.; Chang, W.

    2014-12-01

    High concentrations of aerosols over China lead to strong radiative forcing that is important for both regional and global climate. To understand the representation of aerosols in China in current global climate models, we evaluate extensively the simulated present-day aerosol concentrations and aerosol optical depth (AOD) over China from the 12 models that participated in Atmospheric Chemistry & Climate Model Intercomparison Project (ACCMIP), by using ground-based measurements and satellite remote sensing. Ground-based measurements of aerosol concentrations used in this work include those from the China Meteorological Administration (CMA) Atmosphere Watch Network (CAWNET) and the observed fine-mode aerosol concentrations collected from the literature. The ground-based measurements of AOD in China are taken from the AErosol RObotic NETwork (AERONET), the sites with CIMEL sun photometer operated by Institute of Atmospheric Physics, Chinese Academy of Sciences, and from Chinese Sun Hazemeter Network (CSHNET). We find that the ACCMIP models generally underestimate concentrations of all major aerosol species in China. On an annual mean basis, the multi-model mean concentrations of sulfate, nitrate, ammonium, black carbon, and organic carbon are underestimated by 63%, 73%, 54%, 53%, and 59%, respectively. The multi-model mean AOD values show low biases of 20-40% at studied sites in China. The ACCMIP models can reproduce seasonal variation of nitrate but cannot capture well the seasonal variations of other aerosol species. Our analyses indicate that current global models generally underestimate the role of aerosols in China in climate simulations.

  11. A case study of the radiative effect of aerosols over Europe: EUCAARI-LONGREX

    NASA Astrophysics Data System (ADS)

    Esteve, Anna R.; Highwood, Eleanor J.; Ryder, Claire L.

    2016-06-01

    The radiative effect of anthropogenic aerosols over Europe during the 2008 European Integrated Project on Aerosol Cloud Climate and Air Quality Interactions Long Range Experiment (EUCAARI-LONGREX) campaign has been calculated using measurements collected by the Facility for Airborne Atmospheric Measurements (FAAM) BAe-146 aircraft and radiative transfer modelling. The aircraft sampled anthropogenically perturbed air masses across north-western Europe under anticyclonic conditions with aerosol optical depths ranging from 0.047 to 0.357. For one specially designed "radiative closure" flight, simulated irradiances have been compared to radiation measurements for a case of aged European aerosol in order to explore the validity of model assumptions and the degree of radiative closure that can be attained given the spatial and temporal variability of the observations and their measurement uncertainties. Secondly, the diurnally averaged aerosol radiative effect throughout EUCAARI-LONGREX has been calculated. The surface radiative effect ranged between -3.9 and -22.8 W m-2 (mean -11 ± 5 W m-2), whilst top-of-the-atmosphere (TOA) values were between -2.1 and -12.0 W m-2 (mean -5 ± 3 W m-2). We have quantified the uncertainties in our calculations due to the way in which aerosols and other parameters are represented in a radiative transfer model. The largest uncertainty in the aerosol radiative effect at both the surface and the TOA comes from the spectral resolution of the information used in the radiative transfer model (˜ 17 %) and the aerosol description (composition and size distribution) used in the Mie calculations of the aerosol optical properties included in the radiative transfer model (˜ 7 %). The aerosol radiative effect at the TOA is also highly sensitive to the surface albedo (˜ 12 %).

  12. Stratospheric aerosol properties and their effects on infrared radiation.

    NASA Technical Reports Server (NTRS)

    Remsberg, E. E.

    1973-01-01

    This paper presents a stratospheric aerosol model and infers its effects on terrestrial radiation. Composition of the aerosol is assumed to be concentrated sulfuric acid. An appropriate size distribution has been determined from available size distribution measurements of other investigators. Aerosols composed of concentrated sulfuric acid emit energy in the atmospheric window region of the infrared spectrum, 8-13 microns. Laboratory measurements of optical constant data obtained at room temperature are presented for 75 and 90% aqueous sulfuric acid. Calculations of an aerosol extinction coefficient are then performed by using the above data. Effects of changes in aerosol phase and temperature are discussed but not resolved.

  13. Overview of ACE-Asia Spring 2001 Investigations on Aerosol Radiative Effects and Related Aerosol Properties

    NASA Technical Reports Server (NTRS)

    Russell, Philip B.; Valero, F. P. J.; Flatau, P. J.; Bergin, M.; Holben, B.; Nakajima, T.; Pilewskie, P.; Bergstrom, R.; Hipskind, R. Stephen (Technical Monitor)

    2001-01-01

    A primary, ACE-Asia objective was to quantify the interactions between aerosols and radiation in the Asia-Pacific region. Toward this end, radiometric and related aerosol measurements were made from ocean, land, air and space platforms. Models that predict aerosol fields guided the measurements and are helping integrate and interpret results. Companion overview's survey these measurement and modeling components. Here we illustrate how these components were combined to determine aerosol radiative. impacts and their relation to aerosol properties. Because clouds can obscure or change aerosol direct radiative effects, aircraft and ship sorties to measure these effects depended on predicting and finding cloud-free areas and times with interesting aerosols present. Pre-experiment satellite cloud climatologies, pre-flight aerosol and cloud forecasts, and in-flight guidance from satellite imagery all helped achieve this. Assessments of aerosol regional radiative impacts benefit from the spatiotemporal coverage of satellites, provided satellite-retrieved aerosol properties are accurate. Therefore, ACE-Asia included satellite retrieval tests, as part of many comparisons to judge the consistency (closure) among, diverse measurements. Early results include: (1) Solar spectrally resolved and broadband irradiances and optical depth measurements from the C-130 aircraft and at Kosan, Korea yielded aerosol radiative forcing efficiencies, permitting comparisons between efficiencies of ACE-Asia and INDOEX aerosols, and between dust and "pollution" aerosols. Detailed results will be presented in separate papers. (2) Based on measurements of wavelength dependent aerosol optical depth (AOD) and single scattering albedo the estimated 24-h a average aerosol radiative forcing efficiency at the surface for photosynthetically active radiation (400 - 700 nm) in Yulin, China is approx. 30 W sq m per AOD(500 nm). (3) The R/V Brown cruise from Honolulu to Sea of Japan sampled an aerosol optical

  14. Selected translated abstracts of Russian-language climate-change publications, III aerosols: Issue 164

    SciTech Connect

    Razuvaev, V.N.; Ssivachok, S.G.

    1995-10-01

    This report presents abstracts in Russian and translated into English of important Russian-language literature concerning aerosols as they relate to climate change. In addition to the bibliographic citations and abstracts translated into English, this report presents the original citations and abstracts in Russian. Author and title indexes are included to assist the reader in locating abstracts of particular interest.

  15. Distinct effects of anthropogenic aerosols on the East Asian summer monsoon between multidecadal strong and weak monsoon stages

    DOE PAGES

    Xie, Xiaoning; Wang, Hongli; Liu, Xiaodong; Li, Jiandong; Wang, Zhaosheng; Liu, Yangang

    2016-06-18

    Industrial emissions of anthropogenic aerosols over East Asia have greatly increased in recent decades, and so the interactions between atmospheric aerosols and the East Asian summer monsoon (EASM) have attracted enormous attention. In order to further understand the aerosol-EASM interaction, we investigate the impacts of anthropogenic aerosols on the EASM during the multidecadal strong (1950–1977) and weak (1978–2000) EASM stages using the Community Atmospheric Model 5.1. Numerical experiments are conducted for the whole period, including the two different EASM stages, with present day (PD, year 2000) and preindustrial (PI, year 1850) aerosol emissions, as well as the observed time-varying aerosolmore » emissions. A comparison of the results from PD and PI shows that, with the increase in anthropogenic aerosols, the large-scale EASM intensity is weakened to a greater degree (-9.8%) during the weak EASM stage compared with the strong EASM stage (-4.4%). The increased anthropogenic aerosols also result in a significant reduction in precipitation over North China during the weak EASM stage, as opposed to a statistically insignificant change during the strong EASM stage. Because of greater aerosol loading and the larger sensitivity of the climate system during weak EASM stages, the aerosol effects are more significant during these EASM stages. Moreover, these results suggest that anthropogenic aerosols from the same aerosol emissions have distinct effects on the EASM and the associated precipitation between the multidecadal weak and strong EASM stages.« less

  16. Relative Content of Black Carbon in Submicron Aerosol as a Sign of the Effect of Forest Fire Smokes

    SciTech Connect

    Kozlov, V.S.; Panchenko, M.V.; Yauscheva, E.P.

    2005-03-18

    Biomass burning occurs often in regions containing vast forest tracts and peat-bogs. These processes are accompanied by the emission of a large amount of aerosol particles and crystal carbon (black carbon [BC], soot). BC is the predominant source of solar absorption in atmospheric aerosol, which impacts climate. (Jacobson 2001; Rozenberg 1982). In this paper, we analyze the results of laboratory and field investigations that focused on the relative content of BC in aerosol particles. Main attention is given to the study of possibility using this parameter as an informative sign for estimating the effect of remote forest fire smokes on the near-ground aerosol composition.

  17. Microphysical Effects Determine Macrophysical Response for Aerosol Impacts on Deep Convective Clouds

    SciTech Connect

    Fan, Jiwen; Leung, Lai-Yung R.; Rosenfeld, Daniel; Chen, Qian; Li, Zhanqing; Zhang, Jinqiang; Yan, Hongru

    2013-11-26

    Deep convective clouds (DCCs) play a crucial role in the general circulation and energy and hydrological cycle of our climate system. Anthropogenic and natural aerosol particles can influence DCCs through changes in cloud properties, precipitation regimes, and radiation balance. Modeling studies have reported both invigoration and suppression of DCCs by aerosols, but none has fully quantified aerosol impacts on convection life cycle and radiative forcing. By conducting multiple month-long cloud-resolving simulations with spectral-bin cloud microphysics that capture the observed macro- and micro-physical properties of summer convective clouds in the tropics and mid-latitudes, this study provides the first comprehensive look at how aerosols affect cloud cover, cloud top height (CTH), and radiative forcing. Observations validate these simulation results. We find that microphysical aerosol effects contribute predominantly to increased cloud cover and CTH by inducing larger amount of smaller but longer lasting ice particles in the stratiform/anvils of DCCs with dynamical aerosol effects contributing at most ~ 1/4 of the total increase of cloud cover. The overall effect is a radiative warming in the atmosphere (3 to 5 W m-2) with strong surface cooling (-5 to -8 W m-2). Herein we clearly identified mechanisms more important than and additional to the invigoration effects hypothesized previously that explain the consistent signatures of increased cloud tops area and height by aerosols in DCCs revealed by observations.

  18. The effect of smoke, dust, and pollution aerosol on shallow cloud development over the Atlantic Ocean

    NASA Astrophysics Data System (ADS)

    Kaufman, Yoram J.; Koren, Ilan; Remer, Lorraine A.; Rosenfeld, Daniel; Rudich, Yinon

    2005-08-01

    Clouds developing in a polluted environment tend to have more numerous but smaller droplets. This property may lead to suppression of precipitation and longer cloud lifetime. Absorption of incoming solar radiation by aerosols, however, can reduce the cloud cover. The net aerosol effect on clouds is currently the largest uncertainty in evaluating climate forcing. Using large statistics of 1-km resolution MODIS (Moderate Resolution Imaging Spectroradiometer) satellite data, we study the aerosol effect on shallow water clouds, separately in four regions of the Atlantic Ocean, for June through August 2002: marine aerosol (30°S-20°S), smoke (20°S-5°N), mineral dust (5°N-25°N), and pollution aerosols (30°N- 60°N). All four aerosol types affect the cloud droplet size. We also find that the coverage of shallow clouds increases in all of the cases by 0.2-0.4 from clean to polluted, smoky, or dusty conditions. Covariability analysis with meteorological parameters associates most of this change to aerosol, for each of the four regions and 3 months studied. In our opinion, there is low probability that the net aerosol effect can be explained by coincidental, unresolved, changes in meteorological conditions that also accumulate aerosol, or errors in the data, although further in situ measurements and model developments are needed to fully understand the processes. The radiative effect at the top of the atmosphere incurred by the aerosol effect on the shallow clouds and solar radiation is -11 ± 3 W/m2 for the 3 months studied; 2/3 of it is due to the aerosol-induced cloud changes, and 1/3 is due to aerosol direct radiative effect. Author contributions: Y.J.K., I.K., L.A.R., D.R., and Y.R. designed research; Y.J.K., I.K., and L.A.R. performed research; Y.J.K., I.K., and L.A.R. analyzed data; Y.J.K. wrote the paper; I.K. and L.A.R. also participated in writing the paper; D.R. provided cloud physics context for the analysis; and D.R. and Y.R. participated in data

  19. Global Aerosol Effect Retrieval From Passive Hyperspectral Measurements

    NASA Astrophysics Data System (ADS)

    de Graaf, M.; Tilstra, L. G.; Stammes, P.

    2013-12-01

    Absorbing aerosols can have a significant local direct radiative effect (DRE), while the global average aerosol DRE remains highly uncertain. Modelling studies have shown that the magnitude and sign of the aerosol DRE at the top of the atmosphere (TOA) depend on the scene, especially on the albedo of the scene under the aerosol layer. It changes with cloud fraction, from large positive for overcast conditions when aerosols are present above the cloud, to large negative for clear sky ocean scenes. Observational studies, which are necessary to constrain the model studies, have been scarce. The results of modelling studies depend strongly on the assumed aerosol properties. Observational studies also need to assume aerosol type and geophysical properties to derive aerosol optical properties from radiation measurements. This introduces large uncertainties in the retrieved aerosol DRE. Furthermore, the retrieval of aerosols over clouds from passive instruments is difficult, due to the large optical thickness of clouds. Therefore, observational studies of aerosol direct and indirect effects from passive satellite instruments are invariably restricted to aerosol studies close to the cloud edges. We have developed a method to derive the aerosol DRE for smoke over clouds directly from passive satellite hyperspectral reflectance measurements, independent of aerosol micro- physical property assumptions. This allows us to assess the local aerosol DRE from passive imagery directly on a pixel to pixel basis, even over clouds. The solar radiative absorption by smoke layers is quantified using the TOA reflectance spectrum from the ultraviolet (UV) to the shortwave infrared (SWIR). UV- absorbing aerosols have a strong signature that can be detected using UV reflectance measurements. Since the aerosol extinction optical thickness decreases rapidly with increasing wavelength for smoke, the properties of the scene below the aerosol layer can be retrieved in the SWIR, where aerosol

  20. Aerosol effect on cloud droplet size monitored from satellite.

    PubMed

    Bréon, Francois-Marie; Tanré, Didier; Generoso, Sylvia

    2002-02-01

    Aerosol concentration and cloud droplet radii derived from space-borne measurements are used to explore the effect of aerosols on cloud microphysics. Cloud droplet size is found to be largest (14 micrometers) over remote tropical oceans and smallest (6 micrometers) over highly polluted continental areas. Small droplets are also present in clouds downwind of continents. By using estimates of droplet radii coupled with aerosol load, a statistical mean relationship is derived. The cloud droplet size appears to be better correlated with an aerosol index that is representative of the aerosol column number under some assumptions than with the aerosol optical thickness. This study reveals that the effect of aerosols on cloud microphysics is significant and occurs on a global scale.

  1. Quantifying the effect of organic aerosol aging and intermediate-volatility emissions on regional-scale aerosol pollution in China

    NASA Astrophysics Data System (ADS)

    Zhao, Bin; Wang, Shuxiao; Donahue, Neil M.; Jathar, Shantanu H.; Huang, Xiaofeng; Wu, Wenjing; Hao, Jiming; Robinson, Allen L.

    2016-06-01

    Secondary organic aerosol (SOA) is one of the least understood constituents of fine particles; current widely-used models cannot predict its loadings or oxidation state. Recent laboratory experiments demonstrated the importance of several new processes, including aging of SOA from traditional precursors, aging of primary organic aerosol (POA), and photo-oxidation of intermediate volatility organic compounds (IVOCs). However, evaluating the effect of these processes in the real atmosphere is challenging. Most models used in previous studies are over-simplified and some key reaction trajectories are not captured, and model parameters are usually phenomenological and lack experimental constraints. Here we comprehensively assess the effect of organic aerosol (OA) aging and intermediate-volatility emissions on regional-scale OA pollution with a state-of-the-art model framework and experimentally constrained parameters. We find that OA aging and intermediate-volatility emissions together increase OA and SOA concentrations in Eastern China by about 40% and a factor of 10, respectively, thereby improving model-measurement agreement significantly. POA and IVOCs both constitute over 40% of OA concentrations, and IVOCs constitute over half of SOA concentrations; this differs significantly from previous apportionment of SOA sources. This study facilitates an improved estimate of aerosol-induced climate and health impacts, and implies a shift from current fine-particle control policies.

  2. Quantifying the effect of organic aerosol aging and intermediate-volatility emissions on regional-scale aerosol pollution in China.

    PubMed

    Zhao, Bin; Wang, Shuxiao; Donahue, Neil M; Jathar, Shantanu H; Huang, Xiaofeng; Wu, Wenjing; Hao, Jiming; Robinson, Allen L

    2016-01-01

    Secondary organic aerosol (SOA) is one of the least understood constituents of fine particles; current widely-used models cannot predict its loadings or oxidation state. Recent laboratory experiments demonstrated the importance of several new processes, including aging of SOA from traditional precursors, aging of primary organic aerosol (POA), and photo-oxidation of intermediate volatility organic compounds (IVOCs). However, evaluating the effect of these processes in the real atmosphere is challenging. Most models used in previous studies are over-simplified and some key reaction trajectories are not captured, and model parameters are usually phenomenological and lack experimental constraints. Here we comprehensively assess the effect of organic aerosol (OA) aging and intermediate-volatility emissions on regional-scale OA pollution with a state-of-the-art model framework and experimentally constrained parameters. We find that OA aging and intermediate-volatility emissions together increase OA and SOA concentrations in Eastern China by about 40% and a factor of 10, respectively, thereby improving model-measurement agreement significantly. POA and IVOCs both constitute over 40% of OA concentrations, and IVOCs constitute over half of SOA concentrations; this differs significantly from previous apportionment of SOA sources. This study facilitates an improved estimate of aerosol-induced climate and health impacts, and implies a shift from current fine-particle control policies. PMID:27350423

  3. Quantifying the effect of organic aerosol aging and intermediate-volatility emissions on regional-scale aerosol pollution in China

    PubMed Central

    Zhao, Bin; Wang, Shuxiao; Donahue, Neil M.; Jathar, Shantanu H.; Huang, Xiaofeng; Wu, Wenjing; Hao, Jiming; Robinson, Allen L.

    2016-01-01

    Secondary organic aerosol (SOA) is one of the least understood constituents of fine particles; current widely-used models cannot predict its loadings or oxidation state. Recent laboratory experiments demonstrated the importance of several new processes, including aging of SOA from traditional precursors, aging of primary organic aerosol (POA), and photo-oxidation of intermediate volatility organic compounds (IVOCs). However, evaluating the effect of these processes in the real atmosphere is challenging. Most models used in previous studies are over-simplified and some key reaction trajectories are not captured, and model parameters are usually phenomenological and lack experimental constraints. Here we comprehensively assess the effect of organic aerosol (OA) aging and intermediate-volatility emissions on regional-scale OA pollution with a state-of-the-art model framework and experimentally constrained parameters. We find that OA aging and intermediate-volatility emissions together increase OA and SOA concentrations in Eastern China by about 40% and a factor of 10, respectively, thereby improving model-measurement agreement significantly. POA and IVOCs both constitute over 40% of OA concentrations, and IVOCs constitute over half of SOA concentrations; this differs significantly from previous apportionment of SOA sources. This study facilitates an improved estimate of aerosol-induced climate and health impacts, and implies a shift from current fine-particle control policies. PMID:27350423

  4. An Overview of the 2010 Carbonaceous Aerosol and Radiative Effects Study (CARES) Field Campaign

    NASA Astrophysics Data System (ADS)

    Zaveri, R. A.; Shaw, W. J.; Cziczo, D. J.

    2010-12-01

    The primary objective of the DOE Carbonaceous Aerosol and Radiative Effects Study (CARES) in June 2010 was to investigate the evolution of carbonaceous aerosols of different types and their optical and hygroscopic properties in central California, with a focus on the Sacramento urban plume. Carbonaceous aerosol components, which include black carbon (BC), urban primary organic aerosols (POA), biomass burning aerosols, and secondary organic aerosols (SOA) from both urban and biogenic precursors, have been shown to play a major role in the direct and indirect radiative forcing of climate. However, significant knowledge gaps and uncertainties still exist in the process-level understanding of: 1) SOA formation, 2) BC mixing state evolution, and 3) the optical and hygroscopic properties of fresh and aged carbonaceous aerosols. The CARES 2010 field study was designed to address several specific science questions under these three topics. During summer the Sacramento-Blodgett Forest corridor effectively serves as a mesoscale daytime flow reactor in which the urban aerosols undergo significant aging as they are transported to the northeast by upslope flow. The CARES campaign observation strategy consisted of the DOE G-1 aircraft sampling upwind, within, and outside of the evolving Sacramento urban plume in the morning and again in the afternoon. The G-1 payload consisted of a suite of instruments to measure trace gases, aerosol size distribution, composition, and optical properties. The NASA B-200 aircraft carrying a High Spectral Resolution Lidar (HSRL) and a Research Scanning Polarimeter (RSP) was also deployed to characterize the vertical and horizontal distribution of aerosols and aerosol optical properties. The aircraft measurements were complemented by heavily-instrumented ground sites within the Sacramento urban area and at a downwind site in Cool, California, to characterize the diurnal evolution of meteorological variables, trace gases, aerosol precursors, aerosol

  5. Changes in future air quality, deposition, and aerosol-cloud interactions under future climate and emission scenarios

    NASA Astrophysics Data System (ADS)

    Glotfelty, Timothy; Zhang, Yang; Karamchandani, Prakash; Streets, David G.

    2016-08-01

    treatments. This study indicates that effective climate mitigation and emission control strategies are needed to prevent future health impact and ecosystem stress. Further, studies that are used to develop these strategies should use fully coupled models with sophisticated chemical and aerosol-interaction treatments that can provide a more realistic representation of the atmosphere.

  6. Ground-based remote sensing of aerosol climatology in China: Aerosol optical properties, direct radiative effect and its parameterization

    NASA Astrophysics Data System (ADS)

    Xia, X.; Che, H.; Zhu, J.; Chen, H.; Cong, Z.; Deng, X.; Fan, X.; Fu, Y.; Goloub, P.; Jiang, H.; Liu, Q.; Mai, B.; Wang, P.; Wu, Y.; Zhang, J.; Zhang, R.; Zhang, X.

    2016-01-01

    Spatio-temporal variation of aerosol optical properties and aerosol direct radiative effects (ADRE) are studied based on high quality aerosol data at 21 sunphotometer stations with at least 4-months worth of measurements in China mainland and Hong Kong. A parameterization is proposed to describe the relationship of ADREs to aerosol optical depth at 550 nm (AOD) and single scattering albedo at 550 nm (SSA). In the middle-east and south China, the maximum AOD is always observed in the burning season, indicating a significant contribution of biomass burning to AOD. Dust aerosols contribute to AOD significantly in spring and their influence decreases from the source regions to the downwind regions. The occurrence frequencies of background level AOD (AOD < 0.10) in the middle-east, south and northwest China are very limited (0.4%, 1.3% and 2.8%, respectively). However, it is 15.7% in north China. Atmosphere is pristine in the Tibetan Plateau where 92.0% of AODs are <0.10. Regional mean SSAs at 550 nm are 0.89-0.90, although SSAs show substantial site and season dependence. ADREs at the top and bottom of the atmosphere for solar zenith angle of 60 ± 5° are -16--37 W m-2 and -66--111 W m-2, respectively. ADRE efficiency shows slight regional dependence. AOD and SSA together account for more than 94 and 87% of ADRE variability at the bottom and top of the atmosphere. The overall picture of ADRE in China is that aerosols cool the climate system, reduce surface solar radiation and heat the atmosphere.

  7. Effect of Aerosols on Surface Radiation and Air Quality in the Central American Region Estimated Using Satellite UV Instruments

    NASA Astrophysics Data System (ADS)

    Bhartia, P. K.; Torres, O.; Krotkov, N. A.

    2007-05-01

    Solar radiation reaching the Earth's surface is reduced by both aerosol scattering and aerosol absorption. Over many parts of the world the latter effect can be as large or larger than the former effect, and small changes in the aerosol single scattering albedo can either cancel the former effect or enhance it. In addition, absorbing aerosols embedded in clouds can greatly reduce the amount of radiation reaching the surface by multiple scattering. Though the potential climatic effects of absorbing aerosols have received considerable attention lately, their effect on surface UV, photosynthesis, and photochemistry can be equally important for our environment and may affect human health and agricultural productivity. Absorption of all aerosols commonly found in the Earth's atmosphere becomes larger in the UV and blue wavelengths and has a relatively strong wavelength dependence. This is particularly true of mineral dust and organic aerosols. However, these effects have been very difficult to estimate on a global basis since the satellite instruments that operate in the visible are primarily sensitive to aerosol scattering. A notable exception is the UV Aerosol Index (AI), first produced using NASA's Nimbus-7 TOMS data. AI provides a direct measure of the effect of aerosol absorption on the backscattered UV radiation in both clear and cloudy conditions, as well as over snow/ice. Although many types of aerosols produce a distinct color cast in the visible images, and aerosols absorption over clouds and snow/ice could, in principle be detected from their color, so far this technique has worked well only in the UV. In this talk we will discuss what we have learned from the long-term record of AI produced from TOMS and Aura/OMI about the possible role of aerosols on surface radiation and air quality in the Central American region.

  8. Parameterizations of Cloud Microphysics and Indirect Aerosol Effects

    SciTech Connect

    Tao, Wei-Kuo

    2014-05-19

    1. OVERVIEW Aerosols and especially their effect on clouds are one of the key components of the climate system and the hydrological cycle [Ramanathan et al., 2001]. Yet, the aerosol effect on clouds remains largely unknown and the processes involved not well understood. A recent report published by the National Academy of Science states "The greatest uncertainty about the aerosol climate forcing - indeed, the largest of all the uncertainties about global climate forcing - is probably the indirect effect of aerosols on clouds [NRC, 2001]." The aerosol effect on clouds is often categorized into the traditional "first indirect (i.e., Twomey)" effect on the cloud droplet sizes for a constant liquid water path [Twomey, 1977] and the "semi-direct" effect on cloud coverage [e.g., Ackerman et al., 2000]. Enhanced aerosol concentrations can also suppress warm rain processes by producing a narrow droplet spectrum that inhibits collision and coalescence processes [e.g., Squires and Twomey, 1961; Warner and Twomey, 1967; Warner, 1968; Rosenfeld, 1999]. The aerosol effect on precipitation processes, also known as the second type of aerosol indirect effect [Albrecht, 1989], is even more complex, especially for mixed-phase convective clouds. Table 1 summarizes the key observational studies identifying the microphysical properties, cloud characteristics, thermodynamics and dynamics associated with cloud systems from high-aerosol continental environments. For example, atmospheric aerosol concentrations can influence cloud droplet size distributions, warm-rain process, cold-rain process, cloud-top height, the depth of the mixed phase region, and occurrence of lightning. In addition, high aerosol concentrations in urban environments could affect precipitation variability by providing an enhanced source of cloud condensation nuclei (CCN). Hypotheses have been developed to explain the effect of urban regions on convection and precipitation [van den Heever and Cotton, 2007 and Shepherd

  9. Climatic and ecological impacts of tropospheric sulphate aerosols on the terrestrial carbon cycle

    NASA Astrophysics Data System (ADS)

    Eliseev, Alexey V.

    2015-04-01

    Tropospheric sulphate aerosols (TSA) may oxidise the photosynthesising tissues if they are taken up by plants. A parametrisation of this impact of tropospheric sulphate aerosols (TSA) on the terrestrial gross primary production is suggested. This parametrisation is implemented into the global Earth system model developed at the A.M. Obukhov Institute of the Atmospheric Physics, Russian Academy of Sciences (IAP RAS CM). With this coupled model, the simulations are performed which are forced by common anthropogenic and natural climate forcings based on historical reconstructions followed by the RCP 8.5 scenario. The model response to sulphate aerosol loading is subdivided into the climatic (related to the influence of TSA on the radiative transport in the atmosphere) and ecological (related to the toxic influence of sulphate aerosol on terrestrial plants) impacts. We found that the former basically dominates over the latter on the global scale and modifies the responses of the global vegetation and soil carbon stocks to external forcings by 10%. At regional scale, however, ecological impact may be as much important as the climatic one.

  10. The aerosol radiative effects of uncontrolled combustion of domestic waste

    NASA Astrophysics Data System (ADS)

    Kodros, John K.; Cucinotta, Rachel; Ridley, David A.; Wiedinmyer, Christine; Pierce, Jeffrey R.

    2016-06-01

    Open, uncontrolled combustion of domestic waste is a potentially significant source of aerosol; however, this aerosol source is not generally included in many global emissions inventories. To provide a first estimate of the aerosol radiative impacts from domestic-waste combustion, we incorporate the Wiedinmyer et al. (2014) emissions inventory into GEOS-Chem-TOMAS, a global chemical-transport model with online aerosol microphysics. We find domestic-waste combustion increases global-mean black carbon and organic aerosol concentrations by 8 and 6 %, respectively, and by greater than 40 % in some regions. Due to uncertainties regarding aerosol optical properties, we estimate the globally averaged aerosol direct radiative effect to range from -5 to -20 mW m-2; however, this range increases from -40 to +4 mW m-2 when we consider uncertainties in emission mass and size distribution. In some regions with significant waste combustion, such as India and China, the aerosol direct radiative effect may exceed -0.4 W m-2. Similarly, we estimate a cloud-albedo aerosol indirect effect of -13 mW m-2, with a range of -4 to -49 mW m-2 due to emission uncertainties. In the regions with significant waste combustion, the cloud-albedo aerosol indirect effect may exceed -0.4 W m-2.

  11. A GCM Investigation of Dust Aerosol Impact on the Regional Climate of North Africa and South/East Asia

    NASA Astrophysics Data System (ADS)

    Gu, Y.; Xue, Y.; De Sales, F.; Liou, K. N.

    2015-12-01

    The interactions between dust and other physical processes have been found to play an important role in the dust-induced climate change. However, there are large uncertainties regarding whether, where, and how the dust enhances or suppresses precipitation. The climatic effects of dust aerosols in North Africa and South/East Asia have been investigated using an atmospheric general circulation model, NCEP/GCM/SSiB (Simplified Simple Biosphere Model) and the three-dimensional aerosol data simulated by the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model. GCM simulations show that due to the scattering and absorption of solar radiation by dust particles, surface temperature decreases over both regions, accompanied by a reduced sensible heat flux. However, precipitation responses are different in these two regions. Due to differences in dust location and the associated heating with respect to the rainfall band and circulation, the effect of dust could either enhance or suppress precipitation. Over the North Africa region where dust particles are mainly located to the north of rainfall band, heating of the air column by dust particles forces a stronger ascent motion over dust layers, which induces an anomalous subsidence (or a weakened upward motion) and suppressed cyclonic circulation to its south where precipitation reduces. In South/East Asia, dust particles are located in the upper troposphere over the major rainfall band during the monsoon season, especially Southwest India and the coastal area of Bay of Bengal. Heating of the air column increases upward motion and strengthens cyclonic circulation. Therefore, cloud and precipitation increase over South/East Asia associated with dust effect. During the pre-monsoon season, when dust particles are located to the north of the monsoon rainfall band, the heating effect results in shifting precipitation northward. The anomalous upward motion over dust regions will induce a subsidence to its south and

  12. Absorption and scattering properties of organic carbon versus sulfate dominant aerosols at Gosan climate observatory in Northeast Asia

    NASA Astrophysics Data System (ADS)

    Lim, S.; Lee, M.; Kim, S.-W.; Yoon, S.-C.; Lee, G.; Lee, Y. J.

    2014-08-01

    OC compounds. Under sulfate dominant conditions, the sulfate coating on BC particles likely contributed to the absorption of the longer visible light. Consequently, single scattering albedo (SSA) was higher for the 880 nm group than for the 370 nm group, emphasizing that the relative abundances of absorbing and scattering constituents are also important in estimating the climate effect of aerosols.

  13. Improving Bulk Microphysics Parameterizations in Simulations of Aerosol Effects

    SciTech Connect

    Wang, Yuan; Fan, Jiwen; Zhang, Renyi; Leung, Lai-Yung R.; Franklin, Charmaine N.

    2013-06-05

    To improve the microphysical parameterizations for simulations of the aerosol indirect effect (AIE) in regional and global climate models, a double-moment bulk microphysical scheme presently implemented in the Weather Research and Forecasting (WRF) model is modified and the results are compared against atmospheric observations and simulations produced by a spectral bin microphysical scheme (SBM). Rather than using prescribed aerosols as in the original bulk scheme (Bulk-OR), a prognostic doublemoment aerosol representation is introduced to predict both the aerosol number concentration and mass mixing ratio (Bulk-2M). The impacts of the parameterizations of diffusional growth and autoconversion and the selection of the embryonic raindrop radius on the performance of the bulk microphysical scheme are also evaluated. Sensitivity modeling experiments are performed for two distinct cloud regimes, maritime warm stratocumulus clouds (SC) over southeast Pacific Ocean from the VOCALS project and continental deep convective clouds (DCC) in the southeast of China from the Department of Energy/ARM Mobile Facility (DOE/AMF) - China field campaign. The results from Bulk-2M exhibit a much better agreement in the cloud number concentration and effective droplet radius in both the SC and DCC cases with those from SBM and field measurements than those from Bulk-OR. In the SC case particularly, Bulk-2M reproduces the observed drizzle precipitation, which is largely inhibited in Bulk-OR. Bulk-2M predicts enhanced precipitation and invigorated convection with increased aerosol loading in the DCC case, consistent with the SBM simulation, while Bulk-OR predicts the opposite behaviors. Sensitivity experiments using four different types of autoconversion schemes reveal that the autoconversion parameterization is crucial in determining the raindrop number, mass concentration, and drizzle formation for warm 2 stratocumulus clouds. An embryonic raindrop size of 40 μm is determined as a more

  14. Encapsulation effects on carbonaceous aerosol light absorption

    SciTech Connect

    Sedlacek, A.J.; Onasch, T.; Davidovits, P.; Cross, E.; Mazzoleni, C.

    2010-03-15

    The contribution of aerosol absorption on direct radiative forcing is still an active area of research, in part, because aerosol extinction is dominated by light scattering and, in part, because the primary absorbing aerosol of interest, soot, exhibits complex aging behavior that alters its optical properties. The consequences of this can be evidenced by the work of Ramanathan and Carmichael (2008) who suggest that incorporating the atmospheric heating due to brown clouds (plumes containing soot byproducts from automobiles, biomass burning, wood-burning kitchen stoves, and coal-fired power plants) will increase black carbon (BC) radiative forcing from the Intergovernmental Panel on Climate Change best estimate of 0.34 Wm-2 (±0.25 Wm-2) (IPCC 2007) to 0.9 Wm-2. This noteworthy degree of uncertainty is due largely to the interdependence of BC optical properties on particle mixing state and aggregate morphology, each of which changes as the particle ages in the atmosphere and becomes encapsulated within a coating of inorganic and/or organic substances. In July 2008, a laboratory-based measurement campaign, led by Boston College and Aerodyne, was initiated to begin addressing this interdependence. To achieve insights into the interdependence of BC optical properties on particle mixing state and aggregate morphology, measurements of both the optical and physical properties of flame-generated soot under nascent, coated, and denuded conditions were conducted. This poster presents data on black carbon (BC) light absorption measured by Photothermal Interferometry (Sedlacek and Lee 2007). In addition to examining nascent BC—to provide a baseline measurement—encapsulation with varying thicknesses of either dioctyl sebacate (DOS) or sulfuric acid was conducted to glean insights into the interplay between particle mixing state and optical properties. Additionally, some experiments were carried out where BC was coated and then denuded. In the case of DOS-coated soot, a

  15. Global distribution and climate forcing of marine organic aerosol: 1. Model improvements and evaluation

    SciTech Connect

    Meskhidze, N.; Xu, J.; Gantt, Brett; Zhang, Yang; Nenes, Athanasios; Ghan, Steven J.; Liu, Xiaohong; Easter, Richard C.; Zaveri, Rahul A.

    2011-11-23

    -salt provides diverse results with increases and decreases in the concentration of CCN over different parts of the ocean. The sign of the CCN change due to the addition of marine organics to seasalt aerosol is determined by the relative significance of the increase in mean modal diameter due to addition of mass, and the decrease in particle hygroscopicity due to compositional changes in marine aerosol. Based on emerging evidence for increased CCN concentration over biologically active surface ocean areas/periods, our study suggests that treatment of sea spray in global climate models (GCMs) as an internal mixture of marine organic aerosols and sea-salt will likely lead to an underestimation in CCN number concentration.

  16. The Earth Climate Hyperspectral Observatory: Advances in Cloud and Aerosol Remote Sensing

    NASA Astrophysics Data System (ADS)

    Pilewskie, Peter; Schmidt, Sebastian; Coddington, Odele; Kopp, Greg

    2015-04-01

    Future satellite missions to monitor global change require the establishment of high-accuracy spectrally resolved benchmark data records of reflected shortwave radiation for trend detection and attribution. Not surprisingly, these same attributes also provide substantial improvements in the retrieval of microphysical and optical properties of clouds and aerosols over current discrete-band observations. The NASA Climate Absolute Radiance and Refractivity Observatory (CLARREO) mission, currently in pre-formulation, defines a set of fundamental direct observations of spectrally resolved reflected shortwave and emitted longwave radiation, and GNSS radio occultation in order to detect climate trends and to test and improve climate prediction models. The Earth Climate Hyperspectral Observatory (ECHO), a proposed pathfinder mission to CLARREO, focuses on measuring spectrally resolved Earth-reflected shortwave radiation over a spectral range that comprised approximately 95% of the solar radiative energy incident at the top-of-atmosphere. This paper will report on the ECHO requirements specifically directed at objectives related to cloud and aerosol remote sensing, and more generally, characterizing the physical parameters responsible for the observed spectral and temporal variability in a benchmark data record. These objectives are centered on targeted remote sensing and data assimilation analyses to derive the dominant contributors to the observed spectral, temporal, and spatial perturbations in the reflected shortwave signal. Specific improvements in the retrieval of cloud and aerosol properties due to increased spectral coverage, spectral resolution, and radiometric accuracy will be discussed.

  17. A numerical study of the effect of different aerosol types on East Asian summer clouds and precipitation

    SciTech Connect

    Jiang, Yiquan; Liu, Xiaohong; Yang, Xiuqun; Wang, Minghuai

    2013-05-01

    The impact of anthropogenic aerosol on the East Asian summer monsoon (EASM) is investigated with NCAR CAM5, a state-of-the-art climate model with aerosol’s direct and indirect effects. Results indicate that anthropogenic aerosol tends to cause a weakened EASM with a southward shift of precipitation in East Asia mostly by its radiative effect. Anthropogenic aerosol induced surface cooling stabilizes the boundary layer, suppresses the convection and latent heat release in northern China, and reduces the tropospheric temperature over land and land-sea thermal contrast, thus leading to a weakened EASM. Meanwhile, acting as cloud condensation nuclei (CCN), anthropogenic aerosol can significantly increase the cloud droplet number concentration but decrease the cloud droplet effective radius over Indochina and Indian Peninsulas as well as over southwestern and northern China, inhibiting the precipitation in these regions. Thus, anthropogenic aerosol tends to reduce Southeast and South Asian summer monsoon precipitation by its indirect effect.

  18. Aerosol chemical characterization and role of carbonaceous aerosol on radiative effect over Varanasi in central Indo-Gangetic Plain

    NASA Astrophysics Data System (ADS)

    Tiwari, S.; Dumka, U. C.; Kaskaoutis, D. G.; Ram, Kirpa; Panicker, A. S.; Srivastava, M. K.; Tiwari, Shani; Attri, S. D.; Soni, V. K.; Pandey, A. K.

    2016-01-01

    This study investigates the chemical composition of PM10 aerosols at Varanasi, in the central Indo-Gangetic Plain (IGP) during April to July 2011, with emphasis on examining the contribution of elemental carbon (EC) to the estimates of direct aerosol radiative effect (DARE). PM10 samples are analysed for carbonaceous aerosols (Organic Carbon, OC and EC) and water-soluble ionic species (WSIS: Cl-, SO42-, NO3-, PO42- NH4+, Na+, K+, Mg2+ and Ca2+) and several diagnostic ratios (OC/EC, K+/EC, etc) have been also used for studying the aerosol sources at Varanasi. PM10 mass concentration varies between 53 and 310 μg m-3 (mean of 168 ± 73 μg m-3), which is much higher than the National and International air quality standards. The OC mass concentration varies from 6 μg m-3 to 24 μg m-3 (mean of 12 ± 5 μg m-3; 7% of PM10 mass), whereas EC ranges between 1.0 and 14.3 μg m-3 (4.4 ± 3.9 μg m-3; ˜3% of PM10 mass). The relative low OC/EC of 3.9 ± 2.0 and strong correlation (R2 = 0.82) between them suggest the dominance of primary carbonaceous aerosols. The contribution of WSIS to PM10 is found to be ˜12%, out of which ˜57% and 43% are anions and cations, respectively. The composite DARE estimates via SBDART model reveal significant radiative effect and atmospheric heating rates (0.9-2.3 K day-1). Although the EC contributes only ˜3% to the PM10 mass, its contribution to the surface and atmospheric forcing is significantly high (37-63% and 54-77%, respectively), thus playing a major role in climate implications over Varanasi.

  19. Microphysical effects determine macrophysical response for aerosol impacts on deep convective clouds.

    PubMed

    Fan, Jiwen; Leung, L Ruby; Rosenfeld, Daniel; Chen, Qian; Li, Zhanqing; Zhang, Jinqiang; Yan, Hongru

    2013-11-26

    Deep convective clouds (DCCs) play a crucial role in the general circulation, energy, and hydrological cycle of our climate system. Aerosol particles can influence DCCs by altering cloud properties, precipitation regimes, and radiation balance. Previous studies reported both invigoration and suppression of DCCs by aerosols, but few were concerned with the whole life cycle of DCC. By conducting multiple monthlong cloud-resolving simulations with spectral-bin cloud microphysics that capture the observed macrophysical and microphysical properties of summer convective clouds and precipitation in the tropics and midlatitudes, this study provides a comprehensive view of how aerosols affect cloud cover, cloud top height, and radiative forcing. We found that although the widely accepted theory of DCC invigoration due to aerosol's thermodynamic effect (additional latent heat release from freezing of greater amount of cloud water) may work during the growing stage, it is microphysical effect influenced by aerosols that drives the dramatic increase in cloud cover, cloud top height, and cloud thickness at the mature and dissipation stages by inducing larger amounts of smaller but longer-lasting ice particles in the stratiform/anvils of DCCs, even when thermodynamic invigoration of convection is absent. The thermodynamic invigoration effect contributes up to ~27% of total increase in cloud cover. The overall aerosol indirect effect is an atmospheric radiative warming (3-5 W m(-2)) and a surface cooling (-5 to -8 W m(-2)). The modeling findings are confirmed by the analyses of ample measurements made at three sites of distinctly different environments.

  20. Evaluating Clouds, Aerosols, and their Interactions in Three Global Climate Models using COSP and Satellite Observations

    SciTech Connect

    Ban-Weiss, George; Jin, Ling; Bauer, S.; Bennartz, Ralph; Liu, Xiaohong; Zhang, Kai; Ming, Yi; Guo, Huan; Jiang, Jonathan

    2014-09-23

    Accurately representing aerosol-cloud interactions in global climate models is challenging. As parameterizations evolve, it is important to evaluate their performance with appropriate use of observations. In this work we compare aerosols, clouds, and their interactions in three climate models (AM3, CAM5, ModelE) to MODIS satellite observations. Modeled cloud properties were diagnosed using the CFMIP Observations Simulator Package (COSP). Cloud droplet number concentrations (N) were derived using the same algorithm for both satellite-simulated model values and observations. We find that aerosol optical depth tau simulated by models is similar to observations. For N, AM3 and CAM5 capture the observed spatial pattern of higher values in near-coast versus remote ocean regions, though modeled values in general are higher than observed. In contrast, ModelE simulates lower N in most near-coast versus remote regions. Aerosol- cloud interactions were computed as the sensitivity of N to tau for marine liquid clouds off the coasts of South Africa and Eastern Asia where aerosol pollution varies in time. AM3 and CAM5 are in most cases more sensitive than observations, while the sensitivity for ModelE is statistically insignificant. This widely used sensitivity could be subject to misinterpretation due to the confounding influence of meteorology on both aerosols and clouds. A simple framework for assessing the N – tau sensitivity at constant meteorology illustrates that observed sensitivity can change from positive to statistically insignificant when including the confounding influence of relative humidity. Satellite simulated values of N were compared to standard model output and found to be higher with a bias of 83 cm-3.

  1. Overview of the Chemistry-Aerosol Mediterranean Experiment/Aerosol Direct Radiative Forcing on the Mediterranean Climate (ChArMEx/ADRIMED) summer 2013 campaign

    NASA Astrophysics Data System (ADS)

    Mallet, M.; Dulac, F.; Formenti, P.; Nabat, P.; Sciare, J.; Roberts, G.; Pelon, J.; Ancellet, G.; Tanré, D.; Parol, F.; Denjean, C.; Brogniez, G.; di Sarra, A.; Alados-Arboledas, L.; Arndt, J.; Auriol, F.; Blarel, L.; Bourrianne, T.; Chazette, P.; Chevaillier, S.; Claeys, M.; D'Anna, B.; Derimian, Y.; Desboeufs, K.; Di Iorio, T.; Doussin, J.-F.; Durand, P.; Féron, A.; Freney, E.; Gaimoz, C.; Goloub, P.; Gómez-Amo, J. L.; Granados-Muñoz, M. J.; Grand, N.; Hamonou, E.; Jankowiak, I.; Jeannot, M.; Léon, J.-F.; Maillé, M.; Mailler, S.; Meloni, D.; Menut, L.; Momboisse, G.; Nicolas, J.; Podvin, T.; Pont, V.; Rea, G.; Renard, J.-B.; Roblou, L.; Schepanski, K.; Schwarzenboeck, A.; Sellegri, K.; Sicard, M.; Solmon, F.; Somot, S.; Torres, B.; Totems, J.; Triquet, S.; Verdier, N.; Verwaerde, C.; Waquet, F.; Wenger, J.; Zapf, P.

    2016-01-01

    The Chemistry-Aerosol Mediterranean Experiment (ChArMEx; http://charmex.lsce.ipsl.fr) is a collaborative research program federating international activities to investigate Mediterranean regional chemistry-climate interactions. A special observing period (SOP-1a) including intensive airborne measurements was performed in the framework of the Aerosol Direct Radiative Impact on the regional climate in the MEDiterranean region (ADRIMED) project during the Mediterranean dry season over the western and central Mediterranean basins, with a focus on aerosol-radiation measurements and their modeling. The SOP-1a took place from 11 June to 5 July 2013. Airborne measurements were made by both the ATR-42 and F-20 French research aircraft operated from Sardinia (Italy) and instrumented for in situ and remote-sensing measurements, respectively, and by sounding and drifting balloons, launched in Minorca. The experimental setup also involved several ground-based measurement sites on islands including two ground-based reference stations in Corsica and Lampedusa and secondary monitoring sites in Minorca and Sicily. Additional measurements including lidar profiling were also performed on alert during aircraft operations at EARLINET/ACTRIS stations at Granada and Barcelona in Spain, and in southern Italy. Remote-sensing aerosol products from satellites (MSG/SEVIRI, MODIS) and from the AERONET/PHOTONS network were also used. Dedicated meso-scale and regional modeling experiments were performed in relation to this observational effort. We provide here an overview of the different surface and aircraft observations deployed during the ChArMEx/ADRIMED period and of associated modeling studies together with an analysis of the synoptic conditions that determined the aerosol emission and transport. Meteorological conditions observed during this campaign (moderate temperatures and southern flows) were not favorable to producing high

  2. How shorter black carbon lifetime alters its climate effect.

    PubMed

    Hodnebrog, Øivind; Myhre, Gunnar; Samset, Bjørn H

    2014-01-01

    Black carbon (BC), unlike most aerosol types, absorbs solar radiation. However, the quantification of its climate impact is uncertain and presently under debate. Recently, attention has been drawn both to a likely underestimation of global BC emissions in climate models, and an overestimation of BC at high altitudes. Here we show that doubling present day BC emissions in a model simulation, while reducing BC lifetime based on observational evidence, leaves the direct aerosol effect of BC virtually unchanged. Increased emissions, together with increased wet removal that reduces the lifetime, yields modelled BC vertical profiles that are in strongly improved agreement with recent aircraft observations. Furthermore, we explore the consequences of an altered BC profile in a global circulation model, and show that both the vertical profile of BC and rapid climate adjustments need to be taken into account in order to assess the total climate impact of BC. PMID:25255429

  3. How shorter black carbon lifetime alters its climate effect.

    PubMed

    Hodnebrog, Øivind; Myhre, Gunnar; Samset, Bjørn H

    2014-09-25

    Black carbon (BC), unlike most aerosol types, absorbs solar radiation. However, the quantification of its climate impact is uncertain and presently under debate. Recently, attention has been drawn both to a likely underestimation of global BC emissions in climate models, and an overestimation of BC at high altitudes. Here we show that doubling present day BC emissions in a model simulation, while reducing BC lifetime based on observational evidence, leaves the direct aerosol effect of BC virtually unchanged. Increased emissions, together with increased wet removal that reduces the lifetime, yields modelled BC vertical profiles that are in strongly improved agreement with recent aircraft observations. Furthermore, we explore the consequences of an altered BC profile in a global circulation model, and show that both the vertical profile of BC and rapid climate adjustments need to be taken into account in order to assess the total climate impact of BC.

  4. Volcanic Aerosol Radiative Properties

    NASA Technical Reports Server (NTRS)

    Lacis, Andrew

    2015-01-01

    Large sporadic volcanic eruptions inject large amounts of sulfur bearing gases into the stratosphere which then get photochemically converted to sulfuric acid aerosol droplets that exert a radiative cooling effect on the global climate system lasting for several years.

  5. Aerosol radiative effects in the ultraviolet, visible, and near-infrared spectral ranges using long-term aerosol data series over the Iberian Peninsula

    NASA Astrophysics Data System (ADS)

    Mateos, D.; Antón, M.; Toledano, C.; Cachorro, V. E.; Alados-Arboledas, L.; Sorribas, M.; Costa, M. J.; Baldasano, J. M.

    2014-04-01

    A better understanding of the aerosol radiative properties is a crucial challenge for climate change studies. This study aims to provide a complete characterization of aerosol radiative effects in different spectral ranges within the shortwave (SW) solar spectrum. For this purpose, long-term datasets of aerosol properties from six AERONET stations located in the Iberian Peninsula (Southwestern Europe) are analyzed in term of climatology characterization and trends. Aerosol information is used as input to the libRadtran model in order to determine the aerosol radiative effect at the surface in the ultraviolet (AREUV), visible (AREVIS), near-infrared (ARENIR), and the entire SW range (ARESW) under cloud-free conditions. Over the whole Iberian Peninsula, aerosol radiative effects in the different spectral ranges are: -1.1 < AREUV < -0.7 W m-2, -5.7 < AREVIS < -3.8 W m-2, -2.8 < ARENIR < -1.7 W m-2, and -9.5 < ARESW < -6.1 W m-2. The four variables showed positive statistically significant trends between 2004 and 2012, e.g., ARESW increased +3.6 W m-2 per decade. This fact is linked to the decrease in the aerosol load, which presents a trend of -0.04 per unit of aerosol optical depth at 500 nm per decade, hence a reduction of aerosol effect on solar radiation at the surface is seen. Monthly means of ARE show a seasonal pattern with larger values in spring and summer. The aerosol forcing efficiency (AFE), ARE per unit of aerosol optical depth, is also evaluated in the four spectral ranges. AFE exhibits a dependence on single scattering albedo and a weaker one on Ångström exponent. AFE is larger (in absolute value) for small and absorbing particles. The contributions of the UV, VIS, and NIR ranges to the SW efficiency vary with the aerosol types. Aerosol size determines the fractions of AFEVIS/AFESW and AFENIR/AFESW. VIS range is the dominant region for all types, although non-absorbing large particles cause a more equal contribution of VIS and NIR intervals. The AFEUV

  6. Type-segregated aerosol effects on regional monsoon activity: A study using ground-based experiments and model simulations

    NASA Astrophysics Data System (ADS)

    Vijayakumar, K.; Devara, P. C. S.; Sonbawne, S. M.

    2014-12-01

    Classification of observed aerosols into key types [e.g., clean-maritime (CM), desert-dust (DD), urban-industrial/biomass-burning (UI/BB), black carbon (BC), organic carbon (OC) and mixed-type aerosols (MA)] would facilitate to infer aerosol sources, effects, and feedback mechanisms, not only to improve the accuracy of satellite retrievals but also to quantify the assessment of aerosol radiative impacts on climate. In this paper, we report the results of a study conducted in this direction, employing a Cimel Sun-sky radiometer at the Indian Institute of Tropical Meteorology (IITM), Pune, India during 2008 and 2009, which represent two successive contrasting monsoon years. The study provided an observational evidence to show that the local sources are subject to heavy loading of absorbing aerosols (dust and black carbon), with strong seasonality closely linked to the monsoon annual rainfall cycle over Pune, a tropical urban station in India. The results revealed the absence of CM aerosols in the pre-monsoon as well as in the monsoon seasons of 2009 as opposed to 2008. Higher loading of dust aerosols is observed in the pre-monsoon and monsoon seasons of 2009; majority may be coated with fine BC aerosols from local emissions, leading to reduction in regional rainfall. Further, significant decrease in coarse-mode AOD and presence of carbonaceous aerosols, affecting the aerosol-cloud interaction and monsoon-rain processes via microphysics and dynamics, is considered responsible for the reduction in rainfall during 2009. Additionally, we discuss how optical depth, contributed by different types of aerosols, influences the distribution of monsoon rainfall over an urban region using the Monitoring Atmospheric Composition and Climate (MACC) aerosol reanalysis. Furthermore, predictions of the Dust REgional Atmospheric Model (DREAM) simulations combined with HYSPLIT (HYbrid Single Particle Lagrangian Integrated Trajectory) cluster model are also discussed in support of the

  7. Aerosol effects and corrections in the Halogen Occultation Experiment

    NASA Technical Reports Server (NTRS)

    Hervig, Mark E.; Russell, James M., III; Gordley, Larry L.; Daniels, John; Drayson, S. Roland; Park, Jae H.

    1995-01-01

    The eruptions of Mt. Pinatubo in June 1991 increased stratospheric aerosol loading by a factor of 30, affecting chemistry, radiative transfer, and remote measurements of the stratosphere. The Halogen Occultation Experiment (HALOE) instrument on board Upper Atmosphere Research Satellite (UARS) makes measurements globally for inferring profiles of NO2, H2O, O3, HF, HCl, CH4, NO, and temperature in addition to aerosol extinction at five wavelengths. Understanding and removing the aerosol extinction is essential for obtaining accurate retrievals from the radiometer channels of NO2, H2O and O3 in the lower stratosphere since these measurements are severely affected by contaminant aerosol absorption. If ignored, aerosol absorption in the radiometer measurements is interpreted as additional absorption by the target gas, resulting in anomalously large mixing ratios. To correct the radiometer measurements for aerosol effects, a retrieved aerosol extinction profile is extrapolated to the radiometer wavelengths and then included as continuum attenuation. The sensitivity of the extrapolation to size distribution and composition is small for certain wavelength combinations, reducing the correction uncertainty. The aerosol corrections extend the usable range of profiles retrieved from the radiometer channels to the tropopause with results that agree well with correlative measurements. In situations of heavy aerosol loading, errors due to aerosol in the retrieved mixing ratios are reduced to values of about 15, 25, and 60% in H2O, O3, and NO2, respectively, levels that are much less than the correction magnitude.

  8. Radiative Effects of Aerosols Generated from Biomass Burning, Dust Storms, and Forest Fires

    NASA Technical Reports Server (NTRS)

    Christopher Sundar A.; Vulcan, Donna V.; Welch, Ronald M.

    1996-01-01

    Atmospheric aerosol particles, both natural and anthropogenic, are important to the earth's radiative balance. They scatter the incoming solar radiation and modify the shortwave reflective properties of clouds by acting as Cloud Condensation Nuclei (CCN). Although it has been recognized that aerosols exert a net cooling influence on climate (Twomey et al. 1984), this effect has received much less attention than the radiative forcings due to clouds and greenhouse gases. The radiative forcing due to aerosols is comparable in magnitude to current anthropogenic greenhouse gas forcing but opposite in sign (Houghton et al. 1990). Atmospheric aerosol particles generated from biomass burning, dust storms and forest fires are important regional climatic variables. A recent study by Penner et al. (1992) proposed that smoke particles from biomass burning may have a significant impact on the global radiation balance. They estimate that about 114 Tg of smoke is produced per year in the tropics through biomass burning. The direct and indirect effects of smoke aerosol due to biomass burning could add up globally to a cooling effect as large as 2 W/sq m. Ackerman and Chung (1992) used model calculations and the Earth Radiation Budget Experiment (ERBE) data to show that in comparison to clear days, the heavy dust loading over the Saudi Arabian peninsula can change the Top of the Atmosphere (TOA) clear sky shortwave and longwave radiant exitance by 40-90 W/sq m and 5-20 W/sq m, respectively. Large particle concentrations produced from these types of events often are found with optical thicknesses greater than one. These aerosol particles are transported across considerable distances from the source (Fraser et al. 1984). and they could perturb the radiative balance significantly. In this study, the regional radiative effects of aerosols produced from biomass burning, dust storms and forest fires are examined using the Advanced Very High Resolution Radiometer (AVHRR) Local Area

  9. GCM simulations of volcanic aerosol forcing. Part I: Climate changes induced by stead-state perturbations

    SciTech Connect

    Pollack, J.B. ); Rind, D.; Lacis, A.; Hansen, J.E.; Sato, M.; Ruedy, R. )

    1993-09-01

    The Goddard Institute for Space Studies Climate Model II was used to simulate the response of the climate system to a spatially and temporally constant forcing by volcanic aerosols. The climatic changes produced by differencing this simulation and one made for the present climate with no volcanic aerosol forcing. These climatic changes are also compared with those obtained when CO[sub 2] in the atmosphere was doubled and when the boundary conditions associated with the peak of the last ice age. In all three cases, the absolute magnitude of the change in the globally averaged air temperature at the surface is approximately 5K. The simulations imply a significant cooling of the troposphere and surface can occur at times of closely spaced, multiple, sulfur-rich volcanic explosions that span time scales of decades to centuries, such as occurred at the end of the nineteenth and beginning of the twentieth centuries. The steady-state climate response to volcanic forcing includes a expansion of sea ice, especially Southern Hemisphere; a large increase in surface and planetary albedo at high latitudes; and sizable changes in the annually and zonally averaged air temperature. The climate response to three different forcings is similar in 3 ways: direct radiative forcing accounts for 30% and 25% of the total [delta]T[sub s]; Changes in atmospheric water vapor are the most important positive feedback; Albedo feedback is significant, positive at high latitudes. The climate response to the three forcings also differs. The latitudinal profiles of [delta]T[sub s] differ, reflecting significant variations in the latitudinal profiles of the primary radiative forcing. Changes in eddy kinetic energy, heat transport by atmospheric eddies, and total atmospheric heat transport are quite different. These results raise questions about the ease with which atmospheric heat transport can be parameterized in a simple way in energy climate models. 44 refs., 32 figs.

  10. Aerosol speckle effects on atmospheric pulsed lidar backscattered signals

    NASA Technical Reports Server (NTRS)

    Murty, S. R.

    1989-01-01

    Lidar systems using atmospheric aerosols as targets exhibit return signal amplitude and power fluctuations which indicate speckle effects. The effects of refractive turbulence along the path on the aerosol speckle field propagation and on the decorrelation time are studied for coherent pulsed lidar systems.

  11. Vertical microphysical profiles of convective clouds as a tool for obtaining aerosol cloud-mediated climate forcings

    SciTech Connect

    Rosenfeld, Daniel

    2015-12-23

    Quantifying the aerosol/cloud-mediated radiative effect at a global scale requires simultaneous satellite retrievals of cloud condensation nuclei (CCN) concentrations and cloud base updraft velocities (Wb). Hitherto, the inability to do so has been a major cause of high uncertainty regarding anthropogenic aerosol/cloud-mediated radiative forcing. This can be addressed by the emerging capability of estimating CCN and Wb of boundary layer convective clouds from an operational polar orbiting weather satellite. Our methodology uses such clouds as an effective analog for CCN chambers. The cloud base supersaturation (S) is determined by Wb and the satellite-retrieved cloud base drop concentrations (Ndb), which is the same as CCN(S). Developing and validating this methodology was possible thanks to the ASR/ARM measurements of CCN and vertical updraft profiles. Validation against ground-based CCN instruments at the ARM sites in Oklahoma, Manaus, and onboard a ship in the northeast Pacific showed a retrieval accuracy of ±25% to ±30% for individual satellite overpasses. The methodology is presently limited to boundary layer not raining convective clouds of at least 1 km depth that are not obscured by upper layer clouds, including semitransparent cirrus. The limitation for small solar backscattering angles of <25º restricts the satellite coverage to ~25% of the world area in a single day. This methodology will likely allow overcoming the challenge of quantifying the aerosol indirect effect and facilitate a substantial reduction of the uncertainty in anthropogenic climate forcing.

  12. Effects of aerosols and relative humidity on cumulus clouds

    NASA Astrophysics Data System (ADS)

    Fan, Jiwen; Zhang, Renyi; Li, Guohui; Tao, Wei-Kuo

    2007-07-01

    The influences of the aerosol type and concentration and relative humidity (RH) on cumulus clouds have been investigated using a two-dimensional spectral-bin cloud model. Three simulations are conducted to represent the polluted continental, clean continental, and marine aerosol types. Under the same initial dynamic and thermodynamic conditions, the maritime aerosol case results in more intensive radar reflectivity in both developing and mature stages than the continental aerosol cases, because of enhanced warm rain by collisions and ice processes by deposition growth due to larger droplet sizes and higher supersaturation, respectively. The considerable delay in convective development due to reduced droplet condensation is responsible for the longer cloud lifetime in the marine aerosol case. For the continental case, the most noticeable effects of increasing aerosol number concentrations (with 15 different initial values) are the increases of the cloud droplet number concentration and cloud water content but a decrease in the effective droplet radius. More latent heat release from increasing condensation results in stronger convection and more melting precipitation at the higher aerosol concentrations. Melting precipitation and secondary clouds primarily contribute to enhanced precipitation with increasing aerosols. The precipitation, however, decreases with increasing aerosol in the extremely high aerosol cases (over 5 × 104 cm-3) due to suppression of convection from depleted water vapor and inefficient coalescence. When the initial aerosol concentration exceeds a critical level, most of the cloud properties become less sensitive to aerosols, implying that the aerosol effect on deep convection is more pronounced in relatively clean air than in heavily polluted air. The aerosol effect on the cloud properties is strongly dependent on RH. As the surface RH increases from 40 to 70%, the cloud changes from shallow warm to deep convective types due to a significant

  13. Model-Based Estimation of Sampling-Caused Uncertainty in Aerosol Remote Sensing for Climate Research Applications

    NASA Technical Reports Server (NTRS)

    Geogdzhayev, Igor V.; Cairns, Brian; Mishchenko, Michael I.; Tsigaridis, Kostas; van Noije, Twan

    2014-01-01

    To evaluate the effect of sampling frequency on the global monthly mean aerosol optical thickness (AOT), we use 6 years of geographical coordinates of Moderate Resolution Imaging Spectroradiometer (MODIS) L2 aerosol data, daily global aerosol fields generated by the Goddard Institute for Space Studies General Circulation Model and the chemical transport models Global Ozone Chemistry Aerosol Radiation and Transport, Spectral Radiationtransport Model for Aerosol Species and Transport Model 5, at a spatial resolution between 1.125 deg × 1.125 deg and 2 deg × 3?: the analysis is restricted to 60 deg S-60 deg N geographical latitude. We found that, in general, the MODIS coverage causes an underestimate of the global mean AOT over the ocean. The long-term mean absolute monthly difference between all and dark target (DT) pixels was 0.01-0.02 over the ocean and 0.03-0.09 over the land, depending on the model dataset. Negative DT biases peak during boreal summers, reaching 0.07-0.12 (30-45% of the global long-term mean AOT). Addition of the Deep Blue pixels tempers the seasonal dependence of the DT biases and reduces the mean AOT difference over land by 0.01-0.02. These results provide a quantitative measure of the effect the pixel exclusion due to cloud contamination, ocean sun-glint and land type has on the MODIS estimates of the global monthly mean AOT. We also simulate global monthly mean AOT estimates from measurements provided by pixel-wide along-track instruments such as the Aerosol Polarimetry Sensor and the Cloud-Aerosol LiDAR with Orthogonal Polarization. We estimate the probable range of the global AOT standard error for an along-track sensor to be 0.0005-0.0015 (ocean) and 0.0029-0.01 (land) or 0.5-1.2% and 1.1-4% of the corresponding global means. These estimates represent errors due to sampling only and do not include potential retrieval errors. They are smaller than or comparable to the published estimate of 0.01 as being a climatologically significant

  14. Impact of Aerosols and Atmospheric Thermodynamics on Cloud Properties within the Climate System

    NASA Technical Reports Server (NTRS)

    Matsui, Toshihisa; Masunaga, Hirohiko; Pielke, Roger, Sr.; Tao, Wei-Kuo

    2003-01-01

    A combination of cloud-top and columnar droplet sizes derived from the multi Tropical Rainfall Measurement Mission (TRMM) sensors reveals the sensitivity of the aerosols effect on cloud-precipitation process due to environmental vertical thermodynamic structure. First, the magnitude of aerosol indirect effect could be larger with the analysis of columnar droplet sizes than that derived from the cloud-top droplet sizes, since column-droplet size can account for the broader droplet spectra in the cloud layers. Second, a combination of cloud- top and columnar droplet sizes reveals that the warm rain process is prevented regardless of the aerosols concentration under a high static stability such as when a strong temperature inversion exists, while a high aerosol concentration suppresses the warm rain formulation under a low static stability.

  15. Total aerosol effect: forcing or radiative flux perturbation?

    SciTech Connect

    Lohmann, Ulrike; Storelvmo, Trude; Jones, Andy; Rotstayn, Leon; Menon, Surabi; Quaas, Johannes; Ekman, Annica; Koch, Dorothy; Ruedy, Reto

    2009-09-25

    Uncertainties in aerosol forcings, especially those associated with clouds, contribute to a large extent to uncertainties in the total anthropogenic forcing. The interaction of aerosols with clouds and radiation introduces feedbacks which can affect the rate of rain formation. Traditionally these feedbacks were not included in estimates of total aerosol forcing. Here we argue that they should be included because these feedbacks act quickly compared with the time scale of global warming. We show that for different forcing agents (aerosols and greenhouse gases) the radiative forcings as traditionally defined agree rather well with estimates from a method, here referred to as radiative flux perturbations (RFP), that takes these fast feedbacks and interactions into account. Thus we propose replacing the direct and indirect aerosol forcing in the IPCC forcing chart with RFP estimates. This implies that it is better to evaluate the total anthropogenic aerosol effect as a whole.

  16. Aerosol-Cloud Interactions in the South-East Atlantic: Knowledge Gaps, Planned Observations to Address Them, and Implications for Global Climate Change Modeling

    NASA Technical Reports Server (NTRS)

    Redemann, Jens; Wood, R.; Zuidema, P.; Haywood, J.; Luna, B.; Abel, S.

    2015-01-01

    Southern Africa produces almost a third of the Earth's biomass burning (BB) aerosol particles, yet the fate of these particles and their influence on regional and global climate is poorly understood. Particles lofted into the mid-troposphere are transported westward over the South-East (SE) Atlantic, home to one of the three permanent subtropical Stratocumulus (Sc) cloud decks in the world. The stratocumulus "climate radiators" are critical to the regional and global climate system. They interact with dense layers of BB aerosols that initially overlay the cloud deck, but later subside and are mixed into the clouds. These interactions include adjustments to aerosol-induced solar heating and microphysical effects. As emphasized in the latest IPCC report, the global representation of these aerosol-cloud interaction processes in climate models is one of the largest uncertainty in estimates of future climate. Hence, new observations over the SE Atlantic have significant implications for global climate change scenarios. We discuss the current knowledge of aerosol and cloud property distributions based on satellite observations and sparse suborbital sampling, and describe planned field campaigns in the region. Specifically, we describe the scientific objectives and implementation of the following four synergistic, international research activities aimed at providing a process-level understanding of aerosol-cloud interactions over the SE Atlantic: 1) ORACLES (Observations of Aerosols above Clouds and their interactions), a five-year investigation between 2015 and 2019 with three Intensive Observation Periods (IOP), recently funded by the NASA Earth-Venture Suborbital Program, 2) CLARIFY-2016 (Cloud-Aerosol-Radiation Interactions and Forcing: Year 2016), a comprehensive observational and modeling programme funded by the UK's Natural Environment Research Council (NERC), and supported by the UK Met Office. 3) LASIC (Layered Atlantic Smoke Interactions with Clouds), a funded

  17. Aerosol-cloud interactions in the South-East Atlantic: knowledge gaps, planned observations to address them, and implications for global climate change modeling

    NASA Astrophysics Data System (ADS)

    Redemann, Jens; Wood, Robert; Zuidema, Paquita; Haywood, James; Luna, Bernadette; Abel, Steven

    2015-04-01

    Southern Africa produces almost a third of the Earth's biomass burning (BB) aerosol particles, yet the fate of these particles and their influence on regional and global climate is poorly understood. Particles lofted into the mid-troposphere are transported westward over the South-East (SE) Atlantic, home to one of the three permanent subtropical Stratocumulus (Sc) cloud decks in the world. The stratocumulus "climate radiators" are critical to the regional and global climate system. They interact with dense layers of BB aerosols that initially overlay the cloud deck, but later subside and are mixed into the clouds. These interactions include adjustments to aerosol-induced solar heating and microphysical effects. As emphasized in the latest IPCC report, the global representation of these aerosol-cloud interaction processes in climate models is one of the largest uncertainty in estimates of future climate. Hence, new observations over the SE Atlantic have significant implications for global climate change scenarios. We discuss the current knowledge of aerosol and cloud property distributions based on satellite observations and sparse suborbital sampling, and describe planned field campaigns in the region. Specifically, we describe the scientific objectives and implementation of the following four synergistic, international research activities aimed at providing a process-level understanding of aerosol-cloud interactions over the SE Atlantic: 1) ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS), a five-year investigation between 2015 and 2019 with three Intensive Observation Periods (IOP), recently funded by the NASA Earth-Venture Suborbital Program, 2) CLARIFY-2016 (CLoud-Aerosol-Radiation Interactions and Forcing: Year 2016), a comprehensive observational and modeling programme funded by the UK's Natural Environment Research Council (NERC), and supported by the UK Met Office. 3) LASIC (Layered Atlantic Smoke Interactions with Clouds), a funded

  18. Integration of prognostic aerosol-cloud interactions in a chemistry transport model coupled offline to a regional climate model

    NASA Astrophysics Data System (ADS)

    Thomas, M. A.; Kahnert, M.; Andersson, C.; Kokkola, H.; Hansson, U.; Jones, C.; Langner, J.; Devasthale, A.

    2015-06-01

    To reduce uncertainties and hence to obtain a better estimate of aerosol (direct and indirect) radiative forcing, next generation climate models aim for a tighter coupling between chemistry transport models and regional climate models and a better representation of aerosol-cloud interactions. In this study, this coupling is done by first forcing the Rossby Center regional climate model (RCA4) with ERA-Interim lateral boundaries and sea surface temperature (SST) using the standard cloud droplet number concentration (CDNC) formulation (hereafter, referred to as the "stand-alone RCA4 version" or "CTRL" simulation). In the stand-alone RCA4 version, CDNCs are constants distinguishing only between land and ocean surface. The meteorology from this simulation is then used to drive the chemistry transport model, Multiple-scale Atmospheric Transport and Chemistry (MATCH), which is coupled online with the aerosol dynamics model, Sectional Aerosol module for Large Scale Applications (SALSA). CDNC fields obtained from MATCH-SALSA are then fed back into a new RCA4 simulation. In this new simulation (referred to as "MOD" simulation), all parameters remain the same as in the first run except for the CDNCs provided by MATCH-SALSA. Simulations are carried out with this model setup for the period 2005-2012 over Europe, and the differences in cloud microphysical properties and radiative fluxes as a result of local CDNC changes and possible model responses are analysed. Our study shows substantial improvements in cloud microphysical properties with the input of the MATCH-SALSA derived 3-D CDNCs compared to the stand-alone RCA4 version. This model setup improves the spatial, seasonal and vertical distribution of CDNCs with a higher concentration observed over central Europe during boreal summer (JJA) and over eastern Europe and Russia during winter (DJF). Realistic cloud droplet radii (CD radii) values have been simulated with the maxima reaching 13 μm, whereas in the stand

  19. Remote sensing of aerosols in the Arctic for an evaluation of global climate model simulations

    PubMed Central

    Glantz, Paul; Bourassa, Adam; Herber, Andreas; Iversen, Trond; Karlsson, Johannes; Kirkevåg, Alf; Maturilli, Marion; Seland, Øyvind; Stebel, Kerstin; Struthers, Hamish; Tesche, Matthias; Thomason, Larry

    2014-01-01

    In this study Moderate Resolution Imaging Spectroradiometer (MODIS) Aqua retrievals of aerosol optical thickness (AOT) at 555 nm are compared to Sun photometer measurements from Svalbard for a period of 9 years. For the 642 daily coincident measurements that were obtained, MODIS AOT generally varies within the predicted uncertainty of the retrieval over ocean (ΔAOT = ±0.03 ± 0.05 · AOT). The results from the remote sensing have been used to examine the accuracy in estimates of aerosol optical properties in the Arctic, generated by global climate models and from in situ measurements at the Zeppelin station, Svalbard. AOT simulated with the Norwegian Earth System Model/Community Atmosphere Model version 4 Oslo global climate model does not reproduce the observed seasonal variability of the Arctic aerosol. The model overestimates clear-sky AOT by nearly a factor of 2 for the background summer season, while tending to underestimate the values in the spring season. Furthermore, large differences in all-sky AOT of up to 1 order of magnitude are found for the Coupled Model Intercomparison Project phase 5 model ensemble for the spring and summer seasons. Large differences between satellite/ground-based remote sensing of AOT and AOT estimated from dry and humidified scattering coefficients are found for the subarctic marine boundary layer in summer. Key Points Remote sensing of AOT is very useful in validation of climate models PMID:25821664

  20. Aerosol, Cloud, and Climate: From Observation to Model (457th Brookhaven Lecture)

    SciTech Connect

    Wang, Jian

    2010-05-12

    In the last 100 years, the Earth has warmed by about 1ºF, glaciers and sea ice have been melting more quickly than previously, especially during the past decade, and the level of the sea has risen about 6-8 inches worldwide. Scientists have long been investigating this phenomenon of “global warming,” which is believed to be at least partly due to the increased carbon dioxide (CO2) concentration in the air from burning fossil fuels. Funded by DOE, teams of researchers from BNL and other national labs have been gathering data in the U.S. and internationally to build computer models of climate and weather to help in understanding general patterns, causes, and perhaps, solutions. Among many findings, researchers observed that atmospheric aerosols, minute particles in the atmosphere, can significantly affect global energy balance and climate. Directly, aerosols scatter and absorb sunlight. Indirectly, increased aerosol concentration can lead to smaller cloud droplets, changing clouds in ways that tend to cool global climate and potentially mask overall warming from man-made CO2.

  1. Aerosol, Cloud, and Climate: From Observation to Model (457th Brookhaven Lecture)

    ScienceCinema

    Wang, Jian [Ph.D., Environmental Sciences Department

    2016-07-12

    In the last 100 years, the Earth has warmed by about 1ºF, glaciers and sea ice have been melting more quickly than previously, especially during the past decade, and the level of the sea has risen about 6-8 inches worldwide. Scientists have long been investigating this phenomenon of “global warming,” which is believed to be at least partly due to the increased carbon dioxide (CO2) concentration in the air from burning fossil fuels. Funded by DOE, teams of researchers from BNL and other national labs have been gathering data in the U.S. and internationally to build computer models of climate and weather to help in understanding general patterns, causes, and perhaps, solutions. Among many findings, researchers observed that atmospheric aerosols, minute particles in the atmosphere, can significantly affect global energy balance and climate. Directly, aerosols scatter and absorb sunlight. Indirectly, increased aerosol concentration can lead to smaller cloud droplets, changing clouds in ways that tend to cool global climate and potentially mask overall warming from man-made CO2.

  2. A GCM investigation of dust aerosol impact on the regional climate of North Africa and South/East Asia

    NASA Astrophysics Data System (ADS)

    Gu, Y.; Xue, Y.; De Sales, F.; Liou, K. N.

    2016-04-01

    The climatic effects of dust aerosols in North Africa and South/East Asia have been investigated using an atmospheric general circulation model, NCEP/GCM/SSiB (Simplified Simple Biosphere Model) and the three-dimensional aerosol data simulated by the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model. GCM simulations show that due to the scattering and absorption of solar radiation by dust particles, surface temperature decreases over both regions, accompanied by a reduced sensible heat flux. However, precipitation responses are different in these two regions. Due to differences in dust location and the associated heating with respect to the rainfall band and circulation, the effect of dust could either enhance or suppress precipitation. Over the North Africa region where dust particles are mainly located to the north of rainfall band, heating of the air column by dust particles forces a stronger ascent motion over dust layers, which induces an anomalous subsidence (or a weakened upward motion) and suppressed cyclonic circulation to its south where precipitation reduces. Furthermore, both humidity and cloud decrease due to the heating in the middle troposphere (semi-direct effect). In South/East Asia, dust particles are located in the upper troposphere over the major rainfall band during the monsoon season, especially Southwest India and the coastal area of Bay of Bengal. Heating of the air column increases upward motion and strengthens cyclonic circulation. Humidity also increases due to the draw-in of the low level moist air. Therefore, cloud and precipitation increase over South/East Asia associated with dust effect. During the pre-monsoon season, when dust particles are located to the north of the monsoon rainfall band, the heating effect results in shifting precipitation northward. The heating of air column due to dust particles, not surface cooling, plays the major role in precipitation changes. The anomalous upward motion over dust regions will

  3. Amplification of ENSO effects on Indian summer monsoon by absorbing aerosols

    NASA Astrophysics Data System (ADS)

    Kim, Maeng-Ki; Lau, William K. M.; Kim, Kyu-Myong; Sang, Jeong; Kim, Yeon-Hee; Lee, Woo-Seop

    2016-04-01

    In this study, we present observational evidence, based on satellite aerosol measurements and MERRA reanalysis data for the period 1979-2011, indicating that absorbing aerosols can have strong influence on seasonal-to-interannual variability of the Indian summer monsoon rainfall, including amplification of ENSO effects. We find a significant correlation between ENSO (El Nino Southern Oscillation) and aerosol loading in April-May, with La Nina (El Nino) conditions favoring increased (decreased) aerosol accumulation over northern India, with maximum aerosol optical depth over the Arabian Sea and Northwestern India, indicative of strong concentration of dust aerosols transported from West Asia and Middle East deserts. Composite analyses based on a normalized aerosol index (NAI) show that high concentration of aerosol over northern India in April-May is associated with increased moisture transport, enhanced dynamically induced warming of the upper troposphere over the Tibetan Plateau, and enhanced rainfall over northern India and the Himalayan foothills during May-June, followed by a subsequent suppressed monsoon rainfall over all India, consistent with the elevated heat pump (EHP) hypothesis (Lau et al. in Clim Dyn 26:855-864, 2006. doi: 10.1007/s00382-006-0114-z). Further analyses from sub-sampling of ENSO years, with normal (<1-σ), and abnormal (>1-σ) NAI over northern India respectively show that the EHP may lead to an amplification of the Indian summer monsoon response to ENSO forcing, particularly with respect to the increased rainfall over the Himalayan foothills, and the warming of the upper troposphere over the Tibetan Plateau. Our results suggest that absorbing aerosol, particular desert dusts can strongly modulate ENSO influence, and possibly play important roles as a feedback agent in climate change in Asian monsoon regions.

  4. Climatic Effects of Regional Nuclear War

    NASA Technical Reports Server (NTRS)

    Oman, Luke D.

    2011-01-01

    We use a modern climate model and new estimates of smoke generated by fires in contemporary cities to calculate the response of the climate system to a regional nuclear war between emerging third world nuclear powers using 100 Hiroshima-size bombs (less than 0.03% of the explosive yield of the current global nuclear arsenal) on cities in the subtropics. We find significant cooling and reductions of precipitation lasting years, which would impact the global food supply. The climate changes are large and longlasting because the fuel loadings in modern cities are quite high and the subtropical solar insolation heats the resulting smoke cloud and lofts it into the high stratosphere, where removal mechanisms are slow. While the climate changes are less dramatic than found in previous "nuclear winter" simulations of a massive nuclear exchange between the superpowers, because less smoke is emitted, the changes seem to be more persistent because of improvements in representing aerosol processes and microphysical/dynamical interactions, including radiative heating effects, in newer global climate system models. The assumptions and calculations that go into these conclusions will be described.

  5. Climate missing links: Aqueous greenhouse species in clouds, fogs and aerosols

    SciTech Connect

    Gaffney, J.S.; Marley, N.A.; Cunningham, M.M.

    1991-11-01

    Recently, there has been considerable interest regarding possible greenhouse effects due to combustion and energy-related pollution. This concern has been due to the release and secondary production of greenhouse gases such as carbon dioxide, freons, methane, nitrous oxide, and ozone. These gases can absorb infrared radiation as it comes back from the heated ground and therefore effectively trap the infrared radiation in the troposphere, leading to climatic change. Beyond these gases, clouds, aerosols, and fogs may also play important roles in affecting, the radiation balance by scattering incoming radiation. This work describes the measurement of water soluble infrared absorbers that are known to be derived from pollution. Polluted precipitation is likely to be an important contributor to radiation balance that is currently being neglected. Pollutants characterized include sulfate, nitrate, formate, acetate, oxalate, phenol, p-nitrophenol, ammonium, carbonate, bicarbonate, formaldehyde (dihydroxy methane), methanol, and ethanol. Band positions and band strengths have been determined. These species show measurable infrared absorption bands in the atmospheric window regions (i.e., 900--1600 cm{sup {minus}1}). These data are discussed with regard to the reported discrepancies in the radiatively important water infrared absorption region commonly referred to as the ``foreign broadened continuum.``

  6. Analysis of Atmospheric Aerosol Data Sets and Application of Radiative Transfer Models to Compute Aerosol Effects

    NASA Technical Reports Server (NTRS)

    Schmid, Beat; Bergstrom, Robert W.; Redemann, Jens

    2002-01-01

    This report is the final report for "Analysis of Atmospheric Aerosol Data Sets and Application of Radiative Transfer Models to Compute Aerosol Effects". It is a bibliographic compilation of 29 peer-reviewed publications (published, in press or submitted) produced under this Cooperative Agreement and 30 first-authored conference presentations. The tasks outlined in the various proposals are listed below with a brief comment as to the research performed. Copies of title/abstract pages of peer-reviewed publications are attached.

  7. Novel insights about salting-effects and reactivity of soluble molecules in aqueous aerosols

    NASA Astrophysics Data System (ADS)

    Volkamer, Rainer

    2014-05-01

    Organic carbon in the atmosphere modifies the lifetime of climate active gases such as O3, and CH4 (oxidative capacity), and forms aerosols that affect Earth's radiation balance. Water soluble organic carbon (WSOC) molecules are well established to form secondary organic aerosol (SOA) in cloud water. However, the chemistry and rate of SOA formation in aqueous aerosol is less well known, and is typically ignored in atmospheric models. Aqueous particles provide a very different chemical environment than clouds, i.e., they are the most concentrated aqueous salt solution that can be found on Earth. As a result of high ionic strength, phase separations of inorganic and organic phases, mass transfer limitations and viscosity effects affect the chemistry in aqueous particles, which proceeds via essentially different reaction pathways than in clouds. Of particular importance in this context is the Henry's law partitioning coefficient. Laboratory experiments show activity coefficients of 1/500 for Henry's law partitioning coefficients of glyoxal in concentrated aqueous aerosol- salt solutions. This salting-in mechanism is investigated in laboratory experiments, and shown to be a major driver in the rate of secondary organic aerosol (SOA) formation from the multiphase chemistry of soluble species like glyoxal. This solicited talk will summarize and discuss new experimental findings from simulation chamber experiments, and bulk reactor experiments to assess the Setschenow salting behavior of soluble molecules in different aqueous seed types, and study the effect of anthropogenic triggers such as sulfate and ammonium for the reactivity of multiphase reactions in the aerosol aqueous phase.

  8. Modeling Study of the Effect of Anthropogenic Aerosols on Late Spring Drought in South China

    SciTech Connect

    Hu, Ning; Liu, Xiaohong

    2013-10-01

    In this study, the mechanisms underlying the decadal variability of late spring precipitation in south China are investigated using the latest version 1 of Community Earth System Model (CESM1). We aim to unravel the effects of different climate forcing agents, such as aerosols and greenhouse gases (GHGs), on the decadal variation of precipitation with transient experiments from pre-industry (for year 1850) to present-day (for year 2000). Our results reveal that: (1) CESM1 can reproduce the climatological features of atmospheric circulation and precipitation for the late spring in south China; (2) Only simulations including the forcing of anthropogenic aerosols can reproduce the observed decreasing trend of late spring precipitation from 1950-2000 in south China; (3) Aerosols affect the decadal change of precipitation mainly by altering the large scale atmospheric circulation, and to a less extent by increasing the lower-tropospheric stability to inhibit the convective precipitation; and (4) In comparison, other climate forcing agents, such as GHGs, have much smaller effects on the decadal change of spring precipitation in south China. Key words: precipitation, aerosols, climate change, south China, Community Earth System Model

  9. Effect of anthropogenic sulfate aerosols on low-level cloud albedo over oceans

    NASA Technical Reports Server (NTRS)

    Kim, Youngseung; Cess, Robert D.

    1993-01-01

    By reducing cloud droplet size, anthropogenic sulfate aerosols are capable of increasing cloud albedo and thus possibly changing the climate. To test the detectability of this effect, we examined satellite-measured low-level cloud albedo off the east coasts of North America and Asia at midlatitudes where anthropogenic sulfate sources are large and aerosols are transported eastward over the oceans by prevailing westerlies. The satellite data demonstrate enhanced cloud albedo near the coastal boundaries where sulfate concentrations are large. Similar trends are absent over ocean regions of the Southern Hemisphere that are removed from anthropogenic sulfate sources.

  10. Exploring the Longwave Radiative Effects of Dust Aerosols

    NASA Technical Reports Server (NTRS)

    Hansell, Richard A., Jr.

    2012-01-01

    Dust aerosols not only affect air quality and visibility where they pose a significant health and safety risk, but they can also play a role in modulating the energy balance of the Earth-atmosphere system by directly interacting with local radiative fields. Consequently, dust aerosols can impact regional climate patterns such as changes in precipitation and the evolution of the hydrological cycle. Assessing the direct effect of dust aerosols at the solar wavelengths is fairly straightforward due in part to the relatively large signal-to-noise ratio in broadband irradiance measurements. The longwave (LW) impacts, on the other hand, are rather difficult to ascertain since the measured dust signal level (10 Wm-2) is on the same order as the instrumental uncertainties. Moreover, compared to the shortwave (SW), limited experimental data on the LW optical properties of dust makes it a difficult challenge for constraining the LW impacts. Owing to the strong absorption features found in many terrestrial minerals (e.g., silicates and clays), the LW effects, although much smaller in magnitude compared to the SW, can still have a sizeable impact on the energetics of the Earth-atmosphere system, which can potentially trigger changes in the heat and moisture surface budgets, and dynamics of the atmosphere. The current endeavor is an integral part of an on-going research study to perform detailed assessments of dust direct aerosol radiative effects (DARE) using comprehensive global datasets from NASA Goddards mobile ground-based facility (cf. http://smartlabs.gsfc.nasa.gov/) during previous field experiments near key dust source regions. Here we examine and compare the results from two of these studies: the 2006 NASA African Monsoon Multidisciplinary Activities and the 2008 Asian Monsoon Years. The former study focused on transported Saharan dust at Sal Island (16.73N, 22.93W), Cape Verde along the west coast of Africa while the latter focused on Asian dust at Zhangye China (39

  11. Impact of Cloud-Borne Aerosol Representation on Aerosol Direct and Indirect Effects

    SciTech Connect

    Ghan, Steven J.; Easter, Richard C.

    2006-09-21

    Aerosol particles attached to cloud droplets are much more likely to be removed from the atmosphere and are much less efficient at scattering sunlight than if unattached. Models used to estimate direct and indirect effects of aerosols employ a variety of representations of such cloud-borne particles. Here we use a global aerosol model with a relatively complete treatment of cloud-borne particles to estimate the sensitivity of simulated aerosol, cloud and radiation fields to various approximations to the representation of cloud-borne particles. We find that neglecting transport of cloud-borne particles introduces little error, but that diagnosing cloud-borne particles produces global mean biases of 20% and local errors of up to 40% for many variables of interest. A treatment that predicts the total mass concentration of cloud-borne particles for each mode yields smaller errors and runs 20% faster than the complete treatment.

  12. A satellite view of the direct effect of aerosols on solar radiation at global scale

    NASA Astrophysics Data System (ADS)

    Hatzianastassiou, Nikolaos; Papadimas, Christos D.; Matsoukas, Christos; Fotiadi, Aggeliki; Benas, Nikolaos; Vardavas, Ilias

    2016-04-01

    Aerosols are a key parameter for better understanding and predicting current and future climate change. They are determining, apart from clouds, patterns of solar radiation through scattering and absorption processes. Especially, under cloud-free skies, aerosols are the major modulator of the solar radiation budget of the Earth-atmosphere system. Although significant improvement has been made as to better understanding the direct radiative effect (DRE) of aerosols, there is still a need for further improvement in our knowledge of the DRE spatial and temporal patterns, in particular with respect to extended spatial and temporal coverage of relevant information. In an ongoing rapidly evolving era of great satellite-based achievements, concerning the knowledge of solar radiation budget and its modulators, and with the great progress in obtaining significant information on key aerosol optical properties needed for modeling DRE, it is a great challenge to use all this new aerosol information and to see what is the new acquired scientific knowledge. The objective of this study is to obtain an improved view of global aerosol DRE effects using contemporary accurate data for the important atmospheric and surface parameters determining the solar radiation budget, with emphasis to state of the art aerosol data. Thus, a synergy is made of different datasets providing the necessary input data and of a detailed spectral radiative transfer model (RTM) to compute spectral globally distributed aerosol DREs. Emphasis is given on using highly accurate and well-tested aerosol optical properties. Spectral information on aerosol optical depth (AOD) is taken from retrieved products of the MODerate resolution Imaging Spectroradiometer (MODIS) instrument, while similar information is taken from MODIS for the aerosol asymmetry parameter (AP) over ocean. Information from MODIS is also taken for the aerosol single scattering albedo (SSA). All this information comes from the latest Collection

  13. Effect of secondary organic aerosol amount and condensational behavior on global aerosol size distributions

    NASA Astrophysics Data System (ADS)

    D'Andrea, S. D.; Häkkinen, S. A. K.; Westervelt, D. M.; Kuang, C.; Spracklen, D. V.; Riipinen, I.; Pierce, J. R.

    2013-05-01

    Recent research has shown that secondary organic aerosols (SOA) are major contributors to ultrafine particle growth to climatically relevant sizes, increasing global cloud condensation nuclei (CCN) concentrations within the continental boundary layer. Many models treat SOA solely as semivolatile, which leads to condensation of SOA proportional to the aerosol mass distribution; however, recent closure studies with field measurements show that a significant fraction of SOA condenses proportional to the aerosol surface area, which suggests a very low volatility. Additionally, while many global models contain only biogenic sources of SOA (with emissions generally 10-30 Tg yr-1), recent studies have shown a need for an additional source of SOA around 100 Tg yr-1 correlated with anthropogenic carbon monoxide (CO) emissions is required to match measurements. Here, we explore the significance of these two findings using the GEOS-Chem-TOMAS global aerosol microphysics model. The percent change in the number of particles of size Dp > 40 nm (N40) within the continental boundary layer between the surface-area-and massdistribution condensation schemes, both with the base biogenic SOA only, yielded a global increase of 8% but exceeds 100% in biogenically active regions. The percent change in N40 within the continental boundary layer between the base simulation (19 Tg yr-1) and the additional SOA (100 Tg yr-1) both using the surface area condensation scheme (very low volatility) yielded a global increase of 14%, and a global decrease in the number of particles of size Dp > 10 nm (N10) of 32%. These model simulations were compared to measured data from Hyytiälä, Finland and other global locations and confirmed a decrease in the model-measurement bias. Thus, treating SOA as very low volatile as well as including additional SOA correlated with anthropogenic CO emissions causes a significant global increase in the number of climatically relevant sized particles, and therefore we

  14. Radiative Effects of Carbonaceous and Inorganic Aerosols over California during CalNex and CARES: Observations versus Model Predictions

    NASA Astrophysics Data System (ADS)

    Vinoj, V.; Fast, J. D.; Liu, Y.

    2012-12-01

    Aerosols have been identified to be a major contributor to the uncertainty in understanding the present climate. Most of this uncertainty arises due to the lack of knowledge of their micro-physical and chemical properties as well as how to adequately represent their spatial and temporal distributions. Increased process level understanding can be achieved through carefully designed field campaigns and experiments. These measurements can be used to elucidate the aerosol properties, mixing, transport and transformation within the atmosphere and also to validate and improve models that include meteorology-aerosol-chemistry interactions. In the present study, the WRF-Chem model is used to simulate the evolution of carbonaceous and inorganic aerosols and their impact on radiation during May and June of 2010 over California when two field campaigns took place: the California Nexus Experiment (CalNex) and Carbonaceous Aerosol and Radiative Effects Study (CARES). We merged CalNex and CARES data along with data from operational networks such as, California Air Resources Board (CARB's) air quality monitoring network, the Interagency Monitoring of Protected Visual Environments (IMPROVE) network, the AErosol RObotic NETwork (AERONET), and satellites into a common dataset for the Aerosol Modeling Test bed. The resulting combined dataset is used to rigorously evaluate the model simulation of aerosol mass, size distribution, composition, and optical properties needed to understand uncertainties that could affect regional variations in aerosol radiative forcing. The model reproduced many of the diurnal, multi-day, and spatial variations of aerosols as seen in the measurements. However, regionally the performance varied with reasonably good agreement with observations around Los Angeles and Sacramento and poor agreement with observations in the vicinity of Bakersfield (although predictions aloft were much better). Some aerosol species (sulfate and nitrate) were better represented

  15. Aerosol indirect effects -- general circulation model intercomparison and evaluation with satellite data

    SciTech Connect

    Quaas, Johannes; Ming, Yi; Menon, Surabi; Takemura, Toshihiko; Wang, Minghuai; Penner, Joyce E.; Gettelman, Andrew; Lohmann, Ulrike; Bellouin, Nicolas; Boucher, Olivier; Sayer, Andrew M.; Thomas, Gareth E.; McComiskey, Allison; Feingold, Graham; Hoose, Corinna; Kristjansson, Jon Egill; Liu, Xiaohong; Balkanski, Yves; Donner, Leo J.; Ginoux, Paul A.; Stier, Philip; Feichter, Johann; Sednev, Igor; Bauer, Susanne E.; Koch, Dorothy; Grainger, Roy G.; Kirkevag, Alf; Iversen, Trond; Seland, Oyvind; Easter, Richard; Ghan, Steven J.; Rasch, Philip J.; Morrison, Hugh; Lamarque, Jean-Francois; Iacono, Michael J.; Kinne, Stefan; Schulz, Michael

    2009-04-10

    Aerosol indirect effects continue to constitute one of the most important uncertainties for anthropogenic climate perturbations. Within the international AEROCOM initiative, the representation of aerosol-cloud-radiation interactions in ten different general circulation models (GCMs) is evaluated using three satellite datasets. The focus is on stratiform liquid water clouds since most GCMs do not include ice nucleation effects, and none of the model explicitly parameterizes aerosol effects on convective clouds. We compute statistical relationships between aerosol optical depth (Ta) and various cloud and radiation quantities in a manner that is consistent between the models and the satellite data. It is found that the model-simulated influence of aerosols on cloud droplet number concentration (Nd) compares relatively well to the satellite data at least over the ocean. The relationship between Ta and liquid water path is simulated much too strongly by the models. It is shown that this is partly related to the representation of the second aerosol indirect effect in terms of autoconversion. A positive relationship between total cloud fraction (fcld) and Ta as found in the satellite data is simulated by the majority of the models, albeit less strongly than that in the satellite data in most of them. In a discussion of the hypotheses proposed in the literature to explain the satellite-derived strong fcld - Ta relationship, our results indicate that none can be identified as unique explanation. Relationships similar to the ones found in satellite data between Ta and cloud top temperature or outgoing long-wave radiation (OLR) are simulated by only a few GCMs. The GCMs that simulate a negative OLR - Ta relationship show a strong positive correlation between Ta and fcld The short-wave total aerosol radiative forcing as simulated by the GCMs is strongly influenced by the simulated anthropogenic fraction of Ta, and parameterisation assumptions such as a lower bound on Nd

  16. Modeling Trends in Tropospheric Aerosol Burden & Its Radiative Effects

    EPA Science Inventory

    Large changes in emissions of aerosol precursors have occurred across the southeast U.S., North America, as well as the northern hemisphere. The spatial heterogeneity and contrasting trends in the aerosol burden is resulting in differing effects on regional radiative balance. Mul...

  17. EFFECT OF ACIDITY ON SECONDARY ORGANIC AEROSOL FORMATION FROM ISOPRENE

    EPA Science Inventory

    The effect of particle-phase acidity on secondary organic aerosol (SOA) formation from isoprene is investigated in a laboratory chamber study, in which the acidity of the inorganic seed aerosol was controlled systematically. The observed enhancement in SOA mass concentration is c...

  18. SILAM and MACC reanalysis aerosol data used for simulating the aerosol direct radiative effect with the NWP model HARMONIE for summer 2010 wildfire case in Russia

    NASA Astrophysics Data System (ADS)

    Toll, V.; Reis, K.; Ots, R.; Kaasik, M.; Männik, A.; Prank, M.; Sofiev, M.

    2015-11-01

    Persistent high pressure conditions over the European part of Russia during summer 2010 were responsible for an extended period of hot and dry weather, creating favourable conditions for severe wildfires. The chemical transport model SILAM is used to simulate the dispersion of smoke aerosol for this case. Aerosol fields from SILAM are compared to the Monitoring Atmospheric Composition and Climate (MACC) reanalysis. Moreover, the model output is compared to in situ and remote sensing measurements, paying particular attention to the most intense fire period of August 7 to 9, when the plume reached the Baltic countries and Finland. The maximum observed aerosol optical depth was more than 4 at 550 nm during this time. The aerosol distributions from the SILAM run and the MACC reanalysis are subsequently used in meteorological simulations using the Hirlam Aladin Research for Mesoscale Operational Numerical Weather Prediction in Euromed (HARMONIE) model. The modelling results show a significant reduction of the daily average shortwave radiation fluxes at the surface (up to 125 W/m2) and daily average near-surface temperature (up to 4 °C) through the aerosol direct radiative effect. The simulated near-surface temperature and vertical temperature profile agree better with the observations, when the aerosol direct radiative effect is considered in the meteorological simulation. The boundary layer is more stably stratified, creating poorer dispersion conditions for the smoke.

  19. Interannual variabilities in tropospheric constituents during 2000-2013 simulated in a chemistry-aerosol coupled climate model

    NASA Astrophysics Data System (ADS)

    Sudo, K.; Ito, A.

    2014-12-01

    Global distributions and abundances of tropospheric constituents (O3, CH4, NOy, CO, VOCs, NHx, SOx and aerosols) interannually change under the influences of meteorology (transport, temperature, water vapor, clouds, rain, etc.) and emissions from anthropogenic/natural sources and biomass burning. Given the importance of climate effects of these species as short-lived climate pollutants (SLCPs), there have been increasing number of studies to project future changes in individual constituents and assess impacts of emission reduction in future. Since chemistry climate model is basically used for such purpose, model validation against the observations and precise interpretation/understanding of changing processes in a model are essentially needed. In this study, we investigate interannual variability of tropospheric constituents during the years 2000 to 2013 in a chemistry-aerosol coupled climate model. The base chemical model used in this study is CHASER (Sudo et al., 2002, 2007) coupled with the aerosol model SPRINTARS (Takemura et al., 2006). The CHASER model, also developed in the framework of the MIROC earth system model (MIROC-ESM-CHEM), simulates detailed chemistry in the troposphere and stratosphere with an on-line aerosol simulation including production of particulate nitrate and SOA. We use the NCEP reanalysis data (FNL) for constraining the model's meteorology. Anthropogenic and biomass burning emissions are specified using the HTAP2 and MAC inventories, respectively. For biogenic VOCs emissions, we employ calculation by the land ecosystem/trace gas emission model VISIT (Ito et al., 2008). Our results show that temporal variability (anomaly) in surface and lower tropospheric ozone very clearly correlates with that in CO especially in NH, indicating principal importance of biomass burning emission in determining near-surface O3 variability; surface PM (PM2.5) in NH also coincides with CO. Changes in middle to upper tropospheric O3, on the other hand

  20. Simulating Changes in Tropospheric Aerosol Burden and its Radiative Effects across the Northern Hemisphere: Contrasting Multi-Decadal Trends between Asia and North America

    EPA Science Inventory

    Though aerosol radiative effects have been recognized as some of the largest sources of uncertainty among the forcers of climate change, the verification of the spatial and temporal variability of the magnitude and directionality of aerosol radiative forcing has remained challeng...

  1. Unexpected Benefits of Reducing Aerosol Cooling Effects

    EPA Science Inventory

    Impacts of aerosol cooling are not limited to changes in surface temperature since modulation of atmospheric dynamics resulting from the increased stability can deteriorate local air quality and impact human health. Health impacts from two manifestations of the aerosol direct eff...

  2. Evaluation of cloud microphysical schemes on aerosol indirect effects from different scale models

    NASA Astrophysics Data System (ADS)

    Shiu, C. J.; Chen, Y. H.; Hashino, T.; Tsai, I. C.; Chen, W. T.; Chen, J. P.; Hsu, H. H.

    2014-12-01

    Quantification of aerosol indirect effects in climate modeling remain unresolved and of large uncertainties. The complicated aerosol-cloud-precipitation interactions in climate model are suggested to be quite sensitive to some tunable microphysical parameters such as the threshold radius associated with autoconversion of cloud droplets to rain droplets. More fundamental studies regarding to different microphysical processes used in various cloud microphysical schemes should be devoted, evaluated and investigated. In this study, we apply a synergy of different scale models with the same cloud and aerosol microphysical schemes (Chen and Liu, 2004; Cheng et al., 2007; and Chen et al., 2013) to understand and evaluate how cloud microphysical processes can be influenced by different microphysical schemes and their interaction with aerosols and radiation. These models include Kinematic Driver (KiD), Single Column Model of Community Atmosphere Model (SCAM), Large Eddy Simulation (LES), and NCAR CESM model. Simulation results from these models will be further validated and compared to either field campaign or satellite observations depending on the scale of the models. Off-line satellite simulator approach (i.e. Joint-Simulator) will also be applied for evaluating cloud microphysics against CloudSat and CALIPSO. Such type of synergy of models can be very useful for improvement, development and evaluation of physical parameterizations for global climate prediction and weather forecast in the near future especially for processes related to cloud macrophysics and microphysics.

  3. Direct radiative effect by multicomponent aerosol over China

    SciTech Connect

    Huang, Xin; Song, Yu; Zhao, Chun; Cai, Xuhui; Zhang, Hongsheng; Zhu, Tong

    2015-05-01

    The direct radiative effect (DRE) of multiple aerosol species (sulfate, nitrate, ammonium, black carbon (BC), organic carbon (OC), and mineral aerosol) and their spatiotemporal variations over China were investigated using a fully coupled meteorology–chemistry model (WRF-Chem) for the entire year of 2006. We made modifications to improve model performance, including updating land surface parameters, improving the calculation of transition metal-catalyzed oxidation of SO2, and adding in heterogeneous reactions between mineral aerosol and acid gases. The modified model well reproduced the magnitude, seasonal pattern, and spatial distribution of the measured meteorological conditions, concentrations of PM10 and its components, and aerosol optical depth (AOD). A diagnostic iteration method was used to estimate the overall DRE of aerosols and contributions from different components. At the land surface, all kinds of aerosol species reduced the incident net radiation flux with a total DRE of 10.2 W m-2 over China. Aerosols significantly warm the atmosphere with the national mean DRE of +10.8 W m-2. BC was the leading radiative-heating component (+8.7 W m-2), followed by mineral aerosol (+1.1 W m-2). At the top of the atmosphere (TOA), BC introduced the largest radiative perturbation (+4.5 W m-2), followed by sulfate (-1.4 W m-2). The overall perturbation of aerosols on radiation transfer is quite small over China, demonstrating the counterbalancing effect between scattering and adsorbing aerosols. Aerosol DRE at the TOA had distinct seasonality, generally with a summer maximum and winter minimum, mainly determined by mass loadings, hygroscopic growth, and incident radiation flux.

  4. Aerosol composition and sources during the Chinese Spring Festival: fireworks, secondary aerosol, and holiday effects

    NASA Astrophysics Data System (ADS)

    Jiang, Q.; Sun, Y. L.; Wang, Z.; Yin, Y.

    2015-06-01

    Aerosol particles were characterized by an Aerodyne aerosol chemical speciation monitor along with various collocated instruments in Beijing, China, to investigate the role of fireworks (FW) and secondary aerosol in particulate pollution during the Chinese Spring Festival of 2013. Three FW events, exerting significant and short-term impacts on fine particles (PM2.5), were observed on the days of Lunar New Year, Lunar Fifth Day, and Lantern Festival. The FW were shown to have a large impact on non-refractory potassium, chloride, sulfate, and organics in submicron aerosol (PM1), of which FW organics appeared to be emitted mainly in secondary, with its mass spectrum resembling that of secondary organic aerosol (SOA). Pollution events (PEs) and clean periods (CPs) alternated routinely throughout the study. Secondary particulate matter (SPM = SOA + sulfate + nitrate + ammonium) dominated the total PM1 mass on average, accounting for 63-82% during nine PEs in this study. The elevated contributions of secondary species during PEs resulted in a higher mass extinction efficiency of PM1 (6.4 m2 g-1) than during CPs (4.4 m2 g-1). The Chinese Spring Festival also provides a unique opportunity to study the impact of reduced anthropogenic emissions on aerosol chemistry in the city. Primary species showed ubiquitous reductions during the holiday period with the largest reduction being in cooking organic aerosol (OA; 69%), in nitrogen monoxide (54%), and in coal combustion OA (28%). Secondary sulfate, however, remained only slightly changed, and the SOA and the total PM2.5 even slightly increased. Our results have significant implications for controlling local primary source emissions during PEs, e.g., cooking and traffic activities. Controlling these factors might have a limited effect on improving air quality in the megacity of Beijing, due to the dominance of SPM from regional transport in aerosol particle composition.

  5. Quantifying the temperature-independent effect of stratospheric aerosol geoengineering on global-mean precipitation in a multi-model ensemble

    NASA Astrophysics Data System (ADS)

    Ferraro, Angus J.; Griffiths, Hannah G.

    2016-03-01

    The reduction in global-mean precipitation when stratospheric aerosol geoengineering is used to counterbalance global warming from increasing carbon dioxide (CO2) concentrations has been mainly attributed to the temperature-independent effect of CO2 on atmospheric radiative cooling. We demonstrate here that stratospheric sulphate aerosol itself also acts to reduce global-mean precipitation independent of its effects on temperature. The temperature-independent effect of stratospheric aerosol geoenginering on global-mean precipitation is calculated by removing temperature-dependent effects from climate model simulations of the Geoengineering Model Intercomparison Project (GeoMIP). When sulphate aerosol is injected into the stratosphere at a rate of 5 Tg SO2 per year the aerosol reduces global-mean precipitation by approximately 0.2 %, though multiple ensemble members are required to separate this effect from internal variability. For comparison, the precipitation reduction from the temperature-independent effect of increasing CO2 concentrations under the RCP4.5 scenario of the future is approximately 0.5 %. The temperature-independent effect of stratospheric sulphate aerosol arises from the aerosol’s effect on tropospheric radiative cooling. Radiative transfer calculations show this is mainly due to increasing downward emission of infrared radiation by the aerosol, but there is also a contribution from the stratospheric warming the aerosol causes. Our results suggest climate model simulations of solar dimming can capture the main features of the global-mean precipitation response to stratospheric aerosol geoengineering.

  6. Final Report for Cloud-Aerosol Physics in Super-Parameterized Atmospheric Regional Climate Simulations (CAP-SPARCS)(DE-SC0002003) for 8/15/2009 through 8/14/2012

    SciTech Connect

    Russell, Lynn M; Somerville, Richard C.J.

    2012-11-05

    Improving the representation of local and non-local aerosol interactions in state-of-the-science regional climate models is a priority for the coming decade (Zhang, 2008). With this aim in mind, we have combined two new technologies that have a useful synergy: (1) an aerosol-enabled regional climate model (Advanced Weather Research and Forecasting Model with Chemistry WRF-Chem), whose primary weakness is a lack of high quality boundary conditions and (2) an aerosol-enabled multiscale modeling framework (PNNL Multiscale Aerosol Climate Model (MACM)), which is global but captures aerosol-convection-cloud feedbacks, and thus an ideal source of boundary conditions. Combining these two approaches has resulted in an aerosol-enabled modeling framework that not only resolves high resolution details in a particular region, but crucially does so within a global context that is similarly faithful to multi-scale aerosol-climate interactions. We have applied and improved the representation of aerosol interactions by evaluating model performance over multiple domains, with (1) an extensive evaluation of mid-continent precipitation representation by multiscale modeling, (2) two focused comparisons to transport of aerosol plumes to the eastern United States for comparison with observations made as part of the International Consortium for Atmospheric Research on Transport and Transformation (ICARTT), with the first being idealized and the second being linked to an extensive wildfire plume, and (3) the extension of these ideas to the development of a new approach to evaluating aerosol indirect effects with limited-duration model runs by nudging to observations. This research supported the work of one postdoc (Zhan Zhao) for two years and contributed to the training and research of two graduate students. Four peer-reviewed publications have resulted from this work, and ground work for a follow-on project was completed.

  7. Tropospheric Aerosols

    NASA Astrophysics Data System (ADS)

    Buseck, P. R.; Schwartz, S. E.

    2003-12-01

    It is widely believed that "On a clear day you can see forever," as proclaimed in the 1965 Broadway musical of the same name. While an admittedly beautiful thought, we all know that this concept is only figurative. Aside from Earth's curvature and Rayleigh scattering by air molecules, aerosols - colloidal suspensions of solid or liquid particles in a gas - limit our vision. Even on the clearest day, there are billions of aerosol particles per cubic meter of air.Atmospheric aerosols are commonly referred to as smoke, dust, haze, and smog, terms that are loosely reflect